WO2014081004A1

WO2014081004A1 - Active energy ray-curable resin composition, coating agent composition, and laminate

Info

Publication number: WO2014081004A1
Application number: PCT/JP2013/081484
Authority: WO
Inventors: 篤志辻本
Original assignee: 日本合成化学工業株式会社
Priority date: 2012-11-22
Filing date: 2013-11-22
Publication date: 2014-05-30
Also published as: TW201425465A; TWI625359B; CN104797613A; KR20150090061A

Abstract

An active energy ray-curable resin composition which is characterized by containing (A) a urethane (meth)acrylate compound and (B) a fine particulate synthetic resin filler, a coating agent composition which uses the active energy ray-curable resin composition, and a laminate are provided as an active energy ray-curable resin composition which forms a coating layer that has moist and soft finger tactile, while having excellent workability during a coating process and excellent productivity during a curing process, a coating agent composition which uses the active energy ray-curable resin composition, and a laminate.

Description

Active energy ray-curable resin composition, coating agent composition, and laminate

The present invention relates to an active energy ray-curable resin composition, a coating agent composition, and a laminate, and more specifically, has a moist touch feeling called soft feel and soft touch when used as a cured coating film, and Active energy ray-curable resin composition for forming a cured coating film excellent in appearance and high quality, a coating agent composition using the same, and further a substrate and a coating layer comprising the coating agent composition It is related with the laminated body which has.

Conventionally, polyurethane coating agents containing organic fine particles have been used as coating agents for interior parts such as plastic panels in automobiles in order to give a high-class feeling and a moist touch feeling.

Generally, a polyurethane-based coating agent is a thermosetting type coating agent obtained by reacting a polyol component and an isocyanate component. Since the reactivity of the polyol component and the isocyanate component is high, it is usually used in two liquids. Since both were mixed immediately before application to the material, the workability and productivity were inferior.

Accordingly, various thermosetting polyurethane-based coating agents with improved workability have been developed. For example, Patent Document 1 discloses a first urethane resin obtained by a reaction between a polycarbonate-based polyol and a polyisocyanate. , A second urethane resin obtained by the reaction of a polyether polyol and a polyisocyanate, a crosslinking agent containing two or more carbodiimide groups in one molecule, urethane beads, and surface modification that is an organosilicon compound. In addition, Patent Document 2 contains a curing agent composition (X) containing a specific polyisocyanate and an aliphatic polycarbonate diol (Y) as essential components. NCO group contained in the curing agent composition (X) and O contained in the aliphatic polycarbonate diol (Y) Mixing molar ratio of the base paint curable compositions have been proposed a NCO / OH = 0.8 ~ 2.0.

JP 2007-319836 A JP 2010-13529 A

However, the technique disclosed in Patent Document 1 has been devised to extend the pot life as a paint by using an aqueous dispersion of carbodiimide as a crosslinking agent in order to control the reactivity in an aqueous coating solution. However, in order to cure the coating layer, in addition to the drying conditions at 80 ° C. for 30 minutes, it takes several days in a humidity control atmosphere, so the solution stability (workability) is improved to some extent. However, productivity was still not satisfactory.

In addition, although the technique disclosed in Patent Document 2 is considered to have improved durability of various coating layers as a solvent-based coating liquid, the stability of the coating liquid in which isocyanate and polyol are mixed is sufficient. However, it was thought that this was not the case, and there were still problems in workability.

Therefore, the present invention is a one-part curable resin composition excellent in workability under such a background, and has a soft and soft touch when used as a coating layer. It is another object of the present invention to provide an active energy ray-curable resin composition excellent in workability during coating and productivity during curing, and a coating agent composition using the same.

However, as a result of intensive studies in view of such circumstances, the present inventor has obtained a conventional thermosetting urethane resin as a resin component in a coating composition obtained by adding a fine synthetic resin filler to a resin component. Instead, by using urethane (meth) acrylate having active energy ray curability, an active energy ray curable resin composition excellent in workability during coating and productivity during curing can be obtained and cured. The present invention was completed by finding that the coating film (coating layer) obtained later had a moist and soft touch feeling.

That is, the gist of the present invention relates to an active energy ray-curable resin composition comprising a urethane (meth) acrylate compound (A) and a fine particle synthetic resin filler (B).
The present invention also provides a coating composition comprising the active energy ray-curable resin composition, and a laminate having a substrate and a coating layer comprising the coating composition. .

The active energy ray-curable resin composition of the present invention, when used as a coating agent, becomes an active energy ray-curable resin composition excellent in workability during coating and productivity during curing, and The coating layer obtained after curing has an effect of having a moist and soft touch feeling and is particularly useful as a coating agent.

The present invention is described in detail below.
The active energy ray-curable resin composition of the present invention comprises a urethane (meth) acrylate compound (A) and a fine synthetic resin filler (B).

In the present invention, (meth) acryl means acryl or methacryl, (meth) acryloyl means acryloyl or methacryloyl, and (meth) acrylate means acrylate or methacrylate.

[Urethane (meth) acrylate compound (A)]
The content of the ethylenically unsaturated group of the urethane (meth) acrylate compound (A) used in the present invention is preferably 2 to 10, particularly preferably 2 to 6. If the number of such ethylenically unsaturated groups is too large, the crosslinking density after curing becomes too large, and the coating film tends to be too hard and it is difficult to obtain a moist soft feeling. Since it cannot be obtained, there is a tendency that the surface of the cured coating film is sticky or various durability performances are deteriorated.

The weight average molecular weight of the urethane (meth) acrylate compound (A) used in the present invention is preferably 1,000 to 50,000, particularly preferably 1,500 to 40,000, particularly preferably 2. , 5,000 to 35,000.
If the weight average molecular weight is too small, the crosslink density is relatively increased, so that the surface of the cured coating film is too hard and it is difficult to obtain a moist soft feeling. If it is too large, the viscosity of the curable resin composition is low. There is a tendency to become too high, a sufficient crosslinking density cannot be obtained, the surface of the cured coating film becomes sticky, and various durability tends to decrease.

In addition, said weight average molecular weight is a weight average molecular weight by standard polystyrene molecular weight conversion, a column is put into a high performance liquid chromatography (Nippon Waters Co., Ltd., "Waters 2695 (main body)" and "Waters 2414 (detector)"). (Shodex GPC KF-806L (exclusion limit molecular weight: 2 × 10 ⁷ , separation range: 100 to 2 × 10 ⁷ , theoretical plate number: 10,000 plates / piece, filler material: styrene-divinylbenzene copolymer, filler) It is measured by using three series of particle diameters: 10 μm)).

The viscosity of the urethane (meth) acrylate compound (A) at 60 ° C. is preferably 1,000 to 100,000 mPa · s, and particularly preferably 1,500 to 50,000 mPa · s. When the viscosity is out of the above range, the coatability tends to be lowered.
In addition, the measuring method of a viscosity is based on an E-type viscometer.

The urethane (meth) acrylate compound (A) used in the present invention is obtained by reacting a hydroxyl group-containing (meth) acrylate compound (a1), a polyvalent isocyanate compound (a2) and a polyol compound (a3). A urethane (meth) acrylate compound (A2) obtained by reacting a urethane (meth) acrylate compound (A1) or a hydroxyl group-containing (meth) acrylate compound (a1) and a polyvalent isocyanate compound (a2). Among these, only one type may be used alone, or two or more types may be used in combination.

Among these, urethane synthesized as a relatively low molecular weight in terms of suppressing the stickiness of the coating film when it is used as a cured coating film, and obtaining a crosslinking density that can impart durability to the cured coating film. The (meth) acrylate compound (A2) is preferable, and the urethane (meth) acrylate compound (A1) obtained by reacting the polyol compound (a3) is preferable in terms of imparting flexibility to the cured coating film. .
These are appropriately selected in consideration of imparting various physical properties of the intended cured coating film.

<Urethane (meth) acrylate compound (A1)>
As described above, the urethane (meth) acrylate compound (A1) is obtained by reacting the hydroxyl group-containing (meth) acrylate compound (a1), the polyvalent isocyanate compound (a2), and the polyol compound (a3). . The hydroxyl group-containing (meth) acrylate compound (a1), polyvalent isocyanate compound (a2), and polyol compound (a3), which are compounds for obtaining the urethane (meth) acrylate compound (A1), will be described below in order. .

<Hydroxyl-containing (meth) acrylate compound (a1)>
Examples of the hydroxyl group-containing (meth) acrylate compound (a1) include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, and 4-hydroxybutyl (meth). Acrylates, hydroxyalkyl (meth) acrylates such as 6-hydroxyhexyl (meth) acrylate, 2-hydroxyethyl acryloyl phosphate, 2- (meth) acryloyloxyethyl-2-hydroxypropyl phthalate, caprolactone-modified 2-hydroxyethyl (meth) ) Acrylate, dipropylene glycol (meth) acrylate, fatty acid modified-glycidyl (meth) acrylate, polyethylene glycol mono (meth) acrylate, polypropylene glycol mono (meth) Acrylate, 2-hydroxy-3- (meth) acryloyloxy propyl (meth) acrylate, containing one ethylenically unsaturated group such as (meth) acrylate compound;
(Meth) acrylate compounds containing two ethylenically unsaturated groups such as glycerin di (meth) acrylate, 2-hydroxy-3-acryloyl-oxypropyl methacrylate, and the like;
Pentaerythritol tri (meth) acrylate, caprolactone modified pentaerythritol tri (meth) acrylate, ethylene oxide modified pentaerythritol tri (meth) acrylate, dipentaerythritol penta (meth) acrylate, caprolactone modified dipentaerythritol penta (meth) acrylate, ethylene Examples thereof include (meth) acrylate compounds containing three or more ethylenically unsaturated groups such as oxide-modified dipentaerythritol penta (meth) acrylate.

Among these, a hydroxyl group (meth) acrylate compound having one ethylenically unsaturated group is preferable because it can mitigate cure shrinkage during coating film formation, and more preferably 2-hydroxyethyl (meth). Hydroxyalkyl (meth) acrylates such as acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, caprolactone modified 2- Hydroxyethyl (meth) acrylate, particularly preferably 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, and caprolactone-modified 2-hydroxyethyl (meth) acrylate in terms of excellent reactivity and versatility. .
Moreover, these can be used 1 type or in combination of 2 or more types.

<Polyisocyanate compound (a2)>
Examples of the polyvalent isocyanate compound (a2) include aromatics such as tolylene diisocyanate, diphenylmethane diisocyanate, polyphenylmethane polyisocyanate, modified diphenylmethane diisocyanate, xylylene diisocyanate, tetramethylxylylene diisocyanate, phenylene diisocyanate, and naphthalene diisocyanate. Polyisocyanate;
Aliphatic polyisocyanates such as hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, lysine diisocyanate, lysine triisocyanate;
Cycloaliphatic polyisocyanates such as hydrogenated diphenylmethane diisocyanate, hydrogenated xylylene diisocyanate, isophorone diisocyanate, norbornene diisocyanate, 1,3-bis (isocyanatomethyl) cyclohexane;
Alternatively, trimer compounds or multimeric compounds of these polyisocyanates, allophanate type polyisocyanates, burette type polyisocyanates, water-dispersed polyisocyanates (for example, “Aquanate 100”, “Aquanate 110” manufactured by Nippon Polyurethane Industry Co., Ltd., "Aquanate 200", "Aquanate 210", etc.).

