JP2021161147A - Photocurable ink composition - Google Patents

Abstract

To provide a photocurable ink composition capable of forming a printed film which is hard to break and excellent in thermal yellowing resistance.SOLUTION: The photocurable ink composition at least comprises: (A) a compound represented by the formula (I) in the figure (where x is 0 or 1; R1, R2 and R3 are each independently a hydrogen atom or alkyl group; and R4 is a C1 to C10 organic group); (B) a polyfunctional polymerizable compound with an alicyclic structure; and (C) a photoinitiator.SELECTED DRAWING: None

Description

The present invention relates to a photocurable ink composition, and more particularly to a photocurable ink composition capable of forming a printing film that is not easily cracked and is excellent in heat-resistant yellowing.

In recent years, decoration has been performed using active energy ray-curable ink. Since active energy ray-curable ink is cured by irradiation with active energy rays, ejection defects such as nozzle clogging due to volatilization and drying of water and organic solvent occur as in the case of conventional organic solvent-based ink and water-based ink. It is difficult and quick-drying, so it has the advantage of improving productivity. In particular, in recent years, a colorless and transparent clear ink layer using an active energy ray-curable ink has been formed to protect the ink layer and a new design formation has been proposed.

When a water-based ink or a solvent-based ink is used, the water or solvent is colorless and transparent, and the resin itself tends to become transparent after drying. Therefore, it is relatively easy to form a colorless and transparent clear ink layer. However, since the active energy ray-curable ink contains a monomer and an initiator, it is difficult to make the ink itself colorless and transparent, and the ink layer obtained by reaction-curing these is also prone to yellowing in the reaction process. It is easy to yellow even by heat treatment, and it is easy to yellow due to the influence of unreacted monomers even when the ink is stored or the printed matter changes with time, and it is extremely difficult to form and hold a colorless and transparent clear ink layer. Met.

To solve this problem, Japanese Patent Application Laid-Open No. 2012-207084 (Patent Document 1) uses a specific polymerizable monomer and a photopolymerization initiator to provide excellent curability and multi-base material adhesion while having a low viscosity. It is described that an ink composition having an excellent degree of non-yellowing of printed matter can be provided. Further, Japanese Patent Application Laid-Open No. 2011-177964 (Patent Document 2) forms a clear layer containing an amine-modified reactive oligomer and a monofunctional (meth) acrylate having a glass transition temperature of a cured product of 0 ° C. or lower as a single substance. It is described that the ink composition for use has both adhesion and curability suitable for forming a clear layer of a thick film. Further, in Japanese Patent Application Laid-Open No. 2019-65214 (Patent Document 3), the rate of photocuring with respect to light having a narrow wavelength range from an LED or the like is high, and yellowing does not occur during photocuring. A photocurable clear ink capable of expressing a color tone is disclosed.

Japanese Unexamined Patent Publication No. 2012-207804 Japanese Unexamined Patent Publication No. 2011-177964 JP-A-2019-65214

The present inventor has studied a printing method in which a heat-resistant substrate such as metal, glass, ceramic, or artificial marble is printed, cured, and then the printed matter is further heated. In such an ink composition, there is a problem that the ink layer turns yellow due to heat treatment after printing and curing. The heat treatment performed after printing and curing can solve the problems of odor and stickiness of the ink layer, and can also improve the adhesiveness of the ink layer. Therefore, when printing on a heat-resistant substrate, It is desirable to heat-treat the printed matter.

In addition, it has been proposed to apply various designs such as gloss, matte, lenticular, and three-dimensional effect to the surface of printed matter, but in the heat treatment after printing and curing, the ink layer, especially the thick part, is treated. There is also the problem of cracking and peeling.

Therefore, an object of the present invention is to provide a photocurable ink composition capable of solving the above-mentioned problems of the prior art and forming a printing film which is hard to crack and is excellent in heat-resistant yellowing.

As a result of diligent studies to achieve the above object, the present inventor prints a photocurable ink composition in which a specific silicon-containing compound and a polyfunctional polymerizable compound having an alicyclic structure are blended. We have found that it is possible to form a printed film that is hard to crack and hard to yellow even when it is formed into a thick film by heat treatment after curing, and has completed the present invention.

（式中、ｘは０又は１であり、Ｒ^１、Ｒ^２及びＲ^３はそれぞれ独立して水素原子、又はアルキル基であり、Ｒ^４は炭素数１〜１０の有機基である）で表される化合物と、（Ｂ）脂環構造を有する多官能重合性化合物と、（Ｃ）光重合開始剤を少なくとも含むことを特徴とする。 That is, the photocurable ink composition of the present invention has (A) the following formula (I).

(In the formula, x is 0 or 1, R ¹ , R ² and R ³ are independently hydrogen atoms or alkyl groups, and R ⁴ is an organic group having 1 to 10 carbon atoms). It is characterized by containing at least (B) a polyfunctional polymerizable compound having an alicyclic structure, and (C) a photopolymerization initiator.

A preferred example of the photocurable ink composition of the present invention further contains (D) an ultraviolet absorber, (E) a radical scavenger, or both.

Another preferred example of the photocurable ink composition of the present invention further comprises (F) a polymerizable oligomer having a molecular weight of 1,000 to 20,000.

In another preferred example of the photocurable ink composition of the present invention, the amount of the compound represented by the formula (I) in the ink composition is in the range of 0.1 to 20% by mass.

In another preferable embodiment of the photocurable ink composition of the present invention, in the formula (I), the organic group R ⁴ comprises a (meth) acryloyl groups.

In another preferred example of the photocurable ink composition of the present invention, the photopolymerization initiator (C) comprises at least an acylphosphine oxide-based initiator.

Another preferred example of the photocurable ink composition of the present invention further comprises (G) a colorant.

Another preferred example of the photocurable ink composition of the present invention is a clear ink composition.

According to the present invention, it is possible to provide a photocurable ink composition capable of forming a printing film which is hard to crack and is excellent in heat-resistant yellowing.

The ink composition of the present invention will be described in detail below. The ink composition of the present invention is a photocurable ink composition and contains a specific silicon-containing compound, a polymerizable compound, and a photopolymerization initiator.

In the present specification, the photocurable ink composition means an ink composition that can be cured by irradiation with active energy rays such as ultraviolet rays, visible rays, and electron beams.

（式中、ｘは０又は１であり、Ｒ^１、Ｒ^２及びＲ^３はそれぞれ独立して水素原子、又はアルキル基であり、Ｒ^４は炭素数１〜１０の有機基である）で表される化合物である。上記式（Ｉ）で表される化合物は、付着性の向上を目的として使用される物質であるが、本発明者は、驚くべきことに、式（Ｉ）で表される化合物を用いることで、耐熱黄変性をも向上でき、厚膜を形成した際にも優れた透明性を提供できることを見出した。この点について、本発明者は、インク組成物に式（Ｉ）の化合物を配合すると、式（Ｉ）の化合物は、インク中の重合性化合物と結合し、膜自体の結晶性が高まり、加熱処理後の透明度が向上したものと推察する。本明細書においては、上記式（Ｉ）で表される化合物を（Ａ）ケイ素含有化合物ともいう。 The specific silicon-containing compound used in the ink composition of the present invention is (A) the following formula (I).

(In the formula, x is 0 or 1, R ¹ , R ² and R ³ are independently hydrogen atoms or alkyl groups, and R ⁴ is an organic group having 1 to 10 carbon atoms). It is a compound to be used. The compound represented by the above formula (I) is a substance used for the purpose of improving the adhesiveness, but the present inventor surprisingly uses the compound represented by the formula (I). It has been found that heat-resistant yellowing can be improved and excellent transparency can be provided even when a thick film is formed. In this regard, when the compound of the formula (I) is blended in the ink composition, the compound of the formula (I) binds to the polymerizable compound in the ink, the crystallinity of the film itself is enhanced, and the ink is heated. It is presumed that the transparency after processing has improved. In the present specification, the compound represented by the above formula (I) is also referred to as (A) silicon-containing compound.

In the above formula (I), R ¹ , R ² and R ³ are independently hydrogen atoms or alkyl groups, respectively. Here, the alkyl group may be a straight chain or a branched chain, and an alkyl group having 1 to 4 carbon atoms is preferable, and an alkyl group having 1 to 2 carbon atoms is more preferable. Specific examples include a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group and the like. The alkyl group may be unsubstituted or substituted, but is preferably an unsubstituted alkyl group. Examples of the substituent of the alkyl group include halogen and the like.

