Patent Application
20230312956
The present invention relates to an aqueous pigment dispersion.
In the related art, a method of dispersing a pigment in an aqueous medium in the field of inkjet includes a method using a surfactant, a method of modifying the pigment surface with a hydrophilic group, a method of dispersing a pigment with a hydrophilic resin, and the like.
Among these methods, examination of the method of dispersing a pigment with a hydrophilic resin has been promoted because high dispersion stability is obtained and the aqueous pigment dispersion can have rub resistance. Examples thereof include an aqueous pigment dispersion prepared by dispersing a pigment with a polyurethane resin having an anionic group (Patent Literature 1).
Furthermore, use of pigment printing in the inkjet field allowing printing by Drop On Demand has been expected in recent years. In pigment printing, printing is performed on fabrics pre-treated with an inorganic metal salt, a cationic resin or the like to ensure the practically minimal color developability (image density) of images, while sufficient color developability cannot be demonstrated in fabrics not pre-treated, leading to limitations to fabrics which can be used.
The pigment dispersion prepared according to Patent Literature 1 demonstrates excellent image density when the recording medium is paper, while the color developability of printed materials is still insufficient.
Patent Literature 1: JP 2017-114991 A
An object of the present invention is to provide an aqueous pigment dispersion having high initial dispersion stability and high storage stability and demonstrating high color developability in particularly fabrics not pre-treated.
The present inventors, who have conducted extensive research, have achieved the present invention. Specifically, the present invention is an aqueous pigment dispersion for an aqueous inkjet ink, including a pigment and an aqueous medium, the pigment being dispersed with a polyurethane resin prepared by reacting an active hydrogen atom-containing component (A) with an organic polyisocyanate component (B), the active hydrogen atom-containing component (A) containing a quaternary ammonium compound (a1), the quaternary ammonium compound (a1) being contained in a weight proportion of 12% by weight or more relative to the total weight of the active hydrogen atom-containing component (A) and the organic polyisocyanate component (B).
The present invention can provide an aqueous pigment dispersion having high initial dispersion stability and high storage stability and demonstrating high color developability in particularly fabrics not pre-treated.
The aqueous pigment dispersion according to the present invention is an aqueous pigment dispersion for an aqueous inkjet ink, including a pigment and an aqueous medium, the pigment being dispersed with a polyurethane resin prepared by reacting an active hydrogen atom-containing component (A) with an organic polyisocyanate component (B).
The active hydrogen atom-containing component (A) contains a quaternary ammonium compound (a1), and the quaternary ammonium compound (a1) is contained in a weight proportion of 12% by weight or more relative to the total weight of the active hydrogen atom-containing component (A) and the organic polyisocyanate component (B).
In the polyurethane resin used in the aqueous pigment dispersion according to the present invention, the active hydrogen atom-containing component (A) contains the quaternary ammonium compound (a1). If the quaternary ammonium compound (a1) is contained, aqueous pigment dispersion particles are localized on the surface of an absorptive substrate such as a fabric due to ionic interaction to improve the frequency of presence of the pigment, resulting in an improvement in color developability (=image density).
The quaternary ammonium compound is ionized by an alkyl group covalently bonded to a nitrogen atom, and thus is electrolytically dissociated even after its counter ion is lost. In other words, the aqueous pigment dispersion according to the present invention is stably dispersed even in environments having a pH of 7 or more, and can be established as an inkjet ink.
The quaternary ammonium compound (a1) is a polyatomic ion represented by NR4+ having a positive charge, and can be any compound as long as it contains an active hydrogen atom. Examples thereof include reaction products of an active hydrogen atom-containing component having a tertiary amino group with a quaternarizing agent (a1-2).
Examples of the active hydrogen atom-containing component having a tertiary amino group include tertiary amino group-containing polyols (a1-1), tertiary amino group-containing polycarboxylic acids, tertiary amino group-containing polyamines, tertiary amino group-containing polyamides, tertiary amino group-containing polyurethane compounds, and tertiary amino group-containing polyurea compounds.
Examples of the tertiary amino group-containing polyols (a1-1) include compounds represented by the following Formula (3) and/or Formula (4):
wherein R8 is an alkyl group having 1 to 24 carbon atoms, and R9 and R10 are each independently an alkylene group having 1 to 20 carbon atoms or an oxyalkylene group having 2 to 20 carbon atoms.
wherein R11 and R12 are each independently an alkyl group having 1 to 4 carbon atoms.
Among the tertiary amino group-containing polyols (a1-1), examples of the compound represented by Formula (3) include N-alkyl dialcohol amines, and polyoxyalkylene alkylamine.
In the present invention, “alkyl” encompasses linear and branched alkyl groups. Preferred are linear or branched alkyl groups having 1 to 24 carbon atoms, more preferred are linear or branched alkyl groups having 1 to 12 carbon atoms, and still more preferred are linear or branched alkyl groups having 1 to 4 carbon atoms. In particular, examples of alkyl groups include methyl, ethyl, propyl, isopropyl, n-butyl, 2-(iso-)butyl, secondary (sec-)butyl, tertiary (tert-)butyl, n-pentyl, 2-pentyl, 2-methylbutyl, 3-methylbutyl, 1,2-dimethylpropyl, 1,1-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 2-hexyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethylbutyl, 2-ethylbutyl, 1-ethyl-2-methylpropyl, n-heptyl, 2-heptyl, 3-heptyl, 2-ethylpentyl, 1-propylbutyl, n-octyl, 2-ethylhexyl, 2-propylheptyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, icodecyl, and tetracosyl.
Specific examples of N-alkyl dialcohol amines and polyoxyalkylene alkylamines include N-methyldiethanolamine, N-ethyldiethanolamine, N-butyldiethanolamine, N-tert-butyldiethanolamine, N-lauryldiethanolamine, N-stearyldiethanolamine, and poly(where n=1 to 10) oxyethyleneoleylamine.
Among the tertiary amino group-containing polyols (a1-1), examples of the compound represented by Formula (4) include 3-(diethylamine)-1,2-propanediol.
Examples of the tertiary amino group-containing polycarboxylic acids include, but is not limited to, products terminated with a carboxylic acid group, which are prepared through esterification of the tertiary amino group-containing polyols (a1-1) described above and a polycarboxylic acid. Specifically, examples thereof include products terminated with a carboxylic acid group, which are prepared through dehydration condensation of the N-alkyl dialcohol amines and an aliphatic or aromatic dicarboxylic acid in the molar ratio of functional groups of 1:2. Examples thereof include a reaction product of N-methyldiethanolamine and succinic acid, and a reaction product of N-methyldiethanolamine and terephthalic acid.
Examples of the tertiary amino group-containing polyamines include, but is not limited to, products terminated with an amino group, which are prepared through amidation of the tertiary amino group-containing polycarboxylic acids described above and a polyamine; products terminated with an amino group, which are prepared by urethanizing the tertiary amino group-containing polyols (a1-1) described above and an organic polyisocyanate to prepare isocyanate-terminated products and further adding water to the isocyanate-terminated products; and products terminated with an amino group, which are prepared by further adding a polyamine to the isocyanate-terminated products or the like. Specifically, examples thereof include products terminated with an amino group, which are prepared through dehydration condensation of the N-alkyl dialcohol amines and an aliphatic or aromatic dicarboxylic acid in a molar ratio of functional groups (hydroxyl group:carboxylic acid group) of 1:2 to prepare products terminated with a carboxylic acid group, which are then subjected to dehydration condensation with a polyamine in a molar ratio of functional groups (carboxylic acid group:amino group) of 1:2. Examples thereof also include reaction products, which are prepared by urethanizing the N-alkyl dialcohol amines and an aliphatic or alicyclic or aromatic diisocyanate in a molar ratio of functional groups (hydroxyl group:isocyanate group) of 1:2 and by converting the terminals of the resulting isocyanate-terminated products into an amino group with water; and products terminated with an amino group, which are prepared through dehydration condensation of the isocyanate-terminated products and a polyamine in a molar ratio of functional groups (isocyanate group:amino group) of 1:2. More specifically, examples thereof include products terminated with an amino group, which are prepared through dehydration condensation of N-methyldiethanolamine, succinic acid, and isophoronediamine; products terminated with an amino group, which are prepared through a reaction of N-methyldiethanolamine with isophorone diisocyanate and water; and products terminated with an amino group, which are prepared through a reaction of N-methyldiethanolamine with isophorone diisocyanate and isophoronediamine.
Examples of the tertiary amino group-containing polyamides include, but is not limited to, products terminated with an amide group, which are prepared through a reaction of the tertiary amino group-containing polycarboxylic acids described above with ammonia. Specifically, examples thereof include products terminated with an amide group, which are prepared through dehydration condensation of the N-alkyl dialcohol amines and an aliphatic or aromatic dicarboxylic acid in a molar ratio of functional groups (hydroxyl group:carboxylic acid group) of 1:2, followed by dehydration condensation of the resulting products terminated with a carboxylic acid group and ammonia in a molar ratio of functional groups (carboxylic acid group:ammonia) of 1:1. Specifically, examples thereof include reaction products terminated with an amide group, which are prepared by adding ammonia to a reaction product of N-methyldiethanolamine with succinic acid, followed by dehydration condensation.
Examples of the reaction of the tertiary amino group-containing polycarboxylic acid with ammonia include [1] and [2] below:
Examples of the tertiary amino group-containing polyurethane compounds include, but is not limited to, products prepared through urethanization of the tertiary amino group-containing polyols (a1-1) described above and an organic monoisocyanate in a molar ratio of a hydroxyl group to an isocyanate group of 1:1. Specifically, examples thereof include urethane group-containing products prepared through a reaction of an N-alkyl dialcohol amine with an aliphatic or alicyclic or aromatic monoisocyanate in a molar ratio of functional groups of 1:1. More specifically, examples thereof include reaction products of the N-methyldiethanolamines with phenyl isocyanate.
