JP3223460B2 - Coating composition - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION The present invention relates to a method of producing a substrate having abrasion resistance, surface smoothness, heat resistance,
The present invention relates to a coating material composition capable of forming a crosslinked cured film having excellent chemical resistance, durability, weather resistance, and adhesion to a substrate.

[0002]

2. Description of the Related Art Synthetic resin molded products made of polymethyl methacrylate resin, polymethacrylimide resin, polycarbonate resin, polystyrene resin, AS resin, etc. are lightweight and excellent in impact resistance. Not only that, it also has good transparency, and in recent years, it has been widely used as a plastic material for automobiles, such as headlamps, glazing, and instrument covers. However, on the other hand, these synthetic resin molded products have insufficient abrasion resistance on the surface, and are easily damaged by contact, friction, scratching, etc. with other hard objects. Improving the abrasion resistance of the surface is strongly demanded because it significantly reduces the value of the product or renders the product unusable in a short period of time. Further, when used as the above-mentioned automotive material, its weather resistance is also an important performance.

Various methods for improving the disadvantages of such synthetic resin molded articles have been studied in the past,
For example, a coating material composed of a silicone-based or melamine-based resin composition is applied to the surface of a synthetic resin molded product, and is subjected to heat condensation to form a crosslinked film, thereby improving abrasion resistance. There has been proposed a method of forming a crosslinked film by irradiating an active energy ray after applying a resin composition of the formula (JP-A-56-122840).

However, although the abrasion resistance of the surface of the synthetic resin molded article is improved to some extent by these methods, the former method is insufficient in durability against heat shock, hot water and the like and chemical resistance, and the latter method is insufficient. Although the method (1) is excellent in durability and chemical resistance, it is not satisfactory in weather resistance. In particular, when the weather resistance of the synthetic resin molded product of the base material is essentially poor, such as a polycarbonate resin, even though the weather resistance of the surface-hardened coating itself is good, it passed through the coating. The base material itself is deteriorated by active energy rays such as ultraviolet rays contained in sunlight, and the molded product is significantly yellowed, a cured film on the surface is cracked, or the film is peeled off.

[0005]

SUMMARY OF THE INVENTION The present invention has been made in view of the above background, and has as its object to provide abrasion resistance, surface lubrication, heat resistance, chemical resistance, and durability. An object of the present invention is to provide a coating material composition capable of forming a crosslinked cured film having excellent properties, weather resistance and adhesion to a substrate.

[0006]

The present inventors have conducted intensive studies and found that polypentaerythritol having a (meth) acryloyl group and urethane poly (meth) acryle having a radically polymerizable unsaturated double bond. A coating composition containing a specific ratio of a compound, a cyanurate having a (meth) acryloyl group, an ultraviolet absorber, a hindered amine-based light stabilizer and a photopolymerization initiator is applied to a synthetic resin molded article. The present inventors have found that a synthetic resin molded article excellent in wear resistance and weather resistance can be obtained by curing by irradiation with active energy rays, and completed the present invention.

That is, the present invention relates to (A) at least one kind of monomer selected from poly (meth) acrylates of mono- or polypentaerythritol represented by the following general formula (I): ~ 70 parts by weight,

[0008]

Embedded image

Wherein X ₁₁ , X ₁₂ , X ₁₃ , X ₂₂ , X ₂₃ ,
... at least three of X _n2 , X _n3 , and X ₁₄ are CH
₂ = CR-COO- group, the rest being -OH groups. Also,
n is an integer of 1 to 5, and R represents hydrogen or a methyl group. (B) (meth) acrylates containing hydroxyl groups
And isocyanates having two or more isocyanate groups in the molecule.
Urethane reaction product or molecule with anate compound
Isocyanate having two or more isocyanate groups therein
Polyol, polyester or polyamide geo
After reacting the adduct to synthesize the adduct,
A (meth) actone containing a hydroxyl group in a cyanate group
A urethanation reaction product to which relate is added,
At least two radically polymerizable unsaturated doublets in one molecule
At least one urethane poly (meth) acrylate compound having a bond and a molecular weight of 1,000 to 5,000 ,
50 parts by weight, (C) poly [(meth) acryloyloxyalkyl] (iso) cyanurene represented by formula (II) or (III)
G, 5 to 50 parts by weight,

[0010]

Embedded image

[0011]

Embedded image

[0012] (wherein, X _1, X _2, and X ₃ represents an acryloyl group, a methacryloyl group, a hydrogen atom or an alkyl group, at least two of these are (meth) acryloyl group, R _1, R ₂ and R ₃ each represent an oxyalkylene group having 1 to 4 carbon atoms.) (D) an ultraviolet absorber, 2 to 30 parts by weight, (E) a hindered amino ether light represented by the general formula (IV) Stabilizer, 0.1 to 5 parts by weight,

Embedded image (In the formula, R ₄ and R ₅ may be the same or different and represent an alkyl group having 1 to 12 carbon atoms.) (F) Photopolymerization initiator, 0.1 to 10 parts by weight, , A, B, C, D, E and F are 100 parts by weight).

