JP2006282764A - Ink composition and method for forming image using the same, and recorded article - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an ink composition which is low viscous and has excellent curability and adhesiveness to substrates, can form high quality images having clear hues and high colorability, and is suitable for ink jet recording. <P>SOLUTION: This ink composition is characterized by containing a cation-polymerizable group-having dendritic branched polymer. The ink composition, wherein the dendritic branched polymer is a hyper branched polymer or dendrimer. The ink composition, wherein the cation-polymerizable group is a vinyl ether group, oxirane group or oxetane group. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to an ink composition and an image forming method using the same.

  Water-based ink-jet inks have poor water resistance when printed on plain paper and are likely to bleed. In addition, ink droplets adhere poorly when printed on non-water-absorbing recording media such as plastic. For this reason, image formation could not be performed, and drying of the solvent was extremely slow, so that it was necessary to dry without overlapping the recorded material immediately after printing, and the image was liable to blur.

  Ultraviolet curable inks using polyfunctional monomers with excellent adhesion to recording media have been developed as suitable for printing on non-water-absorbing recording media. Slow and insufficient to form a full color image. In order to solve the drying property, a method using a volatile organic solvent as the solvent of the ink has been carried out, but in order to dry quickly, it is highly flammable, such as methyl ethyl ketone and ethanol, and is also highly volatile. It was necessary to use a solvent.

In order to solve these problems, inkjet inks that are cured and fixed by radiation rather than volatilization of the ink solvent have been developed. For example, Patent Documents 1 to 3 disclose inks containing a monomer having a polymerizable group and an oil-soluble dye. Patent Document 4 discloses a photopolymerizable composition containing a photopolymerizable compound and a photopolymerization initiator. However, these inks have a problem that the curing speed is insufficient. In general, since radical polymerization is inhibited by oxygen, the curability in air and in a thin film is a problem.
Therefore, an ink using cationic polymerization that is not inhibited by oxygen is disclosed. For example, Patent Document 5 discloses an active energy ray-curable composition having oxirane and oxetane, but the curing rate is not sufficient. Patent Document 6 discloses an active energy ray-curable composition having oxirane, oxetane, and vinyl ether with improved curing speed, but has a problem that storage stability deteriorates, and vinyl ether is decomposed. There was a problem of producing acetaldehyde. On the other hand, Patent Document 7 discloses an active energy ray-curable ink using a cyclic compound such as tetrahydrofuran, oxepane, and monocyclic acetal for the purpose of having storage stability, but the curing speed is not sufficient. It was.
JP 2003-221528 A JP 2003-221532 A JP 2003-221530 A JP 2001-222105 A JP 2000-169552 A Japanese Patent Laid-Open No. 2001-220526 JP 2004-10625 A

  The problem to be solved by the present invention is to provide an ink composition that has a low viscosity, is excellent in curability and adhesion to a substrate, and gives a high-quality recorded matter. Another object of the present invention is to provide an image forming method and recorded matter using such an ink composition.

As a result of intensive studies, the present inventors have used a dendritic branched polymer having a polymerizable functional group, thereby having excellent curability and good adhesion to a substrate, and also long-term storage, Alternatively, the inventors have found that an ink composition having low viscosity and excellent ejection stability in ink jet can be obtained even after repeated temperature changes, and the present invention has been completed.
That is, the present invention is as follows.
(1) An ink composition comprising a dendritic polymer having a cationically polymerizable group.
(2) The ink composition according to item (1), wherein the dendritic polymer is a hyperbranched polymer or a dendrimer.
(3) The ink composition according to item (1) or (2), wherein the cationically polymerizable group is a vinyl ether group, an oxirane group, or an oxetane group.
(4) The ink composition according to any one of (1) to (3), wherein the ink composition further contains a photoacid generator.
(5) The ink composition according to any one of (1) to (4), wherein the ink composition further contains a cationically polymerizable compound having at least one of an oxirane group and an oxetane group.
(6) The ink composition according to any one of (1) to (5), wherein the ink composition further contains a colorant.
(7) The ink composition according to item (6), wherein the colorant is a pigment or an oil-soluble dye.
(8) The ink composition according to any one of (1) to (7), which is an ink composition for inkjet recording.
(9) An image recording step of recording an image on a recording material using the ink composition according to any one of (1) to (8);
An image curing step of irradiating and curing an active energy ray on the image recorded on the recording material in the image recording step;
An image forming method comprising:
(10) The image forming method according to (9), wherein the image recording step records the image by inkjet recording in which the ink composition is discharged. And (11) A recorded matter recorded using the ink composition according to any one of (1) to (8).

  In the ink composition of the present invention, by using a dendritic polymer having a cationic polymerizable group, it is possible to increase the curing speed and to have good ink stability. Also, since the ink cure speed is sufficiently fast and the ink stability is good, the ink jet printer is less clogged and has excellent adhesion to the recording medium, and good characters or images can be recorded on the recording medium (printing paper, etc.) Can be recorded. Moreover, since it is a dendritic polymer, the entanglement between molecules is small and it can be adjusted to an appropriate low viscosity. Further, high transparency can be obtained, and a high-quality recorded product can be obtained.

  According to the present invention, an ink composition having excellent curability and stability can be provided. In addition, an image forming method and a recorded matter using such an ink composition can be provided.

Details of the present invention will be described below.
The curable ink composition in the present invention contains a dendritic branched polymer having a cationic polymerizable group. The dendritic polymer is a polymer having a plurality of branched chains in one molecule. In the present invention, a dendrimer, a hyperbranched polymer, a star polymer, or a graft polymer is preferably used. More preferred are polymers. Among these, dendrimers are particularly excellent in terms of physical properties (particularly viscosity) of the ink composition, and hyperbranched polymers are particularly excellent in terms of curability.

  Examples of the dendrimer used in the present invention include G.I. R. Newkome, C.I. N. Moorefield, F.M. "Dendrimers and Dendrons" by Fegtre (2001, published by WILEY-VCH), C.I. J. et al. Hawkeret al; Chem. Soc. , Commun. , 1010 (1990), D.C. A. Tomalia et al; Angew. Chem. Int. Ed. Engl. 29, 138 (1990), C.I. J. et al. Hawker et al; Am. Chem. Soc. 112, p. 7638 (1990), J. Am. M.M. J. et al. It is possible to use what is described in literatures, such as Frechet, Science, 263, 1710 (1994).

  Examples of the dendrimer suitably used in the present invention include dendrimers represented by the following Den-1 to Den-5, but the present invention is not limited thereto. In addition, it is especially preferable that these dendrimers are 2nd generation-4th generation. The dendrimer preferably has a molecular weight of 500 to 50,000, and particularly preferably a molecular weight of 500 to 10,000.

  The hyperbranched polymer used in the present invention is a multibranched polymer synthesized by self-condensation of so-called ABx type molecules having a total of 3 or more of two kinds of substituents in one molecule. For example, hyperbranched polymers described in the book of “Nanotechnology of Branched Polymers” edited by Koji Ishizu (2000, IPC Co., Ltd.) can be mentioned.

Examples of methods for producing these hyperbranched polymers include M.I. As described in Suzuki et al; Macromolecules, 25, 7071 (1992), 31, 1716 (1998), by a ring-opening polymerization of a cyclic compound using a primary amine as a nucleophilic component and a palladium catalyst. Examples include synthesis methods. A polymerizable compound in the present invention can be obtained by adding a known polymerizable functional group to these known dendritic branched polymers.
In the present invention, examples of the hyperbranched polymer suitably used include HP-1 to HP-5 produced by the following production method.

  In the above formula, a, b and c represent copolymer composition ratios and are expressed in mol% (a + b + C = 100). In the present invention, the molecular weight of the hyperbranched polymer is preferably 1000 to 500000, more preferably about 1000 to 100000, and more preferably 2000 to 50000. If the molecular weight is too large, the ink viscosity increases, and the ejection stability during ink jet recording may decrease. Moreover, when molecular weight is too small, sclerosis | hardenability may become inadequate.

The dendritic branched polymer used in the present invention has a cationic polymerizable group.
Examples of the cationic polymerizable group include oxirane group, oxetane group, oxepane group, acetal group, vinyl ether group, styryl group, carbonate group, thiirane group, thietane group, thiocarbonate group, orthoester group, lactone group, and lactam group. Can be mentioned. Among these, a vinyl ether group, a styryl group, an oxirane group, and an oxetane group are particularly preferable from the viewpoint of the polymerization rate in the presence of oxygen and the adhesion to a substrate.

Hereinafter, specific examples of preferable dendritic branched polymers in the present invention will be described. Note that the present invention is not limited to this.
P-1) Reaction product of the exemplified compound Den-2 and p-chloromethylstyrene
P-2) Reaction product of the exemplified compound Den-4 and p-chloromethylstyrene
P-3) Reaction product of Exemplified Compound HP-4 with p-chloromethylstyrene
P-4) Reaction product of the exemplified compound Den-1 and chloroethyl vinyl ether
P-5) Reaction product of Exemplified Compound HP-1 and chloroethyl vinyl ether
P-6) Reaction product of Exemplified Compound HP-2 and chloroethyl vinyl ether
P-7) Reaction product of the exemplified compound HP-5 with 2-hydroxyethyl vinyl ether
P-8) Reaction product of the exemplified compound Den-4 and epichlorohydrin
P-9) Reaction product of the exemplified compound HP-1 and epichlorohydrin
P-10) Reaction product of the exemplified compound HP-2 and epibromohydrin
P-11) Reaction product of Exemplified Compound HP-3 with epibromohydrin
P-12) Reaction product of the exemplified compound Den-5 and 3-ethyl-3-chloromethyl-oxetane
P-13) Reaction product of the exemplified compound HP-1 and 3-ethyl-3-chloromethyl-oxetane
P-14) Reaction product of Exemplified Compound HP-2 and 3-ethyl-3-chloromethyl-oxetane
P-15) Reaction product of the exemplified compound HP-3 and 3-ethyl-3-chloromethyl-oxetane
P-16) Reaction product of Exemplified Compound HP-5 and 3-ethyl-3-hydroxymethyl-oxetane These reactions can all be obtained by heating from room temperature to 100 ° C. in a solvent. It is preferable to use the catalyst.

  The content of the dendritic polymer is preferably 0.5% by mass or more, more preferably 0.5 to 30% by mass, and even more preferably 0.5 to 20% by mass in the ink composition. If the content is too small, the curability may be insufficient, and if the content is too large, the ink ejection property may decrease.

  In the present invention, it is preferable from the viewpoint of ink viscosity to use another polymerizable compound together with the dendritic branched polymer having a polymerizable group. The other polymerizable compound that can be used in combination is preferably a cationic polymerizable compound, and any monomer, oligomer, or polymer species can be used as long as it is a compound having a generally known cationic polymerizable group. The cationic polymerizable compound is not particularly limited, and any known cationic polymerizable compound can be used without any problem. Moreover, the cationically polymerizable compound can be used alone or in combination for the purpose of adjusting the reaction rate, ink physical properties, cured film physical properties and the like.