Examples of the tertiary amino group-containing polyurea compounds include, but is not limited to, urea group-containing products, which are prepared by urethanizing the tertiary amino group-containing polyols (a1-1) and organic polyisocyanate and adding ammonia or an organic monoamine to the resulting isocyanate-terminated products. Specifically, examples thereof include urea group-containing products, which are prepared by urethanizing an N-alkyl dialcohol amine and an aliphatic, alicyclic, or aromatic diisocyanate in a molar ratio of functional groups (hydroxyl group:isocyanate group) of 1:2 and reacting ammonia or monoamine to the resulting product terminated with an isocyanate group in a molar ratio of functional groups (isocyanate group:ammonia or amino group) of 1:1. More specifically, examples thereof include products prepared by reacting N-methyldiethanolamine with isophorone diisocyanate and reacting piperidine with the resulting product terminated with an isocyanate group.
Examples of the quaternarizing agent (a1-2) include halogenated alkyl compounds, dialkyl sulfate compounds, and trialkyl phosphate compounds. Specific examples thereof include ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate. Among these, preferred are dimethyl sulfate and diethyl sulfate from the viewpoint of the reaction rate.
The quaternary ammonium compound (a1) according to the present invention is preferably a compound represented by the following Formula (1) and/or Formula (2):
wherein R1 and R2 are each independently an alkyl group having 1 to 24 carbon atoms, R3 and R4 are each independently an alkylene group having 1 to 20 carbon atoms or an oxyalkylene group having 2 to 20 carbon atoms, and X− is an anion.
wherein R5 to R7 are each independently an alkyl group having 1 to 4 carbon atoms, and X− is an anion.
The quaternary ammonium compound (a1) according to the present invention is preferably a product prepared by reacting a tertiary amino group-containing polyol (a1-1) represented by Formula (3) and/or Formula (4) with a quaternarizing agent (a1-2) in a molar ratio of the compounds of 1:1.
Specific examples of the quaternary ammonium compound (a1) represented by Formula (1) include reaction products of N-methyldiethanolamine with any one of ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate; reaction products of N-ethyldiethanolamine with any one of ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate; reaction products of N-butyldiethanolamine with any one of ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate; reaction products of N-tert-butyldiethanolamine with any one of ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate; reaction products of N-lauryldiethanolamine with any one of ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate; reaction products of N-stearyldiethanolamine with any one of ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate; reaction products of poly(n=1 to 10)oxyethyleneoleylamine with any one of ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate, and the like.
Among these, preferred are reaction products of N-methyldiethanolamine, N-ethyldiethanolamine, N-butyldiethanolamine, N-tert-butyldiethanolamine, N-lauryldiethanolamine, N-stearyldiethanolamine, and poly(n=1 to 10)oxyethyleneoleylamine with dimethyl sulfate or diethyl sulfate, more preferred are reaction products of N-methyldiethanolamine and N-ethyldiethanolamine with dimethyl sulfate or diethyl sulfate, and still more preferred are reaction products of N-methyldiethanolamine with dimethyl sulfate from the viewpoint of the nitrogen atom content relative to the weight of the quaternary ammonium compound (a1) (the viewpoint of hydrophilicity).
The anion in the quaternary ammonium compound (a1) (anion X− in Formulae (1) and (2)) is an anion derived from the quaternarizing agent (a1-2). Examples of the anion include bromide ion (Br−), iodide ion (I−), methyl sulfate ion (CH3OSO3−), ethyl sulfate ion (C2H5OSO3−), propyl sulfate ion (C3H7OSO3−), butyl sulfate ion (C4H9OSO3−), and dimethyl phosphate ion ((CH3O)2PO2−).
Specific examples of the quaternary ammonium compound (a1) represented by Formula (2) include reaction products of 3-(diethylamine)-1,2-propanediol with any one of ethyl bromide, ethyl iodide, dimethyl sulfate, diethyl sulfate, dipropyl sulfate, dibutyl sulfate, and trimethyl phosphate.
Among these, preferred is a reaction product of 3-(diethylamine)-1,2-propanediol with dimethyl sulfate or diethyl sulfate from the viewpoint of the nitrogen atom content relative to the weight of the quaternary ammonium compound (a1) (the viewpoint of hydrophilicity).
According to one aspect, the weight proportion of the quaternary ammonium compound (a1) in the polyurethane resin according to the present invention is 12% by weight or more, preferably 12 to 60% by weight, more preferably 12 to 50% by weight, still more preferably 12 to 42% by weight relative to the total weight of the active hydrogen atom-containing component (A) and the organic polyisocyanate component (B). A weight proportion of the quaternary ammonium compound (a1) of less than 12% by weight results in coarse aqueous pigment dispersion particles, which reduces initial dispersibility.
The active hydrogen atom-containing component (A) may contain a polyol other than the quaternary ammonium compound (a1). Examples of polyols other than the quaternary ammonium compound (a1) include polycarbonate polyols, polyester polyols, polyether polyols, and low molecular weight polyols. The polyol other than the quaternary ammonium compound (a1) preferably includes at least one of polycarbonate polyols, polyester polyols, or polyether polyols, and is more preferably polycarbonate polyol. Particularly preferably, the polycarbonate polyol is a crystalline polycarbonate polyol.
Examples of polycarbonate polyols include polycarbonate polyols prepared by condensing a low molecular weight dihydric alcohol having a number average molecular weight (Mn) of less than 300 and a low molecular carbonate compound (such as a dialkyl carbonate having alkyl groups having 1 to 10 carbon atoms, an alkylene carbonate having an alkylene group having 2 to 6 carbon atoms, or a diaryl carbonate having an aryl group having 6 to 9 carbon atoms) while performing dealcohlation. These low molecular weight dihydric alcohols and these low molecular carbonate compounds each may be used alone or in combination. The low molecular weight dihydric alcohols described above may contain tri- or higher hydric alcohols.
Specific examples of polycarbonate polyols include aliphatic polycarbonate polyols such as polyhexamethylene carbonate diol, polydecamethylene carbonate diol, polypentamethylene carbonate diol, 3-methyl-5-pentane-carbonate diol, polytetramethylene carbonate diol, and poly(tetramethylene/hexamethylene) carbonate diol (such as diols prepared by condensing 1,4-butanediol and 1,6-hexanediol with a dialkyl carbonate while performing dealcohlation). Examples of alicyclic polycarbonate polyols include polycyclohexamethylene carbonate diol, and polynorbornene carbonate diol. Examples of aromatic polycarbonate polyols include poly-1,4-xylylene carbonate diol, bisphenol A-type polycarbonate diol, and bisphenol F-type polycarbonate diol.
Examples of commercial products of polycarbonate polyols include ETERNACOLL UH-200 [polyhexamethylene carbonate diol having an Mn of 2,000, available from UBE Corporation], ETERNACOLL UH-100 [polyhexamethylene carbonate diol having an Mn of 1,000, available from UBE Corporation], ETERNACOLL UC-100 [polycyclohexamethylene carbonate diol having an Mn of 1,000, available from UBE Corporation], BENEBiOL NL2010DB [polydecamethylene carbonate diol having an Mn of 2,000, available from Mitsubishi Chemical Corporation], DURANOL T5651 [polypentamethylene, hexamethylene carbonate diol having an Mn of 1,000, available from Asahi Kasei Chemicals Corporation], and DURANOL G4672 [polytetramethylene, hexamethylene carbonate diol having an Mn of 1,000, available from Asahi Kasei Chemicals Corporation].
According to one aspect, the polycarbonate polyol is more preferably a crystalline polycarbonate polyol.
In the present invention, the term “crystallinity” indicates that the peak top temperature of an endothermic peak is present when the transition temperature of a sample is measured using a differential scanning calorimeter (DSC) by the method according to JIS K7121.
The measurement conditions for the peak top temperature of the endothermic peak are shown below.
The peak top temperature is measured using a differential scanning calorimeter (e.g., Q2000 available from TA Instruments-Waters LLC). The sample is heated from 20° C. to 150° C. at 10° C./min in a first heating operation, and then is cooled from 150° C. to 0° C. at 10° C./min, and subsequently is heated from 0° C. to 150° C. at 10° C./min in a second heating operation. The temperature indicating the top of the endothermic peak in the second heating operation is defined as peak top temperature of the endothermic peak.
If the polyurethane resin contains a polyol component containing a crystalline polycarbonate polyol in its constitutional monomer (constitutional unit), the mechanical strength thereof can be improved, and thus the rub resistance thereof can be improved.
Examples of the crystalline polycarbonate polyol include polycarbonate polyols prepared by condensing a saturated low molecular weight aliphatic or alicyclic dihydric alcohol and a low molecular carbonate compound (such as a dialkyl carbonate having an alkyl group having 1 to 10 carbon atoms, an alkylene carbonate having an alkylene group having 2 to 6 carbon atoms, and a diaryl carbonate having an aryl group having 6 to 9 carbon atoms) while performing dealcohlation. Although these low molecular weight dihydric alcohols may be used in combination and these low molecular carbonate compounds may be used in combination, the content of a single alcohol raw material is preferably 70 to 100% by weight, more preferably 100% by weight from the viewpoint of crystallinity.
Specific examples of the crystalline polycarbonate polyol include polyhexamethylene carbonate diol, polydecamethylene carbonate diol, and polycyclohexamethylene carbonate diol.
Examples of polyester polyols include condensed polyester polyols, polylactone polyols, and castor oil-based polyols.
The condensed polyester polyol is a polyester polyol of a low molecular weight dihydric alcohol having a number average molecular weight (Mn) of less than 300 and a dicarboxylic acid having 2 to 10 carbon atoms or an ester formable derivative thereof.
Examples of usable low molecular weight dihydric alcohols include divalent aliphatic dihydric alcohols having an Mn of less than 300 and low mole adducts of alkylene oxides (hereinafter, abbreviated to AO in some cases) of divalent phenols having an Mn of less than 300.
Examples of the AO include ethylene oxides (hereinafter, abbreviated to EOs in some cases), propylene oxides (hereinafter, abbreviated to POs in some cases), and 1,2-, 1,3-, 2,3-, or 1,4-butylene oxides.