This coating material composition is applied to the surface of a synthetic resin molded article and irradiated with active energy rays to thereby provide abrasion resistance, heat resistance, and chemical resistance having a crosslinked cured film having a thickness of 1 to 30 μm. Thus, a synthetic resin molded article having excellent durability and weather resistance can be obtained. The present invention will be described in detail. First, each component of the coating composition of the present invention will be described.

Regarding the component (A). Component (A), poly (meth) acrylate of mono- or polypentaerythritol, exhibits good polymerization activity upon irradiation with active energy rays and has excellent abrasion resistance having a high crosslinking density. To form a polymer. Therefore, a cured film having excellent wear resistance can be formed on the surface of the base material.

Specific examples of component (A) include pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol tri (meth) acrylate, Dipentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, tripentaerythritol tetra (meth) acrylate Tripentaerythritol penta (meth) acrylate, tripentaerythritol hexa (meth) acrylate, tripentaerythritol hepta (meth) acrylate, tripentaerythritol octa (meth) acrylate Acrylate and the like.

The proportion of the component (A) used is (A) to (F)
The amount is 10 to 70 parts by weight, more preferably 25 to 50 parts by weight, per 100 parts by weight of the total amount of the components. (A) Component amount is 1
If the amount is less than 0 parts by weight, a cured film having sufficient abrasion resistance cannot be obtained. If the amount exceeds 70 parts by weight, cracks are liable to occur in the cured film. Cracks occur. In addition, the heat resistance of the cured film also decreases.

Regarding the component (B). The component (B) is a (meth) acrylate containing a hydroxyl group.
Having two or more isocyanate groups in the relay and the molecule
That isocyanate - urethane reaction raw composition as the door compound, some
Having two or more isocyanate groups in the molecule
Polyol, polyester or polyamide in cyanate
After reacting the diol of the system to synthesize the adduct, the remaining
A hydroxyl group in the isocyanate group
(T) a urethanation reaction product to which acrylate is added
At least two radically polymerizable molecules per molecule
C having a molecular weight of 1,000 to 5,000 having a saturated double bond.
At least one of a urethane poly (meth) acrylate compound;
Is a seed. This urethane poly (meth) acrylate compound
The material is toughness, flexibility, heat resistance and weather resistance of the cured film
It is a component that improves. Urethane poly (meta)
Acrylate, that is, two or more isocyanates in a molecule
Polyols and polyethers areocyanates having a net group
Adduct by reacting steal or polyamide diol
After the synthesis, the remaining isocyanate group is
A (meth) acrylate containing a sil group
The product of the ethane-forming reaction can improve the toughness and flexibility of the cured film.
It is preferable because it can be further improved. In addition, the base of the cured film
From the viewpoint of improving adhesion to materials, these are molecular
A quantity of 1000 to 5000 is used.

Specific examples of the polyisocyanate compound include tolylene diisocyanate, ethylene diisocyanate, 1,2-diisocyanatopropane, 1,3-diisocyanatopropane and 4,4'- Diphenylmethane diisocyanate, xylylene diisocyanate, tetramethyl xylylene diisocyanate, hexamethylene diisocyanate, lysine isocyanate, 4,4'-methylene bis (cyclohexyl) isocyanate, Methylcyclohexane-2,4-diisocyanate, methylcyclohexane-2,6-diisocyanate, 1,3-bis (isocyanatomethyl) cyclohexane, isophorone diisocyanate, trimethylhexamethylene diisocyanate, Tetramethylene diisocyanate, dimer acid diisocyanate, - isocyanatoethyl-2,6
Polyisocyanate monomers such as diisocyanatohexanoate, burettes and trimers thereof, and adducts thereof with various polyols can be given.

The polyol used for the synthesis of the adduct is not particularly limited, and specific examples thereof include ethylene glycol
Propylene glycol, butylene glycol, neopentyl glycol, trimethylolpropane, pentaerythrol, sorbitol, mannitol, glycerin and other alkyl polyols and polyether polyols thereof. And polyester polyols such as polyester polyols and polycaprolactone polyols synthesized from polyhydric alcohols and polybasic acids.

