WO2007055333A1 - 活性エネルギー線硬化型インクジェットインキ - Google Patents
活性エネルギー線硬化型インクジェットインキ Download PDFInfo
- Publication number
- WO2007055333A1 WO2007055333A1 PCT/JP2006/322493 JP2006322493W WO2007055333A1 WO 2007055333 A1 WO2007055333 A1 WO 2007055333A1 JP 2006322493 W JP2006322493 W JP 2006322493W WO 2007055333 A1 WO2007055333 A1 WO 2007055333A1
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- WIPO (PCT)
- Prior art keywords
- energy ray
- ink
- active energy
- photopolymerization initiator
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- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/0081—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using electromagnetic radiation or waves, e.g. ultraviolet radiation, electron beams
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
Definitions
- the present invention relates to an active energy ray-curable inkjet ink which is excellent in stretch processability and free of blocking.
- JP-A-2002-167537 an attempt has been made to develop an ink containing an oligomer in order to improve curability.
- the use of a high molecular weight oligomer reduces the crosslink density in the ink, so a large amount of polyfunctional monomer is used to develop solvent resistance and friction resistance.
- the stretchability of the cured film cannot be obtained sufficiently.
- JP-A-2002-241647 an attempt is made to improve the reactivity of an ink with a photopolymerization initiator in a formulation containing a relatively large amount of polyfunctional monomer.
- the initiator was applied to an ink containing a large amount of the monofunctional monomer of the present invention, the initiator was not able to obtain a sufficient effect for blocking.
- the ink having excellent stretch processability obtained by the conventional technique is used in actual use and has a tack on the printed surface even after curing. Even if the printed matter is blocked or it is forcibly peeled off, marks may remain on the printed matter and the cosmetics may be impaired.
- Blocking-free means that the printed substrate is layered on a cured film that is not only cured, pressed at a linear pressure of 11.5 kgfZcm 2 and a speed of 0.3 m / min, then peeled off and applied to the printed substrate. It means that there is no transcription.
- An object of the present invention is to provide an active energy ray-curable ink for ink jet which is excellent in stretch processability and capable of obtaining a blocking-free printed matter.
- the present invention relates to an active energy ray-curable inkjet ink containing a polymerizable monomer and a photopolymerization initiator, containing a monofunctional monomer in an amount of 50% by weight or more in the polymerizable monomer, and the following [Formula 1]
- the present invention relates to an active energy ray-curable inkjet ink comprising a photopolymerization initiator represented by [Formula 2]. [0011] [Chemical 1]
- Rl, R2, R3, and R4 each independently represent a hydrogen atom, a halogen atom, a hydroxyl group, an amino group, an alkyl group, an alkoxy group, or a phenol group, and n is from 2 to Represents an integer of 10.
- R 1, R 2 and R 3 each independently represents a hydrogen atom, a halogen atom, a hydroxyl group, an amino group, an alkyl group, an alkoxy group or a phenol group.
- the photopolymerization initiator may be oligo (2-hydroxy-2-methyl-1- (4- (1-methylvinyl) phenol) propanone) or 2-hydroxy mono 1-. (4- (4- (2-Hydoxy-2-propyl) -benzyl) -phenol) -2-methyl-propan-1-one .
- the present invention relates to the above active energy ray-curable inkjet ink, wherein the content of the photopolymerization initiator is 2 to 20% by weight based on the polymerizable monomer.
- the present invention provides a second optical weight having an absorption peak in a wavelength range of 350 nm to 395 nm.
- the present invention relates to the above-mentioned active energy ray-curable ink jet ink, which contains a initiator.
- the present invention provides a second photopolymerization initiator power 2, 4, 6 trimethylbenzoyl diphosphine phosphine oxide, or bis (2, 4, 6 trimethylbenzoyl) monophenylphosphine. It is related with the said active energy ray hardening-type inkjet ink which is an oxide.
- the present invention relates to the active energy ray-curable inkjet ink as described above, wherein the ink contains 2 benzyl-1,2 dimethylamino-1- (4-morpholinophenol) -butanone 1.
- the present invention relates to the active energy ray-curable ink-jet ink as described above, wherein the polymerizable monomer contains 30% by weight or more of 2-phenoxychetyl acrylate.