Among these low molecular weight dihydric alcohols which can be used for the condensed polyester polyol, preferred are ethylene glycol, propylene glycol, 1,4-butanediol, neopentyl glycol, 1,6-hexane glycol, 1,9-nonanediol, 1,10-decanediol, EO or PO low mole adducts of bisphenol A, and combinations thereof.
A tri- or higher hydric alcohol and a tri- or higher valent carboxylic acid or an ester formable derivative thereof may be contained as the constitutional components for forming the condensed polyester polyol.
Examples of the dicarboxylic acids having 2 to 10 carbon atoms or ester formable derivatives thereof which can be used in the condensed polyester polyols include aliphatic dicarboxylic acids (such as succinic acid, adipic acid, azelaic acid, sebacic acid, dodecanedioic acid, fumaric acid, and maleic acid), alicyclic dicarboxylic acids (such as dimer acid), aromatic dicarboxylic acids (such as terephthalic acid, isophthalic acid, and phthalic acid), anhydrides thereof (such as succinic anhydride, maleic anhydride, and phthalic anhydride), acid halides thereof (such as adipic acid dichloride), low molecular weight alkyl esters thereof (such as dimethyl succinate and dimethyl phthalate), and combinations thereof. Examples of the tri- or higher valent polycarboxylic acids include trimellitic acid, and pyromellitic acid.
Specific examples of the condensed polyester polyol include polyethylene adipate diol, polybutylene adipate diol, polyhexamethylene adipate diol, polyhexamethylene isophthalate diol, polyhexamethylene terephthalate diol, polyneopentyl adipate diol, polyethylene propylene adipate diol, polyethylene butylene adipate diol, polybutylene hexamethylene adipate diol, polydiethylene adipate diol, poly(polytetramethylene ether)adipate diol, poly(3-methylpentylene adipate) diol, polyethylene azelate diol, polyethylene sebacate diol, polybutylene azelate diol, polybutylene sebacate diol, and polyneopentyl terephthalate diol.
Examples of commercial products of the condensed polyester polyols include SANESTER 2610 [polyethylene adipate diol having an Mn of 1,000, available from Sanyo Chemical Industries, Ltd.], SANESTER 4620 [polytetramethylene adipate diol having an Mn of 2,000, available from Sanyo Chemical Industries, Ltd.], SANESTER 2620 [polyethylene adipate diol having an Mn of 2,000, available from Sanyo Chemical Industries, Ltd.], Kuraray Polyol P-2010 [poly-3-methyl-1,5-pentane adipate diol having an Mn of 2,000], Kuraray Polyol P-3010 [poly-3-methyl-1,5-pentane adipate diol having an Mn of 3,000], Kuraray Polyol P-6010 [poly-3-methyl-1,5-pentane adipate diol having an Mn of 6,000], Kuraray Polyol P-2020 [poly-3-methyl-1,5-pentane terephthalate diol having an Mn of 2,000], and Kuraray Polyol P-2030 [poly-3-methyl-1,5-pentane isophthalate diol having an Mn of 2,000].
Examples of the polylactone polyols include polylactonediol, polycaprolactonediol, polyvalerolactonediol, and polycaprolactone triol.
The polylactonediol is a polyadded product of a lactone added to the low molecular weight dihydric alcohols described above, and examples of lactones include lactones having 4 to 12 carbon atoms (such as γ-butyrolactone, γ-valerolactone, and ε-caprolactone).
Examples of the castor oil-based polyols include castor oil, and modified castor oils modified with a polyol or an AO. The modified castor oil can be prepared through ester exchange between castor oil and a polyol and/or AO addition. Examples of the castor oil-based polyols include castor oil, trimethylolpropane-modified castor oil, pentaerythritol-modified castor oil, and EO (4 to 30 mol) adducts of castor oil.
Examples of the polyether polyols include aliphatic polyether polyols and aromatic ring-containing polyether polyols.
Examples of the aliphatic polyether polyols include polyoxyethylene polyols [such as polyethylene glycol (hereinafter, abbreviated to PEG)], polyoxypropylene polyols [such as polypropylene glycol], polyoxyethylene/propylene polyol, and polytetramethylene ether glycol.
Examples of commercial products of the aliphatic polyether polyols include SANNIX PP-600 [polyoxypropylene glycol having an Mn of 600, available from Sanyo Chemical Industries, Ltd.], PTMG1000 [polytetramethylene ether glycol having an Mn of 1,000, available from Mitsubishi Chemical Corporation], PTMG2000 [polytetramethylene ether glycol having an Mn of 2,000, available from Mitsubishi Chemical Corporation], PTMG3000 [polytetramethylene ether glycol having an Mn of 3,000, available from Mitsubishi Chemical Corporation], PTGL3000 [modified PTMG having an Mn of 3,000, available from HODOGAYA CHEMICAL CO., LTD.], and SANNIX GP-3000 [polypropylene ether triol having an Mn of 3,000, available from Sanyo Chemical Industries, Ltd.].
Examples of the aromatic ring-containing polyether polyols include polyols having a bisphenol structure such as EO adducts of bisphenol A [such as EO 2 mol adduct of bisphenol A, EO 4 mol adduct of bisphenol A, EO 6 mol adduct of bisphenol A, EO 8 mol adduct of bisphenol A, EO 10 mol adduct of bisphenol A, and EO 20 mol adduct of bisphenol A] and PO adducts of bisphenol A [such as PO 2 mol adduct of bisphenol A, PO 3 mol adduct of bisphenol A, and PO 5 mol adduct of bisphenol A]; and EO or PO adducts of resorcin.
Examples of the low molecular weight polyols include the aliphatic diols having 2 to 20 carbon atoms described above. Preferred are diols having 4 to 10 carbon atoms and a branched structure, more preferred are 3-methyl-1,5-pentanediol and neopentyl glycol, and still more preferred is 3-methyl-1,5-pentanediol. Use of a low molecular weight polyol having a branched structure is preferred because the aggregation force between hard segments (urethane bond moieties) in the polyurethane resin is reduced, improving solvent solubility and coating flexibility and enhancing initial dispersibility (particularly reducing the particle size). When the active hydrogen atom-containing component (A) contains a low molecular weight polyol, the low molecular weight polyol is contained in an amount of preferably 0.1 to 4.5% by weight, more preferably 0.3 to 2% by weight relative to the total weight of the active hydrogen atom-containing component (A) and the organic polyisocyanate component (B).
Among these polyols other than the quaternary ammonium compound (a1) described above, the active hydrogen atom-containing component (A) preferably includes at least one selected from the group consisting of polycarbonate polyols, polyester polyols, and polyether polyols, and is more preferably a polycarbonate polyol. Particularly preferably, the polycarbonate polyol is a crystalline polycarbonate polyol.
Examples of the organic polyisocyanate component (B) used in the polyurethane resin include aliphatic polyisocyanates having two or more isocyanate groups and having 2 to 18 carbon atoms (excluding carbons in the isocyanate groups; the same is applied to below), alicyclic polyisocyanates having 4 to 15 carbon atoms, aromatic polyisocyanates having 6 to 20 carbon atoms, aromatic aliphatic polyisocyanates having 8 to 15 carbon atoms, and derivatives of these polyisocyanates (such as isocyanurated products).
These polyisocyanate components may be used alone or in combination.
Examples of the aliphatic polyisocyanates having 2 to 18 carbon atoms include ethylene diisocyanate, tetramethylene diisocyanate, hexamethylene diisocyanate (HDI), dodecamethylene diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, lysine diisocyanate, and 2-isocyanatoethyl 2,6-diisocyanatohexanoate.
Examples of the alicyclic polyisocyanates having 4 to 15 carbon atoms include isophorone diisocyanate (IPDI), dicyclohexylmethane 4,4-diisocyanate (hydrogenated MDI), cyclohexylene diisocyanate, methylcyclohexylene diisocyanate (hydrogenated TDI), bis(2-isocyanatoethyl)-4-cyclohexene-1,2-dicarboxylate, and 2,5- or 2,6-norbornane diisocyanate.
Examples of the aromatic polyisocyanates having 6 to 20 carbon atoms include 1,3- or 1,4-phenylene diisocyanate, 2,4- or 2,6-tolylene diisocyanate (TDI), 4,4′- or 2,4′-diphenylmethane diisocyanate (MDI), 1,5-naphthylene diisocyanate, 4,4′,4″-triphenylmethane triisocyanate, m- or p-isocyanatophenyl sulfonyl isocyanate, and crude MDIs.
Examples of the aromatic aliphatic polyisocyanates having 8 to 15 carbon atoms include m- or p-xylylene diisocyanate (XDI) and α,α,α′,α′-tetramethylxylylene diisocyanate (TMXDI).
From the viewpoint of the initial dispersibility of the aqueous pigment dispersion and mechanical strength of the polyurethane resin, as the organic polyisocyanate component (B), preferred are aromatic polyisocyanates having 6 to 20 carbon atoms and alicyclic polyisocyanates having 4 to 15 carbon atoms, and more preferred are TDI, IPDI, and hydrogenated MDI.
From the viewpoint of a uniform composition distribution of the polyurethane resin and the mechanical strength thereof, the equivalent ratio (NCO/OH) of the isocyanate group contained in the organic polyisocyanate component (B) to the hydroxyl group contained in the active hydrogen atom-containing component (A) is preferably 1.2 to 1.8, more preferably 1.3 to 1.6.
While the active hydrogen atom-containing component (A) described above and the organic polyisocyanate component (B) are essential components of the constitutional monomer (constitutional unit) of the polyurethane resin, the components for forming the constitutional monomer may include a compound other than the active hydrogen atom-containing component (A) and the organic polyisocyanate component (B). Examples of the compound other than the active hydrogen atom-containing component (A) and the organic polyisocyanate component (B) contained in the constitutional monomer include chain extenders, and reaction terminators. These may be used alone or in combination. According to one aspect, the polyurethane resin is preferably a reaction product of a urethane prepolymer with a chain extender, the urethane prepolymer being terminated with an isocyanate group formed by reacting the active hydrogen atom-containing component (A) described above with the organic polyisocyanate component (B).