In the above formula (I), ^{R 4} is an organic group having 1 to 10 carbon atoms. Here, the organic group preferably has at least one functional group that is reactive with the polymerizable compound, such as a carbon-carbon double bond constituting an acryloyl group, a methacryloyl group, a vinyl group or an allyl group. It is more preferable to have one or more polymerizable unsaturated groups, and it is further preferable to have one or more functional groups of an acryloyl group and a methacryloyl group. In addition, in this specification, the term (meth) acryloyl group means an acryloyl group or a methacryloyl group. Here, as the organic group, for example, a methyl group, an ethyl group, a propyl group, an isopropyl group, a hexyl group, an octyl group, a decyl group, a cyclohexyl group, a phenyl group, a vinyl group, an allyl group, 2- (3,4-). Epoxycyclohexyl) ethyl group, 3-glycidoxypropyl group, p-styryl group, 3-methacryloxypropyl group, 3-acryloxypropyl group, N-2- (aminoethyl) -3-aminopropyl group, 3- Examples thereof include an aminopropyl group and an N- (1,3-dimethyl-butylidene) propylamino group.

In the above formula (I), x is 0 or 1.

Specific examples of the silicon-containing compound (A) include methyltrimethoxysilane, methyltriethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, n-propyltrimethoxysilane, diisopropyldimethoxysilane, diisopropyldiethoxysilane, and isopropyltrimethoxy. Silane, isopropyltriethoxysilane, n-hexyltrimethoxysilane, n-hexyltriethoxysilane, n-octyltrimethoxysilane, n-octyltrimethoxysilane, n-decyltrimethoxysilane, n-decyltriethoxysilane, cyclohexyl Methyldimethoxysilane, phenyltriethoxysilane, phenyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, allyltrimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-glycidoxypropyl Methyldimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, 3-glycidoxypropyltriethoxysilane, p-styryltrimethoxysilane, 3-methacryloxypropylmethyldimethoxysilane , 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3-methacryloxypropyltriethoxysilane, 3-acryloxypropyltrimethoxysilane, N-2- (aminoethyl) -3-amino Propylmethyldimethoxysilane, N-2- (aminoethyl) -3-aminopropyltrimethoxysilane, N-2- (aminoethyl) -3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane, 3-amino Examples thereof include propyltriethoxysilane, 3-triethoxysilyl-N- (1,3-dimethyl-butylidene) propylamine, and N-phenyl-3-aminopropyltrimethoxysilane. Among these, methyltrimethoxysilane, n-propyltrimethoxysilane, phenyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-methacryloxy Preferable are propylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3-methacryloxypropyltriethoxysilane, and 3-acryloxypropyltrimethoxysilane.

In the ink composition of the present invention, the amount of the silicon-containing compound (A) is preferably 0.1 to 20% by mass, more preferably 0.5 to 10% by mass, particularly preferably 1 to 5% by mass, and most preferably. Is 2 to 5% by mass. The silicon-containing compound (A) may be used alone or in combination of two or more.

The polymerizable compound used in the ink composition of the present invention is a polymerization of a functional group (for example, a carbon-carbon double bond constituting an acryloyl group, a methacryloyl group, a vinyl group or an allyl group) that exhibits reactivity when irradiated with active energy rays. It is a compound that causes a polymerization reaction via a sex unsaturated group). In addition, in this specification, a polymerizable compound refers to a polymerizable compound excluding the above-mentioned (A) silicon-containing compound. The polymerizable compound may be used alone or in combination of two or more. In the ink composition of the present invention, the amount of the polymerizable compound is preferably 60 to 95% by mass.

In the ink composition of the present invention, the polymerizable compound is classified into a monofunctional polymerizable compound or a polyfunctional polymerizable compound. Here, as the monofunctional polymerizable compound, a monofunctional polymerizable monomer having one functional group exhibiting reactivity when irradiated with active energy rays (for example, a monofunctional polymerizable monomer having one polymerizable unsaturated group) or an activity Examples thereof include a monofunctional polymerizable oligomer having one functional group exhibiting reactivity when irradiated with energy rays (for example, a monofunctional polymerizable oligomer having one polymerizable unsaturated group). Examples of the polyfunctional polymerizable compound include a polyfunctional polymerizable monomer having two or more functional groups exhibiting reactivity when irradiated with active energy rays (for example, a polyfunctional polymerizable monomer having two or more polymerizable unsaturated groups) and an activity. Examples thereof include a polyfunctional polymerizable oligomer having two or more functional groups exhibiting reactivity when irradiated with energy rays (for example, a polyfunctional polymerizable oligomer having two or more polymerizable unsaturated groups).

Specific examples of the monofunctional polymerizable monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxykipropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6. -Hydroxyhexyl (meth) acrylate, polyoxyethylene mono (meth) acrylate, polyoxypropylene mono (meth) acrylate, polyoxybutylene mono (meth) acrylate, stearyl (meth) acrylate, acryloyl morpholine, tridecyl (meth) acrylate, Lauryl (meth) acrylate, dimethylacrylamide, hydroxyethylacrylamide, diethylacrylamide, isopropylacrylamide, dimethylaminopropylacrylamide, diacetoneacrylamide, Nn-butoxymethylacrylamide, N-isobutoxymethylacrylamide, N-methoxymethylacrylamide, N -Methylol acrylamide, N-vinyl caprolactam, decyl (meth) acrylate, phenoxyethyl (meth) acrylate, phenoxydiethylene glycol (meth) acrylate, benzyl (meth) acrylate, isodecyl (meth) acrylate, isobornyl (meth) acrylate, dicyclopenta Nyl (meth) acrylate, dicyclopentenyl (meth) acrylate, octyl (meth) acrylate, isooctyl (meth) acrylate, octyl (meth) acrylate, dicyclopentenyloxyethyl (meth) acrylate, cyclohexyl (meth) acrylate, t- Butylcyclohexyl (meth) acrylate, isoamyl (meth) acrylate, 2-ethylhexyl-diglycol (meth) acrylate, EO (ethylene oxide) modified 2-ethylhexyl (meth) acrylate, neopentyl glycol (meth) acrylic acid benzoic acid ester, N -Vinyl-2-pyrrolidone, N-vinylimidazole, tetrahydrofurfuryl (meth) acrylate, methoxydipropylene glycol (meth) acrylate, (2-methyl-2-ethyl-1,3-dioxolan-4-yl) methyl ( Examples thereof include meth) acrylate, cyclic trimethylol propaneformal (meth) acrylate, and ethoxy-diethylene glycol (meth) acrylate.

Among the above polyfunctional polymerizable monomers, 1,12-dodecanediol di (1,12-dodecanediol di) is a specific example of the polyfunctional polymerizable monomer (bifunctional polymerizable monomer) having two functional groups that show reactivity when irradiated with active energy rays. Meta) acrylate, 1,10-decanediol di (meth) acrylate, 2-methyl-1,8-octanediol di (meth) acrylate, 2-butyl-2-ethyl-1,3-propanediol di (meth) Acrylate, 1,9-nonanediol di (meth) acrylate, 1,8-octanediol di (meth) acrylate, 1,7-heptanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, 1,4-Butanediol di (meth) acrylate, polytetramethylene glycol di (meth) acrylate, 3-methyl-1,5-pentanediol di (meth) acrylate, tricyclodecanedimethanol diacrylate, dimethylolcyclohexanedi Acrylate, neopentyl glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, PO (propylene oxide) modified neopentyl glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate, triethylene glycol Examples thereof include di (meth) acrylate, tripropylene glycol di (meth) acrylate, and dipropylene glycol di (meth) acrylate.

Specific examples of the polyfunctional polymerizable monomer having three or more functional groups exhibiting reactivity when irradiated with active energy rays (trifunctional or higher functional polyfunctional polymerizable monomer) include trimethylpropantri (meth) acrylate and ethoxy. Trimethylol propanetri (meth) acrylate, propoxylated trimethylol propanetri (meth) acrylate, glycerin tri (meth) acrylate ethoxylated, pentaerythritol tetra (meth) acrylate, pentaerythritol tetra (meth) acrylate ethoxylated, EO modified Examples thereof include diglycerin tetra (meth) acrylate, ditrimethylolpropantetra (meth) acrylate, dipentaerythritol hexa (meth) acrylate, and EO-modified dipentaerythritol hexa (meth) acrylate.

