KR20050068563A - Corrosion-resistant composition for treating the surface of aluminum material and coating composition containing the same - Google Patents

Abstract

The present invention relates to an anticorrosive composition for aluminum coating, a method for preparing the same, and a coating composition using the same for preventing corrosion of aluminum products such as aluminum fins used for automobiles or households. In addition, the present invention provides a method for painting the aluminum surface by using the anticorrosive composition for aluminum coating.

The anticorrosive composition for aluminum coating according to the present invention is not only excellent in corrosion resistance to prevent corrosion of the aluminum surface, but also interlayer adhesion and heat resistance, odor resistance, corrosion resistance and workability with a top coat such as a hydrophilic agent applied on the corrosion inhibitor. And moldability are excellent. In addition, it is environmentally friendly because it does not use heavy metals such as chromium that have recently emerged as environmental problems.

Description

Corrosion-resistant composition for treating the surface of aluminum material and coating composition containing the same}

The present invention relates to an anticorrosive agent capable of imparting corrosion resistance to aluminum surfaces such as aluminum fin products used in home appliances and automobiles. More specifically, it is used in the surface of aluminum or aluminum alloy products such as heat dissipation fins used in heat exchangers such as air conditioners or automobiles, and is a corrosion resistant composition that can prevent corrosion of aluminum, and it is possible to harden high temperature baking, in particular, a coating film. The present invention relates to an aqueous anticorrosive composition having excellent hardness and water resistance and excellent processability, which can be coated before molding, and having excellent interlayer adhesion and workability with a hydrophilic agent, a method for preparing the same, and a coating composition using the same.

The materials of fins used in home appliances such as outdoor units or indoor units of air conditioners or automobile air conditioners are generally aluminum or aluminum alloys, which are often used without additional corrosion treatment. However, the aluminum tends to be easily corroded by acid rain resulting from nitric acid or sulfurous acid gas due to air pollution or by contact with salts contained in the atmosphere.

In order to solve this problem, research has been conducted to improve the corrosion resistance by further providing corrosion resistance to the aluminum and improving the interlayer adhesion between the hydrophilic agent and the corrosion agent coated on the corrosion inhibitor. In particular, a method using phosphate treatment or chromate treatment has been proposed. However, the phosphate or chromate treatment has a large amount of waste water treatment costs and adversely affect the safety of the handling agent due to the carcinogenicity of the surface treatment agent itself, it has become internationally regulated.

Japanese Patent Application No. Hei 3-131370 discloses a resin type anticorrosive composition containing a water-soluble chromium compound and water-dispersed silica in a dispersion of an olefin-alpha, beta-ethylenically unsaturated carboxylic acid copolymer. Although this leads to an improvement in corrosion resistance, there is a problem that some white rust occurs when long-term exposure in high humidity atmosphere. In addition, Korean Laid-Open Patent Publication No. 2001-0066133 discloses a one-component type corrosion inhibitor using a water-soluble epoxy-phosphate resin and a curing agent, but the corrosion inhibitor has good corrosion resistance and adhesion but is interlayer with a hydrophilic agent having heat resistance and top coat. Due to poor adhesion, hydrophilic persistence is reduced and heat discoloration may occur.

On the other hand, Korean Laid-Open Patent Publication No. 1998-087035 discloses a composition which can be colored as a non-chromic corrosion resistant coating composition comprising a thiocarbonyl group-containing compound, phosphate ions and water dispersible silica. This can be obtained a variety of colors according to the customer's request, but can give inconvenience to the continuous operation in a multi-component type.

The anticorrosive for aluminum surface treatment containing a large amount of the metal component utilizes the principle of maximizing corrosion resistance by arranging the metal component on the coating film surface after drying. However, while the corrosion resistant agent has an excellent rigidity of the coating film, it is difficult to process and difficult to protect the metal surface due to the poor adhesion to the hydrophilic agent used for aluminum or aluminum alloy.

On the other hand, in the case of non-chromic anticorrosive which does not use a metal, when the hydrophilic agent is applied on the anticorrosive, there is a problem in that the hydrophilicity is weakened or the corrosion resistance is reduced or the workability is poor because it is multi-liquid.

Therefore, in order to solve the above problems, as a corrosion treatment agent for aluminum surface treatment can increase the crosslinking density on the surface of the coating film during the baking process, can be given a corrosion protection effect, and also can obtain a variety of colors according to the customer's requirements Corrosion resistance is required. Also during storage of pigment There should be no precipitation and the hardener is mixed in the paint in one-component type, so a corrosion resistant agent having excellent workability is required.

Accordingly, the present inventors supplement the disadvantages of the adhesive strength with the hydrophilic agent, which is a problem of the conventional anticorrosive containing a metal component as described above, and at the same time, the long-term corrosion resistance and workability, which is a problem of the conventional nonmetallic anticorrosive, Overcoming, the inventors have invented an organic type aluminum corrosion resistant agent which is inexpensive and has excellent processability.

In addition, it is possible to increase the crosslinking density of the coating surface in the baking process to give the corrosion protection effect, to obtain a variety of colors as needed, and as a one-component type that does not precipitate pigment during storage, the curing agent is mixed in the paint A corrosion resistant agent for aluminum surface treatment has been developed which is advantageous for workability.

Accordingly, an object of the present invention is to enable high-temperature baking hardening for a short time as a thin film, and to be excellent in workability and workability, so that continuous PCF coating and sheet coating can be achieved, and corrosion resistance and water resistance can be obtained at the same time. It is possible to provide an anticorrosive agent having improved interlayer adhesion with a hydrophilic agent.

The present invention also provides a method for preparing the above corrosion resistant agent.

It is also an object of the present invention to provide a coating composition containing the above corrosion inhibitor.

The present invention also provides a method for painting an aluminum surface using the coating composition.

The present invention is at least one resin selected from the group consisting of emulsion resin (A), monomer-modified epoxy resin (B), water-soluble urethane resin (C) and water-soluble acrylic resin (D); And at least one of an aqueous melamine resin, a resol-type aqueous phenol resin, and an aqueous benzoguanamine resin as a curing agent.

The anticorrosive composition may be applied to the coating for PCF. The PCF coating refers to a coating method for working a thin film with a reverse roll, etc., and refers to the work of curing the paint while rolling the aluminum steel sheet at a speed of 60 to 80 m / min and passing through a drying furnace of 200 ℃ to 250 ℃.