Specific examples of the (meth) acrylate containing a hydroxyl group include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, and 2-hydroxybutyl (meth) acrylate. −
Addition reaction of monoepoxy compounds such as butyl glycidyl ether, 2-ethylhexyl glycidyl ether and glycidyl methacrylate with (meth) acrylic acid in addition to methacrylate, 4-hydroxybutyl (meth) acrylate and the like. Object, polyethylene glycol, polypropylene glyco-
Mono (meth) acrylic acid esters of polycaprolactonediol, and the like.

The reaction between polyisocyanate, various diols and hydroxyl-containing (meth) acrylate is carried out in the presence of a tin-based catalyst such as n-butyltin dilaurate.
The mixture is heated at 60 to 70 ° C. for several hours, using isocyanate groups and hydroxyl groups in substantially equal amounts. Since the reactants generally have a high viscosity, it is preferable to dilute the reactants with an organic solvent or another diluent monomer during or after the reaction.

The proportion of the component (B) used is (A) to (F)
The amount is 5 to 50 parts by weight, more preferably 15 to 35 parts by weight based on 100 parts by weight of the total amount of the components. When the amount of the component (B) is less than 5 parts by weight, a cured film having sufficient toughness and weather resistance cannot be obtained, and the curability in an air atmosphere becomes poor.
If it exceeds 50 parts by weight, the abrasion resistance decreases.

Regarding the component (C). The component (C), poly [(meth) acryloyloxyalkyl] (iso) cyanurate represented by the general formula (II) or (III), exhibits good polymerization activity upon irradiation with active energy rays, Further, it is a component capable of improving the toughness and heat resistance of a cured film without impairing high wear resistance. Specific examples of the component (C) include di (2-acryloyloxyethyl) isocyanurate, tris (2-acryloyloxyethyl) isocyanurate, di (2-acryloyloxypropyl) isocyanurate, and tris ( 2-acryloyloxypropyl) isocyanurate, di (2
-Acroyloxyethyl) cyanurate, tris (2
-Acryloyloxyethyl) cyanurate, di (2-
Acroyloxypropyl) cyanurate, tris (2
-Acryloyloxypropyl) cyanurate and the like. The proportion of the component (C) used is preferably 5 to 50 parts by weight, more preferably 10 to 100 parts by weight of the total amount of the components (A) to (F).
４０40 parts by weight. When the amount of the component (C) is less than 5 parts by weight, a cured film having sufficient toughness and heat resistance cannot be obtained, and when it exceeds 50 parts by weight, abrasion resistance decreases.

Regarding the component (D). The ultraviolet absorber as the component (D) is not particularly limited, and may be used as long as it is uniformly dissolved in the composition and has good weather resistance. However, good solubility and weather resistance to the composition can be used. From the viewpoint of improving effect, a benzophenone-based compound, a benzotriazole-based compound, a phenyl salicylate-based compound, a compound derived from a phenyl benzoate-based compound, and an ultraviolet absorber having a maximum absorption wavelength in the range of 240 to 380 nm is preferable. A benzophenone-based ultraviolet absorber is used because it can be contained in a large amount in the composition, and a benzotriazole-based ultraviolet absorber is used because it can prevent yellowing of a base material such as polycarbonate. Absorbents are preferred. Most preferably, these two types are used in combination.

Specific examples of component (D) include 2-hydroxybenzophenone, 5-chloro-2-hydroxybenzophenone, 2,4-dihydroxybenzophenone,
-Hydroxy-4-methoxybenzophenone, 2-hydroxy-4-octyloxybenzophenone, 4-dodecyloxy-2-hydroxybenzophenone, 2-hydroxy-4-octadecyloxybenzophenone, 2,2'-
Dihydroxy-4-methoxybenzophenone, 2,2 ′
-Dihydroxy-4,4'-dimethoxybenzophenone, phenyl salicylate, p-tert-butylphenyl salicylate, p- (1,1,3,3-tetramethylbutyl) phenyl salicylate, 3-hydroxyphenylbenzoate Ethate, phenylene-1,3-dibenzoate
G, 2- (2-hydroxy-5'-methylphenyl) benzotriazole, 2- (2-hydroxy-5-ter
t-butylphenyl) -5-chlorobenzotriazo-
2- (2-hydroxy-3,5-di-tert-butylphenyl) benzotriazole, 2- (2-hydroxy-5-tert-butylphenyl) benzotriazole, 2- (2-hydroxy-4 -Octylphenyl)
Benzotriazole and the like, among which,
Benzophenone 2-hydroxy-4-octoxybenzophenone and 2,4-dihydroxybenzophenone, benzotriazole 2- (2-hydroxy-5)
-Tert-butylphenyl) benzotriazole is particularly preferred, and these are more preferably used in combination of two or more.

