KR19980061684A - Photocurable coating film composition excellent in heat resistance and adhesion - Google Patents

Abstract

The present invention is a photocurable coating film composition excellent in heat resistance and adhesion, specifically 10 to 60 parts by weight of melamine acrylate, 10 to 50 parts by weight of polyfunctional acrylate containing a hydroxyl group, 10 to 60 parts by weight of non-reactive resin, reactive It is characterized by containing 10 to 60 parts by weight of monomer, 0.1 to 20 parts by weight of photoinitiator, 0.1 to 10 parts by weight of acid catalyst, 0.1 to 5 parts by weight of leveling agent and a small amount of additive.

The coating composition according to the present invention improves the adhesiveness by using the melamine acrylate, which enables simultaneous curing of heat and ultraviolet rays, and reduces the shrinkage rate, and the reaction of the polyfunctional acrylate containing melamine and hydroxyl groups in the heat curing process. The heat resistance was improved by introducing an unsaturated group through increasing the crosslinking density during UV curing.

Description

Photocurable coating film composition excellent in heat resistance and adhesion

The present invention relates to a photocurable coating composition having excellent heat resistance and adhesion, and more particularly, to a melamine acrylate, a polyfunctional acrylate containing a hydroxyl group, an unreactive resin, a reactive monomer, a photoinitiator, an acid catalyst, a leveling agent, and an additive. Heat-resistant plastic molded articles such as fiber-reinforced plastic (FRP), polybutylene terephthalate (PBT), polyamide (nylon-66), polyphenylene oxide (PPO), or polyphenylene sulfide (PPS) That is, the present invention relates to a photocurable coating composition which is coated on automobiles, electrical / electronics, and other industrial articles to improve the appearance, durability, heat resistance, and other physical properties of molded articles.

Metal vacuum deposition film of automobile lamps reflector and the surface of electronic parts and industrial products requiring heat resistance are coated with metal coating film through undercoat to improve the glossiness of deposited film and increase reflection efficiency.

Conventionally, as such a coating material, a thermosetting paint containing an acrylic thermosetting resin and a silicone resin has been mainly used. However, these thermosetting paints have to be exposed to heat for a long time in order to form a coating film, so that the yield decreases, and the high temperature adversely affects the physical properties such as adhesion, heat resistance, and water resistance of the plastic molded article, and also, there is a problem in operation during coating. Was raised.

In order to solve the above problems, a conventional coating film (paint) composition containing a photocurable oligomer, for example, Korean Patent No. 73183, No. 74985, KCC Application No. 95-68614, US Patent No. 3,782,061, No. 3,850,770 , 3,891,523, 3,907,574, 3,932,356 and 4,301,209, Japanese Patent Nos. 59-117,561, 63-221,119, but the physical properties such as heat resistance, water resistance, chemical resistance, etc. are insufficient. In particular, it was difficult to apply to electronic parts and industrial plastic molded parts requiring heat resistance.

SUMMARY OF THE INVENTION An object of the present invention is to provide a photocurable coating composition having excellent heat resistance and adhesion that is coated on a heat-resistant plastic molded article, ie, automotive, electric / electronic, and other industrial articles to improve the appearance, durability, heat resistance, and other physical properties of the molded article. have.

The photocurable coating composition having excellent heat resistance and adhesion for achieving the object of the present invention is composed of melamine acrylate, a polyfunctional acrylate containing a hydroxyl group, a reactive monomer, a non-reactive resin, a photoinitiator, and the like. The rate allows simultaneous curing of heat and ultraviolet rays, which reduces the curing shrinkage rate, thus improving adhesion and introducing unsaturated groups through the reaction of polyfunctional acrylates containing melamine and hydroxyl groups in the heat curing process. This is improved.

In the present invention, those represented by the following formula (1) and (3) are used as melamine acrylate.

In Formula 1, R ₁ is hydrogen or an alkyl group, n is a number between 0 and 6, and R ₂ is represented by the following formula (2).

In Formula 2, R ₃ is hydrogen or a methyl group, m is a number between 1 and 6.

In Formula 3, R ₁ is hydrogen or an alkyl group, n is a number between 0 and 6, and R ₄ is hydrogen or a methyl group.