  Among these cationically polymerizable compounds, it is preferable to further contain a compound having at least one of an oxirane group and an oxetane group in order to further improve the adhesion. These compounds can be contained in an amount of preferably 5% by mass to 90% by mass with respect to the ink composition, and preferably 20% by mass to 90% by mass from the viewpoint of suppressing volume shrinkage.

  The oxirane group-containing compound (oxirane compound, that is, epoxy compound) and the oxetane group-containing compound (oxetane compound) may be used alone or in combination of two or more. From the viewpoint of improving the curing rate and the degree of curing, it is preferable to use at least one oxetane compound and an oxirane compound in combination. In this case, the content ratio of the oxirane compound and the oxetane compound in the ink composition is preferably 10:90 to 60:40, respectively. An ink composition having a good balance between curability and curing speed can be obtained by setting between these values.

[Oxirane compounds]
Examples of the oxirane compound include aromatic epoxides and alicyclic epoxides. Aromatic epoxides include di- or polyglycidyl ethers produced by the reaction of polyphenols having at least one aromatic nucleus or their alkylene oxide adducts and epichlorohydrin, such as bisphenol A or its alkylene oxides. Examples thereof include di- or polyglycidyl ethers of adducts, di- or polyglycidyl ethers of hydrogenated bisphenol A or alkylene oxide adducts thereof, and novolak type epoxy resins. Here, examples of the alkylene oxide include ethylene oxide and propylene oxide.

Examples of the alicyclic epoxide include cyclohexene oxide obtained by epoxidizing a compound having at least one cycloalkane ring such as cyclohexene or cyclopentene ring with an appropriate oxidizing agent such as hydrogen peroxide or peracid. Preferred examples include cyclopentene oxide-containing compounds.
Examples of the aliphatic epoxide include dihydric polyhydridyl ethers of aliphatic polyhydric alcohols or alkylene oxide adducts thereof, and typical examples thereof include diglycidyl ether of ethylene glycol, diglycidyl ether of propylene glycol or 1,6. -Diglycidyl ether of alkylene glycol such as diglycidyl ether of hexanediol, polyglycidyl ether of polyhydric alcohol such as diglycerin or its alkylene oxide adduct di- or triglycidyl ether, diglycidyl of polyethylene glycol or its alkylene oxide adduct Polyalkylene glycol diglycol represented by diglycidyl ether of ether, polypropylene glycol or its alkylene oxide adduct Jill ether, and the like. Here, examples of the alkylene oxide include ethylene oxide and propylene oxide.
Among these oxirane compounds, aromatic epoxides and alicyclic epoxides are preferable from the viewpoint of excellent curing speed, and alicyclic epoxides are particularly preferable.
Further, among the oxirane compounds, those having a small number of functional groups are preferable because they can simultaneously have solubility and viscosity adjusting effects as described above.

  Examples of monofunctional epoxides used in the present invention include, for example, phenyl glycidyl ether, p-tert-butylphenyl glycidyl ether, butyl glycidyl ether, 2-ethylhexyl glycidyl ether, allyl glycidyl ether, 1,2-butylene oxide, 1 , 3-butadiene monooxide, 1,2-epoxydodecane, epichlorohydrin, 1,2-epoxydecane, styrene oxide, cyclohexene oxide, 3-methacryloyloxymethylcyclohexene oxide, 3-acryloyloxymethylcyclohexene oxide, 3- Examples include vinylcyclohexene oxide.

  Examples of polyfunctional epoxides include, for example, bisphenol A diglycidyl ether, bisphenol F diglycidyl ether, bisphenol S diglycidyl ether, brominated bisphenol A diglycidyl ether, brominated bisphenol F diglycidyl ether, brominated bisphenol S diglycidyl. Ether, epoxy novolac resin, hydrogenated bisphenol A diglycidyl ether, hydrogenated bisphenol F diglycidyl ether, hydrogenated bisphenol S diglycidyl ether, 3,4-epoxycyclohexylmethyl-3 ′, 4′-epoxycyclohexanecarboxylate, 2 -(3,4-epoxycyclohexyl-5,5-spiro-3,4-epoxy) cyclohexane-meta-dioxane, bis (3,4-epoxycyclohexyl) Til) adipate, vinylcyclohexene oxide, 4-vinylepoxycyclohexane, bis (3,4-epoxy-6-methylcyclohexylmethyl) adipate, 3,4-epoxy-6-methylcyclohexyl-3 ', 4'-epoxy-6 '-Methylcyclohexanecarboxylate, methylenebis (3,4-epoxycyclohexane), dicyclopentadiene diepoxide, di (3,4-epoxycyclohexylmethyl) ether of ethylene glycol, ethylenebis (3,4-epoxycyclohexanecarboxylate) , Epoxyhexahydrophthalate dioctyl, epoxyhexahydrophthalate di-2-ethylhexyl, 1,4-butanediol diglycidyl ether, 1,6-hexanediol diglycidyl ether, Reserine triglycidyl ether, trimethylolpropane triglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ethers, 1,1,3-tetradecadiene dioxide, limonene dioxide, 1,2,7,8-di Examples thereof include epoxy octane, 1,2,5,6-diepoxycyclooctane and the like.

[Oxetane compounds]
The oxetane compound in the present invention refers to a compound having an oxetane ring, and arbitrarily selected from known oxetane compounds as described in JP-A Nos. 2001-220526, 2001-310937, and 2003-341217. Can be used.
As the compound having an oxetane ring that can be used in the ink composition of the present invention, a compound having 1 to 4 oxetane rings in its structure is preferable, and as described above, the viscosity and tackiness of the ink composition are particularly preferable. From the viewpoint, it is preferable to use a compound having one or two oxetane rings. By using such a compound, it becomes easy to maintain the viscosity of the ink composition in a good handling property range, and it is possible to obtain high adhesion of the cured ink to the recording medium. .

  Examples of the compound having 1 to 2 oxetane rings in the molecule include compounds represented by the following general formulas (1) to (3).

R ^a1 represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a fluoroalkyl group having 1 to 6 carbon atoms, an allyl group, an aryl group, a furyl group, or a thienyl group. When two R ^a1 are present in the molecule, they may be the same or different.
Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, and a butyl group. Preferred examples of the fluoroalkyl group include those in which any hydrogen of these alkyl groups is substituted with a fluorine atom.
R ^a2 is an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, a group having an aromatic ring, an alkylcarbonyl group having 2 to 6 carbon atoms, or an alkoxycarbonyl having 2 to 6 carbon atoms. Group represents an N-alkylcarbamoyl group having 2 to 6 carbon atoms. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, and a butyl group. Examples of the alkenyl group include a 1-propenyl group, a 2-propenyl group, a 2-methyl-1-propenyl group, and a 2-methyl-2. -Propenyl group, 1-butenyl group, 2-butenyl group, 3-butenyl group and the like, and examples of the group having an aromatic ring include phenyl group, benzyl group, fluorobenzyl group, methoxybenzyl group, phenoxyethyl group and the like. Can be mentioned. As the alkylcarbonyl group, an ethylcarbonyl group, a propylcarbonyl group, a butylcarbonyl group, etc., as an alkoxycarbonyl group, an ethoxycarbonyl group, a propoxycarbonyl group, a butoxycarbonyl group, etc., as an N-alkylcarbamoyl group, Examples thereof include an ethylcarbamoyl group, a propylcarbamoyl group, a butylcarbamoyl group, and a pentylcarbamoyl group.

R ^a3 represents a linear or branched alkylene group, a linear or branched poly (alkyleneoxy) group, a linear or branched unsaturated hydrocarbon group, an alkylene group containing a carbonyl group or a carbonyl group, a carboxyl group Represents an alkylene group containing, an alkylene group containing a carbamoyl group, or a group shown below. Examples of the alkylene group include an ethylene group, a propylene group, and a butylene group. Examples of the poly (alkyleneoxy) group include a poly (ethyleneoxy) group and a poly (propyleneoxy) group. Examples of the unsaturated hydrocarbon group include a propenylene group, a methylpropenylene group, and a butenylene group.

When R ^a3 is the above polyvalent group, R ^a4 is a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a halogen atom, a nitro group, a cyano group, a mercapto group, A lower alkyl carboxyl group, a carboxyl group, or a carbamoyl group is represented.
R ^a5 represents an oxygen atom, a sulfur atom, a methylene group, NH, SO, SO ₂ , C (CF ₃ ) ₂ , or C (CH ₃ ) ₂ .
R ^a6 represents an alkyl group having 1 to 4 carbon atoms or an aryl group. n is an integer of 0-2000. R ^a7 represents an alkyl group having 1 to 4 carbon atoms, an aryl group, or a monovalent group having the following structure. In the following formula, R ^a8 is an alkyl group having 1 to 4 carbon atoms or an aryl group, and m is an integer of 0 to 100.

  Examples of the compound having 3 to 4 oxetane rings include compounds represented by the following general formula (4).

In general formula (4), R ^a1 has the same ^meaning as in general formula (1). In addition, examples of R ^a9 that is a polyvalent linking group include branched alkylene groups having 1 to 12 carbon atoms such as groups represented by A to C below, and branched poly ( An alkyleneoxy) group or a branched polysiloxy group such as a group represented by E below. j is 3 or 4.

In the above A, R ^a10 represents a methyl group, an ethyl group, or a propyl group. Moreover, in said D, p is an integer of 1-10.

  Another embodiment of the oxetane compound that can be suitably used in the present invention includes a compound represented by the following general formula (5) having an oxetane ring in the side chain.

In the general formula (5), R ^a1 and R ^a8 have the same ^{meaning as} in the above formula. R ^a11 is an alkyl group having 1 to 4 carbon atoms such as a methyl group, an ethyl group, a propyl group, or a butyl group, or a trialkylsilyl group, and r is 1 to 4.

