JP4466298B2 - Aqueous resin composition and paint using the same - Google Patents

Description

  The present invention relates to an aqueous resin composition useful for a paint or an adhesive, and a paint using the same.

  Since a large amount of organic solvent is usually used for the paint, the organic solvent is discharged into the atmosphere during painting. These organic solvents cause air pollution, and there is a high risk that these organic solvents cause a fire. In recent years, various efforts have been made to reduce the amount of organic solvent, and high solid paints, powder paints, electron beam / ultraviolet curable paints, water-based paints, and the like have been developed for that purpose. In particular, water-based paints are attracting attention because they use water that is not dangerous and that is highly economical, and that they can be easily converted from conventional coating equipment. However, the conventional water-based paint has a problem that the paint is dried slowly and water resistance and corrosion resistance are inferior.

In order to solve these problems, for example, in a water-based alkyd resin coating, a polymerizable monomer is added in the presence of a method in which a resin component contains a phenol resin, a petroleum resin, an epoxy resin, or a radical polymerization initiator. Attempts have been made to polymerize.
As such an improved resin, there is a water-dilutable vinyl-modified epoxy ester resin obtained by polymerizing a vinyl monomer in the presence of a bisphenol-type epoxy resin and a fatty acid ester. However, paints using this water-dilutable vinyl-modified epoxy ester resin have good water resistance, but have the disadvantages of poor corrosion resistance, poor paint stability, and slow drying (for example, Patent Document 1 and (See Patent Document 2). In addition, an anionic or nonionic emulsifier is used to improve paint stability and water reducibility, but the emulsifier tends to localize on the surface, resulting in a decrease in water resistance (for example, patent documents). 3). There are also paints that use resins obtained by reacting epoxy esters with polybasic acids or their acid anhydrides and then acrylic modification, but these paints are excellent in corrosion resistance but poor in paint stability and drying. (For example, refer to Patent Document 4).
However, recently, there has been an increasing demand for water-based coatings, and there has been an increasing demand for paints having a quick drying property that can be applied even with current solvent type lines. However, if the epoxy resin of the vinyl-modified epoxy resin is increased in molecular weight and Tg is increased to increase the drying property, the flexibility of the coating film is lost and the adhesion to the substrate is decreased, and the corrosion resistance and water resistance are decreased. Moreover, the problem that it becomes difficult to form a film arises.
Furthermore, the water-dispersed acrylic-modified epoxy resin, which is water-modified by modifying amine with epoxy resin and reacting with acrylic, can improve the drying property without reducing the corrosion resistance and water resistance, but the drying property is insufficient. there were. Moreover, although introduction | transduction with an oxazoline group or bridge | crosslinking with an oxazoline group containing aqueous polymer is also possible, the curing temperature needs to be 80 degreeC or more, and the amine which is a neutralizing agent must be made into a highly volatile amine. Although the drying property is improved by blending the acrylic emulsion, there is a problem in the deterioration of the corrosion resistance and the resin stability.

Furthermore, a composition comprising an anionically stabilized emulsion polymer, a polyfunctional amine polymer, and a volatile base has been proposed (see, for example, Patent Document 5). In this composition, the polyfunctional amine is deprotonated from the volatilization of the volatile base, becomes a cationic resin, and the emulsion polymer that has been stabilized in an anionic state becomes unstable, thereby improving the drying property. However, there was a problem in water resistance due to the inclusion of the polyfunctional amine polymer. Moreover, since it was an acrylic emulsion polymer, there was also a problem in corrosion resistance.
As described above, there are still no paints that can be used in the current solvent line, and that have a fast drying property and excellent flexibility, water resistance, corrosion resistance, chemical resistance, and corrosion resistance.
Japanese Patent Publication No. 51-11128 Japanese Examined Patent Publication No. 4-6726 JP 54-30249 A Japanese Patent No. 3000487 Japanese Patent Laid-Open No. 3-157463

  An object of the present invention is to solve these problems, and a specific epoxy ester-modified acrylic emulsion obtained by graft emulsion copolymerization of an epoxy ester resin and an ethylenically unsaturated copolymerization monomer and an amine functional group-containing aqueous resin. Use of the water-based resin composition having excellent flexibility, water resistance, corrosion resistance, chemical resistance, water-based paint composition and excellent drying properties comparable to the solvent system, and this composition It can be used for anti-corrosion paints that require the above characteristics, traffic paints, and the like.