Melamines usable in formulas (1) and (3) include hexamethylolmelamine, hexamethoxymethylolmelamine, hexabutoxymethylolmelamine, monomethoxymethylolmelamine, monobutoxymethylpentamethylolmelamine, dimethoxymethyltetramethyl Olmelamine, dibutoxymethyltetramethylolmelamine, trimethoxymethylpropanemethylolmelamine, tributoxymethylpropanemethylolmelamine, tetramethoxymethyldimethylolmelamine, tetrabutoxymethyldimethylolmelamine, pentamethoxymethyl mono Methylolmelamine, pentabutoxymethylmonomethylolmelamine and the like.

Examples of the monofunctional acrylate containing a hydroxyl group represented by Formula 2 include hydroxy ethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl acrylate, hydroxypropyl methacrylate, hydroxybutyl acrylate and hydroxybutyl Methacrylate, hydroxypentyl acrylate, hydroxypentyl methacrylate, hydroxyhexyl acrylate, hydroxyhexyl methacrylate and the like.

In addition, acrylamide, methacrylamide, and the like may be used as the amide reacting with melamine in the formula (3).

Melamine acrylate of Formula 1 and Formula 3 is a monofunctional acrylate or amide containing a melamine and a hydroxyl group by applying a molar ratio of 1: 0 to 6, an acid catalyst and a polymerization inhibitor are reacted at a temperature of 90 ~ 100 ℃ unsaturated It is obtained by introducing a double bond and removing by-products under vacuum conditions at the completion of the reaction.

The appropriate reaction ratio of the melamine acrylate synthesized in the present invention is preferably a molar ratio of melamine: acrylate or amide 1: 2 to 1: 4.

If it is applied less than 1: 2, the curing property at the time of ultraviolet curing is poor, and the application name adhesion is poor at 1: 4 or more. This melamine acrylate resin is used in 10 to 60 weight% of a coating composition.

The melamine acrylate resin as described above is reacted with a polyfunctional acrylate containing a hydroxyl group for 5 to 20 minutes at 100 to 150 ℃ and the acid catalyst blocked before the ultraviolet curing reaction when applied to the paint. At this time, as the polyfunctional acrylate containing a hydroxyl group, trimethylolpropanediallyl ether, pentaerythritol triallyl ether, trimethylolpropane diacrylate, trimethylolpropane dimethacrylate, triethylolpropane diacrylate, triethylol Propane dimethacrylate, glycerol diacrylate, glycerol dimethacrylate, pentaerythritol triacrylate, pentaerythritol trimethacrylate, dipentaerythritol pentaacrylate, dipentaerythritol pentamethacrylate, etc. It can be used at -50% by weight. If it is used at less than 10% by weight, the adhesion and heat resistance is poor according to the change over time, and if more than 40 parts by weight is used, the paint viscosity is high and workability is poor.

The present invention uses a non-reactive resin in 10 to 60% by weight of the coating film composition to improve adhesion to the base material and the metal film. Alkyd resins, acrylic resins, polyvinylbutylal resins, polyvinyl chloride-polyvinylacetate copolymer resins, and cellulose acetate butyrate resins having good compatibility with the compounds used in the present invention can be used. Especially when the alkyd resin is used, the adhesion is greatly improved. As the alkyd resin in the present invention, a fatty acid and a polyfunctional alcohol are generally prepared by condensation reaction using a suitable catalyst at a temperature of 190 to 250 ° C. The fatty acids used in the preparation of alkyd resins include abietic acid, benzoic acid, p-butylbenzoic acid, caproic acid, caprylic acid, capric acid, castor fat acid, coconut fat acid, 2-ethylhexoic acid, lauric acid , Lyoic acid, linoleic acid, oleic acid, ferragonic acid, soya bean fat acid, tall oil fat acid, adipic acid, crorendic acid, fumaric acid, isophthalic acid, phthalic acid, phthalic hydride, Polyfunctional alcohols include ethylene glycol, propylene glycol, 1,3-butylene glycol, pentanediol, neopentyldiol, hexylene glycol, diethylene glycol, dipropylene glycol, triethylene glycol, glycerol, glycerin, trimethylol Ethane, triethylolpropane, trimethylolpropane, pentaerythritol, dipentaerythritol, sorbitol and the like can be used.

After the thermosetting process, the melamine acrylate resins of Formulas 1 and 3 are UV cured by conventional photoinitiators together with polyfunctional acrylates and reactive monomers.