  Examples of the oxetane compound used in the present invention include mono-functional oxetane such as 3-ethyl-3-hydroxymethyloxetane, 3- (meth) allyloxymethyl-3-ethyloxetane, (3-ethyl-3 -Oxetanylmethoxy) methylbenzene, 4-fluoro- [1- (3-ethyl-3-oxetanylmethoxy) methyl] benzene, 4-methoxy- [1- (3-ethyl-3-oxetanylmethoxy) methyl] benzene, [ 1- (3-Ethyl-3-oxetanylmethoxy) ethyl] phenyl ether, isobutoxymethyl (3-ethyl-3-oxetanylmethyl) ether, isobornyloxyethyl (3-ethyl-3-oxetanylmethyl) ether, isobornyl (3-Ethyl-3-oxetanylmethyl) ether, 2-ethyl Hexyl (3-ethyl-3-oxetanylmethyl) ether, ethyldiethylene glycol (3-ethyl-3-oxetanylmethyl) ether, dicyclopentadiene (3-ethyl-3-oxetanylmethyl) ether, dicyclopentenyloxyethyl (3- Ethyl-3-oxetanylmethyl) ether, dicyclopentenyl (3-ethyl-3-oxetanylmethyl) ether, tetrahydrofurfuryl (3-ethyl-3-oxetanylmethyl) ether, tetrabromophenyl (3-ethyl-3-oxetanyl) Methyl) ether, 2-tetrabromophenoxyethyl (3-ethyl-3-oxetanylmethyl) ether, tribromophenyl (3-ethyl-3-oxetanylmethyl) ether, 2-tribromophenoxyethyl (3-ethyl) Ru-3-oxetanylmethyl) ether, 2-hydroxyethyl (3-ethyl-3-oxetanylmethyl) ether, 2-hydroxypropyl (3-ethyl-3-oxetanylmethyl) ether, butoxyethyl (3-ethyl-3- Oxetanylmethyl) ether, pentachlorophenyl (3-ethyl-3-oxetanylmethyl) ether, pentabromophenyl (3-ethyl-3-oxetanylmethyl) ether, bornyl (3-ethyl-3-oxetanylmethyl) ether, etc. .

  Examples of the polyfunctional oxetane include 3,7-bis (3-oxetanyl) -5-oxa-nonane and 3,3 ′-(1,3- (2-methylenyl) propanediylbis (oxymethylene)) bis. -(3-ethyloxetane), 1,4-bis [(3-ethyl-3-oxetanylmethoxy) methyl] benzene, 1,2-bis [(3-ethyl-3-oxetanylmethoxy) methyl] ethane, 1, 3-bis [(3-ethyl-3-oxetanylmethoxy) methyl] propane, ethylene glycol bis (3-ethyl-3-oxetanylmethyl) ether, dicyclopentenylbis (3-ethyl-3-oxetanylmethyl) ether, tri Ethylene glycol bis (3-ethyl-3-oxetanylmethyl) ether, tetraethylene glycol bis (3-ethyl) -3-Oxetanylmethyl) ether, tricyclodecanediyldimethylene (3-ethyl-3-oxetanylmethyl) ether, trimethylolpropane tris (3-ethyl-3-oxetanylmethyl) ether, 1,4-bis (3- Ethyl-3-oxetanylmethoxy) butane, 1,6-bis (3-ethyl-3-oxetanylmethoxy) hexane, pentaerythritol tris (3-ethyl-3-oxetanylmethyl) ether, pentaerythritol tetrakis (3-ethyl-3 -Oxetanylmethyl) ether, polyethylene glycol bis (3-ethyl-3-oxetanylmethyl) ether, dipentaerythritol hexakis (3-ethyl-3-oxetanylmethyl) ether, dipentaerythritol pentakis (3-ethyl) 3-oxetanylmethyl) ether, dipentaerythritol tetrakis (3-ethyl-3-oxetanylmethyl) ether, caprolactone-modified dipentaerythritol hexakis (3-ethyl-3-oxetanylmethyl) ether, caprolactone-modified dipentaerythritol pentakis ( 3-ethyl-3-oxetanylmethyl) ether, ditrimethylolpropanetetrakis (3-ethyl-3-oxetanylmethyl) ether, EO-modified bisphenol A bis (3-ethyl-3-oxetanylmethyl) ether, PO-modified bisphenol A bis ( 3-ethyl-3-oxetanylmethyl) ether, EO-modified hydrogenated bisphenol A bis (3-ethyl-3-oxetanylmethyl) ether, PO-modified hydrogenated bisphenol A bis (3-ethyl) And polyfunctional oxetanes such as ru-3-oxetanylmethyl) ether and EO-modified bisphenol F (3-ethyl-3-oxetanylmethyl) ether.

[Examples of vinyl ether]
Further, in the present invention, a compound having a vinyl ether group may be further contained in order to impart a degree of curing. In this case, the compound having a vinyl ether group can be present in the ink composition in the range of 1% by mass to 20% by mass from the viewpoint of adjusting the surface physical properties of the cured product and the solubility of the ink composition.
Examples of monofunctional vinyl ethers used in the present invention include, for example, methyl vinyl ether, ethyl vinyl ether, propyl vinyl ether, n-butyl vinyl ether, t-butyl vinyl ether, 2-ethylhexyl vinyl ether, n-nonyl vinyl ether, lauryl vinyl ether, cyclohexyl vinyl ether, Cyclohexylmethyl vinyl ether, 4-methylcyclohexyl methyl vinyl ether, benzyl vinyl ether, dicyclopentenyl vinyl ether, 2-dicyclopentenoxyethyl vinyl ether, methoxyethyl vinyl ether, ethoxyethyl vinyl ether, butoxyethyl vinyl ether, methoxyethoxyethyl vinyl ether, ethoxyethoxyethyl vinyl ether , Methoxy polyethylene Recall vinyl ether, tetrahydrofurfuryl vinyl ether, 2-hydroxyethyl vinyl ether, 2-hydroxypropyl vinyl ether, 4-hydroxybutyl vinyl ether, 4-hydroxymethylcyclohexyl methyl vinyl ether, diethylene glycol monovinyl ether, polyethylene glycol vinyl ether, chloroethyl vinyl ether, chlorobutyl vinyl ether, Examples include chloroethoxyethyl vinyl ether, phenylethyl vinyl ether, phenoxypolyethylene glycol vinyl ether, and the like.

  Examples of polyfunctional vinyl ethers include, for example, ethylene glycol divinyl ether, diethylene glycol divinyl ether, polyethylene glycol divinyl ether, propylene glycol divinyl ether, butylene glycol divinyl ether, hexanediol divinyl ether, bisphenol A alkylene oxide divinyl ether, bisphenol F alkylene oxide. Divinyl ethers such as divinyl ether; trimethylolethane trivinyl ether, trimethylolpropane trivinyl ether, ditrimethylolpropane tetravinyl ether, glycerin trivinyl ether, pentaerythritol tetravinyl ether, dipentaerythritol pentavinyl ether, dipentaerythritol hex Vinyl ether, ethylene oxide-added trimethylolpropane trivinyl ether, propylene oxide-added trimethylolpropane trivinyl ether, ethylene oxide-added ditrimethylolpropane tetravinyl ether, propylene oxide-added ditrimethylolpropane tetravinyl ether, ethylene oxide-added pentaerythritol tetravinyl ether, propylene oxide-added penta And polyfunctional vinyl ethers such as erythritol tetravinyl ether, ethylene oxide-added dipentaerythritol hexavinyl ether, and propylene oxide-added dipentaerythritol hexavinyl ether.

<Photo acid generator>
The ink composition of the present invention preferably contains a photoacid generator. This photoacid generator (hereinafter also referred to as “photocation polymerization initiator”) refers to a compound that generates an acid upon irradiation with actinic rays or actinic radiation to initiate cationic polymerization, and is a known compound or a mixture thereof. Can be appropriately selected and used.
As the photocationic polymerization initiator, those listed below may be used alone or in combination of two or more. The content of the cationic photopolymerization initiator in the ink composition is preferably 0.1 to 20% by mass, and more preferably 0.5 to 10% by mass. When the content of the photocationic polymerization initiator is 0.1% or less, the amount of acid generated is reduced, so that the curability may be lowered. When the content of the photocationic polymerization initiator is 20% or more, the brittleness of the cured product is reduced. And the generation of acid by the remaining initiator may cause a problem, which is not preferable.

  Examples of the photocationic polymerization initiator in the present invention include diazonium salts, phosphonium salts, sulfonium salts, iodonium salts, imide sulfonates, oxime sulfonates, diazodisulfones, disulfones, and o-nitrobenzyl sulfonates.

Further, these photocationic polymerization initiators, or compounds obtained by introducing a group or compound having an equivalent function into the main chain or side chain of the polymer, for example, US Pat. No. 3,849,137, German Patent No. 3914407. JP, 63-26653, JP 55-164824, JP 62-69263, JP 63-146038, JP 63-163452, JP 62-153853, The compounds described in JP-A-63-146029 can be used.
Furthermore, compounds capable of generating an acid by light described in US Pat. No. 3,779,778, European Patent 126,712 and the like can also be used.

  Preferred examples of the photoacid generator that can be used in the present invention include compounds represented by the following general formulas (b1), (b2), and (b3).

In general formula (b1), R ²⁰¹ , R ²⁰² and R ²⁰³ each independently represents an organic group.
X ⁻ represents a non-nucleophilic anion, preferably a sulfonate anion, a carboxylate anion, a bis (alkylsulfonyl) amide anion, a tris (alkylsulfonyl) methide anion, BF ₄ ⁻ , PF ₆ ⁻ , SbF ₆ ⁻ or the following The organic anion which has a carbon atom is preferable.

  Preferable organic anions include organic anions represented by the following formula.

Rc ¹ represents an organic group.
Examples of the organic group in Rc ¹ include those having 1 to 30 carbon atoms, and preferably an alkyl group, a cycloalkyl group, an aryl group, or a plurality of these are a single bond, —O—, —CO ₂ —, —S—. , —SO ₃ —, —SO ₂ N (Rd ¹ ) — and the like.

Rd ¹ represents a hydrogen atom or an alkyl group.
Rc ³ , Rc ⁴ and Rc ⁵ each independently represents an organic group.
Preferred examples of the organic group for Rc ³ , Rc ⁴ , and Rc ⁵ include the same organic groups as those for Rc ¹ , and most preferably a perfluoroalkyl group having 1 to 4 carbon atoms.
Rc ³ and Rc ⁴ may be bonded to form a ring.
Examples of the group formed by combining Rc ³ and Rc ⁴ include an alkylene group and an arylene group. Preferably, it is a C2-C4 perfluoroalkylene group.

As the organic groups of Rc ¹ and Rc ^{3 to} Rc ⁵ , the most preferable one is an alkyl group substituted at the 1-position with a fluorine atom or a fluoroalkyl group, or a phenyl group substituted with a fluorine atom or a fluoroalkyl group. By having a fluorine atom or a fluoroalkyl group, the acidity of the acid generated by light irradiation is increased and the sensitivity is improved.

The carbon number of the organic group as R ²⁰¹ , R ²⁰² and R ²⁰³ is generally 1 to 30, preferably 1 to 20.
Two of R ^{201 to} R ²⁰³ may be bonded to form a ring structure, and the ring may contain an oxygen atom, a sulfur atom, an ester bond, an amide bond, or a carbonyl group. Examples of the group formed by combining two of R ^{201 to} R ²⁰³ include an alkylene group (eg, butylene group, pentylene group).