As used herein, the term (meth) acrylate means methacrylate or acrylate. Further, when the (meth) acrylate is prefixed with a plurality of prefixes such as di (meth) acrylate and tri (meth) acrylate, each (meth) acrylate may be the same or different. good.

In the ink composition of the present invention, the amount of the monofunctional polymerizable monomer is preferably 30 to 90% by mass. In the ink composition of the present invention, the amount of the polyfunctional polymerizable monomer is, for example, 2 to 30% by mass, preferably 5 to 20% by mass. If the content of the polyfunctional monomer is less than 2% by mass, the curability may be lowered, and if it exceeds 30% by mass, the volume shrinkage of the printing film during curing may cause the ink layer at the time of thick film to be easily cracked.

The ink composition of the present invention contains at least (B) a polyfunctional polymerizable compound having an alicyclic structure as a polymerizable compound. By using a polyfunctional polymerizable compound having an alicyclic structure, it is possible to form a printed film that is hard to break even when it is formed into a thick film. In this regard, the present inventor has a polyfunctional polymerizable compound having an alicyclic structure, which has both properties of a cyclic compound and an aliphatic compound. It is presumed that the internal stress of the above can be relaxed and a printed film that is hard to break even when formed into a thick film can be provided. Moreover, it is possible to improve the curability.

As the polyfunctional polymerizable compound having an alicyclic structure (B), a bifunctional polymerizable monomer having an alicyclic structure is preferable, and tricyclodecanedimethanol diacrylate or cyclohexanedimethanol diacrylate is particularly preferable.

In the ink composition of the present invention, the amount of the polyfunctional polymerizable compound having the (B) alicyclic structure is preferably 1 to 50% by mass, more preferably 5 to 40% by mass, and particularly preferably 10 to 30% by mass. %. The polyfunctional polymerizable compound (B) having an alicyclic structure may be used alone or in combination of two or more. If the amount of the polyfunctional polymerizable compound having an alicyclic structure is less than 1% by mass, the curability may decrease, and if it exceeds 50% by mass, the volume shrinkage of the printed film during curing causes the ink to be thick. The layer may be easily cracked.

The ink composition of the present invention preferably contains a nitrogen-containing polymerizable compound as the polymerizable compound. By using the nitrogen-containing polymerizable compound, the adhesiveness of the printing film can be improved. The nitrogen-containing polymerizable compound may cause yellowing of the printed film. However, according to the present invention, the use of the silicon-containing compound (A) can improve heat-resistant yellowing, so that a thick film is formed. It is possible to provide excellent transparency even when it is used.

The nitrogen-containing polymerizable compound is preferably a nitrogen-containing polymerizable monomer. Further, the nitrogen-containing polymerizable compound has, for example, a nitrogen-containing group such as an amino group, an amide group, an imide group, a urea group, and a urethane group. In the ink composition of the present invention, the amount of the nitrogen-containing polymerizable compound is preferably 1 to 30% by mass, more preferably 2 to 20% by mass, and particularly preferably 3 to 10% by mass. The nitrogen-containing polymerizable compound may be used alone or in combination of two or more.

（式中、Ｒ^１は、水素原子又は炭素数が１〜８のアルキル基であり、Ｒ^２は、水素原子又はメチル基である）で表される化合物を含むことが好ましい。上記式（ＩＩ）で表される化合物は、付着性の向上効果が高い。 In the ink composition of the present invention, the nitrogen-containing polymerizable compound is represented by the following formula (II).

(In the formula, R ¹ is a hydrogen atom or an alkyl group having 1 to 8 carbon atoms, and R ² is a hydrogen atom or a methyl group). The compound represented by the above formula (II) has a high effect of improving adhesiveness.

In the above formula (II), R ¹ is a hydrogen atom or an alkyl group having 1 to 8 carbon atoms. Here, the alkyl group may be a straight chain or a branched chain, and an alkyl group having 1 to 4 carbon atoms is preferable. Specific examples include a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group and the like. The alkyl group may be unsubstituted or substituted, but is preferably an unsubstituted alkyl group. Examples of the substituent of the alkyl group include halogen and the like. Further, in the above formula (II), R ² is a hydrogen atom or a methyl group, and is preferably hydrogen.

Specific examples of the compound represented by the above formula (II) preferably include Nn-butoxymethylacrylamide, N-isobutoxymethylacrylamide, N-methoxymethylacrylamide, N-methylolacrylamide and the like.

In the ink composition of the present invention, the amount of the compound represented by the above formula (II) is preferably 1 to 30% by mass, more preferably 2 to 20% by mass, and particularly preferably 3 to 10% by mass. .. The compound represented by the above formula (II) may be used alone or in combination of two or more.

Further, the ink composition of the present invention preferably contains phenoxyethyl acrylate as the polymerizable compound from the viewpoint of lowering the viscosity and improving the ejection property.

Further, the ink composition of the present invention preferably contains a hydroxyl group-containing polymerizable monomer as the polymerizable compound, and more preferably contains a hydroxyl group-containing monofunctional polymerizable monomer, from the viewpoint of improving the adhesiveness. Specific examples of the hydroxyl group-containing polymerizable monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxykipropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, and 6-. Hydroxyhexyl (meth) acrylate, hydroxyethyl acrylamide and the like are preferably mentioned. In the ink composition of the present invention, the amount of the hydroxyl group-containing polymerizable monomer is preferably 1 to 15% by mass. The hydroxyl group-containing polymerizable monomer may be used alone or in combination of two or more.

The ink composition of the present invention preferably contains (F) a polymerizable oligomer as a polymerizable compound. The polymerizable oligomer can provide a printed film that has little volume shrinkage and is not easily cracked when heated even when it is formed into a thick film.

In the ink composition of the present invention, the polymerizable oligomer is preferably an acrylate oligomer. The number of functional groups of the polymerizable oligomer is preferably 2 to 6, and the molecular weight of the polymerizable oligomer is preferably 500 to 30,000, more preferably 1,000 to 20,000. Here, the molecular weight of the polymerizable oligomer is a polystyrene-equivalent weight average molecular weight.

Specific examples of the acrylate oligomer include urethane acrylate oligomer [acrylate oligomer having a plurality of urethane bonds (-NHCOO-)], amino acrylate oligomer [ _{acrylate oligomer having a plurality of amino groups (-NH 2} )], and epoxy acrylate oligomer [epoxy group]. Acrylate oligomer having a plurality of ester bonds [], silicone acrylate oligomer [acrylate oligomer having a plurality of siloxane bonds (-SiO−)], ester acrylate oligomer [acrylate oligomer having a plurality of ester bonds (-COO−)] and butadiene acrylate oligomer [butadiene unit A plurality of acrylate oligomers] and the like. Among these, urethane acrylate oligomers are preferable.

