JP2009287038A - Ultraviolet curable anti-fogging composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an ultraviolet curable anti-fogging composition having highly improved long-lasting anti-fogging performance, allowing thermoforming, and exhibiting excellent abrasion resistance. <P>SOLUTION: The ultraviolet curable anti-fogging composition comprises, a bifunctional urethane acrylate oligomer (a) as a reaction product of an isocyanate compound, which is obtained by reacting polyether diol with an aromatic/alicyclic diisocyanate, and an acrylate monomer having a hydroxyl group, a monomer (b) having two or less functional groups, and at least one kind of component among a dilution solvent and a photopolymerization initiator. The polyether diol is polyethylene oxide or an ethylene oxide-propylene oxide random copolymer containing 60 mol% or more ethylene oxide. A solid content weight ratio (a)/(b) is from 50/50 to 98/2. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

The present invention relates to an ultraviolet curable antifogging composition, in particular, an ultraviolet ray having remarkably improved antifogging performance, excellent durability of the antifogging performance, thermoforming, and excellent wear resistance equivalent to a hard coat. The present invention relates to a curable antifogging composition.

Various plastic materials are used for personal protective equipment such as sports goggles, helmet shields, safety glasses, safety shields, etc. from the viewpoint of lightness, transparency, processability and safety when cracked. For industrial use such as various display devices, instrument covers, lenses, sensor covers, housing use such as partitions and showcases in residential stores, and transportation related uses such as partitions and shelves for automobiles, railway vehicles, instrument covers, window glass, etc. It is used. The plastic materials used in these applications are subject to condensation or cloudiness on the surface when used in the vicinity of breathing, in high-temperature and high-humidity environments, or in environments with a large temperature difference between the front and back surfaces. There is a drawback that convenience and safety are likely to be lowered, such as deterioration of performance and malfunction of sensors.

In order to eliminate this drawback, various studies on anti-fogging treatment have been made. For example, there is a method of forming an antifogging film by applying a composition containing a surfactant as a main component on the surface of a substrate. However, the surfactant is easily eluted only by contact with water, and the antifogging property is lowered in a short period of time, which is impractical in terms of durability. Moreover, the coating film which has surfactant had the problem that the movement to the interface and a protective film occurred during storage, and the external appearance of the product was remarkably impaired.

Therefore, in order to improve the antifogging durability, a method of applying a hydrophilic polymer such as polyhydroxyalkyl (meth) acrylate and providing antifogging properties by a film cured by heat curing has been proposed. Although improvement in the properties is observed, it cannot be said that the anti-fogging performance is sufficient, and the mechanical strength such as wear resistance is practically insufficient, or if it is thermoformed into goggles or the like, it is prevented by the heat during molding. There is a problem that haze decreases.

In order to improve the wear resistance, a method of forming an antifogging film by combining a hydrophilic polymer and a crosslinking agent has been proposed, but the antifogging durability and wear resistance are not sufficient, and thermoforming. There was a problem that the anti-fogging property was sometimes extremely lowered. Further, an anti-fogging composition containing organic silicon has been proposed, and although it has relatively high wear resistance and anti-fogging properties and durability, thermoforming itself cannot be performed and processing such as goggles is performed. There was a problem that it could not be applied to products.

JP-A-56-090876 Japanese Patent Publication No. 53-018347 JP-A-53-028587 Japanese Examined Patent Publication No. 52-047754 Japanese Patent Laid-Open No. 08-176466

The present invention provides an ultraviolet curable antifogging composition that solves the above problems, has a significantly improved antifogging performance, is excellent in durability of the antifogging performance, can be thermoformed, and has excellent wear resistance. The purpose is to do.

As a result of intensive studies, the present inventors have found that the composition of the present invention comprises a composition comprising a specific polyether diol, an isocyanate compound comprising a combination of an aromatic or cycloaliphatic polyisocyanate, and a monomer having 2 or less functional groups. I found that I could achieve my objective.

That is, the present invention relates to a bifunctional urethane acrylate oligomer (a) which is a reaction product of an isocyanate compound obtained by reacting a polyether diol with an aromatic or cycloaliphatic diisocyanate and an acrylate monomer having a hydroxyl group, Ethylene oxide-propylene comprising at least one type of monomer (b) having 2 or less groups, a diluting solvent and a photopolymerization initiator, and the polyether diol containing at least 60 mol% of polyethylene oxide or ethylene oxide The gist is an ultraviolet curable antifogging composition which is an oxide random copolymer and has a solid content weight ratio (a) / (b) of 50/50 to 98/2.