Specific examples of the organic group as R ²⁰¹ , R ²⁰² and R ²⁰³ include corresponding groups in the compounds (b1-1), (b1-2) and (b1-3) described later.
In addition, the compound which has two or more structures represented by general formula (b1) may be sufficient. For example, at least one of ^R 201 ^{to R 203} of the compound represented by the general formula (b1) is at least one directly with ^R 201 ^{to R 203} of another compound represented by formula (b1), or, It may be a compound having a structure bonded through a linking group.

  Further preferred examples of the component (b1) include compounds (b1-1), (b1-2), and (b1-3) described below.

Compound (b1-1) is in which at least one aryl group ^R 201 ^{to R 203} in formula (b1), arylsulfonium compound, i.e., a compound having arylsulfonium as a cation.

In the arylsulfonium compound, all of R ^{201 to} R ²⁰³ may be an aryl group, or a part of R ^{201 to} R ²⁰³ may be an aryl group, and the rest may be an alkyl group or a cycloalkyl group.

  Examples of the arylsulfonium compound include triarylsulfonium compounds, diarylalkylsulfonium compounds, aryldialkylsulfonium compounds, diarylcycloalkylsulfonium compounds, aryldicycloalkylsulfonium compounds, and the like.

  The aryl group of the arylsulfonium compound is preferably an aryl group such as a phenyl group or a naphthyl group, or a heteroaryl group such as an indole residue or a pyrrole residue, more preferably a phenyl group or an indole residue. When the arylsulfonium compound has two or more aryl groups, the two or more aryl groups may be the same or different.

The alkyl group that the arylsulfonium compound has as necessary is preferably a linear or branched alkyl group having 1 to 15 carbon atoms, such as a methyl group, an ethyl group, a propyl group, an n-butyl group, sec. -A butyl group, a t-butyl group, etc. can be mentioned.
The cycloalkyl group that the arylsulfonium compound has as necessary is preferably a cycloalkyl group having 3 to 15 carbon atoms, and examples thereof include a cyclopropyl group, a cyclobutyl group, and a cyclohexyl group.

The aryl group, alkyl group, and cycloalkyl group of R ^{201 to} R ²⁰³ are an alkyl group (eg, having 1 to 15 carbon atoms), a cycloalkyl group (eg, having 3 to 15 carbon atoms), an aryl group (eg, having 6 to 14 carbon atoms). ), An alkoxy group (for example, having 1 to 15 carbon atoms), a halogen atom, a hydroxyl group, or a phenylthio group as a substituent. Preferred substituents are linear or branched alkyl groups having 1 to 12 carbon atoms, cycloalkyl groups having 3 to 12 carbon atoms, and linear, branched or cyclic alkoxy groups having 1 to 12 carbon atoms, and most preferred. Is an alkyl group having 1 to 4 carbon atoms and an alkoxy group having 1 to 4 carbon atoms. The substituent may be substituted with any one of three R ^{201 to} R ²⁰³ , or may be substituted with all three. When R ^{201 to} R ²⁰³ are an aryl group, the substituent is preferably substituted at the p-position of the aryl group.

Next, the compound (b1-2) will be described.
The compound (b1-2) is a compound when R ^{201 to} R ²⁰³ in the formula (b1) each independently represents an organic group that does not contain an aromatic ring. Here, the aromatic ring includes an aromatic ring containing a hetero atom.
The organic group not containing an aromatic ring as R ^{201 to} R ²⁰³ generally has 1 to 30 carbon atoms, preferably 1 to 20 carbon atoms.
R ^{201 to} R ²⁰³ are each independently preferably an alkyl group, a cycloalkyl group, an allyl group, or a vinyl group, more preferably a linear, branched, cyclic 2-oxoalkyl group, or an alkoxycarbonylmethyl group, particularly preferably Is a linear, branched 2-oxoalkyl group.

The alkyl group as R ^{201 to} R ²⁰³ may be either linear or branched, and is preferably a linear or branched alkyl group having 1 to 10 carbon atoms (for example, methyl group, ethyl group, propyl group). Group, a butyl group, a pentyl group), and a linear, branched 2-oxoalkyl group, and an alkoxycarbonylmethyl group are more preferable.

The cycloalkyl group as R ^{201 to} R ²⁰³ preferably includes a cycloalkyl group having 3 to 10 carbon atoms (cyclopentyl group, cyclohexyl group, norbornyl group), and a cyclic 2-oxoalkyl group is more preferable.

Preferred examples of the linear, branched and cyclic 2-oxoalkyl group represented by R ^{201 to} R ²⁰³ include a group having> C═O at the 2-position of the above alkyl group or cycloalkyl group.
The alkoxy group in the alkoxycarbonylmethyl group as R ^{201 to} R ²⁰³ is preferably an alkoxy group having 1 to 5 carbon atoms (methoxy group, ethoxy group, propoxy group, butoxy group, pentoxy group).
R ^{201 to} R ²⁰³ may be further substituted with a halogen atom, an alkoxy group (eg, having 1 to 5 carbon atoms), a hydroxyl group, a cyano group, or a nitro group.

  The compound (b1-3) is a compound represented by the following general formula (b1-3), and is a compound having a phenacylsulfonium salt structure.

In General Formula (b1-3), R ^{1c to} R ^5c each independently represent a hydrogen atom, an alkyl group, a cycloalkyl group, an alkoxy group, or a halogen atom.
R ^6c and R ^7c each independently represents a hydrogen atom, an alkyl group or a cycloalkyl group.
R ^x and R ^y each independently represents an alkyl group, a cycloalkyl group, an allyl group, or a vinyl group.
Any two or more of R ^{1c to} R ^5c , R ^6c and R ^7c , and R ^x and R ^y may be bonded to each other to form a ring structure.
Zc ^- represents a non-nucleophilic anion, in the general formula (b1) X ^- can be the same as the non-nucleophilic anion.

The alkyl group as R ^{1c to} R ^7c may be either linear or branched, and for example, a linear and branched alkyl group having 1 to 20 carbon atoms, preferably 1 to 12 carbon atoms (for example, Methyl group, ethyl group, linear or branched propyl group, linear or branched butyl group, linear or branched pentyl group).

Preferred examples of the cycloalkyl group represented by R ^{1c to} R ^7c include cycloalkyl groups having 3 to 8 carbon atoms (for example, a cyclopentyl group and a cyclohexyl group).

The alkoxy group as R ^{1c to} R ^{5c may} be linear, branched or cyclic, for example, an alkoxy group having 1 to 10 carbon atoms, preferably a linear or branched alkoxy group having 1 to 5 carbon atoms. (For example, methoxy group, ethoxy group, linear or branched propoxy group, linear or branched butoxy group, linear or branched pentoxy group), C3-C8 cyclic alkoxy group (for example, cyclopentyloxy group, cyclohexyloxy group) ).

Examples of the group formed by combining any two or more of R ^{1c to} R ^5c , R ^6c and R ^7c , and R ^x and R ^y include a butylene group and a pentylene group. This ring structure may contain an oxygen atom, a sulfur atom, an ester bond, or an amide bond.

Preferably, any one of R ^{1c to} R ^5c is a linear or branched alkyl group, a cycloalkyl group, or a linear, branched, or cyclic alkoxy group, and more preferably the sum of the carbon number of R ^1c to R ^5c is 2-15. Thereby, solvent solubility improves more and generation | occurrence | production of a particle is suppressed at the time of a preservation | save.

^Examples of the alkyl group and cycloalkyl group as R ^x and R ^y include the same alkyl groups and cycloalkyl groups as R ^{1c to} R ^7c .
R ^x and R ^y are preferably a 2-oxoalkyl group or an alkoxycarbonylmethyl group.
Examples of the 2-oxoalkyl group include a group having> C═O at the 2-position of the alkyl group or cycloalkyl group as R ^{1c to} R ^5c .
The alkoxy group in the alkoxycarbonylmethyl group may be the same as the alkoxy group as R ^1c to R ^5c.

R ^x and R ^y are preferably an alkyl group or cycloalkyl group having 4 or more carbon atoms, more preferably 6 or more, and still more preferably 8 or more alkyl groups or cycloalkyl groups.

In the formula ^{(b2), (b3),} R 204 ~R 207 each independently represents an aryl group, an alkyl group or a cycloalkyl group. X ⁻ represents a non-nucleophilic anion, and examples thereof include the same non-nucleophilic anion as X ^{− in} formula (b1).

The aryl group for R ^{204 to} R ²⁰⁷ is preferably a phenyl group or a naphthyl group, and more preferably a phenyl group.
The alkyl group as R ^{204 to} R ²⁰⁷ may be either linear or branched, and is preferably a linear or branched alkyl group having 1 to 10 carbon atoms (for example, methyl group, ethyl group, propyl group). Group, butyl group, pentyl group). The cycloalkyl group as R ²⁰⁴ to R ²⁰⁷ is preferably, and a cycloalkyl group having 3 to 10 carbon atoms (e.g., cyclopentyl, cyclohexyl, norbornyl).
The R ²⁰⁴ to R ²⁰⁷ are substituents which may have, for example, an alkyl group (for example, 1 to 15 carbon atoms), a cycloalkyl group (for example, 3 to 15 carbon atoms), an aryl group (e.g., 6 carbon atoms 15), alkoxy groups (for example, having 1 to 15 carbon atoms), halogen atoms, hydroxyl groups, phenylthio groups and the like.

  Examples of the photocationic polymerization initiator that may be used further include compounds represented by the following general formulas (b4), (b5), and (b6).

In general formulas (b4) to (b6), Ar ³ and Ar ⁴ each independently represents an aryl group.
R ²⁰⁶ , R ²⁰⁷ and R ²⁰⁸ each independently represents an alkyl group, a cycloalkyl group or an aryl group.
A represents an alkylene group, an alkenylene group or an arylene group.

Preferred examples of the cationic photopolymerization initiator include compounds represented by general formulas (b1) to (b3).
Particularly preferred specific examples of the cationic photopolymerization initiator that can be used in the present invention are listed below.

Further, oxazole derivatives and s-triazine derivatives described in JP-A No. 2002-122994, paragraph numbers [0029] to [0030] are also preferably used.
The onium salt compounds and sulfonate compounds exemplified in JP-A-2002-122994, paragraphs [0037] to [0063] can also be suitably used in the present invention.

[Active energy rays]
As active energy rays for proceeding the polymerization of the ink composition of the present invention, α rays, γ rays, X rays, ultraviolet rays, visible rays, electron rays and the like can be used. Of these, ultraviolet rays and visible rays are preferably used from the viewpoint of cost and safety, and ultraviolet rays are more preferably used.
As a light source for generating ultraviolet rays, low-pressure mercury lamps, high-pressure mercury lamps, short arc discharge lamps, ultraviolet light-emitting diodes, and the like, which are known ultraviolet lamps, can be used. High pressure mercury lamps, metal halide lamps, and xenon lamps belonging to short arc discharge lamps are preferably used. Moreover, an ultraviolet light emitting diode is also preferably used from the viewpoint of energy saving.