Of these, aliphatic diisocyanates such as hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, lysine diisocyanate, hydrogenated diphenylmethane diisocyanate, hydrogenated xylylene diisocyanate, isophorone diisocyanate, norbornene diisocyanate, 1, An alicyclic diisocyanate such as 3-bis (isocyanatomethyl) cyclohexane is preferred, particularly preferably isophorone diisocyanate, hydrogenated diphenylmethane diisocyanate, hydrogenated xylylene diisocyanate, hexamethylene diisocyanate, and more preferably reactive. In addition, isophorone diisocyanate and hexamethylene diisocyanate are excellent in versatility.

<Polyol compound (a3)>
The polyol compound (a3) may be any compound containing two or more hydroxyl groups. For example, an aliphatic polyol, an alicyclic polyol, a polyether polyol, a polyester polyol, a polycarbonate polyol, a polyolefin polyol, Examples thereof include polybutadiene-based polyols, polyisoprene-based polyols, (meth) acrylic polyols, and polysiloxane-based polyols.

The weight-average molecular weight of the polyol compound (a3) is preferably 60 to 20,000, particularly preferably 100 to 15,000, and further preferably 150 to 8,000. If the weight-average molecular weight of the polyol-based compound (a3) is too large, a sufficient crosslinking density cannot be obtained at the time of curing, the cured coating film surface tends to be sticky, and various durability tends to decrease. The curable resin composition tends to be highly viscous and difficult to handle. Moreover, when the weight average molecular weight of a polyol type compound (a3) is too small, the softness | flexibility of the coating film after hardening falls and there exists a tendency for a moist soft touch feeling to be hard to be obtained.

Further, it is preferable that the polyol compound (a3) contains a polyol compound (a3-1) having a weight average molecular weight of less than 500 and a polyol compound (a3-2) having a weight average molecular weight of 500 to 20,000. From the viewpoint of sex.

The weight average molecular weight of the polyol compound (a3-1) is less than 500, preferably 60 to 450, particularly preferably 60 to 400, and further preferably 100 to 300. When the weight average molecular weight of the polyol compound (a3-1) is too large, when it is used as a blended composition, the hydrogen bond pseudo-crosslinking degree peculiar to the urethane bond is lowered, so that durability such as chemical resistance of the cured coating film is reduced. There is a tendency to decrease.

The weight average molecular weight of the polyol compound (a3-2) is 500 to 20,000, preferably 2,000 to 15,000, and particularly preferably 3,000 to 8,000. If the weight average molecular weight of the polyol compound (a3-2) is too small, the molecular weight of the urethane (meth) acrylate compound (A) becomes relatively small. When it is too large, the coating film made of a resin solution that is blended to form an active energy ray-curable composition tends to be sticky. Further, since the polyol compound (a3-2) has a large weight average molecular weight, the reactivity at the time of synthesis becomes poor, so that the reaction time becomes extremely long, and this is not practically preferable as a synthesis condition.

Further, in the weight average molecular weight of the polyol compound, the difference between the polyol compound (a3-1) and the polyol compound (a3-2) is preferably 400 or more, particularly preferably 800 or more, more preferably 1,200 or more. Particularly preferred is 2,000 or more. If the difference is too small, the balance between chemical resistance and elasticity of the cured coating film tends to be inferior, making it difficult to achieve both functions.

The blending ratio (mol ratio) of the polyol compound (a3-1) and the polyol compound (a3-2) is preferably (a3-1) :( a3-2) = 30: 70 to 95: 5, particularly Preferably (a3-1) :( a3-2) = 40: 60 to 90:10, more preferably (a3-1) :( a3-2) = 50: 50 to 85:15.
If the blending ratio of the polyol compound (a3-1) is too large, the viscosity tends to increase too much, and if it is too small, the alkali resistance and ethanol resistance tend to decrease.

Examples of the polyol compound (a3-1) having a weight average molecular weight of less than 500 include ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, trimethylene glycol, dimethylolpropane, neopentyl glycol, 1,2-hexanediol, 2,2-diethyl-1,3-propanediol, 2-butyl-2-ethyl-1,3-propanediol, 1,4-tetramethylenediol, 1,3-tetramethylenediol, 2-methyl-1, 3-trimethylenediol, 1,5-pentamethylenediol, 1,6-hexamethylenediol, 3-methyl-1,5-pentamethylenediol, 2,4-diethyl-1,5-pentamethylenediol, 1, 9-nonanediol, 2-methyl-1,8-o Aliphatic alcohols such as tandiol, ditrimethylolpropane, dipentaerythritol, tripentaerythritol, cyclohexanediols such as 1,4-cyclohexanediol and cyclohexyldimethanol, bisphenols such as bisphenol A, tricyclodecane dimethanol, xylitol And sugar alcohols such as sorbitol and the like, and these can be used alone or in combination of two or more. Of these, neopentyl glycol, 1,2-hexanediol, and tricyclodecane dimethanol are preferably used because of their low crystallinity.

Examples of the polyol compound (a3-2) having a weight average molecular weight of 500 to 20,000 include aliphatic polyols, alicyclic polyols, polyether polyols, polyester polyols, polycarbonate polyols, polyolefin polyols, Examples include polybutadiene polyols, (meth) acrylic polyols, and polysiloxane polyols.

Examples of the aliphatic polyol include ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, trimethylene glycol, dimethylolpropane, neopentyl glycol, 2,2-diethyl-1,3-propanediol, and 2-butyl- 2-ethyl-1,3-propanediol, 1,4-tetramethylenediol, 1,3-tetramethylenediol, 2-methyl-1,3-trimethylenediol, 1,5-pentamethylenediol, 1,6 -Hexamethylenediol, 3-methyl-1,5-pentamethylenediol, 2,4-diethyl-1,5-pentamethylenediol, pentaerythritol diacrylate, 1,9-nonanediol, 2-methyl-1,8 -Two hydroxyl acids such as octanediol , Aliphatic alcohols containing 3 or more hydroxyl groups such as glycerin, trimethylolpropane, trimethylolethane, and the like, and the like. Two or more kinds can be used in combination.

Examples of the alicyclic polyol include cyclohexanediols such as 1,4-cyclohexanediol and cyclohexyldimethanol, hydrogenated bisphenols such as hydrogenated bisphenol A, and tricyclodecane dimethanol. Two or more species can be used in combination.

Examples of the polyether polyol include, for example, polyether glycols containing alkylene structures such as polyethylene glycol, polypropylene glycol, polytetramethylene glycol, polybutylene glycol, polypentamethylene glycol, polyhexamethylene glycol, and the like. A random or block copolymer is mentioned.

Examples of the polyester-based polyol include three types of components: a condensation polymer of a polyhydric alcohol and a polycarboxylic acid; a ring-opening polymer of a cyclic ester (lactone); a polyhydric alcohol, a polycarboxylic acid, and a cyclic ester. And the like.

Examples of the polyhydric alcohol include ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, trimethylene glycol, 1,4-tetramethylene diol, 1,3-tetramethylene diol, 2-methyl-1,3-trimethyl. Methylene diol, 1,5-pentamethylene diol, neopentyl glycol, 1,6-hexamethylene diol, 3-methyl-1,5-pentamethylene diol, 2,4-diethyl-1,5-pentamethylene diol, glycerin , Trimethylolpropane, trimethylolethane, cyclohexanediols (such as 1,4-cyclohexanediol), bisphenols (such as bisphenol A), sugar alcohols (such as xylitol and sorbitol)

Examples of the polyvalent carboxylic acid include aliphatic dicarboxylic acids such as malonic acid, maleic acid, fumaric acid, succinic acid, glutaric acid, adipic acid, suberic acid, azelaic acid, sebacic acid, and dodecanedioic acid; -Alicyclic dicarboxylic acids such as cyclohexanedicarboxylic acid; aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid, orthophthalic acid, 2,6-naphthalenedicarboxylic acid, paraphenylenedicarboxylic acid, trimellitic acid, and the like.

Examples of the cyclic ester include propiolactone, β-methyl-δ-valerolactone, and ε-caprolactone.

Examples of the polycarbonate polyol include a reaction product of a polyhydric alcohol and phosgene; a ring-opening polymer of a cyclic carbonate (such as alkylene carbonate).

Examples of the polyhydric alcohol include polyhydric alcohols exemplified in the description of the polyester-based polyol, and examples of the alkylene carbonate include ethylene carbonate, trimethylene carbonate, tetramethylene carbonate, hexamethylene carbonate, and the like. It is done.

The polycarbonate-based polyol may be a compound having a carbonate bond in the molecule and having a hydroxyl group at the end, and may have an ester bond together with the carbonate bond.

Examples of the polyolefin-based polyol include those having a saturated hydrocarbon skeleton having a homopolymer or copolymer such as ethylene, propylene and butene, and having a hydroxyl group at the molecular end.

Examples of the polybutadiene-based polyol include those having a butadiene copolymer as a hydrocarbon skeleton and having a hydroxyl group at the molecular end.
The polybutadiene-based polyol may be a hydrogenated polybutadiene polyol in which all or part of the ethylenically unsaturated groups contained in the structure thereof are hydrogenated.

Examples of the polyisoprene-based polyol include those having a copolymer of isoprene as a hydrocarbon skeleton and a hydroxyl group at the molecular end.
The polyisoprene-based polyol may be a hydrogenated polyisoprene polyol in which all or part of the ethylenically unsaturated groups contained in the structure is hydrogenated.

Examples of the (meth) acrylic polyol include those having at least two hydroxyl groups in the molecule of the polymer or copolymer of the (meth) acrylic ester. For example, methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, hexyl (meth) acrylate, octyl (meth) acrylate, (meth) acrylic And (meth) acrylic acid alkyl esters such as 2-ethylhexyl acid, decyl (meth) acrylate, dodecyl (meth) acrylate, and octadecyl (meth) acrylate.

Examples of the polysiloxane polyol include dimethyl polysiloxane polyol and methylphenyl polysiloxane polyol.

Among these, aliphatic polyols and alicyclic polyols are preferably used in terms of suppressing stickiness when it becomes a cured coating film, and polyester polyols, polyether polyols, and polycarbonate polyols are preferred in terms of imparting flexibility. Preferably used.

The production method of the urethane (meth) acrylate compound (A1) is usually a reaction of the hydroxyl group-containing (meth) acrylate compound (a1), the polyvalent isocyanate compound (a2), and the polyol compound (a3) with a reactor. The reaction product obtained by reacting the polyol-based compound (a3) and the polyvalent isocyanate-based compound (a2) in advance may be added to the hydroxyl group-containing (meth) acrylate-based compound ( The reaction of a1) is useful in terms of reaction stability and reduction of byproducts.