The ultraviolet curable antifogging composition of the present invention is a bifunctional compound that is a reaction product of an isocyanate compound obtained by reacting a specific polyether diol with an aromatic or cycloaliphatic diisocyanate and an acrylate monomer having a hydroxyl group. Excellent anti-fogging performance by having the urethane acrylate oligomer (a) and the monomer (b) having 2 or less functional groups as the main component and the weight ratio (a) / (b) within a specific range. And has excellent anti-fogging durability, thermoforming, and wear resistance equivalent to that of a hard coat.

The bifunctional urethane acrylate oligomer (a) of the present invention is a reaction product of an isocyanate compound and an acrylate monomer having a hydroxyl group. The isocyanate compound comprises a polyether diol as a polyol and an aromatic or cyclic polyisocyanate. It is obtained by reacting with an aliphatic diisocyanate. As the polyether diol, polyethylene oxide or an ethylene oxide-propylene oxide random copolymer containing 60 mol% or more of ethylene oxide is used.

As described above, the bifunctional urethane acrylate oligomer has a hydrophilic ethylene oxide polymer skeleton or an ethylene oxide-propylene oxide copolymer skeleton as a soft segment, and the hard segment isocyanate has an aromatic structure or a cyclic aliphatic structure. There is. The hydrophilic skeleton of ethylene oxide polymer skeleton or ethylene oxide-propylene oxide copolymer skeleton has good antifogging properties and does not lose its antifogging performance due to elution unlike a surfactant. However, since this ethylene oxide polymer skeleton or ethylene oxide-propylene oxide copolymer skeleton has a flexible molecular structure, it has the effect of softening the coating film and reducing strength such as abrasion resistance. Complementing this defect is an isocyanate skeleton having an aromatic structure or a cycloaliphatic structure that is rigid in molecular structure and can improve the abrasion resistance, hardness, heat resistance, etc. of the coating film. Coating strength such as anti-fogging and abrasion resistance is achieved by the balance between this soft segment, ethylene oxide polymer skeleton or ethylene oxide propylene oxide copolymer skeleton, and hard segment, aromatic structure or cycloaliphatic structure. In addition, anti-fogging properties and durability of the coating film itself can be obtained.

As described above, as the polyether diol of the present invention, polyethylene oxide or an ethylene oxide-propylene oxide random copolymer containing 60 mol% or more of ethylene oxide is used. When the polyether diol does not have an ethylene oxide structure, antifogging properties cannot be obtained. In addition, in the ethylene oxide homostructure, oligomer crystallization is likely to occur and handling may be difficult, and ethylene oxide propylene oxide copolymers that are difficult to crystallize can also be used, but in this case, the molar ratio of ethylene oxide to propylene oxide Is important, and it is necessary to use one containing 60 mol% or more of ethylene oxide. When the content of ethylene oxide is less than 60 mol%, not only the antifogging property is lowered, but also the tackiness of the coating film surface after curing is increased, and problems such as easy adhesion of dust occur. . Therefore, when no problem occurs in handling, it is desirable to select a homostructure of ethylene oxide, and when crystallization or the like becomes a problem in handling, it is desirable to select an ethylene oxide propylene oxide copolymer.

The polyether diol of the present invention can be used with various molecular weights, but it is desirable to use those having an average molecular weight of 400 or more. This is because the antifogging property is further enhanced at an average molecular weight of 400 or more.

The diisocyanate used in the present invention is an aromatic or cycloaliphatic diisocyanate, and examples of the aromatic isocyanate include methylene diphenyl diisocyanate (MDI), tolylene diisocyanate (TDI), xylylene diisocyanate (XDI), naphthylene 1, 5-diisocyanate (NDI), tetramethylene xylylene diisocyanate (TMXDI) and the like. Examples of the cyclic aliphatic isocyanate include isophorone diisocyanate (IPDI), hydrogenated MDI, dicyclohexylmethane diisocyanate (H12MDI), hydrogenated XDI (H6XDI). And the like.