Reactive monomers usable here include 1,6-hexanediol diacrylate, triphenylglycol diacrylate, butanediol diacrylate, 1,3-butylene glycol dimethacrylate, 1,6-hexanediol diol Methacrylate, neopentyl glycol diacrylate, ethylene glycol dimethacrylate, diethylene glycol diacrylate, diethylene glycol dimethacrylate, triethylene glycol diacrylate, polyethylene glycol dimethacrylate, polyethylene glycol di Bifunctional monomers such as methacrylate, dipropylene glycol diacrylate, methoxylated neopentylglycol diacrylate, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, pentaerythritol triacrylate, Ethoxylated Trimethylol Propane Triacrylate, Propylated Trimethylol Trifunctional monomers such as propane triacrylate, glycerylpropylated triacrylate, tris (2-hydroxyethyl) isocyanurate triacrylate, pentaerythritol tetraacrylate, alkoxylated tetraacrylate, and the like. One or more polyfunctional monomers may be used, and the amount thereof is preferably 10 to 60% by weight of the coating composition in consideration of the cured product properties.

As the photoinitiator, conventional polymerization initiators activated by ultraviolet rays are used, and in particular, benzophenone series, benzyldimethyl ketal series, acetophenone series, adrakunone series, thioxanthone series, acylphosphine oxide series, and aminoalkylphenone series 2-hydroxy 1,2-diphenylethanone, 2-ethoxy 1,2-diphenylethanone, 2-isopropyl 1, such as a hydroxyalkyl phenone type, dialkoxy acetophenone type, and a benzyl ketal type, 2-phenylethanone, 2-butoxy 1,2-diphenylethanone, 2-isobutoxy 1,2-diphenylethanone, 2,2-dimethoxy 1,2-diphenylethanone, 2,2 -Dibutoxy 1-phenyl ethanone, 1-hydroxycyclohexylphenyl ketone, dimethoxyhydroxyacetophenone, 1- (4-isopropylphenyl) -2-hydroxy 2-methylpropanone, 2-methyl 1- [4- (methylthio) phenyl] -2-morpholinopropanone, 2-benzyl 2-dimethylamino 1- (4-morpholinophenyl) butanone or 3,6 bis [2-methyl] -2- Morpholino (propanoyl) -butylcarbazole The use, and the amount of use thereof is preferably a coating composition 0.1 to 20% by weight.

The acid catalyst used in the thermosetting reaction uses a blocked type in consideration of paint storage properties. Dinonyl naphthalene sulfonic acid, dinonyl naphthalene disulfonic acid, dodecyl benzene sulfonic acid, paratoluene sulfonic acid, etc. are used as the kind, It is used at 0.1-10 weight% of a coating film composition in consideration of reaction rate.

As a leveling agent, the silicone diacrylate type and silicone polyacrylate type compound are used at 0 to 10 weight% of a coating film composition.

When semi-gloss or matte is required for the coating film composition, the matting agent may be used in an amount of 1 to 10% by weight based on the required gloss.

The painting operation on the plastic molded article is made by spraying, dipping or coating, which can be selected depending on the material of the plastic, the shape of the molded article and the thickness of the coating.

Different viscosity is required depending on the coating method, which can be used by adjusting the viscosity by adding an appropriate amount of volatile solvent. In addition, volatile solvents increase the adhesion of the coating film by giving a chemical impact to the plastic body before curing during painting. In this case, one or two or more kinds of ketones, acetates, aromatic compounds, etc. may be used as the solvent. The usage-amount is used for the varnish / solvent weight ratio as 4/1-1/4.

In addition, as an additive, an antifoamer etc. can be used according to the characteristic of a well-known compound.

Specifically, the coating composition of the present invention is 10 to 60% by weight of melamine acrylate, 10 to 50% by weight of polyfunctional acrylate containing hydroxyl group, 10 to 60% by weight of non-reactive resin, 10 to 60% of reactive monomer, 0.1 to photoinitiator 20 weight%, acid catalyst 0.1-10 weight%, leveling agent 0.1-5 weight%, and a small amount of additives are contained.

