WO2023163064A1 - Ink composition, ink set, recorded matter in which ink composition is applied to base material, recording method, method for producing recorded matter, and inkjet recording device equipped with storage container filled with ink composition - Google Patents

Ink composition, ink set, recorded matter in which ink composition is applied to base material, recording method, method for producing recorded matter, and inkjet recording device equipped with storage container filled with ink composition Download PDF

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Publication number
WO2023163064A1
WO2023163064A1 PCT/JP2023/006539 JP2023006539W WO2023163064A1 WO 2023163064 A1 WO2023163064 A1 WO 2023163064A1 JP 2023006539 W JP2023006539 W JP 2023006539W WO 2023163064 A1 WO2023163064 A1 WO 2023163064A1
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Prior art keywords
ink composition
water
ink
soluble organic
composition according
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PCT/JP2023/006539
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French (fr)
Japanese (ja)
Inventor
保真 齋藤
祐二 牧本
充功 田村
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株式会社Ｄｎｐファインケミカル
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Publication of WO2023163064A1 publication Critical patent/WO2023163064A1/en

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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
    • 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
    • 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
    • C09D11/30—Inkjet printing inks

Definitions

  • the present invention provides an ink composition, an ink set, a recorded matter obtained by applying the ink composition onto a substrate, a recording method, a method for producing a recorded matter, and an ink jet recording method equipped with a container filled with the ink composition. Regarding the device.
  • the inkjet recording method is a recording method in which droplets of an ink composition are directly ejected from very fine nozzles onto a base material such as paper and applied to obtain letters and images.
  • This recording method is easy to reduce size, increase speed, reduce noise, save power, and colorize. , and the range of application has expanded to include commercial printing applications.
  • Aqueous ink compositions in which various coloring materials are dissolved or dispersed in water or a mixture of water and a water-soluble organic solvent are widely used as ink compositions used in inkjet recording systems.
  • Such water-based ink compositions have less impact on the environment than non-aqueous ink compositions containing organic solvents used in the same inkjet recording system, and are non-flammable. Safe for people.
  • the drying temperature can be set high to shorten the drying time rather than extending the drying time. I had to dry it. However, if the drying temperature is high, depending on the base material, warping or the like occurs, so there is also an aspect that the selection range of the base material is narrowed.
  • Patent Document 1 describes a technique related to an inkjet recording method including a step of ejecting an aqueous ink composition containing 2-pyrrolidone and water-insoluble thermoplastic resin particles containing a urethane resin.
  • Japanese Patent Laid-Open No. 2002-100002 describes that the ink jet recording method can obtain an image having high image quality with less bleeding of the ink composition and excellent abrasion resistance.
  • the ink composition contains a resin, it is possible to impart further abrasion resistance to the coating film of the resulting ink composition.
  • An object of the present invention is to provide an ink composition that dries well and improves the scratch resistance of the coating film.
  • the present inventors found that the above problems can be solved by an ink composition containing a water-soluble organic solvent having a predetermined boiling point or less and a resin. was completed. Specifically, the present invention provides the following.
  • An inkjet ink composition containing a water-soluble organic solvent and a resin, at least part of the resin being a dispersible resin, the water-soluble organic solvent having a boiling point of 230°C.
  • the dispersible resin includes acrylic resin, polyurethane resin, polyester resin, vinyl chloride resin, vinyl acetate resin, polyether resin, vinyl chloride vinyl acetate copolymer resin, polyethylene resin, and acrylamide resin.
  • the ink according to any one of (1) to (4), containing one or more resins or copolymer resins selected from the group consisting of resins, epoxy resins, polycarbonate resins, silicone resins, and polystyrene resins. Composition.
  • the water-soluble organic solvent A is an amide solvent having a boiling point of 230° C. or less represented by the following formula (1), a cyclic ester solvent having a boiling point of 230° C. or less represented by the following formula (2), and any one of (1) to (7) containing at least one water-soluble organic solvent A selected from glycol ether solvents having a boiling point of 230° C. or less represented by the following formula (3): ink composition.
  • R 1 is hydrogen or an alkyl group having 1 to 4 carbon atoms
  • R 2 and R 3 are functional groups.
  • R 5 is a carbon chain having an alkylene group having 3 to 5 carbon atoms or a vinylene group
  • R 6 represents hydrogen, an alkyl group having 1 to 2 carbon atoms, or a vinylidene group.
  • R 6 may be present at any position on the carbon chain of R 5 , and may be plural, and R 5 and R 6 may be linked by either a single bond or a multiple bond.
  • R 7 R 9 is hydrogen, an alkyl group, or an acyl group, at least one of which is an alkyl group or an acyl group;
  • R 8 represents an ethylene group or a propylene group;
  • n is 2; Represents an integer of ⁇ 4.
  • the water-soluble organic solvent A is N-ethyl-N-methylformamide, N-methyl-N-propylformamide, N,N-diethylformamide, N-ethyl-N-propylformamide, N,N-dimethyl Acetamide, N-ethyl-N-methylacetamide, N-methyl-N-propylacetamide, N,N-diethylacetamide, N,N-dimethylpropanamide, N-ethyl-N-methylpropanamide, ⁇ -butyrolactone, ⁇ -methylene- ⁇ -butyrolactone, ⁇ -caprolactone, diethylene glycol monoethyl ether, dipropylene glycol monomethyl ether, and diethylene glycol monoisobutyl ether
  • the ink composition according to any one of (1) to (8). .
  • a leveling agent is further included, and the content of the leveling agent is in the range of 0.1 parts by mass or more and 50 parts by mass or less with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition.
  • the ink composition according to any one of (1) to (17).
  • the ink composition according to any one of (1) to (19) or the ink set according to (20) is applied onto a substrate by an inkjet method, and then the ink composition is applied to the ink composition.
  • a method for producing recorded matter comprising applying the ink composition according to any one of (1) to (19) or the ink composition contained in the ink set according to (20) onto a substrate by an inkjet method. .
  • the ink composition of the present invention is highly dry and can form a coating film with high scratch resistance.
  • the ink composition according to the present embodiment is an ink composition for inkjet and contains a water-soluble organic solvent.
  • the water-soluble organic solvent contains one or more water-soluble organic solvents A selected from amide solvents with a boiling point of 230°C or lower, cyclic ester solvents with a boiling point of 230°C or lower, and glycol ether solvents with a boiling point of 230°C or lower. characterized by Such an ink composition containing a predetermined organic solvent having a boiling point of 230° C. or less has high drying properties, and the resulting recorded matter has good scratch resistance.
  • the ink composition according to the present embodiment contains a resin.
  • a water-soluble organic solvent A an amide solvent with a boiling point of 230° C. or lower, a cyclic ester solvent with a boiling point of 230° C. or lower, and a glycol ether solvent with a boiling point of 230° C. or lower
  • it acts as a film-assisting agent.
  • a temperature equal to or higher than a predetermined temperature (minimum film-forming temperature) during film formation of the ink composition, the resin contained in the ink composition can be fused to form a scratch-resistant coating film.
  • a predetermined temperature minimum film-forming temperature
  • the minimum film-forming temperature is generally around the Tg of the resin, but the water-soluble organic solvent A contained in the ink composition makes it possible to lower the minimum film-forming temperature. Even if the drying temperature is as low as the temperature, the resin can be fused on the substrate, and a coating film having sufficient scratch resistance can be formed.
  • the ink composition according to the present embodiment may be a colored ink containing a coloring material.
  • coloring material includes dyes and pigments, such as yellow, magenta, cyan, black, and dyes contained in colored inks that form images such as intermediate colors and light colors thereof, or The concept includes pigments, white dyes or white pigments contained in white ink, and bright pigments contained in metallic ink.
  • the colored inks may be yellow, magenta, cyan, black, and colored inks that form images such as intermediate colors and light colors thereof. Further, the colored ink may be white ink containing a white colorant, metallic ink containing a bright pigment, or the like.
  • the ink composition according to the present embodiment may be a receiving solution containing a cationic compound that is applied to the substrate prior to applying the colored ink to the substrate.
  • it may be a clear ink containing no coloring material, or an overcoat ink for forming an overcoat layer on the surface of a printed matter.
  • the clear ink containing no coloring material may or may not contain a resin.
  • the ink composition according to this embodiment contains a water-soluble organic solvent.
  • the water-soluble organic solvent is 5 parts by mass or more, preferably 20 parts by mass or more, more preferably 50 parts by mass or more, and still more preferably 70 parts by mass in 100 parts by mass of water at 25°C under 1 atmosphere. Parts or more, more preferably 90 parts by mass or more can be dissolved.
  • the water-soluble organic solvent is one or more water-soluble organic solvents A selected from amide solvents with a boiling point of 230°C or lower, cyclic ester solvents with a boiling point of 230°C or lower, and glycol ether solvents with a boiling point of 230°C or lower. contains.
  • the water-soluble organic solvent A will be described below.
  • amide-based solvent with a boiling point of 230°C or lower is an organic is a solvent.
  • amide-based solvents having a boiling point of 230° C. or lower include alkoxyalkylamide-based solvents having an alkoxyalkyl group (C n H 2n+1 —O—C m H 2m —) and alkyl groups having an alkyl group (C n H 2n+1 —).
  • Examples include amide-based solvents and cyclic amide-based solvents having a cyclic structure and a —C( ⁇ O)—N— group in the cyclic structure.
  • the amide-based solvent having a boiling point of 230°C or lower is preferably an alkylamide-based solvent, an alkoxyalkylamide-based solvent, or a cyclic amide-based solvent, and more preferably an alkylamide-based solvent.
  • an alkylamide-based solvent, an alkoxyalkylamide-based solvent, or a cyclic amide-based solvent By containing an alkylamide-based solvent, an alkoxyalkylamide-based solvent, or a cyclic amide-based solvent, the ink composition exhibits the effects of the present invention.
  • alkylamide-based solvent those having, for example, the following structures can be preferably used.
  • R 1 is hydrogen or an alkyl group having 1 to 4 carbon atoms, and R 2 and R 3 are functional groups.
  • R 2 and R 3 are not particularly limited as long as they are functional groups.
  • R 2 and R 3 are preferably hydrogen, an alkyl group, an alkoxy group, a hydroxyalkyl group or a hydroxyl group. more preferably hydrogen or an alkyl group having 1 to 4 carbon atoms.
  • R 2 and R 3 may be the same or different.
  • alkylamide-based solvents in which R 1 to R 3 in formula (1) are hydrogen or alkyl groups include formamide, acetamide, propanamide, butanamide, isobutylamide, pentanamide, and N-methylformamide.
  • R 2 and R 3 in formula (1) are alkoxy groups, hydroxyl groups, and hydroxyalkyl groups
  • R 2 and R 3 in formula (1) are alkoxy groups, hydroxyl groups, and hydroxyalkyl groups
  • examples of those in which R 2 and R 3 in formula (1) are alkoxy groups, hydroxyl groups, and hydroxyalkyl groups include N-ethyl-N-(2-methoxyethyl)formamide and N-methoxymethylformamide. , N-hydroxymethyl-N-methylacetamide, N-(2-hydroxyethyl)-N-methylacetamide, N-methoxymethyl-N-methylformamide, or those having a different carbon number or a branched carbon chain structure etc.
  • N-ethyl-N-methylformamide N-methyl-N-propylformamide, N,N-diethylformamide, N-ethyl-N-propylformamide, N
  • a more selected alkylamide solvent is particularly preferred.
  • alkoxyalkylamide-based solvent for example, among alkylamide-based solvents having an alkylamide-based structure represented by formula (2), those having a boiling point of 230° C. or lower can be preferably used.
  • R 12 is each independently an alkyl group having 1 to 4 carbon atoms
  • R 13 is an alkylene group having 1 to 4 carbon atoms
  • R 10 and R 11 are each independently It is a functional group that may be independent.
  • R 12 is preferably an alkyl group having 1 or more and 2 or less carbon atoms, more preferably an alkyl group having 1 or more and 2 or less carbon atoms.
  • R 13 is preferably an alkylene group having 1 to 3 carbon atoms, more preferably an alkylene group having 1 to 2 carbon atoms.
  • R 10 and R 11 are not particularly limited as long as they are functional groups.
  • R 10 and R 11 are preferably hydrogen, an alkyl group, an alkoxy group, a hydroxyalkyl group, or a hydroxyl group. more preferably hydrogen or an alkyl group having 1 to 4 carbon atoms, more preferably hydrogen or an alkyl group having 1 to 2 carbon atoms
  • alkoxyalkylamide-based solvent 3-methoxy-N,N-dimethylpropanamide, 3-propoxy-N,N-dimethylpropanamide, or the difference in the number of carbon atoms in the alkoxy group or alkyl group or the branched structure of the carbon chain. of those having a boiling point of 230° C. or lower are preferred. Among these, 3-methoxy-N,N-dimethylpropanamide is particularly preferable from the viewpoint of exhibiting the effects of the present invention.
  • the alkylamide solvent those having a boiling point of 230° C. or lower among the cyclic amide solvents represented by the formulas (3) to (5) can be preferably used.
  • R 4 is an optionally branched alkylene group having 3 to 5 carbon atoms
  • R 5 is hydrogen, an alkyl group having 1 to 4 carbon atoms, or an unsaturated hydrocarbon group. represent.
  • R 4 is preferably an alkylene group having 3 or more and 4 or less carbon atoms.
  • R5 is preferably hydrogen, an alkyl group having 1 to 2 carbon atoms, or an unsaturated hydrocarbon group.
  • R 14 is hydrogen, an optionally branched alkyl group having 1 to 4 carbon atoms, or an unsaturated hydrocarbon group, and R 15 represents an alkylene group having 1 to 4 carbon atoms.
  • R 16 and R 17 are each independently hydrogen, an optionally branched alkyl group having 1 to 4 carbon atoms, or an unsaturated hydrocarbon group, and R 18 is 1 to 4 carbon atoms. represents the following optionally branched alkylene group.
  • Cyclic amide solvents include N-vinylmethyloxazolidinone, 1,3-dimethyl-2-pyrrolidone, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, ⁇ -lactam, 4-methoxy-1-methyl -2-pyrrolidinone, N-propyl-2-pyrrolidone, N-methyl-2-piperidinone, or those having a branched carbon chain structure or a different number of carbon atoms in their alkoxy or alkyl groups, those having a boiling point of 230°C or less is preferred.
  • N-methyl-2-pyrrolidone is particularly preferable from the viewpoint of exhibiting the effects of the present invention.
  • a cyclic ester solvent having a boiling point of 230° C. or less can preferably be used, for example, having the following structure.
  • R 5 is a carbon chain having an alkylene group having 3 to 5 carbon atoms or a vinylene group
  • R 6 represents hydrogen, an alkyl group having 1 to 2 carbon atoms, or a vinylidene group.
  • R 6 may be at any position in the carbon chain of R 5 and may be plural, and R 5 and R 6 may be linked by either a single bond or a multiple bond.
  • R 5 is preferably an alkylene group having 4 or more and 5 or less carbon atoms, more preferably an alkylene group having 5 carbon atoms.
  • R 6 is preferably hydrogen or an alkyl group having 1 carbon atom, more preferably hydrogen.
  • R 8 is hydrogen or an alkyl group having 1 to 4 carbon atoms
  • R 9 represents an alkylene group having 1 to 3 carbon atoms.
  • cyclic ester solvents examples include ⁇ -butyrolactone, ⁇ -methylene- ⁇ -butyrolactone, ⁇ -caprolactone, ⁇ -valerolactone, ⁇ -hexanolactone, ⁇ -heptanolactone, ⁇ -valerolactone, ⁇ -hexanolactone, ⁇ -heptalactone, ⁇ -octalactone, ⁇ -nonalactone, ⁇ -decalactone, ⁇ -undecalactone, ⁇ , ⁇ -dimethyl- ⁇ -butyrolactone, ⁇ -methyl- ⁇ -butyrolactone, ⁇ - Crotolactone, ⁇ -methylene- ⁇ -butyrolactone, ⁇ -methyl- ⁇ -butyrolactone, 6-methylvalerolactone, 2,3-butylene carbonate, ethylene carbonate, propylene carbonate, etc. with a boiling point of 230°C or less can be done.
  • Glycol ether solvent with a boiling point of 230°C or less A glycol ether solvent with a boiling point of 230°C or less means that the boiling point is 230°C or less, and the OH groups at one or both ends of the polyalkylene glycol are alkyl or acyl. , is an aryl-substituted organic solvent. Glycol ether solvents having a boiling point of 230° C. or less can preferably be used, for example, having the following structure.
  • R 7 and R 9 are hydrogen, an alkyl group, or an acyl group, at least one of which is an alkyl group or an acyl group.
  • R 8 represents an ethylene group or a propylene group.
  • n represents an integer from 2 to 4.
  • glycol ether solvents include ethylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether, diethylene glycol monomethyl (or ethyl, propyl , isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether, triethylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n -hexyl, 2-ethylhexyl) ether, propylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobut
  • the organic solvent A preferably contains an amide-based solvent having a boiling point of 230° C. or less, and particularly preferably contains an alkylamide-based solvent.
  • the water-soluble organic solvent A may contain two or more water-soluble organic solvents A.
  • an ink composition containing at least two or more amide-based solvents having a boiling point of 230°C or lower, and (2) at least an amide-based solvent having a boiling point of 230°C or lower and a cyclic ester-based solvent having a boiling point of 230°C or lower. and an ink composition containing (3) an amide solvent having a boiling point of 230° C. or less and a glycol ether solvent having a boiling point of 230° C. or less, and (4) a cyclic ester having a boiling point of 230° C. or less and an ink composition containing a glycol ether solvent having a boiling point of 230° C. or lower.
  • water-soluble organic solvents A with a high water/1-octanol partition coefficient (LogP) are preferred.
  • the partition coefficient is an index of the hydrophobicity of an organic solvent, and a higher organic solvent with a higher partition coefficient (LogP) in water/1-octanol means that the organic solvent has relatively higher hydrophobicity. is.
  • An ink composition containing a water-soluble organic solvent A having a boiling point of 230° C. or less has high drying properties and high productivity of the resulting recorded matter. If the treatment is shortened or the drying treatment is performed at a low temperature, the film-forming property of the ink composition containing the dispersible resin is lowered, and the abrasion resistance is relatively lowered.
  • An ink composition containing a dispersible resin by containing a water-soluble organic solvent A having a high water/1-octanol partition coefficient (LogP) that is, a water-soluble organic solvent A having relatively high hydrophobicity
  • the ink composition is capable of forming a coating film having high scratch resistance.
  • the water-soluble organic solvent A having a boiling point of 230° C. or less preferably has a water/1-octanol distribution coefficient (LogP) of ⁇ 0.6 or more, and preferably ⁇ 0.4 or more. is more preferable, and ⁇ 0.3 or more is even more preferable.
  • LogP water/1-octanol distribution coefficient
  • the water-soluble organic solvent A having a boiling point of 230° C. or less preferably has a water/1-octanol distribution coefficient (LogP) of 1.5 or less, more preferably 1.0 or less, and 0.5. More preferably: By containing the water-soluble organic solvent A having a water/1-octanol partition coefficient (LogP) of 1.5 or less, the compatibility with the dispersible resin or the like contained in the ink composition is increased, and the ink composition Good storage stability of the product.
  • LogP water/1-octanol distribution coefficient
  • the boiling point of the water-soluble organic solvent A having a boiling point of 230°C or lower is preferably 220°C or lower, more preferably 210°C or lower. As a result, an ink composition having higher drying properties can be obtained.
  • the boiling point of the water-soluble organic solvent A having a boiling point of 230° C. or lower is preferably 130° C. or higher, more preferably 140° C. or higher, and even more preferably 150° C. or higher. When the boiling point of the water-soluble organic solvent A is 130° C. or higher, it is possible to suppress deterioration in ejection stability due to increased drying properties on the nozzle surface.
  • the content of the water-soluble organic solvent A having a boiling point of 230° C. or lower is not particularly limited, but is preferably in the range of 2% by mass or more, and in the range of 5% by mass or more in the total amount of the ink composition. is more preferable, and 10% by mass or more is even more preferable. As a result, an ink composition having a higher film-forming property of the resin particles is obtained.
  • the content of the water-soluble organic solvent A having a boiling point of 230° C. or less is preferably 40% by mass or less, more preferably 35% by mass or less, and preferably 30% by mass or less in the total amount of the ink composition. More preferred. As a result, an ink composition having good compatibility with other components and good ink storage stability can be obtained.
  • the content of the water-soluble organic solvent A can be controlled according to the content of the dispersible resin contained in the ink composition.
  • the content of the water-soluble organic solvent A with respect to 100 parts by mass of the dispersible resin is preferably 30 parts by mass or more, more preferably 50 parts by mass or more, and 65 parts by mass or more. is more preferred.
  • an ink composition having a higher film-forming property of the resin particles is obtained.
  • the ink composition according to the present embodiment may contain other water-soluble organic solvents different from the water-soluble organic solvent A.
  • water-soluble organic solvents examples include 3-methyl-2-oxazolidinone, 3-ethyl-2-oxazolidinone, 3-methyl-2-pyrrolidinone, 2-pyrrolidone, N-methyl-N-(1-methyl ethyl)formamide, N-hydroxypropyl-N-methylacetamide, 3-butoxy-N,N-dimethylpropanamide, ⁇ -lactam, ⁇ -lactam, ⁇ -caprolactam, N-2-hydroxyethyl-2-pyrrolidone, ethylene Amide solvents such as urea, N-hydroxyethyleneurea, 3-methoxypropanamide, 3-butoxypropanamide, N,N-dibutyl-3-methoxypropanamide, N,N-dibutyl-3-butoxypropanamide; alkyl alcohols having 1 to 5 carbon atoms such as methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol
  • Oxyethylene or oxypropylene copolymer ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, 1,3-propanediol, isobutylene glycol, triethylene glycol, tripropylene glycol, tetraethylene glycol, 2-methyl-1,2 -propanediol, 2-methyl-1,2-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,2-pentanediol, 1,3-pentanediol, 1,2-hexanediol, 1,5-pentanediol, 1,6-hexanediol, 2-methyl-2,4-pentanediol, 3-methyl-1,3-butanediol, 3-methyl-1,5 - diols such as pentanediol and 2-methyl-2,4-pentaned
  • diol-based solvents are preferred, alkanediol-based solvents are more preferred, and 1,2-alkanediol-based solvents are even more preferred.
  • the diol-based solvent is highly miscible with other components contained in the ink composition, and is less volatile than the water-soluble organic solvent A, which has a boiling point of 230° C. or less. It is possible to prevent this, and it is possible to improve the ejection stability.
  • alkanediol-based solvents it is particularly preferable to contain an alkanediol-based solvent having 3 or more and 6 or less carbon atoms and having at least one hydroxyl group at at least one end of the carbon skeleton.
  • the content of the other water-soluble organic solvent is not particularly limited. is more preferably 10% by mass or more, and even more preferably 15% by mass or more. It is preferably 35% by mass or less, more preferably 30% by mass or less, and even more preferably 25% by mass or less, based on the total amount of the ink composition.
  • the ink composition according to this embodiment may contain water.
  • the water content is not particularly limited, but the lower limit of the water content is preferably in the range of 30% by mass or more, more preferably in the range of 45% by mass or more, based on the total amount of the ink composition. , 50% by mass or more.
  • the upper limit of the water content is preferably within the range of 85% by mass or less, more preferably within the range of 80% by mass or less, and within the range of 75% by mass or less in the total amount of the ink composition. is more preferred.
  • the solvent other than water in the ink composition when water is contained, the solvent other than water in the ink composition must be composed of a highly hydrophilic solvent from the standpoint of storage stability.
  • a water-soluble solvent is selected.
  • the drying property tends to deteriorate particularly in low-temperature drying, and the problem of the present invention that the drying property deteriorates occurs more remarkably. will do.
  • the ink composition according to the present embodiment contains an amide-based solvent having a predetermined boiling point or less, even if it is an aqueous ink composition containing water, it becomes possible to improve the drying property, and it is possible to obtain It is possible to increase the productivity of printed matter.
  • the ink composition according to this embodiment contains a resin. Thereby, the scratch resistance of the coating film can be improved.
  • the ink composition according to the present embodiment is used as an overcoat ink, it is possible to impart suitable scratch resistance to a recorded matter by containing a resin.
  • the ink composition according to the present embodiment contains a water-soluble organic solvent A (an amide solvent with a boiling point of 230° C. or lower, a cyclic ester solvent with a boiling point of 230° C. or lower, and a Since it contains a glycol ether solvent), it is possible to fuse the resin on the substrate even at a low drying temperature such as a temperature below the Tg of the resin, and it has sufficient scratch resistance. It is possible to form a coating film having In particular, when the ink composition according to the present embodiment is used as an overcoat ink, it is possible to impart suitable scratch resistance to a recorded matter by containing a resin.
  • a water-soluble organic solvent A an amide solvent with a boiling point of 230° C. or lower, a cyclic ester solvent with a boiling point of 230° C. or lower, and a Since it contains a glycol ether solvent
  • a dispersible resin is contained from the viewpoint of excellent fixability and excellent water resistance of the ink composition layer.
  • the resin can be dispersed as fine resin particles in the ink composition by electrostatic repulsion or steric repulsion, and dispersion stability can be improved.
  • the dispersible resin is a resin that is dispersed in the ink composition in the form of particles, and means a resin that can be dispersed in the ink composition in the form of particles.
  • One or more resins selected from the group consisting of acrylamide-based resins, epoxy-based resins, polycarbonate-based resins, silicone-based resins, and polystyrene-based resins, or copolymer resins, or mixtures thereof can be used. .
  • These are preferable because they can improve not only water resistance but also solvent resistance.
  • at least one of the constituent monomers is an acrylic resin having an acrylic skeleton or a copolymer with an acrylic resin (acrylic copolymer resin).
  • the Tg (glass transition temperature) of the resin contained in the ink composition according to the present embodiment is not particularly limited, it is preferably higher than the drying temperature of the ink composition. Specifically, the Tg of the resin is preferably 50° C. or higher, more preferably 55° C. or higher, and even more preferably 60° C. or higher. Originally, when the Tg of the resin contained in the ink composition increases, the resin cannot be fused onto the substrate unless the drying temperature is increased, and the abrasion resistance and solvent resistance suitable for recorded matter are improved. , it becomes difficult to impart water friction resistance.
  • the ink composition according to the present embodiment contains the water-soluble organic solvent A acting as a film-forming aid, even if it contains a resin having a high Tg, the resin can be fused on the substrate by low-temperature drying. It is possible to impart suitable abrasion resistance, solvent resistance, and water abrasion resistance to the recorded matter.
  • dispersible resins include, for example, ACRYT WEM-031U, WEM-200U, WEM-321, WEM-3000, WEM-202U, WEM-3008 (manufactured by Taisei Fine Chemical Co., Ltd., acrylic-urethane dispersible resin). , AKW107, RKW-500 (manufactured by Taisei Fine Chemical Co., Ltd., acrylic dispersible resin), LUBRIJET N240 (manufactured by Lubrizol, acrylic dispersible resin), Superflex 150, 210, 470, 500M, E2000, E4800, R5002 (No.
  • the content of the resin (dispersible resin) contained in the ink composition is not particularly limited, but the lower limit of the content of the resin is preferably 0.05% by mass or more based on the total amount of the ink composition. , preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and more preferably 1% by mass or more. Thereby, the scratch resistance of the coating film can be further improved.
  • the upper limit of the resin content is preferably 25% by mass or less, more preferably 20% by mass or less, and even more preferably 15% by mass or less, based on the total amount of the ink composition. This makes it possible to improve ejection stability.
  • the average particle size of the dispersible resin is preferably 30 nm or more, more preferably 40 nm or more, and even more preferably 50 nm or more.
  • the average particle size of the dispersible resin is preferably 300 nm or less, more preferably 270 nm or less, and even more preferably 250 nm or less. This makes it easier for the particles of the dispersible resin to fuse with each other, so that the film formability is improved. In addition, it becomes possible to further improve the ejection stability of the inkjet.
  • the resin when the resin is a particulate dispersible resin, the resin particles contained in the ink composition are more densely filled with each other as the water-soluble organic solvent gradually volatilizes during film formation of the ink composition.
  • the average particle size of the dispersible resin is 300 nm or less, the contact area between the densely packed resin particles increases, and the fusion tends to proceed. As a result, the resin particles can be fused together more effectively on the base material, and a coating film with higher scratch resistance can be formed.
  • the ink composition according to the present embodiment contains a water-soluble organic solvent A (an amide solvent with a boiling point of 230° C. or lower, a cyclic ester solvent with a boiling point of 230° C.
  • the average particle size of the dispersible resin can be measured using a concentrated particle size analyzer (manufactured by Otsuka Electronics Co., Ltd., model: FPAR-1000) at a measurement temperature of 25°C.
  • the weight average molecular weight of the dispersible resin is preferably 10,000 or more, more preferably 50,000 or more, and even more preferably 100,000 or more, from the viewpoint of the water resistance of the ink composition layer.
  • the mass average molecular weight of the dispersible resin is preferably 2,000,000 or less, more preferably 1,500,000 or less, and more preferably 1,000,000 or less.
  • the molecular weight of the resin indicates the mass average molecular weight Mw, which is a value measured by GPC (gel permeation chromatography), using "HLC-8120GPC" manufactured by Tosoh Corporation. , can be measured using a polystyrene standard for a calibration curve as a standard.
  • the ink composition according to this embodiment may contain a leveling agent. Although it is not essential that the ink composition according to the present embodiment contains a leveling agent, the inclusion of the leveling agent allows the ink composition applied on the substrate to spread more wetly. The surface area of the interface between the ink composition and the ambient air is increased. As a result, the ink composition according to the present embodiment containing the water-soluble organic solvent A can be dried more effectively, and the effects of the present invention can be exhibited particularly effectively.
  • a leveling agent makes it easier to wet the base material, making density unevenness less likely to occur.
  • the type of leveling agent is not particularly limited.
  • surfactants such as anionic surfactants, nonionic surfactants, silicone (silicon) surfactants, fluorine surfactants, and acetylene glycol surfactants.
  • surfactants such as silicone (silicon)-based surfactants, acetylene glycol-based surfactants, and alkane glycol-based surfactants are preferred.
  • silicone (silicon)-based surfactants acetylene glycol-based surfactants, and alkane glycol-based surfactants are preferred.
  • the liquid repellency with respect to the nozzle plate can be improved.
  • silicone (silicon)-based surfactant the surface of the coating film has good lubricity and the abrasion resistance of the coating film is improved.
  • Emal Latemul
  • Pelex Neoperex
  • Demol all of which are anionic surfactants; manufactured by Kao Corporation
  • Sunol Liporan, Lipon, and Ripal (all of which are anionic surfactants; Lion Co., Ltd.
  • a leveling agent with an HLB value of 15 or less is preferable. If the leveling agent has an HLB value of 15 or less, the leveling agent tends to be oriented at the interface between the ink composition applied on the substrate and the outside air, and the ink composition spreads more easily. The composition dries more effectively.
  • the content of the leveling agent is 10% of the water-soluble organic solvent A having a boiling point of 230° C. or less contained in the ink composition according to the present embodiment. It is preferable to control according to the content.
  • the water-soluble organic solvent A having a boiling point of 230° C. or less is a relatively hydrophobic water-soluble organic solvent among water-soluble organic solvents. ° C. or lower, the leveling agent becomes more likely to dissolve in the water-soluble organic solvent A, and the orientation of the leveling agent at the interface with the outside air may become difficult. Therefore, by appropriately controlling the content according to the content of the water-soluble organic solvent A having a boiling point of 230° C. or less, the ink composition can spread wetly, so that the ink composition can be effectively dried. Become.
  • the content of the leveling agent is preferably in the range of 0.1 parts by mass or more with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. As a result, the ink composition is further wetted and spread, so that the ink composition dries more effectively.
  • the content of the leveling agent is more preferably in the range of 0.3 parts by mass or more, and in the range of 0.6 parts by mass or more with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. It is more preferable that the content is in the range of 1.0 parts by mass or more.
  • the content of the leveling agent is preferably in the range of 50 parts by mass or less with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. This improves the compatibility of the leveling agent with the amide solvent.
  • the content of the leveling agent is more preferably in the range of 49 parts by mass or less, more preferably in the range of 48 parts by mass or less with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. preferable.
  • the ink composition according to this embodiment may contain a coloring material.
  • the ink composition according to the present embodiment does not necessarily contain a coloring material. It is possible to use white ink or metallic ink that will serve as a base layer.
  • the coloring material may be either a dye or a pigment.
  • the pigment that can be used in the ink composition according to the present embodiment is not particularly limited, and examples thereof include organic pigments and inorganic pigments used in conventional ink compositions. These may be used individually by 1 type, or may be used in combination of 2 or more type. Note that the ink composition according to the present embodiment may not contain a coloring material.
  • the dispersion stability of the pigment can be improved by using a dispersant or dispersing aid (pigment derivative), which will be described later.
  • organic pigments include, for example, insoluble azo pigments, soluble azo pigments, derivatives from dyes, phthalocyanine-based organic pigments, quinacridone-based organic pigments, perylene-based organic pigments, perinone-based organic pigments, azomethine-based organic pigments, and anthraquinone-based pigments.
  • Organic pigments (anthrone-based organic pigments), xanthene-based organic pigments, diketopyrrolopyrrole-based organic pigments, dioxazine-based organic pigments, nickel azo-based pigments, isoindolinone-based organic pigments, pyranthrone-based organic pigments, thioindigo-based organic pigments, condensed azo organic solid solution pigments such as organic pigments, benzimidazolone organic pigments, quinophthalone organic pigments, isoindoline organic pigments, quinacridone solid solution pigments, perylene solid solution pigments, and other pigments such as lake pigments and carbon black. be done.
  • C.I. color index
  • azo dyes benzoquinone dyes, naphthoquinone dyes, anthraquinone dyes, cyanine dyes, squarylium dyes, croconium dyes, Merocyanine dyes, stilbene dyes, diarylmethane dyes, triarylmethane dyes, fluorane dyes, spiropyran dye
  • inorganic pigments that can be used in the ink composition according to the present embodiment include titanium oxide, barium sulfate, calcium carbonate, zinc oxide, barium carbonate, silica, talc, clay, synthetic mica, alumina, and zinc.
  • flower, lead sulfate, yellow lead, zinc yellow, red iron oxide (iron (III)), cadmium red, ultramarine blue, dark blue, chromium oxide green, cobalt green, amber, titanium black, aluminum, titanium, indium, synthetic iron black, Inorganic solid solution pigments and the like can be mentioned.
  • the average dispersed particle size of these organic pigments or inorganic pigments is not particularly limited as long as the desired color development is possible. Although it varies depending on the type of pigment, the lower limit of the average dispersed particle diameter of the pigment is preferably in the range of 10 nm or more, preferably 20 nm or more, from the viewpoint of obtaining sufficient coloring power with good dispersion stability of the pigment. It is more preferably within the range, and even more preferably within the range of 30 nm or more.