A chain extender is preferably used in the polyurethane resin. Examples of chain extenders include water, diamines having 2 to 10 carbon atoms (such as ethylenediamine, propylenediamine, hexamethylenediamine, isophoronediamine, toluenediamine, and piperazine), polyalkylene polyamines having 2 to 10 carbon atoms (such as diethylenetriamine, triethylenetetramine, and tetraethylenepentamine), hydrazine or derivatives thereof (dibasic acid dihydrazides such as adipic acid dihydrazide), polyepoxy compounds having 2 to 30 carbon atoms (such as 1,6-hexanediol diglycidyl ether and trimethylolpropane polyglycidyl ether), and amino alcohols having 2 to 10 carbon atoms (such as ethanolamine, diethanolamine, 2-amino-2-methylpropanol, and triethanolamine). As the chain extender, preferred are diamines having 2 to 10 carbon atoms, more preferred are secondary diamines, and still more preferred is isophoronediamine. If the polyurethane resin contains the above-mentioned compound in the constitutional monomer, the aggregation force of the urethane group moiety is increased to reduce the degree of swelling to water. Thus, high wet rubbing fastness is demonstrated. Use of diamines is preferred because generation of carbon dioxide gas is suppressed by extension reaction by amine and the amount of amine carbonate salts generated is reduced to enhance storage stability.
The amount of the chain extender to be used is in the range such that the equivalent ratio of the active hydrogen-containing group in the chain extender to the terminal isocyanate group in the urethane prepolymer is preferably 0.2 to 2, more preferably 0.5 to 1.5.
A reaction terminator can be used in the polyurethane resin as needed. Examples of the reaction terminator include monoalcohols having 1 to 8 carbon atoms (such as methanol, ethanol, isopropanol, cellosolve, and carbitols), and monoamines having 1 to 10 carbon atoms (such as mono- or dialkylamine such as monomethylamine, monoethylamine, monobutylamine, dibutylamine, and monooctylamine; and mono- or dialkanolamines such as monoethanolamine, diethanolamine, and diisopropanolamine).
The polyurethane resin according to the present invention can be prepared by any method, and examples thereof include the methods [1] to [4] below.
The polyurethane resins prepared by the methods [1] to [4] above can be used in preparation of the aqueous pigment dispersion. Among these, more preferred are methods [1] to [3] from the viewpoint of the storage stability of the aqueous pigment dispersion.
Examples of the hydrophilic solvent used in preparation of the polyurethane resin by the method [4] described above include those substantially unreactive with the isocyanate group (ketones such as acetone and ethyl methyl ketone, esters, ethers, amides, and alcohols). Among these, preferred is tetrahydrofuran. The aqueous medium may be water alone, and a mixed solution of water and a hydrophilic solvent can also be used. The weight ratio of the hydrophilic solvent to water (hydrophilic solvent/water) is preferably 0/100 to 50/50, more preferably 35/65 to 45/55.
If the hydrophilic solvent is used, the hydrophilic solvent may be distilled off, as needed, after the polyurethane resin is prepared.
The polyurethane resin is synthesized by a reaction at preferably 20° C. to 150° C., more preferably 60° C. to 110° C., and the reaction time is preferably 2 to 20 hours.
The polyurethane resin can be synthesized in the presence or absence of an organic solvent substantially non-reactive with the isocyanate group. The polyurethane resin terminated with an isocyanate group usually contains 0.5 to 10% of free isocyanate group. Examples of the organic solvent substantially unreactive with the isocyanate group include the hydrophilic solvents listed above. Preferred is tetrahydrofuran.
In preparation of the polyurethane resin, a catalyst usually used in a urethane reaction may be used to accelerate the reaction as needed. Examples of the catalyst include amine catalysts, such as triethylamine, N-ethylmorpholine, triethylenediamine, and cycloamidines described in the specification of U.S. Pat. No. 4,524,104 [such as 1,8-diaza-bicyclo(5,4,0)undecene-7 (available from San-Apro Ltd., DBU)]; tin-based catalysts, such as dibutyltin dilaurate, dioctyltin dilaurate, and tin octylate; and titanium-based catalysts, such as tetrabutyl titanate.
The content of the isocyanate group in the polyurethane resin can be measured by the method specified in JIS K1603-1. In Examples described in this specification, the content (NCO % by weight) of the isocyanate group in the solvent solution was used.
The urea group is contained in a proportion of preferably 0.01 to 0.2% by weight, more preferably 0.05 to 0.1% by weight of the weight of the polyurethane resin. The urea group contained in a proportion of 0.01 to 0.2% by weight (preferably 0.05 to 0.1% by weight) of the weight of the polyurethane resin is preferred because the polyurethane resin contains the urea group in an appropriate amount, leading to compatibility between mechanical strength of the polyurethane resin and the viscosity of the aqueous dispersion.
Examples of the pigment in the present invention include organic and inorganic pigments known in the related art or the like (such as white pigments, black pigments, gray pigments, red pigments, brown pigments, yellow pigments, green pigments, blue pigments, violet pigments, metallic pigments, natural organic pigments, synthetic organic pigments, nitroso pigments, nitro pigments, pigment dye-type azo pigments, azo lakes made from water-soluble dyes, azo lakes made from poorly soluble dyes, lakes made from basic dyes, lakes made from acidic dyes, xanthan lakes, anthraquinone lakes, pigments made from vat dyes, phthalocyanine pigments, and organic pigments such as daylight fluorescent pigments).
Specific examples of the organic and inorganic pigments are listed below.
Examples of white pigments include inorganic pigments such as titanium oxide, zinc oxide, zinc sulfide, antimony oxide, and zirconium oxide. Other than the inorganic pigment, hollow resin fine particles and polymer fine particles can also be used.
The pigment preferably has an average particle size of 200 to 300 nm. If the pigment has an average particle size of less than 200 nm, the hiding power tends to be insufficient. If the pigment has an average particle size of more than 300 nm, the ejection stability tends to be insufficient.
Among these, preferred is use of titanium oxide from the viewpoint of the hiding power. Preferably, titanium oxide also has an average particle size of 200 to 300 nm.
Examples of magenta pigments include, but is not limited to, C.I. Pigment Red 2, C.I. Pigment Red 3, C.I. Pigment Red 5, C.I. Pigment Red 6, C.I. Pigment Red 7, C.I. Pigment Red 15, C.I. Pigment Red 16, C.I. Pigment Red 48:1, C.I. Pigment Red 53:1, C.I. Pigment Red 57:1, C.I. Pigment Red 122, C.I. Pigment Red 123, C.I. Pigment Red 139, C.I. Pigment Red 144, C.I. Pigment Red 149, C.I. Pigment Red 166, C.I. Pigment Red 177, C.I. Pigment Red 178, and C.I. Pigment Red 222.
Examples of yellow pigments include, but is not limited to, C.I. Pigment orange 31, C.I. Pigment orange 43, C.I. Pigment Yellow 12, C.I. Pigment Yellow 13, C.I. Pigment Yellow 14, C.I. Pigment Yellow 15, C.I. Pigment Yellow 17, C.I. Pigment Yellow 74, C.I. Pigment Yellow 93, C.I. Pigment Yellow 94, C.I. Pigment Yellow 128, C.I. Pigment Yellow 138, C.I. Pigment Yellow 155, and C.I. Pigment Yellow 180.
Examples of cyan pigments include, but is not limited to, C.I. Pigment Blue 15, C.I. Pigment Blue 15:2, C.I. Pigment Blue 15:3, C.I. Pigment Blue 15:4, C.I. Pigment Blue 16, C.I. Pigment Blue 60, and C.I. Pigment green 7.
Examples of black pigments include carbon blacks (C.I. Pigment Black 7) such as furnace black, lamp black, acetylene black, and channel black; metals such as copper and iron (C.I. Pigment Black 11); metal compounds such as titanium oxide; and organic pigments such as aniline black (C.I. Pigment Black 1).
In the present invention, the total weight of the pigment and the polyurethane resin in the aqueous pigment dispersion is preferably 10 to 40% by weight, more preferably 20 to 30% by weight from the viewpoint of storage stability.
In the aqueous pigment dispersion according to the present invention, the ratio of the pigment to the polyurethane resin (pigment:polyurethane resin) is preferably 80:20 to 20:80 from the viewpoint of initial dispersibility and rubbing fastness.
In the aqueous pigment dispersion, usually, particles containing a pigment and the polyurethane resin are dispersed in water. For the color pigment, the particle size of particles in the aqueous pigment dispersion is preferably 100 to 200 nm, more preferably 120 to 180 nm from the viewpoint of storage stability and viscosity. For the white pigment, the particle size is preferably 200 to 400 nm, more preferably 220 to 300 nm. In the present invention, the particle size indicates a cumulant average particle size. The particle size can be measured with a light scattering particle size distribution analyzer [such as “DLS-8000” available from Otsuka Electronics Co., Ltd.], and can be determined.
<Method of Preparing Aqueous Pigment Dispersion>
As the method of preparing the aqueous pigment dispersion, methods known in the related art all can be used. Examples of methods known in the related art include a surface polymerization method of adsorbing a monomer on the surface of the pigment dispersion, and polymerizing the monomer; a surface deposition method of dispersing a pigment in a resin solution, adding a poor solvent to the resin, and depositing the resin on the pigment surface; a kneading and pulverization method of melt kneading a pigment and a resin to form a masterbatch, and wet pulverizing the masterbatch into fine particles; a method of simultaneously achieving permeation of a resin solution into pigment aggregates using a high pressure fluid, pulverization by expansion energy when discharged under an atmospheric pressure, and coating; a method of wet pulverizing a pigment and a resin aqueous dispersion into fine particles, and dispersing the fine particles by mechanical energy; and a phase inversion emulsion method of wet pulverizing a resin solution having self-dispersibility to water and a pigment into fine particles, and adding water to the solvent phase of the resin solution to prepare an aqueous pigment dispersion.
Among these methods, methods suitable for preparing the aqueous pigment dispersion according to the present invention are the method of wet pulverizing a pigment and a resin aqueous dispersion into fine particles and dispersing the fine particles by mechanical energy and the phase inversion emulsion method from the viewpoint of initial dispersibility and storage stability.