An acrylate monomer having a hydroxyl group is a monomer having one end, such as 2-hydroxylethyl acrylate, 2-hydroxylpropyl acrylate, 4-hydroxybutyl acrylate, cyclohexanedimethanol monoacrylate, and the like. It is used to add a group to make an ultraviolet curable urethane acrylate oligomer. The added acrylate remains as it is in the process of synthesizing the urethane acrylate oligomer, and serves as a functional group that reacts when irradiated with ultraviolet rays.

The monomer (b) having two or less functional groups in the present invention is for obtaining good adhesion to the base material, has an appropriate compatibility with the base material, and is a bifunctional to be combined. It may be compatible with the urethane acrylate oligomer (a). However, depending on the type of monomer, the antifogging property that is characteristic of the component (a) may be inhibited and reduced. Also, if the compatibility with the base material is too high or the size of the molecule is too small, the monomer will permeate the base material too much due to heating when drying to curing the coating, and adhesion may not be obtained. In addition, the appearance structure such as haze is increased by eroding the base material to roughen the interface structure or the surface becomes uneven. Conversely, if the compatibility is insufficient or the molecule is too large, it is difficult to obtain sufficient adhesion. The following can be mentioned as a monomer which can be used by this invention.

（Ｒ_１は水素原子又はメチル基を示し、Ｒ_２はメチル基またはフェニル基を示し、ｍは５〜２０を示す）

（Ｒ_１は水素原子、炭素数１〜６の直鎖または分岐鎖をもったアルキル基、またはアルキルケトン基を示す）

（ｍはエチレンオキシドの平均付加モル数を示し、４〜２０である）

（ｍとｎはエチレンオキシドの平均付加モル数を示し、ｍ＋ｎが４〜２０である）

（ｍとｎはエチレンオキシドの平均付加モル数を示し、ｍ＋ｎが４〜２０である）

（ｍとｎはエチレンオキシドの平均付加モル数を示し、ｍ＋ｎが４〜２０である） 4-hydroxybutyl acrylate (HBA), N-vinylpyrrolidone (NVP), cyclohexanedimethanol monoacrylate, N-vinylformamide (NVF), acryloylmorpholine (ACMO), methoxypolyethylene glycol (meth) acrylate, phenoxypolyethylene glycol (meth) Acrylate, ethoxy mono (meth) acrylate and acrylamide represented by the following formula (1), acrylic acid amide compound represented by the following formula (2), ethylene oxide diacrylate compound represented by the following formula (3), the following formula Ethoxylated bisphenol A diacrylate represented by (4), ethoxylated hydrogenated bisphenol A diacrylate represented by the following formula (5), ethoxylated cyclohexane diacrylate represented by the following formula (6) Door.

(R ₁ represents a hydrogen atom or a methyl group, R ₂ represents a methyl group or a phenyl group, and m represents 5 to 20)

(R ₁ represents a hydrogen atom, a linear or branched alkyl group having 1 to 6 carbon atoms, or an alkyl ketone group)

(M represents the average number of moles of ethylene oxide added and is 4 to 20)

(M and n represent the average number of moles of ethylene oxide added, and m + n is 4 to 20)

(M and n represent the average number of moles of ethylene oxide added, and m + n is 4 to 20)

(M and n represent the average number of moles of ethylene oxide added, and m + n is 4 to 20)

The weight ratio (a) / (b) between the bifunctional urethane acrylate oligomer (a) and the monomer (b) having 2 or less functional groups is 50/50 to 98/2, more preferably 70/30 to It must be 95/5. If the ratio of (a) is less than 50%, the abrasion resistance of the coating film is extremely lowered, and at the same time, appearance defects such as an increase in haze and irregularities on the appearance surface occur. When the ratio of (b) is less than 2%, the durability adhesion of the coating film is insufficient.

The diluting solvent used in the present invention must be a good solvent of the bifunctional urethane acrylate oligomer (a) and the monomer (b) having 2 or less functional groups, and the antifogging composition as a base material. When the coating film formed by heating is dried by heating, it needs to be sufficiently dried at an appropriate speed capable of maintaining smoothness without deteriorating the appearance.