  • the upper limit of the average dispersed particle size of the pigment is preferably 500 nm or less, more preferably 400 nm or less, and even more preferably 350 nm or less.
  • the average dispersed particle size is 500 nm or less, nozzle clogging of an inkjet head is unlikely to occur, and a uniform image with high reproducibility can be obtained.
  • the average dispersed particle diameter is 10 nm or more, the light resistance of the resulting printed matter can be improved.
  • the average dispersed particle diameter of the pigment is the average particle diameter ( D50).
  • the ink composition according to the present embodiment may contain a luster pigment as a pigment.
  • Luminous pigments include metal-containing luster pigments that are at least one of simple metals such as aluminum, silver, gold, nickel, chromium, tin, zinc, indium, titanium, and copper; metal compounds; alloys and mixtures thereof; Pearl pigments having pearl luster or interference luster such as mica, fish scale foil, bismuth oxychloride, silicon dioxide, metal oxides, metal compounds, and laminates thereof may be mentioned.
  • the glitter pigment preferably has a plate-like shape (also referred to as a fine plate-like shape, a scale-like shape, or the like). This makes it possible to impart a more suitable metallic luster to the subject.
  • the content of the coloring material is preferably 0.05% by mass or more, more preferably 0.08% by mass or more, based on the total amount of the ink composition. is more preferable, and 0.1% by mass or more is even more preferable.
  • the content of the coloring material is preferably 20.0% by mass or less, and 17.0% by mass or less, based on the total amount of the ink composition. is more preferable, and 15.0% by mass or less is even more preferable.
  • the ink composition according to this embodiment may contain a pigment dispersant.
  • the ink composition according to the present embodiment does not necessarily contain a pigment dispersant, but by containing the pigment dispersant together with the pigment, the dispersibility of the pigment can be improved.
  • pigment dispersant means a resin or surfactant that adheres to a part of the pigment surface and has a function of improving the dispersibility of the pigment in the ink composition.
  • the pigment dispersant that can be used in the ink composition according to the present embodiment is not particularly limited.
  • cationic, anionic, nonionic, amphoteric, silicone (silicon), and fluorine surfactants can be used.
  • surfactants polymer surfactants (polymer dispersants) such as those exemplified below are preferred.
  • a water-soluble polymer dispersant can be preferably used as a pigment dispersant that can be used in the ink composition according to the present embodiment.
  • water-soluble polymer dispersants include polyester-, polyacrylic-, polyurethane-, polyamine-, and polycaptolactone-based main chains, and side chains containing amino groups, carboxyl groups, sulfone groups, and hydroxyl groups.
  • (co)polymers of unsaturated carboxylic acid esters such as polyacrylic acid esters; copolymers of aromatic vinyl compounds such as styrene and ⁇ -methylstyrene and unsaturated carboxylic acid esters such as acrylic acid esters; (partial) amine salts, (partial) ammonium salts and (partial) alkylamine salts of (co)polymers of unsaturated carboxylic acids such as polyacrylic acid; hydroxyl group-containing unsaturated carboxylic acid esters such as hydroxyl group-containing polyacrylic acid esters Polyurethanes; Unsaturated polyamides; Polysiloxanes; Long-chain polyaminoamide phosphates; Polyethyleneimine derivatives (poly (lower alkylene imine) and free carboxyl group-containing polyester amides obtained by reaction and their bases); polyallylamine derivatives (polyallylamine and polyester having a free carboxyl group
  • water-soluble polymer dispersant examples include Cray Valley's SMA1440, SMA2625, SMA17352, SMA3840, SMA1000, SMA2000, SMA3000, BASF Japan's JONCRYL67, JONCRYL678, JONCRYL586, JONCRYL611, JONCRYL680, JONCRYL682, JONCRYL690, JONCRYL819, JONCRYL -JDX5050, EFKA4550, EFKA4560, EFKA4585, EFKA5220, EFKA6230, Dispex Ultra PX4575, Lubrizol SOLSPERSE20000, SOLSPERSE27000, SOLSPERSE40000, SOLSPERSE410 00, SOLSPERSE41090, SOLSPERSE43000, SOLSPERSE44000, SOLSPERSE45000, SOLSPERSE46000, SOLSPERSE47000, SOLSPERSE53095, SOLSPERSE54000,
  • the ink composition according to this embodiment may contain a cationic compound.
  • the ink composition according to the present embodiment does not necessarily contain a cationic compound. can do.
  • the coloring ink containing the coloring material is anionic.
  • cationic compounds include polyvalent metal salts (polyvalent metal ions) and cationic resins.
  • Polyvalent metal salts mainly contain ions and anions of polyvalent metals.
  • the concept of "containing a polyvalent metal salt” includes not only those to which a polyvalent metal salt is added during preparation of the receiving solution, but also compounds capable of generating polyvalent metal ions and compounds capable of generating anions. and are added at the time of preparation of the receiving solution to contain the polyvalent metal ions and the anions constituting the polyvalent metal salt.
  • the anion may be an anion of an inorganic substance or an anion of an organic substance.
  • the anions preferably include organic anions.
  • inorganic anions include chloride ions, bromide ions, nitrate ions, and sulfate ions.
  • organic anions include acetic acid, benzoic acid, salicylic acid, 2,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid, dimethylolpropionic acid, pantothenic acid, succinic acid, maleic acid, glutaric acid, Mention may be made of the anions of suberic acid, trimellitic acid, methylmalonic acid.
  • a polyvalent metal ion is an ion of a metal with a valence of at least two. Bleeding of the ink composition can be suppressed by using polyvalent metal ions.
  • polyvalent metal ions include calcium ions, magnesium ions, aluminum ions, titanium ions, iron (II) ions, iron (III) ions, cobalt ions, nickel ions, copper ions, zinc ions, barium ions, strontium ions, and the like. is mentioned.
  • one selected from calcium ions, magnesium ions, nickel ions, zinc ions, and aluminum ions because it has a large interaction with the colorant in the ink composition and has a high effect of suppressing bleeding and unevenness. It is preferable to contain the above.
  • the cationic compound may contain a cationic resin having a cationic group instead of the polyvalent metal salt.
  • cationic resins include resins having cationic groups such as amino groups, ammonium groups, amide groups, and --NHCONH2 groups.
  • a cationic resin can be synthesized by a known method, or a commercially available product can be used.
  • the cationic resin can be synthesized by a known method, or a commercially available product can be used.
  • Examples of commercially available products are as follows: APC-810, 815; D-6010, 6020, 6030, 6040, 6050, 6060, 6080, 6310; FQP-1264 ; RSL-18-22, 4071H, 4400, 8391, 8391H, HD70C, HF70D; WS-72 (manufactured by SNF), Arafix 100, 251S, 255, 255LOX (manufactured by Arakawa Chemical), DK-6810, 6853, 6885 WS-4010, 4011, 4020, 4024, 4027, 4030 (manufactured by Seiko PMC), Senka F-300; Papiogen P-105, P-113, P-271, P-316; Pitchnol QG5A; Myriogen P- 20; Unisense FPA100L, FPA101L, FPA
  • the cationic resin may be a water-soluble cationic resin that dissolves in water or a water-soluble organic solvent, or a dispersible cationic resin that disperses in water or a water-soluble organic solvent.
  • the cationic resin is preferably a dispersible cationic resin.
  • the coating film resistance (scratch resistance) of the ink composition layer can be improved.
  • the cationic compound contains a polyvalent metal ion and a dispersible cationic resin, or the cationic compound contains a water-soluble cationic resin and a dispersible cationic resin. more preferably.
  • the ink composition layer can be coated while suppressing bleeding of the colored ink more effectively.
  • Film resistance shock resistance
  • the content of the cationic compound is not particularly limited. It is preferably in the range of 5% by mass or more, more preferably in the range of 0.8% by mass or more, and even more preferably in the range of 1.0% by mass or more. When the content of the cationic compound is within the range of 0.5% by mass or more based on the total amount of the ink composition, it becomes possible to fix the coloring material more effectively, and the bleeding of the colored ink is effectively suppressed. can do.
  • the upper limit of the content of the cationic compound is preferably within the range of 9% by mass or less, more preferably within the range of 8% by mass or less, and within the range of 7% by mass or less in the total amount of the ink composition. is more preferable. When the content of the cationic compound is within the range of 9% by mass or less based on the total amount of the ink composition, the storage stability of the ink composition is improved.
  • the ink composition may further contain conventionally known additives, if necessary.
  • additives include waxes, viscosity modifiers, pH modifiers, antioxidants, preservatives, antifungal agents, and the like.
  • the method for preparing the ink composition is not particularly limited. , A method in which a pigment and a dispersant are added and dispersed, and then a resin, a surfactant and, if necessary, other ingredients are added. After adding the components of (1), the pigment is dispersed and prepared.
  • the surface tension of the ink composition is not particularly limited, but the upper limit of the static surface tension at 25° C. is preferably 40.0 mN/m or less, more preferably 35.0 mN/m or less, and 32.0 mN/m or less. More preferred.
  • the lower limit of the static surface tension at 25°C is preferably 19.0 mN/m or more, more preferably 20.0 mN/m or more, and even more preferably 21.0 mN/m or more.
  • the static surface tension can be measured, for example, by the Wilhelmy method (DY-300 manufactured by Kyowa Interface Science) at a measurement temperature of 25°C.
  • the conductivity of the ink composition is not particularly limited, it is preferably 2500 ⁇ S/cm or less. By controlling the components of the ink composition so that the electrical conductivity is 2500 ⁇ S/cm or less, it is possible to suppress the interaction between the components and improve the storage stability.
  • the conductivity of the ink composition is preferably 2450 ⁇ S/cm or less, more preferably 2400 ⁇ S/cm or less.
  • the electrical conductivity can be measured at 25° C. with EC Testr 11+ manufactured by Eutech Instruments, for example.
  • the above ink composition may be a colored ink, a metallic ink or the like, a receiving solution containing a cationic compound, or a clear ink containing no coloring material, and may be an overcoat ink.
  • the ink set according to the present embodiment may be an ink set in which these ink compositions are combined.
  • one ink composition contained in the ink set is a colored ink composition (C) containing a coloring material
  • the other ink composition contained in the ink set contains a cationic compound.
  • the ink set that is the receiving solution (P) and one ink composition contained in the ink set are the overcoat inks (O) that form an overcoat layer on the surface of the object, and the other ink compositions contained in the ink set.
  • the ink composition is an ink set that is a receiving solution (P) containing a cationic compound, and one ink composition included in the ink set is a colored ink composition (C) that contains a coloring material, and the ink Other ink compositions included in the set include an ink set that is an overcoat ink (O) that forms an overcoat layer on the surface of a substrate.
  • P receiving solution
  • C colored ink composition
  • O overcoat ink
  • the ink set may be a combination of colored ink compositions (C) containing a coloring material. ink, red ink) or light colored ink compositions (for example, light magenta ink, light cyan ink, light black ink).
  • an ink set containing a white ink composition containing a white colorant, a yellow ink composition, a magenta ink composition, a cyan ink composition, and a black ink composition and a white ink composition containing a white colorant and a yellow ink composition, a magenta ink composition, a cyan ink composition, a black ink composition, and an intermediate color ink composition or a light color ink composition of yellow, magenta, cyan, and black.
  • an ink set containing a metallic ink containing a glitter pigment, a yellow ink composition, a magenta ink composition, a cyan ink composition, and a black ink composition containing a metallic ink containing a glitter pigment and a yellow ink composition
  • a metallic ink containing a glitter pigment and a yellow ink composition A magenta ink composition, a cyan ink composition, a black ink composition, and intermediate color ink compositions or light color ink compositions of yellow, magenta, cyan, and black.
  • the conductivity is preferably 1000 ⁇ S/cm or less. Since the coloring ink composition (C) containing the coloring material contains the coloring material (pigment) in the coloring ink composition (C), the coloring material (pigment) agglomerates and the stability is lowered. tend to
  • the colored ink composition (C) contains components such as a colorant dispersant (pigment dispersant) and a leveling agent (surfactant) that disperse the colorant (pigment) so that the conductivity is 1000 ⁇ S/cm or less. By doing so, it is possible to suppress the interaction between the components (especially between the coloring materials), and it is possible to further improve the stability.
  • the electrical conductivity of the colored ink composition (C) is more preferably 950 ⁇ S/cm or less, even more preferably 900 ⁇ S/cm or less.
  • the electrical conductivity of the overcoat ink (O) is preferably 1000 ⁇ S/cm or less.
  • the overcoat ink (O) that forms the overcoat layer on the surface of the object contains a resin for forming the overcoat layer. tend to decline.
  • the electrical conductivity of the overcoat ink (O) is 1000 ⁇ S/cm or less. interaction can be suppressed, and the stability can be further improved.
  • the conductivity of the overcoat ink (O) is more preferably 950 ⁇ S/cm or less, even more preferably 900 ⁇ S/cm or less.
  • the electrical conductivity of the receiving solution (P) is preferably 1000 ⁇ S/cm or more and 2500 ⁇ S/cm or less. Since the receiving solution (P) contains a cationic compound, the receiving solution (P ) while maintaining the storage stability of the receiving solution (P), it is possible to improve the reactivity with the colored ink (C) and the overcoat ink (O) that land on the receiving solution (P), suppressing bleeding and unevenness. It becomes possible to
  • the electrical conductivity of the receiving solution (P) is more preferably 1050 ⁇ S/cm or higher, more preferably 1100 ⁇ S/cm or higher.
  • the recording method according to the present embodiment is a recording method in which the ink composition described above is applied onto a substrate by an inkjet method.
  • This ink composition contains a water-soluble organic solvent A having a boiling point of 230° C. or less and a resin, and is highly drying and capable of forming a coating film with high scratch resistance.
  • High-speed recording can be achieved by coating the base material with the ink-jet method according to the recording method of the present embodiment. Furthermore, even if recording is performed at a high speed, it is possible to suppress deterioration in abrasion resistance, and as a result, a coating film having high abrasion resistance can be formed.
  • the maximum recording speed in the recording method according to the present embodiment is 7.5 m 2 /h or more in the case of the serial method, although it depends on the type of the base material, the type of the ink jet recording apparatus, and the like. It is preferably 10 m 2 /h or more, more preferably 15 m 2 /h or more. In the case of the single pass method, the speed is preferably 30 m/min or more, more preferably 40 m/min or more, and even more preferably 50 m/min or more.
  • the serial method is a printing method in which the inkjet head is moved in the horizontal direction and the ink is ejected in several batches, while the single-pass method is a method in which the inkjet head is fixed and the substrate passes through the inkjet head once. It is a printing method in which an image is formed by
  • the drying temperature can be recorded at a relatively low temperature. Therefore, it becomes possible to suppress deterioration of scratch resistance due to the organic solvent remaining in the coating film, and as a result, it is possible to form a coating film having high scratch resistance.
  • the drying temperature in the recording method according to the present embodiment may be 80°C or lower, preferably 70°C or lower, and more preferably 60°C or lower.
  • the above-described recording method can also be defined as a method for producing a recorded matter in which the above-described ink composition is applied onto a substrate by an inkjet method.
  • the base material (recording medium) that can be used in the recording method according to the present embodiment is not particularly limited.
  • Various substrates can be used, such as an absorbent substrate such as a woven fabric, or a surface-coated substrate such as a substrate having a receiving layer. The same applies to the base material that can be used in the method of manufacturing a recorded matter according to an embodiment described later.
  • non-absorbent substrates include resin substrates such as polyester resins, polypropylene synthetic paper, polypropylene resins, polyethylene resins, acrylic resins, styrene resins, polycarbonate resins, ABS resins, vinyl chloride resins, polyimide resins, Metal, metal foil coated paper, glass, synthetic rubber, natural rubber and the like can be mentioned.
  • resin substrates such as polyester resins, polypropylene synthetic paper, polypropylene resins, polyethylene resins, acrylic resins, styrene resins, polycarbonate resins, ABS resins, vinyl chloride resins, polyimide resins, Metal, metal foil coated paper, glass, synthetic rubber, natural rubber and the like can be mentioned.
  • absorbent substrates include dry paper, medium-quality paper, high-quality paper, synthetic paper, cotton, synthetic fiber fabric, silk, hemp, fabric, non-woven fabric, leather, and the like.
  • Examples of surface-coated substrates include coated paper, art paper, cast paper, lightweight coated paper, and lightly coated paper.
  • the layer of the ink composition is a layer formed by volatilization of the solvent contained in the ink composition described above.
  • the ink composition contains a coloring material, it becomes a decorative layer forming a desired image or a base layer therefor.
  • the above-described ink composition when used as a receiving solution containing a cationic compound, the above-described ink composition (receiving solution) is applied onto a substrate, and the above-described ink composition (coloring ink) is applied thereon. ) may be applied, or the above-described ink composition (receiving solution) is applied on the substrate, and an ink composition (colored ink) different from the above-described ink composition (colored ink) is applied thereon. You may
  • the ink composition described above when used as an overcoat ink, it becomes an overcoat layer formed on the surface of a recorded matter.
  • the ink composition that forms the recording layer of the recorded matter may be the ink composition described above, or may be an ink composition different from the ink composition described above.
  • An inkjet recording apparatus is an inkjet recording apparatus equipped with a container filled with the ink composition described above.
  • the ink composition described above has high drying property and can form a coating film with high abrasion resistance. Therefore, it is possible to produce recorded matter having high scratch resistance.
  • the storage container mounted on the inkjet recording apparatus is not particularly limited, and examples include containers such as ink bottles, pouches, bag-in-boxes, and drums. Also, these containers may be further housed in a cartridge or the like.
  • the material of the storage container is not particularly limited, and may be a conventionally known resin, or a material containing a part of metal material (for example, an aluminum pouch having an aluminum deposition layer). .
  • this apparatus include a drying mechanism for drying the ink composition after the ink composition is ejected. This makes it possible to effectively remove the volatile components contained in each ink composition and promote film formation of the resin particles.
  • the drying mechanism for drying the ink after ejection is not particularly limited, and may be a heater or the like, or a mechanism for blowing hot air or room temperature air.
  • the ink composition applied on the substrate at a temperature lower than the Tg of the resin contained in the ink composition. Since the above ink composition is highly drying, it can be sufficiently dried even at a temperature lower than the Tg of the resin contained in the ink composition.
  • the ejection method in each ejection part may be any method such as a piezo method, a thermal method, or an electrostatic method.
  • Drying properties of the ink compositions of Examples and Comparative Examples were evaluated. Specifically, after applying 7 g/m 2 of the ink composition onto a vinyl chloride resin substrate with a bar coater, it was placed in an oven at 60° C. and the time until drying was evaluated by touch. The surface was touched with a finger every 30 seconds, and the time until the ink composition stopped adhering was measured, and evaluation was performed based on the following evaluation criteria. The evaluation results are shown in the table below (indicated as "drying property" in the table). Evaluation Criteria A: Dried in 3 minutes. B: Dried in 3.5 to 5 minutes. C: Dried in 5.5 to 7 minutes. D: Dried in 7.5 to 8 minutes. E: Not dried in 8 minutes (out of practical range).
  • Storage stability was evaluated for the ink compositions of Examples and Comparative Examples. Specifically, the ink composition was heated in an oven at 60° C. for one week, and the viscosity before and after heating was measured at a liquid temperature of 25° C., and evaluated based on the following evaluation criteria. The evaluation results are shown in the table below (indicated as "storage stability" in the table). Evaluation Criteria A: Viscosity change rate of 5% or less B: Viscosity change rate of more than 5% and less than 10% C: Viscosity change rate of 10% or more and less than 20% D: Viscosity change rate of 20% or more (outside practical range)
  • Density unevenness Density unevenness was evaluated for recorded matter obtained with the ink compositions of Examples and Comparative Examples. Specifically, the ink composition is filled in an ink cartridge (container), and the ink cartridge (container) is mounted on a serial head type inkjet recording apparatus. A solid image with a droplet size of 6 pl and a printing density of 100% was printed on a vinyl chloride resin substrate, and the presence or absence of density unevenness was visually observed, and evaluation was made based on the following evaluation criteria. The evaluation results are shown in the table below (denoted as "density unevenness" in the table). Evaluation Criteria A: No density unevenness B: Density unevenness C: Image formation not possible due to poor ink wetting (outside practical range)
  • Liquid repellency Liquid repellency was evaluated for the ink compositions of Examples and Comparative Examples. Specifically, the nozzle plate of a 600 dpi printer head in an inkjet recording apparatus is immersed in the ink composition, and the exposed area of the ink composition on the plate after being removed from the liquid surface is visually observed every 30 seconds. was evaluated based on the evaluation criteria of The evaluation results are shown in the table below (indicated as "liquid repellency" in the table). Evaluation criteria A: The exposed area of the plate after 30 seconds is 80% or more B: The exposed area of the plate after 1 minute is 80% or more C: The exposed area of the plate is less than 80% even after 1 minute (outside the practical range)
  • the intermittent discharge properties of the ink compositions of Examples and Comparative Examples were evaluated. Specifically, the ink composition is filled in an ink cartridge (container), the ink cartridge (container) is mounted in a serial head type inkjet recording apparatus, and a nozzle check pattern is printed by the inkjet recording apparatus. Then, after standing still for a certain period of time, the same printing was performed. The presence or absence of missing nozzles was checked before and after standing, and the same printing was repeated until the missing nozzles decreased to less than 10% of the pattern before standing. The evaluation results are shown in the table below (indicated as "intermittent discharge property" in the table).
  • an ink composition containing a water-soluble organic solvent having a predetermined boiling point or lower and a resin can be dried quickly and can improve the scratch resistance of the coating film.
  • the ink compositions of Examples 1, 2, and 4 to 9 containing a leveling agent are good in the "drying property" evaluation of the obtained recorded matter as compared with the ink composition of Example 3 which does not contain a leveling agent. Met.
  • Tg glass transition temperature
  • Example 1 and 18 to 28 in which the type of the water-soluble organic solvent A was changed the water-soluble organic solvent A having a water/1-octanol partition coefficient (LogP) of -0.6 or more was used.
  • the ink compositions of Examples 1, 18 to 22, and 24 to 28 had good scratch resistance even when compared with the ink compositions of Examples 1 and 23.
  • Example 29 receiving solution (P)
  • Example 30 receiving solution (P)
  • Example 34 in which the content of the water-soluble organic solvent A was changed, Examples 1, 35 to 39 in which the content of the water-soluble organic solvent A was in the range of 5% by mass or more
  • the ink composition of Example 34 had even better evaluations of "drying property" and "scratch resistance” than the ink composition of Example 34.
  • the ink compositions of Examples 1 and 34 to 38, in which the content of the water-soluble organic solvent A was in the range of 35% by mass or less were evaluated for "storage stability" even when compared with the ink composition of Example 39. was even better.
  • the ink compositions of Examples 1 and 40 to 44 in which the resin content was changed the ink compositions of Examples 1 and 41 to 44 in which the resin content was in the range of 1.5% by mass or more were Even when compared with the ink composition of Example 40, the "scratch resistance" evaluation was even better.
  • the ink compositions of Examples 1 and 45 containing a dispersible resin having an average particle size of 300 nm or less had even better "scratch resistance" evaluation than the ink composition of Example 46. there were.
  • the “1,3-propanediol” of Example 36 containing N,N-diethylformamide and further containing 1,3-propanediol was changed to 1,2- Examples 141 and 142, in which the alkanediol-based solvent "propylene glycol” was used, gave even better "drying property” evaluations.
  • "1,3-propanediol” of Example 70, which contains ⁇ -caprolactone and further contains 1,3-propanediol, as a cyclic ester-based solvent having a boiling point of 230°C or less is replaced with 1,2-alkanediol.
  • the "1,3-propanediol" of Example 105 which contains dipropylene glycol monomethyl ether and further contains 1,3-propanediol, as a glycol ether-based solvent having a boiling point of 230° C. or less is replaced with 1,2- Examples 145 and 146, in which the alkanediol-based solvent "propylene glycol” was used, gave even better "drying property” evaluations.
  • the ink set of the ink composition containing the water-soluble organic solvent A having a boiling point of 230° C. or less and the resin has high drying property and can improve the abrasion resistance of the coating film. I know you can.
  • Example 29 having a conductivity of 1000 ⁇ S/cm or more and 2500 ⁇ S/cm or less and the ink composition of Example 24 having a conductivity of 1000 ⁇ S/cm or less.
  • Example 134 which contains the ink composition of Example 29 (receiving solution) and the ink set of Comparative Example 11, which does not contain the water-soluble organic solvent A, is compared with the ink set of Comparative Example 11. The evaluations of "fairness”, “bleeding”, and "scratch resistance" were all good.
  • Example 133 containing the ink composition (overcoat ink) of Example 32 containing the water-soluble organic solvent A and the ink composition (cyan ink) of Comparative Example 7 not containing the water-soluble organic solvent A
  • the set was compared with the ink set of Comparative Example 10, which did not contain the ink composition containing the water-soluble organic solvent A, and the "drying property" evaluation, "bleeding” evaluation, and "scratch resistance” evaluation were good. there were. From these results, it was confirmed that the effect of the invention of the present application is achieved by containing the "water-soluble organic solvent A" in at least one ink composition constituting the ink set.
  • the ink sets of Examples 148, 150, 152, 154, 156, 158, 160, 162, and 164 149, 151, 153, 155, 157, 159, 161, and 163, the "scratch resistance" is good.
  • the ink sets of Examples 148, 150, 152, 154, 156, 158, 160, 162 and 164 contain the ink compositions of Examples 142, 144 and 146 containing a silicone surfactant. From this, it was confirmed that an ink set containing an ink composition containing a silicone (silicon)-based surfactant can form a coating film with high scratch resistance.

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Abstract

Provided is an ink composition having high dryability and improved scratch resistance as a coating film.　An inkjet ink composition, wherein the ink composition contains a water-soluble organic solvent and a resin, at least part of the resin being contained as a dispersible resin, and the water-soluble organic solvent containing at least one water-soluble organic solvent A selected from amide solvents having a boiling point of 230°C or lower, cyclic ester solvents having a boiling point of 230°C or lower, and glycol ether solvents having a boiling point of 230°C or lower.

Description

インク組成物、インクセット、インク組成物を基材上に塗布された記録物、記録方法、記録物の製造方法、及びインク組成物が充填された収容容器が搭載されたインクジェット記録装置Ink composition, ink set, recorded matter coated with ink composition on substrate, recording method, method for producing recorded matter, and ink jet recording apparatus equipped with storage container filled with ink composition
　本発明は、インク組成物、インクセット、インク組成物を基材上に塗布された記録物、記録方法、記録物の製造方法、及びインク組成物が充填された収容容器が搭載されたインクジェット記録装置に関する。 The present invention provides an ink composition, an ink set, a recorded matter obtained by applying the ink composition onto a substrate, a recording method, a method for producing a recorded matter, and an ink jet recording method equipped with a container filled with the ink composition. Regarding the device.
　インクジェット記録方式は、非常に微細なノズルからインク組成物の液滴を紙等の基材に直接吐出し、塗布して文字や画像を得る記録方式である。この記録方式は、小型化、高速化、低騒音化、省電力化、カラー化が容易であり、しかも基材に対して非接触印刷が可能であることから、家庭用途のみならず、オフィス用途、商業印刷用途にまで適用範囲が拡大している。 The inkjet recording method is a recording method in which droplets of an ink composition are directly ejected from very fine nozzles onto a base material such as paper and applied to obtain letters and images. This recording method is easy to reduce size, increase speed, reduce noise, save power, and colorize. , and the range of application has expanded to include commercial printing applications.
　インクジェット記録方式に使用されるインク組成物として、各種の色材を水、又は水と水溶性有機溶剤との混合液に溶解、もしくは分散させた水性インク組成物が広く用いられている。このような水を主成分とする水性インク組成物は、同じインクジェット記録方式に使用される有機溶剤を含んだ非水性インク組成物と比較して環境に対する影響が少なく、引火することがないため作業者に対して安全性が高い。 Aqueous ink compositions in which various coloring materials are dissolved or dispersed in water or a mixture of water and a water-soluble organic solvent are widely used as ink compositions used in inkjet recording systems. Such water-based ink compositions have less impact on the environment than non-aqueous ink compositions containing organic solvents used in the same inkjet recording system, and are non-flammable. Safe for people.
　一方、水性インク組成物は前記非水性インク組成物と比較すると乾燥により多くの熱量が必要となるため、生産性の面では乾燥時間を延ばすよりも、乾燥温度を高く設定することにより短時間で乾燥させる必要があった。しかしながら、乾燥温度が高いと基材によっては撓み等が発生するため、基材の選択幅が狭くなってしまうという側面も持ち合わせている。 On the other hand, since the water-based ink composition requires a larger amount of heat for drying than the non-aqueous ink composition, in terms of productivity, the drying temperature can be set high to shorten the drying time rather than extending the drying time. I had to dry it. However, if the drying temperature is high, depending on the base material, warping or the like occurs, so there is also an aspect that the selection range of the base material is narrowed.
　そこで、例えば、特許文献１には、２－ピロリドンと、ウレタン樹脂を含む水不溶性の熱可塑性樹脂粒子と、を含有する水性インク組成物を吐出する工程を含むインクジェット記録方法に関する技術が記載されている。特許文献１には、インクジェット記録方法は、インク組成物の滲みが少なく高画質であり、耐擦過性が優れた画像が得られることが記載されている。 Therefore, for example, Patent Document 1 describes a technique related to an inkjet recording method including a step of ejecting an aqueous ink composition containing 2-pyrrolidone and water-insoluble thermoplastic resin particles containing a urethane resin. there is Japanese Patent Laid-Open No. 2002-100002 describes that the ink jet recording method can obtain an image having high image quality with less bleeding of the ink composition and excellent abrasion resistance.
特開２０１５－０９１６５８号公報JP 2015-091658 A
　さて、インク組成物に樹脂を含有させると、得られるインク組成物の塗膜にさらに耐擦過性を付与することができる。 By the way, if the ink composition contains a resin, it is possible to impart further abrasion resistance to the coating film of the resulting ink composition.
　しかしながら、記録物の生産性を高くしようとして乾燥処理を短くし、あるいは低温で乾燥処理を施すと、インク組成物の乾燥が十分とならないばかりか、均一化した塗膜を形成することができず、これが耐擦過性等の塗膜耐性を低下させてしまうことが本発明者らの研究により明らかとなった。 However, if the drying process is shortened or the drying process is performed at a low temperature in an attempt to increase the productivity of recorded matter, not only is the ink composition not sufficiently dried, but a uniform coating film cannot be formed. The inventors' studies have revealed that this lowers the coating film resistance such as scratch resistance.
　本発明は、乾燥性が高く、塗膜の耐擦過性を向上させるインク組成物を提供することを目的とする。 An object of the present invention is to provide an ink composition that dries well and improves the scratch resistance of the coating film.
　本発明者は、上記課題を解決するために鋭意検討をした結果、所定沸点以下の水溶性有機溶剤と樹脂と、を含有するインク組成物であれば、上記課題を解決できることを見出し、本発明を完成するに至った。具体的には、本発明では、以下のようなものを提供する。 As a result of intensive studies to solve the above problems, the present inventors found that the above problems can be solved by an ink composition containing a water-soluble organic solvent having a predetermined boiling point or less and a resin. was completed. Specifically, the present invention provides the following.
　（１）インクジェット用のインク組成物であって、水溶性有機溶剤と、樹脂と、を含有し、前記樹脂の少なくとも一部を分散性樹脂として含有し、前記水溶性有機溶剤は、沸点２３０℃以下のアミド系溶剤、沸点２３０℃以下の環状エステル系溶剤、及び沸点２３０℃以下のグリコールエーテル系溶剤から選択される少なくとも１つ以上の水溶性有機溶剤Ａを含有するインク組成物。 (1) An inkjet ink composition containing a water-soluble organic solvent and a resin, at least part of the resin being a dispersible resin, the water-soluble organic solvent having a boiling point of 230°C. An ink composition containing at least one water-soluble organic solvent A selected from the following amide solvents, cyclic ester solvents having a boiling point of 230°C or lower, and glycol ether solvents having a boiling point of 230°C or lower.
　（２）前記分散性樹脂１００質量部に対する前記水溶性有機溶剤Ａの含有量は３０質量部以上である（１）に記載のインク組成物。
（１）に記載のインク組成物。 (2) The ink composition according to (1), wherein the content of the water-soluble organic solvent A with respect to 100 parts by mass of the dispersible resin is 30 parts by mass or more.
The ink composition according to (1).
　（３）前記分散性樹脂のＴｇは、インク組成物の乾燥温度よりも高い（１）又は（２）に記載のインク組成物。 (3) The ink composition according to (1) or (2), wherein the Tg of the dispersible resin is higher than the drying temperature of the ink composition.
　（４）　前記分散性樹脂のＴｇは、５０℃以上である（１）から（３）のいずれかに記載のインク組成物。 (4) The ink composition according to any one of (1) to (3), wherein the Tg of the dispersible resin is 50°C or higher.
　（５）前記分散性樹脂は、アクリル系樹脂、ポリウレタン系樹脂、ポリエステル系樹脂、塩化ビニル系樹脂、酢酸ビニル系樹脂、ポリエーテル系樹脂、塩化ビニル酢酸ビニル共重合樹脂、ポリエチレン系樹脂、アクリルアミド系樹脂、エポキシ系樹脂、ポリカーボネート系樹脂、シリコーン系樹脂、及びポリスチレン系樹脂からなる群より選択される１つ以上の樹脂あるいは共重合樹脂を含む（１）から（４）のいずれかに記載のインク組成物。 (5) The dispersible resin includes acrylic resin, polyurethane resin, polyester resin, vinyl chloride resin, vinyl acetate resin, polyether resin, vinyl chloride vinyl acetate copolymer resin, polyethylene resin, and acrylamide resin. The ink according to any one of (1) to (4), containing one or more resins or copolymer resins selected from the group consisting of resins, epoxy resins, polycarbonate resins, silicone resins, and polystyrene resins. Composition.
　（６）前記分散性樹脂は、少なくともアクリル系樹脂、又はアクリル系共重合樹脂を含む（５）に記載のインク組成物。 (6) The ink composition according to (5), wherein the dispersible resin contains at least an acrylic resin or an acrylic copolymer resin.
　（７）前記水溶性有機溶剤Ａの水／１－オクタノールでの分配係数（ＬｏｇＰ）が－０．６以上である（１）から（６）のいずれかに記載のインク組成物。 (7) The ink composition according to any one of (1) to (6), wherein the water/1-octanol partition coefficient (LogP) of the water-soluble organic solvent A is -0.6 or more.