- the present invention relates to the above active energy ray-curable ink-jet ink, wherein the polymerizable monomer contains 5 to 30% by weight of N-Bureu 2 force prolatatam.
- the present invention relates to a printed matter obtained by printing on a printing substrate with the above active energy ray-curable inkjet ink.
- the polymerizable monomer is an active energy ray curing reaction component, and specifically represents a molecule having an ethylenically unsaturated double bond.
- the monofunctional monomer is contained in the polymerizable monomer in an amount of 50% by weight or more.
- the monofunctional monomer content is less than 50% by weight, the stretchability of the cured film is significantly reduced.
- the monofunctional monomer is preferably 70% by weight or more. If further ductility is required, the monofunctional monomer is preferably 80% by weight or more.
- the monofunctional monomer include cyclohexyl acrylate, tetrahydrofurfuryl acrylate, benzyl acrylate, methyl phenoxy cetyl acrylate, 4-tert-butyl cyclohexyl acrylate, force prolatathone modification Tetrahydrofurfuryl acrylate , Tribromophenol acrylate, ethoxylated tribromophenol acrylate, 2-phenoxychhetyl acrylate (or phenoxy polyethylene glycol acrylate, phenoxy polypropylene glycol acrylate, phenoxy polyethylene polypropylene glycol acrylate ), Ataliloylmorpholine, Isovolyl Atarylate, Phenoxyjet Tylene Glycol Atylate, Bialcaprolatatam, Vinylpyrrolidone, 2-Hydroxy-3 Phenoxypropyl Atarylate, 1,4 Cyclohexanedimethanol Mono-Ataryl
- the adhesion to the substrate is increased, 2-phenoxychetyl acrylate having an appropriate ductility, the adhesion to the substrate is increased, and the hardness of the cured film at room temperature.
- Caprolatatam which increases the hardness of the film, and is useful in the case where you want to increase the hardness of the cured film and lower the viscosity of the ink.
- 2-hydroxy-3-phenoxypropyl attalylate contributes to improved flexibility.
- the content of 2-phenoxychetyl acrylate is less than 30% by weight in the polymerizable monomer, the adhesion to the substrate is lowered, which is not preferable.
- the content of burkabu-mouth ratatamum is less than 5% by weight in the polymerizable monomer, the reactivity of the cured film will be lowered, resulting in poor adhesion to the substrate, and if the content is more than 30% by weight. This is preferable because the viscosity stability of the ink deteriorates.
- polyfunctional monomer examples include dimethylol monotricyclodecane diatalate, propoxylated bisphenol A di (meth) acrylate, ethoxylated bisphenol A di (meth) acrylate, and cyclohexane diacrylate.
- the ink containing the photopolymerization initiator represented by [Formula 1] or [Formula 2] has a good curing speed and is effective in obtaining a blocking-free printed matter.
- the photopolymerization initiator often has one cleavage part, but the photopolymerization initiator used in the present invention has two or more cleavage parts.
- the molecular weight of the polymerization reaction product in the cured film can be increased.
- the blocking is considered to be caused by a large amount of unreacted monomers and dimers and trimers that have been polymerized in a low molecular state in the cured film. Therefore, a blocking-free printed matter can be obtained by using a photopolymerization initiator having two or more cleavage sites as the photopolymerization initiator and increasing the molecular weight of the polymerization reaction product in the cured film.
- Photopolymerization initiators are classified into intramolecular bond cleavage type and intermolecular hydrogen abstraction type.
- Photoinitiators represented by [Formula 1] or [Formula 2] of the present invention are large of intramolecular bond cleavage type. It is classified into the acetophenone series, which occupies a part, and has characteristics such as faster polymerization, less yellowing due to photoacids, and better storage stability compared to intermolecular hydrogen abstraction type.
- photopolymerization initiator represented by [Formula 1] or [Formula 2] of the present invention include oligo (2-hydroxy-1-methyl 1- (4- (1-methylvinyl)). (Phenyl) propanone), 2-hydroxy-1- (4- (4-((2-hydroxy-1-methyl-1-propiol) -benzyl) -phenyl) 2-methyl-propane 1-on, etc. Not limited to. In addition, one or two or more photopolymerization initiators can be used.