For the reaction between the polyol compound (a3) and the polyvalent isocyanate compound (a2), known reaction means can be used. At that time, for example, the molar ratio of the isocyanate group in the polyvalent isocyanate compound (a2) to the hydroxyl group in the polyol compound (a3) is usually about 2n: (2n-2) (n is an integer of 2 or more). Thus, after obtaining the terminal isocyanate group-containing urethane (meth) acrylate compound having the isocyanate group remaining, the addition reaction with the hydroxyl group-containing (meth) acrylate compound (a1) is made possible.

The addition reaction of the reaction product obtained by reacting the polyol compound (a3) and the polyvalent isocyanate compound (a2) in advance with the hydroxyl group-containing (meth) acrylate compound (a1) is also a known reaction. Means can be used.

The reaction molar ratio between the reaction product and the hydroxyl group-containing (meth) acrylate compound (a1) is, for example, that the polyisocyanate compound (a2) has two isocyanate groups and the hydroxyl group-containing (meth) acrylate compound (a1). ) Has one hydroxyl group, the reaction product: hydroxyl group-containing (meth) acrylate compound (a1) is about 1: 2, and the polyisocyanate compound (a2) has three isocyanate groups. When the hydroxyl group-containing (meth) acrylate compound (a1) has one hydroxyl group, the reaction product: hydroxyl group-containing (meth) acrylate compound (a1) is about 1: 3.

In the addition reaction between the reaction product and the hydroxyl group-containing (meth) acrylate compound (a1), the reaction is terminated when the residual isocyanate group content in the reaction system is 0.5% by weight or less. A (meth) acrylate compound (A1) is obtained.

In the reaction between the polyol compound (a3) and the polyvalent isocyanate compound (a2), and further in the reaction between the reaction product and the hydroxyl group-containing (meth) acrylate compound (a1), a catalyst is used for the purpose of promoting the reaction. It is also preferable to use, for example, organometallic compounds such as dibutyltin dilaurate, trimethyltin hydroxide, tetra-n-butyltin, zinc octenoate, tin octenoate, cobalt naphthenate, stannous chloride. Metal salts such as stannic chloride, triethylamine, benzyldiethylamine, 1,4-diazabicyclo [2,2,2] octane, 1,8-diazabicyclo [5,4,0] undecene, N, N, N ′, Amine catalysts such as N'-tetramethyl-1,3-butanediamine and N-ethylmorpholine, bismuth nitrate, bibromide In addition to trout, bismuth iodide, bismuth sulfide, etc., organic bismuth compounds such as dibutyl bismuth dilaurate and dioctyl bismuth dilaurate, bismuth 2-ethylhexanoate, bismuth naphthenate, bismuth isodecanoate, bismuth neodecanoate, lauryl Organic acid bismuth such as bismuth acid salt, bismuth maleate, bismuth stearate, bismuth oleate, bismuth linoleate, bismuth acetate, bismuth bisneodecanoate, bismuth disalicylate, bismuth subgallate Examples thereof include bismuth-based catalysts such as salts, among which dibutyltin dilaurate and 1,8-diazabicyclo [5,4,0] undecene are preferable.
It is also preferable to use a zirconium-based catalyst and a liquid zinc-based catalyst in combination.

In the reaction between the polyol compound (a3) and the polyvalent isocyanate compound (a2), and in the reaction between the reaction product and the hydroxyl group-containing (meth) acrylate compound (a1), it reacts with the isocyanate group. Organic solvents having no functional group, for example, esters such as ethyl acetate and butyl acetate, ketones such as methyl ethyl ketone and methyl isobutyl ketone, and organic solvents such as aromatics such as toluene and xylene can be used.

The reaction temperature is usually 30 to 90 ° C., preferably 40 to 80 ° C., and the reaction time is usually 2 to 10 hours, preferably 3 to 8 hours.

The urethane (meth) acrylate compound (A1) preferably has 2 to 10 ethylenically unsaturated groups, particularly preferably 2 to 6 in terms of imparting durability to the cured coating film. Having an ethylenically unsaturated group. If the number of such ethylenically unsaturated groups is too large, the crosslinking density after curing becomes too large, and the coating film tends to be too hard and it is difficult to obtain a moist soft feeling. Since it is difficult to obtain, the cured coating film surface tends to be sticky and the durability performance tends to be lowered.

The weight average molecular weight of the urethane (meth) acrylate compound (A1) is preferably 1,000 to 50,000, more preferably 2,000 to 40,000. If the weight average molecular weight is too small, the cured coating film tends to be brittle, and if it is too large, the viscosity tends to be high and difficult to handle.

As the polyol compound (a3) constituting the urethane (meth) acrylate compound (A1), a polyol compound (a3-1) having a weight average molecular weight of less than 500 and a polyol compound (a3) having a weight average molecular weight of 500 to 20,000 are used. -2), the urethane (meth) acrylate compound (A1) preferably has a weight average molecular weight of 2,500 to 50,000, particularly preferably 2,500 to 40,000, More preferably, it is 3,500 to 30,000.
If the weight average molecular weight is too small, the unsaturated group equivalent in the compounding will increase relatively, and when it is a cured coating film, the hardness difference from the fine synthetic resin filler (B) becomes remarkable, and the external The stress of the curable resin composition tends to be damaged due to the stress that cannot be released, and if it is too large, the viscosity of the curable resin composition tends to be too high, and a sufficient crosslinking density cannot be obtained. There is a tendency that the surface becomes sticky and various durability tends to decrease.

The weight average molecular weight is measured in the same manner as described above.

The viscosity of the urethane (meth) acrylate compound (A1) at 60 ° C. is preferably 1,000 to 100,000 mPa · s, particularly preferably 1,500 to 50,000 mPa · s. When the viscosity is out of the above range, the coatability tends to be lowered.
The viscosity is measured by an E-type viscometer as described above.

<Urethane (meth) acrylate compound (A2)>
The urethane (meth) acrylate compound (A2) in the present invention is obtained by reacting a hydroxyl group-containing (meth) acrylate compound (a1) and a polyvalent isocyanate compound (a2).

The content of ethylenically unsaturated groups in the urethane (meth) acrylate compound (A2) used in the present invention is preferably 2 to 10, particularly preferably 2 to 6. If the number of such ethylenically unsaturated groups is too large, the crosslinking density after curing becomes too large, and the coating film tends to be too hard and it is difficult to obtain a moist soft feeling. Since it is difficult to obtain, the surface of the cured coating film tends to be sticky or the durability performance tends to deteriorate.

In order to adjust the number of ethylenically unsaturated groups, the hydroxyl group-containing (meth) acrylate compound (a1) and the polyvalent isocyanate compound (a2) may be appropriately selected and used. When using a hydroxyl group-containing (meth) acrylate compound (a1) having three ethylenically unsaturated groups and using a diisocyanate compound as the polyvalent isocyanate compound (a2), urethane (meth) acrylate The number of ethylenically unsaturated groups in the compound (A2) is 6.

What is necessary is just to manufacture according to the manufacturing method of the said urethane (meth) acrylate type compound (A1) about the manufacturing method of a urethane (meth) acrylate type compound (A2).

The reaction molar ratio between the polyvalent isocyanate compound (a2) and the hydroxyl group-containing (meth) acrylate compound (a1) is, for example, that the polyisocyanate compound (a2) has two isocyanate groups and has a hydroxyl group content ( When the meth) acrylate compound (a1) has one hydroxyl group, the polyvalent isocyanate compound (a2): hydroxyl group-containing (meth) acrylate compound (a1) is about 1: 2, and the polyisocyanate compound When the compound (a2) has three isocyanate groups and the hydroxyl group-containing (meth) acrylate compound (a1) has one hydroxyl group, the polyvalent isocyanate compound (a2): hydroxyl group-containing (meth) acrylate compound (A1) is about 1: 3.

In the addition reaction between the polyvalent isocyanate compound (a2) and the hydroxyl group-containing (meth) acrylate compound (a1), the reaction is terminated when the residual isocyanate group content in the reaction system is 0.5% by weight or less. By making it, a urethane (meth) acrylate type compound (A2) is obtained.

The weight average molecular weight of the obtained urethane (meth) acrylate compound (A2) is preferably 1,000 to 20,000, and more preferably 1,000 to 10,000. If the weight average molecular weight is too small, the flexibility of the cured coating film tends to be reduced, and a moist soft feeling tends not to be obtained. If it is too large, a sufficient crosslinking density cannot be obtained during curing, and the cured coating film surface It tends to be sticky or the durability tends to decrease.

The above weight average molecular weight is measured in the same manner as described above.

The viscosity of the urethane (meth) acrylate compound (A2) at 60 ° C. is preferably 1,000 to 30,000 mPa · s, particularly preferably 1,000 to 20,000 mPa · s. When the viscosity is out of the above range, the coatability tends to be lowered.
The viscosity is measured by an E-type viscometer as described above.

[Fine particle synthetic resin filler (B)]
Examples of the fine particle synthetic resin filler (B) in the present invention include nitrogen atom-containing synthetic resin fillers such as nylon filler, polyurethane filler, polyurea filler, polyamideimide filler, polyacrylamide filler;
Polyolefin resin fillers such as polyethylene filler and polypropylene filler;
Poly (meth) acrylic filler, polybutyl (meth) acrylic filler, (meth) acrylic group-containing synthetic resin filler consisting of a single polymerization component such as polystyrene filler, (meth) acrylic group-containing synthetic resin consisting of two or more polymerization components (Meth) acrylic synthetic resin fillers such as fillers;
Sulfur atom-containing synthetic resin filler such as polyphenylene sulfide filler and polyethersulfone filler;
Fluorine atom-containing synthetic resin filler such as polytetrafluoroethylene filler;
An epoxy group-containing synthetic resin filler comprising an epoxy resin;
Polycarbonate resin filler;
Examples of the filler include composite synthetic resin fillers and core-shell multilayer fillers.

Among these, a nitrogen atom-containing synthetic resin filler and a polyolefin resin filler are preferable. Nitrogen atom-containing synthetic resin filler preferably has excellent affinity with urethane (meth) acrylate compound (A), particle aggregation stability, sedimentation stability, moist soft coating and elasticity It is a polyurethane filler because it is easy to do, and a polyethylene filler is preferable as the polyolefin resin filler. Furthermore, in order to give a moist touch feeling to the cured coating film, it is preferable to use the polyurethane filler and the polyethylene filler in combination.

Examples of the nylon filler include those manufactured by Toray Industries, Inc. (trade names: “SP-10”, “SP-500”, “TR-1”, “TR-2”, “842-P48”, “842-P70”). , “842-P80”).

Examples of the polyurethane filler include cross-linked urethane beads manufactured by Negami Kogyo Co., Ltd. (trade names: “Art Pearl C Series”, “Art Pearl P Series”, “Art Pearl JB Series”, “Art Pearl U Series”, “Art” "Pearl CE Series", "Art Pearl AK Series", "Art Pearl HI Series", "Art Pearl MM Series", "Art Pearl FF Series", "Art Pearl TK Series", "Art Pearl C-TH Series", " Art Pearl RW-Z series "," Art Pearl RU-V series "," Art Pearl BP series ").