　（８）前記水溶性有機溶剤Ａは、以下の式（１）で表される沸点２３０℃以下のアミド系溶剤、以下の式（２）で表される沸点２３０℃以下の環状エステル系溶剤、及び、以下の式（３）で表される沸点２３０℃以下のグリコールエーテル系溶剤から選択される少なくとも１つ以上の水溶性有機溶剤Ａを含有する（１）から（７）のいずれかに記載のインク組成物。
Figure JPOXMLDOC01-appb-C000004
 （式（１）中、Ｒ１は水素、若しくは炭素数１～４のアルキル基であり、Ｒ２、Ｒ３は官能基である。）
Figure JPOXMLDOC01-appb-C000005
 （式（６）中、Ｒ５は、炭素数３以上５以下のアルキレン基又はビニレン基を有する炭素鎖であり、Ｒ６は、水素若しくは炭素数１以上２以下のアルキル基又はビニリデン基を表す。Ｒ６は、Ｒ５の炭素鎖であればどの位置でも、複数あってもよく、Ｒ５とＲ６は単結合又は多重結合のいずれの結合で繋がっていてもよい。）
Figure JPOXMLDOC01-appb-C000006
 　（式（８）中、Ｒ７Ｒ９は、水素、若しくはアルキル基、アシル基であり少なくとも一方はアルキル基、若しくはアシル基である、Ｒ８は、エチレン基又はプロピレン基を表す。ｎは２～４の整数を表す。） (8) The water-soluble organic solvent A is an amide solvent having a boiling point of 230° C. or less represented by the following formula (1), a cyclic ester solvent having a boiling point of 230° C. or less represented by the following formula (2), and any one of (1) to (7) containing at least one water-soluble organic solvent A selected from glycol ether solvents having a boiling point of 230° C. or less represented by the following formula (3): ink composition.
Figure JPOXMLDOC01-appb-C000004
 (In formula (1), R 1 is hydrogen or an alkyl group having 1 to 4 carbon atoms, and R 2 and R 3 are functional groups.)
Figure JPOXMLDOC01-appb-C000005
 (In formula (6), R 5 is a carbon chain having an alkylene group having 3 to 5 carbon atoms or a vinylene group, and R 6 represents hydrogen, an alkyl group having 1 to 2 carbon atoms, or a vinylidene group. R 6 may be present at any position on the carbon chain of R 5 , and may be plural, and R 5 and R 6 may be linked by either a single bond or a multiple bond.)
Figure JPOXMLDOC01-appb-C000006
 (In formula (8), R 7 R 9 is hydrogen, an alkyl group, or an acyl group, at least one of which is an alkyl group or an acyl group; R 8 represents an ethylene group or a propylene group; n is 2; Represents an integer of ~4.)
　（９）前記水溶性有機溶剤Ａは、Ｎ－エチル－Ｎ－メチルホルムアミド、Ｎ－メチル－Ｎ－プロピルホルムアミド、Ｎ，Ｎ－ジエチルホルムアミド、Ｎ－エチル－Ｎ－プロピルホルムアミド、Ｎ，Ｎ－ジメチルアセトアミド、Ｎ－エチル－Ｎ－メチルアセトアミド、Ｎ－メチル－Ｎ－プロピルアセトアミド、Ｎ，Ｎ－ジエチルアセトアミド、Ｎ，Ｎ－ジメチルプロパンアミド、Ｎ－エチル－Ｎ－メチルプロパンアミド、γ－ブチロラクトン、α－メチレン－γ－ブチロラクトン、ε－カプロラクトン、ジエチレングリコールモノエチルエーテル、ジプロピレングリコールモノメチルエーテル、及びジエチレングリコールモノイソブチルエーテルからなる群より選択される（１）から（８）のいずれかに記載のインク組成物。 (9) The water-soluble organic solvent A is N-ethyl-N-methylformamide, N-methyl-N-propylformamide, N,N-diethylformamide, N-ethyl-N-propylformamide, N,N-dimethyl Acetamide, N-ethyl-N-methylacetamide, N-methyl-N-propylacetamide, N,N-diethylacetamide, N,N-dimethylpropanamide, N-ethyl-N-methylpropanamide, γ-butyrolactone, α -methylene-γ-butyrolactone, ε-caprolactone, diethylene glycol monoethyl ether, dipropylene glycol monomethyl ether, and diethylene glycol monoisobutyl ether The ink composition according to any one of (1) to (8). .
　（１０）さらにアルカンジオール系溶剤を含有する（１）から（９）のいずれかに記載のインク組成物。 (10) The ink composition according to any one of (1) to (9), further containing an alkanediol solvent.
　（１１）前記水溶性有機溶剤Ａは、少なくとも２種以上の沸点２３０℃以下のアミド系溶剤を含有する（１０）に記載のインク組成物。 (11) The ink composition according to (10), wherein the water-soluble organic solvent A contains at least two amide-based solvents having a boiling point of 230°C or less.
　（１２）前記アルカンジオール系溶剤は、炭素数が３以上６以下であり、炭素骨格の少なくとも一方の末端に水酸基を備えるアルカンジオール系溶剤を含有する（１１）に記載のインク組成物。 (12) The ink composition according to (11), wherein the alkanediol-based solvent has 3 or more and 6 or less carbon atoms and has a hydroxyl group at at least one end of the carbon skeleton.
　（１３）前記水溶性有機溶剤Ａは、少なくとも２種以上の水溶性有機溶剤Ａを含有する（１）から（１２）のいずれかに記載のインク組成物。 (13) The ink composition according to any one of (1) to (12), wherein the water-soluble organic solvent A contains at least two or more water-soluble organic solvents A.
　（１４）前記水溶性有機溶剤Ａは、少なくとも２種以上の沸点２３０℃以下のアミド系溶剤を含有する（１３）に記載のインク組成物。 (14) The ink composition according to (13), wherein the water-soluble organic solvent A contains at least two amide-based solvents having a boiling point of 230°C or less.
　（１５）前記水溶性有機溶剤Ａは、少なくとも沸点２３０℃以下のアミド系溶剤と、沸点２３０℃以下の環状エステル系溶剤と、を含有する（１３）に記載のインク組成物。 (15) The ink composition according to (13), wherein the water-soluble organic solvent A contains at least an amide solvent with a boiling point of 230°C or lower and a cyclic ester solvent with a boiling point of 230°C or lower.
　（１６）前記水溶性有機溶剤Ａは、少なくとも沸点２３０℃以下のアミド系溶剤と、沸点２３０℃以下のグリコールエーテル系溶剤と、を含有する（１３）に記載のインク組成物。 (16) The ink composition according to (13), wherein the water-soluble organic solvent A contains at least an amide solvent with a boiling point of 230°C or lower and a glycol ether solvent with a boiling point of 230°C or lower.
　（１７）前記水溶性有機溶剤Ａは、少なくとも、沸点２３０℃以下の環状エステル系溶剤と、沸点２３０℃以下のグリコールエーテル系溶剤と、を含有する（１３）に記載のインク組成物。 (17) The ink composition according to (13), wherein the water-soluble organic solvent A contains at least a cyclic ester solvent with a boiling point of 230°C or less and a glycol ether solvent with a boiling point of 230°C or less.
　（１８）さらにレベリング剤を含有し、前記レベリング剤の含有量は、前記インク組成物に含まれる前記水溶性有機溶剤Ａ１００質量部に対して０．１質量部以上５０質量部以下の範囲である（１）から（１７）のいずれかに記載のインク組成物。 (18) A leveling agent is further included, and the content of the leveling agent is in the range of 0.1 parts by mass or more and 50 parts by mass or less with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. The ink composition according to any one of (1) to (17).
　（１９）導電率が２５００μＳ／ｃｍ以下である（１）から（１８）のいずれかに記載のインク組成物。 (19) The ink composition according to any one of (1) to (18), which has a conductivity of 2500 μS/cm or less.
　（２０）（１）から（１９）のいずれかに記載のインク組成物を含むインクセット。 (20) An ink set containing the ink composition according to any one of (1) to (19).
　（２１）（１）から（１９）のいずれかに記載のインク組成物、又は（２０）に記載のインクセットに含まれるインク組成物が基材上に塗布された記録物。 (21) A recorded matter in which the ink composition according to any one of (1) to (19) or the ink composition contained in the ink set according to (20) is applied onto a substrate.
　（２２）（１）から（１９）のいずれかに記載のインク組成物、又は（２０）に記載のインクセットに含まれるインク組成物をインクジェット法により基材上に塗布する記録方法。 (22) A recording method in which the ink composition according to any one of (1) to (19) or the ink composition contained in the ink set according to (20) is applied onto a substrate by an inkjet method.
　（２３）（１）から（１９）のいずれかに記載のインク組成物、又は（２０）に記載のインクセットをインクジェット法により基材上に塗布し、その後、前記インク組成物を該インク組成物に含まれる樹脂のＴｇよりも低い温度で乾燥する記録方法。 (23) The ink composition according to any one of (1) to (19) or the ink set according to (20) is applied onto a substrate by an inkjet method, and then the ink composition is applied to the ink composition. A recording method that dries at a temperature lower than the Tg of the resin contained in an object.
　（２４）（１）から（１９）のいずれかに記載のインク組成物、又は（２０）に記載のインクセットに含まれるインク組成物をインクジェット法により基材上に塗布する記録物の製造方法。 (24) A method for producing recorded matter, comprising applying the ink composition according to any one of (1) to (19) or the ink composition contained in the ink set according to (20) onto a substrate by an inkjet method. .
　（２５）（１）から（１９）のいずれかに記載のインク組成物、又は（２０）に記載のインクセットに含まれるインク組成物が充填された収容容器が搭載されたインクジェット記録装置。 (25) An inkjet recording apparatus equipped with a container filled with the ink composition according to any one of (1) to (19) or the ink composition contained in the ink set according to (20).
　本発明のインク組成物は、乾燥性が高く、耐擦過性の高い塗膜を形成することができる。 The ink composition of the present invention is highly dry and can form a coating film with high scratch resistance.
　以下、本発明の具体的な実施形態について、詳細に説明するが、本発明は、以下の実施形態に何ら限定されるものではなく、本発明の目的の範囲内において、適宜変更を加えて実施することができる。 Hereinafter, specific embodiments of the present invention will be described in detail, but the present invention is not limited to the following embodiments at all, and can be implemented with appropriate modifications within the scope of the purpose of the present invention. can do.
　＜インク組成物＞
　本実施の形態に係るインク組成物は、インクジェット用のインク組成物であって、水溶性有機溶剤を含有する。 <Ink composition>
The ink composition according to the present embodiment is an ink composition for inkjet and contains a water-soluble organic solvent.
　そして、水溶性有機溶剤は、沸点２３０℃以下のアミド系溶剤、沸点２３０℃以下の環状エステル系溶剤、沸点２３０℃以下のグリコールエーテル系溶剤から選ばれる１つ以上の水溶性有機溶剤Ａを含有することを特徴とする。このような、沸点が２３０℃以下の所定の有機溶剤を含有するインク組成物であれば、乾燥性が高く、得られる記録物の耐擦過性が良好となる。 The water-soluble organic solvent contains one or more water-soluble organic solvents A selected from amide solvents with a boiling point of 230°C or lower, cyclic ester solvents with a boiling point of 230°C or lower, and glycol ether solvents with a boiling point of 230°C or lower. characterized by Such an ink composition containing a predetermined organic solvent having a boiling point of 230° C. or less has high drying properties, and the resulting recorded matter has good scratch resistance.
　さらに、本実施の形態に係るインク組成物は樹脂を含有する。樹脂を含むインク組成物である場合には、水溶性有機溶剤Ａ（沸点２３０℃以下のアミド系溶剤、沸点２３０℃以下の環状エステル系溶剤、及び沸点２３０℃以下のグリコールエーテル系溶剤）が造膜助剤として作用することが本発明の研究により明らかとなった。一般にインク組成物の製膜時に所定の温度（最低造膜温度）以上の温度を加えることでインク組成物に含まれる樹脂が融着して耐擦過性の有する塗膜を形成することが可能となる。特に、この樹脂が粒子状の分散性樹脂である場合には、樹脂粒子同士の融着の度合いにより塗膜の状態は大きく変化するので、最低造膜温度と乾燥温度との関係は、塗膜の耐擦過性により強く影響する。 Furthermore, the ink composition according to the present embodiment contains a resin. In the case of an ink composition containing a resin, a water-soluble organic solvent A (an amide solvent with a boiling point of 230° C. or lower, a cyclic ester solvent with a boiling point of 230° C. or lower, and a glycol ether solvent with a boiling point of 230° C. or lower) is used. It has been found by the studies of the present invention that it acts as a film-assisting agent. In general, by applying a temperature equal to or higher than a predetermined temperature (minimum film-forming temperature) during film formation of the ink composition, the resin contained in the ink composition can be fused to form a scratch-resistant coating film. Become. In particular, when this resin is a particulate dispersible resin, the state of the coating film varies greatly depending on the degree of fusion between the resin particles. have a stronger effect on the scratch resistance of
　この最低造膜温度は、樹脂のＴｇ付近となることが一般的ではあるが、インク組成物に含まれる水溶性有機溶剤Ａにより最低造膜温度を下げることが可能となり、例えば樹脂のＴｇ以下の温度のような低温での乾燥温度であっても、樹脂を基材上で融着させることが可能となり、十分に耐擦過性の有する塗膜を形成することができる。 The minimum film-forming temperature is generally around the Tg of the resin, but the water-soluble organic solvent A contained in the ink composition makes it possible to lower the minimum film-forming temperature. Even if the drying temperature is as low as the temperature, the resin can be fused on the substrate, and a coating film having sufficient scratch resistance can be formed.
　なお、本実施の形態に係るインク組成物は、色材を含有する着色インクであってもよい。本明細書において「色材」とは、染料及び顔料を含むものであり、例えば、イエロー、マゼンタ、シアン、ブラック、及びこれらの中間色や淡色のような画像を形成する着色インクに含まれる染料又は顔料や、ホワイトインクに含まれる白色染料又は白色顔料や、メタリックインクに含まれる光輝性顔料をも含む概念として使用する。 Note that the ink composition according to the present embodiment may be a colored ink containing a coloring material. As used herein, the term “coloring material” includes dyes and pigments, such as yellow, magenta, cyan, black, and dyes contained in colored inks that form images such as intermediate colors and light colors thereof, or The concept includes pigments, white dyes or white pigments contained in white ink, and bright pigments contained in metallic ink.
　この着色インクは、イエロー、マゼンタ、シアン、ブラック、及びこれらの中間色や淡色のような画像を形成する着色インクであってもよい。また、着色インクは、白色色材を含むホワイトインクであってもよく、光輝性顔料を含むメタリックインク等であってもよい。 The colored inks may be yellow, magenta, cyan, black, and colored inks that form images such as intermediate colors and light colors thereof. Further, the colored ink may be white ink containing a white colorant, metallic ink containing a bright pigment, or the like.
　また、本実施の形態に係るインク組成物は、基材に着色インクを塗布するのに先立ち、基材に塗布され、カチオン性の化合物を含む受理溶液であってもよい。さらに、色材を含有しないクリアインクであってもよいし、記録物の表面にオーバーコート層を形成するためのオーバーコートインクであってもよい。なお、色材を含有しないクリアインクは樹脂を含有していてもしていなくともよい。 In addition, the ink composition according to the present embodiment may be a receiving solution containing a cationic compound that is applied to the substrate prior to applying the colored ink to the substrate. Furthermore, it may be a clear ink containing no coloring material, or an overcoat ink for forming an overcoat layer on the surface of a printed matter. The clear ink containing no coloring material may or may not contain a resin.
　以下、本実施の形態に係るインク組成物に含まれる各成分について説明する。 Each component contained in the ink composition according to the present embodiment will be described below.
　［水溶性有機溶剤］
　本実施の形態に係るインク組成物は水溶性有機溶剤を含有する。本明細書において水溶性有機溶剤とは、２５℃の水１００質量部中に、１気圧下で５質量部以上、好ましくは２０質量部以上、より好ましくは５０質量部以上、更に好ましくは７０質量部以上、更になお好ましくは９０質量部以上溶解することができるものをいう。 [Water-soluble organic solvent]
The ink composition according to this embodiment contains a water-soluble organic solvent. In this specification, the water-soluble organic solvent is 5 parts by mass or more, preferably 20 parts by mass or more, more preferably 50 parts by mass or more, and still more preferably 70 parts by mass in 100 parts by mass of water at 25°C under 1 atmosphere. Parts or more, more preferably 90 parts by mass or more can be dissolved.
　そして、この水溶性有機溶剤は、沸点２３０℃以下のアミド系溶剤、沸点２３０℃以下の環状エステル系溶剤、沸点２３０℃以下のグリコールエーテル系溶剤から選ばれる１つ以上の水溶性有機溶剤Ａを含有する。以下では、その水溶性有機溶剤Ａについて説明する。 The water-soluble organic solvent is one or more water-soluble organic solvents A selected from amide solvents with a boiling point of 230°C or lower, cyclic ester solvents with a boiling point of 230°C or lower, and glycol ether solvents with a boiling point of 230°C or lower. contains. The water-soluble organic solvent A will be described below.
　（水溶性有機溶剤Ａ）
　（１）沸点が２３０℃以下のアミド系溶剤
　沸点が２３０℃以下のアミド系溶剤とは、沸点が２３０℃以下であって、－Ｃ（＝Ｏ）－Ｎ－基（アミド結合）を有する有機溶剤である。沸点が２３０℃以下のアミド系溶剤としては、アルコキシアルキル基（ＣｎＨ２ｎ＋１－Ｏ－ＣｍＨ２ｍ－）を有するアルコキシアルキルアミド系溶剤や、アルキル基（ＣｎＨ２ｎ＋１－）を有するアルキルアミド系溶剤や、環状構造を有し、その環状構造に－Ｃ（＝Ｏ）－Ｎ－基を有する環状アミド系溶剤が挙げられる。 (Water-soluble organic solvent A)
(1) Amide-based solvent with a boiling point of 230°C or lower An amide-based solvent with a boiling point of 230°C or lower is an organic is a solvent. Examples of amide-based solvents having a boiling point of 230° C. or lower include alkoxyalkylamide-based solvents having an alkoxyalkyl group (C n H 2n+1 —O—C m H 2m —) and alkyl groups having an alkyl group (C n H 2n+1 —). Examples include amide-based solvents and cyclic amide-based solvents having a cyclic structure and a —C(═O)—N— group in the cyclic structure.
　沸点が２３０℃以下のアミド系溶剤としては、アルキルアミド系溶剤、アルコキシアルキルアミド系溶剤、又は環状アミド系溶剤であることが好ましく、アルキルアミド系溶剤であることがさらに好ましい。アルキルアミド系溶剤、アルコキシアルキルアミド系溶剤、又は環状アミド系溶剤を含有することで、本発明の効果を特に奏するインク組成物となる。 The amide-based solvent having a boiling point of 230°C or lower is preferably an alkylamide-based solvent, an alkoxyalkylamide-based solvent, or a cyclic amide-based solvent, and more preferably an alkylamide-based solvent. By containing an alkylamide-based solvent, an alkoxyalkylamide-based solvent, or a cyclic amide-based solvent, the ink composition exhibits the effects of the present invention.
（（アルキルアミド系溶剤））
　アルキルアミド系溶剤とは、アルキル基（ＣｎＨ２ｎ＋１－）と－Ｃ（＝Ｏ）－Ｎ－基（アミド結合）を有する化合物であって、水素若しくはアルキル基と－Ｃ（＝Ｏ）－Ｎ－基から構成された化合物からなる溶剤である。アルキルアミド系溶剤は、例えば以下の構造を有するものを好ましく用いることができる。 ((alkylamide solvent))
An alkylamide solvent is a compound having an alkyl group (C n H 2n+1 -) and a -C(=O)-N- group (amide bond), wherein hydrogen or an alkyl group and -C(=O)- It is a solvent consisting of a compound composed of N-groups. As the alkylamide-based solvent, those having, for example, the following structures can be preferably used.
Figure JPOXMLDOC01-appb-C000007
 （式（１）中、Ｒ１は水素、若しくは炭素数１～４のアルキル基であり、Ｒ２，Ｒ３は官能基である。）
Figure JPOXMLDOC01-appb-C000007
 (In formula (1), R 1 is hydrogen or an alkyl group having 1 to 4 carbon atoms, and R 2 and R 3 are functional groups.)
　Ｒ２，Ｒ３は官能基であれば特に限定されないが、例えば、Ｒ２，Ｒ３は、水素、アルキル基、アルコキシ基、ヒドロキシアルキル基、水酸基であることが好ましく、水素、あるいはアルキル基であることがより好ましく、水素、あるいは炭素数１～４のアルキル基であることがさらに好ましい。なお、Ｒ２，Ｒ３は同一であっても異なっていてもよい。 R 2 and R 3 are not particularly limited as long as they are functional groups. For example, R 2 and R 3 are preferably hydrogen, an alkyl group, an alkoxy group, a hydroxyalkyl group or a hydroxyl group. more preferably hydrogen or an alkyl group having 1 to 4 carbon atoms. R 2 and R 3 may be the same or different.
　アルキルアミド系溶剤としては、前記式（１）のＲ１～Ｒ３が水素、あるいはアルキル基で構成される例として、ホルムアミド、アセトアミド、プロパンアミド、ブタンアミド、イソブチルアミド、ペンタンアミド、Ｎ－メチルホルムアミド、Ｎ－メチルアセトアミド、Ｎ－メチルプロパンアミド、Ｎ－メチルブタンアミド、Ｎ－メチルイソブチルアミド、Ｎ－メチルペンタンアミド、Ｎ－エチルホルムアミド、Ｎ－エチルアセトアミド、Ｎ－エチルプロパンアミド、Ｎ－エチルブタンアミド、Ｎ－エチルイソブチルアミド、Ｎ－エチルペンタンアミド、Ｎ－プロピルホルムアミド、Ｎ－プロピルアセトアミド、Ｎ－プロピルプロパンアミド、Ｎ－プロピルブタンアミド、Ｎ－プロピルイソブチルアミド、Ｎ－プロピルペンタンアミド、Ｎ－イソプロピルホルムアミド、Ｎ－イソプロピルアセトアミド、Ｎ－イソプロピルプロパンアミド、Ｎ－イソプロピルブタンアミド、Ｎ－イソプロピルイソブチルアミド、Ｎ－イソプロピルペンタンアミド、Ｎ－ブチルホルムアミド、Ｎ－ブチルアセトアミド、Ｎ－ブチルプロパンアミド、Ｎ－ブチルブタンアミド、Ｎ－ブチルイソブチルアミド、Ｎ－ブチルペンタンアミド、Ｎ，Ｎ－ジメチルホルムアミド、Ｎ，Ｎ－ジメチルアセトアミド、Ｎ，Ｎ－ジメチルプロパンアミド、Ｎ，Ｎ－ジメチルブタンアミド、Ｎ，Ｎ－ジメチルイソブチルアミド、Ｎ，Ｎ－ジメチルペンタンアミド、Ｎ，Ｎ－ジエチルホルムアミド、Ｎ，Ｎ－ジエチルアセトアミド、Ｎ，Ｎ－ジエチルプロパンアミド、Ｎ，Ｎ－ジエチルブタンアミド、Ｎ，Ｎ－ジエチルイソブチルアミド、Ｎ，Ｎ－ジエチルペンタンアミド、Ｎ，Ｎ－ジプロピルホルムアミド、Ｎ，Ｎ－ジプロピルアセトアミド、Ｎ，Ｎ－ジプロピルプロパンアミド、Ｎ，Ｎ－ジプロピルブタンアミド、Ｎ，Ｎ－ジプロピルイソブチルアミド、Ｎ，Ｎ－ジプロピルペンタンアミド、Ｎ，Ｎ－ジイソプロピルホルムアミド、Ｎ，Ｎ－ジイソプロピルアセトアミド、Ｎ，Ｎ－ジイソプロピルプロパンアミド、Ｎ，Ｎ－ジイソプロピルブタンアミド、Ｎ，Ｎ－ジイソプロピルイソブチルアミド、Ｎ，Ｎ－ジイソプロピルペンタンアミド、Ｎ，Ｎ－ジブチルホルムアミド、Ｎ，Ｎ－ジブチルアセトアミド、Ｎ，Ｎ－ジブチルプロパンアミド、Ｎ，Ｎ－ジブチルブタンアミド、Ｎ，Ｎ－ジブチルイソブチルアミド、Ｎ，Ｎ－ジブチルペンタンアミド、Ｎ－エチル－Ｎ－メチルホルムアミド、Ｎ－エチル－Ｎ－メチルアセトアミド、Ｎ－エチル－Ｎ－メチルプロパンアミド、Ｎ－エチル－Ｎ－メチルブタンアミド、Ｎ－エチル－Ｎ－メチルイソブチルアミド、Ｎ－エチル－Ｎ－メチルペンタンアミド、Ｎ－メチル－Ｎ－プロピルホルムアミド、Ｎ－メチル－Ｎ－プロピルアセトアミド、Ｎ－メチル－Ｎ－プロピルプロパンアミド、Ｎ－メチル－Ｎ－プロピルブタンアミド、Ｎ－メチル－Ｎ－プロピルイソブチルアミド、Ｎ－メチル－Ｎ－プロピルペンタンアミド、Ｎ－エチル－Ｎ－プロピルホルムアミド、Ｎ－エチル－Ｎ－プロピルアセトアミド、Ｎ－エチル－Ｎ－プロピルプロパンアミド、Ｎ－エチル－Ｎ－プロピルブタンアミド、Ｎ－エチル－Ｎ－プロピルイソブチルアミド、Ｎ－エチル－Ｎ－プロピルペンタンアミド、あるいはこれらアルキル基の炭素数違いや炭素鎖が分岐構造を有するものなどが挙げられる。 Examples of alkylamide-based solvents in which R 1 to R 3 in formula (1) are hydrogen or alkyl groups include formamide, acetamide, propanamide, butanamide, isobutylamide, pentanamide, and N-methylformamide. , N-methylacetamide, N-methylpropanamide, N-methylbutanamide, N-methylisobutyramide, N-methylpentanamide, N-ethylformamide, N-ethylacetamide, N-ethylpropanamide, N-ethylbutane Amide, N-ethylisobutyramide, N-ethylpentanamide, N-propylformamide, N-propylacetamide, N-propylpropanamide, N-propylbutanamide, N-propylisobutyramide, N-propylpentanamide, N- Isopropylformamide, N-isopropylacetamide, N-isopropylpropanamide, N-isopropylbutanamide, N-isopropylisobutyramide, N-isopropylpentanamide, N-butylformamide, N-butylacetamide, N-butylpropanamide, N- Butylbutanamide, N-butylisobutyramide, N-butylpentanamide, N,N-dimethylformamide, N,N-dimethylacetamide, N,N-dimethylpropanamide, N,N-dimethylbutanamide, N,N- dimethylisobutyramide, N,N-dimethylpentanamide, N,N-diethylformamide, N,N-diethylacetamide, N,N-diethylpropanamide, N,N-diethylbutanamide, N,N-diethylisobutyramide, N,N-diethylpentanamide, N,N-dipropylformamide, N,N-dipropylacetamide, N,N-dipropylpropanamide, N,N-dipropylbutanamide, N,N-dipropylisobutyramide , N,N-dipropylpentanamide, N,N-diisopropylformamide, N,N-diisopropylacetamide, N,N-diisopropylpropanamide, N,N-diisopropylbutanamide, N,N-diisopropylisobutyramide, N, N-diisopropylpentanamide, N,N-dibutylformamide, N,N-dibutylacetamide, N,N-dibutylpropanamide, N,N-dibutylbutanamide, N,N-dibutylisobutylamide, N,N-dibutylpentane amides, N-ethyl-N-methylformamide, N-ethyl-N-methylacetamide, N-ethyl-N-methylpropanamide, N-ethyl-N-methylbutanamide, N-ethyl-N-methylisobutyramide, N-ethyl-N-methylpentanamide, N-methyl-N-propylformamide, N-methyl-N-propylacetamide, N-methyl-N-propylpropanamide, N-methyl-N-propylbutanamide, N- methyl-N-propylisobutyramide, N-methyl-N-propylpentanamide, N-ethyl-N-propylformamide, N-ethyl-N-propylacetamide, N-ethyl-N-propylpropanamide, N-ethyl- Examples include N-propylbutanamide, N-ethyl-N-propylisobutyramide, N-ethyl-N-propylpentanamide, and those having alkyl groups with different numbers of carbon atoms or having branched carbon chains.
　また、前記式（１）のＲ２、Ｒ３がアルコキシ基や、水酸基、ヒドロキシアルキル基となったものの例としては、Ｎ－エチル－Ｎ－（２－メトキシエチル）ホルムアミド、Ｎ－メトキシメチルホルムアミド、Ｎ－ヒドロキシメチル－Ｎ－メチルアセトアミド、Ｎ－（２－ヒドロキシエチル）－Ｎ－メチルアセトアミド、Ｎ－メトキシメチル－Ｎ－メチルホルムアミド、あるいはこれらの炭素数違いや炭素鎖が分岐構造を有するものなどが挙げられる。この中でも、本発明の効果を特に奏するという観点から、Ｎ－エチル－Ｎ－メチルホルムアミド、Ｎ－メチル－Ｎ－プロピルホルムアミド、Ｎ，Ｎ－ジエチルホルムアミド、Ｎ－エチル－Ｎ－プロピルホルムアミド、Ｎ，Ｎ－ジメチルアセトアミド、Ｎ－エチル－Ｎ－メチルアセトアミド、Ｎ－メチル－Ｎ－プロピルアセトアミド、Ｎ，Ｎ－ジエチルアセトアミド、Ｎ，Ｎ－ジメチルプロパンアミド、Ｎ－エチル－Ｎ－メチルプロパンアミドからなる群より選択されるアルキルアミド系溶剤が特に好ましい。 Examples of those in which R 2 and R 3 in formula (1) are alkoxy groups, hydroxyl groups, and hydroxyalkyl groups include N-ethyl-N-(2-methoxyethyl)formamide and N-methoxymethylformamide. , N-hydroxymethyl-N-methylacetamide, N-(2-hydroxyethyl)-N-methylacetamide, N-methoxymethyl-N-methylformamide, or those having a different carbon number or a branched carbon chain structure etc. Among these, N-ethyl-N-methylformamide, N-methyl-N-propylformamide, N,N-diethylformamide, N-ethyl-N-propylformamide, N, The group consisting of N-dimethylacetamide, N-ethyl-N-methylacetamide, N-methyl-N-propylacetamide, N,N-diethylacetamide, N,N-dimethylpropanamide, N-ethyl-N-methylpropanamide A more selected alkylamide solvent is particularly preferred.
　（（アルコキシアルキルアミド系溶剤））
　アルコキシアルキルアミド系溶剤とは、アルコキシアルキル基（ＣｎＨ２ｎ＋１－Ｏ－ＣｎＨ２ｎ－）と－Ｃ（＝Ｏ）－Ｎ－基（アミド結合）を有する化合物からなる溶剤である。アルコキシアルキルアミド系溶剤は、例えば式（２）のアルキルアミド系構造を有するアルキルアミド系溶剤のうち沸点が２３０℃以下のものを好ましく用いることができる。 ((Alkoxyalkylamide-based solvent))
An alkoxyalkylamide-based solvent is a solvent composed of a compound having an alkoxyalkyl group (C n H 2n+1 -O-C n H 2n -) and a -C(=O)-N- group (amide bond). As the alkoxyalkylamide-based solvent, for example, among alkylamide-based solvents having an alkylamide-based structure represented by formula (2), those having a boiling point of 230° C. or lower can be preferably used.
Figure JPOXMLDOC01-appb-C000008
 （式（２）中、Ｒ１２は、それぞれ独立して炭素数１以上４以下のアルキル基であり、Ｒ１３は、炭素数１以上４以下のアルキレン基であり、Ｒ１０、Ｒ１１はそれぞれ独立してもよい官能基である。）
Figure JPOXMLDOC01-appb-C000008
 (In Formula (2), R 12 is each independently an alkyl group having 1 to 4 carbon atoms, R 13 is an alkylene group having 1 to 4 carbon atoms, and R 10 and R 11 are each independently It is a functional group that may be independent.)
　Ｒ１２は、炭素数１以上２以下のアルキル基であることが好ましく、炭素数１以上２以下のアルキル基であることがより好ましい。Ｒ１３は、炭素数１以上３以下のアルキレン基であることが好ましく、炭素数１以上２以下のアルキレン基であることがより好ましい。 R 12 is preferably an alkyl group having 1 or more and 2 or less carbon atoms, more preferably an alkyl group having 1 or more and 2 or less carbon atoms. R 13 is preferably an alkylene group having 1 to 3 carbon atoms, more preferably an alkylene group having 1 to 2 carbon atoms.
　Ｒ１０、Ｒ１１は官能基であれば特に限定されないが、例えば、Ｒ１０、Ｒ１１は、水素、アルキル基、アルコキシ基、ヒドロキシアルキル基、水酸基であることが好ましく、水素、あるいはアルキル基であることがより好ましく、水素、あるいは炭素数１～４のアルキル基であることがさらに好ましく、水素、あるいは炭素数１～２のアルキル基であることが R 10 and R 11 are not particularly limited as long as they are functional groups. For example, R 10 and R 11 are preferably hydrogen, an alkyl group, an alkoxy group, a hydroxyalkyl group, or a hydroxyl group. more preferably hydrogen or an alkyl group having 1 to 4 carbon atoms, more preferably hydrogen or an alkyl group having 1 to 2 carbon atoms
　アルコキシアルキルアミド系溶剤としては、３－メトキシ－Ｎ，Ｎ－ジメチルプロパンアミド、３－プロポキシ－Ｎ，Ｎ－ジメチルプロパンアミド、あるいはこれらのアルコキシ基やアルキル基の炭素数違いや炭素鎖が分岐構造を有するものうち沸点が２３０℃以下のものが好ましい。この中でも、本発明の効果を特に奏するという観点から、３－メトキシ－Ｎ，Ｎ－ジメチルプロパンアミドが特に好ましい。 As the alkoxyalkylamide-based solvent, 3-methoxy-N,N-dimethylpropanamide, 3-propoxy-N,N-dimethylpropanamide, or the difference in the number of carbon atoms in the alkoxy group or alkyl group or the branched structure of the carbon chain. of those having a boiling point of 230° C. or lower are preferred. Among these, 3-methoxy-N,N-dimethylpropanamide is particularly preferable from the viewpoint of exhibiting the effects of the present invention.
　（（環状アミド系溶剤））
　環状アミド系溶剤とは、環状構造を有し、その環状構造に－Ｃ（＝Ｏ）－Ｎ－基を有する化合物からなる溶剤である。アルキルアミド系溶剤は、例えば式（３）～（５）の環状アミド系溶剤のうち沸点が２３０℃以下のものを好ましく用いることができる。 ((Cyclic amide solvent))
A cyclic amide solvent is a solvent composed of a compound having a cyclic structure and a -C(=O)-N- group in the cyclic structure. As the alkylamide solvent, those having a boiling point of 230° C. or lower among the cyclic amide solvents represented by the formulas (3) to (5) can be preferably used.
Figure JPOXMLDOC01-appb-C000009
 （式（３）中、Ｒ４は、炭素数３以上５以下の分岐しても良いアルキレン基であり、Ｒ５は、水素若しくは炭素数１以上４以下のアルキル基または不飽和炭化水素基を表す。）
Figure JPOXMLDOC01-appb-C000009
 (In formula (3), R 4 is an optionally branched alkylene group having 3 to 5 carbon atoms, and R 5 is hydrogen, an alkyl group having 1 to 4 carbon atoms, or an unsaturated hydrocarbon group. represent.)