The proportion of the component (D) used is (A) to (F)
It is 2 to 30 parts by weight, more preferably 5 to 15 parts by weight based on 100 parts by weight of the total amount of the components. When the amount of the component (D) is less than 2 parts by weight, the weather resistance of the cured film and the protection of the base material from ultraviolet rays are not sufficient. The toughness, heat resistance, and wear resistance decrease.

Regarding the component (E). As the (E) component, a hindered amino ether light stabilizer represented by the general formula (IV), bis (1-methoxy-2,2,6,6-tetramethyl-4-piperidyl)
Sebacate, bis (1-ethoxy-2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1-
Propoxy-2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1-butoxy-2,2,2)
6,6-tetramethyl-4-piperidyl) sebacate,
Bis (1-pentyloxy-2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1-hexyloxy-2,2,6,6-tetramethyl-4-piperidyl) sebacate, Bis (1-heptyloxy-2,2,
6,6-tetramethyl-4-piperidyl) sebacate,
Bis (1-octoxy-2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1-nonyloxy-2,2,6,6-tetramethyl-4-piperidyl) sebacate, Bis (1-decanyloxy-2,2,6,6-
Tetramethyl-4-piperidyl) sebacate, bis (1
-Dodecyloxy-2,2,6,6-tetramethyl-4-
Among them, bis (1-octoxy-2,2,6,6-tetramethyl-4-piperidyl) sebacate is particularly preferable. Component (E) is used in an amount of 0.1 to 5 parts by weight, more preferably 0.1 to 5 parts by weight, per 100 parts by weight of the total of components (A) to (F).
It is 5 to 2 parts by weight. When the amount of the component (E) is less than 0.1 part by weight, the weather resistance and durability of the cured film are insufficient, and
If the amount is more than 10 parts by weight, curing of the coating itself becomes insufficient, and the toughness, heat resistance and abrasion resistance of the cured coating decrease.

Regarding the component (F). As the photopolymerization initiator as the component (F), benzoin,
Benzoin monomethyl ether, benzoin isopropyl ether, acetoin, benzyl, benzophenone,
p-methoxybenzophenone, diethoxyacetophenone, benzyldimethylketal, 2,2-diethoxyacetophenone, 1-hydroxycyclohexylphenylketone, methylphenylglyoxylate, ethylphenylglyoxylate, 2-hydroxy- 2-methyl-
Carbonyl compounds such as 1-phenylpropan-1-one; sulfur compounds such as tetramethylthiuram monosulfide and tetramethylthiuram disulfide; and 2,4,6
Acylphosphine oxides such as -trimethylbenzoyldiphenylphosphine oxide. These are used in one kind or in a mixture of two or more kinds. Among these, benzophenone, benzoin isopropyl ether, methylphenylglyoxylate
And benzyldimethylketal is more preferred. Component (F) is used in an amount of 0.1 to 10 parts by weight, preferably 1 to 100 parts by weight of the total of components (A) to (F).
-5 parts by weight. If the amount of the component (F) is less than 0.1 part by weight, the curability will be insufficient, and if it exceeds 10 parts by weight, the cured film will be colored and the weather resistance will be reduced.

The coating composition of the present invention comprises the above (A)
It comprises the components of (B), (C), (D), (E) and (F), and if necessary, an organic solvent, an antioxidant, a yellowing inhibitor, a blueing agent, a pigment, Various additives such as a leveling agent, an antifoaming agent, a thickener, an anti-settling agent, an antistatic agent, and an anti-fogging agent may be contained. The organic solvent is preferably selected and used depending on the type of the base material. That is, when polycarbonate is used as the base material, isobutano-
It is preferable to use a combination of three types of solvents such as alcohol solvents such as alcohol, ester solvents such as n-butyl acetate and diethylene glycol acetate, and cellosolve solvents such as ethyl cellosolve. The use amount of the solvent is preferably 20 to 800 parts by weight based on 100 parts by weight of the coating composition.

