JP2007045058A - Active energy curable type inkjet recorder - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an active energy curable type inkjet recorder which forms a high-quality image by suppressing a visible unnecessary surface structure. <P>SOLUTION: The active energy curable type inkjet recorder comprises: an image recording section having an inkjet head for forming an image by discharging ink on a recording medium; a carrying means for carrying the recording medium to a down stream of the inkjet head; and a resin layer forming means for forming a film consisting of resin particles on the recording medium wherein an image is drawn by the inkjet head, and ink is cured by an active energy irradiation means. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

  The present invention relates to an active energy curable ink jet recording apparatus that forms an image on a recording medium by ink jet using ink that is cured by the active energy of an electron beam or ultraviolet light.

An active energy curable ink jet recording apparatus that discharges ink that is cured by active energy such as electron beam or ultraviolet ray onto a recording medium using an ink jet head and cures the ink by energy irradiation to form an image is environmentally friendly. It has features such as high-definition images that can be recorded on various recording media at high speed and that are difficult to bleed. In particular, an apparatus using ultraviolet curable ink has been developed from the viewpoint of easy handling of a light source, compactness, and the like. On the other hand, the ink ejected onto the recording medium is cured in a raised state on the recording medium, and there is a problem in that an unnecessary structure is visually recognized and image quality is deteriorated. In order to solve this problem, an image is formed on a recording medium with a curable ink, cured or thickened by irradiation, and then pressed with a material that is smooth and has a higher surface energy than the recording medium. Discloses an apparatus for smoothing the surface.
JP 2003-276178 A

  The present invention has been made in view of the above-mentioned problems. As an object thereof, an active energy curable ink jet recording apparatus that forms an image on a recording medium by ink jetting an ink that is cured by active energy irradiation is unnecessary. An object of the present invention is to provide an active energy curable ink jet recording apparatus capable of forming a high quality image while suppressing the surface structure.

The above-mentioned subject concerning the present invention is attained by the following composition.
(1) An active energy curable ink jet recording apparatus for forming an image of ink curable by active energy on a recording medium by ink jetting,
An image recording unit that cures an image formed by ejecting the ink onto the recording medium by an inkjet head by energy irradiation of an active energy irradiation unit;
Conveying means for conveying the recording medium downstream of the inkjet head;
An active energy curable ink jet recording apparatus comprising resin layer forming means for forming a resin layer on an image surface on a recording medium formed and cured by the image recording unit.
(2) The resin layer forming means is disposed at a position facing the rotary electrodeposited body on which the charged resin particles are electrodeposited and the rotary electrodeposited body through the recording medium, and cooperates with the rotary electrodeposited body. 2. The active energy curable ink jet recording apparatus according to claim 1, further comprising: a thermal transfer body that thermally transfers the charged resin particles that are electrodeposited on the rotating electrodeposition body onto the recording medium.
By providing the resin layer forming means for forming the resin layer on the recording medium drawn by the ink jet head and having the ink cured by the active energy irradiation means, it is unnecessary by smoothing the surface structure that can be visually recognized. The surface structure is suppressed and high-quality image formation becomes possible.
In particular, the resin layer is formed by transferring a liquid toner containing charged resin particles to the ink discharge formation surface of the recording medium. This resin layer is preferably transparent, but white can also be applied.

  According to the present invention, it is possible to form an image with high image quality by suppressing the unnecessary surface structure generated due to the overlap and uneven distribution of the ink ejected imagewise on the recording medium. An active energy curable ink jet recording apparatus can be provided.

Embodiments of the present invention will be described below with reference to the drawings.
FIG. 1 is a schematic view of an active energy curable ink jet recording apparatus according to an embodiment of the present invention.
In the figure, in the casing 12 of the active energy curable ink jet recording apparatus 10, a recording medium storage unit 20 for storing a plurality of sheet-like recording media S of the same size and a storage medium S from the storage unit 20. A transport unit 30 that takes out the recording medium, a scanning transport unit 40 that performs scanning while holding the recording medium S carried by the transport unit 30 in the recording position range, and a recording medium S that is held and transferred and scanned by the scanning transport unit 40. An image recording unit 50 that performs inkjet image recording and active energy (ultraviolet light in this embodiment) irradiation fixing, and a tray 90 to which a recording medium S that has been recorded by the image recording unit 50 is sent out are provided. . A cartridge mounting unit 70 is connected to the image recording unit 50 for supplying ink. The cartridge mounting unit 70 is detachably equipped with a cartridge described later.

  In the recording medium storage unit 20, a storage cassette 22 for storing the recording medium S is detachably disposed at the bottom of the casing 12 of the active energy curable ink jet recording apparatus 10, and the recording medium S of a different size can be supplied by replacement. it can. The recording medium storage unit 20 may be configured to mount a plurality of cassettes.

  The transport unit 30 includes a feed roller 32 that comes into contact with the leading end of the recording medium S in the storage cassette 22 set in the housing 12 in the insertion direction, and further scans and transports the recording medium S fed out by the feed roller 32. Conveying roller pairs 34 and 36 for conveying to the section 40 are provided.

  The scanning conveyance unit 40 includes a conveyance belt 48 that is stretched and driven by three belt rollers 42, 44, and 46. The conveyance belt 48 is driven in the X direction from the upstream belt roller 44 to the downstream belt roller 46, and the recording medium S is placed and conveyed on the conveyance belt 48 between the upstream belt roller 44 and the downstream belt roller 46. Is done. The conveyor belt 48 is cleaned of dust and the like attached to its surface by the cleaning roller 43.

  In the image recording unit 50, a head unit 52 to which the cartridge mounting unit 70 is connected for supplying ink is provided with the tip of the ejection unit facing the conveyance belt 48 at an image recording position 48P. A head driver 54 is connected to the head unit 52 to control the ejection amount of each ink color. A cartridge mounting portion 70 is connected to these head units 52 for supplying ink. In addition, an infrared irradiation unit 56 is disposed immediately after the image recording position 48P and downstream of the head unit 52, and gives strong active energy sufficient for the ink to get on the recording medium S and to be cured immediately thereafter. The head unit 52 is a full-line head having an array of the lengths in the width direction of the recording medium S, and a piezo type is applied to each nozzle.

  Cartridges 71a, 71b, 71c, 71d, and 71e are mounted on the cartridge mounting unit 70, and these cartridges are respectively W (white), Y (yellow), M (magenta), C (cyan), and K ( Black) ink is stored. Each cartridge 71a, 71b, 71c, 71d, 71e can be connected to the head unit 52 through the ink supply path 72 at the time of mounting.

  In the ultraviolet irradiation unit 56, in order to use the strong light for curing the ink as described above, the exhaust cooling unit 80 is disposed at the upper part in the casing 12 in order to suppress the temperature rise in the casing 12. Yes.

  A separation claw 92 is disposed downstream of the position where the recording medium S is separated from the conveyance belt 48 (downstream belt roller 46 in the present embodiment), and promotes the separation of the recording medium S from the conveyance belt 48.