Examples of the diluting solvent include methyl cellosolve, ethyl cellosolve, propylene glycol monomethyl ether, propylene glycol monoethyl, which have relatively medium drying rates, such as methanol, ethanol, isopropanol, n-propanol, and isobutanol, which have relatively high drying rates. Ether, n-butanol, diacetone alcohol, butyl cellosolve, propylene glycol monomethyl ether acetate, etc., which have a relatively slow drying rate, can be used alone or in combination. It is also possible to mix a small amount of ketones, esters, and aromatic hydrocarbon solvents to the extent that they do not affect the solubility of (a) and (b). Examples of ketones, esters, and aromatic hydrocarbon solvents include methyl ethyl ketone, methyl isobutyl ketone, ethyl acetate, butyl acetate, xylene, and toluene.

The photopolymerization initiator used in the present invention has a function as a polymerization initiator when the photopolymerizable compound is cured by ultraviolet rays, and known ones can be used. For example, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether and other benzoin or benzoin alkyl ethers, benzophenone, benzoylbenzoic acid and other aromatic ketones, benzyl and other alphage carbonyls, benzyldimethyl ketal, benzyl diethyl Benzyl ketals such as ketals, acetophenone, 1- (4-dodecylphenyl) -2-hydroxy-2-methylpropan-1-one, 1-hydroxycyclohexyl phenyl ketone, 2-hydroxy-2-methyl-1-phenyl- 1-propan-1-one, 1- (4-isopropylphenyl) -2-hydroxy-2-methyl-propan-1-one, 2-methyl-1- [4- (methylthio) phenyl] -2-morpholinopropa Acetophenones such as N-1, anthraquinones such as 2-methylanthraquinone, 2-ethylanthraquinone and 2-t-butylanthraquinone, thioxanthones such as 2,4-dimethylthioxanthone, 2-isopropylthioxanthone and 2,4-diisopropylthioxanthone , Alpha-siloximes such as 1-phenyl-1,2-propanedione-2- (o-ethoxycarbonyl) oxime, amines such as ethyl p-dimethylaminobenzoate, isoamyl p-dimethylaminobenzoate, etc. Can be used. Of these, acetophenones such as 2-hydroxy-2-methyl-1-phenyl-1-propan-1-one and aromatic ketones such as benzophenone are particularly preferable.

For the purpose of slightly improving the initial antifogging performance, a surfactant may be supplementarily added to the antifogging composition of the present invention. The surfactant that can be added can be selected from general nonionic surfactants, anionic surfactants, cationic surfactants, zwitterionic surfactants, and the like. Among these, nonionic surfactants or anionic surfactants are particularly preferable, and combinations thereof are also preferable.

Further, in the present invention, in order to obtain wettability and uniformity of the coating film on the base material at the time of coating, surface smoothness and surface slip property of the cured coating film, a silicone system, an acrylic copolymer system, etc. It is preferable to add the surface conditioner.

As the silicone-based surface conditioner, polydimethylsiloxane or a modified silicone-based one obtained by modifying it is used. As the modified silicone, a polyether-modified product, an alkyl-modified product, a polyester-modified product and the like are preferable, and a polyether-modified product is particularly preferable. Moreover, it is also possible to use these in combination.

The anti-fogging coating film which consists of an anti-fogging composition of this invention can be obtained in the process of mixing-dilution-application-drying-hardening of a composition. The thickness of the coating film is 5 μm or more and 80 μm or less. From the viewpoint of anti-fogging properties, the thicker the coating, the better. However, if it exceeds 80 μm, the curability of the coating will decrease, and the wear resistance and adhesion will decrease. Cannot be obtained. Moreover, as a coating method, a roll coater, a spray coater, a curtain flow coater, a slit die coater, etc. having a horizontal type coating and conveying facility are suitable.

After the antifogging composition of the present invention is applied to the substrate, the temperature of the substrate and the atmosphere is raised, and after sufficiently diluting the diluting solvent, ultraviolet rays are irradiated to cure the coating film. For the ultraviolet irradiation, a general electroded or electrodeless high-pressure ultraviolet lamp or metal halide lamp can be used.

Although general transparent plastics can be used as the base material, it is assumed to be used in the present invention, such as sports goggles, helmet shields, safety glasses, and safety shields for human bodies, and various display devices and instrument covers. Polycarbonate resin is used in industrial applications such as lenses and sensor covers, residential applications such as partitions and showcases in residential stores, and transportation-related applications such as partitions and shelves, instrument covers, and window glass. It is most preferable to use a material from the viewpoints of lightness, transparency, workability, and resistance to cracking and safety when cracked. Other common transparent resins such as polymethyl methacrylate, polyethylene terephthalate, and polyvinyl chloride can also be used.