- the photopolymerization initiator represented by [Formula 1] and the photopolymerization initiator represented by [Formula 2] can be used together to increase the curing rate. It can be much faster.
- the photopolymerization initiator is preferably contained in an amount of 2 to 20% by weight based on the polymerizable monomer. If it is less than 2% by weight, the curing rate is remarkably deteriorated, and if it is more than 20% by weight, not only the curing rate is different from that of 10% by weight, but also a dissolution residue may occur. Even if heat is applied to melt the undissolved residue, there is a problem that the viscosity of the ink rises and the ink jetting properties deteriorate.
- the present invention provides 350 ⁇ ! It is preferable to use a second photopolymerization initiator having an absorption peak in the wavelength range of ⁇ 395 nm.
- the penetration depth of the irradiated light becomes longer, so Curing of is promoted.
- the curing rate was improved as a result of using a photopolymerization initiator having an absorption peak in the above wavelength range.
- the absorption spectrum was measured with a spectrophotometer (U-3300 manufactured by HITACHI) using a 1 cm stone cell in which 0.1% by weight of the photopolymerization initiator was dissolved in acetonitrile.
- the absorption peak described in the present invention means a peak having an absorbance of 0.5 or more under the above measurement conditions.
- the acylphosphine oxide photopolymerization initiator is most often the second photopolymerization initiator under the above measurement conditions, having an absorption peak with an intensity of 0.5 or more in the wavelength range of 350 nm to 395 nm.
- an intensity of 0.5 or more in the wavelength range of 350 nm to 395 nm Favored ,.
- the second photopolymerization initiator of the present invention includes 2, 4, 6 trimethylbenzoyl diphosphine phosphine oxide, bis (2, 4, 6 trimethylbenzoyl) monophenylphosphine oxide, and the like. Although it is mentioned, it is not limited to this. Moreover, the said photoinitiator can use 1 type (s) or 2 or more types.
- the ink of the present invention contains 2 benzil 2 dimethylamino 1- (4 morpholino vinyl) -butanone 1 in addition to the second photopolymerization initiator, so that the curing speed is remarkably improved.
- This combination of photopolymerization initiators has the effect of remarkably increasing the curing speed.
- it since it has yellowing property, when it is used for clear ink and white ink, if added over 5%, it is applied after the weather resistance test. The color of the film can change.
- a bifunctional monomer can be more suitably used as the polyfunctional monomer.
- the active energy rays in the present invention are ultraviolet rays. Specifically, metal lines such as metal lamps, ride lamps, high-pressure mercury lamps, electrodeless ultraviolet lamps, etc. that are irradiated with force, but are not limited thereto.
- the ink shown in the present invention refers to a liquid that is printed or coated on the surface of a substrate. When this ink does not contain a coloring component, it can be used as a coating application, and can also be used as a single coating layer or laminated with an ink containing a colorant described below.
- various fillers can be added with a resin component in order to impart durability, molding processability such as hardness and scratch resistance of the cured film, or control of wrinkles and design properties.
- fillers include extender pigments such as calcium carbonate, barium sulfate, spherical silica, hollow silica, and resin beads.
- resin component any resin that is inert to the active energy line can be used.
- polyurethane resin for example, polyvinyl chloride resin, vinyl chloride-vinyl acetate copolymer), ethylene acetate butyl copolymer, polyester resin, Poly (meth) acrylic resin, polyketone resin, polyvinyl resin (for example, polyvinylacetal resin, polyvinyl petital resin, polybylpyrrolidone resin), cellulose resin (for example, CAB resin, CAP And the like.
- the type and composition in consideration of ink jet suitability.
- coating by other printing methods such as silk screen printing, gravure printing, offset printing, or spray coating may be performed.
- the coating material used in general printing applications other than the ink of the present invention for example, silk screen printing, gravure printing, offset printing, etc. includes the colorant of the present invention. It may be laminated on the ink layer, or a separately formed coating layer (film, etc.) may be transferred by lamination, or lamination using a spray coating material or the like.