  A transfer unit 60 is disposed downstream of the scanning conveyance unit 40. The recording medium S is peeled from the transport belt 48 by the peeling claw 92 and then transported to the transfer unit 60 along the transport path 94. The transfer means 60 includes a conductive roller 62 that is a rotary electrodeposition body, a heat roller 64 that is a thermal transfer body, and a colorless liquid toner 68 that is stored in a metal container 66 and into which the conductive roller 62 is immersed. The It should be noted that a roller pair or the like may be provided upstream of the transfer unit 60 to induce a change in direction of the recording medium S.

  On the conductive roller 62, substantially transparent charged resin particles are electrodeposited by a colorless liquid toner 68 stored in a metal container 66. The conductive roller 62 is rotated by a driving unit (not shown) to transfer the colorless liquid toner 68 onto the image forming surface of the recording medium S.

The heat roller 64 is disposed at a position facing the conductive roller 62, and the substantially transparent charged resin particles electrodeposited on the conductive roller 62 by cooperating with the conductive roller 62 are recorded on the recording medium S. To heat and pressure.
A final transport unit 96 and a tray 90 are disposed downstream of the transfer unit 60 and accommodates the recording medium S transported from the transfer unit 60.

  As another configuration of the recording medium storage unit 20 described above, a cassette for supplying a recording medium wound around a roll may be used. In this case, a cutter that cuts the recording medium into a desired length is disposed instead of the feed roller 32 of the transport unit 30.

  In the present embodiment, the head unit 52 is a full-line head in which inkjet nozzles are arranged in the width direction of the recording medium S. However, the head unit 52 is configured to be a scanning head or a multi-channel type that performs vertical scanning in the conveyance direction of the recording medium S. It is also possible to adopt. When the scanning head is used, the ultraviolet irradiation unit is provided so as to move together with the scanning head. In this embodiment, the ink jet recording position is transported by the transport belt. However, as another configuration, the recording medium may be transported on the platen at the ink jet recording position while being sandwiched between transport rollers. it can. The platen can be a fixed type or a movable type.

Next, regarding the present embodiment, the transfer unit 60 will be described in detail with reference to the drawings.
FIG. 2A is an enlarged view centering on the transfer unit 60, and FIG. 2B is a cross-sectional view of the recording medium S carried out from the transfer unit 60.

  As shown in FIG. 2A, in the transfer unit 60, the conductive roller 62 is electrically connected to the power supply unit 63. As a result, substantially transparent charged resin particles are electrodeposited on the conductive roller 62. Thus, by providing a resin layer by electrodeposition, a resin layer excellent in thickness uniformity can be formed at high speed. At this time, the conductive roller 62 can be heated to a predetermined temperature (40 to 50 ° C.) to promote the coating of the colorless liquid toner 68 before the thermal pressure transfer, and the simple transfer of the resin layer can be performed. It becomes possible.

  The transfer means 60 transfers the colorless liquid toner 68 onto the image 65 drawn on the recording medium S that has been peeled off from the conveying belt 48 by the peeling claw 92 and cured with ink, and simultaneously with the conductive roller 62 by the heat roller 64. The transfer layer 67 made of substantially transparent charged resin particles electrodeposited in cooperation is transferred onto the recording medium S by thermal pressure. As transfer conditions at this time, the surface temperature of the heat roller is preferably 50 to 100 ° C., and the pressure is preferably about 0.1 MPa to 1.0 MPa. By setting the transfer condition within such a range, a high-quality image can be obtained without deformation of the recording medium.

  As shown in FIG. 2B, the transfer layer 67 that has been thermally transferred to the recording medium S creates a smooth surface covering the unevenness of the image 65, thereby smoothing the surface structure that can be visually recognized. As a result, an unnecessary surface structure can be suppressed and high-quality image formation can be performed.

  In addition, since the uneven image 65 is covered with the transfer layer 67, the light resistance of the image 65 can be improved and the durability against damage such as scratches can be improved. In this embodiment, the transfer layer 67 is colorless and transparent. However, the present invention is not limited to this. For example, even when the base color is white, the transfer layer 67 can be used.

  In the transfer means 60, as a component of the liquid toner 68, particles mainly containing a thermoplastic resin are dispersed and supplied in the electrically insulating liquid, so that the transfer layer has a uniform thickness. The film can be easily transferred while easily adjusting the film.

In this method, particles mainly containing a resin constituting the transfer layer are dispersed and supplied in an electric insulating solvent having an electric resistance of 10 ⁸ Ω · cm or more and a relative dielectric constant of 3.5 or less. The film thickness is preferable in that it can be easily prepared uniformly and thinly. Specific examples of the insulating solvent include linear or branched aliphatic hydrocarbons, alicyclic hydrocarbons, aromatic hydrocarbons, and halogen-substituted products thereof. For example, octane, isooctane, decane, isodecane, decalin, nonane, dodecane, isododecane, cyclohexane, cyclooctane, cyclodecane, benzene, toluene, xylene, mesitylene, Isopar E, Isopar G, Isopar H, Isopar L (Isopar; Exxon products) Name), shell sol 70, shell sol 71 (shell sol; trade name of Shell Oil), Amsco OMS, Amsco 460 solvent (Amsco; trade name of Spirits), etc. can be used alone or in combination. When compound (S) coexists, dimethylpolysiloxane oil (KF-96; Shin-Etsu Silicone, TSF451; manufactured by Toshiba Silicone Co., Ltd.), methyl hydrogen polysiloxane oil (KF-99, TSF484 etc.), methyl Silicon oils such as phenyl polysiloxane oil (KF50, TSF437, etc.) are also used.

  Hereinafter, the resin transfer layer of this embodiment will be described in detail. The transfer layer mainly containing the thermoplastic resin is preferably translucent or white, but is not particularly limited. When the image to be transferred after being transferred to the transfer material is a color image (particularly a full color image), a colorless and transparent transfer layer is usually used.

The weight average molecular weight of the thermoplastic resin in this transfer layer is preferably in the range of 1 × 10 ³ to 1 × 10 ⁵ , more preferably 3 × 10 ^{3 to} 5 × 10 ⁴ . The glass transition temperature of the thermoplastic resin is preferably -20 ° C to 50 ° C, more preferably -10 ° C to 40 ° C.

  In the present invention, any thermoplastic resin satisfying the above properties may be used. Specifically, olefin polymers and copolymers, vinyl chloride copolymers, vinylidene chloride copolymers, vinyl alkanoate polymers and copolymers. Polymers, allyl alkanoic acid polymers and copolymers, polymers and copolymers of styrene and its derivatives, olefin-styrene olefin-unsaturated carboxylic acid ester copolymers, acrylonitrile copolymers, methacrylonitrile copolymers , Alkyl vinyl ether copolymers, acrylic ester polymers and copolymers, methacrylic ester polymers and copolymers, styrene-acrylic ester copolymers, styrene-methacrylic ester copolymers, itaconic acid Diester polymers and copolymers, maleic anhydride copolymers, acrylamide copolymers, meta Rilamide copolymer, hydroxyl group-modified silicone resin, polycarbonate resin, ketone resin, polyester resin, silicone resin, amide resin, hydroxyl group and carboxyl group-modified polyester resin, butyral resin, polyvinyl acetal resin, cyclized rubber-methacrylate ester copolymer , A cyclized rubber-acrylic acid ester copolymer, a copolymer containing a heterocyclic ring (for example, a furan ring, a tetrahydrofuran ring, a thiophene ring, a dioxane ring, a dioxofuran ring, a lactone ring, a benzofuran ring, a benzothiophene ring , 1,3-dioxetane ring, etc.), cellulose resin, fatty acid-modified cellulose resin, epoxy resin and the like.