<Adjustment of urethane acrylate>
(1) 150 parts of tolylene diisocyanate (TDI) and polyoxyethylene diol 350 having an average molecular weight of 400 in a 1 liter four-necked flask equipped with a thermometer, stirrer, inert gas inlet, air inlet and reflux condenser The parts were charged and reacted at 80 ° C. for 5 hours under a nitrogen atmosphere. Thereafter, the mixture was cooled to 40 ° C., 150 parts of 2-hydroxyethyl acrylate was then added, and the mixture was reacted at 80 ° C. for 4 hours in an air atmosphere to obtain a bifunctional urethane acrylate oligomer (1).
(2) Although it is the same as said (1), the isocyanate which is aliphatic diisocyanate was made into 150 parts of hexamethylene diisocyanate (HDI), and the bifunctional urethane acrylate oligomer (2) was obtained.
(3) Similar to (1) above, but with a polyether diol of 300 parts of polyoxypropylene diol having an average molecular weight of 600, a bifunctional urethane acrylate oligomer (3) was obtained.
(4) Similar to (1) above, but with 300 parts of a random copolymer of polyoxyethylene diol and polyoxypropylene diol having an average molecular weight of 600 and containing 70 mol% of ethylene oxide, a bifunctional urethane An acrylate oligomer (4) was obtained.
(5) Similar to (1) above, but with 300 parts of a random copolymer of polyoxyethylene diol and polyoxypropylene diol having an average molecular weight of 600 and containing 50 mol% of ethylene oxide, a bifunctional urethane An acrylate oligomer (5) was obtained.

<Example 1>
Each component used is as follows.
(A): Bifunctional urethane acrylate oligomer (1)
(B): Bisphenol A diacrylate diluting solvent having an average addition mole number of ethylene oxide of 10: 1: 1 solution photopolymerization initiator of isopropyl alcohol and methyl cellosolve: 2-hydroxy-2-methyl-1-phenyl-propane-1- 1: 1 mixture of ON and 1- [4- (2-hydroxy) -phenyl] -2-hydroxy-2-methyl-1-propan-1-one,

In addition, a polyether-modified polydimethylsiloxane solution (manufactured by BYK Chemie, trade name BYK-306) was used as a silicone-based surface conditioner.

The solid content weight ratio (a) / (b) was blended so as to be 80/20, and further diluted with the above diluting solvent so that these components were 40% by weight in the solution. At this time, a photopolymerization initiator previously dissolved in methyl cellosolve was added as a part of the diluent solvent so that the solid content ratio was 4%. Further, 0.1 part by weight of a silicone surface conditioner was added to 100 parts by weight of the composition. The composition was sufficiently stirred and mixed, and then stored in a sealed container.

A transparent polycarbonate sheet having a plate thickness of 1.5 mm (“Polyca Ace” manufactured by Chuchu Plastic Industry Co., Ltd.) was prepared as a substrate, and the composition was applied using a metal bar coater so that the dry film thickness was 30 μm. Next, the coated polycarbonate sheet was placed in a hot air circulation oven at 50 ° C. and dried. After drying for 20 minutes, a polycarbonate sheet is placed on a conveyor at a speed of 5 m / min using a 160 W / cm high-pressure mercury lamp (USHIO Inc.), and the polycarbonate sheet is irradiated with ultraviolet rays at a distance of 15 cm between the mercury lamp and the polycarbonate sheet. And the composition was cured. The performance of the sheet on which the antifogging coating film was formed was evaluated as follows.