[Polymerization inhibitor]
In the present invention, it is preferable to use in combination with a polymerization inhibitor that inhibits the progress of polymerization other than cationic polymerization in order to effectively progress the polymerization by the photocationic polymerization initiator.
Suitable polymerization inhibitors include phenolic hydroxyl group-containing compounds and quinones, N-oxide compounds, piperidine 1-oxyl free radical compounds, pyrrolidine 1-oxyl free radical compounds, N-nitrosophenylhydroxylamines, and cations. It is a compound selected from the group consisting of dyes. Preferred polymerization inhibitors include haloid quinone, p-methoxyphenol, di-t-butyl-p-cresol, pyrogallol, resorcinol, catechol, t-butylcatechol, hydroquinone, benzoquinone, 4,4-thiobis (3-methyl-6- t-butylphenol), 2,2'-methylenebis (4-methyl-6-t-butylphenol), 2,2,6,6-tetramethylpiperidine and its derivatives, di-t-butylnitroxide, 2,2,6 1,6-tetramethylpiperidine-N-oxide and its derivatives, such as piperidine 1-oxyl free radical, 2,2,6,6-tetramethylpiperidine 1-oxyl free radical, 4-oxo-2,2,6,6 -Tetramethylpiperidine 1-oxyl free radical, 4-hydroxy-2,2,6,6-tetramethyl Peridine 1-oxyl free radical, 4-acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl free radical, 4-maleimido-2,2,6,6-tetramethylpiperidine 1-oxyl free radical, 4 -Phosphonoxy-2,2,6,6-tetramethylpiperidine 1-oxyl free radical, 3-carboxy-2,2,5,5-tetramethylpyrrolidine 1-oxyl free radical, N-nitrosophenylhydroxylamine cerium Salt, N-nitrosophenylhydroxylamine aluminum salt, crystal violet, methyl violet, ethyl violet and Victoria pure blue BOH. The addition amount of the polymerization inhibitor is preferably about 0.01% by mass to about 5% by mass with respect to the mass of the ink composition.

[Colorant]
A colorant can be preferably added to the ink composition of the present invention in order to form a visible image.
There is no restriction | limiting in particular in the coloring agent which can be used here, According to a use, well-known various color materials and (pigment, dye) can be selected suitably, and can be used. For example, when forming an image excellent in weather resistance, a pigment is preferable. As the dye, both water-soluble dyes and oil-soluble dyes can be used as long as they are soluble in the polymerizable compound. In the present invention, in order to form an image, the ink composition of the present invention preferably contains a pigment or an oil-soluble dye as a colorant.
These colorants are preferably added in an amount of 0.5 to 20% by mass in the ink composition, more preferably 1 to 15% by mass, and still more preferably 5 to 15% by mass.

The pigment preferably used in the present invention will be described.
[Pigment]
The pigment is not particularly limited, and all commercially available organic and inorganic pigments or pigments dispersed in an insoluble resin or the like as a dispersion medium, or the resin is grafted onto the pigment surface Can be used. Moreover, what dye | stained the resin particle with dye can be used.
Examples of these pigments include, for example, “Spirit of Pigments” edited by Seijiro Ito (2000), W. Herbst, K. Hunger, “Industrial Organic Pigments”, JP 2002-12607 A, JP 2002-188025 A. Examples thereof include pigments described in JP-A No. 2003-26978 and JP-A No. 2003-342503.

  Specific examples of organic pigments and inorganic pigments that can be used in the present invention include C.I. I. Pigment Yellow 1 (Fast Yellow G etc.), C.I. I. A monoazo pigment such as C.I. Pigment Yellow 74; I. Pigment Yellow 12 (disaji yellow AAA, etc.), C.I. I. Disazo pigments such as C.I. Pigment Yellow 17; I. Non-benzidine type azo pigments such as CI Pigment Yellow 180; I. Azo lake pigments such as C.I. Pigment Yellow 100 (eg Tartrazine Yellow Lake); I. Condensed azo pigments such as CI Pigment Yellow 95 (Condensed Azo Yellow GR, etc.); I. Acidic dye lake pigments such as C.I. Pigment Yellow 115 (such as quinoline yellow lake); I. Basic dye lake pigments such as CI Pigment Yellow 18 (Thioflavin Lake, etc.), anthraquinone pigments such as Flavantron Yellow (Y-24), isoindolinone pigments such as Isoindolinone Yellow 3RLT (Y-110), and quinophthalone yellow Quinophthalone pigments such as (Y-138), isoindoline pigments such as isoindoline yellow (Y-139), C.I. I. Nitroso pigments such as C.I. Pigment Yellow 153 (nickel nitroso yellow, etc.); I. And metal complex salt azomethine pigments such as CI Pigment Yellow 117 (copper azomethine yellow, etc.).

  C. As a thing which exhibits red or magenta color, C.I. I. Monoazo pigments such as CI Pigment Red 3 (Toluidine Red, etc.); I. Disazo pigments such as C.I. Pigment Red 38 (Pyrazolone Red B, etc.); I. Pigment Red 53: 1 (Lake Red C, etc.) and C.I. I. Azo lake pigments such as C.I. Pigment Red 57: 1 (Brilliant Carmine 6B); I. Condensed azo pigments such as C.I. Pigment Red 144 (condensed azo red BR, etc.); I. Acidic dye lake pigments such as C.I. Pigment Red 174 (Phloxine B Lake, etc.); I. Basic dye lake pigments such as C.I. Pigment Red 81 (Rhodamine 6G 'lake, etc.); I. Anthraquinone pigments such as C.I. Pigment Red 177 (eg, dianthraquinonyl red); I. Thioindigo pigments such as C.I. Pigment Red 88 (Thioindigo Bordeaux, etc.); I. Perinone pigments such as C.I. Pigment Red 194 (perinone red, etc.); I. Perylene pigments such as C.I. Pigment Red 149 (perylene scarlet, etc.); I. Pigment violet 19 (unsubstituted quinacridone), C.I. I. Quinacridone pigments such as CI Pigment Red 122 (quinacridone magenta, etc.); I. Isoindolinone pigments such as CI Pigment Red 180 (isoindolinone red 2BLT, etc.); I. And alizarin lake pigments such as CI Pigment Red 83 (Mada Lake, etc.).

  As a pigment exhibiting blue or cyan, C.I. I. Disazo pigments such as C.I. Pigment Blue 25 (Dianisidine Blue, etc.); I. Phthalocyanine pigments such as C.I. Pigment Blue 15 (phthalocyanine blue, etc.); I. Acidic dye lake pigments such as C.I. Pigment Blue 24 (Peacock Blue Lake, etc.); I. Basic dye lake pigments such as C.I. Pigment Blue 1 (Viclotia Pure Blue BO Lake, etc.); I. Anthraquinone pigments such as C.I. Pigment Blue 60 (Indantron Blue, etc.); I. And alkali blue pigments such as CI Pigment Blue 18 (Alkali Blue V-5: 1).

As a pigment exhibiting green, C.I. I. Pigment green 7 (phthalocyanine green), C.I. I. Phthalocyanine pigments such as C.I. Pigment Green 36 (phthalocyanine green); I. And azo metal complex pigments such as CI Pigment Green 8 (Nitroso Green).
As a pigment exhibiting orange, C.I. I. An isoindoline pigment such as C.I. Pigment Orange 66 (isoindoline orange); I. And anthraquinone pigments such as CI Pigment Orange 51 (dichloropyrantron orange).

Examples of the black pigment include carbon black, titanium black, and aniline black.
Specific examples of the white pigment include basic lead carbonate (2PbCO ₃ Pb (OH) ₂ , so-called silver white), zinc oxide (ZnO, so-called zinc white), titanium oxide (TiO ₂ , so-called titanium white), Strontium titanate (SrTiO ₃ , so-called titanium strontium white) or the like can be used.

  Here, titanium oxide has a smaller specific gravity than other white pigments, a large refractive index, and is chemically and physically stable, so that it has a large hiding power and coloring power as a pigment. Excellent durability against other environments. Therefore, it is preferable to use titanium oxide as the white pigment. Of course, other white pigments (may be other than the listed white pigments) may be used as necessary.

For dispersion of the pigment, for example, a dispersion device such as a ball mill, a sand mill, an attritor, a roll mill, a jet mill, a homogenizer, a paint shaker, a kneader, an agitator, a Henschel mixer, a colloid mill, an ultrasonic homogenizer, a pearl mill, or a wet jet mill is used. Can do.
It is also possible to add a dispersant when dispersing the pigment. Examples of the dispersant include a hydroxyl group-containing carboxylic acid ester, a salt of a long-chain polyaminoamide and a high molecular weight acid ester, a salt of a high molecular weight polycarboxylic acid, a high molecular weight unsaturated acid ester, a high molecular weight copolymer, a modified polyacrylate, an aliphatic polyacrylate. Carboxylic acid, naphthalenesulfonic acid formalin condensate, polyoxyethylene alkyl phosphate ester, pigment derivative and the like. It is also preferable to use a commercially available polymer dispersant such as the Solsperse series from Zeneca.
Moreover, it is also possible to use a synergist according to various pigments as a dispersion aid. These dispersants and dispersion aids are preferably added in an amount of 1 to 50 parts by mass with respect to 100 parts by mass of the pigment.

  In the ink composition, as a dispersion medium for various components such as pigments, a solvent may be added, and the cationic polymerizable compound that is a low molecular weight component without a solvent may be used as a dispersion medium. The ink composition of the invention is a radiation curable ink, and is preferably solvent-free in order to be cured after the ink is applied onto a recording medium. This is because if the solvent remains in the cured ink image, the solvent resistance is deteriorated or a problem of VOC (Volatile Organic Compound) of the remaining solvent occurs. From such a viewpoint, it is preferable to use a cationically polymerizable compound as the dispersion medium, and in particular, to select a cationically polymerizable monomer having the lowest viscosity from the viewpoint of improving dispersibility and handling properties of the ink composition.

  The average particle diameter of the pigment particles is preferably 0.08 to 0.5 μm, and the selection of the pigment, the dispersant, the dispersion medium, the dispersion conditions, and the filtration so that the maximum particle diameter is 10 μm or less, preferably 3 μm or less. Set conditions. By controlling the particle size, clogging of the head nozzle can be suppressed, and ink storage stability, ink transparency, and curing sensitivity can be maintained.