In the anticorrosive composition according to the present invention, the resins (A), (B), (C) and (D) are preferably contained in an amount of 60 to 99% by weight based on the total weight of the composition. Depending on the resin, the number average molecular weight is 30,000 to 200,000, the hydroxyl value is 10 to 120 mg KOH / g, and the acid value is preferably 30 to 85 mg KOH / g. Moreover, it is good that glass transition temperature (Tg) is -20-60 degreeC. For this purpose, the resin can be prepared using a unsaturated functional monomer having a hydroxyl value of 10 to 120 mg KOH / g and an acid value of 30 to 85 mg KOH / g as a functional monomer.

According to the present invention, an emulsion resin (A) synthesized using an unsaturated double bond monomer, a functional monomer, an emulsifier, etc .;

A bisphenol A modified epoxy resin having an epoxy equivalent of 450 to 4000 is esterified with an acrylic resin or a styrene-acrylic copolymer resin containing a carboxyl group or a hydroxy group (block copolymer); Or a monomer-modified epoxy resin (B) prepared by graft polymerization of an unsaturated double bond monomer or a functional monomer on the bisphenol A-modified epoxy resin in the presence of a peroxide initiator;

A water-soluble urethane in which a polyester polyol resin or a polyether polyol resin prepared by using a polyhydric alcohol and a polybasic acid is introduced into an isocyanate group together with DMPA or DMBA by an amphoteric solvent to dissolve and dissolve the urethane bond. Resin (C); And

A water-soluble acrylic resin (D) used in the presence of an amphoteric solvent in which an unsaturated double-bonding monomer or a functional monomer was copolymerized with an initiator and neutralized with an amine for more stable dispersion in an aqueous phase. Used as a resin for anticorrosive

In addition, as a hardening | curing agent, resol type aqueous phenol resin, aqueous melamine resin, or aqueous benzoguanamine resin can be used. It is preferable to contain the said hardening | curing agent as much as 1-40 weight part with respect to 100 parts of corrosion resistance compositions.

In addition to the hardening agent, an emulsifier, an antibacterial agent, an antifungal agent, a coloring agent (coloring agent), etc. can be added to the said anticorrosive composition. For reference, the colorant preferably contains 0.1 to 5.0 parts by weight based on 100 parts by weight of the corrosion resistant composition. As such a colorant, an organic or inorganic pigment can be used individually or in mixture as needed for coloration.

The anticorrosive composition according to the present invention is a thin film coated on the aluminum surface, showing excellent corrosion resistance and interlayer adhesion with a hydrophilic agent. When the composition is applied to an aluminum coating, the paint has excellent corrosion resistance, processability, interlayer adhesion, workability, and coloring ability, and in particular, improves interlayer adhesion with an organic hydrophilic agent or an inorganic hydrophilic agent which is a top coat. It can provide hydrophilic persistence and good corrosion resistance.

It is preferable to coat the said anticorrosive composition so that dry coating amount may be about 0.8-1.6 g / m <2> on an aluminum plate. If the dry coating amount is 0.8 g / m 2 or less, the corrosion resistance may be deteriorated. If the dry coating film amount is 1.6 g / m 2 or more, the amount of application of the hydrophilic agent decreases, resulting in insufficient hydrophilicity. Preferably, when carrying out the so-called PCF (PCF) coating method which works with a thin film by a reverse roll so that a dry coat amount may be about 1.0-1.4 g / m <2>, a clean film without bubbles and streaks can be obtained.

Hereinafter, each component will be described in detail.

(A) emulsion resin

The emulsion resin according to the present invention preferably has a number average molecular weight of 30,000 to 200,000, a hydroxyl value of 10 to 120 mg KOH / g, an acid value of 30 to 85 mg KOH / g, and a functional unsaturated monomer. It is good to be manufactured. Specifically, a styrene-acrylic copolymer emulsion resin or a pure acrylic emulsion resin having a glass transition temperature (Tg) of -20 to 60 ° C is suitable, and it is preferable to have a dissolving power in water.

The emulsion resin (A) used in the present invention is a functional monomer containing 30 to 90 parts by weight of an aromatic vinyl monomer, a methacrylate ester monomer or an acrylate ester monomer containing an unsaturated double bond and a hydroxyl group or a carboxyl group. 5 to 30 parts by weight may be obtained by radical polymerization in the presence of an emulsifier, an initiator and ion-exchanged water. Preferably, as a milky white emulsion resin having a solid content of 30% to 55%, a pH of 6 to 9 and a viscosity of 500 to 4500 cps, an acrylic single or styrene-acrylic copolymer having a number average molecular weight of 30,000 to 200,000 can be obtained. .

As the monomer containing the unsaturated double bond, there are mainly functional monomers having a hydroxyl group and a carboxyl group, an acrylic or methacrylic ester monomer, an aromatic vinyl monomer, and the like. Examples of the carboxyl group-containing monomers include acrylic acid, methacrylic acid, itaconic acid, and fumaric acid. As hydroxyl-containing monomer, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxyamyl (meth) acrylate, 2-hydroxy-3- phenoxy propylacryl Latex, 2-hydroxy butyl (meth) acrylate, 2- (meth) acryloyloxy ethyl 2-hydroxy ethyl phthalate, 3-chloro-2-hydroxy propyl methacrylate, 2-hydroxy hexyl (meth And hydroxy alkyl (meth) acrylates such as) acrylate. Examples of the acryl or methacrylate monomers include methacrylates having 1 to 18 alkyl ester carbon atoms, for example, methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, lauryl methacrylate, and the like. Examples of the acrylates having 1 to 18 alkyl ester carbon atoms include methyl acrylate, ethyl acrylate, n-butyl acrylate, lauryl acrylate and the like. Aromatic vinyl monomers include styrene, vinyltoluene, alphamethylstyrene, and the like. Other functional monomers include glycidyl methacrylate monomers, 2-methacryloyloxyethyl phosphate monomers or derivatives thereof, N-metholacryl amide monomers or derivatives thereof, and 2-acrylamido-2 methylpropanesyl. Phosphonic acid monomers or derivatives thereof, trifluoroethyl methacrylate monomers or derivatives thereof, phenoxy ethyl acrylate monomers or derivatives thereof, 2-acryloyloxy ethyl lycinate monomers or derivatives thereof and the like.

If the functional monomer is used in an amount less than 5 parts by weight, the adhesion to the aluminum surface tends to be inferior. If it is used in an amount of 30 parts by weight or more, the reactivity becomes poor, resulting in abnormal particles, and lack of miscibility with the curing agent. Therefore, it is preferable to use within the range of 6-20 weight part.