　Ｒ４は、炭素数３以上４以下のアルキレン基であることが好ましい。Ｒ５は、水素若しくは炭素数１以上２以下のアルキル基または不飽和炭化水素基であることが好ましい。 R 4 is preferably an alkylene group having 3 or more and 4 or less carbon atoms. R5 is preferably hydrogen, an alkyl group having 1 to 2 carbon atoms, or an unsaturated hydrocarbon group.
Figure JPOXMLDOC01-appb-C000010
 （式（４）中、Ｒ１４は水素若しくは炭素数１以上４以下の分岐しても良いアルキル基または不飽和炭化水素基であり、Ｒ１５は炭素数１以上４以下のアルキレン基を表す。）
Figure JPOXMLDOC01-appb-C000010
 (In formula (4), R 14 is hydrogen, an optionally branched alkyl group having 1 to 4 carbon atoms, or an unsaturated hydrocarbon group, and R 15 represents an alkylene group having 1 to 4 carbon atoms. )
Figure JPOXMLDOC01-appb-C000011
 （式（５）中、Ｒ１６、Ｒ１７はそれぞれ独立して、水素若しくは炭素数１以上４以下の分岐しても良いアルキル基または不飽和炭化水素基でありＲ１８は炭素数１以上４以下の分岐しても良いアルキレン基を表す。
Figure JPOXMLDOC01-appb-C000011
 (In Formula (5), R 16 and R 17 are each independently hydrogen, an optionally branched alkyl group having 1 to 4 carbon atoms, or an unsaturated hydrocarbon group, and R 18 is 1 to 4 carbon atoms. represents the following optionally branched alkylene group.
　環状アミド系溶剤としては、Ｎ－ビニルメチルオキサゾリジノン、１，３－ジメチル－２－ピロリドン、Ｎ-メチル－２－ピロリドン、Ｎ－エチル－２－ピロリドン、β－ラクタム、４－メトキシ－１－メチル－２－ピロリジノン、Ｎ－プロピル－２－ピロリドン、Ｎ－メチル－２－ピペリジノン、あるいはこれらのアルコキシ基やアルキル基の炭素数違いや炭素鎖が分岐構造を有するものうち沸点が２３０℃以下のものが好ましい。この中でも、本発明の効果を特に奏するという観点から、Ｎ-メチル－２－ピロリドンが特に好ましい。 Cyclic amide solvents include N-vinylmethyloxazolidinone, 1,3-dimethyl-2-pyrrolidone, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, β-lactam, 4-methoxy-1-methyl -2-pyrrolidinone, N-propyl-2-pyrrolidone, N-methyl-2-piperidinone, or those having a branched carbon chain structure or a different number of carbon atoms in their alkoxy or alkyl groups, those having a boiling point of 230°C or less is preferred. Among these, N-methyl-2-pyrrolidone is particularly preferable from the viewpoint of exhibiting the effects of the present invention.
　（２）沸点２３０℃以下の環状エステル系溶剤
　沸点が２３０℃以下の環状エステル系溶剤とは、沸点が２３０℃以下であって、環状構造を有し、その環状構造に－Ｃ（＝Ｏ）－Ｏ－基を有する有機溶剤である。沸点２３０℃以下の環状エステル系溶剤は、例えば以下の構造を有するものを好ましく用いることができる。 (2) Cyclic ester solvent with a boiling point of 230° C. or less A cyclic ester solvent with a boiling point of 230° C. or less has a boiling point of 230° C. or less and has a cyclic structure in which —C (=O) It is an organic solvent having an —O— group. A cyclic ester solvent having a boiling point of 230° C. or less can preferably be used, for example, having the following structure.
Figure JPOXMLDOC01-appb-C000012
 （式（６）中、Ｒ５は、炭素数３以上５以下のアルキレン基又はビニレン基を有する炭素鎖であり、Ｒ６は、水素若しくは炭素数１以上２以下のアルキル基又はビニリデン基を表す。Ｒ６は、Ｒ５の炭素鎖であればどの位置でも、複数あってもよく、Ｒ５とＲ６は単結合又は多重結合のいずれの結合で繋がっていてもよい。）
Figure JPOXMLDOC01-appb-C000012
 (In formula (6), R 5 is a carbon chain having an alkylene group having 3 to 5 carbon atoms or a vinylene group, and R 6 represents hydrogen, an alkyl group having 1 to 2 carbon atoms, or a vinylidene group. R 6 may be at any position in the carbon chain of R 5 and may be plural, and R 5 and R 6 may be linked by either a single bond or a multiple bond.)
　Ｒ５は、炭素数４以上５以下のアルキレン基であることが好ましく、炭素数５のアルキレン基であることがより好ましい。Ｒ６は、水素若しくは炭素数１のアルキル基であることが好ましく、水素であることがより好ましい。 R 5 is preferably an alkylene group having 4 or more and 5 or less carbon atoms, more preferably an alkylene group having 5 carbon atoms. R 6 is preferably hydrogen or an alkyl group having 1 carbon atom, more preferably hydrogen.
Figure JPOXMLDOC01-appb-C000013
 （式（７）中、Ｒ８は、水素若しくは炭素数１以上４以下のアルキル基であり、Ｒ９は、炭素数１以上３以下のアルキレン基を表す。）
Figure JPOXMLDOC01-appb-C000013
 (In formula (7), R 8 is hydrogen or an alkyl group having 1 to 4 carbon atoms, and R 9 represents an alkylene group having 1 to 3 carbon atoms.)
　このような環状エステル系溶剤としては、例えば、γ－ブチロラクトン、α－メチレン－γ－ブチロラクトン、ε－カプロラクトン、γ－バレロラクトン、γ－ヘキサノラクトン、γ－ヘプタノラクトン、δ－バレロラクトン、δ－ヘキサノラクトン、δ－ヘプタラクトン、δ－オクタラクトン、δ－ノナラクトン、δ－デカラクトン、δ－ウンデカラクトン、γ,γ－ジメチル－γ－ブチロラクトン、α－メチル－γ－ブチロラクトン、γ－クロトラクトン、α－メチレン－γ－ブチロラクトン、β－メチル－γ－ブチロラクトン、６-メチルバレロラクトン、２，３－ブチレンカーボネート、エチレンカーボネート、プロピレンカーボネート等のうち沸点が２３０℃以下のものを挙げることができる。 Examples of such cyclic ester solvents include γ-butyrolactone, α-methylene-γ-butyrolactone, ε-caprolactone, γ-valerolactone, γ-hexanolactone, γ-heptanolactone, δ-valerolactone, δ-hexanolactone, δ-heptalactone, δ-octalactone, δ-nonalactone, δ-decalactone, δ-undecalactone, γ,γ-dimethyl-γ-butyrolactone, α-methyl-γ-butyrolactone, γ- Crotolactone, α-methylene-γ-butyrolactone, β-methyl-γ-butyrolactone, 6-methylvalerolactone, 2,3-butylene carbonate, ethylene carbonate, propylene carbonate, etc. with a boiling point of 230°C or less can be done.
　（３）沸点２３０℃以下のグリコールエーテル系溶剤
　沸点が２３０℃以下のグリコールエーテル系溶剤とは、沸点が２３０℃以下であって、ポリアルキレングリコールの片末端もしくは両末端のＯＨ基がアルキルやアシル、アリール置換された有機溶剤である。沸点２３０℃以下のグリコールエーテル系溶剤は、例えば以下の構造を有するものを好ましく用いることができる。 (3) Glycol ether solvent with a boiling point of 230°C or less A glycol ether solvent with a boiling point of 230°C or less means that the boiling point is 230°C or less, and the OH groups at one or both ends of the polyalkylene glycol are alkyl or acyl. , is an aryl-substituted organic solvent. Glycol ether solvents having a boiling point of 230° C. or less can preferably be used, for example, having the following structure.
Figure JPOXMLDOC01-appb-C000014
 　（式（８）中、Ｒ７、Ｒ９は、水素、若しくはアルキル基、アシル基であり、少なくとも一方はアルキル基、若しくはアシル基である。Ｒ８は、エチレン基又はプロピレン基を表す。ｎは２～４の整数を表す。）
Figure JPOXMLDOC01-appb-C000014
 (In Formula (8), R 7 and R 9 are hydrogen, an alkyl group, or an acyl group, at least one of which is an alkyl group or an acyl group. R 8 represents an ethylene group or a propylene group. n represents an integer from 2 to 4.)
　このようなグリコールエーテル系溶剤としては、エチレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテル、ジエチレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテル、トリエチレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテル、プロピレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテル、ジプロピレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテル、トリプロピレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテル等のモノアルキルエーテル類；ジエチレングリコールジメチルエーテル、ジエチレングリコールジエチルエーテル、ジエチレングリコールエチルメチルエーテル、トリエチレングリコールジメチルエーテル、トリエチレングリコールジエチルエーテル、トリエチレングリコールエチルメチルエーテル、テトラエチレングリコールジメチルエーテル、テトラエチレングリコールジエチルエーテル、テトラエチレングリコールエチルメチルエーテル、プロピレングリコールジメチルエーテル、プロピレングリコールジエチルエーテル、プロピレングリコールエチルメチルエーテル、ジプロピレングリコールジメチルエーテル、ジプロピレングリコールジエチルエーテル、ジプロピレングリコールエチルメチルエーテル、トリプロピレングリコールジメチルエーテル、トリプロピレングリコールジエチルエーテル、トリプロピレングリコールエチルメチルエーテル等の多価アルコールのジアルキルエーテル類；エチレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテルアセテート、ジエチレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテルアセテート、トリエチレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテルアセテート、プロピレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテルアセテート、ジプロピレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテルアセテート、トリプロピレングリコールモノメチル（又はエチル、プロピル、イソプロピル、ｎ－ブチル、イソブチル、ｔ－ブチル、ペンチル、ｎ－ヘキシル、２－エチルヘキシル）エーテルアセテート、エチレングリコールジアセテート、ジエチレングリコールジアセテート、プロピレングリコールジアセテート、ジプロピレングリコールジアセテート等のアセテート類等であって沸点２３０℃以下のものを挙げることができる。 Such glycol ether solvents include ethylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether, diethylene glycol monomethyl (or ethyl, propyl , isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether, triethylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n -hexyl, 2-ethylhexyl) ether, propylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether, dipropylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether, tripropylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, monoalkyl ethers such as n-hexyl, 2-ethylhexyl) ether; diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol ethyl methyl ether, triethylene glycol dimethyl ether, triethylene glycol diethyl ether, triethylene glycol ethyl methyl ether, tetraethylene glycol dimethyl ether , tetraethylene glycol diethyl ether, tetraethylene glycol ethyl methyl ether, propylene glycol dimethyl ether, propylene glycol diethyl ether, propylene glycol ethyl methyl ether, dipropylene glycol dimethyl ether, dipropylene glycol diethyl ether, dipropylene glycol ethyl methyl ether, tripropylene glycol Dialkyl ethers of polyhydric alcohols such as dimethyl ether, tripropylene glycol diethyl ether, tripropylene glycol ethyl methyl ether; ethylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl , 2-ethylhexyl) ether acetate, diethylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether acetate, triethylene glycol monomethyl (or ethyl, propyl) , isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether acetate, propylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n -hexyl, 2-ethylhexyl) ether acetate, dipropylene glycol monomethyl (or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether acetate, tripropylene glycol monomethyl ( or ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, n-hexyl, 2-ethylhexyl) ether acetate, ethylene glycol diacetate, diethylene glycol diacetate, propylene glycol diacetate, dipropylene glycol diacetate, etc. and the like having a boiling point of 230° C. or less.
　上述した水溶性有機溶剤Ａとして沸点２３０℃以下のアミド系溶剤、沸点２３０℃以下の環状エステル系溶剤、及び沸点２３０℃以下のグリコールエーテル系溶剤からなる群より選択される少なくとも１つを含有するインク組成物であれば、最低造膜温度を下げる効果をより効果的に享受することが可能となる。その中でも、有機溶剤Ａとして沸点が２３０℃以下のアミド系溶剤を含有することが好ましく、アルキルアミド系溶剤を含有することが特に好ましい。 Contains at least one selected from the group consisting of amide solvents with a boiling point of 230° C. or lower, cyclic ester solvents with a boiling point of 230° C. or lower, and glycol ether solvents with a boiling point of 230° C. or lower as the water-soluble organic solvent A described above. With the ink composition, it is possible to more effectively enjoy the effect of lowering the minimum film-forming temperature. Among them, the organic solvent A preferably contains an amide-based solvent having a boiling point of 230° C. or less, and particularly preferably contains an alkylamide-based solvent.
　また、水溶性有機溶剤Ａは、２種以上の水溶性有機溶剤Ａを含んでいてもよい。具体的には、（１）少なくとも２種以上の沸点２３０℃以下のアミド系溶剤を含有するインク組成物（２）少なくとも沸点２３０℃以下のアミド系溶剤と、沸点２３０℃以下の環状エステル系溶剤と、を含有するインク組成物や（３）沸点２３０℃以下のアミド系溶剤と、沸点２３０℃以下のグリコールエーテル系溶剤と、を含有するインク組成物や（４）沸点２３０℃以下の環状エステル系溶剤と、沸点２３０℃以下のグリコールエーテル系溶剤を含有するインク組成物が挙げられる。 In addition, the water-soluble organic solvent A may contain two or more water-soluble organic solvents A. Specifically, (1) an ink composition containing at least two or more amide-based solvents having a boiling point of 230°C or lower, and (2) at least an amide-based solvent having a boiling point of 230°C or lower and a cyclic ester-based solvent having a boiling point of 230°C or lower. and an ink composition containing (3) an amide solvent having a boiling point of 230° C. or less and a glycol ether solvent having a boiling point of 230° C. or less, and (4) a cyclic ester having a boiling point of 230° C. or less and an ink composition containing a glycol ether solvent having a boiling point of 230° C. or lower.
　水溶性有機溶剤Ａのなかでも、水／１－オクタノールでの分配係数（ＬｏｇＰ）が高い水溶性有機溶剤Ａであることが好ましい。分配係数は、有機溶剤の疎水性の指標であり、水／１－オクタノールでの分配係数（ＬｏｇＰ）が高い有機溶剤であるほど、疎水性が相対的に高い有機溶剤であることを意味するものである。 Among the water-soluble organic solvents A, water-soluble organic solvents A with a high water/1-octanol partition coefficient (LogP) are preferred. The partition coefficient is an index of the hydrophobicity of an organic solvent, and a higher organic solvent with a higher partition coefficient (LogP) in water/1-octanol means that the organic solvent has relatively higher hydrophobicity. is.
　沸点が２３０℃以下の水溶性有機溶剤Ａを含有するインク組成物であれば、乾燥性が高く、得られる記録物の生産性が高いものであるが、記録物の生産性を高くしようとして乾燥処理を短くし、あるいは低温で乾燥処理を施すと、分散性樹脂を含有するインク組成物の造膜性が低下し、耐擦過性が相対的に低下することとなる。 An ink composition containing a water-soluble organic solvent A having a boiling point of 230° C. or less has high drying properties and high productivity of the resulting recorded matter. If the treatment is shortened or the drying treatment is performed at a low temperature, the film-forming property of the ink composition containing the dispersible resin is lowered, and the abrasion resistance is relatively lowered.
　水／１－オクタノールでの分配係数（ＬｏｇＰ）が高い水溶性有機溶剤Ａ（すなわち、疎水性が相対的に高い水溶性有機溶剤Ａ）を含有することにより、分散性樹脂を含有するインク組成物の造膜性が良好となり、結果として耐擦過性の高い塗膜を形成することが可能なインク組成物となる。 An ink composition containing a dispersible resin by containing a water-soluble organic solvent A having a high water/1-octanol partition coefficient (LogP) (that is, a water-soluble organic solvent A having relatively high hydrophobicity) As a result, the ink composition is capable of forming a coating film having high scratch resistance.
　具体的には、沸点が２３０℃以下の水溶性有機溶剤Ａは、水／１－オクタノールでの分配係数（ＬｏｇＰ）が－０．６以上であることが好ましく、－０．４以上であることがより好ましく、－０．３以上であることがさらに好ましい。水／１－オクタノールでの分配係数（ＬｏｇＰ）が－０．６以上である水溶性有機溶剤Ａを含有することで、より耐擦過性に優れるインク組成物となる。 Specifically, the water-soluble organic solvent A having a boiling point of 230° C. or less preferably has a water/1-octanol distribution coefficient (LogP) of −0.6 or more, and preferably −0.4 or more. is more preferable, and −0.3 or more is even more preferable. By containing the water-soluble organic solvent A having a water/1-octanol partition coefficient (LogP) of −0.6 or more, the ink composition has more excellent scratch resistance.
　沸点が２３０℃以下の水溶性有機溶剤Ａは、水／１－オクタノールでの分配係数（ＬｏｇＰ）が１．５以下であることが好ましく、１．０以下であることがより好ましく、０．５以下であることがさらに好ましい。水／１－オクタノールでの分配係数（ＬｏｇＰ）が１．５以下である水溶性有機溶剤Ａを含有することで、インク組成物に含まれる分散性樹脂等との相溶性が高くなってインク組成物の保存安定性が良好となる。 The water-soluble organic solvent A having a boiling point of 230° C. or less preferably has a water/1-octanol distribution coefficient (LogP) of 1.5 or less, more preferably 1.0 or less, and 0.5. More preferably: By containing the water-soluble organic solvent A having a water/1-octanol partition coefficient (LogP) of 1.5 or less, the compatibility with the dispersible resin or the like contained in the ink composition is increased, and the ink composition Good storage stability of the product.
　沸点が２３０℃以下の水溶性有機溶剤Ａの沸点は、２２０℃以下であることが好ましく、２１０℃以下であることがより好ましい。これにより、より乾燥性が高いインク組成物となる。沸点が２３０℃以下の水溶性有機溶剤Ａの沸点は、１３０℃以上であることが好ましく、１４０℃以上であることがより好ましく、１５０℃以上であることがさらに好ましい。水溶性有機溶剤Ａの沸点は、１３０℃以上であることにより、ノズル面での乾燥性が高くなることによる吐出安定性の低下を抑制することが可能となる。 The boiling point of the water-soluble organic solvent A having a boiling point of 230°C or lower is preferably 220°C or lower, more preferably 210°C or lower. As a result, an ink composition having higher drying properties can be obtained. The boiling point of the water-soluble organic solvent A having a boiling point of 230° C. or lower is preferably 130° C. or higher, more preferably 140° C. or higher, and even more preferably 150° C. or higher. When the boiling point of the water-soluble organic solvent A is 130° C. or higher, it is possible to suppress deterioration in ejection stability due to increased drying properties on the nozzle surface.
　沸点が２３０℃以下の水溶性有機溶剤Ａの含有量は、とくに限定されるものではないが、インク組成物全量中２質量％以上の範囲であることが好ましく、５質量％以上の範囲であることがより好ましく、１０質量％以上であることがさらに好ましい。これにより、樹脂粒子の造膜性がより高いインク組成物となる。 The content of the water-soluble organic solvent A having a boiling point of 230° C. or lower is not particularly limited, but is preferably in the range of 2% by mass or more, and in the range of 5% by mass or more in the total amount of the ink composition. is more preferable, and 10% by mass or more is even more preferable. As a result, an ink composition having a higher film-forming property of the resin particles is obtained.
　沸点が２３０℃以下の水溶性有機溶剤Ａの含有量は、インク組成物全量中４０質量％以下であることが好ましく、３５質量％以下であることがより好ましく、３０質量％以下であることがさらに好ましい。これにより、他の成分との相溶性が良く、インクの保存安定性が良いインク組成物となる。 The content of the water-soluble organic solvent A having a boiling point of 230° C. or less is preferably 40% by mass or less, more preferably 35% by mass or less, and preferably 30% by mass or less in the total amount of the ink composition. More preferred. As a result, an ink composition having good compatibility with other components and good ink storage stability can be obtained.
　また、上述した通り、水溶性有機溶剤Ａは造膜助剤として作用するため、インク組成物に含有される分散性樹脂の含有量に応じて水溶性有機溶剤Ａの含有量を制御することが好ましい。具体的には、分散性樹脂１００質量部に対する前記水溶性有機溶剤Ａの含有量は３０質量部以上であることが好ましく、５０質量部以上であることがより好ましく、６５質量部以上であることがさらに好ましい。これにより、樹脂粒子の造膜性がより高いインク組成物となる。 Further, as described above, since the water-soluble organic solvent A acts as a film-forming aid, the content of the water-soluble organic solvent A can be controlled according to the content of the dispersible resin contained in the ink composition. preferable. Specifically, the content of the water-soluble organic solvent A with respect to 100 parts by mass of the dispersible resin is preferably 30 parts by mass or more, more preferably 50 parts by mass or more, and 65 parts by mass or more. is more preferred. As a result, an ink composition having a higher film-forming property of the resin particles is obtained.
　（その他の水溶性有機溶剤）
　本実施の形態に係るインク組成物には、水溶性有機溶剤Ａとは異なるその他の水溶性有機溶剤を含有してもよい。 (Other water-soluble organic solvents)
The ink composition according to the present embodiment may contain other water-soluble organic solvents different from the water-soluble organic solvent A.
　そのような水溶性有機溶剤としては、例えば、３－メチル－２－オキサゾリジノン、３－エチル－２－オキサゾリジノン、３－メチル－２－ピロリジノン、２－ピロリドン、Ｎ－メチル－Ｎ－（１－メチルエチル）ホルムアミド、Ｎ－ヒドロキシプロピル－Ｎ－メチルアセトアミド、３－ブトキシ－Ｎ，Ｎ－ジメチルプロパンアミド、β-ラクタム、δ-ラクタム、ε-カプロラクタム、Ｎ－２－ヒドロキシエチル－２－ピロリドン、エチレン尿素、Ｎ－ヒドロキシエチレン尿素、３－メトキシプロパンアミド、３－ブトキシプロパンアミド、Ｎ，Ｎ－ジブチル－３－メトキシプロパンアミド、Ｎ，Ｎ－ジブチル－３－ブトキシプロパンアミド、等のアミド系溶剤；メチルアルコール、エチルアルコール、ｎ－プロピルアルコール、イソプロピルアルコール、ｎ－ブチルアルコール、ｓｅｃ－ブチルアルコール、ｔｅｒｔ－ブチルアルコール、イソブチルアルコール、ｎ－ペンタノール等の炭素数１～５のアルキルアルコール類、３－メトキシ－３－メチル－１－ブタノール、３－メトキシ－１－プロパノール、１－メトキシ－２－プロパノール、３－メトキシ－ｎ－ブタノール等の１価のアルコール類、アセトン、メチルエチルケトン、メチル－ｎ－プロピルケトン、メチルイソプロピルケトン、メチル－ｎ－ブチルケトン、メチルイソブチルケトン、メチル－ｎ－アミルケトン、メチルヘキシルケトン、メチルイソアミルケトン、ジエチルケトン、エチル－ｎ－プロピルケトン、エチルイソプロピルケトン、エチル－ｎ－ブチルケトン、エチルイソブチルケトン、ジ－ｎ－プロピルケトン、ジイソブチルケトン、シクロペンタノン、シクロヘキサノン、メチルシクロヘキサノン、イソホロン、アセチルケトン等のケトン又はケトアルコール類、テトラヒドロフラン、ジオキサン等のエーテル類、ポリエチレングリコール、ポリプロピレングリコール等のオキシエチレン又はオキシプロピレン共重合体、エチレングリコール、プロピレングリコール、ジエチレングリコール、ジプロピレングリコール、１，３－プロパンジオール、イソブチレングリコール、トリエチレングリコール、トリプロピレングリコール、テトラエチレングリコール、２－メチル－１，２－プロパンジオール、２－メチル－１，２－プロパンジオール、１，２－ブタンジオール、１，３－ブタンジオール、１，４－ブタンジオール、１，２－ペンタンジオール、１，３－ペンタンジオール、１，２－ヘキサンジオール、１，５－ペンタンジオール、１，６－ヘキサンジオール、２－メチル－２，４－ペンタンジオール、３－メチル－１，３－ブタンジオール、３－メチル－１，５－ペンタンジオール、２－メチル－２，４－ペンタンジオール等のジオール類；グリセリン、トリメチロールエタン、トリメチロールプロパン、１，２，６－ヘキサントリオール等のトリオール類；メソエリスリトール、ペンタエリスリトール等の４価アルコール類；モノエタノールアミン、ジエタノールアミン、トリエタノールアミン、Ｎ－メチルエタノールアミン、Ｎ－エチルエタノールアミン、Ｎ－ブチルエタノールアミン、Ｎ－メチルジエタノールアミン、Ｎ－エチルジエタノールアミン、Ｎ－ブチルジエタノールアミン等のアルカノールアミン類、酢酸メチル、酢酸エチル、酢酸－ｎ－プロピル、酢酸イソプロピル、酢酸－ｎ－ブチル、酢酸イソブチル、酢酸ヘキシル、酢酸オクチル等の酢酸エステル類、乳酸メチル、乳酸エチル、乳酸ブチル、乳酸プロピル、乳酸エチルヘキシル、乳酸アミル、乳酸イソアミル等の乳酸エステル類、シュウ酸ジメチル、シュウ酸ジエチル、マロン酸ジメチル、マロン酸ジエチル、マロン酸ジプロピル、コハク酸ジメチル、コハク酸ジエチル、グルタル酸ジメチル、グルタル酸ジエチルなどの二塩基酸エステル類、ｎ－ヘキサン、イソヘキサン、ｎ－ノナン、イソノナン、ドデカン、イソドデカン等の飽和炭水素類、１－ヘキセン、１－ヘプテン、１－オクテン等の不飽和炭化水素類、シクロヘキサン、シクロヘプタン、シクロオクタン、シクロデカン、デカリン等の環状飽和炭化水素類、シクロヘキセン、シクロヘプテン、シクロオクテン、１，１，３，５，７－シクロオクタテトラエン、シクロドデセン等の環状不飽和炭化水素類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、Ｎ－メチルモルホリン、Ｎ－エチルモルホリン、Ｎ－ヒドロキシエチルモルホリン、４－アセチルモルホリン、Ｎ－ホルミルモルホリンなどのモルホリン類、テルペン系溶剤など、一般的な有機溶剤であって、水溶性有機溶剤Ａに該当しないものを挙げることができる。組み合わせる樹脂や分散剤などに応じて、適切なＨＳＰ値の溶剤を選択することが好ましい。 Examples of such water-soluble organic solvents include 3-methyl-2-oxazolidinone, 3-ethyl-2-oxazolidinone, 3-methyl-2-pyrrolidinone, 2-pyrrolidone, N-methyl-N-(1-methyl ethyl)formamide, N-hydroxypropyl-N-methylacetamide, 3-butoxy-N,N-dimethylpropanamide, β-lactam, δ-lactam, ε-caprolactam, N-2-hydroxyethyl-2-pyrrolidone, ethylene Amide solvents such as urea, N-hydroxyethyleneurea, 3-methoxypropanamide, 3-butoxypropanamide, N,N-dibutyl-3-methoxypropanamide, N,N-dibutyl-3-butoxypropanamide; alkyl alcohols having 1 to 5 carbon atoms such as methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, isobutyl alcohol, n-pentanol; Monohydric alcohols such as methoxy-3-methyl-1-butanol, 3-methoxy-1-propanol, 1-methoxy-2-propanol, 3-methoxy-n-butanol, acetone, methyl ethyl ketone, methyl-n-propyl ketone, methyl isopropyl ketone, methyl-n-butyl ketone, methyl isobutyl ketone, methyl-n-amyl ketone, methylhexyl ketone, methyl isoamyl ketone, diethyl ketone, ethyl-n-propyl ketone, ethyl isopropyl ketone, ethyl-n-butyl ketone, Ketones or ketoalcohols such as ethyl isobutyl ketone, di-n-propyl ketone, diisobutyl ketone, cyclopentanone, cyclohexanone, methylcyclohexanone, isophorone, acetyl ketone, ethers such as tetrahydrofuran and dioxane, polyethylene glycol, polypropylene glycol, etc. Oxyethylene or oxypropylene copolymer, ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, 1,3-propanediol, isobutylene glycol, triethylene glycol, tripropylene glycol, tetraethylene glycol, 2-methyl-1,2 -propanediol, 2-methyl-1,2-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,2-pentanediol, 1,3-pentanediol, 1,2-hexanediol, 1,5-pentanediol, 1,6-hexanediol, 2-methyl-2,4-pentanediol, 3-methyl-1,3-butanediol, 3-methyl-1,5 - diols such as pentanediol and 2-methyl-2,4-pentanediol; triols such as glycerin, trimethylolethane, trimethylolpropane and 1,2,6-hexanetriol; 4 such as mesoerythritol and pentaerythritol Hydric alcohols; alkanolamines such as monoethanolamine, diethanolamine, triethanolamine, N-methylethanolamine, N-ethylethanolamine, N-butylethanolamine, N-methyldiethanolamine, N-ethyldiethanolamine, N-butyldiethanolamine Acetic esters such as methyl acetate, ethyl acetate, n-propyl acetate, isopropyl acetate, n-butyl acetate, isobutyl acetate, hexyl acetate, octyl acetate, methyl lactate, ethyl lactate, butyl lactate, propyl lactate, lactic acid Lactate esters such as ethylhexyl, amyl lactate and isoamyl lactate; Dibasic acid esters, saturated hydrocarbons such as n-hexane, isohexane, n-nonane, isononane, dodecane, and isododecane, unsaturated hydrocarbons such as 1-hexene, 1-heptene, and 1-octene, cyclohexane, cyclohexane cyclic saturated hydrocarbons such as heptane, cyclooctane, cyclodecane and decalin; cyclic unsaturated hydrocarbons such as cyclohexene, cycloheptene, cyclooctene, 1,1,3,5,7-cyclooctatetraene and cyclododecene; benzene; General organic solvents such as aromatic hydrocarbons such as toluene and xylene, morpholines such as N-methylmorpholine, N-ethylmorpholine, N-hydroxyethylmorpholine, 4-acetylmorpholine and N-formylmorpholine, and terpene solvents. Solvents other than the water-soluble organic solvent A can be mentioned. It is preferable to select a solvent with an appropriate HSP value according to the resin, dispersant, etc. to be combined.
　その中でも、ジオール系溶剤であることが好ましく、アルカンジオール系溶剤であることがより好ましく、１，２－アルカンジオール系溶剤であることがさらに好ましい。ジオール系溶剤は、インク組成物に含まれる他の含有成分との混和性が高く、かつ沸点が２３０℃以下の水溶性有機溶剤Ａに比べて揮発性が低いため、ヘッドノズル面での乾燥を防ぐことが可能となり、吐出安定性を高めることができる。 Among them, diol-based solvents are preferred, alkanediol-based solvents are more preferred, and 1,2-alkanediol-based solvents are even more preferred. The diol-based solvent is highly miscible with other components contained in the ink composition, and is less volatile than the water-soluble organic solvent A, which has a boiling point of 230° C. or less. It is possible to prevent this, and it is possible to improve the ejection stability.
　アルカンジオール系溶剤のなかでも、炭素数が３以上６以下であり、炭素骨格の少なくとも一方の末端に少なくとも１つの水酸基を備えるアルカンジオール系溶剤を含有することが特に好ましい。 Among the alkanediol-based solvents, it is particularly preferable to contain an alkanediol-based solvent having 3 or more and 6 or less carbon atoms and having at least one hydroxyl group at at least one end of the carbon skeleton.
　その他の水溶性有機溶剤を含有する場合、その他の水溶性有機溶剤の含有量は、特に限定されないが、例えば、インク組成物全量中１質量％以上であることが好ましく、５質量％以上であることがより好ましく、１０質量％以上であることがさらに好ましく、１５質量％以上であることがさらになお好ましい。インク組成物全量中３５質量％以下であることが好ましく、３０質量％以下であることがより好ましく、２５質量％以下であることがさらに好ましい。 When the other water-soluble organic solvent is contained, the content of the other water-soluble organic solvent is not particularly limited. is more preferably 10% by mass or more, and even more preferably 15% by mass or more. It is preferably 35% by mass or less, more preferably 30% by mass or less, and even more preferably 25% by mass or less, based on the total amount of the ink composition.
　［水］
　本実施の形態に係るインク組成物は、水を含有してもよい。水の含有量は、とくに限定されないが、水の含有量の下限は、インク組成物全量中３０質量％以上の範囲内であることが好ましく、４５質量％以上の範囲内であることがより好ましく、５０質量％以上の範囲内であることがさらに好ましい。水の含有量の上限は、インク組成物全量中８５質量％以下の範囲内であることが好ましく、８０質量％以下の範囲内であることがより好ましく、７５質量％以下の範囲内であることがさらに好ましい。 [water]
The ink composition according to this embodiment may contain water. The water content is not particularly limited, but the lower limit of the water content is preferably in the range of 30% by mass or more, more preferably in the range of 45% by mass or more, based on the total amount of the ink composition. , 50% by mass or more. The upper limit of the water content is preferably within the range of 85% by mass or less, more preferably within the range of 80% by mass or less, and within the range of 75% by mass or less in the total amount of the ink composition. is more preferred.
　特に、水を含有する場合、保存安定性の面からインク組成物の水以外の溶媒は親水性が高い溶剤で構成する必要があり、必然的にジオール系溶剤に代表される比較的高沸点の水溶性溶媒が選択される。溶媒が水と親水性が高い溶剤だけで構成される水性インク組成物の場合、特に低温乾燥においては乾燥性が悪化する傾向があり、乾燥性が悪化するという本発明の課題がより顕著に発生することになる。所定沸点以下のアミド系溶剤を含有する本実施の形態に係るインク組成物であれば、水を含有する水性インク組成物であっても、乾燥性を高くすることができるようになり、得られる記録物の生産性を高くすることが可能となる。 In particular, when water is contained, the solvent other than water in the ink composition must be composed of a highly hydrophilic solvent from the standpoint of storage stability. A water-soluble solvent is selected. In the case of an aqueous ink composition in which the solvent is composed of only water and a highly hydrophilic solvent, the drying property tends to deteriorate particularly in low-temperature drying, and the problem of the present invention that the drying property deteriorates occurs more remarkably. will do. As long as the ink composition according to the present embodiment contains an amide-based solvent having a predetermined boiling point or less, even if it is an aqueous ink composition containing water, it becomes possible to improve the drying property, and it is possible to obtain It is possible to increase the productivity of printed matter.
　［樹脂］
　本実施の形態に係るインク組成物は、樹脂を含有する。これにより、塗膜の耐擦過性を向上させることができる。特に、本実施の形態に係るインク組成物をオーバーコートインクとする場合、樹脂を含有することで、記録物に好適な耐擦過性を付与することが可能となる。 [resin]
The ink composition according to this embodiment contains a resin. Thereby, the scratch resistance of the coating film can be improved. In particular, when the ink composition according to the present embodiment is used as an overcoat ink, it is possible to impart suitable scratch resistance to a recorded matter by containing a resin.