That is, this invention mix | blends the polymeric vinyl monomer mixture containing ethylenically unsaturated carboxylic acid in presence of water and an epoxy ester resin, and uses the reactive emulsifier which has an ethylenically unsaturated group as an emulsifier. The present invention relates to an aqueous resin composition comprising an epoxy ester-modified vinyl polymer emulsion obtained by emulsion polymerization and addition of an amine, and (B) an amine functional group-containing aqueous resin.
Further, the present invention provides an epoxy ester resin having an acid value of 30 or less obtained by addition condensation of 30 to 70% by weight of a fatty acid and 70 to 30% by weight of an epoxy resin, with the total amount of fatty acid and epoxy resin being 100% by weight. It is related with said aqueous resin composition which is an epoxy ester resin.
The present invention also relates to the above aqueous resin composition, wherein the epoxy ester-modified vinyl polymer emulsion is adjusted to pH 8 to 12 by adding an amine.
Moreover, this invention mix | blends 95-40 weight% of polymerizable vinyl monomer mixtures containing ethylenically unsaturated carboxylic acid in presence of (A) water and epoxy ester resin 5-60 weight%, and is ethylenic as an emulsifier. It contains an epoxy ester-modified vinyl polymer emulsion having an acid value of 10 to 50 obtained by emulsion polymerization using a reactive emulsifier having an unsaturated group and adding an amine, and (B) an amine functional group-containing aqueous resin. The above-mentioned aqueous resin composition.
Moreover, this invention relates to the coating material containing said aqueous resin composition.

  The aqueous resin composition and coating composition of the present invention are excellent in water resistance of the coating film and remarkably excellent in corrosion resistance and drying property.

  The epoxy ester resin used in the present invention is obtained by adding and condensing a fatty acid and an epoxy resin. This addition and condensation reaction can be performed according to a known method. As the fatty acids used in the present invention, fatty acids having an ethylenically unsaturated double bond are usually preferred. For example, fatty acids derived from dry oil or semi-dry oil and synthetic fatty acids are used. Examples thereof include fatty acids obtained from tung oil, soybean oil, linseed oil, castor oil, dehydrated castor oil, safflower oil, cottonseed oil, and the like, and versatic acid obtained by synthesis (trade name, manufactured by Shell Chemical Co., Ltd.). Although it is preferable to use a fatty acid derived from a drying oil or a semi-drying oil because it can provide room temperature curability, a fatty acid that can be derived from a non-drying oil may be used. These fatty acids are used alone or in combination of two or more. The double bond of fatty acid has oxidative polymerizability by a dryer or the like, and also serves as a grafting point when the vinyl polymer is modified.

  The epoxy resin used in the present invention is not particularly limited as long as it has two or more epoxy groups in one molecule. For example, aromatic epoxy resins such as bisphenol A type or F type epoxy resins are used. Yes, for example, Epicoat 828, Epicoat 1001, Epicoat 1004, Epicoat 1007, Epicoat 1009 (all are trade names of Japan Epoxy Resin), Epomic R140, (trade names of Mitsui Chemicals), YD-011, YD-014, YD -017, YD-019, and the like. In addition, an aliphatic epoxy compound having a glycidyl group can also be used, for example, an alkylene glycol such as ethylene glycol or propylene glycol, a fat such as polyethylene glycol, polypropylene glycol, tetremethylene glycol, neopentyl glycol, or 1,6-hexanediol. Polyglycidyl ethers of aliphatic polyol compounds such as di- or triglycidyl ethers of aliphatic triol compounds such as diglycidyl ether, trimethylolpropane and glycerin of aromatic diol compounds, pentaerythritol, sorbitol, glycerin dimer and multimers, and adipine And diglycidyl esters of aliphatic dibasic acids such as acids and tetramethylene dicarboxylic acids. 100-1000 are preferable and, as for the epoxy equivalent of an epoxy resin, 150-500 are more preferable. One or more of these epoxy resins are used.

  In order to further introduce an ethylenic double bond capable of reacting with the polymerizable vinyl monomer mixture into the epoxy ester resin, an unsaturated polybasic acid such as an unsaturated dibasic acid having an ethylenically unsaturated double bond or a derivative thereof is used. It may be used. Examples thereof include fumaric acid, maleic acid, itaconic acid, citraconic acid, lower alkyl esters thereof (for example, alkyl esters having an alkyl group having 1 to 4 carbon atoms), acid anhydrides thereof, and the like. .