The emulsifier is preferably a mixture of ionic emulsifiers or nonionic emulsifiers, 1 to 10 parts by weight is used. If it is 1 part by weight or less, the amount of emulsifier is small, the size of the particles is large, adhesion and corrosion resistance is poor, the progress of surface corrosion is relatively fast, and if it is 10 parts by weight or more, the particle size is small, the viscosity is high, making paint difficult and bubbles are generated. Not only does this happen, but the parcels are not made smoothly, so workability is reduced. Preferably 1 to 5 parts by weight is good, the ratio of ionic / nonionic is 4/6 to 2/8 weight ratio is good.

Ionic emulsifiers include alkyl sulfate type, such as sodium lauryl sulfate, ammonium lauryl sulfate, sodium 2-ethylhexyl sulfate, sodium tridecyl sulfate, and ether sulfate types such as sodium tridecyl ether sulfate, alkylphenol Ethoxylate sulfate sodium salt, alkylphenol ethoxylate sulfide ammonium salt, and phosphate ether type include aromatic phosphate esters and aliphatic phosphate esters, and sulfonate type sodium dodecyl benzene sulfonate, disodium Alkyl diphenyl oxide sulfonate, sodium alpha olefin sulfonate, and the like, and sulfo lacsinate types include sodium alkyl ether sulfosulcinate, sodium nonylphenyl ether sulforuccinate, sodium bistridecyl sulfosulcinate, and the like. have.

The emulsifier can be applied to all other resins (B), (C) and (D) as well.

As the radical polymerization initiator, ammonium per sulfate (APS), sodium per sulfate (SPS), or potassium persulfate (KPS) is used in an amount of 0.1 to 2.0 parts by weight, and a buffer, a neutralizer, a protective colloid, and the like may be used.

As a hardening | curing agent, 5-40 weight part is used with respect to 100 weight part of emulsion resins individually or in mixture of a resol type | mold aqueous phenol resin and an aqueous melamine resin. If the amount is 5 parts by weight or less, the corrosion resistance after the coating film is formed, and more than 40 parts by weight appears relatively poor workability. It is preferable to use an aqueous melamine curing agent, and it is preferable to use as much as 6 to 32 parts by weight.

(B) Monomer modified epoxy resin

The monomer-modified epoxy resin (B) is an esterification polymerization reaction of a bisphenol A-modified epoxy resin having an epoxy equivalent of 450 to 4000 with an acrylic resin or a styrene-acrylic copolymer resin containing a functional unsaturated monomer, or as a peroxide polymerization initiator. The bisphenol A modified epoxy resin may be obtained by graft polymerization of an unsaturated double bond monomer or a functional monomer, followed by dispersion in an aqueous medium.

Specifically, the monomer-modified epoxy resin is an esterification reaction of a bisphenol A epoxy resin having an epoxy equivalent of 450 to 4000 in the presence of a basic catalyst with a styrene-acrylic copolymer resin or a pure acrylic resin using a monomer having an unsaturated double bond. Or copolymerize the monomer having an unsaturated double bond to the epoxy resin by graft polymerization, neutralize with a neutralizing agent, disperse with ion-exchanged water to a solid content of 20 to 30 weight, and then at a constant temperature. By adding a curing agent and curing, a water dispersion monomer (acrylic resin) modified epoxy copolymer having a pH of 6 to 9 and a solid acid value of 30 to 120 can be obtained.

The ratio of epoxy / acrylic resin and epoxy / monomer is preferably 20/80 to 90/10, and 70/30 to 80/20 is preferable. If the ratio of epoxy / acrylic is 20/80 or less, adhesion to the aluminum surface is poor and corrosion resistance and interlayer adhesion with the top are weakened, resulting in poor hydrophilic persistence. If it is 90/10 or more, the viscosity of the paint is increased, and splashing and cobweb phenomenon may appear due to roll marking or high-speed rotation of the roll during roll work, which is not preferable. The monomer containing an unsaturated double bond has a carboxyl group, but preferably contains 5 to 15 parts by weight, preferably 8 to 12 parts by weight. If the carboxyl group content is 5 parts by weight or less, the water solubility is poor and does not become water-dispersible, and the shelf life of the paint is deteriorated. If the content is 15 parts by weight or more, the viscosity increases due to the excess acid not participating in the reaction, and a viscosity change occurs during storage. do. To facilitate water dispersion, a neutralizing agent may be used as DMEA (dimethylethanolamine) or TEA (triethylamine), aqueous ammonia or 2 amino 2 methyl propanol.

As the unsaturated double bond monomer, an acrylate or methacrylate ester monomer, an aromatic vinyl monomer, a hydroxyl group-containing monomer, or the like can be used. As the initiator, it is advantageous to use benzoyl peroxide, which is easy to radically polymerize at 80 ° C to 120 ° C. In addition, dicumyl peroxide, tertiary butyl peroxy 2-ethyl hexanoate, AIBN (2,2'-Azobisisobutyronitrile) and the like can be used.

The content of the solid content is 15 to 25 parts by weight is good, the ion exchange water or amphoteric solvent is used as the dispersion medium, the ion exchange water is preferably contained by 75 to 95 parts by weight relative to the dispersion medium. If the content is 75 parts by weight or less, the amount of solvent in the finished product is a lot of odor generated by the evaporation can be a problem in the working environment and difficult to adjust the viscosity. If the amount is more than 95 parts by weight, the solvent may be insufficient, and a film may be formed around the roll during the roll operation due to evaporation of the solvent, resulting in foreign matters, and teeing or roll marking may occur on the painted surface.

As a hardening | curing agent, aqueous melamine, aqueous phenol, aqueous benzoguanamine, etc. can be used, It is comparatively preferable to use an aqueous phenol resin. This is because the corrosion resistance is superior to other types and the effect can be obtained even using a small amount. It is preferable to use 3-30 weight part of hardening | curing agents with respect to 100 weight part of monomer-modified epoxy resins, and it is relatively preferable to use 3-30 weight part in the case of a phenol hardening | curing agent, and 5-30 weight part in the case of a melamine hardening agent.

The resol type aqueous phenol resin usable in the present invention can be obtained by reacting phenol or phenols with formaldehyde or formaldehyde in the presence of a catalyst, and can be obtained by introducing a methylol group. Some of the methylol groups introduced may be alkyl etherified.