　さらに、本実施の形態に係るインク組成物は、造膜助剤として作用する水溶性有機溶剤Ａ（沸点２３０℃以下のアミド系溶剤、沸点２３０℃以下の環状エステル系溶剤、及び沸点２３０℃以下のグリコールエーテル系溶剤）を含有するため、例えば樹脂のＴｇ以下の温度のような低温での乾燥温度であっても、樹脂を基材上で融着させることが可能となり、十分に耐擦過性の有する塗膜を形成することが可能となる。特に、本実施の形態に係るインク組成物をオーバーコートインクとする場合、樹脂を含有することで、記録物に好適な耐擦過性を付与することが可能となる。 Furthermore, the ink composition according to the present embodiment contains a water-soluble organic solvent A (an amide solvent with a boiling point of 230° C. or lower, a cyclic ester solvent with a boiling point of 230° C. or lower, and a Since it contains a glycol ether solvent), it is possible to fuse the resin on the substrate even at a low drying temperature such as a temperature below the Tg of the resin, and it has sufficient scratch resistance. It is possible to form a coating film having In particular, when the ink composition according to the present embodiment is used as an overcoat ink, it is possible to impart suitable scratch resistance to a recorded matter by containing a resin.
　樹脂としては、定着性に優れ、インク組成物の層の耐水性に優れる点から分散性樹脂を含有する。また、分散性樹脂を形成することによって、樹脂が静電反発力や立体反発力によって樹脂微粒子としてインク組成物中に分散することができ、分散安定性を向上させることが可能となる。なお、分散性樹脂とは、インク組成物中に粒子状に分散した樹脂であり、粒子状の樹脂がインク組成物に分散可能な樹脂を意味する。 As the resin, a dispersible resin is contained from the viewpoint of excellent fixability and excellent water resistance of the ink composition layer. In addition, by forming a dispersible resin, the resin can be dispersed as fine resin particles in the ink composition by electrostatic repulsion or steric repulsion, and dispersion stability can be improved. The dispersible resin is a resin that is dispersed in the ink composition in the form of particles, and means a resin that can be dispersed in the ink composition in the form of particles.
　具体的には、アクリル系樹脂、スチレン－アクリル系樹脂、ポリウレタン系樹脂、ポリエステル系樹脂、塩化ビニル系樹脂、酢酸ビニル系樹脂、ポリエーテル系樹脂、塩化ビニル酢酸ビニル共重合樹脂、ポリエチレン系樹脂、アクリルアミド系樹脂、エポキシ系樹脂、ポリカーボネート系樹脂、シリコーン系樹脂、ポリスチレン系樹脂からなる群より選択される１つ以上の樹脂あるいは共重合樹脂を含むものあるいはこれらの混合物を含むものを用いることができる。これらのものは耐水性に加えて耐溶剤性も向上させることができる点で好ましい。中でも、吐出安定性、耐水性及び耐溶剤性に優れたものとすることができることから、構成モノマーの少なくとも１つ以上にアクリル骨格を有するアクリル樹脂又はアクリル樹脂との共重合体（アクリル系共重合樹脂）を含むものであることが好ましい。 Specifically, acrylic resins, styrene-acrylic resins, polyurethane resins, polyester resins, vinyl chloride resins, vinyl acetate resins, polyether resins, vinyl chloride vinyl acetate copolymer resins, polyethylene resins, One or more resins selected from the group consisting of acrylamide-based resins, epoxy-based resins, polycarbonate-based resins, silicone-based resins, and polystyrene-based resins, or copolymer resins, or mixtures thereof can be used. . These are preferable because they can improve not only water resistance but also solvent resistance. Among them, since it can be excellent in ejection stability, water resistance and solvent resistance, at least one of the constituent monomers is an acrylic resin having an acrylic skeleton or a copolymer with an acrylic resin (acrylic copolymer resin).
　本実施の形態に係るインク組成物に含まれる樹脂のＴｇ（ガラス転移温度）は、とくに限定されるものではないが、インク組成物の乾燥温度よりも高いことが好ましい。具体的には、樹脂のＴｇは５０℃以上であることが好ましく、５５℃以上であることがより好ましく、６０℃以上であることがさらに好ましい。本来であれば、インク組成物に含まれる樹脂のＴｇが高くなると乾燥温度を高くしなければ樹脂を基材上に融着させることができず、記録物に好適な耐擦過性や耐溶剤性、耐水摩擦性を付与することが難しくなる。造膜助剤として作用する水溶性有機溶剤Ａを含有する本実施の形態に係るインク組成物であれば、高いＴｇを有する樹脂を含有していても低温乾燥で樹脂を基材上で融着させることが可能となり、記録物に好適な耐擦過性や耐溶剤性、耐水摩擦性を付与することが可能となる。 Although the Tg (glass transition temperature) of the resin contained in the ink composition according to the present embodiment is not particularly limited, it is preferably higher than the drying temperature of the ink composition. Specifically, the Tg of the resin is preferably 50° C. or higher, more preferably 55° C. or higher, and even more preferably 60° C. or higher. Originally, when the Tg of the resin contained in the ink composition increases, the resin cannot be fused onto the substrate unless the drying temperature is increased, and the abrasion resistance and solvent resistance suitable for recorded matter are improved. , it becomes difficult to impart water friction resistance. As long as the ink composition according to the present embodiment contains the water-soluble organic solvent A acting as a film-forming aid, even if it contains a resin having a high Tg, the resin can be fused on the substrate by low-temperature drying. It is possible to impart suitable abrasion resistance, solvent resistance, and water abrasion resistance to the recorded matter.
　市販の分散性樹脂としては、例えば、アクリットＷＥＭ－０３１Ｕ、ＷＥＭ－２００Ｕ、ＷＥＭ－３２１、ＷＥＭ－３０００、ＷＥＭ－２０２Ｕ、ＷＥＭ－３００８、（大成ファインケミカル（株）製、アクリル－ウレタン分散性樹脂）、ＡＫＷ１０７、ＲＫＷ－５００（大成ファインケミカル（株）製、アクリル分散性樹脂）、ＬＵＢＲＩＪＥＴ　Ｎ２４０（ルーブリゾール製、アクリル分散性樹脂）、スーパーフレックス１５０、２１０、４７０、５００Ｍ、Ｅ２０００、Ｅ４８００、Ｒ５００２（第一工業製薬（株）製、ウレタン分散性樹脂）、ビニブラン７００、７０１、７１１、７３７、７４７（日信化学（株）製、塩化ビニル－アクリル分散性樹脂）、ビニブラン２７０６、２６８５（日信化学（株）製、アクリル分散性樹脂）、モビニール７４３Ｎ、６５２０、６６００、６８２０、７４７０、７７２０、（ジャパンコーティングレジン社製、アクリル分散性樹脂）、ＰＲＩＭＡＬ　ＡＣ-２６１Ｐ、　ＡＣ-８１８（ダウ・ケミカル社製　アクリル樹脂）、ＮｅｏＣｒｙｌ　Ａ２０９１、Ａ２０９２、Ａ６３９、Ａ６５５、Ａ６６２（ＤＳＭ　Ｃｏａｔｉｎｇ　Ｒｅｓｉｎ社製　スチレン－アクリル樹脂）、ＱＥ－１０４２、ＫＥ－１０６２（星光ＰＭＣ社製　スチレン－アクリル分散性樹脂）、ＪＥ－１０５６（星光ＰＭＣ社製　アクリル樹脂）、ＪＯＮＣＲＹＬ７１９９、ＰＤＸ－７６３０Ａ（ＢＡＳＦジャパン社製　スチレン－アクリル分散性樹脂）、シャリーヌＲ１７０ＢＸ（日信化学工業社製　シリコーン－アクリル分散性樹脂）、タケラックＷ－６０１０（三井化学社製　ウレタン分散性樹脂）、エリーテル ＫＡ-５０７１Ｓ（ユニチカ社製　ポリエステル分散性樹脂）等を例示することができるが、これらに限定されるものではない。 Commercially available dispersible resins include, for example, ACRYT WEM-031U, WEM-200U, WEM-321, WEM-3000, WEM-202U, WEM-3008 (manufactured by Taisei Fine Chemical Co., Ltd., acrylic-urethane dispersible resin). , AKW107, RKW-500 (manufactured by Taisei Fine Chemical Co., Ltd., acrylic dispersible resin), LUBRIJET N240 (manufactured by Lubrizol, acrylic dispersible resin), Superflex 150, 210, 470, 500M, E2000, E4800, R5002 (No. Ichi Kogyo Pharmaceutical Co., Ltd., urethane dispersing resin), Vinyblan 700, 701, 711, 737, 747 (manufactured by Nissin Chemical Co., Ltd., vinyl chloride-acrylic dispersing resin), Vinyblan 2706, 2685 (Nissin Chemical Co., Ltd., acrylic dispersion resin), Movinyl 743N, 6520, 6600, 6820, 7470, 7720, (Japan Coating Resin Co., acrylic dispersion resin), PRIMAL AC-261P, AC-818 (Dow Chemical Company) acrylic resin), NeoCryl A2091, A2092, A639, A655, A662 (styrene-acrylic resin manufactured by DSM Coating Resin), QE-1042, KE-1062 (styrene-acrylic dispersion resin manufactured by Seiko PMC), JE-1056 (manufactured by Seiko PMC, acrylic resin), JONCRYL7199, PDX-7630A (manufactured by BASF Japan, styrene-acrylic dispersible resin), Charine R170BX (manufactured by Nissin Chemical Industry Co., Ltd., silicone-acrylic dispersible resin), Takelac W-6010 (Mitsui Kagaku Co., Ltd. urethane dispersing resin), Elitel KA-5071S (Unitika Co., Ltd. polyester dispersing resin), etc. can be exemplified, but are not limited to these.
　インク組成物に含まれる樹脂（分散性樹脂）の含有量は、特に限定されるものではないが、樹脂の含有量の下限は、インク組成物全量中０．０５質量％以上であることが好ましく、０．１質量％以上であることが好ましく、更に０．５質量％以上であることが好ましく、１質量％以上がより好ましい。これにより、塗膜の耐擦過性をさらに向上させることができる。樹脂の含有量の上限は、インク組成物全量中２５質量％以下であることが好ましく、中でも、２０質量％以下であることがより好ましく、１５質量％以下であることがさらに好ましい。これにより、吐出安定性を高めることが可能となる。 The content of the resin (dispersible resin) contained in the ink composition is not particularly limited, but the lower limit of the content of the resin is preferably 0.05% by mass or more based on the total amount of the ink composition. , preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and more preferably 1% by mass or more. Thereby, the scratch resistance of the coating film can be further improved. The upper limit of the resin content is preferably 25% by mass or less, more preferably 20% by mass or less, and even more preferably 15% by mass or less, based on the total amount of the ink composition. This makes it possible to improve ejection stability.
　分散性樹脂の平均粒子径は、３０ｎｍ以上が好ましく、４０ｎｍ以上がより好ましく、５０ｎｍ以上がさらに好ましい。分散性樹脂の平均粒子径は、３００ｎｍ以下が好ましく、２７０ｎｍ以下がより好ましく、２５０ｎｍ以下がさらに好ましい。これにより分散性樹脂の粒子同士の融着が進行し易くなるため造膜性も良好となる。またインクジェットの吐出安定性をさらに高めることが可能となる。 The average particle size of the dispersible resin is preferably 30 nm or more, more preferably 40 nm or more, and even more preferably 50 nm or more. The average particle size of the dispersible resin is preferably 300 nm or less, more preferably 270 nm or less, and even more preferably 250 nm or less. This makes it easier for the particles of the dispersible resin to fuse with each other, so that the film formability is improved. In addition, it becomes possible to further improve the ejection stability of the inkjet.
　さらに、樹脂が粒子状の分散性樹脂であると、インク組成物の製膜時で水溶性有機溶剤が徐々に揮発するにつれて、インク組成物に含まれる樹脂粒子同士がより密に充填されることとなるが、分散性樹脂の平均粒子径が３００ｎｍ以下であることにより、密に充填された樹脂粒子同士の接触面積が大きくなり、融着が進行し易くなる。これにより、基材上でより効果的に粒子樹脂同士を融着させることができるようになり、より耐擦過性の高い塗膜を形成することが可能である。しかも、本実施の形態に係るインク組成物は、造膜助剤として作用する水溶性有機溶剤Ａ（沸点２３０℃以下のアミド系溶剤、沸点２３０℃以下の環状エステル系溶剤、及び沸点２３０℃以下のグリコールエーテル系溶剤）を含有するため、例えば樹脂のＴｇ以下の温度のような低温での乾燥温度であっても、樹脂を基材上で融着させることが可能となる。なお、本実施形態において、分散性樹脂の平均粒子径は、測定温度２５℃にて濃厚系粒径アナライザー（大塚電子（株）製、型式：ＦＰＡＲ－１０００）を用いて測定することができる。 Furthermore, when the resin is a particulate dispersible resin, the resin particles contained in the ink composition are more densely filled with each other as the water-soluble organic solvent gradually volatilizes during film formation of the ink composition. However, when the average particle size of the dispersible resin is 300 nm or less, the contact area between the densely packed resin particles increases, and the fusion tends to proceed. As a result, the resin particles can be fused together more effectively on the base material, and a coating film with higher scratch resistance can be formed. Moreover, the ink composition according to the present embodiment contains a water-soluble organic solvent A (an amide solvent with a boiling point of 230° C. or lower, a cyclic ester solvent with a boiling point of 230° C. or lower, and a (glycol ether-based solvent), it is possible to fuse the resin on the substrate even at a low drying temperature such as a temperature below the Tg of the resin. In the present embodiment, the average particle size of the dispersible resin can be measured using a concentrated particle size analyzer (manufactured by Otsuka Electronics Co., Ltd., model: FPAR-1000) at a measurement temperature of 25°C.
　分散性樹脂の質量平均分子量は、インク組成物の層の耐水性の観点から、１００００以上が好ましく、５００００以上がより好ましく、１０００００以上がさらに好ましい。分散性樹脂の質量平均分子量は、インク組成物での分散安定性の観点から、２００００００以下が好ましく、１５０００００以下がより好ましく、１００００００以下がより好ましい。なお、本実施形態において樹脂の分子量は、質量平均分子量Ｍｗを示すものであり、ＧＰＣ（ゲルパーミエーションクロマトグラフィー）により測定された値であり、東ソー（株）製の「ＨＬＣ－８１２０ＧＰＣ」にて、校正曲線用ポリスチレンスタンダードを標準にして測定することができる。 The weight average molecular weight of the dispersible resin is preferably 10,000 or more, more preferably 50,000 or more, and even more preferably 100,000 or more, from the viewpoint of the water resistance of the ink composition layer. From the viewpoint of dispersion stability in the ink composition, the mass average molecular weight of the dispersible resin is preferably 2,000,000 or less, more preferably 1,500,000 or less, and more preferably 1,000,000 or less. In the present embodiment, the molecular weight of the resin indicates the mass average molecular weight Mw, which is a value measured by GPC (gel permeation chromatography), using "HLC-8120GPC" manufactured by Tosoh Corporation. , can be measured using a polystyrene standard for a calibration curve as a standard.
　［レベリング剤］
　本実施の形態に係るインク組成物にはレベリング剤を含有してもよい。本実施の形態に係るインク組成物は、レベリング剤を含有することは必須の構成ではないが、レベリング剤を含有することで、基材上に塗布されたインク組成物がより濡れ広がるようになりインク組成物と外気との界面の表面積が増えるようになる。これにより、水溶性有機溶剤Ａを含有する本実施の形態に係るインク組成物がより効果的に乾燥するようになり、本発明の効果を特に効果的に奏するようになる。 [Leveling agent]
The ink composition according to this embodiment may contain a leveling agent. Although it is not essential that the ink composition according to the present embodiment contains a leveling agent, the inclusion of the leveling agent allows the ink composition applied on the substrate to spread more wetly. The surface area of the interface between the ink composition and the ambient air is increased. As a result, the ink composition according to the present embodiment containing the water-soluble organic solvent A can be dried more effectively, and the effects of the present invention can be exhibited particularly effectively.
　さらに、レベリング剤を含有することで、基材に濡れ易くなるため濃度ムラは生じ難くなる。 In addition, the inclusion of a leveling agent makes it easier to wet the base material, making density unevenness less likely to occur.
　本実施の形態に係るインク組成物にレベリング剤を含有する場合、レベリング剤の種類は特に限定されない。例えば、アニオン系界面活性剤、非イオン性界面活性剤、シリコーン（シリコン）系界面活性剤、フッ素系界面活性剤、アセチレングリコール系界面活性剤等の界面活性剤を挙げることができる。これらのなかでもシリコーン（シリコン）系界面活性剤、アセチレングリコール系界面活性剤、アルカングリコール系界面活性剤等の界面活性剤であることが好ましい。これにより、ノズルプレートに対する撥液性を向上させることができる。さらに、シリコーン（シリコン）系界面活性剤を含有することにより、塗膜表面の滑り性が良好となって塗膜の耐擦過性が向上する。 When the ink composition according to the present embodiment contains a leveling agent, the type of leveling agent is not particularly limited. Examples thereof include surfactants such as anionic surfactants, nonionic surfactants, silicone (silicon) surfactants, fluorine surfactants, and acetylene glycol surfactants. Among these, surfactants such as silicone (silicon)-based surfactants, acetylene glycol-based surfactants, and alkane glycol-based surfactants are preferred. Thereby, the liquid repellency with respect to the nozzle plate can be improved. Further, by containing a silicone (silicon)-based surfactant, the surface of the coating film has good lubricity and the abrasion resistance of the coating film is improved.
　具体例としては、エマール、ラテムル、ペレックス、ネオペレックス、デモール（いずれも、アニオン系界面活性剤；花王株式会社製）、サンノール、リポラン、ライポン、リパール（いずれも、アニオン系界面活性剤；ライオン株式会社製）、ノイゲン、エパン、ソルゲン（いずれも非イオン性界面活性剤；第一工業製薬株式会社製）エマルゲン、アミート、エマゾール（いずれも非イオン性界面活性剤；花王株式会社製）、ナロアクティー、エマルミン、サンノニック（いずれも非イオン性界面活性剤；三洋化成工業株式会社製）、サーフィノール１０４、８２、４２０、４４０、４６５、４８５、ＴＧ、２５０２、ＳＥ－Ｆ、１０７Ｌ、ダイノール３６０、ダイノール６０４、ダイノール６０７（いずれも、アセチレングリコール系界面活性剤；エボニック社製）、ダイノール９６０（アセチレングリコール系とシリコン系界面活性剤の配合物；エボニック社製）、サーフィノールＡＤ０１（アルカングリコール系界面活性剤；エボニック社製）、オルフィンＥ１００４、Ｅ１０１０、ＰＤ００４、ＥＸＰ４３００（いずれも、アセチレングリコール系界面活性剤；日信化学工業株式会社製）、メガファック（フッ素系界面活性剤；ＤＩＣ株式会社製）、サーフロン（フッ素系界面活性剤；ＡＧＣセイミケミカル社製）、ＢＹＫ３０２、３０６、３０７、３３１、３３３、３４５、３４６、３４７、３４８、３４９、３４２０、３４５０、３４５１、３４５５、３４５６（いずれもシリコーン（シリコン）系界面活性剤；ビックケミー社製）、ＫＰ－１１０、１１２、３２３、３４１、６００４（いずれもシリコーン（シリコン）系界面活性剤；信越化学株式会社製）、シルフェイスＳＡＧ００２、シルフェイスＳＡＧ００５、シルフェイスＳＡＧ００８、シルフェイスＳＡＧ０１４、シルフェイスＳＡＧ５０３Ａ、シルフェイスＳＪＭ－００２、シルフェイスＳＪＭ－００３（いずれもシリコーン（シリコン）系界面活性剤；日信化学工業（株）製）、ＴＥＧＯ　ＦＬＯＷ　４２５、ＴＥＧＯ　Ｇｌｉｄｅ　１００、１１０、１３０、４１０、４３２、４４０、４５０、４８２、４９０、４９２、４９４、４９６、ＺＧ４００、ＴＥＧＯ　Ｔｗｉｎ　４０００、ＴＥＧＯ　Ｔｗｉｎ　４１００、ＴＥＧＯ　Ｔｗｉｎ　４２００、ＴＥＧＯ　Ｗｅｔ　２４０、ＫＬ２４５、２５０、２６０、２６５、２７０、２８０、（いずれもシリコーン（シリコン）系界面活性剤；エボニック社製）、ＴＥＧＯ　Ｗｅｔ　５００、５０５、５１０、５２０（いずれもノニオン系界面活性剤；エボニック社製）などが挙げられる。 Specific examples include Emal, Latemul, Pelex, Neoperex, Demol (all of which are anionic surfactants; manufactured by Kao Corporation), Sunol, Liporan, Lipon, and Ripal (all of which are anionic surfactants; Lion Co., Ltd. company), Noigen, Epan, Solgen (all nonionic surfactants; Daiichi Kogyo Seiyaku Co., Ltd.) Emulgen, Amit, Emsol (all nonionic surfactants; Kao Corporation), Naloacty , Emalmin, Sannonic (both nonionic surfactants; manufactured by Sanyo Chemical Industries, Ltd.), Surfynol 104, 82, 420, 440, 465, 485, TG, 2502, SE-F, 107L, Dynol 360, Dynol 604, Dynol 607 (both are acetylene glycol-based surfactants; manufactured by Evonik), Dynol 960 (mixture of acetylene glycol-based and silicon-based surfactants; manufactured by Evonik), Surfynol AD01 (alkane glycol-based surfactant agent; manufactured by Evonik), Olfine E1004, E1010, PD004, EXP4300 (all of which are acetylene glycol-based surfactants; manufactured by Nissin Chemical Industry Co., Ltd.), Megafac (fluorine-based surfactant; manufactured by DIC Corporation), Surflon (fluorosurfactant; manufactured by AGC Seimi Chemical Co., Ltd.), BYK302, 306, 307, 331, 333, 345, 346, 347, 348, 349, 3420, 3450, 3451, 3455, 3456 (all silicone )-based surfactant; manufactured by BYK Chemie), KP-110, 112, 323, 341, 6004 (all silicone (silicon)-based surfactants; manufactured by Shin-Etsu Chemical Co., Ltd.), Silface SAG002, Silface SAG005, Sil Face SAG008, Silface SAG014, Silface SAG503A, Silface SJM-002, Silface SJM-003 (all silicone (silicon) surfactants; manufactured by Nissin Chemical Industry Co., Ltd.), TEGO FLOW 425, TEGO Glide 100, 110, 130, 410, 432, 440, 450, 482, 490, 492, 494, 496, ZG400, TEGO Twin 4000, TEGO Twin 4100, TEGO Twin 4200, TEGO Wet 240, KL245, 250, 260, 265 , 270, 280 (all silicone surfactants; manufactured by Evonik), TEGO Wet 500, 505, 510, 520 (all nonionic surfactants; manufactured by Evonik).
　そのなかでもＨＬＢ値が１５以下であるレベリング剤であることが好ましい。ＨＬＢ値が１５以下であるレベリング剤であれば、基材上に塗布されたインク組成物と外気との界面にレベリング剤が配向しやすくなり、インク組成物がより濡れ広がるようになるので、インク組成物がさらに効果的に乾燥するようになる。 Among them, a leveling agent with an HLB value of 15 or less is preferable. If the leveling agent has an HLB value of 15 or less, the leveling agent tends to be oriented at the interface between the ink composition applied on the substrate and the outside air, and the ink composition spreads more easily. The composition dries more effectively.
　また、本実施の形態に係るインク組成物にレベリング剤を含有する場合、レベリング剤の含有量は、本実施の形態に係るインク組成物に含まれる沸点が２３０℃以下の水溶性有機溶剤Ａの含有量に応じて制御することが好ましい。沸点が２３０℃以下の水溶性有機溶剤Ａは水溶性有機溶剤のなかでも比較的疎水性の水溶性有機溶剤であるので、特にＨＬＢ値が低いレベリング剤がインク組成物に含まれると沸点が２３０℃以下の水溶性有機溶剤Ａに溶け込みやすくなり、外気との界面にレベリング剤が配向し難くなる場合がある。そのため、沸点が２３０℃以下の水溶性有機溶剤Ａの含有量に応じて適切に含有量を制御することでインク組成物が濡れ広がるようになるので、インク組成物が効果的に乾燥するようになる。 Further, when the ink composition according to the present embodiment contains a leveling agent, the content of the leveling agent is 10% of the water-soluble organic solvent A having a boiling point of 230° C. or less contained in the ink composition according to the present embodiment. It is preferable to control according to the content. The water-soluble organic solvent A having a boiling point of 230° C. or less is a relatively hydrophobic water-soluble organic solvent among water-soluble organic solvents. ° C. or lower, the leveling agent becomes more likely to dissolve in the water-soluble organic solvent A, and the orientation of the leveling agent at the interface with the outside air may become difficult. Therefore, by appropriately controlling the content according to the content of the water-soluble organic solvent A having a boiling point of 230° C. or less, the ink composition can spread wetly, so that the ink composition can be effectively dried. Become.
　レベリング剤の含有量は、インク組成物に含まれる水溶性有機溶剤Ａ１００質量部に対して０．１質量部以上の範囲であることが好ましい。これにより、インク組成物がさらに濡れ広がるようになるので、インク組成物がさらに効果的に乾燥するようになる。なお、レベリング剤の含有量は、インク組成物に含まれる水溶性有機溶剤Ａ１００質量部に対して、０．３質量部以上の範囲であることがより好ましく、０．６質量部以上の範囲であることがさらに好ましく、１．０質量部以上の範囲であることがさらになお好ましい。 The content of the leveling agent is preferably in the range of 0.1 parts by mass or more with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. As a result, the ink composition is further wetted and spread, so that the ink composition dries more effectively. The content of the leveling agent is more preferably in the range of 0.3 parts by mass or more, and in the range of 0.6 parts by mass or more with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. It is more preferable that the content is in the range of 1.0 parts by mass or more.
　また、レベリング剤の含有量は、インク組成物に含まれる水溶性有機溶剤Ａ１００質量部に対して５０質量部以下の範囲であることが好ましい。これにより、レベリング剤のアミド系溶剤に対する相溶性が向上する。なお、レベリング剤の含有量は、インク組成物に含まれる水溶性有機溶剤Ａ１００質量部に対して、４９質量部以下の範囲であることがより好ましく、４８質量部以下の範囲であることがさらに好ましい。 Also, the content of the leveling agent is preferably in the range of 50 parts by mass or less with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. This improves the compatibility of the leveling agent with the amide solvent. The content of the leveling agent is more preferably in the range of 49 parts by mass or less, more preferably in the range of 48 parts by mass or less with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. preferable.
　［色材］
　本実施の形態に係るインク組成物には色材を含有してもよい。本実施の形態に係るインク組成物は、色材を含有することは必須の構成ではないが、色材を含有することで、所望の画像パターンを形成するような着色インクにすることや、その下地層となるようなホワイトインクやメタリックインクにすることが可能となる。色材としては、染料であっても顔料であってもよい [Color material]
The ink composition according to this embodiment may contain a coloring material. The ink composition according to the present embodiment does not necessarily contain a coloring material. It is possible to use white ink or metallic ink that will serve as a base layer. The coloring material may be either a dye or a pigment.
　本実施の形態に係るインク組成物において、用いることのできる顔料は特に限定されず、従来のインク組成物に使用されている有機顔料又は無機顔料等が挙げられる。これらは１種単独で用いても、２種以上を組み合わせて用いてもよい。なお、本実施の形態に係るインク組成物は、色材を含有しなくともよい。本実施の形態に係るインク組成物において顔料を用いる場合には、後述する分散剤や分散助剤（顔料誘導体）を使用することで、顔料の分散安定性を向上させることができる。 The pigment that can be used in the ink composition according to the present embodiment is not particularly limited, and examples thereof include organic pigments and inorganic pigments used in conventional ink compositions. These may be used individually by 1 type, or may be used in combination of 2 or more type. Note that the ink composition according to the present embodiment may not contain a coloring material. When a pigment is used in the ink composition according to the present embodiment, the dispersion stability of the pigment can be improved by using a dispersant or dispersing aid (pigment derivative), which will be described later.
　具体的な有機顔料としては、例えば、不溶性アゾ顔料、溶性アゾ顔料、染料からの誘導体、フタロシアニン系有機顔料、キナクリドン系有機顔料、ペリレン系有機顔料、ペリノン系有機顔料、アゾメチン系有機顔料、アントラキノン系有機顔料（アントロン系有機顔料）、キサンテン系有機顔料、ジケトピロロピロール系有機顔料、ジオキサジン系有機顔料、ニッケルアゾ系顔料、イソインドリノン系有機顔料、ピランスロン系有機顔料、チオインジゴ系有機顔料、縮合アゾ系有機顔料、ベンズイミダゾロン系有機顔料、キノフタロン系有機顔料、イソインドリン系有機顔料、キナクリドン系固溶体顔料、ペリレン系固溶体顔料等の有機固溶体顔料、その他の顔料として、レーキ顔料やカーボンブラック等が挙げられる。 Specific organic pigments include, for example, insoluble azo pigments, soluble azo pigments, derivatives from dyes, phthalocyanine-based organic pigments, quinacridone-based organic pigments, perylene-based organic pigments, perinone-based organic pigments, azomethine-based organic pigments, and anthraquinone-based pigments. Organic pigments (anthrone-based organic pigments), xanthene-based organic pigments, diketopyrrolopyrrole-based organic pigments, dioxazine-based organic pigments, nickel azo-based pigments, isoindolinone-based organic pigments, pyranthrone-based organic pigments, thioindigo-based organic pigments, condensed azo organic solid solution pigments such as organic pigments, benzimidazolone organic pigments, quinophthalone organic pigments, isoindoline organic pigments, quinacridone solid solution pigments, perylene solid solution pigments, and other pigments such as lake pigments and carbon black. be done.
　有機顔料をカラーインデックス（Ｃ．Ｉ．）ナンバーで例示すると、Ｃ．Ｉ．ピグメントイエロー１、２、３、１２、１３、１４、１６、１７、２０、２４、７３、７４、７５、８３、９３、９５、９７、９８、１０９、１１０、１１４、１１７、１２０、１２５、１２８、１２９、１３０、１３７、１３８、１３９、１４７、１４８、１５０、１５１、１５３、１５４、１５５、１６６、１６８、１８０、１８５、２１３、２１４、Ｃ．Ｉ．ピグメントレッド５、７、９、１２、４８、４８：２、４８：３、４９、５２、５３、５７、５７：１、９７、１１２、１２２、１２３、１４６、１４９、１５０、１６８、１７６、１７７、１８０、１８４、１８５、１９２、２０２、２０６、２０８、２０９、２１３、２１５、２１６、２１７、２２０、２２３、２２４、２２６、２２７、２２８、２３８、２４０、２５４、２５５、２６９、２９１、Ｃ．Ｉ．ピグメントオレンジ１６、３６、４３、５１、５５、５９、６１、６４、７１、７３、Ｃ．Ｉ．ピグメントバイオレット１９、２３、２９、３０、３７、４０、５０、Ｃ．Ｉ．ピグメントブルー１５、１５：１、１５：３、１５：４、１５：６、１６、２２、６０、６４、Ｃ．Ｉ．ピグメントグリーン７、３６、５８、５９、６２、６３、Ｃ．Ｉ．ピグメントブラウン２３、２５、２６、Ｃ．Ｉ．ピグメントブラック７等が挙げられる。 When organic pigments are exemplified by color index (C.I.) numbers, C.I. I. Pigment Yellow 1, 2, 3, 12, 13, 14, 16, 17, 20, 24, 73, 74, 75, 83, 93, 95, 97, 98, 109, 110, 114, 117, 120, 125, 128, 129, 130, 137, 138, 139, 147, 148, 150, 151, 153, 154, 155, 166, 168, 180, 185, 213, 214, C.I. I. Pigment Red 5, 7, 9, 12, 48, 48:2, 48:3, 49, 52, 53, 57, 57:1, 97, 112, 122, 123, 146, 149, 150, 168, 176, 177, 180, 184, 185, 192, 202, 206, 208, 209, 213, 215, 216, 217, 220, 223, 224, 226, 227, 228, 238, 240, 254, 255, 269, 291, C. I. Pigment Orange 16, 36, 43, 51, 55, 59, 61, 64, 71, 73, C.I. I. pigment violet 19, 23, 29, 30, 37, 40, 50, C.I. I. Pigment Blue 15, 15:1, 15:3, 15:4, 15:6, 16, 22, 60, 64, C.I. I. Pigment Green 7, 36, 58, 59, 62, 63, C.I. I. Pigment Brown 23, 25, 26, C.I. I. Pigment Black 7 and the like.
　本実施の形態に係るインク組成物において、用いることのできる染料の具体例としては、アゾ系染料、ベンゾキノン系染料、ナフトキノン系染料、アントラキノン系染料、シアニン系染料、スクアリリウム系染料、クロコニウム系染料、メロシアニン系染料、スチルベン系染料、ジアリールメタン系染料、トリアリールメタン系染料、フルオラン系染料、スピロピラン系染料、フタロシアニン系染料、インジゴイド等のインジゴ系染料、フルギド系染料、ニッケル錯体系染料、及びアズレン系染料が挙げられる。 Specific examples of dyes that can be used in the ink composition according to the present embodiment include azo dyes, benzoquinone dyes, naphthoquinone dyes, anthraquinone dyes, cyanine dyes, squarylium dyes, croconium dyes, Merocyanine dyes, stilbene dyes, diarylmethane dyes, triarylmethane dyes, fluorane dyes, spiropyran dyes, phthalocyanine dyes, indigo dyes such as indigoids, fulgide dyes, nickel complex dyes, and azulene dyes dyes.
　本実施の形態に係るインク組成物において、用いることのできる無機顔料の具体例としては、酸化チタン、硫酸バリウム、炭酸カルシウム、酸化亜鉛、炭酸バリウム、シリカ、タルク、クレー、合成マイカ、アルミナ、亜鉛華、硫酸鉛、黄色鉛、亜鉛黄、べんがら（赤色酸化鉄（ＩＩＩ））、カドミウム赤、群青、紺青、酸化クロム緑、コバルト緑、アンバー、チタンブラック、アルミニウム、チタン、インジウム、合成鉄黒、無機固溶体顔料等を挙げることができる。 Specific examples of inorganic pigments that can be used in the ink composition according to the present embodiment include titanium oxide, barium sulfate, calcium carbonate, zinc oxide, barium carbonate, silica, talc, clay, synthetic mica, alumina, and zinc. Flower, lead sulfate, yellow lead, zinc yellow, red iron oxide (iron (III)), cadmium red, ultramarine blue, dark blue, chromium oxide green, cobalt green, amber, titanium black, aluminum, titanium, indium, synthetic iron black, Inorganic solid solution pigments and the like can be mentioned.