Among these, transparent fine particles are preferable as those capable of obtaining a transparent to white coating film as a cured coating film without impairing photocurability, and those having a white appearance as a fine particle appearance are preferable. Specifically, as such filler, Art Pearl C-400T, Art Pearl C-600T, Art Pearl C-800T, Art Pearl P-400T, Art Pearl P-600T, Art Pearl P-800T, Art Pearl JB-400T, Art Pearl JB-600T, Art Pearl JB-800T, Art Pearl U-600T, Art Pearl CE-400T, Art Pearl CE-800T, Art Pearl AK-300TR, Art Pearl AK-400TR, Art Pearl AK-800TR, Art Pearl HI-400T, Art Pearl MM-120T, Art Pearl FF-421T, Art Pearl FF-411T, Art Pearl FF-413T, Art Pearl TK-600T, Art Pearl C-600TH, Art Pearl RZ-600T, Art Pearl RY- 600T, Art Pearl RT-600T, Art Pearl RX-600T, Art Pearl RW-600T, Art Pearl RZ-600T, Art Pearl RV-600T, Art Pearl RU-600T, Art Pearl RV-600T, Art Pearl BP-600T Can be mentioned.

Examples of the polyamideimide resin filler include those manufactured by Toray Industries, Inc. (trade name: “Trepearl PAI”).

The polyethylene filler is preferably a solvent-dispersed polyethylene filler. For example, polyethylene wax and modified polyethylene wax (trade names; “Micro Flat UN-8”, “Micro Flat PEX-101” manufactured by Koyo Chemical Co., Ltd.) , “Micro Flat B-501”), polyethylene wax manufactured by Big Chemie Japan, and modified polyethylene wax (trade names; “CERAFLOUR928”, “CERAFLOUR950”, “CERAFLOUR988”, “CERAFLOUR990”, “CERAFLOUR991”, “CERAFLOUR995”) ”,“ CERACOL39 ”,“ CERAFAK111 ”,“ CERAMAT250 ”,“ CERAMAT258 ”,“ MINERPOL221 ”), and the like.

The above-mentioned polypropylene filler is preferably a solvent dispersion type, and examples thereof include a polypropylene wax manufactured by Big Chemie Japan, a modified polypropylene wax (trade name “CERAFLOUR970”), and the like.

Examples of the (meth) acrylic group-containing synthetic resin filler include acrylic beads manufactured by Negami Kogyo Co., Ltd. (trade names; “Art Pearl GR Series”, “Art Pearl SE Series”, “Art Pearl G Series”, “Art Pearl” GS series "," Art Pearl J series "," Art Pearl MF series "," Art Pearl BE series "). Among these, transparent fine particles are preferable as those capable of obtaining a transparent to white coating film as a cured coating film without impairing photocurability, and those having a white appearance as a fine particle appearance are preferable. Specifically as such filler, Art Pearl GR-300T, Art Pearl GR-400T, Art Pearl GR-600T, Art Pearl GR-800T, Art Pearl SE-020T, Art Pearl SE-010T, Art Pearl SE-006T, Art Pearl G-400T, Art Pearl G-800T, Art Pearl GS-310T, Art Pearl GS-350T, Art Pearl GS-850TC, Art Pearl J-4P, Art Pearl J-5P, Art Pearl J-7P, Art Pearl Examples include J-4PY, Art Pearl J-6PF, Art Pearl J-7PY, Art Pearl MF-0063, and Art Pearl BE-006T.

Examples of the sulfur atom-containing synthetic resin filler include polyphenylene sulfide resin fine particles (trade name: “Trepearl PPS”), polyethersulfone resin (trade name: “Trepearl PES”) manufactured by Toray Industries, Inc.

Examples of the fluorine atom-containing synthetic resin filler include polyethylene manufactured by Koyo Chemical Co., Ltd., and polytetrafluoroethylene mixed wax (trade name: “Micro-flat PF-8”), manufactured by Big Chemie Japan Co., Ltd. Fluoroethylene wax (trade names; “CERAFLOUR980”, “CERAFLOUR981”), polyethylene-polytetrafluoroethylene mixed wax (trade name; “CERAFLOUR997”), polytetrafluoroethylene-modified polyethylene wax (trade name; “CERAFLOUR998”, "CERACOL607"), polytetrafluoroethylene microparticles manufactured by Kitamura (trade names: "KTL-8N", "KTL-8F", "KTL-9S", "KTL-10N", "KTL-20N") It is done.

Examples of the epoxy group-containing synthetic resin filler include those manufactured by Toray Industries, Inc. (trade name: “Trepearl EP”).

Examples of the polycarbonate resin filler include those manufactured by Koyo Chemical Co., Ltd. (trade name: “Micro-flat MA-07N”).

The average particle size of the fine particle synthetic resin filler (B) in the present invention is preferably 1 to 30 μm, particularly preferably 2 to 20 μm, and further preferably 4 to 15 μm.
If the average particle size is too small, the gloss of the cured coating film tends to be high, and there is a tendency that it is difficult to feel a high-grade appearance, and if it is too large, the wear contact becomes large and wear resistance decreases, and the cured surface Since the unevenness becomes large and rough, it tends to be difficult to obtain a moist and soft touch feeling.

Since the fine synthetic resin filler (B) is substantially spherical, the particle diameter can be determined using a sphere as a basic shape, and generally the number average particle diameter, length average particle diameter, area average Although there are particle diameter, volume average particle diameter, etc., the average particle diameter of the present invention is a volume average particle diameter usually used, and the volume average particle diameter is measured by a laser diffraction / scattering type particle size distribution meter. .

The true specific gravity of the fine synthetic resin filler (B) is preferably 0.8 to 2.3, particularly preferably 0.8 to 2, and further preferably 0.8 to 1.5.
If the true specific gravity is too large, fine particles will settle in the drying step after coating and tend not to appear as surface irregularities. If it is too small, mixing of the urethane (meth) acrylate compound (A) tends to be difficult. .

Examples of the method for producing the fine particle synthetic resin filler (B) include a method for directly producing a fine particle synthetic resin by polymerizing a monomer by suspension polymerization, emulsion polymerization, seed polymerization, and the like, and various methods. There is a method of mechanically pulverizing a normal synthetic resin produced by the above method into fine particles.
Among these, the polymerization method is preferable in that fine particles having a uniform shape, particularly spherical particles having excellent fluidity and dispersibility can be obtained.

The glass transition temperature (Tg) of the fine particle synthetic resin filler (B) in the present invention is preferably −140 to 40 ° C., particularly preferably −135 to 20 ° C., more preferably −130 to 0 ° C. is there.
If the glass transition temperature is too low, the coating surface tends to be too sticky, and if it is too high, a rubbery and moist soft feeling tends to be hardly obtained on the coating surface.

The glass transition temperature can be measured by using a temperature modulation DSC (DSC2920 manufactured by TA Instruments). Measurement conditions are such that a sample of about 1 to 5 mg is enclosed in a dedicated aluminum pan, and the temperature is raised within a range of −100 ° C. to 100 ° C. and 3 ° C./min.

The content (solid content) of the particulate synthetic resin filler (B) in the present invention is preferably 25 to 400 parts by weight with respect to 100 parts by weight of the urethane (meth) acrylate compound (A). The amount is particularly preferably 30 to 350 parts by weight, and further preferably 35 to 250 parts by weight. If the content of the fine-particle synthetic resin filler (B) is too large, the wear of the cured coating film tends to be extremely lowered, and the coating surface tends to be rough. There is a tendency that a touch feeling is difficult to obtain.

The content (solid content) of the polyurethane filler is preferably 25 to 400 parts by weight, particularly preferably 30 to 300 parts by weight, with respect to 100 parts by weight of the urethane (meth) acrylate compound (A). More preferably, it is 35 to 250 parts by weight. If the polyurethane filler content is too high, the wear of the cured coating film tends to be extremely reduced, the surface of the coating film tends to be rough, and the amount is too small. There is.

Furthermore, as a content ratio (weight ratio of solid content) when the polyurethane filler and the polyethylene filler are used in combination, the polyethylene filler is 0.1 to 70 parts by weight with respect to 100 parts by weight of the polyurethane filler. The amount is preferably 0.5 to 50 parts by weight, more preferably 1 to 30 parts by weight.
If the content of the polyethylene filler in the polyurethane filler is too small, the softness of the coating film is lowered, and the glossiness tends to be impaired due to the increase in gloss, and if it is too much, the scratch resistance performance of the cured coating film is reduced. It tends to be easier.

In addition, in the regulation of the above content, when the fine particle synthetic resin filler (B) is a dispersion such as a solvent, it is specified as a weight in terms of solid content.

The active energy ray-curable resin composition of the present invention contains the urethane (meth) acrylate compound (A) and the fine particle synthetic resin filler (B) as essential components. By forming a network structure by crosslinking by irradiation, it is possible to adjust the balance between hardness and flexibility in the coating film and to improve durability such as water resistance and heat resistance. C) is preferably blended.

[Ethylenically unsaturated monomer (C)]
The ethylenically unsaturated monomer (C) may be any ethylenically unsaturated monomer (excluding the urethane (meth) acrylate compound (A)) having one or more ethylenically unsaturated groups in one molecule. , For example, a monofunctional monomer, a bifunctional monomer, a trifunctional or higher monomer.

The monofunctional monomer may be any monomer containing one ethylenically unsaturated group. For example, styrene, vinyl toluene, chlorostyrene, α-methylstyrene, methyl (meth) acrylate, ethyl (meth) acrylate, acrylonitrile , Vinyl acetate, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, phenoxyethyl (meth) acrylate, 2-phenoxy-2-hydroxypropyl (meth) acrylate 2-hydroxy-3-phenoxypropyl (meth) acrylate, 3-chloro-2-hydroxypropyl (meth) acrylate, glycerol mono (meth) acrylate, glycidyl (meth) acrylate, lauryl (meth) acrylate Rate, cyclohexyl (meth) acrylate, isobornyl (meth) acrylate, tricyclodecanyl (meth) acrylate, dicyclopentenyl (meth) acrylate, n-butyl (meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate , Octyl (meth) acrylate, nonyl (meth) acrylate, decyl (meth) acrylate, isodecyl (meth) acrylate, dodecyl (meth) acrylate, n-stearyl (meth) acrylate, benzyl (meth) acrylate, phenol ethylene oxide modified ( Phthalic acid derivatives such as (meth) acrylate, nonylphenol propylene oxide modified (meth) acrylate, 2- (meth) acryloyloxy-2-hydroxypropyl phthalate -Efester (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, carbitol (meth) acrylate, benzyl (meth) acrylate, caprolactone-modified 2-hydroxyethyl (meth) acrylate, butoxyethyl (meth) acrylate, allyl (meth) acrylate Acryloylmorpholine, 2-hydroxyethylacrylamide, N-methylol (meth) acrylamide, N-vinylpyrrolidone, 2-vinylpyridine, 2- (meth) acryloyloxyethyl acid phosphate monoester, and the like.