  For example, published by Nikkan Kogyo Shimbun “Plastics Materials Course Series” Volumes 1 to 18 (1981), Kinki Chemical Association Vinyl Division “Polyvinyl Chloride” published by Nikkan Kogyo Shimbun (1988), Eizo Omori “Functions” Acrylic Resin ”published by Techno System (1985), Eiichiro Takiyama“ Polyester Resin Handbook ”published by Nikkan Kogyosha (1988), edited by Kazuo Yuki“ Saturated Polyester Resin Handbook ”published by Nikkan Kogyo Shimbun (1989), The Polymer Society of Japan “Polymer Data Handbook <Application>” Chapter 1 Rofukan (1986), Yuji Harasaki's “Latest Binder Technology Handbook” Chapter 2 General Technology Center (1985), etc. It is specifically exemplified.

Next, the “electrodeposition” method of this embodiment will be described.
In the present embodiment, a thermoplastic resin is electrodeposited on the surface of the photoreceptor in the form of resin particles, and a uniform thin film is formed by, for example, heating to form a transfer layer. Therefore, the thermoplastic resin particles need to have either a positive charge or a negative charge, and the charge polarity is arbitrarily determined.

  The resin particles have a range satisfying the above-mentioned physical properties, and the average particle size is usually in the range of 0.01 μm to 15 μm, preferably 0.05 μm to 5 μm, more preferably 0.1 μm to 1 μm. Range. The particles may be in the form of particle powder (dry type) or non-aqueous dispersed resin particles (wet type). Preferably, non-aqueous dispersed resin particles that can easily adjust the film thickness of the peeling transfer layer to a thin film with a uniform thickness can be used.

The electrodeposition amount of the thermoplastic resin particles on the recording material can be arbitrarily adjusted by the voltage applied to the external bias, the voltage application time, and the like. Then, after electrodeposition, the thermoplastic resin particles are formed into a film to form a transfer layer. The electrodeposition amount of the transfer layer at this time is preferably in the range of 0.1 to 10 g / m ² , more preferably 0.5 to 5 g / m ² . When the film thickness is too thin, the structure is visually recognized, and when it is too thick, the translucency tends to be lowered. Further, by warming the conductive roller 62 to about 40 to 50 ° C. during electrodeposition, the colorless liquid toner 68 can be formed into a film immediately after electrodeposition.

  As described above, the transfer means, which is the resin forming means of this embodiment, and the resin layer formation thereof have been described. However, in the present invention, if the resin material can be used, processes other than electrodeposition are possible. For example, a layer can be formed by a coating roller or a coater.

  Here, the “active energy” referred to in the present invention is not particularly limited as long as it can impart energy capable of generating a starting species in the ink composition by the irradiation, and broadly includes α rays, Including gamma rays, X-rays, ultraviolet rays, visible rays, electron beams, and the like. Among these, from the viewpoints of curing sensitivity and device availability, ultraviolet rays and electron beams are preferable, and ultraviolet rays are particularly preferable. Therefore, the ink composition of the present invention is preferably an ink composition that can be cured by irradiation with ultraviolet rays.

In the inkjet recording apparatus of the present invention, the peak wavelength of the active energy depends on the absorption characteristics of the sensitizing dye in the ink composition, but is, for example, 200 to 600 nm, preferably 300 to 450 nm, and more preferably 350 to It is suitable that it is 450 nm. In addition, the (a) electron transfer type initiation system of the ink composition of the present invention has sufficient sensitivity even with low output active energy. Therefore, the output of active energy is, for example, 2,000 mJ / cm ² or less, preferably 10 to 2,000 mJ / cm ² , more preferably 20 to 1,000 mJ / cm ² , and still more preferably 50 to 800 mJ. An irradiation energy of / cm ² is appropriate. The active energy exposure surface illuminance (the maximum illuminance of the surface of the recording medium) is, for example, 10 to 2,000 mW / cm ^2, preferably, suitably be irradiated at 20 to 1,000 mW / cm ² is there.
In particular, in the ink jet recording apparatus of the present invention, irradiation with active energy generates ultraviolet rays having an emission wavelength peak of 390 to 420 nm and a maximum illuminance of 10 to 1,000 mW / cm ^{2 on the} surface of the recording medium. The light emitting diode is preferably irradiated.

In the ink jet recording apparatus of the present invention, it is appropriate that the active energy is applied to the ink composition ejected on the recording medium, for example, 0.01 to 120 seconds, preferably 0.1 to 90 seconds. It is.
Further, in the ink jet recording apparatus of the present invention, the ink composition is heated to a constant temperature, and the time from the landing of the ink composition to the recording medium to the irradiation of the active energy is 0.01 to 0.5 seconds. Preferably, the time is 0.01 to 0.3 seconds, more preferably 0.01 to 0.15 seconds. Thus, by controlling the time from the landing of the ink composition to the recording medium to the irradiation of the active energy to an extremely short time, it is possible to prevent the landed ink composition from bleeding before curing. .

  In order to obtain a color image using the ink jet recording apparatus of the present invention, it is preferable to superimpose in order from the color with the lowest brightness. By overlapping in this way, the active energy can easily reach the lower ink, and good curing sensitivity, reduction of residual monomers, reduction of odor, and improvement of adhesion can be expected. In addition, although irradiation with active energy can be performed by injecting all the colors and exposing them together, exposure for each color is preferable from the viewpoint of promoting curing.

  Since the inkjet head of the present invention is a piezo-type inkjet head, multi-size dots of 0.5 to 100 pl, preferably 1 to 30 pl, for example, 320 × 320 to 4000 × 4000 dpi, preferably 400 × 400 are used. It can be driven to emit at a resolution of ˜2400 × 2400 dpi. In the present invention, dpi represents the number of dots per 2.54 cm.

  Further, as described above, since the active energy curable ink such as the ink composition of the present invention desirably has a constant temperature for the discharged ink composition, from the ink supply tank to the inkjet head portion, It is preferable to perform temperature control by heat insulation and heating. 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 heat energy, it is preferable to insulate from other parts and reduce the heat capacity of the entire heating unit.

  Further, mercury lamps and gas / solid lasers are mainly used as active energy sources, and mercury lamps and metal halide lamps are widely known as ultraviolet light curable ink jets. Furthermore, replacement with a GaN-based semiconductor ultraviolet light emitting device is very useful industrially and environmentally. Furthermore, LED (UV-LED) and LD (UV-LD) are small, have a long lifetime, high efficiency, and low cost, and are expected as radiation sources for active energy curable ink jets.

  Further, as described above, a light emitting diode (LED) and a laser diode (LD) can be used as the active energy source. In particular, when an ultraviolet light source is required, an ultraviolet LED and an ultraviolet LD can be used. For example, Nichia Corporation has introduced a purple LED whose main emission spectrum has a wavelength between 365 nm and 420 nm. Further, when shorter wavelengths are required, US Pat. No. 6,084,250 discloses an LED that can emit active energy centered between 300 nm and 370 nm. Other ultraviolet LEDs are also available and can emit radiation in different ultraviolet bands. A particularly preferable active energy source in the present invention is a UV-LED, and a UV-LED having a peak wavelength of 350 to 420 nm is particularly preferable.