　これらの有機顔料又は無機顔料の平均分散粒径は、所望の発色が可能なものであれば特に限定されるものではない。顔料の種類によっても異なるが、顔料の分散安定性が良好で、充分な着色力を得る点から、顔料の平均分散粒径の下限は、１０ｎｍ以上の範囲内であることが好ましく、２０ｎｍ以上の範囲内であることがより好ましく、３０ｎｍ以上の範囲内であることがさらに好ましい。顔料の平均分散粒径の上限は、５００ｎｍ以下の範囲内であることが好ましく、４００ｎｍ以下の範囲内であることがより好ましく、３５０ｎｍ以下の範囲内であることがさらに好ましい。平均分散粒径が５００ｎｍ以下であれば、インクジェットヘッドのノズル目詰まりを起こしにくく、再現性の高い均質な画像を得ることができる。平均分散粒径が１０ｎｍ以上であれば、得られる印刷物の耐光性を良好なものとすることができる。なお、本実施形態において、顔料の平均分散粒径は、濃厚系粒径アナライザー（大塚電子（株）製、型式：ＦＰＡＲ－１０００））を用いて２５℃の条件下で測定した平均粒子径（Ｄ５０）である。 The average dispersed particle size of these organic pigments or inorganic pigments is not particularly limited as long as the desired color development is possible. Although it varies depending on the type of pigment, the lower limit of the average dispersed particle diameter of the pigment is preferably in the range of 10 nm or more, preferably 20 nm or more, from the viewpoint of obtaining sufficient coloring power with good dispersion stability of the pigment. It is more preferably within the range, and even more preferably within the range of 30 nm or more. The upper limit of the average dispersed particle size of the pigment is preferably 500 nm or less, more preferably 400 nm or less, and even more preferably 350 nm or less. If the average dispersed particle size is 500 nm or less, nozzle clogging of an inkjet head is unlikely to occur, and a uniform image with high reproducibility can be obtained. When the average dispersed particle diameter is 10 nm or more, the light resistance of the resulting printed matter can be improved. In the present embodiment, the average dispersed particle diameter of the pigment is the average particle diameter ( D50).
　本実施の形態に係るインク組成物は、顔料として光輝性顔料を含有してもよい。光輝性顔料としては、アルミニウム、銀、金、ニッケル、クロム、錫、亜鉛、インジウム、チタン、銅等の単体金属；金属化合物；合金およびそれら混合物の少なくとも１種である金属含有光輝性顔料や、雲母、魚鱗箔、酸塩化ビスマス、二酸化ケイ素、金属酸化物、金属化合物、およびそれらの積層等の真珠光沢や干渉光沢を有するパール顔料を挙げることができる。 The ink composition according to the present embodiment may contain a luster pigment as a pigment. Luminous pigments include metal-containing luster pigments that are at least one of simple metals such as aluminum, silver, gold, nickel, chromium, tin, zinc, indium, titanium, and copper; metal compounds; alloys and mixtures thereof; Pearl pigments having pearl luster or interference luster such as mica, fish scale foil, bismuth oxychloride, silicon dioxide, metal oxides, metal compounds, and laminates thereof may be mentioned.
　本実施の形態に係るインク組成物に光輝性顔料を含有する場合、光輝性顔料は平板状（微細板状、鱗片状等とも表される）であることが好ましい。これにより、被体により好適な金属調の光沢を付与することができる。 When the ink composition according to the present embodiment contains a glitter pigment, the glitter pigment preferably has a plate-like shape (also referred to as a fine plate-like shape, a scale-like shape, or the like). This makes it possible to impart a more suitable metallic luster to the subject.
　本実施の形態に係るインク組成物に色材を含有する場合、色材の含有量は、インク組成物全量中０．０５質量％以上であることが好ましく、０．０８質量％以上であることがより好ましく、０．１質量％以上であることがさらに好ましい。本実施の形態に係るインク組成物に色材を含有する場合、色材の含有量は、インク組成物全量中２０．０質量％以下であることが好ましく、１７．０質量％以下であることがより好ましく、１５．０質量％以下であることがさらに好ましい。 When the ink composition according to the present embodiment contains a coloring material, the content of the coloring material is preferably 0.05% by mass or more, more preferably 0.08% by mass or more, based on the total amount of the ink composition. is more preferable, and 0.1% by mass or more is even more preferable. When the ink composition according to the present embodiment contains a coloring material, the content of the coloring material is preferably 20.0% by mass or less, and 17.0% by mass or less, based on the total amount of the ink composition. is more preferable, and 15.0% by mass or less is even more preferable.
　［顔料分散剤］
　本実施の形態に係るインク組成物には顔料分散剤を含有してもよい。本実施の形態に係るインク組成物は、顔料分散剤を含有することは必須の構成ではないが、顔料とともに顔料分散剤を含有することで、顔料の分散性を向上させることができる。ここで顔料分散剤とは、顔料表面の一部に付着することでインク組成物内での顔料の分散性を向上させる機能を有する樹脂又は界面活性剤のことを意味する。 [Pigment Dispersant]
The ink composition according to this embodiment may contain a pigment dispersant. The ink composition according to the present embodiment does not necessarily contain a pigment dispersant, but by containing the pigment dispersant together with the pigment, the dispersibility of the pigment can be improved. Here, the term "pigment dispersant" means a resin or surfactant that adheres to a part of the pigment surface and has a function of improving the dispersibility of the pigment in the ink composition.
　本実施の形態に係るインク組成物において、用いることのできる顔料分散剤は特に限定されない。例えば、カチオン系、アニオン系、ノニオン系、両性、シリコーン（シリコン）系、フッ素系等の界面活性剤を使用できる。界面活性剤の中でも、次に例示するような高分子界面活性剤（高分子分散剤）が好ましい。 The pigment dispersant that can be used in the ink composition according to the present embodiment is not particularly limited. For example, cationic, anionic, nonionic, amphoteric, silicone (silicon), and fluorine surfactants can be used. Among surfactants, polymer surfactants (polymer dispersants) such as those exemplified below are preferred.
　本実施の形態に係るインク組成物において用いることのできる顔料分散剤としては、水溶性高分子分散剤を好ましく用いることができる。水溶性高分子分散剤としては、例えば、ポリエステル系、ポリアクリル系、ポリウレタン系、ポリアミン系、ポリカプトラクトン系の主鎖を有し、側鎖に、アミノ基、カルボキシル基、スルホン基、ヒドロキシル基等の極性基を有する分散剤等が挙げられる。例えば、ポリアクリル酸エステル等の不飽和カルボン酸エステルの（共）重合体類；スチレン、α－メチルスチレン等の芳香族ビニル化合物とアクリル酸エステル等の不飽和カルボン酸エステルの共重合体類；ポリアクリル酸等の不飽和カルボン酸の（共）重合体の（部分）アミン塩、（部分）アンモニウム塩や（部分）アルキルアミン塩類；水酸基含有ポリアクリル酸エステル等の水酸基含有不飽和カルボン酸エステルの（共）重合体やそれらの変性物；ポリウレタン類；不飽和ポリアミド類；ポリシロキサン類；長鎖ポリアミノアミドリン酸塩類；ポリエチレンイミン誘導体（ポリ（低級アルキレンイミン）と遊離カルボキシル基含有ポリエステルとの反応により得られるアミドやそれらの塩基）；ポリアリルアミン誘導体（ポリアリルアミンと、遊離のカルボキシル基を有するポリエステル、ポリアミド又はエステルとアミドの共縮合物（ポリエステルアミド）の３種の化合物の中から選ばれる１種以上の化合物とを反応させて得られる反応生成物）等が挙げられる。中でも、（メタ）アクリル系樹脂を含有する水溶性高分子分散剤が、インク組成物の分散安定性と、印刷物の画像鮮明性の観点から好ましい。 A water-soluble polymer dispersant can be preferably used as a pigment dispersant that can be used in the ink composition according to the present embodiment. Examples of water-soluble polymer dispersants include polyester-, polyacrylic-, polyurethane-, polyamine-, and polycaptolactone-based main chains, and side chains containing amino groups, carboxyl groups, sulfone groups, and hydroxyl groups. and dispersing agents having polar groups such as For example, (co)polymers of unsaturated carboxylic acid esters such as polyacrylic acid esters; copolymers of aromatic vinyl compounds such as styrene and α-methylstyrene and unsaturated carboxylic acid esters such as acrylic acid esters; (partial) amine salts, (partial) ammonium salts and (partial) alkylamine salts of (co)polymers of unsaturated carboxylic acids such as polyacrylic acid; hydroxyl group-containing unsaturated carboxylic acid esters such as hydroxyl group-containing polyacrylic acid esters Polyurethanes; Unsaturated polyamides; Polysiloxanes; Long-chain polyaminoamide phosphates; Polyethyleneimine derivatives (poly (lower alkylene imine) and free carboxyl group-containing polyester amides obtained by reaction and their bases); polyallylamine derivatives (polyallylamine and polyester having a free carboxyl group, polyamide or co-condensation product of ester and amide (polyesteramide)) reaction products obtained by reacting with one or more compounds) and the like. Among them, a water-soluble polymer dispersant containing a (meth)acrylic resin is preferable from the viewpoint of the dispersion stability of the ink composition and the image clarity of the printed matter.
　水溶性高分子分散剤の具体例としては、Ｃｒａｙ　Ｖａｌｌｅｙ製ＳＭＡ１４４０、ＳＭＡ２６２５、ＳＭＡ１７３５２、ＳＭＡ３８４０、ＳＭＡ１０００、ＳＭＡ２０００、ＳＭＡ３０００、ＢＡＳＦジャパン社製ＪＯＮＣＲＹＬ６７、ＪＯＮＣＲＹＬ６７８、ＪＯＮＣＲＹＬ５８６、ＪＯＮＣＲＹＬ６１１、ＪＯＮＣＲＹＬ６８０、ＪＯＮＣＲＹＬ６８２、ＪＯＮＣＲＹＬ６９０、ＪＯＮＣＲＹＬ８１９、ＪＯＮＣＲＹＬ－ＪＤＸ５０５０、ＥＦＫＡ４５５０、ＥＦＫＡ４５６０、ＥＦＫＡ４５８５、ＥＦＫＡ５２２０、ＥＦＫＡ６２３０、Ｄｉｓｐｅｘ　Ｕｌｔｒａ　ＰＸ４５７５、ルーブリゾール社製ＳＯＬＳＰＥＲＳＥ２００００、ＳＯＬＳＰＥＲＳＥ２７０００、ＳＯＬＳＰＥＲＳＥ４００００、ＳＯＬＳＰＥＲＳＥ４１０００、ＳＯＬＳＰＥＲＳＥ４１０９０、ＳＯＬＳＰＥＲＳＥ４３０００、ＳＯＬＳＰＥＲＳＥ４４０００、ＳＯＬＳＰＥＲＳＥ４５０００、ＳＯＬＳＰＥＲＳＥ４６０００、ＳＯＬＳＰＥＲＳＥ４７０００、ＳＯＬＳＰＥＲＳＥ５３０９５、ＳＯＬＳＰＥＲＳＥ５４０００、ＳＯＬＳＰＥＲＳＥ６４０００、ＳＯＬＳＰＥＲＳＥ６５０００、ＳＯＬＳＰＥＲＳＥ６６０００、ＳＯＬＳＰＥＲＳＥ　Ｊ４００、ＳＯＬＳＰＥＲＳＥ　Ｗ１００、ＳＯＬＳＰＥＲＳＥ　Ｗ２００、ＳＯＬＳＰＥＲＳＥ　Ｗ３２０、ＳＯＬＳＰＥＲＳＥ　ＷＶ４００、ビックケミー社製ＡＮＴＩ－ＴＥＲＲＡ－２５０、ＢＹＫＪＥＴ－９１５０、ＢＹＫＪＥＴ－９１５１、ＢＹＫＪＥＴ－９１５２、ＢＹＫＪＥＴ－９１７０、ＤＩＳＰＥＲＢＹＫ－１０２、ＤＩＳＰＥＲＢＹＫ－１６８、ＤＩＳＰＥＲＢＹＫ－１８０、ＤＩＳＰＥＲＢＹＫ－１８４、ＤＩＳＰＥＲＢＹＫ－１８５、ＤＩＳＰＥＲＢＹＫ－１８７、ＤＩＳＰＥＲＢＹＫ－１９０、ＤＩＳＰＥＲＢＹＫ－１９１、ＤＩＳＰＥＲＢＹＫ－１９３、ＤＩＳＰＥＲＢＹＫ－１９４Ｎ、ＤＩＳＰＥＲＢＹＫ－１９８、ＤＩＳＰＥＲＢＹＫ－１９９、ＤＩＳＰＥＲＢＹＫ－２０１０、ＤＩＳＰＥＲＢＹＫ－２０１２、ＤＩＳＰＥＲＢＹＫ－２０１３、ＤＩＳＰＥＲＢＹＫ－２０１４、ＤＩＳＰＥＲＢＹＫ－２０１５、ＤＩＳＰＥＲＢＹＫ－２０１８、ＤＩＳＰＥＲＢＹＫ－２０１９、ＤＩＳＰＥＲＢＹＫ－２０５５、ＤＩＳＰＥＲＢＹＫ－２０６０、ＤＩＳＰＥＲＢＹＫ－２０６１、ＤＩＳＰＥＲＢＹＫ－２０８１、ＤＩＳＰＥＲＢＹＫ－２０９６、エボニック社製ＴＥＧＯ　ＤＩＳＰＥＲＳ６５０、ＴＥＧＯ　ＤＩＳＰＥＲＳ６５１、ＴＥＧＯ　ＤＩＳＰＥＲＳ６５２、ＴＥＧＯ　ＤＩＳＰＥＲＳ６５５、ＴＥＧＯ　ＤＩＳＰＥＲＳ６６０Ｃ、ＴＥＧＯ　ＤＩＳＰＥＲＳ６７０、ＴＥＧＯ　ＤＩＳＰＥＲＳ７１５Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７４０Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７４１Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７５０Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７５２Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７５５Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７５７Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７６０Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７６１Ｗ、ＴＥＧＯ　ＤＩＳＰＥＲＳ７６５Ｗ、ＺＥＴＡＳＰＥＲＳＥ１７０、ＺＥＴＡＳＰＥＲＳＥ１７９、ＺＥＴＡＳＰＥＲＳＥ１８２、ＺＥＴＡＳＰＥＲＳＥ３１００、ＺＥＴＡＳＰＥＲＳＥ３４００、ＺＥＴＡＳＰＥＲＳＥ３７００、ＺＥＴＡＳＰＥＲＳＥ３８００、サンノプコ社製ＳＮディスパーサント２０１０、ＳＮディスパーサント２０６０、ＳＮディスパーサント４２１５、ＳＮディスパーサント５０２７、ＳＮディスパーサント５０２９、ＳＮディスパーサント５０３４、ＳＮディスパーサント５４６８、ノプコール５２００、ノプコサントＫ、ノプコサントＲ、ノプコスパース４４－Ｃ、ノプコスパース６１００、ノプコスパース６１５０等が挙げられる。 Specific examples of the water-soluble polymer dispersant include Cray Valley's SMA1440, SMA2625, SMA17352, SMA3840, SMA1000, SMA2000, SMA3000, BASF Japan's JONCRYL67, JONCRYL678, JONCRYL586, JONCRYL611, JONCRYL680, JONCRYL682, JONCRYL690, JONCRYL819, JONCRYL -JDX5050, EFKA4550, EFKA4560, EFKA4585, EFKA5220, EFKA6230, Dispex Ultra PX4575, Lubrizol SOLSPERSE20000, SOLSPERSE27000, SOLSPERSE40000, SOLSPERSE410 00, SOLSPERSE41090, SOLSPERSE43000, SOLSPERSE44000, SOLSPERSE45000, SOLSPERSE46000, SOLSPERSE47000, SOLSPERSE53095, SOLSPERSE54000, SOLSPERSE64000, SOLSPERSE65000, SOLSPERSE66000 , SOLSPERSE J400, SOLSPERSE W100, SOLSPERSE W200, SOLSPERSE W320, SOLSPERSE WV400, BYK-Chemie ANTI-TERRA-250, BYKJET-9150, BYKJET-9151, BYKJET-9152, BYKJET-917 0, DISPERBYK-102, DISPERBYK-168, DISPERBYK -180, DISPERBYK-184, DISPERBYK-185, DISPERBYK-187, DISPERBYK-190, DISPERBYK-191, DISPERBYK-193, DISPERBYK-194N, DISPERBYK-198, DISPERBYK-199, DISPERBYDIK-2010, DISPERBY K-2012, DISPERBYK-2013 , DISPERBYK-2014, DISPERBYK-2015, DISPERBYK-2018, DISPERBYK-2019, DISPERBYK-2055, DISPERBYK-2060, DISPERBYK-2061, DISPERBYK-2081, DISPERBYK-2096, Evonik TEGO DISPER S650, TEGO DISPERS651, TEGO DISPERS652, TEGO DISPERS 655, TEGO DISPERS 660C, TEGO DISPERS 670, TEGO DISPERS 715W, TEGO DISPERS 740W, TEGO DISPERS 741W, TEGO DISPERS 750W, TEGO DISPERS 752W, TEGO DISPERS 755W, TEGO DISPERS 75 7W, TEGO DISPERS760W, TEGO DISPERS761W, TEGO DISPERS765W, ZETASPERSE170, ZETASPERSE179, ZETASPERSE182, ZETASPERSE3100, ZETASPERSE3400, ZETASPERSE3700, ZETASPERSE 3800, San Nopco SN Dispersant 2010, SN Dispersant 2060, SN Dispersant 4215, SN Dispersant 5027, SN Dispersant 5029, SN Dispersant 5034, SN Dispersant 5468, NOPCOL 5200, NOPCOSANT K, NOPCOSANT R, NOPCOSPERS 44-C, Nopcos Perth 6100, Nopcos Perth 6150 and the like.
　［カチオン性の化合物］
　本実施の形態に係るインク組成物にはカチオン性の化合物を含有してもよい。本実施の形態に係るインク組成物は、カチオン性の化合物を含有することは必須の構成ではないが、カチオン性の化合物を含有することで、本実施の形態に係るインク組成物を受理溶液にすることができる。一般的に色材を含む着色インクがアニオン性であり、基材に着色インクを塗布するのに先立ち、カチオン性の化合物を含む受理溶液を基材に塗布することで、カチオン性の化合物により色材を凝集させることが可能となって、着色インクのにじみを抑制することができる。 [Cationic compound]
The ink composition according to this embodiment may contain a cationic compound. The ink composition according to the present embodiment does not necessarily contain a cationic compound. can do. In general, the coloring ink containing the coloring material is anionic. By applying a receiving solution containing a cationic compound to the substrate prior to applying the coloring ink to the substrate, the cationic compound can color the ink. It becomes possible to agglomerate the material, and it is possible to suppress the bleeding of the colored ink.
　カチオン性の化合物としては、多価金属塩（多価金属のイオン）やカチオン性の樹脂を挙げることができる。 Examples of cationic compounds include polyvalent metal salts (polyvalent metal ions) and cationic resins.
　多価金属塩は、主に多価金属のイオンと、陰イオンと、を含有する。なお、「多価金属塩を含有する」という概念は、受理溶液作製時において多価金属塩を添加するもののみならず、多価金属イオンを生成し得る化合物と、陰イオンを生成し得る化合物と、を受理溶液作製時に添加することにより多価金属塩を構成する多価金属のイオンと、陰イオンと、を含有することとなった態様も含む概念である。 Polyvalent metal salts mainly contain ions and anions of polyvalent metals. The concept of "containing a polyvalent metal salt" includes not only those to which a polyvalent metal salt is added during preparation of the receiving solution, but also compounds capable of generating polyvalent metal ions and compounds capable of generating anions. and are added at the time of preparation of the receiving solution to contain the polyvalent metal ions and the anions constituting the polyvalent metal salt.
　陰イオンは、無機物の陰イオンであってもよく、有機物の陰イオンであってもよい。陰イオンの分散性、及び受理溶液の保存安定性及び吐出安定性の観点から、陰イオンは、有機物の陰イオンを含むことが好ましい。 The anion may be an anion of an inorganic substance or an anion of an organic substance. From the viewpoint of the dispersibility of the anions and the storage stability and discharge stability of the receiving solution, the anions preferably include organic anions.
　無機物の陰イオンの具体例としては、塩化物イオン、臭化物イオン、硝酸イオン、硫酸イオン等を挙げることができる。 Specific examples of inorganic anions include chloride ions, bromide ions, nitrate ions, and sulfate ions.
　有機物の陰イオンの具体例としては、酢酸、安息香酸、サリチル酸、２、４－ジヒドロキシ安息香酸、２、５－ジヒドロキシ安息香酸、ジメチロールプロピオン酸、パントテン酸、コハク酸、マレイン酸、グルタル酸、スベリン酸、トリメリット酸、メチルマロン酸の陰イオンを挙げることができる。 Specific examples of organic anions include acetic acid, benzoic acid, salicylic acid, 2,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid, dimethylolpropionic acid, pantothenic acid, succinic acid, maleic acid, glutaric acid, Mention may be made of the anions of suberic acid, trimellitic acid, methylmalonic acid.
　多価金属イオンとは、価数が少なくとも２価以上の金属のイオンをいう。多価金属イオンを用いることでインク組成物のにじみを抑制することができる。多価金属イオンとしては、例えばカルシウムイオン、マグネシウムイオン、アルミニウムイオン、チタンイオン、鉄（ＩＩ）イオン、鉄（ＩＩＩ）イオン、コバルトイオン、ニッケルイオン、銅イオン、亜鉛イオン、バリウムイオン、ストロンチウムイオン等が挙げられる。なかでも、インク組成物中の色材との相互作用が大きく、滲みやムラを抑制する効果が高くなることから、カルシウムイオン、マグネシウムイオン、ニッケルイオン、亜鉛イオン、アルミニウムイオンより選択される１種以上を含有することが好ましい。 A polyvalent metal ion is an ion of a metal with a valence of at least two. Bleeding of the ink composition can be suppressed by using polyvalent metal ions. Examples of polyvalent metal ions include calcium ions, magnesium ions, aluminum ions, titanium ions, iron (II) ions, iron (III) ions, cobalt ions, nickel ions, copper ions, zinc ions, barium ions, strontium ions, and the like. is mentioned. Among them, one selected from calcium ions, magnesium ions, nickel ions, zinc ions, and aluminum ions, because it has a large interaction with the colorant in the ink composition and has a high effect of suppressing bleeding and unevenness. It is preferable to contain the above.
　また、カチオン性の化合物は、多価金属塩の代わりにカチオン基を有するカチオン性の樹脂を含有したものであってもよい。カチオン性の樹脂としては、アミノ基、アンモニウム基、アミド基、－ＮＨＣＯＮＨ２基等のカチオン基を有する樹脂が挙げられる。カチオン性の樹脂は、公知の方法により合成することも、市販品を使用することもできる。 Moreover, the cationic compound may contain a cationic resin having a cationic group instead of the polyvalent metal salt. Examples of cationic resins include resins having cationic groups such as amino groups, ammonium groups, amide groups, and --NHCONH2 groups. A cationic resin can be synthesized by a known method, or a commercially available product can be used.
　カチオン性の樹脂は、公知の方法により合成することも、市販品を使用することもできる。以下に市販品を例示すると、ＡＰＣ－８１０，８１５；Ｄ－６０１０，６０２０、６０３０、６０４０、６０５０、６０６０、６０８０、６３１０、ＤＥＣ－５０，５３、５６，６５；ＦＬ－１４、４２，４４ＬＦ、６１、２０９９，２２５０，２２７３、２３５０、２５５０、２５６５、２５９９、２６５０、２８５０、２９４９、３０５０、３１５０、４３４０、４４２０、４４４０、４４５０、４５２０、４５３０、４５３５、４５４０、４６２０、４８２０；ＦＱＰ－１２６４；ＲＳＬ－１８－２２，４０７１Ｈ，４４００，８３９１、８３９１Ｈ、ＨＤ７０Ｃ、ＨＦ７０Ｄ；ＷＳ－７２（ＳＮＦ社製）、アラフィックス１００、２５１Ｓ、２５５、２５５ＬＯＸ（荒川化学社製）、ＤＫ－６８１０、６８５３、６８８５；ＷＳ－４０１０、４０１１、４０２０、４０２４、４０２７、４０３０（星光ＰＭＣ社製）、センカＦ－３００；パピオゲンＰ－１０５、Ｐ－１１３、Ｐ－２７１、Ｐ－３１６；ピッチノールＱＧ５Ａ；ミリオゲンＰ－２０；ユニセンスＦＰＡ１００Ｌ、ＦＰＡ１０１Ｌ、ＦＰＡ１０２Ｌ、ＦＰＡ１０００Ｌ、ＦＰＡ１００１Ｌ、ＦＰＡ１００ＬＵ、ＦＰＡ１０２ＬＵ、ＦＰＡ１０００ＬＵ；ユニセンスＦＣＡ１０００Ｌ、ＦＣＡ１００１Ｌ、ＦＣＡ１００２Ｌ、ＦＣＡ１００３Ｌ、ＦＣＡ５０００Ｌ；ユニセンスＫＣＡ１００Ｌ、ＫＣＡ１００ＬＵ、ＫＣＡ１０００ＬＵ、ＫＣＡ１００１ＬＵ；ユニセンスＫＨＥ１００Ｌ、ＫＨＥ１０１Ｌ、ＫＨＥ１０２Ｌ、Ｅ１０４Ｌ、ＫＨＥ１０５Ｌ、ＫＨＥ１０７Ｌ、ＫＨＥ１０００Ｌ、ＫＨＥ１００１Ｌ；ユニセンスＫＨＰ１０Ｐ、ＫＨＰ１１Ｌ、ＫＨＰ１０ＬＵ、ＫＨＰ１１ＬＵ、ＫＨＰ１２ＬＵ、ＫＨＰ２０ＬＵ：ユニセンスＫＨＦ１０Ｌ、ＫＨＦ１１Ｌ；ユニセンスＦＰＶ１０００Ｌ、ＦＰＶ１０００ＬＵ；ユニセンスＦＣＶ１０００Ｌ；ユニセンスＺＣＡ１０００Ｌ、ＺＣＡ１００１Ｌ、ＺＣＡ１００２Ｌ、ＺＣＡ５０００Ｌ；ユニセンスＫＰＶ１００ＬＵ、ＫＰＶ１０００ＬＵ（センカ社製）、パラロック４１０Ｋ１０１、４１０Ｋ１１１、４２０Ｋ３０８、４２０Ｋ３００、４６０Ｋ３１３、４６０Ｋ３１８、４７０Ｋ３０８、４８０Ｋ３００、４９０Ｋ３００、４９０Ｋ３０９、５００Ｋ３０Ｅ、５００Ｋ４０Ｅ、５９Ｄ、９２０ＡＰ５００、９７５ＡＰ５００、ＰＤ７００、ＰＤ７１４Ｌ、ＰＤ７１４Ｓ、Ｐ６００、（浅田化学社製）、スミレーズレジン６５０（３０）、６７５Ａ、６６１５、ＳＬＸ－１（田岡化学工業社製）、ＥＰ－１１３７；ＭＺ－４７７、４８０；ＮＳ－３１０Ｘ、６２５ＸＣ（高松油脂社製）、ＰＡＡ－Ｄ１１－ＨＣＬ、Ｄ１９－ＨＣＬ，Ｄ４１－ＨＣＬ、Ｄ１９Ａ；ＰＡＡ－ＨＣＬ－０３、０５、３Ｌ、１０Ｌ；ＰＡＡ－１１１２ＣＬ、２１ＣＬ、ＡＣ５０５０Ａ、Ｎ５０５０ＣＬ、ＳＡ；ＰＡＳ－Ａ－１、５；ＰＡＳ－Ｈ－１Ｌ、５Ｌ、１０Ｌ；ＰＡＳ－Ｊ－８１、８１Ｌ；ＰＡＳ－Ｍ－１、１Ａ、１Ｌ；ＰＡＳ－２１、２１ＣＬ，２２ＳＡ－４０、２４、９２、９２Ａ、８８０、２２０１ＣＬ、２４０１（ニットーボーメディカル社製）、ＰＰ－１７(明成化学社製)；カチオマスターＰＤ－１、７、３０、Ａ、ＰＤＴ－２、ＰＥ－１０、ＰＥ－３０、ＤＴ－ＥＨ、ＥＰＡ－ＳＫ０１、ＴＭＨＭＤＡ－Ｅ（四日市合成社製）、ジェットフィックス３６Ｎ、３８Ａ、５０５２（里田化工社製）、モビニール３５００、６９１０、６９４０、６９５０、６９５１、７８２０（ジャパンコーティングレジン社製）、ＣＴＷ－１１３Ｓ、ＷＥＭ－５０５Ｃ、ＷＢＲ－２１２２Ｃ、アクリットＵＷ－５５０ＣＳ、ＵＷ－２２３ＳＸ（大成ファインケミカル社製）、ＡＰ－１３５０、ＡＥ－８０３、ＡＥ－８２１、ＡＭ－３５００（レゾナック社製）、ハイドランＣＰ－７０５０、ＣＰ－７５２０（ＤＩＣ社製）、スーパーフレックス６２０、６５０（第一工業製薬社製）、ビニブラン７０１ＦＥ５０（日信化学社製）、ポリゾールＡＰ-１３５０（昭和電工社製）などとなる。なお、カチオン性の樹脂は、インク組成物（受理溶液）中に溶解した状態で存在していても、樹脂微粒子として分散された状態で存在していてもよい。 　The cationic resin can be synthesized by a known method, or a commercially available product can be used. Examples of commercially available products are as follows: APC-810, 815; D-6010, 6020, 6030, 6040, 6050, 6060, 6080, 6310; FQP-1264 ; RSL-18-22, 4071H, 4400, 8391, 8391H, HD70C, HF70D; WS-72 (manufactured by SNF), Arafix 100, 251S, 255, 255LOX (manufactured by Arakawa Chemical), DK-6810, 6853, 6885 WS-4010, 4011, 4020, 4024, 4027, 4030 (manufactured by Seiko PMC), Senka F-300; Papiogen P-105, P-113, P-271, P-316; Pitchnol QG5A; Myriogen P- 20; Unisense FPA100L, FPA101L, FPA102L, FPA1000L, FPA1001L, FPA100LU, FPA102LU, FPA1000LU; Unisense FCA1000L, FCA1001L, FCA1002L, FCA1003L, FCA5000L; Unisense KCA100L, KCA1 00LU, KCA1000LU, KCA1001LU; Unisense KHE100L, KHE101L, KHE102L, E104L, KHE105L, KHE107L, KHE1000L, KHE1001L; Unisense KHP10P, KHP11L, KHP10LU, KHP11LU, KHP12LU, KHP20LU: Unisense KHF10L, KHF11L; Unisense FPV1000L, FPV1000LU; Unisense FCV1000L; Sense ZCA1000L, ZCA1001L, ZCA1002L, ZCA5000L; Unisense KPV100LU, KPV1000LU (manufactured by Senka) , Paralock 410K101, 410K111, 420K308, 420K300, 460K313, 460K318, 470K308, 480K300, 490K300, 490K309, 500K30E, 500K40E, 59D, 920AP500, 975AP500, PD7 00, PD714L, PD714S, P600, (manufactured by Asada Chemical Co., Ltd.), violet resin 650 (30), 675A, 6615, SLX-1 (manufactured by Taoka Chemical Co., Ltd.), EP-1137; MZ-477, 480; HCL, D41-HCL, D19A; PAA-HCL-03, 05, 3L, 10L; PAA-1112CL, 21CL, AC5050A, N5050CL, SA; PAS-A-1,5; PAS-H-1L, 5L, 10L; PAS-J-81, 81L; PAS-M-1, 1A, 1L; PAS-21, 21CL, 22SA-40, 24, 92, 92A, 880, 2201CL, 2401 (manufactured by Nittobo Medical), PP-17 ( Meisei Chemical Co., Ltd.); Catiomaster PD-1, 7, 30, A, PDT-2, PE-10, PE-30, DT-EH, EPA-SK01, TMHMDA-E (manufactured by Yokkaichi Gosei Co., Ltd.), Jetfix 36N, 38A, 5052 (manufactured by Satoda Kako), Movinyl 3500, 6910, 6940, 6950, 6951, 7820 (manufactured by Japan Coating Resin), CTW-113S, WEM-505C, WBR-2122C, Acryt UW-550CS, UW -223SX (manufactured by Taisei Fine Chemical Co., Ltd.), AP-1350, AE-803, AE-821, AM-3500 (manufactured by Resonac), Hydran CP-7050, CP-7520 (manufactured by DIC), Superflex 620, 650 ( Daiichi Kogyo Seiyaku Co., Ltd.), Vinyblan 701FE50 (Nissin Chemical Co., Ltd.), Polysol AP-1350 (Showa Denko Co., Ltd.), and the like. The cationic resin may exist in the ink composition (receiving solution) in a dissolved state or in a dispersed state as fine resin particles.
　カチオン性の樹脂は、水や水溶性有機溶剤に溶解する水溶性のカチオン性の樹脂であっても、水や水溶性有機溶剤中で分散する分散性のカチオン性の樹脂であってもよい。この中でも、カチオン性の樹脂が分散性のカチオン性の樹脂であることが好ましい。分散性のカチオン性の樹脂を含有することにより、インク組成物の層の塗膜耐性（耐擦過性）を向上させることができる。この中でも、カチオン性の化合物として、多価金属イオン及び分散性のカチオン性の樹脂を含有するか、またはカチオン性の化合物として、水溶性のカチオン性の樹脂及び分散性のカチオン性の樹脂を含有することがさらに好ましい。このように多価金属イオン（若しくは水溶性のカチオン性の樹脂）及び分散性のカチオン性の樹脂を併用することで、着色インクのにじみをより効果的に抑制しつつインク組成物の層の塗膜耐性（耐擦過性）を向上させることができる。 The cationic resin may be a water-soluble cationic resin that dissolves in water or a water-soluble organic solvent, or a dispersible cationic resin that disperses in water or a water-soluble organic solvent. Among these, the cationic resin is preferably a dispersible cationic resin. By containing a dispersible cationic resin, the coating film resistance (scratch resistance) of the ink composition layer can be improved. Among them, the cationic compound contains a polyvalent metal ion and a dispersible cationic resin, or the cationic compound contains a water-soluble cationic resin and a dispersible cationic resin. more preferably. By using a polyvalent metal ion (or a water-soluble cationic resin) and a dispersible cationic resin together in this way, the ink composition layer can be coated while suppressing bleeding of the colored ink more effectively. Film resistance (scratch resistance) can be improved.