The coating composition of the present invention can be applied to a substrate by brush coating, spray coating, dip coating, spin coating, curtain coating, or the like.
It is preferable to apply the coating composition by adding an appropriate organic solvent from the viewpoints of application workability of the coating composition, smoothness and uniformity of the coating, and improvement in adhesion of the cured coating to the substrate. The coating composition of the present invention crosslinks and forms a cured film by irradiation with active energy rays after being applied to a substrate. When the composition is cured by irradiation with active energy rays, the coating composition is coated on a substrate so as to have a thickness of 1 to 50 μm, preferably 3 to 20 μm, and a high-pressure mercury lamp, a metal halide lamp or the like is used. , 100 to 400 nm of ultraviolet light for 1000 to 50
Irradiation is performed so as to be 00 mJ / cm ² . The irradiation atmosphere may be air or an inert gas such as nitrogen or argon.

The coating composition of the present invention can be used for modifying the surface of various synthetic resin molded articles as a base material, and the synthetic resin molded articles have conventionally been used to improve the abrasion resistance and weather resistance. Various kinds of thermoplastic resins and thermosetting resins which are desired can be used. Specifically, polymethyl methacrylic resin, polycarbonate resin, polyester resin, poly (polyester) carbonate resin, polystyrene resin, ABS resin, AS resin, polyamide resin, polyarylate resin,
Polymethacrylimide resins, polyallyldiglycol-carbonate resins and the like can be mentioned. Above all, polymethyl methacrylic resin, polycarbonate resin, polystyrene resin and polymethacrylimide resin are excellent in transparency and strongly required to improve abrasion resistance, so it is particularly preferable to apply the coating material composition of the present invention. It is valid. The synthetic resin molded articles include sheet-shaped molded articles, film-shaped molded articles, and various injection molded articles made of these resins.

[0032]

The present invention will be described in more detail with reference to the following Examples and Comparative Examples. In the examples, “parts” means “parts by weight”. The measurement and evaluation in the examples were performed by the following methods. (1) Appearance of cured film The appearance of the composition after application and curing was visually evaluated. A sample having a smooth and transparent surface was rated as ○, a portion having cloudiness was rated as Δ, and a sample with whitening or clouding was rated as ×. (2) Abrasion resistance A steel wool of ♯000 was attached to the tip of a cylinder having a diameter of 25 mm, and was brought into contact with a horizontally placed sample surface.
After 50 reciprocal abrasions with a load of, the diffuse transmittance (haze value) was measured to determine the abrasion resistance. The criteria for the wear resistance are as follows. …: Increased haze value = 0 to 0.5: almost no scratches Δ: increased haze value = 0.5 to 3.0: slightly damaged. C: Increased haze value = 3.0 or more: Severely damaged.

(3) Adhesion A cross cut reaching the substrate at 1 mm intervals is made in the cured film, 100 cross-cuts of 1 mm ² are made, a cello tape is stuck thereon, and the cross-cut is peeled off. Eyes counted. When no peeling was observed, the number of peels was 1 to 50.
The specimens were evaluated as Δ, and those having 51 to 100 peels were evaluated as ×. (4) Heat resistance The coated plate sample was placed in a 120 ° C. hot air drier for 24 hours.
The appearance change of the cured film was visually observed.が な い indicates no change, △ indicates a small crack, and × indicates a crack on the entire surface of the coated plate. (5) Weather resistance Using a sunshine car bon weather meter (manufactured by Suga Test Instruments, WEL-SUN-HC-B type) weather tester, a cycle of black panel temperature 63 ± 3 ° C., rainfall 12 minutes, irradiation 48 minutes. Tested. 2000 hours, 25
Changes in the cured film after exposure for 00 hours were observed, and the adhesion was tested. (A) Regarding discoloration of the appearance, ○ indicates no discoloration, Δ indicates slight yellowing, and X indicates large yellowing. (B) Regarding the occurrence of cracks and the peeling of the film, 無 indicates that there was no crack and X indicates that it did.

Examples 1 to 5 and Comparative Examples 1 to 5 The coating material compositions were prepared at the compounding ratios shown in Tables 1 and 2, and a polycarbonate resin plate having a thickness of 3 mm (manufactured by GE Corporation, trade name:
Lexan LS-II) was spray-coated so that the cured film had a thickness of 8 μm. After volatilizing the organic solvent by heating, using a high-pressure mercury lamp in air, the wavelength of 340 n
Irradiation was performed at an energy of 3000 mJ / cm ² with an integrated light amount of m to 380 nm to obtain a cured coating film. The evaluation results of the obtained coating film are shown in Tables 1 and 2.