The following are known as acrylate oligomers.
Beam set 502H, beam set 505A-6, beam set 550B, beam set 575, beam set AQ-17 (manufactured by Arakawa Chemical Industry Co., Ltd.),
AH-600, UA-306H, UA-306T, UA-306I, UA-510H, UF-8001G (manufactured by Kyoeisha Chemical Co., Ltd.),
CN910, CN959, CN963, CN964, CN965NS, CN966NS, CN969NS, CN980NS, CN981NS, CN982, CN983NS, CN985, CN991NS, CN996NS, CN2920, CN2921, CN9881NS, CN2920, CN2921, CN9881NS, CN8883NS, CN9801NS CN9028, CN9030, CN9178NS, CN9290, CN9893NS, CN929, CN989NS, CN968NS, CN9006NS, CN9010NS, CN9025, CN9026, CN9039, CN9062, CN91110NS, CN9029, CN8885NS, CN9013NS, CN9885NS, CN9013NS, CN97895NS, CN9013NS, CN97895NS, CN9013NS CN971, CN972, CN975NS, CN9165 (manufactured by Sartmer),
U-2PPA, U-6LPA, U-10HA, U-10PA, UA-1100H, U-15HA, UA-53H, UA-33H, U-200PA, UA-200PA, UA-160TM, UA-290TM, UA- 4200, UA-4400, UA-122P (manufactured by Shin-Nakamura Chemical Industry Co., Ltd.),
New Frontier R-1235, R-1220, RST-201, RST-402, R-1301, R-1304, R-1214, R-1302XT, GX-8801A, R-1603, R-1150D (Daiichi Kogyo Seiyaku) Made by the company),
EBECRYL204, EBECRYL205, EBECRYL210, EBECRYL215, EBECRYL220, EBECRYL230, EBECRYL244, EBECRYL245, EBECRYL264, EBECRYL265, EBECRYL270, EBECRYL280 / 15IB, EBECRYL284, EBECRYL285, EBECRYL294 / 25HD, EBECRYL1259, EBECRYL1290, KRM8200, EBECRYL4820, EBECRYL4858, EBECRYL5129, EBECRYL8210, EBECRYL8254, EBECRYL8301R, EBECRYL8307, EBECRYL8402, EBECRYL8405, EBECRYL8411, EBECRYL8465, EBECRYL8800, EBECRYL8804, EBECRYL8807, EBECRYL9260, EBECRYL9270, EBECRYL7735, EBECRYL8296, EBECRYL8452, EBECRYL8904, EBECRYL8311, EBECRYL8701, EBECRYL8667 (manufactured by Daicel-Orunekusu Co., Ltd.),
UV-1700B, UV-6300B, UV-7550B, UV-7600B, UV-7605B, UV-7610B, UV-7630B, UV-7640B, UV-7650B, UV-6630B, UV-7000B, UV-7510B, UV- 7461TE,
UV-2000B, UV-2750B, UV-3000B, UV-3200B, UV-3300B, UV-3310B, UV-3700B, UV6640B (manufactured by Nippon Synthetic Chemistry Co., Ltd.),
Art Resins UN-333, UN-350, UN-1255, UN-2600, UN-2700, UN-5590, UN-6060PTM, UN-6200, UN-6202, UN-6300, UN-6301, UN-7600, UN-7700, UN-9000PEP, UN-9200A, UN-3320HA, UN-3320HC, UN-904, UN-906S (manufactured by Negami Kogyo Co., Ltd.)

In the ink composition of the present invention, the amount of the polymerizable oligomer is preferably 1 to 20% by mass, more preferably 5 to 15% by mass. The polymerizable oligomer may be used alone or in combination of two or more. (F) By containing 1% by mass or more of the polymerizable oligomer, it is possible to effectively prevent the formation of a thick film and cracking during heating, and it is possible to improve the weather resistance of the ink. It becomes easy to adjust the ink to the head suitable viscosity.

The (C) photopolymerization initiator used in the ink composition of the present invention has an action of initiating the polymerization of the above-mentioned polymerizable compound by being irradiated with active energy rays. The amount of the photopolymerization initiator (C) is preferably 1 to 25% by mass, more preferably 3 to 20% by mass, and even more preferably 3 to 15% by mass in the ink composition. (C) If the content of the photopolymerization initiator is less than 1% by mass, the printing layer may be poorly cured, and if it exceeds 25% by mass, precipitates are generated at a low temperature and ink ejection becomes unstable. May become. Further, in order to accelerate the initiation reaction of (C) the photopolymerization initiator, it is also possible to use an auxiliary agent such as a photosensitizer in combination.

Examples of the (C) photopolymerization initiator include benzophenone-based compounds, acetophenone-based compounds, thioxanthone-based compounds, and phosphine oxide-based compounds. From the viewpoint of curability, the wavelength of the activated energy ray to be irradiated and the start of photopolymerization. It is preferable that the absorption wavelengths of the agents overlap as much as possible. In particular, the (C) photopolymerization initiator preferably contains an acylphosphine oxide-based initiator from the viewpoint of improving yellowing resistance during heating. Although the printed film of the acylphosphine oxide-based initiator is more likely to yellow than other initiators when cured by irradiation with active energy rays, its transparency is improved by the subsequent heat treatment. The photopolymerization initiator (C) may be used alone or in combination of two or more.

(C) As a specific example of the photopolymerization initiator,
2,2-dimethoxy-1,2-diphenylethane-1-one,
1-Hydroxy-cyclohexyl-phenyl-ketone,
2-Hydroxy-2-methyl-1-phenylpropane-1-one,
Benzophenone,
1- [4- (2-Hydroxyethoxy) -phenyl] -2-hydroxy-2-methyl-1-propane-1-one,
2-Hydroxy-1- {4- [4- (2-hydroxy-2-methylpropionyl) -benzyl] -phenyl} -2-methyl-propan-1-one,
Phenyl Glyoxylic Acid Methyl Ester,
2-Methyl-1- [4- (methylthio) phenyl] -2-morpholinopropane-1-one,
2-Benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone,
2-Dimethylamino-2- (4-methyl-benzyl) -1- (4-morpholin-4-yl-phenyl) -butane-1-one,
Bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide,
Bis (2,6-dimethoxybenzoyl) -2,4,4-trimethyl-pentylphosphine oxide,
2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide,
1,2-octanedione, 1- [4- (phenylthio) -2- (O-benzoyloxime)],
Etanone, 1- [9-ethyl-6- (2-methylbenzoyl) -9H-carbazole-3-yl]-, 1- (O-acetyloxime),
2,4-Diethylthioxanthone,
2-Isopropylthioxanthone,
2-Chlorothioxanthone and the like can be mentioned.

Among these, from the viewpoint of ink curability, 2,2-dimethoxy-1,2-diphenylethane-1-one, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone, Bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide, bis (2,6-dimethoxybenzoyl) -2,4,4-trimethyl-pentylphosphine oxide, 2,4,6-trimethylbenzoyl-diphenyl -Phosphine oxide and 2,4-diethylthioxanthone are preferable, and from the viewpoint of improving yellowing resistance during heating, bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide, bis (2,) 6-Dimethoxybenzoyl) -2,4,4-trimethyl-pentylphosphine oxide, and 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide are preferred, with 2,4,6-trimethylbenzoyl-diphenyl-phosphine. Oxides are particularly preferred.

The ink composition of the present invention preferably contains either (D) an ultraviolet absorber or (E) a radical scavenger, or both (D) an ultraviolet absorber and (E) a radical scavenger.

(D) The ultraviolet absorber has an effect of absorbing ultraviolet rays and preventing deterioration due to ultraviolet rays. Examples of the (D) ultraviolet absorber include cyanoacrylate-based compounds, benzophenone-based compounds, benzoate-based compounds, benzotriazole-based compounds, hydroxyphenyltriazine-based compounds, benziliden camphor-based compounds, inorganic fine particles, and the like. A hydroxyphenyltriazine-based compound having a shorter wavelength is preferable from the viewpoint of ink curability. From the viewpoint of curability, it is preferable that the wavelength of the active energy ray to be irradiated and the absorption wavelength of the (D) ultraviolet absorber do not overlap as much as possible.

(D) As a specific example of the ultraviolet absorber,
2,4-Dihydroxybenzophenone,
2-Hydroxy-4-methoxybenzophenone,
2-Hydroxy-4-methoxybenzophenone-5-sulfonic acid,
2-Hydroxy-4-octoxybenzophenone,
2-Hydroxy-4-dodecyloxybenzophenone-2-hydroxy-4-benzyloxybenzophenone,
Bis (5-benzoyl-4-hydroxy-2-methoxyphenyl) methane,
2,2'-Dihydroxy-4-methoxybenzophenone,
2,2'-Dihydroxy-4,4'-dimethoxybenzophenone,
2,2', 4,4'-tetrahydroxybenzophenone,
2-Hydroxy-4-methoxy-2'-carboxybenzophenone,
2- (2'-Hydroxy-5'-methylphenyl) benzotriazole 2- [2'-hydroxy-3', 5'-bis (α, α- (dimethylbenzyl) phenyl] benzotriazole,
2- (2'-Hydroxy-3', 5'-di-t-butylphenyl) benzotriazole,
2- (2'-Hydroxy-3'-t-Butyl-5'-Methylphenyl) -5-chlorobenzotriazole,
2- (2'-Hydroxy-3', 5'-di-t-butylphenyl) -5-chlorobenzotriazole,
2- (2'-Hydroxy-3', 5'-di-t-amylphenyl) benzotriazole,
2- (2'-Hydroxy-5'-t-octylphenyl) benzotriazole,
2,2'-Methylene-bis [4- (1,1,3,3-tetramethylbutyl) -6- (2N-benzotriazole-2-yl) phenol],
Condensation of methyl-3- [3-t-butyl-5- (2H-benzotriazole-2-yl) -4-hydroxyphenyl] propionate and polyethylene glycol,
2- (2-Hydroxyphenyl) benzotriazole,
2- (2'-Hydroxy-5'-methylphenyl) benzotriazole,
2,6-di-t-butylphenyl-3', 5'-di-t-butyl-4'-hydroxybenzoate,
Hexadecyl-3,5-di-t-butyl-4-hydroxybenzoate and the like can be mentioned.