- the ink of the present invention contains a coloring component
- it can be used as a material for displaying graphics, characters, photographs, and the like.
- dyes and pigments have been widely used as the coloring component, but pigments are often used especially for weather resistance.
- carbon black examples include “Special Black 350, 250, 100, 550, 5, 4, 4A, 6” “PrintexU, V, 140U, 140V, 95, 90, 85, 80, 75, 5 5, 45, 40, P, 60, L6, L, 300, 30, 3, 35, 25, A, G '', Cabot's ⁇ REGAL 400R, 660R, 330R, 250R '' ⁇ MOGUL E , L "," MA7, 8, 11, 7 “manufactured by Mitsubishi 7, 100, 100R, 100S, 220, 230 '' ⁇ # 2700, # 2650, # 2600, # 200, # 235 0, # 2300, # 2200, # 1000, # 990, # 980, # 970, # 960, # 950, # 900, # 850, # 750, # 650, # 52, # 50, # 47, # 45, # 45 # 44, # 40, # 33, # 332, # 30, # 25, # 20 , # 10,
- the ratio of the pigment to the total ink is 0.2 to 15 parts by weight for organic pigments such as yellow, magenta, cyan, and black with respect to 100 parts by weight of the ink.
- organic pigments such as yellow, magenta, cyan, and black
- a dispersant for stabilizing the dispersion of fillers and pigments and other additives for imparting various functions can be used.
- the dispersing agent can be selected according to the force dispersibility in which various dispersing agents such as a polymer dispersing agent and a low molecular dispersing agent are present.
- a pigment derivative can be used as a dispersion aid.
- additives that can be used include wettability modifiers, surface tension modifiers, antifoaming agents, slipping agents, antiblocking agents, and ultraviolet light inhibitors that are conventionally used. Any of the dispersants, dispersion aids, and additives can be selected according to the intended use, and in the present invention, the deviation is not limited.
- oligo means a molecule having 2 to 10 repeating units.
- the present invention includes hydroquinone, p-methoxyphenol, t-butylcatechol, pyrogallol, butylhydroxytoluene and the like in order to increase the stability of the viscosity of the ink over time and the stability in the recording apparatus. It is preferable to blend the polymerization inhibitor in an amount of 0.01% to 5% by weight in the ink.
- the active energy ray-curable ink-jet ink of the present invention includes a plasticizer, a surface conditioner, an ultraviolet ray inhibitor, a light stabilizer, and an additive agent such as an anti-oxidation agent such as dibutylhydroxytoluene as necessary.
- an additive agent such as an anti-oxidation agent such as dibutylhydroxytoluene as necessary.
- One or more types can be used.
- the ink of the present invention is printed on a printing substrate by an inkjet discharge apparatus.
- the printing substrate used in the present invention is not particularly limited, but plastic substrates such as polycarbonate, hard vinyl chloride, soft vinyl chloride, polystyrene, foamed polystyrene, PMMA, polypropylene, polyethylene, and PET are mixed. Or modified products, metal substrates such as glass and stainless steel, and wood.
- the ink of the present invention can be used as a set of a plurality of different pigments, for example, four, five, six, seven or the like.
- yellow, magenta, cyan, black, yellow, magenta, cyan, white, etc. can be exemplified.
- the ink of the present invention is particularly suitable for printing on transparent substrates such as polycarbonate, PMMA, polypropylene, polyethylene, PET, and glass by using a photopolymerization initiator represented by [Formula 1]. Can be used. In addition, it can be more suitably used for printing on polycarbonate, PET, and polypropylene in applications that require weather resistance, such as when used outdoors.
- the present invention it is possible to provide a block-free printed matter having good stretch processability using an inkjet printing method.
- the ink of the present invention prevents blocking during stacking. It is possible to provide a printed matter having a cosmetic appearance using conventional equipment without printing.
- the result of the active energy ray-curable ink for inkjet use of the present invention is excellent in stretch processability and free of blocking.
- Inkjet printing which has been considered difficult to deform in the past, is capable of processing printed matter into various shapes and providing beautiful printed matter without additional equipment such as heat treatment 'topcoat'.
- the application can be greatly expanded to print nameplates that require post-printing workability and cosmetics.