Particularly preferred are 20-30% by weight of melamine acrylate, 15-25% by weight of polyfunctional acrylate containing hydroxyl group, 20-40% by weight of non-reactive resin, and reactive monomer in consideration of physical properties such as heat resistance, adhesion and water resistance. 25 to 35% by weight, 4 to 10% by weight photoinitiator, 2 to 8% by weight acid catalyst, 0.5 to 1% by weight leveling agent and a small amount of additives.

As mentioned above, in the present invention, a multifunctional acrylate containing a melamine acrylate and a hydroxyl group and a reactive monomer are used. As the content of the double melamine acrylate and the polyfunctional acrylate increases, the crosslinking density of the coating film increases, thereby increasing heat resistance. And physical properties such as water resistance are good.

Hereinafter, the present invention will be described in detail through examples.

In the following examples, the properties of the photocurable coating composition using melamine acrylate synthesis and synthesized melamine acrylate resin, hydroxyl-containing polyfunctional acrylate, non-reactive resin, reactive monomer are compared with the comparative example to obtain the effect of the present invention. Let's look at it.

Preparation of Melamine Acrylate

Preparation Example 1

In a four-necked flask equipped with a thermometer, 736 parts by weight of hexamethoxymethylolmelamine (MONSANTO, product name: RESIMENE 747), 258 parts by weight of hydroxyethyl acrylate, 1 part by weight of paratoluenesulphonic acid as a reaction catalyst, and a polymerization inhibitor 5 parts by weight of monomethylhydroquinone is added and the reaction is maintained at 90 ° C. At the completion of the reaction, the temperature was raised to 110 ° C. to remove the by-product methyl alcohol through a vacuum apparatus to prepare melamine acrylate.

Preparation Example 2

770 parts by weight of hydrobutoxymethylolmelamine (MONSANTO, product name: RESIMENE 757) and 224 parts by weight of hydroxyethyl acrylate, 1 part by weight of paradoluenesulphonic acid as a reaction catalyst in a four-necked round flask equipped with a thermometer. 5 parts by weight of monomethylhydroquinone as an inhibitor is added and the reaction is maintained at 90 ° C. At the completion of the reaction, the temperature was raised to 110 ° C. to remove butyl alcohol, a byproduct, through a vacuum apparatus, to prepare melamine acrylate.

Preparation Example 3

Hydromethoxymethylolmelamine (MONSANTO, product name: RESIMENE 757) 730 parts by weight, 264 parts by weight of acrylamide, 1 part by weight of paratoluenesulphonic acid as reaction catalyst, monomethyl as polymerization inhibitor 5 parts by weight of hydroquinone is added and the reaction is maintained at 90 ° C. Upon completion of the reaction, the temperature is raised to 110 ° C. to remove the by-product methyl alcohol through a vacuum apparatus to prepare melamine acrylate.

Example 1

350 parts by weight of the melamine atylate synthesized in Preparation Example 1, 210 parts by weight of trimethylolpropane triacrylate (UCB, product name: TMPTA), 120 parts by weight of trimethylolpropane diacrylate, rheology alkyd resin (Korea Chemical, Product name: R1466 using SOYABIN OIL) 45 parts by weight of 1-hydroxycyclohexylphenyl ketone (CIBA-GEIGY, Switzerland, product name: IRGACURE 184) after stirring at 50 ° C., paratoluenesulphonic acid (KING company, product name) : NACURE 2530] 35 parts by weight of silicone polyacrylate (UCB, Belgium, product name: EBECRYL 350), 5 parts by weight of a mixed solvent of methyl ethyl ketone, toluene, and butyl acetate were thoroughly stirred to prepare a photocurable coating composition. .

Example 2

310 parts by weight of melamine acrylate synthesized in Preparation Example 2, 210 parts by weight of trimethylolpropane triacrylate (UCB, product name: TMPTA), trimethylolpropane diacrylate), rheological alkyd resin (Korea Chemical, Product name: R1466 using SOYABIN OIL) 45 parts by weight of 1-hydroxycyclohexylphenyl ketone (CIBA-GEIGY, Switzerland, product name: IRGACURE 184) after stirring at 50 ° C., paratoluenesulphonic acid (KING company, Product name: NACURE 2530) 35 parts by weight, silicone polyacrylate (UCB, Belgium, product name: EBECRYL 350) 5 parts by weight, a mixed solvent of methyl ethyl ketone, toluene, butyl acetate 115 parts by weight was thoroughly stirred to prepare a photocurable coating composition It was.