In the ink composition of the present invention, the amount of the (D) ultraviolet absorber is preferably 0.1 to 15% by mass, more preferably 0.1 to 10% by mass, still more preferably 0, from the viewpoint of weather resistance. It is preferably in the range of 2 to 5% by mass. If the amount of UV absorber is too large, the print layer may not be sufficiently cured. The (D) ultraviolet absorber may be used alone or in combination of two or more, but the (D) ultraviolet absorber preferably contains at least two types of ultraviolet absorbers. By using a plurality of types of ultraviolet absorbers having different structures, the effect of the ultraviolet absorber can be further sustained.

(E) The radical scavenger can capture free radicals and the like to improve photostability. Further, a substance having a function of reacting with free radicals and preventing a polymerization reaction from occurring (so-called polymerization inhibitor) is also included in the (E) radical scavenger. Examples of the (E) radical scavenger include hindered amine compounds, hydroquinone compounds, phenol compounds, phenothiazine compounds, nitroso compounds, N-oxyl compounds and the like, and in particular, hindered amine light stabilizers (HALS) are used. preferable.

Specific examples of the (E) radical trapping agent include bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate and 1- {2- (3- (3,5-di-t-butyl). -4-Hydroxyphenyl) propionyloxy) ethyl} -2,2,6,6-tetramethylpiperidine, 8-acetyl-3-dodecyl-7,7,9,9-tetramethyl-1,3,8-triazaspiro {4.5} Hindered amine compounds such as decane-2,4-dione, phenol, o-, m- or p-cresol, 2-t-butyl-4-methylphenol, 6-t-butyl-2,4 -Dimethylphenol, 2,6-di-t-butyl-4-methylphenol, 2-t-butylphenol, 4-t-butylphenol, 2,4-di-t-butylphenol, 2-methyl-4-t-butylphenol , 4-t-butyl-2,6-dimethylphenol and other phenolic compounds, hydroquinone, hydroquinone monomethyl ether, methylhydroquinone, 2,5-di-t-butylhydroquinone, 2-methyl-p-hydroquinone, 2,3 -Dimethylhydroquinone, trimethylhydroquinone 4-methylbenzcatechin, t-butylhydroquinone, 3-methylbenzcatechin, 2-methyl-p-hydroquinone, 2,3-dimethylhydroquinone, trimethylhydroquinone, t-butylhydroquinone, benzoquinone, t- Hydroquinone compounds such as butyl-p-benzoquinone and 2,5-diphenyl-p-benzoquinone, phenothiazine compounds such as phenothiazine, N-nitroso-N-phenylhydroxylamine ammonium, N-nitroso-N-phenylhydroxylamine aluminum salt Nitroso compounds such as 4-hydroxy-2,2,6,6-tetramethyl-piperidin-N-oxyl, 4-oxo-2,2,6,6-tetramethyl-piperidin-N-oxyl, 4- Examples thereof include N-oxyl compounds such as methoxy-2,2,6,6-tetramethyl-piperidin-N-oxyl.

In the ink composition of the present invention, the amount of the (E) radical scavenger is preferably 0.01 to 20% by mass, more preferably 0.05 to 10% by mass, and particularly preferably 0, from the viewpoint of weather resistance. It is in the range of 1 to 5% by mass. Too much radical scavenger can cause poor curing. (E) The radical scavenger may be used alone or in combination of two or more.

The ink composition of the present invention may contain a (G) colorant such as a dye or a pigment, but in that case, it is preferable to contain a pigment from the viewpoint of weather resistance. For example, it is also possible to make a metallic ink by using a metal pigment or a pearl pigment. The content of the (G) colorant is, for example, 0.1 to 15% by mass in the ink composition. Further, the (G) colorant may be used alone or in combination of two or more. In the case of clear ink, it is preferable not to blend a pigment having high coloring power, and in the case of blending, it is preferably 1% by mass or less.

(G) As a specific example of the colorant,
C. I. Pigment Yellow 1, 2, 3, 4, 5, 6, 7, 9, 10, 12, 13, 14, 15, 16, 17, 24, 32, 34, 35, 36, 37, 41, 42, 43, 49, 53, 55, 60, 61, 62, 63, 65, 73, 74, 75, 77, 81, 83, 87, 93, 94, 95, 97, 98, 99, 100, 101, 104, 105, 106, 108, 109, 110, 111, 113, 114, 116, 117, 119, 120, 123, 124, 126, 127, 128, 129, 130, 133, 138, 139, 150, 151, 152, 153, 154, 155, 165, 167, 168, 169, 170, 172, 173, 174, 175, 176, 179, 180, 181, 182, 183, 184, 185, 191, 193, 194, 199, 205, 206, 209, 212, 213, 214, 215, 219,
C. I. Pigment Orange 1, 2, 3, 4, 5, 13, 15, 16, 17, 19, 20, 21, 24, 31, 34, 36, 38, 40, 43, 46, 48, 49, 51, 60, 61, 62, 64, 65, 66, 67, 68, 69, 71, 72, 73, 74, 81,
C. I. Pigment Red 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 14, 15, 16, 17, 18, 21, 22, 23, 31, 32, 38, 41, 48, 48: 1, 48: 2, 48: 3, 48: 4, 48: 5, 49, 52, 52: 1, 52: 2, 53: 1, 54, 57: 1, 58, 60: 1, 63, 64: 1, 68, 81: 1, 83, 88, 89, 95, 101, 104, 105, 108, 112, 114, 119, 122, 123, 136, 144, 146, 147, 149, 150, 164, 166, 168, 169, 170, 171, 172, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 187, 188, 190, 193, 194, 200, 202, 206, 207, 208, 209, 210, 211, 213, 214, 216, 220, 220, 221, 224, 226, 237, 238, 239, 242, 245, 247, 248, 251, 253, 254, 255, 256, 257, 258, 260, 262, 263, 264, 266, 268, 269, 270, 271, 272, 279,
C. I. Pigment Violet 1, 2, 3, 3: 1, 3: 3, 5: 1, 13, 15, 16, 17, 19, 23, 25, 27, 29, 31, 32, 36, 37, 38, 42, 50,
C. I. Pigment Blue 1, 15, 15: 1, 15: 2, 15: 3, 15: 4, 15: 5, 15: 6, 16, 17: 1, 24, 24: 1, 25, 26, 27, 28, 29, 36, 56, 60, 61, 62, 63, 75, 79, 80,
C. I. Pigment Green 1, 4, 7, 8, 10, 15, 17, 26, 36, 50,
C. I. Pigment Brown 5, 6, 23, 24, 25, 32, 41, 42,
C. I. Pigment Black 1, 6, 7, 9, 10, 11, 20, 26, 28, 31, 32, 34,
C. I. Pigment White 1, 2, 4, 5, 6, 7, 11, 12, 18, 19, 21, 22, 23, 26, 27, 28,
Examples include aluminum flakes, glass flakes, pearl pigments and hollow particles.

Among these, from the viewpoint of weather resistance and color reproducibility of the print layer,
C. I. Pigment Black 7,
C. I. Pigment Blue 15: 3, C.I. I. Pigment Blue 15: 4, C.I. I. Pigment Blue 28,
C. I. Pigment Red 101, C.I. I. Pigment Red 122, C.I. I. Pigment Red 202, C.I. I. Pigment Red 254, C.I. I. Pigment Red 282,
C. I. Pigment Violet 19,
C. I. Pigment White 6,
C. I. Pigment Yellow 42, C.I. I. Pigment Yellow 120, C.I. I. Pigment Yellow 138, C.I. I. Pigment Yellow 139, C.I. I. Pigment Yellow 150, C.I. I. Pigment Yellow 151, C.I. I. Pigment Yellow 155, C.I. I. Pigment Yellow 213 is preferred.

From the viewpoint of ejection stability, the pigment particles dispersed in the ink composition preferably have a volume average particle diameter of 0.05 to 0.4 μm and a volume maximum particle diameter of 0.2 to 1 μm. .. If the volume average particle size is larger than 0.4 μm and the volume maximum particle size is larger than 1 μm, it tends to be difficult to stably eject the ink composition. The volume average particle size and the volume maximum particle size can be measured by a measuring device using a dynamic light scattering method.