- the active energy ray curable ink for ink jet of the present invention is used for interior and exterior printing applications that require cosmetics, non-printing applications such as printing on CDs and DVDs, and printing on flexible substrates. Suitable for printing on permeable substrates!
- Pigment Dispersion A was prepared with the following composition.
- a dispersion was prepared by adding a pigment and a dispersant to a monomer and stirring the mixture until it became uniform using a speed mixer or the like, and then dispersing the obtained mill base with a horizontal sand mill for about 1 hour.
- Pigment Dispersion B was prepared with the following composition.
- the production method of the dispersion was prepared by the same production method as that of Dispersion A.
- Pigment Dispersion C was prepared with the following composition.
- the production method of the dispersion was prepared by the same production method as that of Dispersion A.
- Pigment Dispersion D was prepared with the following composition.
- the production method of the dispersion was prepared by the same production method as that of Dispersion A.
- Pigment Dispersion E was prepared with the following composition.
- the production method of the dispersion was prepared by the same production method as that of Dispersion A.
- 'Typeta PF740 Ishihara Sangyo silica treatment 1.0%, alumina treatment 2.0% white pigment
- Adhesion to the substrate was achieved by applying cellophane tape to the portion of the cured coating that had been cross-cut into 100 squares at lmm intervals, rubbing it with the top surface eraser, and sufficiently adhering the cellophane tape to the coated surface. Later, the degree of adhesion of the coated film to the substrate when the cellophane tape was peeled at 90 ° was also judged.
- the evaluation criteria are as follows.
- ⁇ ⁇ The force remaining in 100 squares when 100 squares are damaged.
- polycarbonate was overlaid on the cured film, and after pressing with an air laminator at a linear pressure of 11.5 kgfZcm 2 and a speed of 0.3 mZmin, the film was peeled off and the state of the polycarbonate was visually observed.
- Ink is ejected onto a polycarbonate plate with an inkjet ejection device to a thickness of 10 m.
- UV light is irradiated with a 120 WZcm, high pressure mercury lamp from Rison Toshiba Lighting, and then cured.
- the curing speed was evaluated from the conveyor speed when it was determined that the film was cured without any streaks remaining on the cured film by the finger sliding on the film.
- the evaluation criteria are as follows.
- Evaluation method of viscosity stability Measure the viscosity of the ink immediately after preparation, and measure the viscosity again after a 2-day accelerated test in a 60 ° C atmosphere.
- the evaluation criteria are as follows.
- the viscosity was measured using an E-type viscometer under the conditions of 25 ° C. and 20 rpm.
- Examples 1 to 13 are examples in which a monofunctional monomer is blended in an amount of 50% by weight or more. All of the stretch ratios are 20% or more, which is an indication of the presence or absence of stretch processability, and are excellent in stretch processability. I can say that. If the stretching ratio is less than 20%, cracking or breakage will occur even if it is a relatively small process such as punching or folding, and requires deformation. In these examples, since the photopolymerization initiator represented by [Formula 1] or [Formula 2] is used as the photopolymerization initiator, excellent results were shown in the blocking test. The
- Examples 2 to 13 are examples in which the addition amount of the monofunctional monomer is further increased than that in Example 1, and the ink has a stretching ratio of 90% or more and higher stretch workability.
- Example 5 the blocking property, adhesion, stretch ratio, etc. are excellent, and the combination of initiators is excellent! /, So the curing speed is greatly improved.
- Example 6 the curing rate is remarkably increased by using the photopolymerization initiator represented by [Formula 1] and the photopolymerization initiator represented by [Formula 2] in combination.
- Example 7 because the photopolymerization initiator having an absorption peak on the shorter wavelength side than 350 nm is blended as the second photopolymerization initiator, ultraviolet light does not reach the inside of the film, and the dense photopolymerization initiator. Wearability is slightly reduced.
- Example 8 as the second photopolymerization initiator, a photopolymerization initiator having an absorption peak at a wavelength longer than 395 nm was used as the second photopolymerization initiator. Inhibited, the effect of oligo (2-hydroxy-1,2-methyl-1,4- (1- (methylvinyl) phenyl) propanone) is diminished, and the curing speed and adhesion are reduced.