<Appearance>
The cured coating film was visually observed and evaluated as follows.
◎: The surface of the coating is smooth and transparent from any angle. ○: The surface of the coating is smooth. Things △: The coating film surface is not smooth or looks cloudy when viewed from an oblique direction, and has practical problems. ×: The coating film surface is rough, or even when the flat surface is viewed from the front, it is cloudy, and is completely practical. Something without.
<Anti-fogging property 1>
Expiration was blown on the surface of the sheet 5 times, and the degree of cloudiness was visually observed and evaluated as follows.
◯: No cloudiness is observed even when the exhalation is blown three times or more. Δ: Exhalation is not observed even if the exhalation is blown once or twice, but clouding is observed when the exhalation is blown three times or more.
X: Clouding is observed when exhalation is blown once.
<Anti-fogging property 2>
Only for those evaluated as “A” and “B” in the evaluation of the “anti-fogging property 1”, the anti-fogging time was measured according to European standard EN168 and evaluated as follows.
A: Anti-fogging time over 20 seconds (remarkably improved anti-fogging property)
○: Antifogging time 15 seconds to 20 seconds or less (excellent antifogging property)
Δ: Anti-fogging time 5 to 15 seconds or less (weak anti-fogging property, limited use)
X: Anti-fogging time 5 seconds or less (very low anti-fogging property and no practicality)
<Initial adhesion of coating film>
A cross-cut tape method (based on JIS K5400) was performed, and the following evaluation was performed according to the number of squares that were not peeled off.
A: 100 (very strong adhesion)
○: 80 to 99 (adhesiveness having no practical problem)
Δ: 50 to 79 (highly likely to cause practical problems)
X: 20-49 (adhesion is weak and there is no practicality at all)
XX: Largely peeled to 0-19 or outside the grid (no adhesion)
<Abrasion resistance>
According to ASTM D1044, a Taber-type wear test (CS10F wear wheel, load 500 g, 300 revolutions) was performed, and a hard coat (hard coat polycarbonate plate / Chuchu Plastics Co., Ltd. EC100R base material) was evaluated at the same time. 5 mm) and evaluated as follows.
A: Change in haze is hard coat value + 5% or less (excellent wear resistance equivalent to hard coat)
○: Haze change + hard coat value + more than 5% to 10% (excellent wear resistance, no problem in practical use)
Δ: Haze change is more than the value of hard coat + 10% to 15% (although there is wear resistance, there is a possibility of practical problems)
X: Haze change is more than the value of hard coat + 15% to no wear resistance, and there is a problem in practical use)
<Thermoformability>
The sample was softened by heating in a hot air circulation oven set at 170 ° C. for 7 minutes, and immediately after removal, the sample was cooled to near room temperature by attaching it to a wooden cylinder with a radius of 30 mm with a nell cloth with the coating surface facing outward. The single curved surface was molded by keeping it as it was, and then the appearance was observed and evaluated as follows.
○: No occurrence of cracks or peeling of coating film or change in appearance (excellent moldability)
X: Changes in appearance such as occurrence of cracks or peeling of the coating film, white turbidity or rough skin (no formability)
<Durable adhesion of coating film>
In the above-mentioned evaluation of “initial adhesion of coating film”, only samples with ○ and ◎ were immersed in boiling water for 60 minutes, wiped off moisture and dried at room temperature for 2 hours or more, Evaluation by eye tape method as follows. However, this evaluation was not performed for those having an initial evaluation result of “antifogging property 2” of Δ or ×.
A: 90 to 100 (very strong adhesion)
○: 60 to 89 (adhesiveness having no practical problem)
Δ: 30 to 59 (highly likely to cause practical problems)
X: 0 to 29 (problematic problem)
<Anti-fogging durability 1 / warm water>
After immersing the sample in warm water of 60 ° C. for 100 hours, the above “antifogging property 2” was evaluated except for the case where peeling (entire surface or part) of the coating film occurred, and the evaluation was as follows. However, this evaluation was not performed for those having an initial evaluation result of “antifogging property 2” of Δ or ×.
A: The same anti-fogging property as the initial one (good anti-fogging durability)
○: Anti-fogging property one rank lower than the initial one, and the result is Δ to ○ (some anti-fogging durability, which may limit the use)
X: Two or more ranks lower than the initial value, or the result is x (inferior in antifogging durability)
XX: The anti-fogging property 2 could not be evaluated because peeling occurred on the entire surface or a part of the coating film (the coating film itself has a problem with durability or durability adhesion)
<Anti-fog durability 2 / Heat resistance>
The sample was allowed to stand in a hot air circulation oven at 80 ° C. for 100 hours, and then the above “antifogging property 2” was evaluated except for the case where peeling (entire or partial) of the coating film occurred. .
A: The same anti-fogging property as the initial one (good anti-fogging durability)
○: Anti-fogging property one rank lower than the initial one, and the result is Δ to ○ (some anti-fogging durability, which may limit the use)
X: Two or more ranks lower than the initial value, or the result is x (inferior in antifogging durability)
XX: The anti-fogging property 2 could not be evaluated because peeling occurred on the entire surface or a part of the coating film (the coating film itself has a problem with durability or durability adhesion)
<Anti-fog durability 3 / Heat-resistant formability>
About the said molded article, said "anti-fogging property 2" is evaluated. However, this evaluation was not performed for those having an initial evaluation result of “antifogging property 2” of Δ or ×.
◎: The same anti-fogging property as before heat molding (good anti-fogging durability)
○: Antifogging property that is one rank lower than that before heat molding, with a result of Δ to ○ (a degree of antifogging durability that may limit the use)
X: Two ranks lower than before heat molding, or the result is x (inferior in antifogging durability)