  The use amount of the unsaturated polybasic acid having an ethylenically unsaturated double bond or a derivative thereof is 10 parts by weight or less, for example, 0.1 to 10 weights with respect to 100 parts by weight of the total amount of all acid components and epoxy resin components. Parts, preferably 7 parts by weight or less, for example 1 to 7 parts by weight, and more preferably 5 parts by weight or less. When the amount exceeds 10 parts by weight, the polymerizable vinyl monomer is excessively grafted to the resin, so that the coating film performance tends to deteriorate.

  The blending ratio of the fatty acid and the epoxy resin used in the epoxy ester resin is preferably 30 to 70% by weight, preferably 40 to 60% by weight, with the total amount of the fatty acid and the epoxy resin being 100% by weight, from the viewpoint of drying and corrosion resistance. % Is more preferable, and the epoxy resin is preferably 70 to 30% by weight, more preferably 60 to 40% by weight. Moreover, 30 or less are preferable from the point of water resistance, and, as for the acid value of the epoxy ester resin obtained, 10-25 are more preferable.

  The epoxy ester resin is obtained by reacting the epoxy resin with a fatty acid and an unsaturated polybasic acid used as necessary, and the reaction method is an addition or condensation reaction by a known method. For example, what is necessary is just to heat the mixture of an epoxy resin, a fatty acid, and the unsaturated polybasic acid used as needed at 130-250 degreeC for 5 to 10 hours. This reaction may be performed in an organic solvent such as xylene and toluene. The reaction of the epoxy resin with the fatty acid and the unsaturated polybasic acid used as necessary may be carried out at the same time, or after reacting a part of the epoxy resin with the acid component and reacting with another acid component. Also good. For example, after reacting an epoxy resin and a fatty acid, an unsaturated polybasic acid may be added and reacted.

  A polymerizable vinyl monomer mixture is blended in the presence of water and an epoxy ester resin, and emulsion polymerization is performed using an emulsifier. The emulsifier used for emulsion polymerization in the present invention is a reactive emulsifier having an ethylenically unsaturated group from the viewpoint of water resistance and corrosion resistance. As such an emulsifier, for example, Antox MS60 (manufactured by Nippon Emulsifier), Adekaria soap SE10N (manufactured by Asahi Denka Kogyo), Eleminol JS2, Eleminol RS30 (manufactured by Sanyo Chemical), HS10, 20, 1025 (Daiichi Kogyo Kagaku) Anionic reactive emulsifiers having an ethylenically unsaturated group such as Adekaria Soap NE10,20,30, 40 (Asahi Denka Kogyo), RN10,20 (Daiichi Kogyo Kagaku) etc. There is an emulsifier. These reactive emulsifiers can be used alone or in combination of two or more. Moreover, it can also be used in combination with the normal emulsifier which does not have an ethylenically unsaturated group as needed. A smaller amount of these reactive emulsifiers is preferable from the viewpoint of water resistance and corrosion resistance, and 0.5 to 5% by weight (active ingredient) is appropriate for the resin solid content of the epoxy ester-modified vinyl polymer emulsion. is there.

The polymerizable vinyl monomer mixture used in the present invention contains an ethylenically unsaturated carboxylic acid as an essential component. Examples of the ethylenically unsaturated carboxylic acid include α, β-monoethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, maleic acid, maleic anhydride, fumaric acid, crotonic acid, and itaconic acid. The ethylenically unsaturated carboxylic acid is preferably blended so that the acid value of the resin solid content of the epoxy ester-modified vinyl polymer emulsion is 10 to 60, more preferably 20 to 50. Here, when the acid value is less than 10, the stability of the paint may be insufficient, and when it exceeds 60, the water resistance and corrosion resistance of the coating film may be inferior. Further, examples of the polymerizable vinyl monomer other than the ethylenically unsaturated carboxylic acid used in the present invention include methacrylic acid or acrylic acid ester, α, β-monoethylenically unsaturated carboxylic acid hydroxyalkyl ester, and the like.
For example, methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, tert-butyl acrylate, isobutyl acrylate, 2-ethylhexyl acrylate, etc. Examples include methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, tert-butyl methacrylate, isobutyl methacrylate, 2-ethylhexyl methacrylate, and the like. Examples of the ester include 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, and the like. Also, styrene, vinyl toluene, α-methyl styrene, vinyl acetate, glycidyl acrylate, glycidyl methacrylate, acrylamide, methacrylamide, N, N-diethylacrylamide, N, N-diethylmethacrylamide, acrylonitrile, methacrylonitrile, polyethylene Glycol monoacrylate or methacrylate phosphates can also be used. These are appropriately selected according to the required characteristics, and are used alone or in combination of two or more.