- Example 9 even though the monofunctional monomer was 50% by weight or more in the polymerizable monomer, 2-phenoxychetyl acrylate was 30% by weight or less, and as a result, the adhesion decreased.
- Example 10 a force vinyl whose monofunctional monomer is 50% by weight in the polymerizable monomer By using force prolamtam, the reactivity deteriorates and the curing speed, adhesion and blocking are reduced.
- Example 11 when the monofunctional monomer is 50% by weight in the polymerizable monomer and the strength vinyl force prolamtam is 30% by weight or more in the polymerizable monomer, the stability of the viscosity is deteriorated.
- the printed material which was printed using the ink described in Example 1 and then laminated and coated using the ink described in Example 11 or 12 had excellent blocking properties and a ductility of 37%. Furthermore, when the ink described in Example 1 is replaced with any of the inks described in Examples 2-11, a printed matter having a high and ductility of 90% or more and excellent blocking properties can be obtained. It was.
- Comparative Example 1 As a result of the monofunctional monomer being 40% by weight in the polymerizable monomer, the stretching ratio does not reach 20%, and it cannot be said that the ink has excellent stretch processability. A high content of lead to poor adhesion.
- 1-hydroxy monocyclohexyl monophenol monoketone which is the same photophenone photopolymerization initiator as used in the present invention
- Comparative Examples 2 to 5 show that when a photopolymerization initiator having only one cleavage part is used, the reaction rate is sufficient even when the addition amount is increased or in combination with other initiators. This suggests that you can make blocking-free inks! /
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Ink Jet (AREA)
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002629157A CA2629157A1 (en) | 2005-11-11 | 2006-11-10 | Active energy beam-curable inkjet ink |
US12/093,242 US20090117343A1 (en) | 2005-11-11 | 2006-11-10 | Active energy beam-curable inkjet ink |
JP2007544202A JP5520445B2 (ja) | 2005-11-11 | 2006-11-10 | 活性エネルギー線硬化型インクジェットインキ |
EP06823315A EP1967557B1 (en) | 2005-11-11 | 2006-11-10 | Active energy beam-curable inkjet ink |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2005327134 | 2005-11-11 | ||
JP2005-327134 | 2005-11-11 |
Publications (1)
Publication Number | Publication Date |
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WO2007055333A1 true WO2007055333A1 (ja) | 2007-05-18 |
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ID=38023327
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2006/322493 WO2007055333A1 (ja) | 2005-11-11 | 2006-11-10 | 活性エネルギー線硬化型インクジェットインキ |
Country Status (7)
Country | Link |
---|---|
US (1) | US20090117343A1 (ja) |
EP (1) | EP1967557B1 (ja) |
JP (1) | JP5520445B2 (ja) |
KR (1) | KR101092788B1 (ja) |
CN (1) | CN101305060A (ja) |
CA (1) | CA2629157A1 (ja) |
WO (1) | WO2007055333A1 (ja) |
Cited By (13)
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JP2009120834A (ja) * | 2007-11-12 | 2009-06-04 | Sakata Corp | 光硬化型インクジェット印刷用インク組成物 |