[Recording medium]
The recording medium to which the ink composition of the present invention can be applied is not particularly limited, and various kinds of non-absorbing resin materials used for ordinary non-coated paper, coated paper, so-called soft packaging, or the like. A resin film formed into a film can be used, and examples of the various plastic films include PET film, OPS film, OPP film, ONy film, PVC film, PE film, and TAC film. In addition, examples of the plastic that can be used as the recording medium material include polycarbonate, acrylic resin, ABS, polyacetal, PVA, and rubbers. Metals and glasses can also be used as the recording medium.
In the ink composition of the present invention, when a material with low thermal shrinkage at the time of curing is selected, the adhesive property between the cured ink composition and the recording medium is excellent. Films that tend to curl and deform, such as heat-shrinkable PET film, OPS film, OPP film, ONy film, PVC film, etc., have the advantage that a high-definition image can be formed.

Below, each component used for the ink composition which can be used by this invention is demonstrated sequentially.
[Ink composition]
The ink composition used in the present invention is an ink composition that can be cured by irradiation with active energy, and examples thereof include a cationic polymerization ink composition, a radical polymerization ink composition, and a water-based ink composition. These compositions will be described in detail below.

[Cationically-polymerized ink composition]
The cationic polymerization ink composition contains (a) a cationic polymerizable compound and (b) a compound that generates an acid upon irradiation with active energy. If desired, it may further contain (d) an organic acidic component having a pKa value of 2 to 6, (e) a colorant, and the like.
Hereafter, each component used for a cationic polymerization type ink composition is demonstrated one by one.

[(A) Cationic polymerizable compound]
The (a) cationic polymerizable compound used in the present invention is not particularly limited as long as it is a compound that causes a polymerization reaction by an acid generated from a compound that generates an acid by irradiation of active energy (b) described later and cures. Various known cationic polymerizable monomers known as photo cationic polymerizable monomers can be used. Examples of the cationic polymerizable monomer include JP-A-6-9714, JP-A-2001-31892, JP-A-2001-40068, JP-A-2001-55507, JP-A-2001-310938, JP-A-2001-310937, and JP-A-2001-220526. Examples thereof include epoxy compounds, vinyl ether compounds, oxetane compounds and the like.

Examples of the epoxy compound include aromatic epoxides, alicyclic epoxides, and aromatic 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.

  As the alicyclic epoxide, cyclohexene oxide obtained by epoxidizing a compound having at least one cycloalkane ring such as cyclohexene or cyclopentene ring with a suitable oxidizing agent such as hydrogen peroxide or peracid. Or a cyclopentene oxide containing compound is mentioned preferably.

  Examples of the aliphatic epoxide include dihydric polyglycidyl ethers of aliphatic polyhydric alcohols or alkylene oxide adducts thereof. Typical examples include diglycidyl ether of ethylene glycol, diglycidyl ether of propylene glycol or diglycidyl ether of alkylene glycol such as diglycidyl ether of 1,6-hexanediol, di- or tri- or di- or tri-glycol or adducts thereof. Polyglycidyl ether of polyhydric alcohol such as glycidyl ether, diglycidyl ether of polyethylene glycol or alkylene oxide adduct thereof, diglycidyl ether of polyalkylene glycol represented by diglycidyl ether of polypropylene glycol or alkylene oxide adduct thereof, etc. Can be mentioned. Here, examples of the alkylene oxide include ethylene oxide and propylene oxide.

The epoxy compound may be monofunctional or polyfunctional.
Examples of monofunctional epoxy compounds that can be 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 -Vinylcyclohexene oxide etc. are mentioned.

  Examples of polyfunctional epoxy compounds 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, and 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′-epoxycyclohexanecarboxy 2- (3,4-epoxycyclohexyl-5,5-spiro-3,4-epoxy) cyclohexane-meta-dioxane, bis (3,4-epoxycyclo) Xylmethyl) 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, ethylene glycol di (3,4-epoxycyclohexylmethyl) ether, ethylenebis (3,4-epoxycyclohexanecarboxylate) , Epoxyhexahydrophthalate dioctyl, epoxyhexahydrophthalate di-2-ethylhexyl, 1,4-butanediol diglycidyl ether, 1,6-hexanediol diglycidyl ether Glycerin triglycidyl ether, trimethylolpropane triglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ethers, 1,1,3-tetradecadiene dioxide, limonene dioxide, 1,2,7,8- Examples include diepoxyoctane and 1,2,5,6-diepoxycyclooctane.

  Among these epoxy compounds, aromatic epoxides and alicyclic epoxides are preferable from the viewpoint of excellent curing speed, and alicyclic epoxides are particularly preferable.

  Examples of the vinyl ether compound include ethylene glycol divinyl ether, diethylene glycol divinyl ether, triethylene glycol divinyl ether, propylene glycol divinyl ether, dipropylene glycol divinyl ether, butanediol divinyl ether, hexanediol divinyl ether, cyclohexanedimethanol divinyl ether, Di- or trivinyl ether compounds such as methylolpropane trivinyl ether, ethyl vinyl ether, n-butyl vinyl ether, isobutyl vinyl ether, octadecyl vinyl ether, cyclohexyl vinyl ether, hydroxybutyl vinyl ether, 2-ethylhexyl vinyl ether, cyclohexane dimethanol monovinyl ether, n-propyl Pills vinyl ether, isopropyl vinyl ether, isopropenyl ether -O- propylene carbonate, dodecyl vinyl ether, diethylene glycol monovinyl ether, and octadecyl vinyl ether.

The vinyl ether compound may be monofunctional or polyfunctional.
Specifically, examples of monofunctional vinyl ethers 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 , Methoxypolyethyleneglycol 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 thereof include chloroethoxyethyl vinyl ether, phenylethyl vinyl ether, phenoxypolyethylene glycol vinyl ether and the like.

  Examples of polyfunctional vinyl ethers include 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, and bisphenol F. Divinyl ethers such as alkylene oxide divinyl ether; trimethylolethane trivinyl ether, trimethylolpropane trivinyl ether, ditrimethylolpropane tetravinyl ether, glycerin trivinyl ether, pentaerythritol tetravinyl ether, dipentaerythritol pentavinyl ether, dipentaerythritol Hexavinyl 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 addition Examples thereof include polyfunctional vinyl ethers such as pentaerythritol tetravinyl ether, ethylene oxide-added dipentaerythritol hexavinyl ether, and propylene oxide-added dipentaerythritol hexavinyl ether.

  As the vinyl ether compound, a di- or trivinyl ether compound is preferable from the viewpoints of curability, adhesion to a recording medium, surface hardness of the formed image, and the like, and a divinyl ether compound is particularly preferable.