　インク組成物にカチオン性の化合物を含有させる場合、カチオン性の化合物の含有量としては、特に限定されるものではないが、カチオン性の化合物の含有量の下限は、インク組成物全量中０．５質量％以上の範囲内であることが好ましく、０．８質量％以上の範囲内であることがより好ましく、１．０質量％以上の範囲内であることがさらに好ましい。カチオン性の化合物の含有量がインク組成物全量中０．５質量％以上の範囲内であることで、色材をより効果的に定着することが可能となり、着色インクのにじみを効果的に抑制することができる。カチオン性の化合物の含有量の上限は、インク組成物全量中９質量％以下の範囲内であることが好ましく、８質量％以下の範囲内であることがより好ましく、７質量％以下の範囲内であることがさらに好ましい。カチオン性の化合物の含有量がインク組成物全量中９質量％以下の範囲内であることで、インク組成物の保存安定性が向上する。 When the ink composition contains a cationic compound, the content of the cationic compound is not particularly limited. It is preferably in the range of 5% by mass or more, more preferably in the range of 0.8% by mass or more, and even more preferably in the range of 1.0% by mass or more. When the content of the cationic compound is within the range of 0.5% by mass or more based on the total amount of the ink composition, it becomes possible to fix the coloring material more effectively, and the bleeding of the colored ink is effectively suppressed. can do. The upper limit of the content of the cationic compound is preferably within the range of 9% by mass or less, more preferably within the range of 8% by mass or less, and within the range of 7% by mass or less in the total amount of the ink composition. is more preferable. When the content of the cationic compound is within the range of 9% by mass or less based on the total amount of the ink composition, the storage stability of the ink composition is improved.
　［その他の成分］
　インク組成物は、必要に応じて、さらに、従来公知の添加剤を含んでもよい。添加剤としては、例えば、ワックス、粘度調整剤、ｐＨ調整剤、酸化防止剤、防腐剤、防黴剤等が挙げられる。 [Other ingredients]
The ink composition may further contain conventionally known additives, if necessary. Examples of additives include waxes, viscosity modifiers, pH modifiers, antioxidants, preservatives, antifungal agents, and the like.
　＜インク組成物の調製方法＞
　インク組成物の調製方法は、特に限定されない例えば、水溶性有機溶媒に自己分散型の顔料、樹脂、界面活性剤及び必要に応じてその他の成分を添加して調製する方法、水溶性有機溶媒に、顔料と分散剤を加えて分散した後、樹脂、界面活性剤及び必要に応じてその他の成分を添加して調製する方法水溶性有機溶媒に顔料と樹脂と界面活性剤と必要に応じてその他の成分を添加した後、顔料を分散して調製する方法等が挙げられる。 <Method for preparing ink composition>
The method for preparing the ink composition is not particularly limited. , A method in which a pigment and a dispersant are added and dispersed, and then a resin, a surfactant and, if necessary, other ingredients are added. After adding the components of (1), the pigment is dispersed and prepared.
　インク組成物の表面張力は、特に限定されないが、２５℃における静的表面張力の上限は、４０．０ｍＮ／ｍ以下が好ましく、３５．０ｍＮ／ｍ以下がより好ましく、３２．０ｍＮ／ｍ以下がさらに好ましい。２５℃における静的表面張力の下限は、１９．０ｍＮ／ｍ以上が好ましく、２０．０ｍＮ／ｍ以上がより好ましく、２１．０ｍＮ／ｍ以上がさらに好ましい。なお、静的表面張力は、例えば測定温度２５℃にてＷｉｌｈｅｌｍｙ法（協和界面科学製　ＤＹ－３００）で測定することができる。 The surface tension of the ink composition is not particularly limited, but the upper limit of the static surface tension at 25° C. is preferably 40.0 mN/m or less, more preferably 35.0 mN/m or less, and 32.0 mN/m or less. More preferred. The lower limit of the static surface tension at 25°C is preferably 19.0 mN/m or more, more preferably 20.0 mN/m or more, and even more preferably 21.0 mN/m or more. The static surface tension can be measured, for example, by the Wilhelmy method (DY-300 manufactured by Kyowa Interface Science) at a measurement temperature of 25°C.
　インク組成物の導電率は、特に限定されないが、２５００μＳ／ｃｍ以下であることが好ましい。導電率が２５００μＳ／ｃｍ以下となるようにインク組成物の成分を制御することで、成分同士の相互作用を抑制することが可能となり、保存安定性を向上させることが可能となる。 Although the conductivity of the ink composition is not particularly limited, it is preferably 2500 μS/cm or less. By controlling the components of the ink composition so that the electrical conductivity is 2500 μS/cm or less, it is possible to suppress the interaction between the components and improve the storage stability.
　インク組成物の導電率は、２４５０μＳ／ｃｍ以下であることが好ましく、２４００μＳ／ｃｍ以下であることがより好ましい。なお、導電率は、例えば、Ｅｕｔｅｃｈ　Ｉｎｓｔｒｕｍｅｎｔｓ製、ＥＣ　Ｔｅｓｔｒ　１１＋で２５℃にて測定することができる。 The conductivity of the ink composition is preferably 2450 μS/cm or less, more preferably 2400 μS/cm or less. The electrical conductivity can be measured at 25° C. with EC Testr 11+ manufactured by Eutech Instruments, for example.
　＜インクセット＞
　上記のインク組成物は、着色インクであっても、メタリックインク等であっても、カチオン性の化合物を含む受理溶液であっても、色材を含有しないクリアインクであっても、オーバーコートインクであってもよい。本実施の形態に係るインクセットは、これらのインク組成物を組み合わせたインクセットとしてもよい。 <Ink set>
The above ink composition may be a colored ink, a metallic ink or the like, a receiving solution containing a cationic compound, or a clear ink containing no coloring material, and may be an overcoat ink. may be The ink set according to the present embodiment may be an ink set in which these ink compositions are combined.
　その中でも、例えば、インクセットに含まれる１のインク組成物は、色材を含有する着色インク組成物（Ｃ）であり、インクセットに含まれる他のインク組成物は、カチオン性の化合物を含む受理溶液（Ｐ）であるインクセットや、インクセットに含まれる１のインク組成物は、被体の表面にオーバーコート層を形成するオーバーコートインク（Ｏ）であり、インクセットに含まれる他のインク組成物は、カチオン性の化合物を含む受理溶液（Ｐ）であるインクセットや、インクセットに含まれる１のインク組成物は、色材を含有する着色インク組成物（Ｃ）であり、インクセットに含まれる他のインク組成物は、被体の表面にオーバーコート層を形成するオーバーコートインク（Ｏ）であるインクセットを挙げることができる。 Among them, for example, one ink composition contained in the ink set is a colored ink composition (C) containing a coloring material, and the other ink composition contained in the ink set contains a cationic compound. The ink set that is the receiving solution (P) and one ink composition contained in the ink set are the overcoat inks (O) that form an overcoat layer on the surface of the object, and the other ink compositions contained in the ink set. The ink composition is an ink set that is a receiving solution (P) containing a cationic compound, and one ink composition included in the ink set is a colored ink composition (C) that contains a coloring material, and the ink Other ink compositions included in the set include an ink set that is an overcoat ink (O) that forms an overcoat layer on the surface of a substrate.
　また、色材を含有する着色インク組成物（Ｃ）同士を組み合わせたインクセットであってもよく、例えば、イエロー、マゼンタ、シアン、ブラック、及びこれらの中間色（例えば、オレンジインク、グリーンインク、ブルーインク、レッドインク）や淡色（例えば、ライトマゼンタインク、ライトシアンインク、ライトブラックインク）の着色インク組成物のような複数のインク組成物を組み合わせたインクセットであってもよい。また、白色色材を含有する白色インク組成物と、イエローインク組成物、マゼンタインク組成物、シアンインク組成物、ブラックインク組成物と、を含むインクセットや、白色色材を含有する白色インク組成物と、イエローインク組成物、マゼンタインク組成物、シアンインク組成物、ブラックインク組成物と、イエロー、マゼンタ、シアン、ブラックの中間色インク組成物や淡色インク組成物を含むインクセットであってもよい。さらに、光輝性顔料を含むメタリックインクと、イエローインク組成物、マゼンタインク組成物、シアンインク組成物、ブラックインク組成物と、を含むインクセットや、光輝性顔料を含むメタリックインクと、イエローインク組成物、マゼンタインク組成物、シアンインク組成物、ブラックインク組成物と、イエロー、マゼンタ、シアン、ブラックの中間色インク組成物や淡色インク組成物を含むインクセットであってもよい。 Further, the ink set may be a combination of colored ink compositions (C) containing a coloring material. ink, red ink) or light colored ink compositions (for example, light magenta ink, light cyan ink, light black ink). Further, an ink set containing a white ink composition containing a white colorant, a yellow ink composition, a magenta ink composition, a cyan ink composition, and a black ink composition, and a white ink composition containing a white colorant and a yellow ink composition, a magenta ink composition, a cyan ink composition, a black ink composition, and an intermediate color ink composition or a light color ink composition of yellow, magenta, cyan, and black. . Furthermore, an ink set containing a metallic ink containing a glitter pigment, a yellow ink composition, a magenta ink composition, a cyan ink composition, and a black ink composition, and a metallic ink containing a glitter pigment and a yellow ink composition A magenta ink composition, a cyan ink composition, a black ink composition, and intermediate color ink compositions or light color ink compositions of yellow, magenta, cyan, and black.
　そして、着色インク組成物（Ｃ）（イエロー、マゼンタ、シアン、ブラック、及びこれらの中間色や淡色の着色インク組成物や白色色材を含む白インク、光輝性顔料を含むメタリックインクを含む。）の導電率は、１０００μＳ／ｃｍ以下であることが好ましい。色材を含有する着色インク組成物（Ｃ）は、色材を着色インク組成物（Ｃ）中で色材（顔料）を含有するため、色材（顔料）同士が凝集して安定性が低下する傾向がある。着色インク組成物（Ｃ）の導電率は、１０００μＳ／ｃｍ以下となるように色材（顔料）を分散させる色材分散剤（顔料分散剤）やレベリング剤（界面活性剤）等の成分を含有させることで、成分同士（特に色材同士）の相互作用を抑制することが可能となり、安定性をさらに向上させることが可能となる。 and the colored ink composition (C) (yellow, magenta, cyan, black, and intermediate and light colored ink compositions thereof, white ink containing a white colorant, and metallic ink containing a bright pigment). The conductivity is preferably 1000 μS/cm or less. Since the coloring ink composition (C) containing the coloring material contains the coloring material (pigment) in the coloring ink composition (C), the coloring material (pigment) agglomerates and the stability is lowered. tend to The colored ink composition (C) contains components such as a colorant dispersant (pigment dispersant) and a leveling agent (surfactant) that disperse the colorant (pigment) so that the conductivity is 1000 μS/cm or less. By doing so, it is possible to suppress the interaction between the components (especially between the coloring materials), and it is possible to further improve the stability.
　着色インク組成物（Ｃ）の導電率は、９５０μＳ／ｃｍ以下であることがより好ましく、９００μＳ／ｃｍ以下であることがさらに好ましい。 The electrical conductivity of the colored ink composition (C) is more preferably 950 μS/cm or less, even more preferably 900 μS/cm or less.
　また、オーバーコートインク（Ｏ）の導電率は、１０００μＳ／ｃｍ以下であることが好ましい。被体の表面にオーバーコート層を形成するオーバーコートインク（Ｏ）は、オーバーコート層を形成するための樹脂を含有するため、オーバーコートインク（Ｏ）中で樹脂同士が凝集して安定性が低下する傾向がある。オーバーコートインク（Ｏ）の導電率は、１０００μＳ／ｃｍ以下となるように色材（顔料）を分散させるレベリング剤（界面活性剤）等の成分を含有させることで、成分同士（特に樹脂同士）の相互作用を抑制することが可能となり、安定性をさらに向上させることが可能となる。 Also, the electrical conductivity of the overcoat ink (O) is preferably 1000 μS/cm or less. The overcoat ink (O) that forms the overcoat layer on the surface of the object contains a resin for forming the overcoat layer. tend to decline. The electrical conductivity of the overcoat ink (O) is 1000 μS/cm or less. interaction can be suppressed, and the stability can be further improved.
　オーバーコートインク（Ｏ）の導電率は、９５０μＳ／ｃｍ以下であることがより好ましく、９００μＳ／ｃｍ以下であることがさらに好ましい。 The conductivity of the overcoat ink (O) is more preferably 950 μS/cm or less, even more preferably 900 μS/cm or less.
　また、受理溶液（Ｐ）の導電率は、１０００μＳ／ｃｍ以上２５００μＳ／ｃｍ以下であることが好ましい。受理溶液（Ｐ）は、カチオン性の化合物を含むため、受理溶液（Ｐ）の導電率が、１０００μＳ／ｃｍ以上２５００μＳ／ｃｍ以下となるようにカチオン性の化合物を含むことで、受理溶液（Ｐ）の保存安定性を維持しつつ、受理溶液（Ｐ）の上に着弾される着色インク（Ｃ）やオーバーコートインク（Ｏ）との反応性を向上させることが可能となり、滲みやムラを抑制することが可能となる。 Also, the electrical conductivity of the receiving solution (P) is preferably 1000 μS/cm or more and 2500 μS/cm or less. Since the receiving solution (P) contains a cationic compound, the receiving solution (P ) while maintaining the storage stability of the receiving solution (P), it is possible to improve the reactivity with the colored ink (C) and the overcoat ink (O) that land on the receiving solution (P), suppressing bleeding and unevenness. It becomes possible to
　受理溶液（Ｐ）の導電率は、１０５０μＳ／ｃｍ以上であることがより好ましく、１１００μＳ／ｃｍ以上であることがさらに好ましい。 The electrical conductivity of the receiving solution (P) is more preferably 1050 μS/cm or higher, more preferably 1100 μS/cm or higher.
　＜記録方法＞
　本実施の形態に係る記録方法は、上述したインク組成物をインクジェット法により基材上に塗布する記録方法である。 <Recording method>
The recording method according to the present embodiment is a recording method in which the ink composition described above is applied onto a substrate by an inkjet method.
　このインク組成物は、沸点が２３０℃以下の水溶性有機溶剤Ａと、樹脂と、を含有しており、乾燥性が高く、耐擦過性の高い塗膜を形成することができるものであるので、本実施の形態に係る記録方法によりインクジェット法により基材上に塗布することにより、高速で記録することが可能となる。さらに、高速で記録しても、耐擦過性の低下を抑制することが可能となり、結果として耐擦過性の高い塗膜を形成することができる。 This ink composition contains a water-soluble organic solvent A having a boiling point of 230° C. or less and a resin, and is highly drying and capable of forming a coating film with high scratch resistance. High-speed recording can be achieved by coating the base material with the ink-jet method according to the recording method of the present embodiment. Furthermore, even if recording is performed at a high speed, it is possible to suppress deterioration in abrasion resistance, and as a result, a coating film having high abrasion resistance can be formed.
　具体的には、本実施の形態に係る記録方法における記録速度における最高速度は、基材の種類やインクジェット記録装置の種類等にもよるが、シリアル方式の場合は７．５ｍ２／ｈ以上であることが好ましく、１０ｍ２／ｈ以上であることがより好ましく、１５ｍ２／ｈ以上であることがさらに好ましい。シングルパス方式の場合は３０ｍ／ｍｉｎ以上であることが好ましく、４０ｍ／ｍｉｎ以上であることがより好ましく、５０ｍ／ｍｉｎ以上であることがさらに好ましい。なお、シリアル方式とは、インクジェットヘッドを左右方向に移動させ数回に分けてインクを吐出する方式印刷であり、シングルパス方式とは、インクジェットヘッドを固定させ、基材をインクジェットヘッドに１度通過させることにより画像を形成する印刷方式である。 Specifically, the maximum recording speed in the recording method according to the present embodiment is 7.5 m 2 /h or more in the case of the serial method, although it depends on the type of the base material, the type of the ink jet recording apparatus, and the like. It is preferably 10 m 2 /h or more, more preferably 15 m 2 /h or more. In the case of the single pass method, the speed is preferably 30 m/min or more, more preferably 40 m/min or more, and even more preferably 50 m/min or more. The serial method is a printing method in which the inkjet head is moved in the horizontal direction and the ink is ejected in several batches, while the single-pass method is a method in which the inkjet head is fixed and the substrate passes through the inkjet head once. It is a printing method in which an image is formed by
　また、この沸点が２３０℃以下の水溶性有機溶剤Ａの水／１－オクタノールでの分配係数（ＬｏｇＰ）が－０．６以上である場合には、乾燥温度を比較的低温で記録しても、塗膜中に残留する有機溶剤による耐擦過性の低下を抑制することが可能となり、結果として耐擦過性の高い塗膜を形成することができる。 In addition, when the water-soluble organic solvent A having a boiling point of 230° C. or less has a water/1-octanol distribution coefficient (LogP) of −0.6 or more, the drying temperature can be recorded at a relatively low temperature. Therefore, it becomes possible to suppress deterioration of scratch resistance due to the organic solvent remaining in the coating film, and as a result, it is possible to form a coating film having high scratch resistance.
　具体的には、本実施の形態に係る記録方法における乾燥温度は、８０℃以下、好ましくは、７０℃以下さらに好ましくは６０℃以下であってもよい。 Specifically, the drying temperature in the recording method according to the present embodiment may be 80°C or lower, preferably 70°C or lower, and more preferably 60°C or lower.
　＜記録物の製造方法＞
　上述した記録方法は、上述したインク組成物をインクジェット法により基材上に塗布する記録物の製造方法と定義することもできる。 <Manufacturing Method of Recorded Matter>
The above-described recording method can also be defined as a method for producing a recorded matter in which the above-described ink composition is applied onto a substrate by an inkjet method.
　＜記録物＞
　上述した実施形態の記録物の製造方法により製造された記録物を構成する各層について説明する。具体的に、上記のインク組成物、又は上記のインクセットに含まれるインク組成物が基材上に塗布された記録物である。以下、記録物を構成する媒体（記録媒体）やインク組成物の層について説明する。 <Records>
Each layer constituting the recorded matter manufactured by the method for manufacturing the recorded matter of the above-described embodiment will be described. Specifically, it is a recorded matter in which the above ink composition or the ink composition contained in the above ink set is applied onto a substrate. The medium (recording medium) and the ink composition layer constituting the recorded matter will be described below.
　［媒体（記録媒体）］
　本実施の形態に係る記録方法に使用することのできる基材（記録媒体）としては、特に限定はされず、樹脂基材、金属板、ガラスなどの非吸収性基材であっても、紙や布帛などの吸収性基材であっても、受容層を備える基材のような表面塗工が施された基材であってもよく、種々の基材を使用することができる。後述する実施の形態に係る記録物の製造方法に使用することのできる基材についても同様である。 [Medium (recording medium)]
The base material (recording medium) that can be used in the recording method according to the present embodiment is not particularly limited. Various substrates can be used, such as an absorbent substrate such as a woven fabric, or a surface-coated substrate such as a substrate having a receiving layer. The same applies to the base material that can be used in the method of manufacturing a recorded matter according to an embodiment described later.
　非吸収性基材としては、ポリエステル系樹脂、ポリプロピレン系合成紙、ポリプロピレン系樹脂、ポリエチレン系樹脂、アクリル樹脂、スチレン樹脂、ポリカーボネート樹脂、ＡＢＳ樹脂、塩化ビニル樹脂、ポリイミド樹脂等の樹脂基材や、金属、金属箔コート紙、ガラス、合成ゴム、天然ゴム等を挙げることができる。 Examples of non-absorbent substrates include resin substrates such as polyester resins, polypropylene synthetic paper, polypropylene resins, polyethylene resins, acrylic resins, styrene resins, polycarbonate resins, ABS resins, vinyl chloride resins, polyimide resins, Metal, metal foil coated paper, glass, synthetic rubber, natural rubber and the like can be mentioned.
　吸収性基材としては、更紙、中質紙、上質紙、合成紙、綿、化繊織物、絹、麻、布帛、不織布、皮革等を挙げることができる。 Examples of absorbent substrates include dry paper, medium-quality paper, high-quality paper, synthetic paper, cotton, synthetic fiber fabric, silk, hemp, fabric, non-woven fabric, leather, and the like.
　表面塗工が施された基材としてはコート紙、アート紙、キャスト紙、軽量コート紙、微塗工紙等を挙げることができる。 Examples of surface-coated substrates include coated paper, art paper, cast paper, lightweight coated paper, and lightly coated paper.
　［インク組成物の層］
　インク組成物の層とは、上述したインク組成物に含まれる溶媒が揮発することにより形成される層である。例えば、インク組成物に色材を含有した場合には、所望の画像を形成する加飾層やその下地層となる。 [Ink composition layer]
The layer of the ink composition is a layer formed by volatilization of the solvent contained in the ink composition described above. For example, when the ink composition contains a coloring material, it becomes a decorative layer forming a desired image or a base layer therefor.
　また、上述したインク組成物をカチオン性の化合物を含む受理溶液とする場合には、基材上に上述したインク組成物（受理溶液）を塗布し、その上に上述したインク組成物（着色インク）を塗布してもよいし、基材上に上述したインク組成物（受理溶液）を塗布し、その上に上述したインク組成物（着色インク）とは異なるインク組成物（着色インク）を塗布してもよい。 Further, when the above-described ink composition is used as a receiving solution containing a cationic compound, the above-described ink composition (receiving solution) is applied onto a substrate, and the above-described ink composition (coloring ink) is applied thereon. ) may be applied, or the above-described ink composition (receiving solution) is applied on the substrate, and an ink composition (colored ink) different from the above-described ink composition (colored ink) is applied thereon. You may
　また、上述したインク組成物をオーバーコートインクとする場合には、記録物の表面に形成されるオーバーコート層となる。なお、この場合、記録物が備える記録層を形成するインク組成物は、上述したインク組成物であってもよいし、上述したインク組成物とは異なるインク組成物であってもよい。 Also, when the ink composition described above is used as an overcoat ink, it becomes an overcoat layer formed on the surface of a recorded matter. In this case, the ink composition that forms the recording layer of the recorded matter may be the ink composition described above, or may be an ink composition different from the ink composition described above.
　＜インクジェット記録装置＞
　本実施の形態に係るインクジェット記録装置は、上述したインク組成物が充填された収容容器が搭載されたインクジェット記録装置である。上述したインク組成物は乾燥性が高く、耐擦過性の高い塗膜を形成することができるものであるので、上述したインク組成物が充填された収容容器が搭載されたインクジェット記録装置により高速であって、耐擦過性の高い記録物を製造することが可能となる。 <Inkjet recording device>
An inkjet recording apparatus according to the present embodiment is an inkjet recording apparatus equipped with a container filled with the ink composition described above. The ink composition described above has high drying property and can form a coating film with high abrasion resistance. Therefore, it is possible to produce recorded matter having high scratch resistance.
　なお、インクジェット記録装置に搭載される収容容器とは、とくに限定されず、例えば、インクボトル、パウチ、バッグインボックス、ドラム等の容器を挙げることができる。また、これらの容器をさらにカートリッジ等に収容したものであってもよい。収容容器の材質としては、とくに限定されず、従来公知の樹脂製であってもよいし、その一部の金属材料を含む材質（例えば、アルミ蒸着層を備えたアルミパウチ）であってもよい。 The storage container mounted on the inkjet recording apparatus is not particularly limited, and examples include containers such as ink bottles, pouches, bag-in-boxes, and drums. Also, these containers may be further housed in a cartridge or the like. The material of the storage container is not particularly limited, and may be a conventionally known resin, or a material containing a part of metal material (for example, an aluminum pouch having an aluminum deposition layer). .
　またこの装置には、インク組成物の吐出後にインク組成物を乾燥する乾燥機構を備えることが好ましい。これによりそれぞれのインク組成物に含まれる揮発成分を効果的に除去し、樹脂粒子の造膜を促進することが可能となる。 In addition, it is preferable that this apparatus include a drying mechanism for drying the ink composition after the ink composition is ejected. This makes it possible to effectively remove the volatile components contained in each ink composition and promote film formation of the resin particles.
　インクの吐出後に該インクを乾燥する乾燥機構としては特に制限はされず、ヒーター等であってもよいし、熱風や常温の風を送風する機構であってもよい。 The drying mechanism for drying the ink after ejection is not particularly limited, and may be a heater or the like, or a mechanism for blowing hot air or room temperature air.
　そのなかでも、インク組成物に含まれる樹脂のＴｇよりも低い温度で基材上に塗布されたインク組成物を乾燥することが好ましい。上記のインク組成物は乾燥性の高いものであるので、インク組成物に含まれる樹脂のＴｇよりも低い温度で乾燥させても十分に乾燥させることができる。 Among them, it is preferable to dry the ink composition applied on the substrate at a temperature lower than the Tg of the resin contained in the ink composition. Since the above ink composition is highly drying, it can be sufficiently dried even at a temperature lower than the Tg of the resin contained in the ink composition.
　また、それぞれの吐出部における吐出方式は、ピエゾ方式、サーマル方式、静電方式等のいずれの方式であってもよい。 Also, the ejection method in each ejection part may be any method such as a piezo method, a thermal method, or an electrostatic method.
　以下、実施例により、本発明を更に詳細に説明するが、本発明はこれらの記載に何ら制限を受けるものではない。 The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these descriptions.
　１．インク組成物の調製
　各材料を下記表に示す割合（単位は質量％）になるように混合し、室温（２０～２５℃）にて１時間撹拌した。その後、メンブレンフィルターを用いて濾過を行い、実施例及び比較例のインク組成物を調製した。 1. Preparation of Ink Composition Each material was mixed so that the ratio (unit: % by mass) shown in the table below was obtained, and the mixture was stirred at room temperature (20 to 25° C.) for 1 hour. Thereafter, filtration was performed using a membrane filter to prepare ink compositions of Examples and Comparative Examples.
　２．インク組成物の評価
　（乾燥性）
　実施例及び比較例のインク組成物について乾燥性を評価した。具体的には、インク組成物を塩化ビニル樹脂基材上にバーコーターで７ｇ／ｍ２塗布した後、６０℃オーブン内に入れ、乾燥するまでの時間を指触評価した。３０秒毎に指触し、インク組成物が付着しなくなる時間を測定し、以下の評価基準に基づき評価を行った。評価結果を下記表に記載した（表中、「乾燥性」と表記）。
　評価基準
　Ａ：３分で乾燥した。
　Ｂ：３．５～５分で乾燥した。
　Ｃ：５．５～７分で乾燥した。
　Ｄ：７．５～８分で乾燥した。
Ｅ：８分で乾燥しなかった（実用範囲外）。 2. Evaluation of ink composition (drying property)
Drying properties of the ink compositions of Examples and Comparative Examples were evaluated. Specifically, after applying 7 g/m 2 of the ink composition onto a vinyl chloride resin substrate with a bar coater, it was placed in an oven at 60° C. and the time until drying was evaluated by touch. The surface was touched with a finger every 30 seconds, and the time until the ink composition stopped adhering was measured, and evaluation was performed based on the following evaluation criteria. The evaluation results are shown in the table below (indicated as "drying property" in the table).
Evaluation Criteria A: Dried in 3 minutes.
B: Dried in 3.5 to 5 minutes.
C: Dried in 5.5 to 7 minutes.
D: Dried in 7.5 to 8 minutes.
E: Not dried in 8 minutes (out of practical range).
　（保存安定性）
　実施例及び比較例のインク組成物について保存安定性を評価した。具体的には、インク組成物を６０℃オーブン内で１週間加温し、液温２５℃で測定した加温前後の粘度を測定し、以下の評価基準に基づき評価を行った。評価結果を下記表に記載した（表中、「保存安定性」と表記）。
　評価基準
　Ａ：粘度変化率５％以下
　Ｂ：粘度変化率５％超１０％未満
　Ｃ：粘度変化率１０％以上２０％未満
　Ｄ：粘度変化率２０％以上（実用範囲外） (Storage stability)
Storage stability was evaluated for the ink compositions of Examples and Comparative Examples. Specifically, the ink composition was heated in an oven at 60° C. for one week, and the viscosity before and after heating was measured at a liquid temperature of 25° C., and evaluated based on the following evaluation criteria. The evaluation results are shown in the table below (indicated as "storage stability" in the table).
Evaluation Criteria A: Viscosity change rate of 5% or less B: Viscosity change rate of more than 5% and less than 10% C: Viscosity change rate of 10% or more and less than 20% D: Viscosity change rate of 20% or more (outside practical range)
　（濃度ムラ）
　実施例及び比較例のインク組成物により得られた記録物について濃度ムラを評価した。具体的には、インク組成物をインクカートリッジ（収容容器）に充填し、そのインクカートリッジ（収容容器）をシリアルヘッド方式のインクジェット記録装置に搭載し、そのインクジェット記録装置により、解像度６００×９００ｄｐｉ、液滴サイズ６ｐｌ、印字濃度１００％のベタ画像を塩化ビニル樹脂基材上に印刷し、濃度ムラの有無を目視で観察し、以下の評価基準に基づき評価を行った。評価結果を下記表に記載した（表中、「濃度ムラ」と表記）。
　評価基準
　Ａ：濃度ムラ無し
　Ｂ：濃度ムラ有り
　Ｃ：インクの濡れが悪く画像形成できず（実用範囲外） (Density unevenness)
Density unevenness was evaluated for recorded matter obtained with the ink compositions of Examples and Comparative Examples. Specifically, the ink composition is filled in an ink cartridge (container), and the ink cartridge (container) is mounted on a serial head type inkjet recording apparatus. A solid image with a droplet size of 6 pl and a printing density of 100% was printed on a vinyl chloride resin substrate, and the presence or absence of density unevenness was visually observed, and evaluation was made based on the following evaluation criteria. The evaluation results are shown in the table below (denoted as "density unevenness" in the table).
Evaluation Criteria A: No density unevenness B: Density unevenness C: Image formation not possible due to poor ink wetting (outside practical range)
　（撥液性）
　実施例及び比較例のインク組成物について撥液性を評価した。具体的には、インクジェット記録装置における６００ｄｐｉのプリンターヘッドのノズルプレートをインク組成物に浸漬させ、液面から取出した後のプレートに対するインク組成物の露出面積を３０秒毎に目視で観察し、以下の評価基準に基づき評価を行った。評価結果を下記表に記載した（表中、「撥液性」と表記）。
　評価基準
　Ａ：３０秒後のプレートの露出面積が８０％以上
　Ｂ：１分後のプレートの露出面積が８０％以上
　Ｃ：１分後でもプレートの露出面積が８０％未満（実用範囲外） (liquid repellency)
Liquid repellency was evaluated for the ink compositions of Examples and Comparative Examples. Specifically, the nozzle plate of a 600 dpi printer head in an inkjet recording apparatus is immersed in the ink composition, and the exposed area of the ink composition on the plate after being removed from the liquid surface is visually observed every 30 seconds. was evaluated based on the evaluation criteria of The evaluation results are shown in the table below (indicated as "liquid repellency" in the table).
Evaluation criteria A: The exposed area of the plate after 30 seconds is 80% or more B: The exposed area of the plate after 1 minute is 80% or more C: The exposed area of the plate is less than 80% even after 1 minute (outside the practical range)
　（間欠吐出性）
　実施例及び比較例のインク組成物について間欠吐出性を評価した。具体的には、インク組成物をインクカートリッジ（収容容器）に充填し、そのインクカートリッジ（収容容器）をシリアルヘッド方式のインクジェット記録装置に搭載して、そのインクジェット記録装置により、ノズルチェックパターンを印刷し、一定時間静置後に同様の印刷を行った。静置前後でノズル欠け有無を確認し、静置前のパターンに対するノズル欠けが１０％未満になるまで同印刷を繰り返し、その回数により吐出性を以下の評価基準に基づき評価を行った。評価結果を下記表に記載した（表中、「間欠吐出性」と表記）。
　評価基準
　Ａ：静置後の印刷１回目でノズル欠け１０％以下
　Ｂ：静置後の印刷２回目でノズル欠け１０％以下
　Ｃ：静置後の印刷３回目でノズル欠け１０％以下
　Ｄ：静置後の印刷４回目でノズル欠け１０％以下
　Ｅ：静置後の印刷４回目でノズル欠け１１％以上（実用範囲外） (intermittent discharge)
The intermittent discharge properties of the ink compositions of Examples and Comparative Examples were evaluated. Specifically, the ink composition is filled in an ink cartridge (container), the ink cartridge (container) is mounted in a serial head type inkjet recording apparatus, and a nozzle check pattern is printed by the inkjet recording apparatus. Then, after standing still for a certain period of time, the same printing was performed. The presence or absence of missing nozzles was checked before and after standing, and the same printing was repeated until the missing nozzles decreased to less than 10% of the pattern before standing. The evaluation results are shown in the table below (indicated as "intermittent discharge property" in the table).
Evaluation criteria A: Nozzle missing 10% or less in the first printing after standing B: Nozzle missing 10% or less in the second printing after standing C: Nozzle missing 10% or less in the third printing after standing D: Still Nozzle missing 10% or less in the 4th printing after placing E: Nozzle missing 11% or more in the 4th printing after standing still (out of practical range)
　（耐擦過性）
　実施例及び比較例のインク組成物により得られた記録物について耐擦過性を評価した。具体的には、乾燥性評価同様の方法でインクを基材にバーコーターで７ｇ／ｍ２塗布した後６０℃で８分乾燥した塗膜を作製した。学振型摩擦堅牢度試験機ＩＩ型、加重１ｋｇ、当布：金巾３号の条件で試験後塗膜の外観を観察した。
　Ａ：１００回後に外観変化無し
　Ｂ：５０回後に外観変化無し・１００回後にやや外観変化有り
　Ｃ：２５回後に外観変化無し・５０回後にやや外観変化有り
　Ｄ：１０回後に外観変化無し・２５回後にやや外観変化有り
Ｅ：１０回後に外観変化有り（実用範囲外） (Scratch resistance)
The scratch resistance of recorded matter obtained with the ink compositions of Examples and Comparative Examples was evaluated. Specifically, a coating film was prepared by applying 7 g/m 2 of ink to a base material with a bar coater in the same manner as for evaluation of dryness, followed by drying at 60° C. for 8 minutes. After the test, the external appearance of the coating film was observed under the conditions of Gakushin type rubbing fastness tester type II, weight of 1 kg, and cloth: Kanawa No. 3.