Example 3

350 parts by weight of the melamine acrylate synthesized in Preparation Example 3, 210 parts by weight of trimethylolpropane triacrylate (UCB, product name: TMPTA), 120 parts by weight of trimethylolpropane diacrylate, rheological alkyd resin (Korea Chemical, product name) : R1466 using SOYABIN OIL) 45 parts by weight of 1-hydroxycyclohexylphenyl ketone (CIBA-GEIGY, Switzerland, product name: IRGACURE 184) after stirring at 50 ° C., paratoluenesulphonic acid (KING company, product name) : NACURE 2530] 35 parts by weight, 5 parts by weight of silicone polyacrylate (Belgium UCB, product name: EBECRYL 350), 75 parts by weight of a mixed solvent of methyl ethyl ketone, toluene and butyl acetate were thoroughly stirred to prepare a photocurable coating composition. It was.

Example 4

350 parts by weight of melamine acrylate synthesized in Preparation Example 1, dipentaerythritol hexaacrylate (Shinjeungchon Chemical Co., Ltd., DPHA) 210 parts by weight, trimethylolpropane diacrylate 120 parts by weight, rheology alkyd resin (Korea Chemical) Product name: R1466 using SOYABIN OIL) 160 parts by weight at 50 ° C. and then 1-hydroxycyclohexyl phenyl ketone (CIBA-GEIGY, Switzerland, product name: IRGACURE 184) 45 parts by weight, paratoluenesulphonic acid (KING) , Product name: NACURE 2530) 35 parts by weight, silicon polyacrylate (Belgium UCB, product name: EBECRYL 350) 5 parts by weight, a mixed solvent of methyl ethyl ketone, toluene, butyl acetate 75 parts by weight after fully stirring the photocurable coating composition Was prepared.

Example 5

350 parts by weight of the melamine acrylate synthesized in Preparation Example 1, 210 parts by weight of 1,6-hexanediol acrylate (Miwon, product name: HDDA), 120 parts by weight of trimethylolpropane diacrylate, rheology alkyd resin (Korea Chemical) Product name: R1466 using SOYABIN OIL) After stirring at 50 ° C, 1-hydroxycyclohexylphenyl ketone (CIBA-GEIGY, Switzerland, product name: IRGACURE 184) 45 parts by weight, paratoluenesulphonic acid (KING , Product name: NACURE 2530) 35 parts by weight, silicon polyacrylate (Belgium UCB, product name: EBECRYL 350) 5 parts by weight, a mixed solvent of methyl ethyl ketone, toluene, butyl acetate 75 parts by weight after fully stirring the photocurable coating composition Was prepared.

Comparative Example 1

Photocurable coating composition was prepared in the same composition, content and method as in Example 1, except that 350 parts by weight of melamine acrylate was replaced with urethane resin (UCB, product name: EB284).

Comparative Example 2

Photocurable coating composition was prepared in the same composition, content and method as in Example 1 except that the rheology-alkyd resin was used by replacing 160 parts by weight of an acrylic resin (ICI, product name: B728).

The photocurable coating composition prepared in the above Examples and Comparative Examples was applied to the metal vacuum deposition of the automobile headlamp reflector to perform a physical property comparison test.

In the physical property test, methyl ethyl ketone (MEK) and toluene, which are mixed solvents, were diluted to 50% by weight in a coating composition for spray coating. Apply a 20 μm thick coating on the fiber-reinforced plastic test piece, which is a headlamp material, by spray coating, and hot-air-dried at 120 ° C. for 10 minutes, and then UV-cured at 800 mJ / cm 2 of curing energy (UV irradiation device: manufactured by American American Violet Corporation). After that, vacuum is deposited on the vacuum degree of 10 to 40 Torr (vacuum deposition machine: manufactured by Hanil). Physical property test results are shown in Table 1.

Comparison table of physical properties according to Examples and Comparative Examples Properties Example 1 Example 2 Example 3 Example 4 Example 5 Comparative Example 1 Comparative Example 2 Heat resistance ○ ○ ○ ○ △ × △ Adhesion 100/100 100/100 100/100 90/100 100/100 80/100 50/100 Hot water resistance 100/100 100/100 100/100 80/100 80/100 60/100 30/100 Chemical resistance Acid resistance ○ ○ ○ ○ ○ △ ○ Alkali resistance ○ ○ ○ ○ ○ △ ○ Saline resistance ○ ○ ○ ○ ○ △ △

In Table 1, the appearance of the coating film after the test was good ○, the development of cracks in the coating film after the test △, the crack and whitening phenomenon occurred in the coating film after the test is indicated by ×.