  The amount of the epoxy ester resin used in the production of the epoxy ester-modified vinyl polymer emulsion is 5 to 60% by weight (the polymerizable vinyl monomer mixture) when the total amount of the epoxy ester resin and the polymerizable vinyl monomer mixture is 100% by weight. 95 to 40% by weight), and more preferably 10 to 60% by weight. When the amount of the epoxy ester resin is less than 5% by weight, the room temperature curability and the corrosion resistance may be inferior, and when it exceeds 60% by weight, the stability during the emulsion polymerization may be inferior. The epoxy ester-modified acrylic emulsion can be produced by a known emulsion polymerization. It is also useful to perform emulsion polymerization after forcibly dispersing an epoxy ester resin containing an emulsifier in water with a homogenizer or the like. Chain transfer agents such as carbon tetrachloride and mercaptans can also be used for molecular weight control. In addition, free radical initiators such as ammonium persulfate, hydrogen peroxide, t-butyl hydroperoxide and / or alkali metal salts can be used. The amount used is preferably 0.05 to 30 parts by weight with respect to 100 parts by weight of the total monomers.

The amount of water used for the emulsion polymerization is preferably 50 to 500 parts by weight, and more preferably 100 to 300 parts by weight with respect to 100 parts by weight of the total monomers. The emulsion polymerization is preferably performed at 10 to 90 ° C. for 30 minutes to 5 hours.
Moreover, it is preferable to perform the synthesis and emulsion polymerization of the epoxy ester resin in an inert atmosphere such as nitrogen gas.

The emulsion after the emulsion polymerization is neutralized with an amine such as ammonia, triethylamine, dimethylaminoethanol, etc. to obtain a stable emulsion resin. The amount of amine used is preferably more than the amount that neutralizes the amount of carboxyl groups in the emulsion before neutralization, and is preferably 2.5 to 6 equivalents, and 3 to 5 equivalents relative to 1 equivalent of carboxyl groups. Is more preferable. The pH of the epoxy ester-modified vinyl polymer emulsion obtained by neutralization is preferably 8 to 12, and more preferably 10 to 11.
By performing emulsion polymerization using water without using an organic solvent, there is an effect of reducing the amount of the organic solvent.

  The epoxy ester-modified vinyl polymer emulsion thus obtained can be used in combination with water and an organic solvent such as butyl cellosolve, ethyl cellosolve, isopropyl cellosolve, 3-methyl-3-methoxybutanol, isopropanol and butanol. .

As the amine functional group-containing aqueous resin used in the present invention, a polymer containing a monomer having a tertiary amino group is used. In the present specification, the aqueous resin is a resin using water as a medium, and may be either water-soluble or water-dispersible resin. The amine functional group-containing aqueous resin can be obtained by solution polymerization in a neutral, alkaline, or acidic aqueous medium. The amount of the amino group-containing monomer of the amino functional group-containing aqueous resin is preferably 40% by weight or more, and can be used alone or copolymerized with other vinyl monomers. When another vinyl monomer is used in combination, the amino group-containing monomer amount is preferably 40 to 100 parts by weight, and more preferably 60 to 100 parts by weight with respect to 100 parts by weight of the vinyl monomer.
The amino group-containing monomer used in the amine functional group-containing aqueous resin is, for example, an ethylenically unsaturated monomer such as an amide of ethylenically unsaturated carboxylic acid such as acrylic acid or methacrylic acid, maleic acid, crotonic acid, fumaric acid or itaconic acid. Saturated dicarboxylic acid half amides, α, β-unsaturated carboxylic acid dialkylaminoalkyl esters, alkylaminoalkyl esters, aminoalkyl esters, aminoalkoxyalkyl esters and the like are preferred.