The ink composition of the present invention may further contain a pigment dispersant, if necessary, in order to disperse the pigment. The content of the pigment dispersant is, for example, 0.1 to 15% by mass in the ink composition. Further, the pigment dispersant may be used alone or in combination of two or more.

Specific examples of the pigment dispersant include
ANTI-TERRA-U, ANTI-TERRA-U100,
ANTI-TERRA-204, ANTI-TERRA-205,
DISPERBYK-101, DISPERBYK-102,
DISPERBYK-103, DISPERBYK-106,
DISPERBYK-108, DISPERBYK-109,
DISPERBYK-110, DISPERBYK-111,
DISPERBYK-112, DISPERBYK-116,
DISPERBYK-130, DISPERBYK-140,
DISPERBYK-142, DISPERBYK-145,
DISPERBYK-161, DISPERBYK-162,
DISPERBYK-163, DISPERBYK-164,
DISPERBYK-166, DISPERBYK-167,
DISPERBYK-168, DISPERBYK-170,
DISPERBYK-171, DISPERBYK-174,
DISPERBYK-180, DISPERBYK-182,
DISPERBYK-183, DISPERBYK-184,
DISPERBYK-185, DISPERBYK-2000,
DISPERBYK-2001, DISPERBYK-2008,
DISPERBYK-2009, DISPERBYK-2020,
DISPERBYK-2025, DISPERBYK-2050,
DISPERBYK-2070, DISPERBYK-2096,
DISPERBYK-2150, DISPERBYK-2155,
DISPERBYK-2163, DISPERBYK-2164,
BYK-P104, BYK-P104S, BYK-P105,
BYK-9076, BYK-9077, BYK-220S, BYKJET-9150, BYKJET-9151 (all manufactured by Big Chemie Japan),
Solspace 3000, Solspace 5000,
Solspace 9000, Solspace 11200,
Solspace13240, Solspace13650,
Solspace13940, Solspace16000,
Solspace 17000, Solspace 18000,
Solspace 20000, Solspace 21000,
Solspace24000SC, Solspace24000GR,
Solspace26000, Solspace27000,
Solspace28000, Solspace32000,
Solspace32500, Solspace32550,
Solspace32600, Solspace33000,
Solspace34750, Solspace35100,
Solspace35200, Solspace36000,
Solspace 36600, Solspace 37500,
Solspace 38500, Solspace 39000,
Solspace 41000, Solspace 54000,
Solspace 55000, Solspace 56000,
Solspace71000, Solspace76500,
Solspace X300 (above, manufactured by Lubrizol),
Disparon DA-7301, Disparon DA-325, Disparon DA-375, Disparon DA-234 (all manufactured by Kusumoto Kasei Co., Ltd.),
Floren AF-1000, Floren DOPA-15B, Floren DOPA-15BHFS, Floren DOPA-17HF, Floren DOPA-22, Floren DOPA-33, Floren G-600, Floren G-700, Floren G-700AMP, Floren G-700DMEA, Floren G-820, Floren G-900, Floren GW-1500, Floren KDG-2400, Floren NC-500, Floren WK-13E, (all manufactured by Kyoeisha Chemical Co., Ltd.),
TEGO Dispers 610, TEGO Dispers 610S,
TEGO Dispers 630, TEGO Dispers 650,
TEGO Dispers 652, TEGO Dispers 655,
TEGO Dispers 662C, TEGO Dispers 670,
TEGO Dispers 685, TEGO Dispers 700,
TEGO Dispers 710, TEGO Dispers 740W,
LIPOTIN A, LIPOTIN BL,
LIPOTIN DB, LIPOTIN SB (all manufactured by Evonik Degusa),
PB821, PB822, PN411, PA111 (all manufactured by Ajinomoto Fine Techno Co., Ltd.),
Texahole 963, Texahole 964, Texahole 987, Texahole P60, Texahole P61, Texahole P63, Texahole 3250, Texahole SF71, Texahole UV20, Texahole UV21 (all manufactured by Cognis),
Examples thereof include BorchiGenSN88 and BorchiGen0451 (all manufactured by Bocious).

The ink composition of the present invention may further contain a surface conditioner from the viewpoint of improving wettability and the like. As used herein, the surface conditioner means a substance that has a hydrophilic part and a hydrophobic part in the molecular structure and can adjust the surface tension of the ink composition by adding it.

Specific examples of the surface conditioner that can be used in the ink composition of the present invention include anionic surface conditioners such as dialkyl sulfosuccinates, alkylnaphthalene sulfonates, and fatty acid salts, polyoxyethylene alkyl ethers, and polyoxyethylene. Nonionic surface conditioners such as alkylallyl ethers, acetylene glycols, polyoxyethylene / polyoxypropylene block copolymers, cationic surface conditioners such as alkylamine salts and quaternary ammonium salts, acrylic surface conditioners, Examples include silicon-based surface conditioners and fluorine-based surface conditioners. In particular, a silicon-based surface conditioner or an acrylic surface conditioner is preferable, and commercially available products such as Big Chemie, Evonik, and Toray Dow Corning can be used. Further, in the case of a silicone-based surface conditioner, it is preferable that the silicone-based surface conditioner is a polyether-modified silicone oil and has an HLB of 7.6 to 12.

The amount of the surface conditioner in the ink composition of the present invention can be appropriately selected depending on the intended use, but is preferably 0.01 to 1% by mass in the ink composition, for example. The surface conditioner may be used alone or in combination of two or more.

As a specific example of the above surface conditioner,
BYK-300, BYK-302, BYK-306, BYK-307, BYK-310, BYK-313, BYK-315N, BYK-320, BYK-322, BYK-323, BYK-325, BYK-326, BYK- 330, BYK-331, BYK-333, BYK-342, BYK-345, BYK-346, BYK-347, BYK-348, BYK-349, BYK-350, BYK-354, BYK-355, BYK-356, BYK-358N, BYK-361N, BYK-370, BYK-375, BYK-377, BYK-378, BYK-381, BYK-392, BYK-394, BYK-399, BYK-3440, BYK-3441, BYK- 3455, BYK-3550, BYK-3560, BYK-3565, BYK-3760, BYK-DYNWET 800N, BYK-SILCLEAN 3700, BYK-SILCLEAN 3701, BYK-SILCLEAN 3720, BYK-UV3500, BYK-UV3500, BYK-UV3500 BYK-UV3530, BYK-UV3535, BYK-UV3570, BYK-UV3575, BYK-UV3576 (all manufactured by Big Chemie Japan),
TEGO Flow 300, TEGO Flow 370, TEGO Flow 425, TEGO Flow ATF 2, TEGO Flow ZFS 460, TEGO Glide 100, TEGO Glide 110, TEGO Glide 110, TEGO Glide 130, TEGO TEGO Glide 432, TEGO Glide 435, TEGO Glide 440, TEGO Glide 450, TEGO Glide 482, TEGO Glide A 115, TEGO Glide B 1484, TEGO Glide B 1484, TEGO Glide ZG 400
501W ADDITIVE, FZ-2104, FZ-2110, FZ-2123, FZ-2164, FZ-2191, FZ-2203, FZ-2215, FZ-2222, FZ-5609, L-7001, L-7002, L-7604 , OFX-0193, OFX-0309 FLUID, OFX-5221 FLUID, SF 8410 FLUID, SH3771, SH 3746 FLUID, SH 8400 FLUID, SH 8700 FLUID, Y-7006 (all manufactured by Toray Dow Corning),
KF-351A, KF-352A, KF-353, KF-354L, KF-355A, KF-615A, KF-640, KF-642, KF-643, KF-644, KF-945, KF-6004, KF- Examples thereof include 6011, KF-6012, KF-6015, KF-6017, KF-6020, KF-6204, X-22-2516, and X-22-4515 (all manufactured by Shin-Etsu Chemical Co., Ltd.).

Among these, from the viewpoint of structure and HLB, 501W ADDITIVE, FZ-2104, FZ-2123, FZ-2215, L-7002, OFX-0309 FLUID, OFX-5221 FLUID, SH 8400 FLUID, KF-351A, KF- 353, KF-355A, KF-615A, KF-642, KF-644, KF-6004, KF-6011, KF-6204 are preferable.

The ink composition of the present invention has other components such as an antioxidant, a plasticizer, a rust preventive, a solvent, a non-reactive polymer, a filler, an antifoaming agent, a charge control agent, a stress relaxant, a penetrant, and a derivative. Additives such as a light material, a bright material, a magnetic material, and a phosphor may be used as needed.