Physical property test was carried out in the following manner. Heat resistance was measured after 96 hours in the oven at 180 ℃, adhesion was measured by the J D 0202 (JIS D 0202) test method, hot water resistance was measured after 240 hours in hot water 40 ℃ ℃ Measured. In addition, acid resistance among chemical resistance was immersed in 1% sulfuric acid solution at room temperature for 10 minutes, alkali resistance was immersed in 1% sodium hydroxide solution at room temperature for 10 minutes, and salt resistance was measured after 10 minutes in 3% sodium chloride solution at room temperature. It was.

As can be seen in Table 1, when using the melamine acrylate according to the present invention, the heat resistance and water resistance were good compared to those using the urethane acrylate, and the adhesiveness when the alkyd resin was used was better than that when the acrylic resin was used. In addition, when using the multifunctional acrylate in the reactive monomer, the heat resistance and water resistance is better than when using the bifunctional acrylate, but the curing shrinkage rate is large, poor adhesion.

As described in detail above, the coating film composition according to the present invention can improve the adhesion, heat resistance, water resistance, chemical resistance when used in the electrical components and various industrial products and other materials that require heat resistance.

Claims (14)

10 to 60 parts by weight of melamine acrylate, 10 to 50 parts by weight of polyfunctional acrylate containing a hydroxyl group, 10 to 60 parts by weight of non-reactive resin, 10 to 60 parts by weight of reactive monomer, 0.1 to 20 parts by weight of photoinitiator, 0.1 to 20 parts of acid catalyst The photocurable coating film composition excellent in heat resistance and adhesiveness containing 10 weight part, 0.1-5 weight part of leveling agents, and a small amount of additives. The photocurable coating composition of claim 1, wherein the melamine acrylate is a compound represented by Chemical Formulas 1 and 3. [Formula 1] (In Formula 1, R ₁ is hydrogen or an alkyl group, n is a number between 0 and 6, R ₂ is represented by the formula (2).) [Formula 2] (In Formula 2, R ₃ is hydrogen or a methyl group, m is a number of 1 to 6 different.) [Formula 3] (In Formula 3, R ₁ is hydrogen or an alkyl group, n is a number between 0 and 6, and R ₄ is hydrogen or a methyl group.) The melamine used in the preparation of the melamine acrylate is hexamethylolmelamine, hexamethoxymethylolmelamine, hexabutoxymethylolmelamine, monomethoxymethylpentamethylolmelamine, monobutoxymethylmethylol Melamine, dimethoxymethyltetramethylolmelamine, dibutoxymethyltetramethylolmelamine, trimethoxymethylpropamethylolmelamine, tributoxymethylpropamethylolmelamine, tetramethoxymethyldimethylolmelamine, tetrabutoximevetyl A photocurable coating composition having excellent heat resistance and adhesiveness, characterized in that it is one selected from dimethylol melamine, pentamethoxymethyl monomethylolmelamine, and pentabutoxymethylmonomethylolmelamine. The compound of claim 2, wherein R ₂ is hydroxy methyl acrylate, hydroxy methacrylate, hydroxy ethyl acrylate, hydroxy ethyl methacrylate, hydroxy propyl acrylate, hydroxy propyl methacrylate, hydroxy butyl Excellent heat resistance and adhesion properties characterized in that it is one selected from acrylate, hydroxy butyl methacrylate, hydroxyethyl acrylate, hydroxypentyl methacrylate, hydroxy hexyl acrylate, hydroxy hexyl methacrylate Burnable coating composition. The photocurable coating composition according to claim 2, wherein the amide used in the melamine acrylate synthesis of Chemical Formula 3 is acrylamide or methacrylamide. The polyfunctional acrylate containing a hydroxyl group used for thermosetting of melamine acrylate is trimethylolpropanediallyl ether, pentaerythritol allyl ether, trimethylolpropane diacrylate, trimethylolpropane dimethacryl. Rate, triethylol diacrylate, triethylol dimethacrylate, glycerol