The method of dispersing a pigment and a resin aqueous dispersion by mechanical energy and the phase inversion emulsion method are also preferred from the viewpoint of fastness because a polyurethane resin having self-dispersibility to form a coating adsorbs on surfaces of pigment particles or form a coating thereon, and thus, the pigment as a color material can be fixed on the substrate without adding any other binder resin to the ink.
More preferred is the phase inversion emulsion method from the viewpoint of storage stability because it provides a structure in which the pigment surface is covered with the resin. Such a structure reduces the frequency that the pigment surface is exposed to the ink, and leads to dispersed particles having no composition distribution. Moreover, the structure hardly changes.
The method of dispersing a pigment and a resin aqueous dispersion by mechanical energy and the phase inversion emulsion method are also preferred from the viewpoint of fastness because a polyurethane resin having self-dispersibility to form a coating adsorbs on surface of pigment particles or pigment particles are modified with a polyurethane resin having self-dispersibility to form a coating, and thus, the pigment as a color material can be fixed on the substrate without adding any other binder resin to the ink.
More preferred is the phase inversion emulsion method from the viewpoint of storage stability because the pigment surface is modified with a resin, thereby reducing the frequency that the pigment surface is exposed to the ink, leading to dispersed particles having no composition distribution and obstruction of change in structure.
In the aqueous pigment dispersion according to the present invention, the polyurethane resin adsorbs on or adheres to surfaces of pigment particles, which alone are hardly dispersed in the aqueous medium. Thereby, pigment particles to which the resin adheres are dispersed in the aqueous medium. It is inferred that the pigment particles to which the resin adheres are resin-coated pigment particles in which peripheries of the pigment particles are coated with the polyurethane resin.
Specific examples of the method of preparing the aqueous pigment dispersion include preparation methods [A] to [C] below.
Thereafter carboxyl groups are neutralized with a neutralizer, and the polyurethane resin is emulsion dispersed in the form of a salt in an aqueous medium.
Then, a chain extender and/or a reaction terminator is reacted with isocyanate groups in the polyurethane resin, and the hydrophilic solvent is distilled off as needed.
Thereafter carboxyl groups are neutralized with a neutralizer, and the polyurethane resin is emulsion dispersed in the form of a salt in an aqueous medium and the hydrophilic solvent is distilled off as needed.
In the production methods [A] to [C], the apparatus used in synthesis of the polyurethane resin can be used as an apparatus used in mixing and homogenizing. Examples of the dispersing machine used in mechanical disintegration include paint shakers, ball mills, sand mills, and nano mills, and specifically include Dyno-Mill (available from SHINMARU ENTERPRISES CORPORATION), and TSU-6U (available from Aimex Co., Ltd.).
In the methods [A] and [B] of preparing the aqueous pigment dispersion, any apparatus can be used for emulsion dispersion in the aqueous medium, and examples thereof include emulsifying machines of types described below:
The aqueous pigment dispersion can contain additives such as an emulsifier, a cross-linking agent, a weather stabilizer, and a smoothing agent as needed. These additives may be used alone or in combination. The amount of the additives to be used is preferably 15% by weight or less, more preferably 10% by weight or less, still more preferably 5% by weight or less based on the total weight of the pigment and the polyurethane resin.
According to one aspect, preferably, the aqueous pigment dispersion according to the present invention contains an emulsifier. The aqueous pigment dispersion according to the present invention containing an emulsifier demonstrates more favorable storage stability and dry rubbing fastness after the aqueous pigment dispersion is heated. The emulsifier is preferably added during preparation of the aqueous pigment dispersion.
When the emulsifier is used during preparation of the aqueous pigment dispersion, the emulsifier may be added at any timing in the preparation. According to one aspect, from the viewpoint of dispersibility of the pigment and stability of the aqueous dispersion, the emulsifier is preferably added before or during dispersing the pigment in the polyurethane resin. The emulsifier may be added one or both of the solvent solution of the polyurethane resin and the aqueous medium. When the emulsifier is reactive with the urethane prepolymer, it is preferably added to the aqueous medium. The amount of the emulsifier to be added is preferably 0.2 to 10% by weight, more preferably 0.3 to 6% by weight based on the weight of the pigment.
Examples of the emulsifier include nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, and other emulsion dispersants. These emulsifiers may be used alone or in combination. Among these, preferred are nonionic surfactants.
Examples of nonionic surfactants include aliphatic alcohol (8 to 24 carbon atoms) AO (2 to 8 carbon atoms) adducts (degree of polymerization=1 to 100), polyhydric alcohol (3 to 18 carbon atoms) AO (2 to 8 carbon atoms) adducts (degree of polymerization=1 to 100), (poly)oxyalkylene (2 to 8 carbon atoms, degree of polymerization=1 to 100) higher fatty acid (8 to 24 carbon atoms) esters [such as mono- or difatty acid polyethylene glycol esters such as monooleic acid polyethylene glycol esters (HLB=6 to 17), monostearic acid polyethylene glycol esters (HLB=8 to 15), distearic acid polyethylene glycol esters (HLB=8 to 14)], polyvalent (di- to deca- or higher valent) alcohol fatty acid (8 to 24 carbon atoms) esters [such as glycerol monostearate, ethylene glycol monostearate, and fatty acid sorbitan esters (sorbitan monooleate and sorbitan monolaurate)], (poly)oxyalkylene (2 to 8 carbon atoms, degree of polymerization=1 to 100) polyvalent (di- to deca- or higher valent) alcohol higher fatty acid (8 to 24 carbon atoms) esters [such as polyoxyethylene sorbitan monolaurate (HLB=10 to 16), polyoxyethylene methyl glucoside dioleate (HLB=17)], fatty acid alkanolamides [such as 1:1 type coconut oil fatty acid diethanolamide, 1:1 type lauric acid diethanolamide], (poly)oxyalkylene (2 to 8 carbon atoms, degree of polymerization=1 to 100) alkyl (1 to 22 carbon atoms) phenyl ethers, (poly)oxyalkylenes (2 to 8 carbon atoms, degree of polymerization=1 to 100) alkyl (8 to 24 carbon atoms) aminoethers, and alkyl (8 to 24 carbon atoms) dialkyl(1 to 6 carbon atoms) amine oxides [such as lauryl dimethyl amine oxide].
Among these, preferred are aliphatic alcohol (8 to 24 carbon atoms) AO (2 to 8 carbon atoms) adducts (HLB=5 to 18), polyhydric alcohol (3 to 18 carbon atoms) AO (2 to 8 carbon atoms) adducts (HLB=11 to 24), sorbitan monooleate, and mono- or difatty acid polyethylene glycol esters such as monooleic acid polyethylene glycol esters (HLB=6 to 17), monostearic acid polyethylene glycol ester (HLB=8 to 15), and distearic acid polyethylene glycol esters (HLB=8 to 14).
According to one aspect, because of high dry rubbing fastness and high stability under heating, the aqueous pigment dispersion according to the present invention preferably contains a nonionic surfactant. Preferred nonionic surfactants are aliphatic alcohol (8 to 24 carbon atoms) AO (2 to 8 carbon atoms) adducts (HLB=5 to 18), polyhydric alcohol (3 to 18 carbon atoms) AO (2 to 8 carbon atoms) adducts (HLB=11 to 24), monooleic acid sorbitan, and monooleic acid polyethylene glycol esters (HLB=6 to 17)
Examples of anionic surfactants include ether carboxylic acids having a hydrocarbon group having 8 to 24 carbon atoms or salts thereof [such as sodium lauryl ether acetate and (poly)oxyethylene (the number of moles of EO to be added: 1 to 100) sodium lauryl ether acetate]; sulfuric acid esters or ether sulfuric acid esters having a hydrocarbon group having 8 to 24 carbon atoms and salts thereof [such as sodium lauryl sulfate, sodium (poly)oxyethylene (the number of moles of EO to be added: 1 to 100) lauryl sulfate, (poly)oxyethylene (the number of moles of EO to be added: 1 to 100) lauryl sulfuric acid triethanolamine, and (poly)oxyethylene (the number of moles of EO to be added: 1 to 100) coconut oil fatty acid monoethanolamide sodium sulfate]; sulfonates having a hydrocarbon group having 8 to 24 carbon atoms [such as sodium dodecylbenzenesulfonate]; sulfosuccinic acid salts having one or two hydrocarbon groups having 8 to 24 carbon atoms; phosphoric acid esters or ether phosphoric acid esters having a hydrocarbon group having 8 to 24 carbon atoms and salts thereof [such as sodium lauryl phosphate and (poly)oxyethylene (the number of moles of EO to be added: 1 to 100) sodium lauryl ether phosphate]; fatty acid salts having a hydrocarbon group having 8 to 24 carbon atoms [such as sodium laurate and triethanolamine laurate]; and acylated amino acid salts such as hydrocarbon group having 8 to 24 carbon atoms [such as coconut oil fatty acid methyl taurine sodium, coconut oil fatty acid sarcosine sodium, coconut oil fatty acid sarcosine triethanolamine, N-coconut oil fatty acid acyl-L-glutamic acid triethanolamine, N-coconut oil fatty acid acyl-L-glutamic acid sodium, and lauroyl methyl-β-alanine sodium].
Examples of cationic surfactants include quaternary ammonium salt type cationic surfactants [such as stearyltrimethylammonium chloride, behenyltrimethylammonium chloride, distearyldimethylammonium chloride, and lanolin fatty acid aminopropyl ethyl dimethyl ammonium ethylsulfate], and amine salt type cationic surfactants [such as lactic acid salt of diethylaminoethyl stearamide, dilaurylamine hydrochloride, and oleylamine lactate].
Examples of amphoteric surfactants include betaine type amphoteric surfactants [such as coconut oil fatty acid amide propyl dimethylamino acetic acid betaine, lauryl dimethylamino acetic acid betaine, 2-alkyl-N-carboxymethyl-N-hydroxyethyl imidazolinium betaine, lauryl hydroxy sulfobetaine, and sodium lauroyl amideethyl hydroxyethyl carboxymethyl betaine hydroxypropyl phosphate], and amino acid type amphoteric surfactants [such as sodium β-lauryl aminopropionate].