[dye]
Next, the dyes preferably used as the colorant in the present invention will be described.
The dye can be appropriately selected from conventionally known compounds (dyes). Specific examples include dyes described in paragraphs [0023] to [0089] of JP-A No. 2002-114930.

  Examples of yellow dyes include, for example, phenols, naphthols, anilines, pyrazolones, pyridones, aryl or heteryl azo dyes having open-chain active methylene compounds as coupling components, for example, open-chain active methylene compounds as coupling components Azomethine dyes having, for example, methine dyes such as benzylidene dyes and monomethine oxonol dyes, for example, quinone dyes such as naphthoquinone dyes and anthraquinone dyes, and other dyes include quinophthalone dyes, nitro, Nitroso dyes, acridine dyes, acridinone dyes and the like can be mentioned.

  Examples of the magenta dye include phenols, naphthols, anilines, pyrazolones, pyridones, pyrazolotriazoles, and ring-closing active methylene compounds (for example, dimedone, barbituric acid, 4-hydroxycoumarin) as coupling components. Derivatives), electron-rich heterocycles (eg, pyrrole, imidazole, thiophene, thiazole derivatives), or aryl or heteryl azo dyes, eg, azomethine dyes having pyrazolones, pyrazolotriazoles as coupling components, eg, arylidene dyes, styryl Dyes, merocyanine dyes, methine dyes such as oxonol dyes, carbonium dyes such as diphenylmethane dyes, triphenylmethane dyes, xanthene dyes, such as naphthoquinone, anthraquinone, anthrone Quinone dyes such Rapiridon, it can be mentioned condensed polycyclic dyes such as, for example, dioxazine dye.

  Examples of cyan dyes include azomethine dyes such as indoaniline dyes and indophenol dyes, cyanine dyes, oxonol dyes, polymethine dyes such as merocyanine dyes, diphenylmethane dyes, triphenylmethane dyes, carbonium dyes such as xanthene dyes, Examples of phthalocyanine dyes and anthraquinone dyes include phenols, naphthols, anilines, pyrrolopyrimidin-one, aryl or heteryl azo dyes having pyrrolotriazin-one derivatives, and indigo / thioindigo dyes as coupling components.

  Each of the dyes may exhibit yellow, magenta, and cyan colors only after a part of the chromophore is dissociated. In this case, the counter cation is an inorganic cation such as an alkali metal or ammonium. Alternatively, it may be an organic cation such as pyridinium, quaternary ammonium salt, or a cationic polymer having a partial structure thereof.

  The dye used in the present invention is preferably oil-soluble. Specifically, it means that the solubility in water at 25 ° C. (the mass of the dye dissolved in 100 g of water) is 1 g or less, preferably 0.5 g or less, more preferably 0.1 g or less. Therefore, a so-called water-insoluble oil-soluble dye is preferably used.

The dye used in the present invention preferably has an oil-solubilizing group introduced into the above-described dye mother core in order to dissolve the necessary amount in the ink composition.
As the oil-solubilizing group, long chain, branched alkyl group, long chain, branched alkoxy group, long chain, branched alkylthio group, long chain, branched alkylsulfonyl group, long chain, branched acyloxy group, long chain, branched alkoxycarbonyl group, Long chain, branched acyl group, long chain, branched acylamino group long chain, branched alkylsulfonylamino group, long chain, branched alkylaminosulfonyl group and these long chains, aryl groups containing branched substituents, aryloxy groups, aryloxycarbonyl Group, arylcarbonyloxy group, arylaminocarbonyl group, arylaminosulfonyl group, arylsulfonylamino group and the like.
In addition, for water-soluble dyes having carboxylic acid and sulfonic acid, long chain, branched alcohol, amine, phenol, aniline derivatives are used as oil-solubilizing alkoxycarbonyl groups, aryloxycarbonyl groups, alkylaminosulfonyl groups, A dye may be obtained by conversion to an arylaminosulfonyl group.

  The oil-soluble dye preferably has a melting point of 200 ° C. or lower, more preferably has a melting point of 150 ° C. or lower, and still more preferably has a melting point of 100 ° C. or lower. By using an oil-soluble dye having a low melting point, the precipitation of dye crystals in the ink composition is suppressed, and the storage stability of the ink composition is improved.

  Further, it is desirable that the oxidation potential is high in order to improve fading, particularly resistance to oxidizing substances such as ozone and curing characteristics. For this reason, as the oil-soluble dye used in the present invention, those having an oxidation potential of at least 1.0 V (vs SCE) are preferably used. The oxidation potential is preferably higher, the oxidation potential is more preferably 1.1 V (vs SCE) to 2.0 V, and particularly preferably 1.15 V (vs SCE) to 2.0 V.

As the yellow dye, a compound having a structure represented by the general formula (Y-I) described in JP-A No. 2004-250483 is preferable.
Particularly preferred dyes are dyes represented by general formulas (Y-II) to (Y-IV) described in paragraph [0034] of JP-A No. 2004-250483. And the compounds described in paragraph numbers [0060] to [0071] of JP-A-250483. The oil-soluble dye of the general formula (Y-I) described in the publication may be used not only for yellow but also for any color ink such as black ink and red ink.

The magenta dye is preferably a compound having a structure represented by the general formulas (3) and (4) described in JP-A No. 2002-114930. Specific examples include paragraphs of JP-A No. 2002-114930. Examples include the compounds described in [0054] to [0073].
Particularly preferred dyes are azo dyes represented by the general formulas (M-1) to (M-2) described in paragraph numbers [0084] to [0122] of JP-A No. 2002-121414, and specific examples Examples thereof include compounds described in paragraph numbers [0123] to [0132] of JP-A No. 2002-121414. The oil-soluble dyes represented by the general formulas (3), (4) and (M-1) to (M-2) described in the publication are used not only for magenta but also for any color ink such as black ink and red ink. May be.

  Examples of the cyan dye include dyes represented by formulas (I) to (IV) described in JP-A No. 2001-181547, and paragraphs [0063] to [0078] of JP-A No. 2002-121414. The dyes represented by the general formulas (IV-1) to (IV-4) described above are preferred, and specific examples include paragraph numbers [0052] to [0066] of JP-A No. 2001-181547. Examples thereof include the compounds described in paragraph Nos. [0079] to [0081] of Kai 2002-121414.

  Particularly preferred dyes are phthalocyanine dyes represented by general formulas (CI) and (C-II) described in paragraphs [0133] to [0196] of JP-A No. 2002-121414, A phthalocyanine dye represented by formula (C-II) is preferred. Specific examples thereof include the compounds described in JP-A No. 2002-121414, paragraph numbers [0198] to [0201]. The oil-soluble dyes of the formulas (I) to (IV), (IV-1) to (IV-4), (CI) and (C-II) are not only cyan but also black ink or green ink. It may be used for inks of any color.

(Oxidation potential)
The oxidation potential value (Eox) of the dye in the present invention can be easily measured by those skilled in the art. Regarding this method, for example, “New Instrumental Methods in Electrochemistry” by P. Delahay (1954, published by Interscience Publishers), AJBard et al. “Electrochemical Methods” (1980, published by John Wiley & Sons), Akira Fujishima et al. It is described in the book "Electrochemical measurement method" (1984, published by Gihodo Publishing Co., Ltd.).

Specifically, the oxidation potential is measured by placing a test sample in a solvent such as dimethylformamide or acetonitrile containing a supporting electrolyte such as sodium perchlorate or tetrapropylammonium perchlorate in the range of 1 × 10 ⁻² to 1 × 10 ⁻⁶ mol / It is measured as a value relative to SCE (saturated calomel electrode) using various voltammetry (polarography using a dropping mercury electrode, cyclic voltammetry, a method using a rotating disk electrode, etc.). Although this value may be deviated by several tens of mil volts due to the influence of the liquid potential difference or the liquid resistance of the sample solution, the reproducibility of the potential can be guaranteed by inserting a standard sample (for example, hydroquinone).

  In the present invention, SCE (saturated calomel) is used as a reference electrode in N, N-dimethylformamide (concentration of dye is 0.001 mol / liter) containing 0.1 mol / liter of tetrapropylammonium perchlorate as a supporting electrolyte. Electrode), a value measured using a graphite electrode as a working electrode and a platinum electrode as a counter electrode (vsSCE) was defined as the oxidation potential of the dye.

The value of Eox represents the ease of electron transfer from the sample to the electrode, and the greater the value (the higher the oxidation potential), the more difficult the electron transfer from the sample to the electrode, in other words, the less easily oxidized. In relation to the structure of the compound, the oxidation potential becomes more noble by introducing an electron withdrawing group, and the oxidation potential becomes lower by introducing an electron donating group. In the present invention, in order to lower the reactivity with ozone as an electrophile, it is desirable to introduce an electron withdrawing group into the dye skeleton to make the oxidation potential more noble.
Specific examples of preferable dyes used in the present invention are shown below, but the dyes used in the present invention are not limited to the following specific examples.

[Other ingredients]
Hereinafter, various additives that can be contained in the ink composition of the present invention as needed are described.
[Ultraviolet absorber]
From the viewpoint of improving the weather resistance of the resulting image and preventing discoloration, an ultraviolet absorber can be used.
Examples of the ultraviolet absorber are described in JP-A-58-185679, JP-A-61-190537, JP-A-2-782, JP-A-5-97075, JP-A-9-34057, and the like. Benzotriazole compounds, benzophenone compounds described in JP-A No. 46-2784, JP-A No. 5-194433, US Pat. No. 3,214,463, etc., JP-B Nos. 48-30492 and 56-21141 Cinnamic acid compounds described in JP-A-10-88106, JP-A-4-298503, JP-A-8-53427, JP-A-8-239368, JP-A-10-182621, JP The triazine compounds described in JP-A-8-501291, Research Disclosure No. Examples thereof include compounds described in No. 24239, compounds that emit ultraviolet light by absorbing ultraviolet rays typified by stilbene and benzoxazole compounds, so-called fluorescent brighteners, and the like.
The amount added is appropriately selected according to the purpose, but is generally about 0.01 to 10% by mass of the ink composition.

〔Antioxidant〕
An antioxidant can be added to improve the stability of the ink composition. Examples of the antioxidant include European Published Patent No. 223739, No. 309401, No. 309402, No. 310551, No. 310552, No. 4594416, German Published Patent No. 3435443. JP, 54-85535, 62-262417, 63-113536, 63-163351, JP-A-2-262654, JP-A-2-71262, Examples thereof include those described in Kaihei 3-121449, JP-A-5-61166, JP-A-5-119449, US Pat. No. 4,814,262, US Pat. No. 4,980,275, and the like.
The addition amount is appropriately selected according to the purpose, but is generally about 0.001 to 1% by mass of the ink composition.