The oxetane compound in the present invention refers to a compound having an oxetane ring, and a known oxetane compound can be arbitrarily selected and used as described in JP-A Nos. 2001-220526, 2001-310937, and 2003-341217. .
The compound having an oxetane ring that can be used in the ink composition of the present invention is preferably a compound having 1 to 4 oxetane rings in the structure. By using such a compound, it becomes easy to maintain the viscosity of the ink composition within a good handling range, and obtain high adhesion between the cured ink composition and the recording medium. Can do.

The compound having such an oxetane ring is described in detail in the above-mentioned JP-A No. 2003-341217, paragraph numbers [0021] to [0084], and the compounds described therein can be suitably used in the present invention.
Among the oxetane compounds used in the present invention, it is preferable to use a compound having one oxetane ring from the viewpoint of the viscosity and tackiness of the ink composition.

In the ink composition of the present invention, these cationic polymerizable compounds may be used alone or in combination of two or more, but from the viewpoint of effectively suppressing shrinkage during ink curing. Is preferably a combination of at least one compound selected from an oxetane compound and an epoxy compound and a vinyl ether compound.
The content of the (a) cationic polymerizable compound in the ink composition is suitably 10 to 95% by mass, preferably 30 to 90% by mass, and more preferably 50 to 85%, based on the total solid content of the composition. It is the range of mass%.

[(B) Compound that generates acid upon irradiation with active energy]
The ink composition of the present invention contains a compound that generates an acid upon irradiation with radiation (hereinafter, appropriately referred to as “photoacid generator”).
Examples of the photoacid generator that can be used in the present invention include photoinitiators for photocationic polymerization, photoinitiators for photoradical polymerization, photodecolorants for dyes, photochromic agents, and light used for microresists. (400-200 nm ultraviolet rays, far ultraviolet rays, particularly preferably g-line, h-line, i-line, KrF excimer laser beam), ArF excimer laser beam, electron beam, X-ray, molecular beam, ion beam, etc. A compound capable of generating can be appropriately selected and used.

  Examples of such a photoacid generator include an onium salt such as a diazonium salt, an ammonium salt, a phosphonium salt, an iodonium salt, a sulfonium salt, a selenonium salt, an arsonium salt, or the like, which decomposes upon irradiation with radiation to generate an acid. Halogen compounds, organometallic / organic halides, photoacid generators having o-nitrobenzyl type protecting groups, compounds that generate sulfonic acids by photolysis, such as iminosulfonates, disulfone compounds, diazoketosulfones And diazodisulfone compounds.

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

(B) A photo-acid generator can be used individually by 1 type or in combination of 2 or more types.
The content of the (b) photoacid generator in the ink composition is preferably 0.1 to 20% by mass, more preferably 0.5 to 10% by mass, and still more preferably in terms of the total solid content of the ink composition. Is 1-7 mass%.

  In the ink composition of the present invention, various additives can be used in combination with the essential components according to the purpose. These optional components will be described.

[(D) Organic acidic component having a pKa value of 2 to 6]
In the ink composition of the present invention, (d) an organic acidic component having a pKa value of 2 to 6 (hereinafter sometimes simply referred to as “organic acidic component”) can be added. The organic acidic component (d) having a pKa value of 2 to 6 used in the present invention corresponds to a qualitatively weakly acidic organic compound. When the pKa of the organic acidic component is larger than 6, the sensitivity is lowered when it is added to the ink composition of the present invention. In the present invention, it is preferable to apply an organic acidic component having a pKa value of 2 to 6.

  Specific examples of the organic acidic component having a pKa value of 2 to 6 include carboxylic acids. Examples of carboxylic acids include acetic acid, phenylacetic acid, phenoxyacetic acid, methoxypropionic acid, lactic acid, hexanoic acid, heptanoic acid, octanoic acid, palmitic acid, stearic acid, oleic acid, linolenic acid, cyclopropylcarboxylic acid, cyclobutanecarboxylic acid. Acid, cyclopentanecarboxylic acid, cyclohexanecarboxylic acid, 1-adamantanecarboxylic acid, 1,3-adamantanedicarboxylic acid, norbornene-2,3-dicarboxylic acid, abietic acid, trans-retinoic acid, cyclohexylacetic acid, dicyclohexylacetic acid, Adamantane acetic acid, malonic acid, malonic acid monomethyl ester, fumaric acid, maleic acid, maleic acid monomethyl ester, itaconic acid, crotonic acid, succinic acid, adipic acid, sebacic acid, glycolic acid, diglycolic acid, mandelin , Tartaric acid, malic acid, arginic acid, cinnamic acid, methoxycinnamic acid, 3,5-dimethoxycinnamic acid, benzoic acid, salicylic acid, 4-hydroxybenzoic acid, gallic acid, 3-nitrobenzoic acid, 3-chloro Benzoic acid, 4-vinylbenzoic acid, t-butylbenzoic acid, 1-naphthoic acid, 1-hydroxy-2-naphthoic acid, fluorenone-2-carboxylic acid, 9-anthracenecarboxylic acid, 2-anthraquinonecarboxylic acid, phthalic acid , Phthalic acid monomethyl ester, isophthalic acid, terephthalic acid, trimellitic acid, trimellitic acid monomethyl ester, and other aliphatic or aromatic monocarboxylic acids, dicarboxylic acids, and tricarboxylic acids having 1 to 20 carbon atoms. However, it is not limited to this.

[(E) Colorant]
The ink composition of the present invention can form a visible image by adding a colorant. For example, when forming an image area of a lithographic printing plate, it is not always necessary to add it, but it is also preferable to use a colorant from the viewpoint of plate inspection of the obtained lithographic printing plate.
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, but oil-soluble dyes are preferred.

[Pigment]
The pigment preferably used in the present invention will be described.
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, “Pigment Dictionary” (2000), edited by Seijiro Ito. Herbst, K.M. Hunger “Industrial Organic Pigments”, JP 2002-12607 A, JP 2002-188025 A, JP 2003-26978 A, and JP 2003-342503 A3.

  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 an orange color, 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 dispersing 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. be able to.
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 copolymer, a modified polyacrylate, an aliphatic Examples thereof include polyvalent carboxylic acids, naphthalene sulfonic acid formalin condensates, polyoxyethylene alkyl phosphate esters, and pigment derivatives. 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, or the solvent-free low molecular weight component (a) cationic polymerizable compound may be used as a dispersion medium. However, the ink composition of the present invention is a radiation curable ink, and is preferably solventless in order to cure the ink after it is applied to 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, as the dispersion medium, (a) a cationically polymerizable compound is used, and among them, it is preferable to select a cationically polymerizable monomer having the lowest viscosity in terms of dispersion suitability and handling properties of the ink composition. .

The average particle size of the pigment is preferably 0.02 to 4 μm, more preferably 0.02 to 2 μm, and more preferably 0.02 to 1.0 μm.
Selection of pigments, dispersants, and dispersion media, dispersion conditions, and filtration conditions are set so that the average particle diameter of the pigment particles falls within the above preferred range. 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〕
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. Accordingly, so-called water-insoluble oil-soluble dyes are 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 noble (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 1.0 V (vs SCE) or more are preferably used. The oxidation potential is preferably higher, the oxidation potential is more preferably 1.1 V (vs SCE) or more, and particularly preferably 1.15 V (vs SCE) or more.