A: No change in appearance after 100 times B: No change in appearance after 50 times Slight change in appearance after 100 times C: No change in appearance after 25 times Slight change in appearance after 50 times D: No change in appearance after 10 times 25 Slight change in appearance after rotation E: Change in appearance after 10 rotations (outside practical range)
Figure JPOXMLDOC01-appb-T000015
Figure JPOXMLDOC01-appb-T000015
Figure JPOXMLDOC01-appb-T000016
Figure JPOXMLDOC01-appb-T000016
Figure JPOXMLDOC01-appb-T000017
Figure JPOXMLDOC01-appb-T000017
Figure JPOXMLDOC01-appb-T000018
Figure JPOXMLDOC01-appb-T000018
Figure JPOXMLDOC01-appb-T000019
Figure JPOXMLDOC01-appb-T000019
Figure JPOXMLDOC01-appb-T000020
Figure JPOXMLDOC01-appb-T000020
Figure JPOXMLDOC01-appb-T000021
Figure JPOXMLDOC01-appb-T000021
Figure JPOXMLDOC01-appb-T000022
Figure JPOXMLDOC01-appb-T000022
Figure JPOXMLDOC01-appb-T000023
Figure JPOXMLDOC01-appb-T000023
Figure JPOXMLDOC01-appb-T000024
Figure JPOXMLDOC01-appb-T000024
Figure JPOXMLDOC01-appb-T000025
Figure JPOXMLDOC01-appb-T000025
Figure JPOXMLDOC01-appb-T000026
Figure JPOXMLDOC01-appb-T000026
Figure JPOXMLDOC01-appb-T000027
Figure JPOXMLDOC01-appb-T000027
Figure JPOXMLDOC01-appb-T000028
Figure JPOXMLDOC01-appb-T000028
Figure JPOXMLDOC01-appb-T000029
Figure JPOXMLDOC01-appb-T000029
　上記表から分かるように、所定沸点以下の水溶性有機溶剤と樹脂と、を含有するインク組成物であれば、乾燥性が高く、塗膜の耐擦過性を向上させることができることが分かる。 As can be seen from the above table, an ink composition containing a water-soluble organic solvent having a predetermined boiling point or lower and a resin can be dried quickly and can improve the scratch resistance of the coating film.
　また、レベリング剤を含まない実施例３のインク組成物と比較してレベリング剤を含む実施例１、２、４～９のインク組成物は得られる記録物の「乾燥性」評価において良好なものであった。 In addition, the ink compositions of Examples 1, 2, and 4 to 9 containing a leveling agent are good in the "drying property" evaluation of the obtained recorded matter as compared with the ink composition of Example 3 which does not contain a leveling agent. Met.
　また、樹脂の種類を変更させた実施例１、１０～１７のインク組成物において、Ｔｇ（ガラス転移温度）は、５０℃以上の樹脂を含む実施例１、１０、１２、１３、１５～１７のインク組成物は、実施例１１、１４のインク組成物と比較しても耐擦過性評価が良好であった。 Further, in the ink compositions of Examples 1, 10 to 17 in which the type of resin was changed, Tg (glass transition temperature) of Examples 1, 10, 12, 13, 15 to 17 containing resins of 50° C. or higher The ink composition of No. 2 had good scratch resistance evaluation even when compared with the ink compositions of Examples 11 and 14.
　また、水溶性有機溶剤Ａの種類を変更させた実施例１、１８～２８において、水／１－オクタノールでの分配係数（ＬｏｇＰ）が－０．６以上である水溶性有機溶剤Ａを含有する実施例１、１８～２２、２４～２８のインク組成物は、実施例１、２３のインク組成物と比較しても耐擦過性評価が良好であった。 Further, in Examples 1 and 18 to 28 in which the type of the water-soluble organic solvent A was changed, the water-soluble organic solvent A having a water/1-octanol partition coefficient (LogP) of -0.6 or more was used. The ink compositions of Examples 1, 18 to 22, and 24 to 28 had good scratch resistance even when compared with the ink compositions of Examples 1 and 23.
　また、導電率が１０００μＳ／ｃｍ以上２５００μＳ／ｃｍ以下であり実施例２９のインク組成物（受理溶液（Ｐ））は、実施例３０のインク組成物（受理溶液（Ｐ））と比較しても保存安定性が良好であった。 Further, the ink composition of Example 29 (receiving solution (P)) having a conductivity of 1000 μS/cm or more and 2500 μS/cm or less was compared with the ink composition of Example 30 (receiving solution (P)). Good storage stability.
　また、水溶性有機溶剤Ａの含有量を変更した実施例１、３４～３９のインク組成物において、水溶性有機溶剤Ａの含有量が５質量％以上の範囲である実施例１、３５～３９のインク組成物は、実施例３４のインク組成物と比較しても「乾燥性」評価及び「耐擦過性」評価はさらに良好なものであった。また、水溶性有機溶剤Ａの含有量が３５質量％以下の範囲である実施例１、３４～３８のインク組成物は、実施例３９のインク組成物と比較しても「保存安定性」評価はさらに良好なものであった。 Further, in the ink compositions of Examples 1, 34 to 39 in which the content of the water-soluble organic solvent A was changed, Examples 1, 35 to 39 in which the content of the water-soluble organic solvent A was in the range of 5% by mass or more The ink composition of Example 34 had even better evaluations of "drying property" and "scratch resistance" than the ink composition of Example 34. In addition, the ink compositions of Examples 1 and 34 to 38, in which the content of the water-soluble organic solvent A was in the range of 35% by mass or less, were evaluated for "storage stability" even when compared with the ink composition of Example 39. was even better.
　また、樹脂の含有量を変更した実施例１、４０～４４のインク組成物において、樹脂の含有量が１．５質量％以上の範囲である実施例１、４１～４４のインク組成物は、実施例４０のインク組成物と比較しても「耐擦過性」評価はさらに良好なものであった。また、樹脂の含有量が２０質量％以下の範囲である実施例１、４０～４３のインク組成物は、実施例４４のインク組成物と比較しても「間欠吐出性」評価はさらに良好なものであった。 In addition, in the ink compositions of Examples 1 and 40 to 44 in which the resin content was changed, the ink compositions of Examples 1 and 41 to 44 in which the resin content was in the range of 1.5% by mass or more were Even when compared with the ink composition of Example 40, the "scratch resistance" evaluation was even better. In addition, the ink compositions of Examples 1 and 40 to 43, in which the resin content was in the range of 20% by mass or less, were even more favorable in the evaluation of "intermittent ejection property" compared with the ink composition of Example 44. It was something.
　また、平均粒子径が３００ｎｍ以下の分散性樹脂を含有する実施例１、４５のインク組成物は、実施例４６のインク組成物と比較しても「耐擦過性」評価はさらに良好なものであった。 In addition, the ink compositions of Examples 1 and 45 containing a dispersible resin having an average particle size of 300 nm or less had even better "scratch resistance" evaluation than the ink composition of Example 46. there were.
　なお、水溶性有機溶剤Ａを「沸点２３０℃以下の環状エステル系溶剤」に変更した実施例４７～８０のインク組成物や「沸点２３０℃以下のグリコールエーテル系溶剤」に変更した実施例８１～１１５のインク組成物についても実施例１～４６のインク組成物と同様の傾向が見られた。 The ink compositions of Examples 47 to 80 in which the water-soluble organic solvent A was changed to a "cyclic ester solvent having a boiling point of 230°C or less" and Examples 81 to 80 in which a "glycol ether solvent having a boiling point of 230°C or less" were used. The ink composition No. 115 showed the same tendency as the ink compositions of Examples 1-46.
　また、沸点が２３０℃以下のアミド系溶剤として、Ｎ,Ｎ－ジエチルホルムアミドを含有し、さらに１，３－プロパンジオールを含有する実施例３６の「１，３－プロパンジオール」を１，２－アルカンジオール系溶剤である「プロピレングリコール」に変更した実施例１４１，１４２は、「乾燥性」評価はさらに良好なものであった。同様に、沸点２３０℃以下の環状エステル系溶剤として、ε-カプロラクトンを含有し、さらに１，３－プロパンジオールを含有する実施例７０の「１，３－プロパンジオール」を１，２－アルカンジオール系溶剤である「プロピレングリコール」に変更した実施例１４３、１４４は、「乾燥性」評価はさらに良好なものであった。同様に、沸点２３０℃以下のグリコールエーテル系溶剤として、ジプロピレングリコールモノメチルエーテルを含有し、さらに１，３－プロパンジオールを含有する実施例１０５の「１，３－プロパンジオール」を１，２－アルカンジオール系溶剤である「プロピレングリコール」に変更した実施例１４５、１４６は、「乾燥性」評価はさらに良好なものであった。 Further, as the amide-based solvent having a boiling point of 230° C. or lower, the “1,3-propanediol” of Example 36 containing N,N-diethylformamide and further containing 1,3-propanediol was changed to 1,2- Examples 141 and 142, in which the alkanediol-based solvent "propylene glycol" was used, gave even better "drying property" evaluations. Similarly, "1,3-propanediol" of Example 70, which contains ε-caprolactone and further contains 1,3-propanediol, as a cyclic ester-based solvent having a boiling point of 230°C or less is replaced with 1,2-alkanediol. Examples 143 and 144 in which the system solvent "propylene glycol" was changed had even better "drying property" evaluations. Similarly, the "1,3-propanediol" of Example 105, which contains dipropylene glycol monomethyl ether and further contains 1,3-propanediol, as a glycol ether-based solvent having a boiling point of 230° C. or less is replaced with 1,2- Examples 145 and 146, in which the alkanediol-based solvent "propylene glycol" was used, gave even better "drying property" evaluations.
　一方、樹脂を含有しない比較例１のインク組成物は、「耐擦過性」評価が劣るものであり、水溶性有機溶剤Ａを含有しない比較例２～９のインク組成物は、「耐擦過性」評価及び「乾燥性」評価に劣るものであり、本願発明の効果を奏するものとはなっていない。 On the other hand, the ink composition of Comparative Example 1 containing no resin was inferior in the evaluation of "scratch resistance", and the ink compositions of Comparative Examples 2 to 9 containing no water-soluble organic solvent A had "scratch resistance "Evaluation" and "Dryness" evaluation are inferior, and the effect of the present invention is not exhibited.
　３．インクセットの評価
　上記のインク組成物を組み合わせたインクセットについて評価を行った。 3. Evaluation of Ink Set An ink set in which the ink compositions described above were combined was evaluated.
　（乾燥性）
　上記のインク組成物を組み合わせたインクセットについて乾燥性を評価した。具体的には、シリアルヘッド方式のインクジェット印刷装置を使用して、基材として塩化ビニル樹脂又は透明塩化ビニル樹脂の表面に前処理インクと、白インクと、シアンインクと、オーバーコートインクと、をこの順に吐出して、解像度６００×９００ｄｐｉ、液滴サイズ６ｐｌ、印字濃度１００％のベタ画像の印刷物を製造した。印刷直後の印刷物を６０℃オーブン内に入れ、乾燥するまでの時間を指触評価した。３０秒毎に指触し、インク組成物が付着しなくなる時間を測定し、以下の評価基準に基づき評価を行った。
　評価基準
　Ａ：３分で乾燥した。
　Ｂ：３．５～５分で乾燥した。
　Ｃ：５．５～７分で乾燥した。
　Ｄ：７．５～８分で乾燥した。
Ｅ：８分で乾燥しなかった（実用範囲外）。 (dryness)
An ink set in which the above ink compositions were combined was evaluated for drying properties. Specifically, using a serial head type inkjet printer, pretreatment ink, white ink, cyan ink, and overcoat ink are applied to the surface of vinyl chloride resin or transparent vinyl chloride resin as a substrate. By discharging in this order, a solid image print having a resolution of 600×900 dpi, a droplet size of 6 pl, and a print density of 100% was produced. Immediately after printing, the printed matter was placed in an oven at 60° C., and the time until drying was evaluated by touch. The surface was touched with a finger every 30 seconds, and the time until the ink composition stopped adhering was measured, and evaluation was performed based on the following evaluation criteria.
Evaluation Criteria A: Dried in 3 minutes.
B: Dried in 3.5 to 5 minutes.
C: Dried in 5.5 to 7 minutes.
D: Dried in 7.5 to 8 minutes.
E: Not dried in 8 minutes (out of practical range).
　（滲み）
　上記のインク組成物を組み合わせたインクセットについて滲みを評価した。具体的には、シリアルヘッド方式のインクジェット印刷装置を使用して、基材として塩化ビニル樹脂又は透明塩化ビニル樹脂の表面に前処理インクと、白インクと、シアンインクと、オーバーコートインクと、をこの順に吐出して、解像度６００×９００ｄｐｉ、液滴サイズ６ｐｌ、シアンインク以外のインクは印字濃度１００％のベタ画像、シアンインクは４～８ポイントの文字画像の印刷物を製造し、６０℃で乾燥した後の印字の滲みを目視で評価し、以下の評価基準に基づき評価を行った。評価結果を下記表に記載した（表中、「滲み」と表記）。
　評価基準
　Ａ：４ｐｔサイズまでが鮮明
　Ｂ：６ｐｔサイズまでが鮮明
　Ｃ：８ｐｔサイズまでが鮮明
　Ｄ：８ｐｔサイズが不鮮明（実用範囲外） (blur)
Bleeding was evaluated for an ink set in which the above ink compositions were combined. Specifically, using a serial head type inkjet printer, pretreatment ink, white ink, cyan ink, and overcoat ink are applied to the surface of vinyl chloride resin or transparent vinyl chloride resin as a substrate. Discharge in this order to produce a print with a resolution of 600 x 900 dpi, a droplet size of 6 pl, a solid image with a print density of 100% for inks other than cyan ink, and a character image of 4 to 8 points for cyan ink, and dry at 60 ° C. After printing, bleeding was visually evaluated and evaluated based on the following evaluation criteria. The evaluation results are shown in the table below (indicated as "bleeding" in the table).
Evaluation criteria A: clear up to 4pt size B: clear up to 6pt size C: clear up to 8pt size D: unclear up to 8pt size (out of practical range)
　（耐擦過性）
　上記のインク組成物を組み合わせたインクセットについて耐擦過性を評価した。具体的には、上記のインクセットにおける乾燥性と同様に印字濃度１００％のベタ画像の印刷物を製造し、６０℃で８分乾燥後、印刷直後のインク組成物の塗布面の塗膜に対して学振型摩擦堅牢度試験機ＩＩ型、加重１ｋｇ、当布：金巾３号の条件で塗膜の外観を観察した。評価結果を下記表に記載した（表中、「耐擦過性」と表記）。
　Ａ：１００回後に外観変化無し
　Ｂ：７５回後に外観変化無し・１００回後にやや外観変化有り
　Ｃ：５０回後に外観変化無し・７５回後にやや外観変化有り
　Ｄ：２５回後に外観変化無し・５０回後にやや外観変化有り
　Ｅ：２５回後に外観変化有り（実用範囲外） (Scratch resistance)
An ink set in which the above ink compositions were combined was evaluated for scratch resistance. Specifically, a solid image print having a print density of 100% is produced in the same manner as in the drying properties of the ink set described above, and after drying at 60° C. for 8 minutes, the coating film on the coated surface of the ink composition immediately after printing is The appearance of the coating film was observed under the conditions of a Gakushin type rubbing fastness tester type II, a load of 1 kg, and a cloth of No. 3. The evaluation results are shown in the table below (indicated as "scratch resistance" in the table).
A: No change in appearance after 100 times B: No change in appearance after 75 times Slight change in appearance after 100 times C: No change in appearance after 50 times Slight change in appearance after 75 times D: No change in appearance after 25 times 50 Slight change in appearance after rotation E: Change in appearance after 25 rotations (outside practical range)
Figure JPOXMLDOC01-appb-T000030
Figure JPOXMLDOC01-appb-T000030
　上記表から分かるように、沸点が２３０℃以下の水溶性有機溶剤Ａと樹脂とを含有するインク組成物のインクセットであれば、乾燥性が高く、塗膜の耐擦過性を向上させることができることが分かる。 As can be seen from the above table, the ink set of the ink composition containing the water-soluble organic solvent A having a boiling point of 230° C. or less and the resin has high drying property and can improve the abrasion resistance of the coating film. I know you can.
　また、導電率が、１０００μＳ／ｃｍ以上２５００μＳ／ｃｍ以下の範囲にある実施例２９のインク組成物（受理溶液）と、導電率が１０００μＳ／ｃｍ以下の範囲にある実施例２４のインク組成物と、を含む実施例１１７のインクセットは、実施例１３５のインクセットと比較しても、「滲み」評価は良好なものであった。 Further, the ink composition (receiving solution) of Example 29 having a conductivity of 1000 μS/cm or more and 2500 μS/cm or less and the ink composition of Example 24 having a conductivity of 1000 μS/cm or less. The ink set of Example 117 containing .
　また、水溶性有機溶剤Ａを含む実施例３２のインク組成物（オーバーコートインク）と、水溶性有機溶剤Ａを含まない比較例７のインク組成物（シアンインク）と、水溶性有機溶剤Ａを含む実施例２９のインク組成物（受理溶液）と、を含む実施例１３４のインクセットは、水溶性有機溶剤Ａを含むインク組成物を含まない比較例１１のインクセットを比較して、「乾燥性」評価、「滲み」評価、「耐擦過性」評価は良好であった。また、水溶性有機溶剤Ａを含む実施例３２のインク組成物（オーバーコートインク）と、水溶性有機溶剤Ａを含まない比較例７のインク組成物（シアンインク）とを含む実施例１３３のインクセットは、水溶性有機溶剤Ａを含むインク組成物を含まない比較例１０のインクセットを比較して、「乾燥性」評価、「滲み」評価、「耐擦性耐擦過性」評価は良好であった。これらの結果から、インクセットを構成する少なくとも１つのインク組成物が「水溶性有機溶剤Ａ」を含有することで、本願発明の効果を奏するインクセットであることが確認された。 Further, the ink composition (overcoat ink) of Example 32 containing the water-soluble organic solvent A, the ink composition (cyan ink) of Comparative Example 7 not containing the water-soluble organic solvent A, and the water-soluble organic solvent A The ink set of Example 134, which contains the ink composition of Example 29 (receiving solution) and the ink set of Comparative Example 11, which does not contain the water-soluble organic solvent A, is compared with the ink set of Comparative Example 11. The evaluations of "fairness", "bleeding", and "scratch resistance" were all good. Further, the ink of Example 133 containing the ink composition (overcoat ink) of Example 32 containing the water-soluble organic solvent A and the ink composition (cyan ink) of Comparative Example 7 not containing the water-soluble organic solvent A The set was compared with the ink set of Comparative Example 10, which did not contain the ink composition containing the water-soluble organic solvent A, and the "drying property" evaluation, "bleeding" evaluation, and "scratch resistance" evaluation were good. there were. From these results, it was confirmed that the effect of the invention of the present application is achieved by containing the "water-soluble organic solvent A" in at least one ink composition constituting the ink set.
　また、実施例１３９～１４６のインク組成物を含む実施例１４７～１６４のインクセットにおいて、実施例１４８，１５０，１５２，１５４、１５６、１５８、１６０、１６２、１６４のインクセットは、実施例１４７、１４９、１５１、１５３，１５５、１５７、１５９、１６１、１６３のインクセットと比較しても「耐擦過性」が良好となっている。そして、実施例１４８，１５０，１５２，１５４、１５６、１５８、１６０、１６２、１６４のインクセットは、シリコーン系界面活性剤を含む実施例１４２，１４４，１４６のインク組成物を含むものである。このことから、シリコーン（シリコン）系界面活性剤を含有するインク組成物を含むインクセットであれば、耐擦過性の高い塗膜を形成できることが確認された。 Further, in the ink sets of Examples 147 to 164 containing the ink compositions of Examples 139 to 146, the ink sets of Examples 148, 150, 152, 154, 156, 158, 160, 162, and 164 , 149, 151, 153, 155, 157, 159, 161, and 163, the "scratch resistance" is good. The ink sets of Examples 148, 150, 152, 154, 156, 158, 160, 162 and 164 contain the ink compositions of Examples 142, 144 and 146 containing a silicone surfactant. From this, it was confirmed that an ink set containing an ink composition containing a silicone (silicon)-based surfactant can form a coating film with high scratch resistance.

Claims (25)

  1. 　インクジェット用のインク組成物であって、
    　水溶性有機溶剤と、樹脂と、を含有し、
    　前記樹脂の少なくとも一部を分散性樹脂として含有し、
    　前記水溶性有機溶剤は、沸点２３０℃以下のアミド系溶剤、沸点２３０℃以下の環状エステル系溶剤、及び沸点２３０℃以下のグリコールエーテル系溶剤から選択される少なくとも１つ以上の水溶性有機溶剤Ａを含有する
    　インク組成物。     An ink composition for inkjet,
    containing a water-soluble organic solvent and a resin,
    containing at least part of the resin as a dispersible resin;
    The water-soluble organic solvent is at least one water-soluble organic solvent A selected from amide solvents with a boiling point of 230°C or lower, cyclic ester solvents with a boiling point of 230°C or lower, and glycol ether solvents with a boiling point of 230°C or lower. An ink composition containing
  2. 　前記分散性樹脂１００質量部に対する前記水溶性有機溶剤Ａの含有量は３０質量部以上である
    　請求項１に記載のインク組成物。     The ink composition according to claim 1, wherein the content of the water-soluble organic solvent A is 30 parts by mass or more relative to 100 parts by mass of the dispersible resin.
  3. 　前記分散性樹脂のＴｇは、インク組成物の乾燥温度よりも高い
    　請求項１又は２に記載のインク組成物。     The ink composition according to claim 1 or 2, wherein Tg of the dispersible resin is higher than the drying temperature of the ink composition.
  4. 　前記分散性樹脂のＴｇは、５０℃以上である
    　請求項１から３のいずれかに記載のインク組成物。     The ink composition according to any one of claims 1 to 3, wherein the dispersible resin has a Tg of 50°C or higher.
  5. 　前記分散性樹脂は、アクリル系樹脂、ポリウレタン系樹脂、ポリエステル系樹脂、塩化ビニル系樹脂、酢酸ビニル系樹脂、ポリエーテル系樹脂、塩化ビニル酢酸ビニル共重合樹脂、ポリエチレン系樹脂、アクリルアミド系樹脂、エポキシ系樹脂、ポリカーボネート系樹脂、シリコーン系樹脂、及びポリスチレン系樹脂からなる群より選択される１つ以上の樹脂あるいは共重合樹脂を含む
    　請求項１から４のいずれかに記載のインク組成物。     The dispersible resins include acrylic resins, polyurethane resins, polyester resins, vinyl chloride resins, vinyl acetate resins, polyether resins, vinyl chloride vinyl acetate copolymer resins, polyethylene resins, acrylamide resins, epoxy resins. 5. The ink composition according to any one of claims 1 to 4, comprising one or more resins or copolymer resins selected from the group consisting of polystyrene-based resins, polycarbonate-based resins, silicone-based resins, and polystyrene-based resins.
  6. 　前記分散性樹脂は、少なくともアクリル系樹脂、又はアクリル系共重合樹脂を含む
    　請求項５に記載のインク組成物。     6. The ink composition according to claim 5, wherein the dispersible resin contains at least an acrylic resin or an acrylic copolymer resin.
  7. 　前記水溶性有機溶剤Ａの水／１－オクタノールでの分配係数（ＬｏｇＰ）が－０．６以上である
    　請求項１から６のいずれかに記載のインク組成物。     7. The ink composition according to claim 1, wherein the water-soluble organic solvent A has a water/1-octanol partition coefficient (LogP) of −0.6 or more.
  8. 　前記水溶性有機溶剤Ａは、以下の式（１）で表される沸点２３０℃以下のアミド系溶剤、以下の式（２）で表される沸点２３０℃以下の環状エステル系溶剤、及び、以下の式（３）で表される沸点２３０℃以下のグリコールエーテル系溶剤から選択される少なくとも１つ以上の水溶性有機溶剤Ａを含有する
    　請求項１から７のいずれかに記載のインク組成物。
    Figure JPOXMLDOC01-appb-C000001
     （式（１）中、Ｒ１は水素、若しくは炭素数１～４のアルキル基であり、Ｒ２，Ｒ３は官能基である。）
    Figure JPOXMLDOC01-appb-C000002
     （式（６）中、Ｒ５は、炭素数３以上５以下のアルキレン基又はビニレン基を有する炭素鎖であり、Ｒ６は、水素若しくは炭素数１以上２以下のアルキル基又はビニリデン基を表す。Ｒ６は、Ｒ５の炭素鎖であればどの位置でも、複数あってもよく、Ｒ５とＲ６は単結合又は多重結合のいずれの結合で繋がっていてもよい。）
    Figure JPOXMLDOC01-appb-C000003
     　（式（８）中、Ｒ７、Ｒ９は、水素、若しくはアルキル基、アシル基であり少なくとも一方はアルキル基、若しくはアシル基である、Ｒ８は、エチレン基又はプロピレン基を表す。ｎは２～４の整数を表す。）     The water-soluble organic solvent A includes an amide solvent having a boiling point of 230° C. or less represented by the following formula (1), a cyclic ester solvent having a boiling point of 230° C. or less represented by the following formula (2), and 8. The ink composition according to any one of claims 1 to 7, comprising at least one water-soluble organic solvent A selected from glycol ether solvents having a boiling point of 230°C or less represented by the formula (3) of:
    Figure JPOXMLDOC01-appb-C000001
     (In formula (1), R 1 is hydrogen or an alkyl group having 1 to 4 carbon atoms, and R 2 and R 3 are functional groups.)
    Figure JPOXMLDOC01-appb-C000002
     (In formula (6), R 5 is a carbon chain having an alkylene group having 3 to 5 carbon atoms or a vinylene group, and R 6 represents hydrogen, an alkyl group having 1 to 2 carbon atoms, or a vinylidene group. R 6 may be present at any position on the carbon chain of R 5 , and may be plural, and R 5 and R 6 may be linked by either a single bond or a multiple bond.)
    Figure JPOXMLDOC01-appb-C000003
     (In formula (8), R 7 and R 9 are hydrogen, an alkyl group, or an acyl group, and at least one of them is an alkyl group or an acyl group. R 8 represents an ethylene group or a propylene group. n is represents an integer from 2 to 4.)
  9. 　前記水溶性有機溶剤Ａは、Ｎ－エチル－Ｎ－メチルホルムアミド、Ｎ－メチル－Ｎ－プロピルホルムアミド、Ｎ，Ｎ－ジエチルホルムアミド、Ｎ－エチル－Ｎ－プロピルホルムアミド、Ｎ，Ｎ－ジメチルアセトアミド、Ｎ－エチル－Ｎ－メチルアセトアミド、Ｎ－メチル－Ｎ－プロピルアセトアミド、Ｎ，Ｎ－ジエチルアセトアミド、Ｎ，Ｎ－ジメチルプロパンアミド、Ｎ－エチル－Ｎ－メチルプロパンアミド、γ－ブチロラクトン、α－メチレン－γ－ブチロラクトン、ε－カプロラクトン、ジエチレングリコールモノエチルエーテル、ジプロピレングリコールモノメチルエーテル、及びジエチレングリコールモノイソブチルエーテルからなる群より選択される
    　請求項１から８のいずれかに記載のインク組成物。     The water-soluble organic solvent A includes N-ethyl-N-methylformamide, N-methyl-N-propylformamide, N,N-diethylformamide, N-ethyl-N-propylformamide, N,N-dimethylacetamide, N -ethyl-N-methylacetamide, N-methyl-N-propylacetamide, N,N-diethylacetamide, N,N-dimethylpropanamide, N-ethyl-N-methylpropanamide, γ-butyrolactone, α-methylene- 9. The ink composition according to any one of claims 1 to 8, which is selected from the group consisting of γ-butyrolactone, ε-caprolactone, diethylene glycol monoethyl ether, dipropylene glycol monomethyl ether, and diethylene glycol monoisobutyl ether.
  10. 　さらにアルカンジオール系溶剤を含有する
    　請求項１から９のいずれかに記載のインク組成物。     10. The ink composition according to any one of Claims 1 to 9, further comprising an alkanediol solvent.
  11. 　前記水溶性有機溶剤Ａは、少なくとも２種以上の沸点２３０℃以下のアミド系溶剤を含有する
    　請求項１０に記載のインク組成物。     11. The ink composition according to claim 10, wherein the water-soluble organic solvent A contains at least two kinds of amide-based solvents having a boiling point of 230°C or less.
  12. 　前記アルカンジオール系溶剤は、炭素数が３以上６以下であり、炭素骨格の少なくとも一方の末端に水酸基を備えるアルカンジオール系溶剤を含有する
    　請求項１１に記載のインク組成物。     12. The ink composition according to claim 11, wherein the alkanediol-based solvent contains an alkanediol-based solvent having 3 or more and 6 or less carbon atoms and having a hydroxyl group at at least one end of the carbon skeleton.
  13. 　前記水溶性有機溶剤Ａは、少なくとも２種以上の水溶性有機溶剤Ａを含有する
    　請求項１から１２のいずれかに記載のインク組成物。     13. The ink composition according to any one of claims 1 to 12, wherein the water-soluble organic solvent A contains at least two or more water-soluble organic solvents A.
  14. 　前記水溶性有機溶剤Ａは、少なくとも２種以上の沸点２３０℃以下のアミド系溶剤を含有する
    　請求項１３に記載のインク組成物。     14. The ink composition according to claim 13, wherein the water-soluble organic solvent A contains at least two amide-based solvents having a boiling point of 230°C or less.
  15. 　前記水溶性有機溶剤Ａは、少なくとも沸点２３０℃以下のアミド系溶剤と、沸点２３０℃以下の環状エステル系溶剤と、を含有する
    　請求項１３に記載のインク組成物。     The ink composition according to claim 13, wherein the water-soluble organic solvent A contains at least an amide solvent having a boiling point of 230°C or lower and a cyclic ester solvent having a boiling point of 230°C or lower.
  16. 　前記水溶性有機溶剤Ａは、少なくとも沸点２３０℃以下のアミド系溶剤と、沸点２３０℃以下のグリコールエーテル系溶剤と、を含有する
    　請求項１３に記載のインク組成物。     14. The ink composition according to claim 13, wherein the water-soluble organic solvent A contains at least an amide solvent having a boiling point of 230°C or lower and a glycol ether solvent having a boiling point of 230°C or lower.
  17. 　前記水溶性有機溶剤Ａは、少なくとも、沸点２３０℃以下の環状エステル系溶剤と、沸点２３０℃以下のグリコールエーテル系溶剤と、を含有する
    　請求項１３に記載のインク組成物。     14. The ink composition according to claim 13, wherein the water-soluble organic solvent A contains at least a cyclic ester solvent having a boiling point of 230°C or lower and a glycol ether solvent having a boiling point of 230°C or lower.
  18. 　さらにレベリング剤を含有し、
    　前記レベリング剤の含有量は、前記インク組成物に含まれる前記水溶性有機溶剤Ａ１００質量部に対して０．１質量部以上５０質量部以下の範囲である
    　請求項１から１７のいずれかに記載のインク組成物。     Furthermore, it contains a leveling agent,
    18. The content of the leveling agent is in the range of 0.1 parts by mass or more and 50 parts by mass or less with respect to 100 parts by mass of the water-soluble organic solvent A contained in the ink composition. ink composition.
  19. 　導電率が２５００μＳ／ｃｍ以下である
    　請求項１から１８のいずれかに記載のインク組成物。     19. The ink composition according to any one of claims 1 to 18, which has a conductivity of 2500 [mu]S/cm or less.
  20. 　請求項１から１９のいずれかに記載のインク組成物を含む
    　インクセット。     An ink set comprising the ink composition according to any one of claims 1 to 19.
  21. 　請求項１から１９のいずれかに記載のインク組成物、又は請求項２０に記載のインクセットに含まれるインク組成物が基材上に塗布された
    　記録物。     21. A recorded matter obtained by applying the ink composition according to any one of claims 1 to 19 or the ink composition contained in the ink set according to claim 20 to a substrate.
  22. 　請求項１から１９のいずれかに記載のインク組成物、又は請求項２０に記載のインクセットに含まれるインク組成物をインクジェット法により基材上に塗布する
    　記録方法。     21. A recording method, wherein the ink composition according to any one of claims 1 to 19 or the ink composition contained in the ink set according to claim 20 is applied onto a substrate by an inkjet method.
  23. 　請求項１から１９のいずれかに記載のインク組成物、又は請求項２０に記載のインクセットをインクジェット法により基材上に塗布し、その後、前記インク組成物を該インク組成物に含まれる樹脂のＴｇよりも低い温度で乾燥する
    　記録方法。     The ink composition according to any one of claims 1 to 19 or the ink set according to claim 20 is applied onto a substrate by an inkjet method, and then the ink composition is applied to the resin contained in the ink composition. A recording method that dries at a temperature below the Tg of the
  24. 　請求項１から１９のいずれかに記載のインク組成物、又は請求項２０に記載のインクセットに含まれるインク組成物をインクジェット法により基材上に塗布する
    　記録物の製造方法。     21. A method for producing a recorded matter, wherein the ink composition according to any one of claims 1 to 19 or the ink composition contained in the ink set according to claim 20 is applied onto a substrate by an inkjet method.
  25. 　請求項１から１９のいずれかに記載のインク組成物、又は請求項２０に記載のインクセットに含まれるインク組成物が充填された収容容器が搭載された
    　インクジェット記録装置。     21. An inkjet recording apparatus equipped with a container filled with the ink composition according to any one of claims 1 to 19 or the ink composition contained in the ink set according to claim 20.
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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005015672A (en) * 2003-06-27 2005-01-20 Toyo Ink Mfg Co Ltd Nonaqueous inkjet ink for polyvinyl chloride resin sheet
JP2006045450A (en) * 2004-08-09 2006-02-16 Konica Minolta Holdings Inc Inkjet ink and method for inkjet recording
JP2008216866A (en) * 2007-03-07 2008-09-18 Seiko Epson Corp Composition for forming liquid crystal alignment layer and method for manufacturing liquid crystal display device
JP2012224658A (en) * 2011-04-15 2012-11-15 Konica Minolta Ij Technologies Inc Inkjet ink and inkjet recording method
JP2013091711A (en) * 2011-10-25 2013-05-16 Konica Minolta Ij Technologies Inc Functional inkjet ink and method for forming functional coating film
JP2014185207A (en) * 2013-03-22 2014-10-02 Seiko Epson Corp Nonaqueous ink composition for inkjet recording and inkjet recording method
WO2021201149A1 (en) * 2020-03-31 2021-10-07 株式会社Ｄｎｐファインケミカル Non-aqueous ink composition, inkjet recording method, and method for manufacturing printed matter
JP2021187095A (en) * 2020-06-02 2021-12-13 セイコーエプソン株式会社 White ink composition and recording method

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005015672A (en) * 2003-06-27 2005-01-20 Toyo Ink Mfg Co Ltd Nonaqueous inkjet ink for polyvinyl chloride resin sheet
JP2006045450A (en) * 2004-08-09 2006-02-16 Konica Minolta Holdings Inc Inkjet ink and method for inkjet recording
JP2008216866A (en) * 2007-03-07 2008-09-18 Seiko Epson Corp Composition for forming liquid crystal alignment layer and method for manufacturing liquid crystal display device
JP2012224658A (en) * 2011-04-15 2012-11-15 Konica Minolta Ij Technologies Inc Inkjet ink and inkjet recording method
JP2013091711A (en) * 2011-10-25 2013-05-16 Konica Minolta Ij Technologies Inc Functional inkjet ink and method for forming functional coating film
JP2014185207A (en) * 2013-03-22 2014-10-02 Seiko Epson Corp Nonaqueous ink composition for inkjet recording and inkjet recording method
WO2021201149A1 (en) * 2020-03-31 2021-10-07 株式会社Ｄｎｐファインケミカル Non-aqueous ink composition, inkjet recording method, and method for manufacturing printed matter
JP2021187095A (en) * 2020-06-02 2021-12-13 セイコーエプソン株式会社 White ink composition and recording method

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