In addition to the monofunctional monomer, there may be mentioned Michael adduct of acrylic acid or 2-acryloyloxyethyl dicarboxylic acid monoester. Examples of the Michael adduct of acrylic acid include acrylic acid dimer, methacrylic acid dimer, acrylic acid trimer. Methacrylic acid trimer, acrylic acid tetramer, methacrylic acid tetramer and the like. Examples of 2-acryloyloxyethyl dicarboxylic acid monoester which is a carboxylic acid having a specific substituent include 2-acryloyloxyethyl succinic acid monoester, 2-methacryloyloxyethyl succinic acid monoester, and 2-acryloyloxyethyl. Examples thereof include phthalic acid monoester, 2-methacryloyloxyethyl phthalic acid monoester, 2-acryloyloxyethyl hexahydrophthalic acid monoester, and 2-methacryloyloxyethyl hexahydrophthalic acid monoester. Furthermore, oligoester acrylate is also mentioned.

The bifunctional monomer may be any monomer containing two ethylenically unsaturated groups. For example, ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate, polyethylene glycol Di (meth) acrylate, propylene glycol di (meth) acrylate, dipropylene glycol di (meth) acrylate, polypropylene glycol di (meth) acrylate, butylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, ethylene oxide Modified bisphenol A type di (meth) acrylate, propylene oxide modified bisphenol A type di (meth) acrylate, 1,6-hexanediol di (meth) acrylate 1,6-hexanediol ethylene oxide modified di (meth) acrylate, 1,9-nonanediol di (meth) acrylate, glycerin di (meth) acrylate, pentaerythritol di (meth) acrylate, ethylene glycol diglycidyl ether di (Meth) acrylate, diethylene glycol diglycidyl ether di (meth) acrylate, diglycidyl phthalate di (meth) acrylate, hydroxypivalic acid modified neopentyl glycol di (meth) acrylate, isocyanuric acid ethylene oxide modified diacrylate, 2- ( And (meth) acryloyloxyethyl acid phosphate diester.

The tri- or higher functional monomer may be any monomer containing three or more ethylenically unsaturated groups. For example, trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) Acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, tri (meth) acryloyloxyethoxytrimethylolpropane, glycerin polyglycidyl ether poly (meth) acrylate, isocyanuric acid ethylene oxide modified triacrylate, ethylene Oxide-modified dipentaerythritol penta (meth) acrylate, ethylene oxide-modified dipentaerythritol hexa (meth) acrylate, ethylene Koxide modified pentaerythritol tri (meth) acrylate, ethylene oxide modified pentaerythritol tetra (meth) acrylate, caprolactone modified dipentaerythritol penta (meth) acrylate, caprolactone modified dipentaerythritol hexa (meth) acrylate, caprolactone modified pentaerythritol tri (meth) ) Acrylate, caprolactone-modified pentaerythritol tetra (meth) acrylate, succinic acid-modified pentaerythritol tri (meth) acrylate, and the like.

These ethylenically unsaturated monomers (C) may be used alone or in combination of two or more. In addition, the ethylenically unsaturated monomer (C) may be separately added to the urethane (meth) acrylate compound (A) or the fine particle synthetic resin filler (B), or may be urethane (meth) acrylate. As a production raw material for the compound (A), a part of the compound (A) may be left in the system during production.

Among the ethylenically unsaturated monomers (C), monofunctional monomers and bifunctional monomers are preferable, there is no aromatic ring, yellowing of the coating film can be suppressed, and cyclohexyl (meth) acrylate and isobornyl are highly versatile. (Meth) acrylate, dicyclopentenyl (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, diethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, dipropylene glycol di ( Particularly preferred are meth) acrylate, neopentyl glycol di (meth) acrylate, and 1,6-hexanediol di (meth) acrylate.

It is also preferable to use a hydroxyl group-containing ethylenically unsaturated monomer. Specific examples include 2-hydroxyethyl (meth) acrylate and 2-hydroxypropyl (meta) because they have no aromatic ring and suppress yellowing of the coating film. ) Acrylate, 2-hydroxybutyl (meth) acrylate, caprolactone-modified 2-hydroxyethyl (meth) acrylate, pentaerythritol tri (meth) acrylate, dipentaerythritol penta (meth) acrylate, particularly preferably 2-hydroxyethyl ( From the viewpoint of versatility, (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, and caprolactone-modified 2-hydroxyethyl (meth) acrylate are preferable.

In the present invention, the content of the ethylenically unsaturated monomer (C) is preferably 0 to 500 parts by weight, particularly 5 to 500 parts by weight with respect to 100 parts by weight of the urethane (meth) acrylate compound (A). It is preferably 350 parts by weight, more preferably 10 to 150 parts by weight. If the content of the ethylenically unsaturated monomer (C) is too large, in the case of a monofunctional monomer, the coated film becomes sticky, and in the case of a monomer having two or more functions, the cured film becomes too hard. There is a tendency that it is difficult to obtain a moist and soft touch feeling.

[Photopolymerization initiator (D)]
In the present invention, in addition to the urethane (meth) acrylate compound (A) and the fine synthetic resin filler (B), a photopolymerization initiator (D) is added in order to efficiently cure with active energy rays. It is preferable to contain.

Examples of the photopolymerization initiator (D) include diethoxyacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, benzyldimethyl ketal, 4- (2-hydroxyethoxy) phenyl- (2- Hydroxy-2-propyl) ketone, 1-hydroxycyclohexylphenylketone, 2-methyl-2-morpholino (4-thiomethylphenyl) propan-1-one, 2-benzyl-2-dimethylamino-1- (4-morpholino) Acetophenones such as phenyl) butanone and 2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propanone oligomers; benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin isobutyl ether Benzoi etc. Benzophenone, methyl o-benzoylbenzoate, 4-phenylbenzophenone, 4-benzoyl-4'-methyl-diphenyl sulfide, 3,3 ', 4,4'-tetra (t-butylperoxycarbonyl) benzophenone, 2 , 4,6-Trimethylbenzophenone, 4-benzoyl-N, N-dimethyl-N- [2- (1-oxo-2-propenyloxy) ethyl] benzenemethananium bromide, (4-benzoylbenzyl) trimethylammonium chloride Benzophenones such as 2-isopropylthioxanthone, 4-isopropylthioxanthone, 2,4-diethylthioxanthone, 2,4-dichlorothioxanthone, 1-chloro-4-propoxythioxanthone, 2- (3-dimethylamino-2-hydroxy) -3,4 Thioxanthones such as dimethyl-9H-thioxanthone-9-one mesochloride; 2,4,6-trimethylbenzoyl-diphenylphosphine oxide, bis (2,6-dimethoxybenzoyl) -2,4,4-trimethyl-pentylphos And acylphosphine oxides such as fin oxide and bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide. In addition, as for these photoinitiators (D), only 1 type may be used independently and 2 or more types may be used together.

These auxiliary agents include triethanolamine, triisopropanolamine, 4,4′-dimethylaminobenzophenone (Michler ketone), 4,4′-diethylaminobenzophenone, 2-dimethylaminoethylbenzoic acid, 4-dimethylaminobenzoic acid. Ethyl, ethyl 4-dimethylaminobenzoate (n-butoxy), isoamyl 4-dimethylaminobenzoate, 2-ethylhexyl 4-dimethylaminobenzoate, 2,4-diethylthioxanthone, 2,4-diisopropylthioxanthone Etc. can be used in combination.

Among these, benzyl dimethyl ketal, 1-hydroxycyclohexyl phenyl ketone, benzoin isopropyl ether, 4- (2-hydroxyethoxy) -phenyl (2-hydroxy-2-propyl) ketone, 2-hydroxy-2-methyl-1- It is preferable to use phenylpropan-1-one.

As content of a photoinitiator (D), it is 0.1 with respect to 100 weight part of urethane (meth) acrylate type-compounds (A) (when it contains an ethylenically unsaturated monomer (C)). It is preferably ˜40 parts by weight, particularly preferably 1 to 20 parts by weight, particularly preferably 2 to 20 parts by weight.
If the content of the photopolymerization initiator (D) is too small, curing tends to be poor, and if it is too much, the solution stability tends to decrease such as precipitation when used as a coating agent, and embrittlement or coloring may occur. Problems tend to occur.

Thus, the active energy ray containing the urethane (meth) acrylate compound (A) of the present invention and the particulate synthetic resin filler (B), preferably further containing an ethylenically unsaturated monomer (C) and a photopolymerization initiator (D). Although a curable resin composition is obtained, a leveling agent (E), a surface conditioner, a polymerization inhibitor, etc. can be further added as needed.

As the leveling agent (E), a known general leveling agent can be used as long as it has an action of imparting wettability to fine particles when the fine particles are wetted and dispersed in a solution such as a solvent. Silicone-modified resins, fluorine-modified resins, alkyl-modified resins, and the like can be used.

Commercially available products of the leveling agent (E) include, for example, Megafac series manufactured by DIC (MCF350-5, F472, F476, F445, F444, F443, F178, F470, F475, F479, F477, F482, F486, TF1025, F478, F178K, etc.);
X22-3710, X22-162C, X22-3701E, X22160AS, X22170DX, X224015, X22176DX, X22-176F, X224272, KF8001, X22-2000, etc. manufactured by Shin-Etsu Chemical Co., Ltd .;
FM4421, FM0425, FMDA26, FS1265, etc. manufactured by Chisso Corporation;
BY16-750, BY16880, BY16848, SF8427, SF8421, SH3746, SH8400, SF3771, SH3749, SH3748, SH8410, etc. manufactured by Toray Dow Corning;
Momentive Performance Materials Japan TSF series (TSF4460, TSF4440, TSF4445, TSF4450, TSF4446, TSF4453, TSF4452, TSF4730, TSF4770, etc.), FGF502, SILWETL77, SILWTLWETL700L , SILWETL7200, SILWETL7210, SILWETL7220, SILWETL7230, SILWETL7500, SILWETL7510, SILWETL7600, SILWETL7602, SILWETL7604, SILWETL7604, SILWETL7605, SI WETL7607, SILWETL7622, SILWETL7644, SILWETL7650, SILWETL7657, SILWETL8500, SILWETL8600, SILWETL8610, SILWETL8620, SILWETL720) or the like;
Neos Inc.'s Fantient Series (FTX218, 250, 245M, 209F, 222F, 245F, 208G, 218G, 240G, 206D, 240D, etc.), KB Series, etc .;
BYK333, 300, etc. manufactured by Big Chemie Japan;
KL600 manufactured by Kyoeisha Chemical Co., etc.

Examples of the surface conditioner include alkyd resins and cellulose acetate butyrate.
Such alkyd resin and cellulose acetate butyrate have an effect of imparting a film-forming property at the time of coating and a solution viscosity adjusting effect.

Examples of the polymerization inhibitor include p-benzoquinone, naphthoquinone, tolquinone, 2,5-diphenyl-p-benzoquinone, hydroquinone, 2,5-di-t-butylhydroquinone, methylhydroquinone, hydroquinone monomethyl ether, mono-t- Examples thereof include butyl hydroquinone and pt-butyl catechol.