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 the general formulas (Y-II) to (Y-IV) described in paragraph [0034] of JP-A No. 2004-250483. And the compounds described in paragraphs [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 inks of any color 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 cyan dyes 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) are listed as preferable examples, and specific examples include paragraph numbers [0052] to [0066] in 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. The ink may be used for any color ink.

  These colorants are preferably added in an amount of 1 to 20% by mass in terms of solid content in the ink composition, and more preferably 2 to 10% by mass.

[Other ingredients]
The various additives used as necessary are described below.
[Ultraviolet absorber]
In the present invention, an ultraviolet absorber can be used from the viewpoint of improving the weather resistance of the obtained image and preventing discoloration.
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. 5-194843, 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.
Although the addition amount is appropriately selected according to the purpose, it is generally about 0.5 to 15% by mass in terms of solid content.

[Sensitizer]
A sensitizer may be added to the ink composition of the present invention as necessary for the purpose of improving the acid generation efficiency of the photoacid generator and increasing the photosensitive wavelength. Any sensitizer may be used as long as the photoacid generator is sensitized by an electron transfer mechanism or an energy transfer mechanism. Preferably, aromatic polycondensed compounds such as anthracene, 9,10-dialkoxyanthracene, pyrene and perylene, aromatic ketone compounds such as acetophenone, benzophenone, thioxanthone and Michlerketone, and heterocyclic compounds such as phenothiazine and N-aryloxazolidinone Is mentioned. The addition amount is appropriately selected according to the purpose, but is generally 0.01 to 1 mol%, preferably 0.1 to 0.5 mol%, based on the photoacid generator.

〔Antioxidant〕
An antioxidant can be added to improve the stability of the ink composition. Examples of the antioxidant include European published patents, 223739, 309401, 309402, 310551, 310552, 359416, and 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 0.1 to 8% by mass in terms of solid content.

[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, VII, I to J, No. 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 according to the purpose, but is generally about 0.1 to 8% by mass in terms of solid content.

[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.

〔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, and the amount is preferably 0.1 to 5% by mass, more preferably 0.1 to 3% by mass with respect to the whole ink composition. % Range.

[Polymer compound]
Various polymer compounds can be added to the ink composition of the present invention in order to adjust film physical properties. Examples of polymer compounds include acrylic polymers, polyvinyl butyral resins, polyurethane resins, polyamide resins, polyester resins, epoxy resins, phenol resins, polycarbonate resins, polyvinyl butyral resins, polyvinyl formal resins, shellacs, vinyl resins, acrylic resins. Rubber resins, waxes and other natural resins can be used. Two or more of these may be used in combination. Of these, vinyl copolymer obtained by copolymerization of acrylic monomers is preferred. Furthermore, a copolymer containing “carboxyl group-containing monomer”, “methacrylic acid alkyl ester”, or “acrylic acid alkyl ester” as a structural unit is also preferably used as the copolymer composition of the polymer binder.

[Surfactant]
A surfactant may be added to the ink composition of the present invention.
Examples of the surfactant include those described in JP-A Nos. 62-173463 and 62-183457. For example, anionic surfactants such as dialkylsulfosuccinates, alkylnaphthalenesulfonates, 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.

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 a tackifier, specifically, a high molecular weight adhesive polymer (for example, (meth) acrylic acid and an alkyl group having 1 to 20 carbon atoms) described in JP-A-2001-49200, 5-6p. An ester with an alcohol having, an ester of (meth) acrylic acid and an alicyclic alcohol having 3 to 14 carbon atoms, a copolymer comprising an ester of (meth) acrylic acid and an aromatic alcohol having 6 to 14 carbon atoms) Or a low molecular weight tackifying resin having a polymerizable unsaturated bond.

[Preferred physical properties of ink composition]
The ink composition of the present invention preferably has an ink viscosity of 7 to 30 mPa · s, more preferably 7 to 20 mPa · s at the temperature at the time of ejection in consideration of ejection properties, and is in the above range. It is preferable to adjust the composition ratio appropriately. The ink viscosity at 25 to 30 ° C. is 35 to 500 mPa · s, preferably 35 to 200 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 to 30 ° C. is less than 35 mPa · s, the effect of preventing bleeding is small, and conversely if it is greater than 500 mPa · s, there is a problem 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 the wettability is preferably 30 mN / m or less.

The ink composition of the present invention thus adjusted is suitably used as an ink for inkjet recording. When used as an ink for ink jet recording, the ink composition is ejected onto a recording medium by an ink jet printer, and then the ejected ink composition is irradiated with radiation and cured to perform recording.
In the printed 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. Therefore, in addition to image formation with ink, for example, an ink receiving layer (image image of a lithographic printing plate) Part), and can be used for various purposes.

[Radical polymerization ink composition]
The radical polymerization ink composition contains a radical polymerizable compound and a polymerization initiator. If desired, it may further contain a sensitizing dye, a coloring material, and the like.
Hereinafter, each component used for the radical polymerization ink composition will be sequentially described.

[Radically polymerizable compound]
Examples of the radically polymerizable compound include compounds having an ethylenically unsaturated bond capable of addition polymerization as described below.

[Compound having an ethylenically unsaturated bond capable of addition polymerization]
Examples of compounds having addition-polymerizable ethylenically unsaturated bonds that can be used in the ink composition of the present invention include unsaturated carboxylic acids (eg, acrylic acid, methacrylic acid, itaconic acid, crotonic acid, isocrotonic acid, maleic acid Etc.) and an aliphatic polyhydric alcohol compound, an amide of the unsaturated carboxylic acid and an aliphatic polyamine compound, and the like.

  Specific examples of the monomer of an ester of an aliphatic polyhydric alcohol compound and an unsaturated carboxylic acid include acrylic acid esters such as ethylene glycol diacrylate, triethylene glycol diacrylate, 1,3-butanediol diacrylate, and tetramethylene glycol. Diacrylate, propylene glycol diacrylate, neopentyl glycol diacrylate, trimethylolpropane triacrylate, trimethylolpropane tri (acryloyloxypropyl) ether, trimethylolethane triacrylate, hexanediol diacrylate, 1,4-cyclohexanediol di Acrylate, Tetraethylene glycol diacrylate, Pentaerythritol diacrylate, Pentaerythritol triacrylate , Pentaerythritol tetraacrylate, dipentaerythritol diacrylate, dipentaerythritol hexaacrylate, sorbitol triacrylate, sorbitol tetraacrylate, sorbitol pentaacrylate, sorbitol hexaacrylate, tri (acryloyloxyethyl) isocyanurate, polyester acrylate oligomer.

  Methacrylic acid esters include tetramethylene glycol dimethacrylate, triethylene glycol dimethacrylate, neopentyl glycol dimethacrylate, trimethylolpropane trimethacrylate, trimethylolethane trimethacrylate, ethylene glycol dimethacrylate, 1,3-butanediol dimethacrylate, Hexanediol dimethacrylate, pentaerythritol dimethacrylate, pentaerythritol trimethacrylate, pentaerythritol tetramethacrylate, dipentaerythritol dimethacrylate, dipentaerythritol hexamethacrylate, sorbitol trimethacrylate, sorbitol tetramethacrylate, bis [p- (3-methacryloxy 2-hydroxypro ) Phenyl] dimethyl methane, bis - [p- (acryloxyethoxy) phenyl] dimethylmethane. Itaconic acid esters include ethylene glycol diitaconate, propylene glycol diitaconate, 1,3-butanediol diitaconate, 1,4-butanediol diitaconate, tetramethylene glycol diitaconate, pentaerythritol diitaconate And sorbitol tetritaconate.