[Anti-fading agent]
In the ink composition of the present invention, various organic and metal complex anti-fading agents can be used. Examples of the organic anti-fading agent include hydroquinones, alkoxyphenols, dialkoxyphenols, phenols, anilines, amines, indanes, chromans, alkoxyanilines, and heterocycles. Examples of the metal complex anti-fading agent include nickel complexes and zinc complexes. No. 17643, No. VII, I to J, ibid. 15162, ibid. No. 18716, page 650, left column, ibid. No. 36544, page 527, ibid. No. 307105, page 872, ibid. The compounds described in the patent cited in No. 15162 and the compounds included in the general formulas and compound examples of representative compounds described in JP-A-62-215272, pages 127 to 137 can be used. .
The addition amount is appropriately selected depending on the purpose, but is generally about 0.001 to 5% by mass of the ink composition.

[Conductive salts]
Conductive salts such as potassium thiocyanate, lithium nitrate, ammonium thiocyanate, and dimethylamine hydrochloride can be added to the ink composition of the present invention for the purpose of controlling ejection properties.
The addition amount is appropriately selected according to the purpose, but is generally about 0.001 to 1.0% by mass of the ink composition.

〔solvent〕
In order to improve the adhesion to the recording medium, it is also effective to add a very small amount of an organic solvent to the ink composition of the present invention.
Examples of the solvent include ketone solvents such as acetone, methyl ethyl ketone, and diethyl ketone, alcohol solvents such as methanol, ethanol, 2-propanol, 1-propanol, 1-butanol, and tert-butanol, and chlorine such as chloroform and methylene chloride. Solvents, aromatic solvents such as benzene and toluene, ester solvents such as ethyl acetate, butyl acetate and isopropyl acetate, ether solvents such as diethyl ether, tetrahydrofuran and dioxane, glycols such as ethylene glycol monomethyl ether and ethylene glycol dimethyl ether And ether solvents.
In this case, it is effective to add the solvent within a range that does not cause the problem of solvent resistance and VOC. % Range.

[Polymer compound]
Various polymer compounds can be added to the ink composition in order to adjust film properties. Examples of the polymer compound include styrene polymers, acrylic polymers, cyclic ether polymers, polyvinyl butyral resins, polyurethane resins, polyamide resins, polyester resins, epoxy resins, phenol resins, polycarbonate resins, polyvinyl butyral resins, and polyvinyl formal resins. Shellac, vinyl resin, acrylic resin, rubber resin, wax, and other natural resins can be used. Two or more of these may be used in combination. Of these, copolymerization of styrene monomers, acrylic monomers, and cyclic ethers is preferred. Furthermore, as a copolymer composition of the polymer binder, a copolymer containing “cyclic ether group-containing monomer” and “vinyl ether group-containing monomer” as a structural unit is also preferably used.
The addition amount is appropriately selected according to the purpose, but is generally about 0.01 to 10.0% by mass of the ink composition.

[Surfactant]
Examples of the surfactant include those described in JP-A Nos. 62-173463 and 62-183457. For example, anionic surfactants such as dialkyl sulfosuccinates, alkyl naphthalene sulfonates, fatty acid salts, polyoxyethylene alkyl ethers, polyoxyethylene alkyl allyl ethers, acetylene glycols, polyoxyethylene / polyoxypropylene blocks Nonionic surfactants such as copolymers, and cationic surfactants such as alkylamine salts and quaternary ammonium salts. An organic fluoro compound may be used in place of the surfactant. The organic fluoro compound is preferably hydrophobic. Examples of the organic fluoro compounds include fluorine surfactants, oily fluorine compounds (eg, fluorine oil) and solid fluorine compound resins (eg, tetrafluoroethylene resin). No. (columns 8 to 17) and those described in JP-A Nos. 62-135826.
The addition amount is appropriately selected according to the purpose, but is generally about 0.001 to 5.0% by mass of the ink composition.

In addition to this, if necessary, for example, leveling additives, matting agents, waxes for adjusting film physical properties, polymerization to inhibit the adhesion to recording media such as polyolefin and PET, and the like, The tackifier which does not do can be contained.
As the tackifier, specifically, a high molecular weight adhesive polymer described in JP-A-2001-49200, 5-6p (for example, (meth) acrylic acid and an alkyl group having 1 to 20 carbon atoms). An ester with an alcohol having, an ester of (meth) acrylic acid with an alicyclic alcohol having 3 to 14 carbon atoms, a copolymer comprising an ester of (meth) acrylic acid with an aromatic alcohol having 6 to 14 carbon atoms) And a low molecular weight tackifying resin having a polymerizable unsaturated bond.

  The ink composition of the present invention preferably has an ink viscosity of 50 mPa · s or less, more preferably 30 mPa · s or less at the temperature at the time of ejection in consideration of ejection properties. It is preferable to adjust and determine the composition ratio. The ink viscosity at 25 ° C. is 10 to 300 mPa · s, preferably 10 to 100 mPa · s. By setting the viscosity at room temperature high, even when a porous recording medium is used, ink penetration into the recording medium can be prevented, uncured monomer can be reduced, and odor can be reduced. Dot bleeding at the time of landing can be suppressed, and as a result, the image quality is improved. If the ink viscosity at 25 ° C. is less than 10 mPa · s, the effect of preventing bleeding is small. Conversely, if the ink viscosity is more than 500 mPa · s, problems may occur in the delivery of the ink liquid.

  The surface tension of the ink composition of the present invention is preferably 20 to 30 mN / m, more preferably 23 to 28 mN / m. When recording on various recording media such as polyolefin, PET, coated paper, and non-coated paper, 20 mN / m or more is preferable from the viewpoint of bleeding and penetration, and 30 mN / m or less is preferable in terms of wettability.

The ink composition of the present invention can be suitably used as an ink for inkjet recording. There are no particular restrictions on the ink jet recording method, for example, a charge control method that ejects ink using electrostatic attraction, a drop-on-demand method (pressure pulse method) that uses the vibration pressure of a piezo element, and an electrical signal that is acoustic Either an acoustic ink jet system that irradiates ink by irradiating it with ink instead of using a beam, or a thermal ink jet system that uses ink to form bubbles by heating the ink and use the generated pressure. Also good. The inkjet recording method includes a method of ejecting a large number of low-density inks called photo inks in a small volume, a method of improving image quality using a plurality of inks having substantially the same hue and different concentrations, and colorless and transparent. A method using ink.
Among these, the ink is suitable as a drop-on-demand type (pressure pulse type) ink jet recording ink using a piezo element.

<Image forming method and recorded matter thereof>
The image forming method of the present invention includes an image recording step of recording an image on a recording material using the ink composition of the present invention described above, and curing by irradiating the recorded image with active energy rays (active rays). And an image curing step to be provided. In the present invention, a polymerizable compound that contributes to imaging by using an active energy ray in an image curing step and recording an image on a recording material in an image recording step and then irradiating the recorded image with the active energy ray. As the polymerization and curing proceed, the image is cured well and an image having high fastness can be formed.
In the recorded matter obtained with this ink, the image portion is cured by irradiation with radiation such as ultraviolet rays, and the strength of the image portion is excellent. For example, it can be used as an ink receiving layer (image portion) of a lithographic printing plate. it can.

  In the image recording step, it is preferable to apply an ink jet recording method using an ink jet printer. Specifically, an aspect in which the image is inkjet-recorded by discharging an ink composition in the image recording step is preferable. In the ink jet recording method, image recording is performed on a recording material using the ink composition of the present invention, but there are no particular restrictions on the ink discharge nozzles (for example, for an ink jet printer) used at that time, and the purpose and application It can be appropriately selected according to the like. There is no restriction | limiting in particular in an inkjet recording system, and it is as above-mentioned specifically.

  In the image curing step, an exposure process for accelerating polymerization and curing can be performed using a light source that emits active energy rays in a wavelength region corresponding to the sensitive wavelength of the ink composition. Specifically, a light source that emits active rays belonging to a wavelength region of 240 to 450 nm, for example, LD, LED, fluorescent lamp, low-pressure mercury lamp, high-pressure mercury lamp, metal halide lamp, carbon arc lamp, xenon lamp, chemical lamp, etc. It can be suitably performed. Preferred light sources include LEDs, high pressure mercury lamps, and metal halide lamps. What is necessary is just to select an exposure time and light quantity suitably according to the grade of the polymerization hardening of the polymeric compound which concerns on this invention.

[Inkjet recording method and inkjet recording apparatus]
Next, an ink jet recording method and an ink jet recording apparatus that can be suitably employed in the present invention will be described below.

  In the ink jet recording method of the present invention, recording is performed using the ink for ink jet recording, but there are no particular limitations on the ink nozzles and the like used at that time, and they can be appropriately selected according to the purpose. The ink jet recording method described in paragraph No. (0247) of JP-A No. 2001-279141 can be used. Particularly preferred are the charge control method, pressure pulse method, and acoustic ink jet method.

  In the inkjet recording method, the ink composition is heated to 40 to 80 ° C., and the viscosity of the ink composition is lowered to 50 mPa · s or less, preferably 30 mPa · s or less, and then ejected. By using this, high injection stability can be realized. In general, radiation curable ink compositions generally have a higher viscosity than aqueous inks, so that the viscosity fluctuation range due to temperature fluctuations during printing is large. This viscosity variation of the ink composition directly affects the droplet size and droplet ejection speed as it is, which causes image quality deterioration. Therefore, it is necessary to keep the ink composition temperature as constant as possible during printing. is there. The control range of the ink composition temperature is preferably set temperature ± 5 ° C., more preferably set temperature ± 2 ° C., and further preferably set temperature ± 1 ° C.

  The ink jet recording apparatus preferably includes a means for stabilizing the temperature of the ink composition, and the part to be kept at a constant temperature is all of the piping system and members from the ink tank (intermediate tank if there is an intermediate tank) to the nozzle ejection surface. Is the target.

  The temperature control method is not particularly limited, but for example, it is preferable to provide a plurality of temperature sensors in each piping portion and perform heating control according to the ink composition flow rate and the environmental temperature. Moreover, it is preferable that the head unit to be heated is thermally shielded or insulated so that the apparatus main body is not affected by the temperature from the outside air. In order to shorten the printer start-up time required for heating or to reduce the loss of thermal energy, it is preferable to insulate from other parts and reduce the heat capacity of the entire heating unit.

  Next, preferable irradiation conditions for radiation will be described. A basic irradiation method is disclosed in JP-A-60-132767. Specifically, a light source is provided on both sides of the head unit, and the head and the light source are scanned by a shuttle method. Irradiation is performed after a certain period of time after ink landing. Further, the curing is completed by another light source that is not driven. In WO99 / 54415, as an irradiation method, a method using an optical fiber or a method in which a collimated light source is applied to a mirror surface provided on the side surface of the head unit to irradiate the recording unit with UV light is disclosed. In the present invention, these irradiation methods can be used.