The active energy ray curable resin composition of the present invention includes oil, antioxidant, flame retardant, antistatic agent, stabilizer, reinforcing agent, abrasive, inorganic fine particles, polymer compound (acrylic resin, polyester resin). , Epoxy resin, etc.) can also be blended.

The active energy ray-curable resin composition of the present invention is also preferably used by blending an organic solvent (F) and adjusting the viscosity. Examples of the organic solvent (F) include alcohols such as methanol, ethanol, propanol, n-butanol and i-butanol, ketones such as acetone, methyl isobutyl ketone, methyl ethyl ketone and cyclohexanone, cellosolves such as ethyl cellosolve, Aromatics such as toluene and xylene, glycol ethers such as propylene glycol monomethyl ether, acetates such as methyl acetate, ethyl acetate and butyl acetate, and diacetone alcohol. These organic solvents may be used alone or in combination of two or more.

The active energy ray-curable resin composition of the present invention can be usually diluted to 3 to 60% by weight using the organic solvent (F) and applied to a substrate.

In producing the active energy ray-curable resin composition of the present invention, the urethane (meth) acrylate compound (A), the fine synthetic resin filler (B), and the ethylenically unsaturated monomer used as necessary (C) About the mixing method of a photoinitiator (D) and a leveling agent (E), it does not specifically limit and can be mixed by various methods.

The active energy ray-curable resin composition of the present invention is effectively used as a curable resin composition for coating film formation having a moist and soft touch feeling to various base materials, and active energy ray curing After applying the functional resin composition to the substrate (after further drying if the composition diluted with an organic solvent is applied), it is cured by irradiation with active energy rays. The coating method is not particularly limited, and examples thereof include wet coating methods such as spraying, showering, dipping, flow coating, gravure coating, roll coating, spin coating, dispenser, ink jet, and screen printing. .

As such active energy rays, rays such as far ultraviolet rays, ultraviolet rays, near ultraviolet rays, infrared rays, electromagnetic waves such as X rays and γ rays, electron beams, proton rays, neutron rays, etc. can be used. Curing by ultraviolet irradiation is advantageous from the viewpoint of easy availability and price. In addition, when performing electron beam irradiation, it can harden | cure even without using a photoinitiator (D).

As a method of curing by ultraviolet irradiation, a high pressure mercury lamp that emits light in a wavelength range of 150 to 450 nm, an ultrahigh pressure mercury lamp, a carbon arc lamp, a metal halide lamp, a xenon lamp, a chemical lamp, an electrodeless discharge lamp, an LED, etc. Irradiation of about 30 to 3,000 mJ / cm ² may be performed.
After the ultraviolet irradiation, heating can be performed as necessary to complete the curing.

The coating film thickness (film thickness after curing) is usually preferably 1 to 50 μm, particularly preferably 2 to 40 μm, more preferably 5 to 30 μm.

Examples of the base material to which the active energy ray-curable resin composition of the present invention is applied include polyolefin resins, polyester resins, polycarbonate resins, acrylonitrile butadiene styrene copolymers (ABS), polystyrene resins, and polyamides. Resins, etc. and their molded products (films, sheets, cups, etc.), metal substrates (metal deposition layers, metal plates (copper, stainless steel (SUS304, SUSBA, etc.), aluminum, zinc, magnesium, etc.)), glass, etc. , And those composite substrates.

The active energy ray-curable resin composition comprising the urethane (meth) acrylate compound (A) of the present invention and the fine particle-like synthetic resin filler (B) has a moist touch feeling called soft feel and soft touch. In addition, it is possible to form a cured coating film having a high-class feeling on the appearance of the cured coating film. The active energy ray-curable resin composition of the present invention is very useful as a coating agent (painting in the non-optical field), and has improved workability (solution storage stability) and productivity (production speed) during coating. Has an excellent effect and is very useful.

The coating agent composition preferably contains 2 to 60% by weight of urethane (meth) acrylate compound (A), particularly preferably 3 to 40% by weight, and more preferably 5 to 30% by weight of the entire coating agent composition. % By weight. In addition, the coating agent composition may or may not contain an organic solvent.
If the content of the urethane (meth) acrylate compound (A) is too small, it tends to be difficult to obtain a moist and soft touch feeling, and if it is too much, the wear property of the cured coating film tends to be extremely lowered. is there.

Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to the following examples unless it exceeds the gist. In the examples, “parts” and “%” mean weight standards.

Prior to Examples and Comparative Examples, the following were produced as urethane (meth) acrylate compounds (A).

<Production Example 1: Urethane (meth) acrylate compound (A1-1)>
In a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser, and a nitrogen gas inlet, 13.2 g (0.06 mol) of isophorone diisocyanate, 82.1 g (hydroxyl value 54 mgKOH / g) 0.04 g of hydroquinone methyl ether as a polymerization inhibitor and 0.02 g of dibutyltin dilaurate as a reaction catalyst and reacted at 60 ° C. for 3 hours to give 4.7 g (0.04 mol) of 2-hydroxyethyl acrylate, Was reacted at 60 ° C. for 3 hours, and when the residual isocyanate group became 0.3% or less, the reaction was terminated, and the bifunctional urethane acrylate (A1-1) (weight average molecular weight (Mw): 16,500 )

<Production Example 2: Urethane (meth) acrylate compound (A1-2)>
In a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser, and a nitrogen gas blowing port, isophorone diisocyanate 16.1 g (0.07 mol), bifunctional polyester polyol (hydroxyl value 54 mg KOH / g) 75.2 g (0 0.04 g of hydroquinone methyl ether as a polymerization inhibitor and 0.02 g of dibutyltin dilaurate as a reaction catalyst, reacted at 60 ° C. for 3 hours, 8.6 g (0.07 mol) of 2-hydroxyethyl acrylate, Was reacted at 60 ° C. for 3 hours, and when the residual isocyanate group became 0.3% or less, the reaction was terminated. Bifunctional urethane acrylate (A1-2) (weight average molecular weight (Mw): 9,500) )

<Production Example 3: Urethane (meth) acrylate compound (A1-3)>
Hydrogenated xylylene diisocyanate 16.1 g (0.08 mol), bifunctional polyester polyol (hydroxyl value 63.9 mgKOH / g) in a four-necked flask equipped with a thermometer, stirrer, water-cooled condenser, and nitrogen gas inlet 73.7 g (0.04 mol), hydroquinone methyl ether 0.02 g as a polymerization inhibitor and 0.02 g of dibutyltin dilaurate as a reaction catalyst were charged and reacted at 60 ° C. for 3 hours to obtain 9.9 g of 2-hydroxyethyl acrylate (0 0.09 mol), and reacted at 60 ° C. for 3 hours. The reaction was terminated when the residual isocyanate group became 0.3% or less, and the bifunctional urethane acrylate (A1-3) (weight average molecular weight (Mw ): 10,400).

<Production Example 4: Urethane (meth) acrylate compound (A1-4)>
Hydrogenated xylylene diisocyanate 30.0 g (0.13 mol), bifunctional polycarbonate polyol (hydroxyl value 139.4 mg KOH / g) in a four-necked flask equipped with a thermometer, stirrer, water-cooled condenser, and nitrogen gas inlet 54.2 g (0.07 mol), 0.02 g of hydroquinone methyl ether as a polymerization inhibitor and 0.02 g of dibutyltin dilaurate as a reaction catalyst were charged and reacted at 60 ° C. for 3 hours to obtain 15.9 g (0 .14 mol) was reacted at 60 ° C. for 3 hours, and the reaction was terminated when the residual isocyanate group became 0.3% or less, and the bifunctional urethane acrylate (A1-4) (weight average molecular weight (Mw ): 5,000).

<Production Example 5: Urethane (meth) acrylate compound (A1-5)>
Isocyanate compound (reaction product of (a2) and (a3)) ("Duranate E402" hexamethylene diisocyanate adduct made by Asahi Kasei Chemicals Co., Ltd.) in a four-necked flask equipped with a thermometer, stirrer, water-cooled condenser and nitrogen gas inlet 78 g of type, 0.056 mol), 22 g (a1) (0.17 mol) of 2-hydroxyethyl acrylate, 0.02 g of hydroquinone methyl ether as a polymerization inhibitor, 0 dibutyltin laurate as a reaction catalyst 0.02 g was added and the internal temperature was raised to 70 ° C., followed by reaction for 3 hours. The reaction was terminated when the residual isocyanate group was 0.3% or less, and the urethane (meth) acrylate compound (A1-5) (Weight average molecular weight (Mw): 3,700) was obtained.

<Production Example 6: Urethane (meth) acrylate compound (A2-1)>
Into a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser and a nitrogen gas inlet, an isocyanate compound (a2) (an isocyanate compound composed of a trimer of “Coronate HX” hexamethylene diisocyanate manufactured by Nippon Polyurethane Industry Co., Ltd., 0 0.02 mol) is charged with 42.2 g, polycaprolactone-modified hydroxyl group-containing acrylate compound (a1) (48.5 g (0.21 mol) of “SC1010A” manufactured by MIWON), and 0.2 g of hydroquinone methyl ether as a polymerization inhibitor. Then, 0.02 g of dibutyltin laurate was added as a reaction catalyst, and the internal temperature was raised to 70 ° C., followed by reaction for 3 hours. Further, 9.3 g of SC1010A was added, and the mixture was maintained at 70 ° C. for 1 hour, and the remaining isocyanate When the group becomes 0.3% or less, the reaction is terminated and urethane (medium A) Acrylate compound (A2-1) (weight average molecular weight (Mw): 3,500) was obtained.
The urethane (meth) acrylate compound (A2-1) contains 9.3% of the polycaprolactone-modified hydroxyl group-containing acrylate compound “SC1010A” as the ethylenically unsaturated monomer (C-1).

<Production Example 7: Urethane (meth) acrylate compound (A2-2)>
Into a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser and a nitrogen gas inlet, an isocyanate compound (a2) (an isocyanate compound composed of a trimer of “Coronate HX” hexamethylene diisocyanate manufactured by Nippon Polyurethane Industry Co., Ltd., 0 .10 mol) 60.4 g, 2-hydroxypropyl acrylate (a1) 39.6 g (0.30 mol), hydroquinone methyl ether 0.2 g as a polymerization inhibitor, dibutyltin laurate as a reaction catalyst 0.02 g was added, and the internal temperature was raised to 70 ° C., followed by reaction for 3 hours, held at 70 ° C. for 1 hour, and when the remaining isocyanate group became 0.3% or less, the reaction was terminated. ) Acrylate compound (A2-2) (weight average molecular weight (Mw): 2,200) was obtained.

<Production Example 8: Urethane (meth) acrylate compound (A2-3)>
Into a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser, and a nitrogen gas blowing port, an isocyanate compound (a2) (“Desmodur N3200” manufactured by Bayer MaterialScience, a biuret-modified type of hexamethylene diisocyanate, 0.06 mol) ), 35.8 g of polycaprolactone-modified hydroxyl group-containing acrylate compound (a1) (65.8 g (0.19 mol) of “M100D” manufactured by MIWON), 0.2 g of hydroquinone methyl ether as a polymerization inhibitor, reaction catalyst Then, 0.02 g of dibutyltin laurate was added and the internal temperature was adjusted to 70 ° C., followed by reaction for 3 hours. When the remaining isocyanate group became 0.3% or less, the reaction was terminated, and urethane (meth) acrylate Compound (A2-3) (weight average molecular weight (Mw): 3, 00) was obtained.