Components of the phenol resin include orthocresol, paracresol, parabutyl phenol, paraethylphenol, 3,4 xylenol, paranonylphenol, paraethylamphenol, paracyclohexylphenol, 2 , 5 xylenol, para-amyl phenol, oxooxy benzoic acid, bifunctional phenols of the type and monofunctional 2,4 xylenol, 2,6 xylenol and tetrafunctional bisphenol A, alkyl bisphenol A, and the like. Can be. These can be used individually by 1 type or in combination of 2 or more types, and can mix and use 2 or more types. Formaldehydes may be formaldehyde or derivatives thereof such as paraformaldehyde, trioxane, hexamine, etc., and may be used in solid or liquid form and may be used alone or in combination. The molecular weight is 300 to 800, the Gardner viscosity is 2 to 20 seconds, diluted with ion-exchanged water and some lower alcohol, the solid content is 35 to 60% by weight, and the pH is 8 to 11. When the molecular weight is 300 or less, the curing degree is improved, the hardness of the coating film is high, the aluminum workability is inferior, and when it is 800 or more, the leveling tends to be lowered.

(C) water-soluble urethane resin

The water-soluble urethane-modified resin is prepared by dissolving a polyester polyol resin or a polyether polyol resin in an amphoteric solvent together with DMPA or DMBA and introducing an isocyanate group to neutralize the aqueous solution after introducing a urethane bond. Can be.

Specifically, the water-soluble urethane resin is introduced into a polyester polyol or polyether polyol having a molecular weight of about 200 to 3000, preferably 300 to 2500, to introduce a hydrophilic part of DMPA or DMBA together with the polyol. After the urethane isocyanate reaction is neutralized with dimethylethanolamine (N, N-Dimethyethanolamine, DMEA) can be prepared by dispersing in ionized water.

Since the water-soluble urethane resin according to the present invention should have excellent adhesion and corrosion resistance and excellent storage stability, an appropriate amount of amphoteric solvent, such as butyl cellosol portion, ethyl cellosol portion, butyl carbitol, methyl carbitol, etc. To completely dissolve the hydrophilic part of DMPA or DMBA for water dispersion in a polyester polyol or polyether polyol having a molecular weight of 200 to 3000, preferably 300 to 2500, consisting of a polyhydric alcohol and a polybasic acid. A urethane reaction was carried out by introducing an isocyanate group capable of reacting with a water-soluble urethane resin polymer in which dimethylethanolamine (N, N-Dimethyethanolamine, DMEA) was added as a neutralizing agent in the same molar ratio as the hydrophilic portion and dispersed in ion-exchanged water. Can be obtained. It is preferable that the amphoteric solvent does not exceed 20 parts by weight in the diluting solvent, and therefore it is preferable to recover the excess amphoteric solvent. If it exceeds 20 parts by weight, environmental problems occur due to pigment storage and baking of the finished product anticorrosive. However, some amphoteric solvent is required to prevent film formation on the roll and to control the drying speed. Compatibility with the hydrophilic agent and interlayer adhesion are influenced by the amount of DMPA or DMBA, and it is relatively advantageous to use 3 to 8 parts by weight. 4 to 6 parts by weight is preferable, and 3 parts by weight or less is inferior in water solubility, and 8 parts by weight or more weakens bubble generation and water resistance. In addition, in order to increase the binding strength with the hydrophilic agent it may be effective to contain some hydroxyl or amide groups.

The aqueous melamine resin or the aqueous phenol resin used as the curing agent is preferably used in an amount of 5 to 35 parts by weight based on 100 parts by weight of the water-soluble urethane, and preferably 5 to 20 parts by weight.

(D) water-soluble acrylic resin

The water-soluble acrylic resin may be prepared by carrying out acrylic copolymerization of a water-soluble and reactive functional monomer with an initiator in the presence of an amphoteric solvent and neutralizing it with an amine for more stable dispersion in an aqueous phase.

The water-soluble acrylic resin used in the present invention is relatively difficult to adjust the color of the finished product, while the physical properties of the coating film after curing is easy to adjust the viscosity. Therefore, it is advantageous to use the mixture with other types of aqueous resins, and when used alone, it is appropriate that the molecular weight is about 2,000 to 20,000. It is preferable to use glass transition temperature at -20 degreeC-60 degreeC. Especially 0 degreeC-30 degreeC is preferable. The processability of the coating film after bake hardening below -20 ℃ is good, but the strength is low, so it is easy to be contaminated on the surface of aluminum coating, and the amount of curing agent must be increased to increase the hardness. Above 60 ° C, the film may be formed on the roll before the baking is dried, and an excessive amount of organic solvent may be used to prevent the film from being formed, which may cause environmental problems and roll marking due to the film.

The monomer having an unsaturated double bond to be used must be capable of controlling rheology even with a reactive hydroxyl group, a carboxyl group for dispersing water, and a low solids, giving pigment miscibility, giving a coloring power, and having a functional monomer compatible with a hydrophilic agent. It is preferable to mix and use about 40 weight part. As the monomer that can be used functionally, the same monomers or derivatives thereof used in the emulsion resin (A) may be used.

In addition, the glass transition temperature can be controlled by using an acrylate or methacrylate monomer or an aromatic vinyl monomer.

As the organic solvent, water-soluble butyl cellosol moiety, ethyl cellosol moiety, butyl carbitol, methyl carbitol, ethyl carbitol, isopropane alcohol, methanol and ethanol may be used alone or in combination. It should not exceed 40 parts by weight. This is because it can affect the storage stability of the finished product and the color of the anticorrosive agent as well as the odor upon baking. Therefore, it is better to recover and use the excess solvent after the reaction and to use it in a range that does not affect the stability of water dispersion or water solubility after neutralization with a neutralizing agent. The acid value of the finished product is 35 to 120 mg KOH / g, the hydroxyl value is in the range of 10 to 120 mg KOH / g.

This is because even when the water-soluble acrylic resin is used alone, sufficient corrosion resistance can be obtained by forming sufficient crosslinking with the curing agent, that is, the melamine resin, the resol-type aqueous phenol resin and the aqueous benzoguanamine resin.

EMBODIMENT OF THE INVENTION Hereinafter, the coating method of the resin composition for aluminum surface nose corrosion of this invention is demonstrated concretely.

The coating method of the present invention can be suitably applied to a paint for aluminum surface anticorrosive. As a coating method, there is a method of baking after baking the aluminum surface and baking, and then baking after dipping, but roll coating is easy for workability and easy post-processing.