  Examples of crotonic acid esters include ethylene glycol dicrotonate, tetramethylene glycol dicrotonate, pentaerythritol dicrotonate, and sorbitol tetradicrotonate. Examples of isocrotonic acid esters include ethylene glycol diisocrotonate, pentaerythritol diisocrotonate, and sorbitol tetraisocrotonate. Examples of maleic acid esters include ethylene glycol dimaleate, triethylene glycol dimaleate, pentaerythritol dimaleate, and sorbitol tetramaleate. Furthermore, the mixture of the above-mentioned ester monomer can also be mention | raise | lifted. Specific examples of amide monomers of aliphatic polyvalent amine compounds and unsaturated carboxylic acids include methylene bis-acrylamide, methylene bis-methacrylamide, 1,6-hexamethylene bis-acrylamide, 1,6-hexa. Examples include methylene bis-methacrylamide, diethylenetriamine trisacrylamide, xylylene bisacrylamide, and xylylene bismethacrylamide.

As another example, a vinyl compound containing a hydroxyl group represented by the following general formula (A) is added to a polyisocyanate compound having two or more isocyanate groups per molecule described in JP-B-48-41708. Examples thereof include vinyl urethane compounds containing two or more polymerizable vinyl groups in one molecule to which a monomer is added. CH ₂ = C (R) COOCH ₂ CH (R ′) OH (A) (where R and R ′ represent H or CH ₃ )
Further, as described in JP-A-51-37193, urethane acrylates, JP-A-48-64183, JP-B-49-43191, JP-B-52-30490, etc. Polyfunctional acrylates and methacrylates such as polyester acrylates and epoxy acrylates obtained by reacting an epoxy resin with (meth) acrylic acid can be used. Furthermore, Journal of Japan Adhesion Association vol.20, No. 7, pages 300 to 308 (1984) as photocurable monomers and oligomers can also be used. In the present invention, these monomers may be used in a chemical form such as a prepolymer, that is, a dimer, a trimer and an oligomer, or a mixture thereof and a copolymer thereof.

  The amount of the radical polymerizable compound used is usually 1 to 99.99%, preferably 5 to 90.0%, more preferably 10 to 70%, based on all components of the ink composition. Mass%).

(Photopolymerization initiator)
Next, the photopolymerization initiator used in the radical polymerization ink composition of the present invention will be described.
The photopolymerization initiator in the present invention is a compound that undergoes a chemical change through the action of light or interaction with the electronically excited state of a sensitizing dye to generate at least one of radicals, acids, and bases. It is.

  Preferred photopolymerization initiators include (a) aromatic ketones, (b) aromatic onium salt compounds, (c) organic peroxides, (d) hexaarylbiimidazole compounds, (e) ketoxime ester compounds, f) borate compounds, (g) azinium compounds, (h) metallocene compounds, (i) active ester compounds, (j) compounds having a carbon halogen bond, and the like.

[Sensitizing dye]
In the present invention, a sensitizing dye may be added for the purpose of improving the sensitivity of the photopolymerization initiator. Examples of preferred sensitizing dyes include those belonging to the following compounds and having an absorption wavelength in the 350 nm to 450 nm region.
Polynuclear aromatics (eg, pyrene, perylene, triphenylene), xanthenes (eg, fluorescein, eosin, erythrosine, rhodamine B, rose bengal), cyanines (eg, thiacarbocyanine, oxacarbocyanine), merocyanines ( For example, merocyanine, carbomerocyanine), thiazines (eg, thionine, methylene blue, toluidine blue), acridines (eg, acridine orange, chloroflavin, acriflavine), anthraquinones (eg, anthraquinone), squalium (eg, squalium) ), Coumarins (eg 7-diethylamino-4-methylcoumarin).

[Co-sensitizer]
Further, the ink of the present invention may contain a known compound having a function of further improving sensitivity or suppressing polymerization inhibition by oxygen as a co-sensitizer.

  Examples of such co-sensitizers include amines such as MR Sander et al., “Journal of Polymer Society”, Vol. 10, page 3173 (1972), Japanese Examined Patent Publication No. 44-20189, Japanese Patent Laid-Open No. 51-82102. Publication, JP 52-134692, JP 59-138205, JP 60-84305, JP 62-18537, JP 64-33104, Research Disclosure 33825 Specifically, triethanolamine, p-dimethylaminobenzoic acid ethyl ester, p-formyldimethylaniline, p-methylthiodimethylaniline and the like can be mentioned.

  Other examples include thiols and sulfides, for example, thiol compounds described in JP-A-53-702, JP-B-55-500806, JP-A-5-142772, and JP-A-56-75643. Specific examples include disulfide compounds, and specific examples include 2-mercaptobenzothiazole, 2-mercaptobenzoxazole, 2-mercaptobenzimidazole, 2-mercapto-4 (3H) -quinazoline, β-mercaptonaphthalene, and the like.

  Other examples include amino acid compounds (eg, N-phenylglycine), organometallic compounds described in Japanese Patent Publication No. 48-42965 (eg, tributyltin acetate), and hydrogen described in Japanese Patent Publication No. 55-34414. Donors, sulfur compounds described in JP-A-6-308727 (eg, trithiane), phosphorus compounds described in JP-A-6-250387 (diethylphosphite, etc.), Si-- described in Japanese Patent Application No. 6-191605 H, Ge-H compound, etc. are mentioned.

  Moreover, it is preferable to add 200-20000 ppm of a polymerization inhibitor from a viewpoint of improving storability. The ink for ink jet recording of the present invention is preferably ejected by heating and lowering the viscosity in the range of 40 to 80 ° C., and a polymerization inhibitor is preferably added to prevent clogging of the head due to thermal polymerization. Examples of the polymerization inhibitor include hydroquinone, benzoquinone, p-methoxyphenol, TEMPO, TEMPOL, and cuperon Al.

[Others]
In addition, known compounds can be used as necessary. For example, surfactants, leveling additives, matting agents, polyester resins for adjusting film properties, polyurethane resins, vinyl resins, acrylic resins. Resin, rubber resin, wax and the like can be appropriately selected and used. In order to improve the adhesion to a recording medium such as polyolefin or PET, it is also preferable to contain a tackifier that does not inhibit the polymerization. Specifically, high molecular weight adhesive polymers described in JP-A-2001-49200, 5-6p (for example, esters of (meth) acrylic acid and alcohols having an alkyl group having 1 to 20 carbon atoms) , An ester of (meth) acrylic acid and an alicyclic alcohol having 3 to 14 carbon atoms, a copolymer formed of an ester of (meth) acrylic acid and an aromatic alcohol having 6 to 14 carbon atoms), A low molecular weight tackifying resin having a saturated bond.

  It is also effective to add a trace amount of organic solvent in order to improve the adhesion to the recording medium. 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.