The following were prepared as fine-particle synthetic resin filler (B).
(B-1): Polyurethane fine particles (average particle size 6.2 μm: glass transition temperature −52 ° C.)
(B-2): Polyurethane fine particles (average particle size 16.7 μm: glass transition temperature −34 ° C.)
(B-3): polyurethane fine particles (average particle size 6.5 μm: glass transition temperature −34 ° C.)
(B-4): polyurethane fine particles (average particle size 13.5 μm: glass transition temperature −13 ° C.)
(B-5): Polyethylene wax (particle size 5-10 μm)

Moreover, the following non-synthetic resin fillers were prepared as comparative fillers for the fine particulate synthetic resin filler (B).
(B′-1: for comparative example): fumed silica (particle diameter 50 nm)

The following were prepared as the photopolymerization initiator (D).
(D-1): 1-hydroxy-cyclohexyl-phenyl-ketone (manufactured by BASF Japan, Irgacure 184)

The following were prepared as the leveling agent (E).
(E-1): Polyether-modified polydimethylsiloxane (BYK-UV3510, manufactured by BYK Japan)

[Example 1]
100 parts of the bifunctional urethane (meth) acrylate compound (A1-1) obtained in Production Example 1 above, 65.9 parts of fine synthetic resin filler (B-1), fine synthetic resin filler (B- 5) 0.5 parts (solid content), 6.8 parts of photopolymerization initiator (D-1), and 2.7 parts of leveling agent (E-1) are mixed to a solids concentration of 50% using ethyl acetate. Thus, an active energy ray-curable resin composition was obtained.

[Example 2]
100 parts of the bifunctional urethane (meth) acrylate compound (A1-2) obtained in Production Example 2 above, 67.0 parts of fine particle synthetic resin filler (B-3), fine particle synthetic resin filler (B- 5) 2.6 parts (solid content), 6.9 parts of photopolymerization initiator (D-1), and 2.7 parts of leveling agent (E-1) are mixed to a solids concentration of 50% using ethyl acetate. Thus, an active energy ray-curable resin composition was obtained.

Example 3
100 parts of bifunctional urethane (meth) acrylate compound (A1-3) obtained in Production Example 3 above, 65.9 parts of fine particle synthetic resin filler (B-1), fine particle synthetic resin filler (B- 5) 0.5 parts (solid content), 6.8 parts of photopolymerization initiator (D-1), and 2.7 parts of leveling agent (E-1) are mixed to a solids concentration of 50% using ethyl acetate. Thus, an active energy ray-curable resin composition was obtained.

Example 4
100 parts of the bifunctional urethane (meth) acrylate compound (A1-4) obtained in Production Example 4 above, 65.9 parts of fine synthetic resin filler (B-1), fine synthetic resin filler (B- 5) 0.5 parts (solid content), 6.8 parts of photopolymerization initiator (D-1), and 2.7 parts of leveling agent (E-1) are mixed to a solids concentration of 50% using ethyl acetate. Thus, an active energy ray-curable resin composition was obtained.

Example 5
100 parts of urethane (meth) acrylate compound (A1-5) obtained in Production Example 5 above, 67.2 parts of fine particle synthetic resin filler (B-2), fine particle synthetic resin filler (B-5) 3.3 parts (solid content), 6.9 parts of photopolymerization initiator (D-1), and 2.2 parts of leveling agent (E-1) were adjusted to a solid content concentration of 50% using ethyl acetate. The active energy ray-curable resin composition was obtained by blending.

Example 6
100 parts of urethane (meth) acrylate compound (A1-5) obtained in Production Example 5 above, 67.2 parts of fine particle synthetic resin filler (B-3), fine particle synthetic resin filler (B-5) 3.3 parts (solid content), 6.9 parts of photopolymerization initiator (D-1), and 2.2 parts of leveling agent (E-1) were adjusted to a solid content concentration of 50% using ethyl acetate. The active energy ray-curable resin composition was obtained by blending.

Example 7
100 parts of urethane (meth) acrylate compound (A2-1) obtained in Production Example 6 above, 67.2 parts of fine synthetic resin filler (B-1), fine synthetic resin filler (B-5) 3.3 parts (solid content), 6.9 parts of photopolymerization initiator (D-1), and 2.2 parts of leveling agent (E-1) were adjusted to a solid content concentration of 50% using ethyl acetate. The active energy ray-curable resin composition was obtained by blending.

Example 8
100 parts of urethane (meth) acrylate compound (A2-1) obtained in Production Example 6 above, 67.2 parts of fine synthetic resin filler (B-2), fine synthetic resin filler (B-5) 3.3 parts (solid content), 6.9 parts of photopolymerization initiator (D-1), and 2.2 parts of leveling agent (E-1) were adjusted to a solid content concentration of 50% using ethyl acetate. The active energy ray-curable resin composition was obtained by blending.

Example 9
100 parts of urethane (meth) acrylate compound (A2-1) obtained in Production Example 6 above, 67.2 parts of fine particle synthetic resin filler (B-1), photopolymerization initiator (D-1) 6. Nine parts and 2.8 parts of a leveling agent (E-1) were blended using ethyl acetate to a solid content concentration of 50% to obtain an active energy ray-curable resin composition.

Example 10
100 parts of urethane (meth) acrylate compound (A2-2) obtained in Production Example 7 above, 65.9 parts of fine particle synthetic resin filler (B-1), fine particle synthetic resin filler (B-5) 0.5 parts (solid content), 6.8 parts of photopolymerization initiator (D-1), and 2.7 parts of leveling agent (E-1) were adjusted to a solid content concentration of 50% using ethyl acetate. The active energy ray-curable resin composition was obtained by blending.

Example 11
100 parts of urethane (meth) acrylate compound (A2-3) obtained in Production Example 8 above, 65.9 parts of fine synthetic resin filler (B-1), fine synthetic resin filler (B-5) 0.5 parts (solid content), 6.8 parts of photopolymerization initiator (D-1), and 2.7 parts of leveling agent (E-1) were adjusted to a solid content concentration of 50% using ethyl acetate. The active energy ray-curable resin composition was obtained by blending.

[Comparative Example 1]
In Example 5, the fine synthetic resin fillers (B-2) and (B-5) and the leveling agent (E-1) were not blended, and the blending amount of the photopolymerization initiator (D-1) was 4 An active energy ray-curable resin composition was obtained in the same manner as in Example 5 except that the parts were changed to parts.

[Comparative Example 2]
In Example 7, the synthetic resin fillers (B-1) and (B-5) in fine particles and the leveling agent (E-1) were not blended, and the blending amount of the photopolymerization initiator (D-1) was 4 An active energy ray-curable resin composition was obtained in the same manner as in Example 7 except that the part was changed to part.

[Comparative Example 3]
In Example 3, fine synthetic resin fillers (B-1) and (B-5) were changed to 6.2 parts of (B′-1), and the blending amount of the photopolymerization initiator (D-1) Was changed to 4.3 parts and the amount of the leveling agent (E-1) was changed to 1.8 parts to obtain an active energy ray-curable resin composition in the same manner as in Example 3.

The active energy ray-curable resin compositions obtained in Examples 1 to 11 and Comparative Examples 1 to 3 are polycarbonate substrates (manufactured by Nippon Test Panel Co., Ltd.) so that the cured coating film has a thickness of 10 μm using an applicator. After drying at 90 ° C. for 3 minutes, using a high pressure mercury lamp lamp 80W and one lamp, UV irradiation of 2 passes at a conveyor speed of 3.4 m / min from a height of 18 cm (accumulated dose 800 mJ / cm ² ) to obtain a cured coating film.

Using the above cured coating film, the soft film properties, substrate adhesion, and surface hardness of the cured coating film were evaluated as follows.

<Soft feel (finger feeling)>
The soft feeling was evaluated by touching the surface of the cured coating film with a hand. The evaluation criteria are as follows. The evaluation results are shown in Table 1 below.
(Evaluation criteria)
A: Good soft feeling (smooth and moist)
○: Good soft feeling (smooth)
X: Soft feeling is not felt (Rough or rough, but there is no soft feeling or the coating surface is sticky)

<Base material adhesion>
Using the cured coating film, a cross-cut tape method was performed according to JIS K 5400 (1990 edition) to evaluate substrate adhesion. The evaluation results are shown in Table 1 below.
(Evaluation criteria)
○: Even after the tape test, all the coating films are in close contact with the substrate (100/100)
X: The coating film is peeled off from the substrate after the tape test (less than 100/100)

<Surface hardness>
Using a human nail tip, a nail scratch test was performed by applying a load of 500 g to the cured coating film while moving it in the longitudinal direction of the nail contact portion, and the practical properties of the coating film surface were evaluated. The evaluation results are shown in Table 1 below.
(Evaluation criteria)
○: Nail scratches do not scratch.
X: The nail scratch is damaged.

Further, in order to evaluate the wear resistance of the cured coating film, the cured coating film of Examples 5 and 7 and Comparative Example 1 were evaluated as follows.

<Abrasion resistance>
The active energy ray-curable resin compositions obtained in the above Examples and Comparative Examples were prepared by using an easy-adhesion PET (manufactured by Toyobo Co., Ltd .; trade name “Cosmo Sunshine A4300”) so that the cured coating film had a thickness of 10 μm with an applicator. After coating at a film thickness of 125 μm and drying at 90 ° C. for 3 minutes, two passes of UV irradiation at a conveyor speed of 3.4 m / min from a height of 18 cm using a high pressure mercury lamp 80 W and one lamp ( An integrated irradiation amount of 800 mJ / cm ² ) was performed to obtain a 100 mm square coating film-forming film.
The obtained coating film-formed film was evaluated for wear resistance under the conditions of 60 rpm, 250 g load, 500 rotations, and wear wheel CS10F using a Taber abrasion tester (manufactured by Tester Sangyo; AB-101 TABERTYPE PE ABRASSION TEST). The evaluation coating was fixed to the sample-installed SUS plate with a double-sided tape. The evaluation results are shown in Table 2 below.
(Evaluation criteria)
Measure and accumulate the coating film defect (exposed base film) part in the wear ring (12.5 mm width) mark of the coating film after evaluation with the ruler, and it is the most for the width of the wear wheel (12.5 mm width) mark A ratio was calculated at a portion having a large numerical value, and a comparative evaluation was performed (cumulative defect portion / wear ring mark (12.5 mm)).
○: Defect rate is less than 30% Δ: Defect rate is 30% or more, less than 50% ×: Defect rate is 50% or more

From the evaluation results in Tables 1 and 2, the active energy ray-curable resin compositions of Examples 1 to 11 in which the urethane (meth) acrylate compound (A) is blended with the fine particle synthetic resin filler (B). Provides a cured coating film that has soft feel and is excellent in wear, adhesion, and hardness, whereas an active energy ray of a comparative example that does not contain fine-particle synthetic resin filler (B) It can be seen that the cured coating film obtained from the curable resin composition is excellent in adhesion and hardness, but inferior in soft feel and abrasion resistance.