Examples of other emulsion dispersants include polyvinyl alcohol, starch and derivatives thereof, cellulose derivatives such as carboxymethyl cellulose, methyl cellulose, and hydroxyethyl cellulose, carboxyl group-containing (co)polymers such as sodium polyacrylate, and emulsion dispersants having a urethane or ester group described in U.S. Pat. No. 5,906,704 [such as a compound of a polylactone polyol and a polyether polyol linked with a polyisocyanate].
When the aqueous pigment dispersion contains the emulsifier, the content is preferably 0.2 to 10% by weight, more preferably 0.3 to 6% by weight based on the weight of the polyurethane resin.
Using the prepared aqueous pigment dispersion, an inkjet ink composition having high rubbing fastness and demonstrating high color developability in particularly fabrics not pre-treated can be obtained.
Other components appropriately selected can be added to the aqueous pigment dispersion or inkjet ink according to the present invention as needed. Examples thereof include dispersants, penetrating agents, pH adjusters, water-dispersible resins, antiseptic and antifungal agents, chelate reagents, rust inhibitors, antioxidants, ultraviolet absorbing agents, oxygen absorbers, and light stabilizers.
According to one aspect, the inkjet ink contains the aqueous pigment dispersion according to the present invention, water, and optionally a water-soluble organic solvent.
According to one aspect, the blending amount of the aqueous pigment dispersion in the inkjet ink is preferably 20 to 80% by weight, more preferably 30 to 70% by weight or more, still more preferably 40 to 60% by weight or more relative to the total amount of the ink.
According to one aspect, the total weight of the pigment and the polyurethane resin in the inkjet ink is preferably 5 to 20% by weight, more preferably 10 to 15% by weight relative to the total amount of the ink from the viewpoint of storage stability.
According to one aspect, the weight of water in the inkjet ink is preferably 50 to 80% by weight, more preferably 60 to 75% by weight relative to the total amount of the ink.
When the medium for the inkjet ink is water, a water-soluble organic solvent can be contained to prevent drying of the ink or improve the dispersion stability of the pigment. Any water-soluble organic solvent can be used, and can be appropriately selected according to the purpose.
Preferably, the water-soluble organic solvent contains a water-soluble solvent (hereinafter, also referred to as “high-boiling point organic solvent”) having a normal boiling point (hereinafter, also simply referred to as “bp”) of 180° C. or more. If a high-boiling point organic solvent is contained, moisture-retaining properties of the nozzle are enhanced, and further the viscosity of the ink can be optimized.
The term “normal boiling point” indicates a boiling point at an atmospheric pressure of 0.101 MPa. High-boiling point organic solvents may be used alone or in combination.
The content of the high-boiling point organic solvent is preferably 1 to 40% by weight, more preferably 5 to 30% by weight, still more preferably 10 to 25% by weight relative to the total amount of the ink.
The water-soluble organic solvent is preferably a polyhydric alcohol. The polyhydric alcohol can be any polyhydric alcohol, which can be appropriately selected as the water-soluble organic solvent according to the purpose. Examples thereof include propylene glycol (bp of 188° C.), dipropylene glycol (bp of 232° C.), 1,5-pentanediol (bp of 242° C.), 3-methyl-1,3-butanediol (bp of 203° C.), 2-methyl-2,4-pentanediol (bp of 197° C.), ethylene glycol (bp of 196° C. to 198° C.), tripropylene glycol (bp of 267° C.), hexylene glycol (bp of 197° C.), 1,6-hexanediol (bp of 253° C. to 260° C.), 1,2-hexanediol (bp of 170° C.), 1,2,6-hexanetriol (bp of 178° C.), 1,2,3-butanetriol, 1,2,4-butanetriol (bp of 190° C. to 191° C./24 hPa), glycerol (bp of 290° C.), diglycerol (bp of 270° C./20 hPa), triethylene glycol (bp of 285° C.), tetraethylene glycol (bp of 324 to 330° C.), diethylene glycol (bp of 245° C.), 1,3-butanediol (bp of 203° C. to 204° C.), and polypropylene glycol (bp of 187° C.)
Other than the water-soluble organic solvent, a different water-soluble organic solvent or a solid wetting agent can be used in combination in the ink as needed, instead of part of these water-soluble organic solvent or in addition to these water-soluble organic solvents.
Examples of the different water-soluble organic solvent or solid wetting agent include polyhydric alcohols, polyhydric alcohol alkylethers, polyhydric alcohol aryl ethers, nitrogen-containing heterocyclic compounds, amides, amines, sulfur-containing compounds, propylene carbonate, ethylene carbonate, and other water-soluble organic solvents.
Examples of the polyhydric alcohols include polyethylene glycol (viscous liquid to solid), trimethylolethane (solid, mp of 199° C. to 201° C.), and trimethylolpropane (solid, mp of 61° C.)
Examples of the polyhydric alcohol alkylethers include ethylene glycol monoethyl ether (bp of 135° C.), ethylene glycol monobutyl ether (bp of 171° C.), diethylene glycol monomethyl ether (bp of 194° C.), diethylene glycol monobutyl ether (bp of 231° C.), ethylene glycol mono-2-ethylhexyl ether (bp of 229° C.), and propylene glycol monoethyl ether (bp of 132° C.)
The ink can contain the water-soluble organic solvent in any amount, which can be appropriately selected according to the purpose. The content is preferably 1 to 50% by weight.
The inkjet ink prepared using the aqueous pigment dispersion according to the present invention preferably contains a surfactant. If the surfactant is contained, ejection properties of the ink can be improved, and wetting and spreading properties can be improved, providing favorable image quality (color developability).
Examples of the surfactant include nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, and other emulsion dispersants. These surfactants may be used alone or in combination. Among these, preferred are nonionic surfactants. Examples of the nonionic surfactants, the anionic surfactants, the cationic surfactants, and the amphoteric surfactants are as listed above.
Preferably, the ink contains a nonionic surfactant as the surfactant. When the ink contains the nonionic surfactant, ejection properties of the ink and wetting and spreading properties can be improved, providing favorable image quality (color developability).
Preferably, as the surfactant, the ink contains an alkylether type nonionic surfactant having an HLB of 5 to 12. When the ink contains the surfactant, ejection properties of the ink and wetting and spreading properties can be improved, providing favorable image quality (color developability). In the present embodiment, the HLB indicates a value determined by a Griffin method.
The content of the surfactant is 0.01 to 10% by weight, more preferably 0.05 to 5% by weight, still more preferably 0.1 to 3% by weight relative to the total amount of the ink.
The ink prepared using the aqueous pigment dispersion according to the present invention has a viscosity at 25° C. of preferably 3.0 to 10.0 mPa·s, more preferably 3.5 to 6.0 mPa·s. The viscosity can be measured using a cone plate viscometer according to conditions specified in Examples.
The inkjet ink containing the aqueous pigment dispersion according to the present invention can be suitably used as inkjet ink for coated paper for printing, inkjet ink for cardboard, and inkjet ink for cotton fabrics, for example. Examples of printing methods using the inkjet ink include, but is not limited to, printing at home, printing in business, sign graphic printing, and printing by pigment printing. Preferably, examples thereof include printing by pigment printing.
Hereinafter, the present invention will be described in detail by way of Examples, but these is not construed as limitations to the present invention. Hereinafter, “parts” indicates parts by weight unless otherwise specified.
836.9 parts of diethylene glycol, 327.3 parts of terephthalic acid, 327.3 parts of isophthalic acid, and 2 parts of titanium diisopropoxy bistriethanol aminato as a condensation catalyst were placed into a reaction tank provided with a cooling tube, a thermometer, a stirrer, and a nitrogen inlet pipe, and were reacted for 3 hours at 200° C. under a nitrogen stream while generated water was being distilled off. These were further reacted at 200° C. for 6 hours under a reduced pressure of 0.5 to 2.5 kPa. When the acid value (mgKOH/g) reached less than 1, the reaction product was extracted from the reaction tank. A polyester polyol having a hydroxyl value (mgKOH/g) of 56.1 was given.
45.1 parts of the polyester polyol, 3.6 parts of 3-methyl-1,5-pentanediol, 7.5 parts of N-methyldiethanolamine as a polyol component having a tertiary amino group in the side chain, 36.9 parts of dicyclohexylmethane-4,4-diisocyanate (hydrogenated MDI) as an organic polyisocyanate component, and 100 parts of tetrahydrofuran as an organic solvent for a reaction were placed into a pressure-resistant reaction container provided with a stirrer and a heater, and were urethanized at 70° C. for 12 hours with stirring. In the next step, 6.9 parts of dimethyl sulfate was placed into the reactor, followed by a reaction at 50° C. for 4 hours to prepare a solvent solution of a polyurethane resin (P-1) containing a quaternary ammonium salt and having an isocyanate group.
45.1 parts of polycarbonate polyol [ETERNACOLL UH-200, available from UBE Corporation], 3.6 parts of 3-methyl-1,5-pentanediol, 7.5 parts of N-methyldiethanolamine as a polyol component having a tertiary amino group in the side chain, 36.9 parts of dicyclohexylmethane-4,4-diisocyanate (hydrogenated MDI) as an organic polyisocyanate component, and 100 parts of tetrahydrofuran as an organic solvent for a reaction were placed into a pressure-resistant reaction container provided with a stirrer and a heater, and were urethanized at 70° C. for 12 hours with stirring. In the next step, 6.9 parts of dimethyl sulfate was placed into the reactor, followed by a reaction at 50° C. for 4 hours to prepare a solvent solution of a polyurethane resin (P-2) containing a quaternary ammonium salt and having an isocyanate group.
Solvent solutions of polyurethane resins (P-3) to (P-12) were prepared in the same manner as in Production Example 2 except that the raw materials used and the amounts thereof were varied as shown in Tables 1-1 to 1-2.