The ink composition of the present invention can be obtained by mixing various components appropriately selected as necessary and using a filter having a pore size of about 1/10 or less of the nozzle diameter of the inkjet printhead to be used, if necessary. It can be prepared by filtering the resulting mixture.

The ink composition of the present invention preferably has a viscosity at 40 ° C. of 5 to 25 mPa · s, and more preferably 5 to 20 mPa · s. When the ink viscosity at 40 ° C. is within the above-specified range, good ejection stability can be obtained. The ink viscosity can be measured using a cone plate type viscometer.

The ink composition of the present invention preferably has a surface tension of 20 to 35 mN / m at 25 ° C., and more preferably 23 to 33 mN / m. When the ink surface tension at 25 ° C. is within the above-specified range, good ejection stability can be obtained. The ink surface tension can be measured by the plate method.

The ink composition of the present invention is preferably a clear ink. In the present specification, the clear ink refers to a clear ink having a light transmittance of 80% or more in a wavelength range of 380 to 800 nm when a film having a thickness of 30 μm is formed, and the light transmittance is preferably 83% or more. , More preferably 85% or more, still more preferably 90% or more. In the present specification, the light transmittance is measured according to JIS K7361-1: 1997 "Plastic-Test method for total light transmittance of transparent material-Part 1: Single beam method".

Next, a preferable example of a method for producing a printed matter using the ink composition of the present invention (hereinafter, also referred to as a method for producing a printed matter of the present invention) will be described, but the present invention is not limited thereto. In the method for producing a printed matter of the present invention, printing is performed on a base material or a layer formed on the base material with the above-mentioned ink composition of the present invention to form a printed layer (preferably a clear layer). Then, it includes a first step of curing the printed layer, and preferably further includes a second step of heating the printed matter obtained by the first step. In the first step, the step of forming the print layer and then curing the print layer may be repeated once or a plurality of times.

The base material is not particularly limited, and paper, coated paper, plastic, vinyl chloride sheet, tarpaulin, corrugated plastic, building board and the like can be used, but when a heating step is included, it can withstand the heating of printed matter described later. It is preferable to use a base material having heat resistance. Examples of such materials include metals such as iron, stainless steel, aluminum, copper, titanium and their alloys, cement, concrete, gypsum, calcium silicate, calcium carbonate, marble, artificial marble, glass, ceramics and the like. However, a combination of two or more of these materials may be used. Further, the surface of the base material may be subjected to pretreatment such as degreasing treatment, chemical conversion treatment and polishing, sealer, primer coating and the like. The surface of the base material may be smooth, may have irregularities, or may be a three-dimensional object. In the present invention, by using a base material having such a material and properties, it can be suitably used especially for furniture, building materials, and small metal objects.

The base material may have a layer (for example, a coating film or a printing film) formed on a part or the whole of the surface thereof, and the layer can be decorated. For example, a coating film formed of a paint, a printing film formed of an ink, a printing film formed of a powder toner, or the like may be formed on a substrate. The layers formed on the base material are resins, colorants such as dyes and pigments, ultraviolet absorbers, radical scavengers, antioxidants, plasticizers, rust inhibitors, fillers, charge control agents, light guide materials, etc. It can contain a bright material, a magnetic material, a phosphor, a wax and the like.

The paints and inks used when forming the layer on the substrate include organic solvent-based paints and inks that use an organic solvent as the main solvent, water-based paints and inks that use water as the main solvent, and light that uses a polymerizable compound. Examples thereof include various paints and inks such as curable paints and inks and powder paints. Here, examples of the components that can be used in the case of the photocurable ink include the components that can be used in the above-mentioned ink composition of the present invention.

In the method for producing a printed matter of the present invention, the means for forming a layer on the substrate is not particularly limited. For example, in the case of paint, various coating means such as air spray, airless spray, roll coater, flow coater, and electrostatic coating can be used. In the case of ink, various printing means such as gravure printing, offset printing, flexographic printing, screen printing, coater printing, and inkjet printing can be used. In the case of powder toner, an electrophotographic development type printing means (specifically, an image forming apparatus such as a copier or a laser printer) can be used.

The printing using the ink composition of the present invention is preferably performed by an inkjet printing method, but is not limited to this, and is not limited to the gravure printing method, the offset printing method, the flexographic printing method, the screen printing method, and the coater method. It is also possible to carry out by various printing methods such as.

In the present specification, printing means applying ink on an object by a printing means, and is not limited to those intended to color the object or draw characters, images, etc., and is not limited to the surface of the object. It is also included that the purpose is to coat the object or to perform a surface treatment on the object. In addition, in this specification, an ink composition for use in an inkjet printing method is also referred to as an inkjet ink.

For inkjet printing, it can be used in various inkjet printers. Examples of the inkjet printer include an inkjet printer that ejects an ink composition by a charge control method or a piezo method. Further, a large-sized inkjet printer, specifically, an inkjet printer for printing on an article produced on an industrial line can also be preferably used.

The printing layer (preferably a clear layer) formed by the ink composition of the present invention is preferably cured by irradiation with light having a peak wavelength in the range of 360 nm or more and 425 nm or less. Here, as the light source, a high-pressure mercury lamp, a metal halide lamp, an LED lamp, or the like can be used. Further, it is preferable that the wavelength of the active energy ray irradiated to cure the print layer overlaps with the absorption wavelength of the photopolymerization initiator. The integrated light intensity of the active energy rays is preferably in the range of ^{100 to 8000 mJ / cm 2.}

The ink composition of the present invention can be subjected to surface finishing such as gloss-like and matte-like by appropriately selecting the ejection conditions for inkjet printing and the subsequent curing conditions. For example, if the ink spreads and then cures after a while, it becomes glossy, and if the ink droplets independently cure in a lenticular shape, it becomes matte.

The thickness of the print layer formed by the ink composition of the present invention is 5 μm or more, preferably 30 μm or more, and more preferably 90 μm or more. The upper limit of the thickness of the print layer is, for example, 500 μm or less.

The printing layer formed by the ink composition of the present invention is formed so as to cover a part or the whole of the surface of the base material or the layer formed on the base material.

When the printing layer formed by the ink composition of the present invention is a clear layer, the clear layer has a light transmittance of 80% or more in the wavelength range of 380 to 800 nm when the thickness is 30 μm. It is preferably 90% or more, and more preferably 90% or more.

As described above, the method for producing a printed matter of the present invention preferably further includes a second step of heating the printed matter obtained by the first step. Specifically, the printed matter obtained through printing using the ink composition of the present invention and subsequent curing is heated. Here, the heat treatment is performed in the range of, for example, 70 ° C. to 300 ° C.

Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to the following examples. In addition, "part" and "%" in Examples and Comparative Examples are based on mass unless otherwise specified.

<Ink preparation method>
A mixture according to the formulation shown in Tables 1 to 3 was obtained and kneaded with a bead mill to homogenize the mixture to prepare an active energy ray-curable inkjet ink.

The details of the ingredients shown in the formulation are shown below.
1) KBM-502, manufactured by Shinetsu Chemical Industry Co., Ltd., 3-methacryloxypropylmethyldimethoxysilane 2) KBE-502, manufactured by Shinetsu Chemical Industry Co., Ltd., 3-methacryloxypropylmethyldiethoxysilane 3) KBM-503, Shinetsu Chemical Industry Co., Ltd. 3-methacryloxypropyltrimethoxysilane 4) KBM-5103, manufactured by Shinetsu Chemical Industry Co., Ltd., 3-acryloxypropyltrimethoxysilane 5) KBM-103, manufactured by Shinetsu Chemical Industry Co., Ltd., phenyltrimethoxysilane 6) Z -8383, Toray Dow Corning Co., Ltd., Methyltriethoxysilane 7) Light Acrylate DCP-A, Kyoeisha Chemical Co., Ltd., Tricyclodecanedimethanol Diacrylate 8) CD406, Sartomer Co., Ltd., Cyclohexanedimethanol Diacrylate 9) Light Acrylate PO-A, Kyoeisha Chemical Co., Ltd., Phenoxyethyl Acrylate 10) Light Acrylate THF-A, Kyoeisha Chemical Co., Ltd., Tetrahydrofurfuryl Acrylate 11) Light Acrylate IB-XA, Kyoeisha Chemical Co., Ltd., Isobornyl Acrylate 12) Light Acrylate 1.6HX-A, manufactured by Kyoeisha Chemical Co., Ltd., 1,6-hexanediol diacrylate 13) NBMA, manufactured by MCC Unitech, Nn-butoxymethylacrylamide 14) light ester HOA, manufactured by Kyoeisha Chemical Co., Ltd., 2-hydroxy Ethyl acrylate 15) 4-HBA, manufactured by Osaka Organic Chemical Industry Co., Ltd., 4-hydroxybutyl acrylate 16) Praxel FA2D, manufactured by Daicel Chemical Industry Co., Ltd., adduct of 2-hydroxyethyl acrylate and ε-caprolactone 17) Praxel FA5, Daicel Additive of 2-hydroxyethyl acrylate and ε-caprolactone manufactured by Kagaku Kogyo Co., Ltd. 18) EBECRYL4265, manufactured by Daicel Ornex, urethane acrylate oligomer, molecular weight 650
19) EBECRYL1290, manufactured by Daicel Ornex, urethane acrylate oligomer, molecular weight 1,000
20) EBECRYL8602, manufactured by Daicel Ornex, urethane acrylate oligomer, molecular weight 2,000
21) SPEEDCURE TPO, Rambson, 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide 22) Omnirad 651, BASF, 2,2-dimethoxy-2-phenylacetophenone 23) Raven 450, Columbian Carbon Japan Black pigment 24) Heliogen Blue L7080, BASF, blue pigment