The coating amount is preferably 0.8 to 1.6 g / m 2, preferably about 1.0 to 1.4 g / m 2, as a dry coating film. If the coating amount is 0.8g or less, the coating amount is difficult to apply uniformly, so the corrosion resistance is inferior. If the coating amount is 1.6g or more, the coating thickness is too thick. Raises the cooling efficiency.

The aluminum surface treatment anticorrosive composition of the present invention is a mixture of an emulsion resin (A), a monomer-modified epoxy resin (B), a water-soluble urethane resin (C), and a water-soluble acrylic resin (D) alone or in combination of two kinds, and examples thereof. For example, an aqueous melamine resin, a resol-type aqueous phenolic resin, and an aqueous benzoguanamine resin can be used alone or in combination to form a coating film having excellent corrosion resistance and processability, which is very useful as an aluminum surface anticorrosive agent, that is, a coating composition for PCF. .

Hereinafter, preferred embodiments of the present invention are illustrated.

The following embodiment is an example of preparing the anticorrosive composition according to the present invention is not limited thereby the scope of the present invention.

<First Embodiment>

It has a number average molecular weight of 30,000 to 200,000, a hydroxyl value of 10 to 120 mgKOH / g, an acid value of 30 to 85 mgKOH / g, and is manufactured using a part of a functional unsaturated monomer, and has a range of cottage (Tg: glass transition temperature) range. Aqueous paint for aluminum corrosion resistant PCF comprising 5-40 parts by weight of a resol type aqueous phenolic resin or an aqueous melamine or benzoguanamine resin crosslinking agent in 100 parts by weight of a styrene-acrylic copolymer emulsion resin or a pure acrylic emulsion resin at -20 to 60 ° C. Composition.

Second Embodiment

Ester polymerization of a bisphenol A modified epoxy resin having an epoxy equivalent of 450 to 4000 and a styrene-acrylic copolymer resin or a pure acrylic resin to which a functional unsaturated monomer is partially applied, or graft polymerization of a functional unsaturated monomer to the bisphenol A modified epoxy resin Aqueous paint for aluminum anticorrosive PCF prepared by containing 1 to 10 parts by weight of a resol-type aqueous phenolic resin or an aqueous melamine or a benzoguanamine resin crosslinking agent with respect to 100 parts by weight of an acrylic modified epoxy resin formed by reacting and dispersing in an aqueous medium. Composition.

Third Embodiment

Hydrophilicity of DMPA or DMBA for Water Dispersion in Polyester Polyols or Polyether Polyols with Molecular Weights of 200 to 3000, preferably 300 to 2500, consisting of polyhydric alcohols and polybasic acids using an amphoteric solvent Water-soluble urethane resin 100 which dissolves the parts completely, introduces an isocyanate group capable of reacting with the polyol, and then disperses by adding dimethylethanolamine (N, N-Dimethyethanolamine, DMEA) in the same molar ratio as the hydrophilic part. The aqueous coating composition for aluminum corrosion inhibitor PCF which contains 5-35 weight part of aqueous melamine or aqueous phenol resin hardening | curing agent in a weight part.

Fourth Embodiment

A styrene-acrylic resin or a pure acrylic resin having a molecular weight of 2000 to 20000 and a titer (Tg: glass transition temperature) of -20 to 60 ° C. using a water-soluble solvent and a radical initiator, and adhesion to aluminum and a hydrophilic agent. To 100 parts by weight of a water-soluble acrylic resin containing a functional monomer for improving interlayer adhesion or at least 5 to 40 parts by weight of a functional monomer capable of improving roll coating workability at a low solid content. Production of the aqueous coating composition for aluminum surface anticorrosive PCF containing 5 to 35 parts by weight of aqueous melamine or aqueous benzoguanamine and aqueous phenol curing agent.

<Fifth embodiment>

In the above embodiments, 5-30 parts by weight of a hydroxyl group, a carboxylic acid group or a phosphoric acid group, a sulferic acid group, an amide group-containing monomer in an unsaturated monomer component of the constituent of the emulsion resin (A), an acrylate or Aqueous resin composition for aluminum surface corrosion inhibitor PCF which contains 70-95 weight part of methacrylate monomers or its derivative monomer, and was manufactured by emulsion-polymerizing using a nonionic emulsifier or an anionic emulsifier individually or in mixture.

Sixth Embodiment

In the above embodiments, the nonionic emulsifier, which is one of the constituent monomer components of the emulsion resin (A), may include an alkylphenol ethoxylate, an aliphatic alcohol ethoxylate system, or a derivative thereof having 8 to 100 moles of ethylene oxide; Aqueous resin for aluminum surface anticorrosive PCF prepared by using 1 to 10 parts by weight of an alkyl sulphate, an ether sulphate, a phosphate ester, a sulfonate, a sulfoxysinate-based derivative or a mixture of 1 to 10 parts by weight or more thereof. Preparation of the composition.

<Seventh embodiment>

In the above embodiments, a carboxylic acid group as an acrylic resin or a monomer which reacts with an epoxy resin of bisphenol A type having an equivalent of 450 to 4,000 of an epoxy resin which is one of the constituents of the monomer (acrylic resin) modified epoxy resin (B). Aqueous resin composition for aluminum surface anticorrosive PCF prepared by using 2 to 10 parts by weight of an unsaturated monomer having at least one or more functional groups in a phosphoric acid group and a sulferic acid group.

Eighth Embodiment

In the above embodiments, the solids weight ratio of the epoxy resin and the unsaturated monomer (acrylic resin) is in the range of 20/80 to 90/10, and consists of a graft polymerization of the monomer or an esterification reaction with the acrylic resin. The aqueous resin composition for aluminum surface anticorrosive PCF whose monomer glass transition temperature is -10 degreeC-90 degreeC.

<Ninth Embodiment>

In the above embodiments, 3 to 8 parts by weight of 100 parts by weight of the DMBA (DMBA) or DMPA (DMPA) in order to facilitate the water dispersion is used, aromatic (toluene diisocyanate) or ali An aqueous resin composition for an aluminum surface anticorrosive PCF obtained by introducing a partic (isophorone diisocyanate) isocyanate group to proceed with a urethane reaction, neutralizing with an amine, and dispersing in ion-exchanged water with high-speed stirring.

Tenth Embodiment

In the above embodiments, a styrene-acrylic resin or pure water containing a hydroxyl group or an acid group alone or in a mixture of components of the water-soluble acrylic resin (D) and having a molecular weight of 2000 to 20000 and a glass transition temperature of -20 ° C to 60 ° C. Aqueous resin composition for aluminum surface corrosion-resistant PCF which consists of acrylic resins.