COMPARATIVE EXAMPLE 6 A coating material composition was prepared at the compounding ratio shown in Table 2 and had a thickness of 3 mm.
Of a cured polymethyl methacrylate resin plate (trade name: Acrypet VH, manufactured by Mitsubishi Rayon Co., Ltd.)
It was spray-painted to a thickness of μm. After volatilizing the organic solvent by heating, using a high-pressure mercury lamp in air,
3000mJ integrated light quantity at wavelength 340nm-380nm
/ Cm ² was irradiated to obtain a cured coating film. Table 2 shows the evaluation results of the obtained coating films.

Example 6 , Comparative Example 7 A coating material composition was prepared at the compounding ratios shown in Tables 1 and 2, and cured to a 3 mm-thick polymethacrylimide resin plate (trade name: PMI, manufactured by Mitsubishi Rayon Co., Ltd.). It was spray-coated so that the subsequent coating film had a thickness of 8 μm. After volatilizing the organic solvent by heating, using a high-pressure mercury lamp in air, the wavelength of 340
Irradiation was performed at an energy of 3000 mJ / cm ² with an integrated light amount of 380 nm to 380 nm to obtain a cured coating film. The evaluation results of the obtained coating film are shown in Tables 1 and 2.

[0037]

[Table 1]

[0038]

[Table 2]

The symbols of the compounds in Table 1 are as follows. DPHA: dipentaerythritol penta acrylate TAIC: tris (2-acryloyloxyethyl) isocyanurate UA1: 2 mol of dicyclohexylmethane diisocyanate, 1 mol of nonabutylene glycol and 2 mol of 2-hydroxyethyl acrylate Urethane acrylate having a molecular weight of 2500 synthesized from TMPTA: trimethylolpropane triacrylate BPN: benzophenone MPG: methylphenylglyoxylate HBPB: 2- (2-hydroxy-5-tert-butylphenyl) benzotriazole DHBP: 2,4-dihydroxy Benzophenone BOTS: bis (1-octoxy-2,2,6,6-tetramethyl-4-piperidyl) sebacate

[0040]

The coating composition of the present invention is applied to various synthetic resin molded articles as a substrate, and is irradiated with active energy such as general ultraviolet rays to deteriorate the substrate. Thus, it is possible to obtain a crosslinked synthetic resin-coated molded article having excellent wear resistance, heat resistance, weather resistance, durability, and chemical resistance.

Continuation of front page (58) Field surveyed (Int.Cl. ⁷ , DB name) C09D 4/02

Claims (1)

(57) [Claims] 1. A poly (meth) acrylic mono- or polypentaerythritol represented by the following general formula (I):
At least one monomer selected from the group consisting of 10 to 70 parts by weight, (Where X ₁₁ , X ₁₂ , X ₁₃ , X ₂₂ , X ₂₃ ,..., X _n2 , X
_n3, and X _14, at least three of CH ₂ = CR-
A COO- group, and the rest are -OH groups. Also, n is 1 to
An integer of 5 and R represents hydrogen or a methyl group; (B) (meth) acrylates containing hydroxyl groups
And isocyanates having two or more isocyanate groups in the molecule.
Urethane reaction product or molecule with anate compound
Isocyanate having two or more isocyanate groups therein
Polyol, polyester or polyamide geo
After reacting the adduct to synthesize the adduct,
A (meth) actone containing a hydroxyl group in a cyanate group
A urethanation reaction product to which relate is added,
At least two radically polymerizable unsaturated doublets in one molecule
At least one urethane poly (meth) acrylate compound having a bond and a molecular weight of 1,000 to 5,000 ,
50 parts by weight, (C) poly [(meth) acryloyloxyalkyl] (iso) cyanurene represented by formula (II) or (III)
G, 5 to 50 parts by weight, Embedded image (Wherein X ₁ , X ₂ and X ₃ represent an acryloyl group, a methacryloyl group, a hydrogen atom or an alkyl group, at least two of which are (meth) acryloyl groups, R ₁ , R ₂ and R ₃ represents an oxyalkylene group having 1 to 4 carbon atoms.) (D) an ultraviolet absorber, 2 to 30 parts by weight, (E) a hindered amino ether light stabilizer represented by the general formula (IV), 0.1-5 parts by weight, (In the formula, R ₄ and R ₅ may be the same or different and represent an alkyl group having 1 to 12 carbon atoms.) (F) Photopolymerization initiator, 0.1 to 10 parts by weight, , A, B, C, D, E, and F are 100 parts by weight in total).