  Dialkylaminoalkyl ester, alkylaminoalkyl ester, aminoalkyl ester, aminoalkoxyalkyl ester of α, β-unsaturated carboxylic acid include dimethylaminoethyl (meth) acrylate, β-aminoethyl (meth) acrylate, t-butyl Aminoethyl (meth) acrylate, dipropylaminoethyl (meth) acrylate, methylaminoethyl (meth) acrylate, N-methyl-N-hydroxyethylaminoethyl (meth) acrylate, N- (mono-n-butyl) aminoethyl (Meth) acrylate, methacryloxyethoxyethylamine, and the like, and various mixtures thereof. Most preferred is dimethylaminoethyl (meth) acrylate.

  The synthesis of the amine functional group-containing aqueous resin is performed by solution polymerization of the above-described amine group-containing monomer in a neutral, alkaline or acidic aqueous medium. Examples of the radical initiator that can be used in the present invention include persulfates such as potassium persulfate and ammonium persulfate, hydrogen peroxide, t-butyl hydroperoxide, benzoyl peroxide, cumene hydroperoxide, dibutyl peroxide, diisopropyl peroxide. Examples include oil-soluble types such as oxydicarbonate and azobisisobutyronitrile. Furthermore, if necessary, a redox system in which a reducing agent such as acidic sodium sulfite, Rongalite, L-ascorbic acid, and ferrous sulfate is used in combination can also be used. A chelating agent such as disodium ethylenediaminetetraacetate can also be used. Although the usage-amount of a polymerization initiator should just be 0.01-10 weight part normally with respect to 100 weight part of all the monomers, Preferably it is 0.1-5 weight part. The polymerization is usually performed at a temperature of 10 to 90 ° C.

  The amount of the amine functional group-containing aqueous resin used is preferably 0.1 to 20% by weight, more preferably 1 to 15% by weight based on the solid content of the epoxy ester-modified acrylic emulsion resin. More preferably, it is weight%. If it is less than 0.1%, the initial drying property may be insufficient, and if it exceeds 20% by weight, it may become more water-soluble and the water resistance may be lowered.

The obtained aqueous resin composition can be used as an aqueous coating as it is, but if necessary, pigment, antifoaming agent, pigment dispersant, plasticizer, organic solvent, water-soluble or water-dispersible resin, metal drying A water-based paint or other paint may be blended with an agent, a surface treatment agent, and the like.
Examples of the pigment include titanium white, carbon black, zinc oxide (antirust pigment), talc (external pigment), and zinc phosphate (antirust pigment).
Examples of the antifoaming agent include BYK-022 (BIC Chemie Co., Ltd. trade name).
Examples of the plasticizer include dimethyl phthalate and dioctyl phthalate.
Examples of the organic solvent include those described above.
Examples of the water-soluble or water-dispersible resin include modified amino resins, epoxy resins, polyester resins, and acrylic resins.

Examples of the metal desiccant (metal dryer) include cobalt naphthenate and lead naphthenate.
Examples of the surface treatment agent include silicon-based slip leveling agents such as BYK-301 (BIC Chemie Co., Ltd. trade name).
In addition, the modified | denatured amino resin and an epoxy resin can be mix | blended with the obtained aqueous resin composition, and it can use as a coating material for baking.
Moreover, using the fatty acid of the said drying oil or semi-drying oil as a fatty acid used for the said fatty acid modified epoxy ester, Furthermore, a metal desiccant is added to the said resin composition for water-based paints, and it uses it as a normal temperature curable coating material. Can do.

As a method for forming a paint, known methods such as a paint shaker method, a roll mill method, a sand mill method, a disperser method, a kneader method, and a high-speed impeller mill method can be used.
The obtained water-based paint can be used for painting in accordance with a normal painting method. In painting, for example, a dipping method, a brush coating method, a spray coating method, a roll coating method, a flow coater coating method, Shibori (or Shigoki) A known coating method such as a coating method or a knife coater coating method can be used.
After coating, the coating film can be dried and cured by natural drying or forced drying by a dryer.
The aqueous resin composition obtained by the production method of the present invention is excellent in corrosion resistance and can be used for paints for coating wood, paper, fiber, plastic, ceramic, iron, non-ferrous metal, glass, concrete and the like. .