diacrylate, glycerol dimethacrylate, pentaerythritol triacrylate, pentaerythritol trimethacrylate, dipentaerythritol pentaacrylate, dipenta Photocurable coating composition excellent in heat resistance and adhesion, characterized in that the one selected from erythritol pentamethacrylate. The non-reactive resin according to claim 1, wherein the non-reactive resin is one selected from alkyd resin, acrylic resin, polybutylene butylal resin, polyvinyl chloride-polyvinylacetate copolymer resin, and cellulose acetate butyrate resin. Photocurable coating film composition excellent in properties. The fatty acid used in the synthesis of the alkyd resin is abietic acid, benzoic acid, P-butylbenzoic acid, caproic acid, caprylic acid, capric acid, castor patic acid, coconut fat acid, 2-ethyl. Hexoic acid, lauric acid, rioleic acid, linoleic acid, oleic acid, ferragonic acid, soya fat acid, tall oil fat acid, adipic acid, crorendic acid, fumaric acid, phthalic acid hard hydride, isophthalic acid, isof Polyfunctional alcohol is ethylene glycol, propylene glycol, 1,3-butylene glycol, pentanediol, neopentyldiol, hexylene glycol, diethylene glycol, dipropylene glycol, tri Photocurable with excellent heat resistance and adhesiveness, characterized in that it is one selected from ethylene glycol, glycerol, glycerin, trimethylol ethane, triethylol propane, trimethylol propane, pentaerythritol, dipentaerythritol, and sorbitol Film composition. The method of claim 1, wherein the reactive monomer is 1,6-hexanediol diacrylate, triphenylglycol diacrylate, butanediol diacrylate, 1,3-butylene glycol dimethacrylate, 1,6-hexanedi All dimethacrylate, neopentyl glycol diacrylate, ethylene glycol dimethacrylate, diethylene glycol diacrylate, triethylene glycol dimethacrylate, polyethylene glycol diacrylate, polyethylene glycol dimethacrylate, dipropylene Bifunctional monomer consisting of glycol diacrylate and ethoxylated neopentyl glycol diacrylate, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, pentaerythritol triacrylate, ethoxylated trimethylolpropane Triacrylate, Propylated Trimethylol Propane Triacrylate, Articles With trifunctional monomers composed of serylpropylated triacrylate, tris (2-hydroxyethyl) isocyanurate triacrylate, pentaerythritol tetraacrylate, alkoxylated tetraacrylate, dipentaerythritol hexaacrylate Photocurable coating composition excellent in heat resistance and adhesion, characterized in that at least one selected from the polyfunctional monomers configured. The photoinitiator of claim 1, wherein the photoinitiator is 2-hydroxy 1,2-diperphenylethanone, 2-ethoxy 1,2-diphenylethanone, 2-isopropyl 1,2-phenylethanone, 2-butoxy 1,2-diphenylethanone, 2-isobutoxy 1,2-diphenylethanone, 2,2-dimethoxy 1,2-diphenylethanone, 2,2-dibutoxy 1-phenylethanone, 1 -Hydroxycyclohexylphenyl ketone, dimethoxyhydroxyhacetophenone, 1- (4-isopropylphenyl) -2-hydroxy 2-methylpropanone, 2-methyl 1-4- (methylthio) phenyl]- 2-morpholinopropanone, 2-benzyl 2-dimethylamino 1- (4-morpholinophenyl) -butanone and 3,6-bis [2-methyl-2-morpholino (propanoyl)] -Photocurable coating composition excellent in heat resistance and adhesion, characterized in that the one selected from butyl carbazole. The photocurable coating composition according to claim 1, wherein the acid catalyst is one selected from dinonyl naphthalene disulfonic acid, dinonyl naphthalene sulfonic acid, dodecylbenzene sulfonic acid, and paratoluene sulfonic acid. The photocurable coating composition according to claim 1, wherein a matting agent is further added and used according to the desired gloss when semi-gloss or matte is required for the coating composition. A heat resistant plastic molded article coated with the photocurable coating film composition excellent in heat resistance and adhesion according to claim 1. A metal vacuum deposition molded article of an electric part and an automobile lamp reflector coated with the photocurable coating composition having excellent heat resistance and adhesion according to claim 1.