<Example 2>
Same as Example 1 except that (a) / (b) is 70/30.

<Example 3>
Same as Example 1 except that (a) / (b) was 95/5.

<Comparative Example 1>
Same as Example 1 except (a) / (b) was 40/60.

<Comparative Example 2>
Same as Example 1, except that (a) / (b) was 100/0.

<Comparative Example 3>
The same as Example 1 except that the bifunctional urethane acrylate oligomer (2) was used instead of (a).

<Comparative example 4>
Similar to Example 1 except that bifunctional urethane acrylate oligomer (3) was used instead of (a)

<Example 4>
The same as Example 1 except that the bifunctional urethane acrylate oligomer (4) was used instead of the bifunctional urethane acrylate oligomer (1).

<Comparative Example 5>
The same as Example 1 except that the bifunctional urethane acrylate oligomer (5) was used instead of (a).

The evaluation results of Examples 1 to 4 and Comparative Examples 1 to 5 are shown in Table 1.

As shown in Table 1, in Examples 1 to 3, where the weight ratio of the bifunctional urethane acrylate oligomer (a) and the monomer (b) having 2 or less functional groups is within the scope of the present invention, It can be seen that the anti-fogging property 1 by the breath test as well as the anti-fogging property 2 by the stricter anti-fogging test of EN168 are excellent. In addition, it can be seen that the anti-fogging property has durability that is not lost in heat and humidity, and that it is excellent in sufficient adhesion to the substrate, moldability, and wear resistance. On the other hand, in Comparative Example 1 or Comparative Example 2 in which the weight ratio of the above (a) and (b) departs from the scope of the present invention, the initial antifogging property is lowered and the abrasion and wear resistance is lowered (comparison). Example 1), durability adhesion and anti-fogging durability were lowered (Comparative Example 2).

In addition, a random copolymer of polyoxyethylene diol and polyoxypropylene diol, which uses a polyether diol containing 70 mol% of ethylene oxide, is evaluated in the same manner as in Example 1 in Example 4 within the scope of the present invention. In comparison example 5 using a random copolymer of polyoxyethylene diol and polyoxypropylene diol containing only 50 mol% of ethylene oxide, which is outside the scope of the present invention, a breath test was obtained. In addition to antifogging property 1 due to the above, the antifogging property 2 according to the stricter antifogging test of EN168 was the lowest rank, and the necessary antifogging property could not be obtained. Moreover, in Comparative Example 5, due to surface tackiness, appearance defects occurred at the time of thermoforming, and could not cope with thermoforming.

In Comparative Example 3 in which a bifunctional urethane acrylate oligomer (2) using a straight chain aliphatic hexamethylene diisocyanate that deviated from the scope of the present invention was used instead of the component (a), excellent antifogging was achieved. However, it is inferior in wear resistance, durability adhesion and anti-fogging durability. Further, in Comparative Example 4 in which a bifunctional urethane acrylate oligomer (3) using polyoxypropylene diol as a diol component deviating from the scope of the present invention was used in place of the component (a), antifogging properties were obtained at all. There wasn't.

Claims (2)

Bifunctional urethane acrylate oligomer (a), which is a reaction product of an isocyanate compound obtained by reacting a polyether diol with an aromatic or cycloaliphatic diisocyanate and an acrylate monomer having a hydroxyl group, the number of functional groups being 2 or less And the polyether diol is an ethylene oxide-propylene oxide random copolymer containing 60 mol% or more of polyethylene oxide or ethylene oxide. The UV curable antifogging composition, wherein the solid content weight ratio (a) / (b) is 50/50 to 98/2. The ultraviolet curable antifogging composition according to claim 1, wherein the polyether diol has an average molecular weight of 400 or more.