  The aqueous resin composition of the present invention described above can be used for paints. Examples of paints include room temperature dry paints by oxidative crosslinking and lacquer paints.

Hereinafter, the present invention will be described more specifically with reference to examples of the present invention and comparative examples thereof, but the present invention is not limited to these examples.
[Production example]
Example of production of epoxy ester-modified vinyl polymer emulsion Epicoat 828, 417 g, dehydrated castor oil fatty acid while introducing inert gas into a glass flask equipped with a stirrer, reflux condenser, inert gas introduction tube, and thermometer 63 g, linseed oil fatty acid 501 g and dimethylethanolamine 1 g were added and reacted at 220 ° C. for 5 hours, then the temperature was lowered to 120 ° C. and maleic acid 20 g was added and reacted for 1 hour to give an epoxy ester resin having an acid value of 10 (A -1) was obtained.
Next, 200 g of the above epoxy ester resin, 40 g of Antox MS 60, and 1465 g of water were added and emulsified in a homogenizer over 5 minutes, transferred to the same flask as in the above production example, heated to 80 ° C., and 2.5 g of ammonium persulfate was added. Added. Separately, a mixed liquid consisting of styrene, 450 g, n-butyl acrylate 80 g, 2-ethylhexyl acrylate 40 g, and methacrylic acid 40 g was charged into a dropping funnel, dropped over 1 hour, kept warm for 2 hours, cooled, and ammonia. The mixture was neutralized with an excess amount of ammonia and adjusted to pH 10. An epoxy ester-modified vinyl polymer emulsion having a heating residue of 40% by weight and an acid value (solid content) of 28 was obtained.

Example of production of amine functional group-containing aqueous resin 295 g of deionized water and acetic acid while introducing an inert gas into a glass flask equipped with a stirrer, reflux condenser, inert gas introduction tube, and thermometer. 5 g was charged, and 1.2 g of an aqueous solution of 0.15% ferrous sulfate and 1.0 g of a 1% aqueous solution of disodium ethylenediaminetetraacetate were mixed and charged into a flask. Thereafter, 100 g of dimethylaminoethyl acrylate and 2.1 g of t-butyl hydroperoxide were mixed and added dropwise over 2 hours together with a mixture of 25 g of deionized water, 0.2 g of acetic acid and 1.2 g of Rongalite. After completion of dropping, 0.25 g of t-butyl hydroperoxide and 0.1 g of Rongalite were added, and the mixture was kept at 75 ° C. for 1 hour. The final product had a solid content of 28.5%, a viscosity of 500 mPa · s, and a pH of 8.0.

[Example 1]
The epoxy ester-modified vinyl polymer emulsion obtained in the above production example and the amine functional group-containing aqueous resin were mixed in the formulation shown in Table 1 to prepare an aqueous resin composition. In Table 1, the amounts of the epoxy ester resin, various polymerizable vinyl monomers, and the amine functional group-containing aqueous resin are each expressed in parts by weight of solid content. Moreover, the coating material was prepared with the coating composition mentioned later, and the evaluation test of the coating film was conducted. The results are shown in Table 2.

[Examples 2 to 6 and Comparative Examples 1 and 2]
Examples 2 to 6 are the same as Example 1 except that the amount of the polymerizable monomer used in the synthesis of the epoxy ester-modified vinyl polymer emulsion and / or the amount of the amine functional group-containing aqueous resin is changed as shown in Table 1. An aqueous resin composition was prepared in the same manner. In Comparative Example 1, an aqueous resin composition was prepared in the same manner as in Example 1 except that only the other polymerizable monomer was used in the amount shown in Table 1 without using the epoxy ester resin. In Comparative Example 2, an aqueous resin composition was prepared in the same manner as in Example 1 except that the amine functional group-containing aqueous resin was not used. The evaluation test of the coating film was conducted in the same manner as in Example 1, and the results are shown in Table 2.