<Eleventh embodiment>

An aluminum coating coating the aluminum surface anticorrosive prepared by the above embodiments, baking the coating, and repainting the hydrophilic agent, characterized by facilitating adhesion and hydrophilic sustainability when painting the hydrophilic agent. Aluminum seal.

<Example>

Hereinafter, the present invention will be described in more detail with reference to Preparation Examples and Comparative Examples. In each example, "parts" and "%" depend on weight basis in principle.

Preparation Example 1 Preparation of Emulsion Resin (A)

600 g of ion-exchanged water, 2 g of sodium lauryl sulfate, 2 g of sodium bicarbonate as a buffer, and 3 g of 40 mol of octyl phenol ethylene oxide were added to the reaction vessel (reaction part), and then the reaction temperature was raised to 70 ° C. Was stirred uniformly to dissolve completely. 20 g of methyl methacrylate monomer, 140 g of styrene monomer, 100 g of butyl monomer, 97 g of methyl methacrylate monomer, 40 g of 2-hydroxy methyl methacrylate monomer, and 3 g of N-methylol acrylamide were added to the dropping tank and stirred uniformly. It was.

10% of the mixed monomers were injected into the reaction unit at 70 ° C, and 0.3 g of APS (ammonium persulfate) was injected to initiate an initial reaction. After heating to 80 ° C. for 10 minutes, the remaining mixed monomer 90% was added dropwise for 3 hours, and then maintained for 1 hour 30 minutes. Cooling to 50 ° C. or less, adjusting the pH to 7-9 with ammonia water, filtering through a 200 mesh filter network, and having a solid content of 99.5% yield, an emulsion resin for corrosion resistance having a mean particle size of 120 nm and a number average molecular weight of 100,000. )

Preparation Example 2 Preparation of Monomer Modified Epoxy Resin (B)

200 g of bisphenol A modified epoxy resin having an epoxy equivalent of 3000 was added to 80 g of a butyl cellosol moiety, and the temperature was raised to 120 ° C to 130 ° C, and maintained until the epoxy resin was completely dissolved. 20 g of methyl methacrylic acid, 20 g of styrene monomer, and 10 g of acrylate monomer were mixed with 2 g of benzoyl peroxide and completely dissolved in the monomer dropping tank, followed by dropwise addition at 120 ° C. for 1 hour, followed by 1 g of benzoyl peroxide at 30 minute intervals. Divided and injected. After maintaining the reaction at 120 ℃, cooled to 70 ℃ and injected with TEA (triethylamine) so that the pH is 7 to 9, and after maintaining for 30 minutes, 740 g of ion-exchanged water is slowly injected to denature the monomer of 25% solids An epoxy resin was obtained. A water-soluble monomer-modified epoxy resin having an average particle diameter of 200 nm and a number average molecular weight of 100,000 µm filtered through a 5 µm guno filter was obtained.

Preparation Example 3 Preparation of Water-Soluble Urethane Resin (C)

267 g of neoffinyl glycol, 293 g of isophthalic acid, 74 g of adipic acid, and 0.2 g of a catalyst (di-n-butyltin oxide) were added to the reaction vessel, followed by heating and stirring, followed by an esterification half while removing the resulting water. The resin with an average molecular weight of 2500 and a hydroxyl value of 56 mg KOH / g and an acid value of 0.5 mg KOH / g was obtained. The obtained resin was diluted with MEK (methyl ethyl ketone) to obtain a polyester polyol resin solution having a solid content of 60%. 80 g of DMBA was added thereto, the temperature was raised to 80 ° C., and completely dissolved. 95 g of TDI (toluene diisocyanate) was dripped over 3 hours, and it confirmed that there was no unreacted NCO after holding for 2 hours at 85 degreeC. 95% or more of the MEK solvent was recovered at the same temperature, and neutralized by adding a TEA neutralizing agent at 60 ° C. or lower, and then ion-exchanged water was injected to prepare a water-soluble urethane resin (C) having a solid content of 35%.

Preparation Example 4 Water-Soluble Acrylic Resin (D)

300 g of butylcarbitol was added to the reaction unit, and the temperature was raised to 103 ° C. In the dropping tank, 54 g of methyl methacrylate monomer, 102 g of methyl methacryl monomer, 90 g of butyl methacrylate monomer, 18 g of 2-hydroxyethyl acrylic monomer, 36 g of 2-ethylhexyl acryl monomer and 6 g of benzoyl peroxide were mixed into a uniform solution. After making, it was dripped at 103 degreeC for 2 hours and 30 minutes, and 3 g of benzoyl peroxides were injected over 4 times over 2 hours. After the temperature was raised to 105 ° C. and maintained for 1 hour, the pH was adjusted to 7-9 with TEA (neutralizing agent) at 60 ° C. or lower, and diluted with ion-exchanged water to obtain a water-soluble acrylic resin (D) having a solid content of 35%. Phosphorus resin solution was obtained.

Example 1 Coating Composition for Aluminum Corrosion Resistant

800 g of the monomer-modified epoxy resin (B) and 2830 g of ion-exchanged water were added to a reaction unit equipped with a stirrer, and uniformly mixed with 3800 g of the emulsion resin (A) obtained in Production Example 1, as a water-soluble phenol resin, Hitanol 7700 (Hitachi Co., Ltd.) 1000 g and 100 g of dimethylethanolamine were added and stirred for 30 minutes in order to make the aqueous dispersion more effective. 20 g of BYK019 (foaming agent) and BYK380 (leveling agent) were respectively injected, and 150 g of the antimicrobial agent zinc-odine 100 (Archi Chemical Co., Ltd.) was injected and stirred uniformly for 30 minutes. 500 g of butyl cellosol and 230 g of LEVANYL BR-LF-50 (Bayer) were added and stirred for 2 hours, and the mixture was lightly stirred at 25% solids, having a viscosity of 15 seconds (pode cup # 4, 25 ° C.) and a pH 8 with a pale blue color. An aqueous coating composition for aluminum corrosion inhibitors was obtained.

<Example 2>

5900 g of the monomer-modified epoxy resin (B) obtained in Preparation Example 2 was uniformly mixed with 800 g of water-soluble acrylic resin (D) and 2500 g of ion-exchanged water, and 500 g of water-soluble melamine resin Cymel 303 (Cytec) and a neutralizer tree for water dispersion. 80 g of ethylamine was added thereto, followed by stirring for 30 minutes. 15 g of Formex 8020 (Degu) and 20 g of Supinol 104H (Air Product) were injected and maintained for 30 minutes while lowering the stirring speed. Then, 250 g of LEVANYL BR-LF-50 (Bayer) was added and stirred uniformly for 2 hours. . As a result, a light blue aqueous anticorrosive composition for light blue aluminum having a solid content of 23% and a viscosity of 18 seconds (pode cup # $, 25 ° C) and a pH of 8.5 was obtained.