<Printing process>
The inks of Examples 1 to 36 and Comparative Examples 1 to 4 were set in an inkjet printer, and the surface of an aluminum base material of 0.8 mm × 100 mm × 50 mm was painted with a white paint for a base layer manufactured by Dai Nippon Toryo Co., Ltd. A stratum is prepared, and a 100 mm × 50 mm image (printing layer) is prepared on the base layer.

<Heat-resistant yellowing>
As described in the above <Printing process>, the aluminum plate was painted with a white paint for a base layer manufactured by Dai Nippon Toryo Co., Ltd. to prepare a base layer. Next, a solid image (thickness: 100 μm) is printed on the base layer by an inkjet printer using an active energy ray-curable inkjet ink, and then an active energy ray having a main wavelength of 360 to 425 nm is 2000 mJ using a metal halide lamp. The image (printing layer) was cured by irradiating with / cm ^2. Next, the surface temperature of the base material was raised to 180 ° C., and heating was performed for 20 minutes at that temperature to prepare a printed matter. Next, the color of the printed layer of the printed matter was measured with a spectrophotometer (SpectroEye, manufactured by X-Rite). In the L * a * b * color system, the b value is an index of yellowness. The b values of the printed portion and the non-printed portion were measured, the difference between these b values was determined, and the heat-resistant yellowing was evaluated according to the following evaluation criteria. Since Examples 25 and 26 are pigment inks, the b values of the printed portion before and after heating were measured, the difference between these b values was determined, and the heat-resistant yellowing was evaluated according to the following evaluation criteria. The results are shown in Tables 1-3.
⊚: Less than 3.0.
◯: 3.0 or more and less than 5.0.
Δ: 5.0 or more and less than 7.0.
X: 7.0 or more.

<Weather resistance>
A printed matter was produced by printing, curing, and heating in the same manner as described in <Heat-resistant yellowing> above except that the thickness of the printed layer was set to 30 μm. Next, a weather resistance test was conducted using an accelerated weather resistance tester conforming to JIS B7753 (Sunshine Weather Meter Method). The test time was 1500 hours. The L, a, and b values of the printed layer before and after the 1500-hour test were measured with a spectrophotometer (SpectroEye, manufactured by X-Rite) to obtain the color difference (ΔE) of the following formula, and the weather resistance was determined according to the following evaluation criteria. Was evaluated. The results are shown in Tables 1-3.
Color difference (ΔE) = [(difference in L value before and after the test) ² + (difference in a value before and after the test) ² + (difference in b value before and after the test) ² ] ^1/2
⊚: Less than 3.0.
◯: 3.0 or more and less than 4.5.
Δ: 4.5 or more and less than 6.
X: 6 or more.

<Crack resistance>
A printed matter was produced by printing, curing, and heating in the same manner as described in <Heat-resistant yellowing> above except that the thickness of the printed layer was changed. The produced printed layer was visually confirmed, and the crack resistance was evaluated according to the following evaluation criteria. Printed matter having print layers having thicknesses of 100 μm, 200 μm, and 300 μm was prepared, respectively. The results are shown in Tables 1-3.
⊚: No crack is confirmed at any of the thicknesses of 300 μm, 200 μm, and 100 μm.
◯: Cracks were confirmed at thicknesses of 300 μm, but no cracks were confirmed at thicknesses of 200 μm and 100 μm.
Δ: Cracks were confirmed at thicknesses of 300 μm and 200 μm, but no cracks were confirmed at thicknesses of 100 μm.
X: Cracks were confirmed at all of the thicknesses of 300 μm, 200 μm, and 100 μm.

<Adhesiveness>
A printed matter was produced by printing, curing, and heating in the same manner as described in <Heat-resistant yellowing> above except that the thickness of the printed layer was set to 30 μm. The printed matter was cross-cut with a width of 1 mm and a width of 100 squares, and the cellophane tape was sufficiently adhered and then peeled off. Adhesion was evaluated according to the following evaluation criteria. The results are shown in Tables 1-3.
⊚: No peeling is confirmed on the cut part.
◯: Less than 5% peeling was confirmed in the cut portion.
Δ: Peeling of 5% or more and less than 20% was confirmed in the cut portion.
X: Peeling of 20% or more was confirmed in the cut portion.

<Bending resistance>
A printed matter was produced by printing, curing, and heating in the same manner as described in <Heat-resistant yellowing> above except that the thickness of the printed layer was set to 30 μm. Next, a 180 ° bending test was performed to visually confirm the degree of cracking and peeling of the printed layer at the bent portion, and the bending resistance was evaluated according to the following evaluation criteria. Here, the 180 ° bending test is a test in which the printed matter is bent 180 ° with the printed surface on the outside, and the presence or absence of cracks in the bent portion is visually evaluated. Further, 0T is defined as a case where the bending portion is bent 180 ° without sandwiching anything inside the bent portion, and 1T is defined as a case where a plate having the same thickness as the test plate is sandwiched and bent. In this test, 3T (that is, sandwiching 3 plates), 4T (that is, sandwiching 4 plates), 5T (that is, 5 plates are sandwiched) using a plate having the same thickness as the aluminum base material. A 180 ° bending test was performed with (sandwiching), and the bending resistance was evaluated according to the following evaluation criteria. A printed layer in which cracking or peeling is not confirmed when the T number is low is excellent in bending resistance. The results are shown in Tables 1-3.
⊚: In the case of 3T, no cracking or peeling of the print layer is confirmed.
◯: In the case of 3T, cracking or peeling of the print layer was confirmed, but in the case of 4T, cracking or peeling of the print layer was not confirmed.
Δ: In the case of 3T and 4T, cracking or peeling of the print layer was confirmed, but in the case of 5T, cracking or peeling of the print layer was not confirmed.
X: In any of 3T, 4T, and 5T, cracking, peeling, or both of the ink is confirmed.

Claims (8)

(A) The following formula (I)

(In the formula, x is 0 or 1, R ¹ , R ² and R ³ are independently hydrogen atoms or alkyl groups, and R ⁴ is an organic group having 1 to 10 carbon atoms). A photocurable ink composition comprising (B) a polyfunctional polymerizable compound having an alicyclic structure, and (C) a photopolymerization initiator at least. The photocurable ink composition according to claim 1, further comprising (D) an ultraviolet absorber, (E) a radical scavenger, or both. The photocurable ink composition according to claim 1 or 2, further comprising (F) a polymerizable oligomer having a molecular weight of 1,000 to 20,000. The photocuring according to any one of claims 1 to 3, wherein the amount of the compound represented by the formula (I) in the ink composition is in the range of 0.1 to 20% by mass. Mold ink composition. In the formula (I), an organic group of R ⁴ is, (meth) characterized in that it comprises an acryloyl group, photocurable ink composition according to any one of claims 1 to 4. The photocurable ink composition according to any one of claims 1 to 5, wherein the photopolymerization initiator (C) contains at least an acylphosphine oxide-based initiator. The photocurable ink composition according to any one of claims 1 to 6, further comprising (G) a colorant. The photocurable ink composition according to any one of claims 1 to 7, which is a clear ink composition.