In addition, as a polyol compound (a3) which is one of the components for obtaining the urethane (meth) acrylate compound (A1), a polyol compound (a3-1) having a weight average molecular weight of less than 500 and a weight average molecular weight of 500 to 20, An example containing 000 polyol compounds (a3-2) will be described below.

Prior to this example, the following were produced as urethane (meth) acrylate compounds (A1).

<Production Example 9: Urethane (meth) acrylate compound (A1-6)>
In a four-necked flask equipped with a thermometer, stirrer, water-cooled condenser, and nitrogen gas inlet, 42.9 g of ethyl acetate, 32.3 g of hydrogenated xylylene diisocyanate (a2), neopentyl glycol (a3-1) (weight) Average molecular weight (Mw) 104) 11.6 g, bifunctional polyester polyol (a3-2) (hydroxyl value 63 mg KOH / g, weight average molecular weight (Mw) 5,000) 49.6 g, hydroquinone methyl ether 0 as a polymerization inhibitor 0.02 g of dibutyltin diaurate as a reaction catalyst was charged and reacted at 60 ° C. for 2 hours, and 6.50 g of 2-hydroxyethyl acrylate (a1) was charged and reacted at 60 ° C. for 3 hours. The reaction was terminated when the level became 0.3% or less, and the urethane (meth) acrylate compound The weight average molecular weight (Mw); 14,000 ethyl acetate solution (A1-6) (solid content of 70%, a viscosity (20 ° C.) of) was obtained 11,000 · s).

<Production Example 10: Urethane (meth) acrylate compound (A1-7)>
In a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser and a nitrogen gas inlet, 42.9 g of ethyl acetate, 29.6 g of hydrogenated xylylene diisocyanate (a2) (0.15 mol), tricyclodecane Methanol (a3-1) (weight average molecular weight (Mw) 196) 19.9 g (0.10 mol), bifunctional polyester polyol (a3-2) (hydroxyl value 63.9 mgKOH / g, weight average molecular weight (Mw) 5,000) 44.5 g (0.025 mol), 0.02 g of hydroquinone methyl ether as a polymerization inhibitor and 0.02 g of dibutyltin dilaurate as a reaction catalyst were charged and reacted at 60 ° C. for 2 hours to give 2-hydroxyethyl acrylate ( a1) 6.0 g (0.052 mol) was charged and reacted at 60 ° C. for 3 hours. The reaction was terminated when it became 3% or less, and an ethyl acetate solution (A1-7) of urethane (meth) acrylate compound (weight average molecular weight (Mw); 14,000) (solid content concentration 70%, viscosity) (20 ° C.) 53,000 mPa · s) was obtained.

<Production Example 11: Urethane (meth) acrylate compound (A1-8)>
In a four-necked flask equipped with a thermometer, stirrer, water-cooled condenser, and nitrogen gas inlet, 42.9 g of ethyl acetate, 32.9 g (0.17 mol) of hydrogenated xylylene diisocyanate (a2), 1,2- Hexanediol (a3-1) (weight average molecular weight (Mw) 118) 13.0 g (0.11 mol), bifunctional polyester polyol (a3-2) (hydroxyl value 63.9 mgKOH / g, weight average molecular weight (Mw) ) 5,000) 48.4 g (0.028 mol), 0.02 g of hydroquinone methyl ether as a polymerization inhibitor and 0.02 g of dibutyltin dilaurate as a reaction catalyst, reacted at 60 ° C. for 2 hours, and 2-hydroxyethyl acrylate (A1) 6.5 g (0.056 mol) was charged and reacted at 60 ° C. for 3 hours. The reaction was terminated at the time when the ratio was less than%, and a urethane (meth) acrylate compound (weight average molecular weight (Mw): 14,000) in ethyl acetate (A1-8) (solid content concentration 70%, viscosity (20 ° C) 123,000 mPa · s).

Next, the following were prepared as the fine particle synthetic resin filler (B).
(B-1): Polyurethane fine particles (average particle size 6.2 μm: glass transition temperature −52 ° C.)
(B-5): Polyethylene wax (particle size 5-10 μm)

The following were prepared as the photopolymerization initiator (D).
(D-1): 1-hydroxy-cyclohexyl-phenyl-ketone (manufactured by BASF Japan, “Irgacure 184”)

The following were prepared as the organic solvent (F).
(F-1): Ethyl acetate (F-2): Isopropyl alcohol

Example 12
27.0 parts of urethane (meth) acrylate compound (A1-6) obtained in Production Example 9 above, 12.7 parts of fine synthetic resin filler (B-1), fine synthetic resin filler (B- 5) 4.9 parts, 1.3 parts of photopolymerization initiator (D-1), 0.5 parts of leveling agent (E-1), 35.9 parts of organic solvent (F-1), organic solvent (F- 2) Using 17.7 parts, it mix | blended so that it might become solid content concentration 40%, and obtained the active energy ray-curable resin composition.

Example 13
27.0 parts of urethane (meth) acrylate compound (A1-7) obtained in Production Example 10 above, 12.7 parts of fine particle synthetic resin filler (B-1), fine particle synthetic resin filler (B- 5) 4.9 parts, 1.3 parts of photopolymerization initiator (D-1), 0.5 parts of leveling agent (E-1), 35.9 parts of organic solvent (F-1), organic solvent (F- 2) Using 17.7 parts, it mix | blended so that it might become solid content concentration 40%, and obtained the active energy ray-curable resin composition.

Example 14
27.0 parts of urethane (meth) acrylate compound (A1-8) obtained in Production Example 11 above, 12.7 parts of fine particle synthetic resin filler (B-1), fine particle synthetic resin filler (B- 5) 4.9 parts, 1.3 parts of photopolymerization initiator (D-1), 0.5 parts of leveling agent (E-1), 35.9 parts of organic solvent (F-1), organic solvent (F- 2) Using 17.7 parts, it mix | blended so that it might become solid content concentration 40%, and obtained the active energy ray-curable resin composition.

The active energy ray-curable resin compositions obtained in Examples 12 to 14 were applied to a polycarbonate substrate (manufactured by Nippon Test Panel Co., Ltd.) with an applicator so that the cured coating film had a thickness of 10 μm, and 90 ° C. After drying for 3 minutes at a high pressure mercury lamp lamp 80W, a single lamp is used to irradiate with 2 passes of ultraviolet light (accumulated dose of 800 mJ / cm ² ) at a conveyor speed of 3.4 m / min from a height of 18 cm to cure. A coating film was obtained.

Using the above-mentioned cured coating film, the soft film properties, substrate adhesion, surface hardness, alkali resistance, and ethanol resistance of the cured coating film were evaluated as follows.

<Soft feel (finger feeling)>
Using the same evaluation criteria as described above, soft feel (finger feeling) is evaluated, and the evaluation results are shown in Table 3 below.

<Base material adhesion>
The substrate adhesion was evaluated using the same evaluation criteria as described above, and the evaluation results are shown in Table 3 below.

<Surface hardness>
Using the cured coating film, the pencil curing degree on the surface of the cured coating film was measured according to JIS K 5600-5-4. The evaluation results are shown in Table 3 below together with the measurement results.
(Evaluation criteria)
○: The pencil hardness is HB or higher hardness x: The pencil hardness is lower than HB

<Alkali resistance>
A 5% NaOH aqueous solution was prepared, and 3 drops (0.1 ml) of a dropper were dropped on one position on the cured coating film, left at room temperature for 5 hours, washed with running water, and the droplet traces were visually confirmed. The evaluation results are shown in Table 3 below.
(Evaluation criteria)
○: No visual indication of dissolution mark ×: Visual observation of coating film abnormality such as dissolution mark

<Ethanol resistance>
On the cured coating film, 3 drops (0.04 ml) of dropper were dropped at one place, left at room temperature for 5 hours, washed with running water, and the droplet traces were visually confirmed. The evaluation results are shown in Table 3 below.
(Evaluation criteria)
○: No visual observation of dissolution mark ×: Visual observation of dissolution mark or coating film abnormality

From the above evaluation results, the active energy ray-curable resin compositions of Examples 12 to 14 in which the fine synthetic resin filler (B) is blended with the urethane (meth) acrylate compound (A1) have a soft feel. It can be seen that a cured coating film that is not only excellent in appearance but also excellent in appearance and excellent in adhesion, hardness, alkali resistance and ethanol resistance can be obtained.

In addition, the formation of these cured coating films is clearly superior to conventional thermosetting paints in that it has low energy, high production rate, and solution stability as a coating agent.

In the above embodiments, specific forms in the present invention have been described. However, the above embodiments are merely examples and are not construed as limiting. Various modifications apparent to those skilled in the art are contemplated to be within the scope of this invention.

When the active energy ray-curable resin composition of the present invention is used as a coating agent, an active energy ray-curable resin composition excellent in workability during coating and productivity during curing can be obtained and cured. The coating layer obtained later has an effect of having a moist and soft touch feeling and is particularly useful as a coating agent in a non-optical field.

Claims

An active energy ray-curable resin composition comprising a urethane (meth) acrylate compound (A) and a fine particle synthetic resin filler (B).
2. The active energy ray-curable resin composition according to claim 1, wherein the urethane (meth) acrylate compound (A) has a weight average molecular weight of 1,000 to 50,000.
The urethane (meth) acrylate compound (A) is obtained by reacting a hydroxyl group-containing (meth) acrylate compound (a1), a polyvalent isocyanate compound (a2), and a polyol compound (a3). The active energy ray-curable resin composition according to claim 1 or 2.
The polyol compound (a3) contains a polyol compound (a3-1) having a weight average molecular weight of less than 500 and a polyol compound (a3-2) having a weight average molecular weight of 500 to 20,000. The active energy ray-curable resin composition described.
The active energy ray-curable resin composition according to any one of claims 1 to 4, wherein the fine particle synthetic resin filler (B) contains at least one of a polyurethane filler and a polyethylene filler.
6. The active energy ray-curable resin composition according to claim 1, wherein the fine particle synthetic resin filler (B) has an average particle diameter of 1 to 30 μm.
The active energy ray-curable resin composition according to any one of claims 1 to 6, wherein the glass transition temperature of the fine-particle synthetic resin filler (B) is -140 to 40 ° C.
8. The fine synthetic resin filler (B) is contained in an amount of 25 to 400 parts by weight with respect to 100 parts by weight of the urethane (meth) acrylate compound (A). Active energy ray-curable resin composition.
A coating agent composition comprising the active energy ray-curable resin composition according to any one of claims 1 to 8.
The coating agent composition according to claim 9, comprising an ethylenically unsaturated monomer (C), a photopolymerization initiator (D), and an organic solvent.
The coating agent composition according to claim 9 or 10, wherein the content of the urethane (meth) acrylate compound (A) is 2 to 60% by weight.
A laminate comprising a substrate and a coating layer comprising the coating agent composition according to any one of claims 9 to 11.