<Example 3>

4290 g of ion-exchanged water was added to the reaction unit, 2000 g of the water-soluble urethane resin (C) obtained in Production Example 3 and 1900 g of the emulsion resin (A) obtained in Production Example 1 were added and mixed uniformly. 750 g of water-soluble melamine resin Cymel 325 (Cytech Co., Ltd.) and 120 g of 2-amino 2methyl propanol were added thereto, followed by uniform stirring for 30 minutes. 15 g of BYK019 (foaming agent) and 15 g of BYK184 (dispersant) were gradually injected while stirring, followed by stirring for 30 minutes. 250g of LEVANYL G-LF-50 (by Bayer) was added thereto, followed by uniform stirring for 2 hours. As a result, a pale green water-based aqueous coating composition having a solid content of 25% and a viscosity of 15 seconds (pode cup # 4, 25 ° C) and pH 8.2 was obtained.

<Example 4>

To 3900 g of the water-soluble urethane resin (C) obtained in Production Example 3, 800 g of the water-soluble acrylic resin (D) obtained in Production Example 4 and 3500 g of ion-exchanged water were uniformly mixed, and 500 g of water-soluble benzoguanamine resin Cymel 1123 (Cytech Co., Ltd.) 80 g of neutralizing agent triethylamine for water dispersion was added and stirred for 30 minutes. 20 g of BYK020 (defoamer) and 20 g of BYK184 (dispersant) are injected and stirred for 30 minutes. 200g of LEVANYL G-LF-50 (by Bayer) was added and stirred uniformly for 2 hours. As a result, an aqueous coating composition for light green aluminum corrosion resistant materials having a solid content of 25% and a viscosity of 18 seconds (pode cup # $, 25 ° C) and pH 8.0 was obtained.

Comparative Example 1

The following paint compositions were prepared to compare long term corrosion resistance and interlayer adhesion.

120 g of propylene glycol, 1050 g of neopentyl glycol, 2900 g of isophthalic acid, 730 g of adipic acid, and 3.0 g of a polymerization catalyst (dibutyltin oxide) were added to the reaction vessel, followed by heating and stirring, and the esterification reaction was carried out while removing the resulting water. When the acid value of the resulting product is 1.0 mg KOH / g or less, the mixture is cooled and the acid value is adjusted to 45 mg KOH / g or less while adding 470 g of trimellitic hydride at a temperature of 130 ° C. or lower and heating up to 180 ° C. 3400 g of cellosol parts and 250 g of dimethylethanolamine were added to obtain a water-soluble polyester resin solution having a solid content of 60%.

Next, 1000 g of the water-soluble polyester resin solution was added to a reactor containing 3600 g of ion-exchanged water, mixed uniformly, and 700 g of water-soluble melamine resin Cymel 303 (Cytech Co., Ltd.) and 60 g of dimethylethanolamine were gradually injected. Stir for minutes. 20 g of BYK020 (foaming agent) and 20 g of BYK184 (dispersant) were injected and 200 g of LEVANYL G-LF-50 (Bayer) was added and stirred for 2 hours, followed by 25% solids and a viscosity of 16 seconds (Pod Cup # 4, 25). C)), a light green aqueous coating composition for aluminum corrosion inhibitors having a pH of 8.0 was obtained.

Test Example 1 Performance Test of Aluminum Corrosion Resistant Composition

The compositions of the respective aqueous corrosion inhibitors obtained in Examples 1 to 4 and Comparative Example 1 were roll-coated on an aluminum plate having a purity of 98% or more with a thickness of 0.1 to 0.2 mm so that the dry coating amount was 1.2 g / m 2, and 240 ° C. (aluminum surface temperature). The coating film performance test was carried out using a coating plate cured by baking for 20 seconds in the).

(Test Methods)

1. Workability: After cutting the coated plate to the size of 150mm in width 100mm 후, fold the contact angle to 0 degrees, rub the bent part with Scotch tape, rub it, remove it, and measure the peeling degree.

2. MEK rubability: After cutting the paint plate to the size of 100mm × 150mm in length, prepare gauze, apply MEK (MK) solvent, rub it until the coated paint shows aluminum plate, and measure the number of times. Was done.

3. Adhesiveness: 100 grids were drawn on the coated aluminum plate at 1mm intervals and made 100 grids, rubbed with strong adhesive tape and rubbed.

4. Water resistance: In order to measure the water resistance of the applied paint, cut the coated aluminum plate to the size of 100mm × 100mm in width × length, measure the weight, and leave it at 80 ℃ ion-exchanged water for 3 hours to change the weight and appearance. The swelling phenomenon was measured and evaluated.

5. Salt water spray resistance: According to the experimental standard of KS D95002, after the continuous spray for 500 hours continuous spraying, the appearance phenomenon of the coating surface was measured and evaluated.

6. Interlayer adhesion: The hydrophilic agent was coated and coated on the aluminum plate so that the dry coating amount was 0.4 g / m 2, and evaluated by measuring workability and hydrophilic persistence after drying. The workability was evaluated by the test method 1, and the hydrophilic persistence was evaluated by measuring the contact angle by 300 cycles of 10 minutes drying after 1 immersion of specimens in ion-exchanged water at room temperature.

7. Heat resistance: The coating plate was cut into a size of 100 mm x 150 mm, and then left in a 200 ° C. oven for 48 hours to measure appearance by visual comparison with the standard plate.

For reference, the hydrophilic agent was SPR-2000 (Samhwa Paint Co., an aqueous product) and the heat curing temperature was evaluated as 240 ℃.

The results obtained in Table 1 are shown.

Example Comparative example One 2 3 4 One Machinability 5 5 5 5 5 MEK rub Episode 17 18 times 18 times Episode 17 Episode 17 Adhesion 100/100 100/100 100/100 100/100 100/100 Water resistance 5 5 5 5 3 Salt water spray resistance R.N 9.5 or higher R.N 9.5 or higher R.N 9.5 or higher R.N 9.5 or higher R.N 9.0 or later Interlayer adhesion 5 5 5 5 4 Heat resistance 5 5 5 5 4

For reference, the numbers in Table 1 are expressed in the order of (excellent) 5 points> 4 points> 3 points> 2 points> 1 point (bad).