  In addition, as a means for preventing a decrease in sensitivity due to the light-shielding effect of the ink color material, it is also preferable to combine a cationic polymerizable monomer having a long polymerization initiator lifetime with a polymerization initiator to obtain a radical-cation hybrid type curable ink. One.

[Water-based ink composition]
The aqueous ink composition contains a polymerizable compound and a water-soluble photopolymerization initiator that generates radicals by the action of radiation. If desired, it may further contain a coloring material and the like.

[Polymerizable compound]
As the polymerizable compound contained in the aqueous ink composition of the present invention, a polymerizable compound contained in a known aqueous ink composition can be used.
A reactive material can be added to the water-based ink composition in order to optimize the formulation considering end-user characteristics such as curing speed, adhesion, and flexibility. Examples of such reactive materials include (meth) acrylate (ie, acrylate and / or methacrylate) monomers and oligomers, epoxides, and oxetanes.
Examples of acrylate monomers include phenoxyethyl acrylate, octyl decyl acrylate, tetrahydrofuryl acrylate, isobornyl acrylate, hexanediol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, polyethylene glycol diacrylate (e.g., tetraethylene glycol). Diacrylate), dipropylene glycol diacrylate, tri (propylene glycol) triacrylate, neopentyl glycol diacrylate, bis (pentaerythritol) hexaacrylate, ethoxylated or propoxylated glycol and polyol acrylate (e.g. propoxylated neopentyl glycol Diacrylate, ethoxylated trimethylol proppant Acrylate), and mixtures thereof.
Examples of acrylate oligomers include ethoxylated polyethylene glycol, ethoxylated trimethylolpropane acrylate and polyether acrylate and ethoxylates thereof, and urethane acrylate oligomers.
Examples of methacrylates include hexanediol dimethacrylate, trimethylolpropane trimethacrylate, triethylene glycol dimethacrylate, diethylene glycol dimethacrylate, ethylene glycol dimethacrylate, 1,4-butanediol dimethacrylate, and mixtures thereof.
The amount of oligomer added is preferably 1 to 80% by weight, more preferably 1 to 10% by weight, based on the total weight of the ink composition.

[Water-soluble photopolymerization initiator that generates radicals by the action of active energy]
The polymerization initiator that can be used in the ink composition of the invention will be described. As an example, for example, a photopolymerization initiator having a wavelength of up to about 400 nm may be mentioned. As such a photopolymerization initiator, for example, a photopolymerization initiator represented by the following general formula (hereinafter referred to as TX), which is a substance having functionality in a long wavelength region, that is, a sensitivity to generate a radical upon receiving ultraviolet rays. In the present invention, it is particularly preferable to select and use them appropriately.

In the above general formulas TX-1 to TX-3, R2 represents — (CH ₂ ) _x — (x = 0 or 1), —O— (CH ₂ ) _y — (y = 1 or 2), substituted or unsubstituted Represents a phenylene group. When R2 is a phenylene group, at least one hydrogen atom in the benzene ring is, for example, a carboxyl group or a salt thereof, a sulfonic acid or a salt thereof, a linear or branched alkyl having 1 to 4 carbon atoms. May be substituted with one or more groups or atoms selected from a group, a halogen atom (fluorine, chlorine, bromine, etc.), an alkoxyl group having 1 to 4 carbon atoms, an aryloxy group such as a phenoxy group, and the like. . M represents a hydrogen atom or an alkali metal (for example, Li, Na, K, etc.). R3 and R4 each independently represents a hydrogen atom or a substituted or unsubstituted alkyl group. Examples of the alkyl group include, for example, a linear or branched alkyl group having about 1 to 10 carbon atoms, particularly about 1 to 3 carbon atoms. Moreover, as an example of the substituent of these alkyl groups, a halogen atom (a fluorine atom, a chlorine atom, an oxalic atom etc.), a hydroxyl group, an alkoxyl group (C1-C3 grade) etc. are mentioned, for example. M represents an integer of 1 to 10.

  Furthermore, in the present invention, a water-soluble derivative (hereinafter abbreviated as IC system) of a photopolymerization initiator Irgacure 2959 (trade name: manufactured by Ciba Specialty Chemicals) having the following general formula may be used. Specifically, IC-1 to IC-3 having the following formulas can be used.

[Material composition of colorant-containing ink]
When the above-described water-soluble polymerizable compound is used in an ink containing a coloring material, the concentration of the polymerization initiator and the polymerizable substance in the ink can be adjusted according to the absorption characteristics of the contained coloring material. preferable. As described above, the amount of water or solvent is in the range of 40% to 90%, preferably in the range of 60% to 75%, based on mass, as the blending amount. Furthermore, the content of the polymerizable compound in the ink is in the range of 1% to 30%, preferably in the range of 5% to 20%, based on the mass, with respect to the total amount of the ink. The polymerization initiator depends on the content of the polymerizable compound, but is generally in the range of 0.1 to 7%, preferably 0.3 to 5% on the mass basis with respect to the total amount of the ink.

  When a pigment is used as the color material of the ink, the concentration of the pure pigment in the ink is generally in the range of 0.3% by mass to 10% by mass with respect to the total amount of the ink. The coloring power of the pigment depends on the dispersion state of the pigment particles, but if it is in the range of about 0.3 to 1%, it becomes a range used as a light-colored ink. On the other hand, if it is more than that, it gives a concentration used for general color coloring.

1 is a schematic configuration diagram of an active energy curable ink jet recording apparatus according to an embodiment of the present invention. (A) is an enlarged view centering on the transfer means, and (b) is a cross-sectional view of the recording medium carried out from the transfer means.

Explanation of symbols

DESCRIPTION OF SYMBOLS 10 Active energy curable inkjet recording device 12 Housing | casing S Recording medium 20 Recording medium storage part 30 Conveyance part 40 Scanning conveyance part 50 Image recording part 60 Transfer part 70 Cartridge mounting part 80 Exhaust cooling part 90 Tray 22 Storage cassette 32 Feed roller 34 , 36 Conveying roller pair 42, 44, 46 Belt roller 48 Conveying belt 48P Image recording position 52 Head unit 54 Head driver 56 Ultraviolet irradiation unit 62 Conductive roller (rotating electrodeposit)
64 Heat roller (thermal transfer member)
67 Transfer layer 68 Liquid toner 71a, 71b, 71c, 71d, 71e Cartridge 92 Peeling claw

Claims (2)

An active energy curable ink jet recording apparatus for forming an image of ink curable by active energy on a recording medium by ink jet,
An image recording unit that cures an image formed by ejecting the ink onto the recording medium by an inkjet head by energy irradiation of an active energy irradiation unit;
Conveying means for conveying the recording medium downstream of the inkjet head;
An active energy curable ink jet recording apparatus comprising resin layer forming means for forming a resin layer on an image surface on a recording medium formed and cured by the image recording unit.   The resin layer forming means is disposed at a position facing the rotating electrodeposition body through the recording medium, and in cooperation with the rotating electrodeposition body on which charged resin particles are electrodeposited. 2. The active energy curable ink jet recording apparatus according to claim 1, further comprising: a thermal transfer body that thermally transfers the charged resin particles electrodeposited on the rotary electrodeposition body onto the recording medium.

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