30 parts of a solvent solution of the polyurethane resin (P-4) prepared in Production Example 4 was added to a vessel provided with a stirrer, and 84.4 parts of water was added with stirring at 200 rpm to disperse the mixture. 0.64 parts of isophoronediamine (IPDA) as a chain extender was added to the resulting dispersion to perform an extension reaction for 30 minutes under stirring, and tetrahydrofuran was distilled off under reduced pressure at 60° C. over 2 hours. The solid concentration was adjusted to 16.7% by weight by adding water to prepare a dispersion of a polyurethane resin (P-13).
57 parts of myristyl alcohol and 0.08 parts of potassium hydroxide were placed into a pressure-resistant reaction container provided with a thermometer, a heating and cooling apparatus, a stirrer, and a cylinder for dropwise addition, followed by purging with nitrogen. Thereafter, the container was sealed, and heated to 140° C. While the pressure was being controlled to 0.5 MPa or less at 140° C. under stirring, 43 parts of ethylene oxide was added dropwise over 5 hours, and was aged at the same temperature for 3 hours to prepare an ethylene oxide 4 mol adduct (O-1) of myristyl alcohol.
36 parts of oleyl alcohol and 0.08 parts of potassium hydroxide were placed into a reaction container similar to that in Production Example 14, followed by purging with nitrogen. Thereafter, the container was sealed, and heated to 140° C. While the pressure was being controlled to 0.5 MPa or less at 140° C. under stirring, 64 parts of ethylene oxide was added dropwise over 5 hours, and was aged at the same temperature for 3 hours to prepare an ethylene oxide 11 mol adduct (O-2) of oleyl alcohol.
15 parts of sorbitol and 0.08 parts of potassium hydroxide were placed into a reaction container similar to that in Production Example 14, followed by purging with nitrogen. Thereafter, the container was sealed, and heated to 140° C. While the pressure was being controlled to 0.5 MPa or less at 140° C. under stirring, 85 parts of ethylene oxide was added dropwise over 5 hours, and was aged at the same temperature for 3 hours to prepare an ethylene oxide 24 mol adduct (O-3) of sorbitol.
39 parts of sorbitol, 61 parts of oleic acid, and 50 parts of xylene as a solvent were placed into a reaction tank provided with a cooling tube, a thermometer, a stirrer, and a nitrogen inlet pipe, and were reacted at 180° C. for 3 hours under a nitrogen stream while generated water was distilled off. When the acid value (mgKOH/g) reached less than 1, the pressure of the reaction system was reduced to remove xylene. Thus, an esterified product (O-4) of sorbitol and oleic acid was prepared.
68 parts of polyoxyethylene monomethyl ether (available from Sigma-Aldrich Corporation, Mn: 550), 32 parts of oleic acid, and 50 parts of xylene as a solvent were placed into a reaction tank provided with a cooling tube, a thermometer, a stirrer, and a nitrogen inlet pipe, and were reacted at 180° C. for 3 hours under a nitrogen stream while generated water was distilled off. When the acid value (mgKOH/g) reached less than 1, the pressure of the reaction system was reduced to remove xylene. Thus, an oleic acid polyethylene glycol ester (O-5) was prepared.
44 parts of polyoxyethylene monomethyl ether (Polyethylene glycol monomethyl ether 220 available from KANTO CHEMICAL CO., INC., Mn: 220), 56 parts of oleic acid, and 50 parts of xylene as a solvent were placed into a reaction tank provided with a cooling tube, a thermometer, a stirrer, and a nitrogen inlet pipe, and were reacted at 180° C. for 3 hours under a nitrogen stream while generated water was distilled off. When the acid value (mgKOH/g) reached less than 1, the pressure of the reaction system was reduced to remove xylene. Thus, an oleic acid polyethylene glycol ester (O-6) was prepared.
Solvent solutions of polyurethane resins (P′-1) to (P′-3) were prepared in the same manner as in Production Example 2 except that the raw materials used and the amounts thereof were varied as shown in Table 1-3.
59 parts of polypropylene glycol-diglycidyl ether (epoxy equivalent: 201 g/equivalent) was placed into a reaction tank provided with a cooling tube, a thermometer, a stirrer, and a nitrogen inlet pipe, and the inside of the vessel was purged with nitrogen and then heated to 70° C. Thereafter, 38 parts of di-n-butylamine was added dropwise with an adding apparatus. After the addition was completed, a reaction was performed at 90° C. for 10 hours. After the reaction was ended, using an infrared spectrophotometer, loss of the absorption peak near 842 cm−1 attributed to the epoxy group of the reaction product was verified. Thus, a tertiary amino group-containing polyol was prepared (the amine value and the hydroxyl value both were 165.5 mgKOH/g).
219.8 parts of 1,4-butanediol, 254.0 parts of neopentyl glycol, 362.0 parts of terephthalic acid, 318.6 parts of adipic acid, and 2 parts of titanium diisopropoxy bistriethanol aminato as a condensation catalyst were placed into a reaction tank provided with a cooling tube, a thermometer, a stirrer, and a nitrogen inlet pipe, and were reacted at 200° C. for 3 hours under a nitrogen stream while generated water was distilled off. These were further reacted at 200° C. for 6 hours under a reduced pressure of 0.5 to 2.5 kPa. When the acid value (mgKOH/g) reached less than 1, the reaction product was extracted from the reaction tank. Thus, a polyester polyol having a hydroxyl value (mgKOH/g) of 58.9 was given.
48.6 parts of polycarbonate polyol [ETERNACOLL UH-200 available from UBE Corporation], 24.2 parts of the above-mentioned polyester polyol (copolymerized product of neopentyl glycol, 1,4-butanediol, terephthalic acid, and adipic acid), 5.8 parts of the above-mentioned tertiary amino group-containing polyol, 19.3 parts of dicyclohexylmethane-4,4-diisocyanate (hydrogenated MDI) as a polyisocyanate component, and 100 parts of ethyl acetate as an organic solvent for a reaction were placed into a pressure-resistant reaction container provided with a stirrer and a heater, and were urethanized at 70° C. for 12 hours with stirring.
After the reaction, 3.2 parts of “Aminosilane A1100” (available from ENEOS NUC Corporation, γ-aminopropyltriethoxysilane) was added, followed by a reaction for 1 hour to prepare an ethyl acetate solution of a urethane prepolymer. In the next step, 1.0 part of hydrazine hydrate was added to the urethane prepolymer solution, followed by a chain extension reaction for 1 hour.
In the next step, 134.6 parts of ethyl acetate and 2.1 parts of dimethyl sulfate were added, and the system was kept at 50° C. for 4 hours. Thereafter, 227.3 parts of water was added with stirring at 200 rpm to disperse the mixture. Ethyl acetate was distilled off under reduced pressure at 60° C. over 2 hours. The solid concentration was adjusted to 16.7% by weight by adding water to prepare a dispersion of a polyurethane resin (P′-4).
The compositions and physical properties value of the polyurethane resins are shown in Tables 1-1 to 1-3.
In Tables 1-1 to 1-3, the weight proportion of the quaternary ammonium compound (a1) was calculated from the following equation:
weight proportion (%) of quaternary ammonium compound (a1)={[(a1-1)+(a1-2)]/[polyol other than quaternary ammonium compound (a1)+(a1-1)+(a1-2)+(B)]}×100
The quaternarizing agent (a1-2) was not used in Comparative Production Examples 1 to 3, and the quaternary ammonium compound (a1) was not present. Thus, the weight proportion (%) is 0%.
30 parts of the solvent solution of the polyurethane resin (P-1) prepared in Production Example 1 and 120 parts of tetrahydrofuran were added to a vessel in a pigment dispersing machine (TSU-6U, available from Aimex Co., Ltd.), and were stirred until the resin was homogeneously dissolved. Next, 10 parts of a cyan pigment [Heliogen Blue D7088 available from BASF SE] and 350 parts of glass beads [ASGB-320, available from AS ONE Corporation] were added, and then the materials were dispersed for 4 hours while 4° C. cooling water was being passed through the jacket.
100 parts of water was added while the resulting dispersed slurry was being stirred at 200 rpm, and the mixture was dispersed. 0.64 parts of isophoronediamine (IPDA) as a chain extender was added to the resulting dispersion under stirring to perform an extension reaction for 30 minutes; thereafter, tetrahydrofuran was distilled off under reduced pressure at 60° C. over 2 hours, and the glass beads were removed through a filter. The solid concentration was adjusted to 25% by weight by adding water to prepare an aqueous pigment dispersion (Q-1).
Aqueous pigment dispersions (Q-2) to (Q-25) were prepared in the same manner as in Example 1 except that the raw materials used and the amounts thereof were varied as shown in Tables 2-1 to 2-3 and 3-1 to 3-3.
In Examples 16 to 25, nonionic surfactants (O-1) to (O-6) were used. When a nonionic surfactant was used, in the beginning of the step shown in Example 1, the nonionic surfactant together with the solvent solution of the polyurethane resin and tetrahydrofuran was added to the vessel of the pigment dispersing machine (TSU-6U, available from Aimex Co., Ltd.), and these were stirred until the resin was homogeneously dissolved.
30 parts of the solvent solution of the polyurethane resin (P-4) prepared in Production Example 4, 50 parts of tetrahydrofuran, and 0.5 parts of the oleic acid polyethylene glycol ester (O-6) prepared in Production Example 19 were added to a vessel in a pigment dispersing machine (TSU-6U, available from Aimex Co., Ltd.), and were stirred until the resin was homogeneously dissolved. 1.51 parts of isophoronediamine (IPDA) as a chain extender was added under stirring to perform an extension reaction for 30 minutes. Next, 10 parts of a cyan pigment [Heliogen Blue D7088 available from BASF SE] and 140 parts of glass beads [ASGB-320, available from AS ONE Corporation] were added, and then were dispersed for 3 hours while 4° C. cooling water was being passed through the jacket.
100 parts of water was added while the resulting dispersed slurry was being stirred at 200 rpm, and the mixture was dispersed. Thereafter, tetrahydrofuran was distilled off under reduced pressure at 60° C. over 2 hours, and the glass beads were removed through a filter. The solid concentration was adjusted to 25% by weight by adding water to prepare an aqueous pigment dispersion (Q-26).