As shown in Table 1, the anticorrosive composition according to the present invention can be seen that not only excellent in water-resistant saline spray resistance compared to the composition of Comparative Example 1 but also excellent in interlayer adhesion and heat resistance.

The aqueous aluminum surface anticorrosive composition of the present invention uses an emulsion resin (A), a monomer (acrylic resin) modified epoxy resin (B), a water-soluble urethane resin (C), and a water-soluble acrylic resin (D) alone or in combination, and a curing agent. As a composition prepared by mixing at least one of an aqueous melamine resin, an aqueous phenolic resin, and an aqueous benzoguanamine resin, it is very useful as an aqueous composition for aluminum surface corrosion inhibitors because it forms a coating film excellent in corrosion resistance and processability.

Claims (14)

60 to 99% by weight of at least one resin selected from the group consisting of an emulsion resin (A), a monomer-modified epoxy resin (B), a water-soluble urethane resin (C), and a water-soluble acrylic resin (D); And 1 to 40% by weight of at least one curing agent selected from the group consisting of an aqueous melamine resin, a resol-type aqueous phenol resin and an aqueous benzoguanamine resin; Anticorrosive composition characterized in that it contains The emulsion resin (A) is prepared by polymerizing an unsaturated monomer having a number average molecular weight of 30,000 to 200,000, a hydroxyl value of 10 to 120 mg KOH / g, and an acid value of 30 to 85 mgKOH / g. And a styrene-acrylic copolymer emulsion resin or a pure acrylic emulsion resin having a glass transition temperature (Tg) of -20 to 60 ° C. The method of claim 1, wherein the monomer-modified epoxy resin (B) is esterified polymerization of a bisphenol A modified epoxy resin having an epoxy equivalent of 450 to 4000 with an acrylic resin or a styrene-acrylic copolymer resin resin containing a functional unsaturated monomer, Or a resin prepared by graft polymerization of the unsaturated monomer on the bisphenol A modified epoxy resin is dispersed in an aqueous medium. The water-soluble urethane resin (C) according to claim 1, wherein DMMP or DMBA is introduced into a polyester polyol or polyether polyol having a molecular weight of 200 to 3000 using an amphoteric solvent. And a water-soluble urethane resin obtained by introducing an isocyanate group to the urethane reaction and then adding a neutralizing agent to disperse the water. The styrene-acrylic resin or acrylic resin according to claim 1, wherein the water-soluble acrylic resin (D) has a molecular weight of 2000 to 20,000 and a glass transition temperature (Tg) of -20 to 60 ° C. Anticorrosive composition, characterized in that it comprises at least 5 to 40 parts by weight of the monomer. 3. The unsaturated monomer according to claim 2, wherein the unsaturated monomer contains 5 to 30% by weight of a monomer containing a hydroxyl group, a carboxyl group, a phosphoryl group, a sulfonyl group, and an amide group, and an acrylate or methacrylate monomer or An anticorrosive composition comprising as much as 70 to 95% by weight of a derivative monomer. 6. The monomer according to any one of claims 2, 3 and 5, wherein the monomer is acryl acid, metaacrylic acid, fumaric acid, maleic acid, itaconic acid as a carboxyl group-containing monomer, and 2-hydroxyl as a monomer-containing monomer. Chill (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxyamyl (meth) acrylate, 2-hydroxy-3-phenoxy propylate, 2-hydroxy butyl (meth) acrylic Alkyl ester carbon number as a latex, 2-acryloyloxy ethyl 2-hydroxy ethyl phthalate, 3-chloro-2-hydroxy propyl methacrylate, 2-hydroxy hexyl (meth) acrylate acrylic or methacrylate monomer Methyl methacrylate of 1 to 18, ethyl methacrylate, n-butyl methacrylate, lauryl methacrylate alkyl ester Acrylate having 1 to 18 carbon atoms Surmethyl acrylate, ethyl acrylate, n-butyl acrylate, lauryl acrylate Aromatic vinyl monomers, styrene monomer, alpha methyl styrene monomer, vinyl toluene monomer Functional monomers, glycidyl methacrylate monomer, 2-methacryl Loyloxyethyl phosphate monomers and derivatives thereof, N-metholacryl amide monomers or derivatives thereof, 2-acrylamido-2 methylpropanesulfonic acid monomers and derivatives thereof, trifluoroethyl methacrylate monomers and derivatives thereof, A phenoxy ethyl acrylate monomer and derivatives thereof, and a 2-acryloyloxy ethyl rosinate monomer and a derivative thereof. The anticorrosive composition according to claim 1, wherein the anticorrosive composition comprises alkylphenol ethoxylates, aliphatic alcohol ethoxylates as nonionic emulsifiers, sodium lauryl sulfate, ammonium lauryl sulfate, sodium 2-ethylhexyl sulfate and Alkyl sulfates including sodium tridecyl sulfate, ether sulfates including sodium tridecyl ether sulfate, phosphate esters including aromatic phosphate esters and aliphatic phosphate esters, sodium dodecyl benzene sulfonate, sodium alpha olefin sulfonate And sulfonates comprising disodium alkyldiphenyl oxide sulfonate, sodium alkylether sulfosulcinate, and sulfouccisinate including sodium nonylphenyl ether sulforuccinate. Characteristic Anticorrosive composition which consists of. The anticorrosive composition according to claim 3, wherein the ratio of the epoxy resin and the acrylic resin and the ratio of the epoxy resin and the monomer are in a weight ratio of 2: 8 to 9: 1. The anticorrosive composition of claim 4, wherein the amount of DMPA or DMBA is included in an amount of 3 to 8 parts by weight based on 100 parts by weight of the resin. The anticorrosive composition according to claim 1, further comprising 0.1 to 5.0 parts by weight of an antimicrobial agent or an antifungal agent, or 0.1 to 5.0 parts by weight of an organic or inorganic pigment as a colorant. The anticorrosive composition according to claim 1, wherein the anticorrosive composition is for aluminum coating. In corrosion-resistant coating method of aluminum, The coating of the anticorrosive composition according to any one of claims 1 to 12 is coated on aluminum and the coating is baked, and the baking temperature is 230 to 250 ° C. and a speed of 40 to 90 m / min by a roll operation. Coating method, characterized in that the dry coating amount is 0.8 to 1.6 g / m 2. The coating method according to claim 13, wherein the hydrophilic agent is recoated as a top coat on the dry coating film of the corrosion resistant composition.