JP2009263525A (ja) * | 2008-04-25 | 2009-11-12 | National Printing Bureau | 樹脂組成物、インキ組成物及びその印刷物 |
JP2009263524A (ja) * | 2008-04-25 | 2009-11-12 | National Printing Bureau | 樹脂組成物、インキ組成物及びその印刷物 |
EP2345703A1 (en) | 2010-01-14 | 2011-07-20 | FUJIFILM Corporation | Inkjet ink composition and inkjet recording method |
JP2011207960A (ja) * | 2010-03-29 | 2011-10-20 | Toyo Ink Sc Holdings Co Ltd | 活性エネルギー線硬化型白色インクジェットインク組成物 |
JP2012052046A (ja) * | 2010-09-02 | 2012-03-15 | Sekisui Chem Co Ltd | インクジェット用硬化性組成物及びプリント配線板の製造方法 |
JP2012087298A (ja) * | 2010-09-24 | 2012-05-10 | Sekisui Chem Co Ltd | インクジェット用硬化性組成物及び電子部品の製造方法 |
JP2015014008A (ja) * | 2014-10-06 | 2015-01-22 | 積水化学工業株式会社 | インクジェット用硬化性組成物及びプリント配線板の製造方法 |
JP2015083656A (ja) * | 2013-09-17 | 2015-04-30 | 株式会社リコー | 活性エネルギー線硬化型インク、インク入りインクカートリッジ、画像乃至硬化物の形成方法、及び画像乃至硬化物の形成装置 |
JP2016028143A (ja) * | 2015-08-19 | 2016-02-25 | 積水化学工業株式会社 | インクジェット用硬化性組成物及びプリント配線板の製造方法 |
JP2017140845A (ja) * | 2010-12-17 | 2017-08-17 | 日立マクセル株式会社 | インクジェット記録用プライマー |
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JP2009120834A (ja) * | 2007-11-12 | 2009-06-04 | Sakata Corp | 光硬化型インクジェット印刷用インク組成物 |
JP2009263525A (ja) * | 2008-04-25 | 2009-11-12 | National Printing Bureau | 樹脂組成物、インキ組成物及びその印刷物 |
JP2009263524A (ja) * | 2008-04-25 | 2009-11-12 | National Printing Bureau | 樹脂組成物、インキ組成物及びその印刷物 |
US8562123B2 (en) | 2010-01-14 | 2013-10-22 | Fujifilm Corporation | Inkjet ink composition and inkjet recording method |
EP2345703A1 (en) | 2010-01-14 | 2011-07-20 | FUJIFILM Corporation | Inkjet ink composition and inkjet recording method |
JP2011207960A (ja) * | 2010-03-29 | 2011-10-20 | Toyo Ink Sc Holdings Co Ltd | 活性エネルギー線硬化型白色インクジェットインク組成物 |
JP2012052046A (ja) * | 2010-09-02 | 2012-03-15 | Sekisui Chem Co Ltd | インクジェット用硬化性組成物及びプリント配線板の製造方法 |
JP2012087298A (ja) * | 2010-09-24 | 2012-05-10 | Sekisui Chem Co Ltd | インクジェット用硬化性組成物及び電子部品の製造方法 |
JP2017140845A (ja) * | 2010-12-17 | 2017-08-17 | 日立マクセル株式会社 | インクジェット記録用プライマー |
JP2015083656A (ja) * | 2013-09-17 | 2015-04-30 | 株式会社リコー | 活性エネルギー線硬化型インク、インク入りインクカートリッジ、画像乃至硬化物の形成方法、及び画像乃至硬化物の形成装置 |
JP2020023702A (ja) * | 2013-09-17 | 2020-02-13 | 株式会社リコー | 活性エネルギー線硬化型インクジェット用インク、インク入りインクカートリッジ、画像乃至硬化物の形成方法、及び画像乃至硬化物の形成装置 |
JP2015014008A (ja) * | 2014-10-06 | 2015-01-22 | 積水化学工業株式会社 | インクジェット用硬化性組成物及びプリント配線板の製造方法 |
JP2016028143A (ja) * | 2015-08-19 | 2016-02-25 | 積水化学工業株式会社 | インクジェット用硬化性組成物及びプリント配線板の製造方法 |
JP2020007565A (ja) * | 2019-09-20 | 2020-01-16 | セイコーエプソン株式会社 | 紫外線硬化型インクジェット組成物及び収容体 |
JP7107293B2 (ja) | 2019-09-20 | 2022-07-27 | セイコーエプソン株式会社 | インクジェット方法、及びインクジェット装置 |
Also Published As
Publication number | Publication date |
---|---|
EP1967557B1 (en) | 2012-02-29 |
KR20080069680A (ko) | 2008-07-28 |
JPWO2007055333A1 (ja) | 2009-04-30 |
KR101092788B1 (ko) | 2011-12-09 |
CN101305060A (zh) | 2008-11-12 |
JP5520445B2 (ja) | 2014-06-11 |
US20090117343A1 (en) | 2009-05-07 |
EP1967557A4 (en) | 2010-04-28 |
EP1967557A1 (en) | 2008-09-10 |
CA2629157A1 (en) | 2007-05-18 |
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