Evaluation (paint composition) parts by weight carbon (trade name: MA-100, manufactured by Mitsubishi Kasei Co., Ltd.) 7.5
LF Bow PW-2 (rust preventive pigment, manufactured by Kikuchi Dye Co., Ltd.) 10.0
Zinc Hana No. 1 (rust preventive pigment, Sakai Chemical Co., Ltd.) 10.0
LMS200 (external pigment, manufactured by Fuji Talc Co., Ltd.) 123.0
3-Methyl-3-methoxybutanol 16.0
Surfynol 104 (pigment dispersant, manufactured by Nissin Chemical Industry Co., Ltd.) 3.5
BYK022 (antifoaming agent, manufactured by BYK Chemie) 0.3
Aqueous resin composition (solid content) 100.0
DICnate 3111 (metal dryer, manufactured by Dainippon Ink and Chemicals, Inc.) 4.5

  The paint dispersed by the paint shaker is adjusted to a viscosity of 16 seconds with a thinner, and the untreated steel sheet (made by Nippon Test Panel Co., Ltd., trade name: SPCC-SD) is adjusted to a dry film thickness of 30 μm by air spray on the untreated steel sheet Plate, thickness: 0.8 mm), and after 5 days of drying at 20 ° C., a coating film evaluation test (based on JIS K 5400) was performed.

(Evaluation methods)
(1) Pencil hardness According to the pencil scratch test method of JIS K 5400, the result was shown by the hardness symbol of the pencil in which the coating film was not torn.
(2) Drying After coating at 5 ° C. and 20 ° C., the curing time (unit: minutes) is determined by finger touch (JIS K 5625).
(3) Adhesion with substrate (cross-cut)
100 squares of 1 mm square were cut with a cutter, and after peeling with cello tape (registered trademark), the remaining meshes of the remaining coating film were indicated.

(4) Water-resistant spot Time until ion-exchanged water is dripped onto the test plate with a dropper and the trace disappears (unit: minutes)
(5) Flexibility The coating plate was bent at 3φ, and the presence or absence of cracks in the bent portion was confirmed. “Good” indicates that there are no abnormalities such as cracks.

(6) Water resistance The test plate was immersed in ion-exchanged water at 20 ° C. for 7 days, and the presence or absence of whitening, swelling, and secondary adhesion on the coating film surface was visually determined. In the evaluation of whitening, ○ indicates that there is no whitening, and Δ indicates that it is slightly whitened. Good swelling indicates that there is no swelling. The secondary adhesion 100/100 indicates that there is no peeling after making 100 squares in 1 m × 1 m and peeling off the tape.
Indicates.
(7) Salt spray (corrosion resistance)
According to the salt water resistance spray test of JIS K 5400, a cut part was formed on the test plate, the amount of rust from the cut part after spraying with salt water for 480 hours was measured, and the blister and the blister width were visually observed. The rust amount ○ indicates that rust has not occurred, x indicates that rust has occurred on the entire surface, and Δ indicates that rust has partially occurred.

   As seen in Examples 1 to 6, the aqueous resin composition of the present invention is excellent in flexibility, water resistance, corrosion resistance, chemical resistance, drying property and the like. Although the comparative example 1 is a case where an epoxy ester resin is not used, corrosion resistance is inferior. Although the comparative example 2 is a case where an amine functional group containing aqueous resin is not used, dryness is remarkably bad.

Claims (4)

(A) A polymerizable vinyl monomer mixture containing an ethylenically unsaturated carboxylic acid is blended in the presence of water and an epoxy ester resin, and emulsion polymerization is performed using a reactive emulsifier having an ethylenically unsaturated group as an emulsifier. An aqueous resin composition comprising an epoxy ester-modified vinyl polymer emulsion adjusted to pH 10 to 11 and (B) an amine functional group-containing aqueous resin.   The epoxy ester resin is an epoxy ester resin having an acid value of 30 or less obtained by addition condensation of 30 to 70% by weight of a fatty acid and 70 to 30% by weight of an epoxy resin, where the total amount of fatty acid and epoxy resin is 100% by weight. Item 12. The aqueous resin composition according to Item 1. (A) A reaction having 95 to 40% by weight of a polymerizable vinyl monomer mixture containing an ethylenically unsaturated carboxylic acid in the presence of 5 to 60% by weight of water and an epoxy ester resin, and having an ethylenically unsaturated group as an emulsifier An epoxy ester-modified vinyl polymer emulsion adjusted to pH 10 to 11 and an acid value of 10 to 50 by adding an amine, and (B) an amine functional group-containing aqueous resin. The aqueous resin composition according to claim 1 or 2 . The coating material containing the aqueous resin composition in any one of Claims 1-3 .