  In the present invention, the ink composition is heated to a constant temperature, and the time from landing to irradiation is desirably 0.01 to 0.5 seconds, preferably 0.01 to 0.3 seconds, and more preferably Preferably, radiation is applied after 0.01 to 0.15 seconds. Thus, by controlling the time from landing to irradiation to an extremely short time, it is possible to prevent the landing ink from bleeding before being cured. In addition, since the ink composition can be exposed to a porous recording medium before reaching the deep part where the light source does not reach, residual unreacted monomer can be suppressed, and as a result, odor can be reduced. Can do. By using the inkjet recording method described above and the ink composition of the present invention in combination, a great synergistic effect is brought about. In particular, when an ink composition having an ink viscosity of 10 to 300 mPa · s at 25 ° C. is used, a great effect can be obtained. By adopting such a recording method, the dot diameter of the landed ink can be kept constant even on various recording media having different surface wettability, and the image quality is improved. In addition, in order to obtain a color image, it is preferable to superimpose in order from the color with the lowest brightness. When inks with low lightness are stacked, it is difficult for the irradiation rays to reach the lower ink, and inhibition of curing sensitivity, increase of residual monomers, generation of odor, and deterioration of adhesion tend to occur. Irradiation can be performed by injecting all colors and exposing them together, but exposure for each color is preferable from the viewpoint of curing acceleration.

  There is no restriction | limiting in particular as an inkjet recording device used for this invention, A commercially available inkjet recording device can be used. That is, in the present invention, recording can be performed on a recording material using a commercially available inkjet recording apparatus.

[Recording material]
As the recording material, either an ink-permeable recording material or an ink-impermeable recording material can be used.

  Examples of the ink-permeable recording material include plain paper, inkjet exclusive paper, coated paper, electrophotographic co-paper, cloth, non-woven fabric, porous film, and polymer absorber. These are described as “recording materials” in Japanese Patent Application Laid-Open No. 2001-181549.

  From the viewpoint of effectively expressing the effects of the present invention, it is preferable to use a non-ink-permeable (non-absorbing) recording material. Examples of the ink-impermeable recording material include art paper, synthetic resin, rubber, resin-coated paper, glass, metal, earthenware, and wood. In addition, in terms of adding each function, a base material obtained by combining a plurality of these materials can also be used.

As the synthetic resin, any synthetic resin can be used. For example, polyester resins such as polyethylene terephthalate and polybutadiene terephthalate; polyolefin resins such as polyvinyl chloride, polystyrene, polyethylene, polyurethane, and polypropylene; and acrylic resins, Examples include polycarbonate, acrylonitrile-butadiene-styrene copolymer, diacetate, triacetate, polyimide, cellophane, and celluloid.
There is no restriction | limiting in particular about the shape of the base material using a synthetic resin, and its thickness, Any of a film form, a card | curd shape, or a block shape may be sufficient, and it can select suitably according to the desired objective. The synthetic resin may be either transparent or opaque.

  As the usage form of the synthetic resin, it is one of the preferred forms used in the form of a film used for so-called soft packaging, and various non-absorbable plastics and films thereof can be used. Examples of various plastics films include PET films, OPS films, OPP films, ONy films, PVC films, PE films, and TAC films.

  Examples of the resin-coated paper include a paper support in which one side or both sides of the paper is coated with a polyolefin resin and the like, and a paper support in which both sides of the paper are laminated with a polyolefin resin is particularly preferable.

  As described above, the recorded matter of the present invention can be obtained by image recording using the ink composition of the present invention (the image forming method of the present invention). The recorded matter of the present invention has a high-quality image excellent in color development and sharpness because the ink used for image formation contains fine pigment particles uniformly and stably dispersed, and the weather resistance of the image Because of its excellent properties, it can be applied to a wide range of fields.

  EXAMPLES Hereinafter, although this invention is demonstrated concretely based on an Example, this invention is not limited to these Examples. In the examples, “%” is based on weight unless otherwise specified.

[Examples 1-9, Comparative Examples 1-6]
Exemplified compounds P-4, P-10, and P-16 described below, a polymerizable compound, a polymerization initiator, and a colorant were mixed with stirring in parts by mass shown in Table 1 to obtain a dye ink or a pigment ink. The pigment ink was prepared by putting a pigment (PR122), a polymerizable compound, and a dispersant “SORPERSE 24000GR” (Avecia) into a disperser motor mill M50 (Eiger) and zirconia beads having a diameter of 0.65 mm. And a dispersion liquid that was dispersed for 6 hours at a peripheral speed of 9 m / s was used.
In addition, the numerical value in a following formula means mol%. Moreover, the weight average molecular weight of P-10 was 8000, and the weight average molecular weight of P-16 was 12000.

[Evaluation of ink composition]
(1. Viscosity)
The viscosity of each inkjet ink at 40 ° C. was measured using an E-type viscometer (manufactured by Toki Sangyo).
A: Less than 30 mPas B: 30 mPas or more, less than 100 mPas C: 100 mPas or more (a level causing a discharge problem)

(2. Discharge stability)
After the ink was continuously printed for 60 minutes by an ink jet printer, A was evaluated for ejection without any problem, B was evaluated for some satellites, and C was evaluated for missing nozzles.
The obtained ink composition was printed on art paper with an inkjet printer (printing density 300 dpi, droplet ejection frequency 4 kHz, nozzle number 64), and then an energy of 15 mJ / cm ^{2 with} a Deep UV lamp (US-7, SP-7). A print sample was obtained by exposure under the following conditions.
Samples 10 minutes after printing were evaluated for the following evaluation items 3 to 5.

(3. Curability)
The printed surface was evaluated by a tack-free test. When the cured film was touched with a finger, the case where there was no stickiness was evaluated as A, the case where there was slightly stickiness was evaluated as B, and the case where it was extremely sticky was evaluated as C.
In the evaluation of A, even when a print sample prepared in the same manner except that the exposure energy by the Deep UV lamp was 7.5 mJ / cm ² was evaluated, the case where there was no stickiness was evaluated as S.

(4. Adhesiveness)
After cutting the cut surface in a grid pattern with a cutter, an adhesive tape was attached to the surface of the cured film, and then the remaining state of the cured film on the substrate when the adhesive tape was peeled was visually observed. The case where peeling was not observed was evaluated as A, the case where partial peeling was observed was evaluated as B, the case where remarkable peeling was observed was evaluated as C, and the case where curing was insufficient and could not be evaluated was evaluated as D.

(5. Light resistance evaluation)
The photo paper on which the image is formed is irradiated with xenon light (100,000 lx) for 3 days using a weather meter (Atlas C.165), and the image density before and after the xenon irradiation is measured using a reflection densitometer (X-Rite 310TR). It was measured and evaluated as a dye residual ratio. The reflection density was fixed at 1.0 and measured. The evaluation was made in three stages, with A being a dye residual ratio of 80% or more, B being less than 80%, and C being less than 70%.

(6. Transparency)
The obtained ink composition was printed on a PET (polyethylene terephthalate) film with an inkjet printer (printing density 300 dpi, droplet ejection frequency 4 kHz, nozzle number 64), and then a deep UV lamp (USHIO, SP-7) was used to print 15 mJ / exposure under conditions such that the energy of cm ^2, and obtain a printed sample.
The haze of the obtained print sample was measured with a haze meter (manufactured by Suga Test Instruments). A case where the haze was less than 20% was evaluated as A, a case where the haze was 20 to 60% was evaluated as B, and a case where the haze was 60% or more was evaluated as C.
Each evaluation result is shown in Table 1.

Details of the compounds other than the exemplified compounds in the table are as follows.
* 1: 3,7-bis (3-oxetanyl) -5-oxa-nonane (OXT-221, manufactured by Toagosei Co., Ltd.)
* 2: 3,4-epoxycyclohexylmethyl-3 ′, 4′-epoxycyclohexanecarboxylate (Celoxide 2021A, manufactured by Daicel UCB)
* 3: 1,4-bis [[(3-ethyloxetane-3-yl) methoxy] methyl] benzene (OXT-121, manufactured by Toagosei Co., Ltd.)
* 4: CN2300 (acryloyl group-containing hyperbranched polyester, Sartomer)
* 5: HDDA (1,6-hexanediol diacrylate, manufactured by Daicel UCB)
* 6: DEGDA (diethylene glycol diacrylate)
* 7: Photocationic polymerization initiator, triphenylsulfonium salt (UVI-6992, manufactured by Dow Chemical Company)
* 8: Photoradical polymerization initiator, acylphosphine oxide (TOP-L, manufactured by BASF Japan)
* 9: Compound M-1 oxidation potential 1.39V (measured with ALS Model 610A manufactured by CH Instruments)
* 10: Compound Y-1 oxidation potential 1.15V (measured with ALS Model 610A manufactured by CH Instruments)
* 11: PR-122 (quinacridone pigment)

As shown in Table 1, when the ink composition of this example containing a dendritic polymer having a cationic polymerizable group was used, ink viscosity, ejection stability, curability, adhesion, and With respect to light resistance, a favorable evaluation can be obtained, ink stability is excellent, a good image can be formed, and the ink has excellent curability and adhesion to a recording medium when a dye is used as a colorant. It was possible to provide a recording ink, an ink jet recording method, and a recorded matter.
Further, such an ink composition is less clogged, and furthermore, the ink has good transparency even when it is printed on a transparent support after curing.
On the other hand, the ink composition of the comparative example could not satisfy both curability and ink viscosity. Moreover, in the hyperbranched polymer having a radical polymerizable group, the curability is improved, but the transparency and adhesion of the printed image are insufficient.

Claims (11)

  An ink composition comprising a dendritic polymer having a cationically polymerizable group.   The ink composition according to claim 1, wherein the dendritic polymer is a hyperbranched polymer or a dendrimer.   The ink composition according to claim 1, wherein the cationically polymerizable group is a vinyl ether group, an oxirane group, or an oxetane group.   The ink composition according to claim 1, wherein the ink composition further contains a photoacid generator.   The ink composition according to any one of claims 1 to 4, wherein the ink composition further contains a cationically polymerizable compound having at least one of an oxirane group or an oxetane group.   The ink composition according to any one of claims 1 to 5, wherein the ink composition further contains a colorant.   The ink composition according to claim 6, wherein the colorant is a pigment or an oil-soluble dye.   It is an ink composition for inkjet recording, The ink composition of any one of Claims 1-7. An image recording step of recording an image on a recording material using the ink composition according to claim 1;
An image curing step of irradiating and curing an active energy ray on the image recorded on the recording material in the image recording step;
An image forming method comprising:   The image forming method according to claim 9, wherein the image recording step records the image by inkjet recording in which the ink composition is discharged. A recorded matter recorded using the ink composition according to any one of claims 1 to 8.