90 parts of the dispersion of the polyurethane resin (P-13) prepared in Production Example 13, 0.5 parts of the oleic acid polyethylene glycol ester (O-6) prepared in Production Example 19, 10 parts of a cyan pigment [Heliogen Blue D7088 available from BASF SE], and 140 parts of glass beads [ASGB-320, available from AS ONE Corporation] were added to a vessel in a pigment dispersing machine (TSU-6U, available from Aimex Co., Ltd.), and were dispersed for 3 hours while 4° C. cooling water was being passed through the jacket. Next, the glass beads were removed through a filter. The solid concentration was adjusted to 25% by weight by adding water to prepare an aqueous pigment dispersion (Q-27).
Aqueous pigment dispersions (Q′-1) to (Q′-3) were prepared in the same manner as in Example 1 except that the raw materials used and the amounts thereof were varied as shown in Table 4.
90 parts of the dispersion of the polyurethane resin (P′-4) prepared in Comparative Production Example 4, 10 parts of a cyan pigment [Heliogen Blue D7088 available from BASF SE], and 140 parts of glass beads [ASGB-320, available from AS ONE Corporation] were added to a vessel of a pigment dispersing machine (TSU-6U, available from Aimex Co., Ltd.), and were dispersed for 3 hours while 4° C. cooling water was being passed through the jacket. Next, the glass beads were removed through a filter. The solid concentration was adjusted to 25% by weight by adding water to prepare an aqueous pigment dispersion (Q′-4).
For the aqueous pigment dispersions prepared in Examples and Comparative Examples, the amounts (parts) of the materials blended, values indicating physical properties, and the results of evaluation are shown in Tables 2-1 to 2-3, 3-1 to 3-3 and 4.
Hereinafter, methods of measuring and evaluating the resulting aqueous pigment dispersions will be described.
For the aqueous pigment dispersions (Q-1) to (Q-27) and (Q′-1) to (Q′-4) prepared in Examples 1 to 27 and Comparative Examples 1 to 4, the particle size was measured with a light scattering particle size distribution analyzer [“ELSZ-1000” available from Otsuka Electronics Co., Ltd.], and the obtained cumulant average particle size was defined as the particle size.
For the aqueous pigment dispersions (Q-1) to (Q-27) and (Q′-1) to (Q′-4) prepared in Examples 1 to 27 and Comparative Examples 1 to 4, 0.1% by weight of each aqueous pigment dispersion was added to a heated gelatin aqueous solution, and was homogenized. Thereafter, the solution was cooled to room temperature, and was further cooled in a refrigerator for 2 hours or more to be solidified.
The solidified sample was cut out with a microtome into a thin layer sample, which was stained with a polyurethane resin by phosphotungstic acid stain. A TEM image of the stained sample was observed, and the shapes of the observed particles were confirmed based on their circularity. The shape was evaluated according to the following criteria:
For the aqueous pigment dispersions (Q-1) to (Q-27) and (Q′-1) to (Q′-4) prepared in Examples 1 to 27 and Comparative Examples 1 to 4, 50.0 parts of each aqueous pigment dispersion, 15.0 parts of glycerol, 1.0 part of triethylene glycol butyl ether (BTG), 0.5 parts of OLFINE E1010 (available from Nissin Chemical Industry Co., Ltd.), and 33.5 parts of water were homogenously mixed, and insolubles were removed through a filter. Thus, inks (R-1) to (R-27) for evaluation and Comparative inks (R′-1) to (R′-4) were prepared.
The aqueous pigment dispersion (Q′-3) in which a tertiary amine salt was used could not be evaluated as the ink because it caused aggregation in a basic pH.
In “Dispersibility after adjustment of ink composition (pH: 8)”, the case where particles of the aqueous pigment dispersion were dispersed in the ink is indicated as Good, and the case where particles of the aqueous pigment dispersion were aggregated in the ink is indicated as Poor.
For each of the inks prepared above, the initial dispersibility of the ink was evaluated from the results of measurement of the particle size of the aqueous pigment dispersion in the ink and the ink viscosity.
The particle size of the aqueous pigment dispersion in the ink containing a color pigment (cyan, magenta, yellow, or black pigment in Examples and Comparative Example) was evaluated according to the following criteria:
The particle size of the aqueous pigment dispersion in the ink containing a white pigment was evaluated according to the following criteria:
The ink viscosity was evaluated according to the following criteria:
From the results of measurement of the particle size and the viscosity, the initial dispersibility of the ink was evaluated according to the following criteria:
It was measured by the same method as that for the aqueous pigment dispersion.
The ink (R′-3), which was aggregated, was excluded from the analysis.
For the inks (R-1) to (R-27) for evaluation and Comparative inks (R′-1), (R′-2), and (R′-4), the viscosity was measured on the following conditions using the following apparatus:
The ink (R′-3), which was aggregated, was excluded from the analysis.
The ink was left to stand for 5 days in an air-circulating dryer at a temperature set to 60° C., and storage stability of the ink was evaluated from a rate of change of the particle size of the aqueous pigment dispersion in the ink before and after the test and that of the ink viscosity before and after the test.
The rate of changes are calculated from the following expressions:
rate of change (%) of particle size of aqueous pigment dispersion in ink: (S2−S1)/S1×100
rate of change (%) of ink viscosity: (V2−V1)/V1×100
Evaluation was performed according to the following criteria for evaluation.
The inks for evaluation (R-1) to (R-14), (R-16) to (R-24), and (R-26) to (R-27) and Comparative inks (R′-1), (R′-2), and (R′-4) were printed on a plain cotton broadcloth [cotton: 100% by mass] using a modified machine of an inkjet printer PX-G930 available from Seiko Epson Corporation, and were dried at 160° C. for 10 minutes to prepare test pieces (21 cm×28 cm) of the plain cotton broadcloth having a pigment and the polyurethane resin applied thereonto. The dry rubbing fastness was evaluated according to JIS L0849-2. Each of the test pieces was rubbed 100 times in a reciprocating manner under a load of 200 g. The density of the transferred ink in the #3 shirting was measured in nine points of the test piece with a spectrocolorimeter [X-rite938 available from X-Rite, Inc.], and the average of the results of measurement was defined as the density of the transferred ink. The density of the transferred ink was evaluated according to the following criteria, and the results are shown in Tables 2-1 to 2-3, 3-1 to 3-3 and 4. A lower density of the transferred ink indicates higher dry rubbing fastness.
The density of the transferred ink of 0.15 or less indicates that the ink is at a practical level.
The inks for evaluation (R-15) and (R-25) were printed on a black plain cotton broadcloth [black cotton: 100% by mass] with a modified machine of an inkjet printer PX-G930 available from Seiko Epson Corporation, and were dried at 160° C. for 10 minutes to prepare test pieces (21 cm×28 cm) of the black plain cotton broadcloth having the pigment and the polyurethane resin applied thereonto.
The dry rubbing fastness was evaluated according to JIS L0849-2. Each of the test pieces was rubbed 100 times in a reciprocating manner under a load of 200 g. The pigment-printed surface of the test piece before and after rubbing was measured in nine points of the test piece with a spectrocolorimeter [X-rite938 available from X-Rite, Inc.], and the average of differences between the results of measurement before and after rubbing was defined as ΔL*. The ΔL* was evaluated according to the following criteria, and the results are shown in Tables 2-3 and 3-3. A lower ΔL* indicates higher rubbing fastness.
The inks for evaluation (R-1) to (R-14), (R-16) to (R-24), and (R-26) to (R-27) and Comparative inks (R′-1), (R′-2), and (R′-4) were printed on a plain cotton broadcloth [cotton: 100% by mass] with a modified machine of an inkjet printer PX-G930 available from Seiko Epson Corporation, and were dried at 160° C. for 10 minutes to prepare test pieces (21 cm×28 cm) of the plain cotton broadcloth having the pigment and the polyurethane resin applied thereonto. The wet rubbing fastness was evaluated according to JIS L0849-2. Each of the test pieces was rubbed 100 times in a reciprocating manner under a load of 200 g. The density of the transferred ink in the #3 shirting was measured in nine points of the test piece with a spectrocolorimeter [X-rite938 available from X-Rite, Inc.], and the average of the results of measurement was defined as the density of the transferred ink. The density of the transferred ink was evaluated according to the following criteria, and the results are shown in Tables 2-1 to 2-3, 3-1 to 3-3 and 4. A lower density of the transferred ink indicates higher wet rubbing fastness.
A density of the transferred ink of 0.25 or less indicates that the ink is at a practical level.
The inks for evaluation (R-15) and (R-25) were printed on a black plain cotton broadcloth [black cotton: 100% by mass] with a modified machine of an inkjet printer PX-G930 available from Seiko Epson Corporation, and were dried at 160° C. for 10 minutes to prepare test pieces (21 cm×28 cm) of the black plain cotton broadcloth having the pigment and the polyurethane resin applied thereonto. The wet rubbing fastness was evaluated according to JIS L0849-2. Each of the test pieces was rubbed 100 times in a reciprocating manner under a load of 200 g. The pigment-printed surface of the test piece before and after rubbing was measured in nine points of the test piece with a spectrocolorimeter [X-rite938 available from X-Rite, Inc.], and the average of differences between the results of measurement before and after rubbing was defined as ΔL*. The ΔL* was evaluated according to the following criteria, and the results are shown in Tables 2-3 and 3-3. A lower ΔL* indicates higher rubbing fastness.
The inks for evaluation (R-1) to (R-14), (R-16) to (R-24), and (R-26) to (R-27) and Comparative inks (R′-1), (R′-2), and (R′-4) were printed on a plain cotton broadcloth [cotton: 100% by mass] with a modified machine of an inkjet printer PX-G930 available from Seiko Epson Corporation, and were dried at 160° C. for 10 minutes to prepare test pieces (21 cm×28 cm) of the plain cotton broadcloth having the pigment and the polyurethane resin applied thereonto. The image density was measured in nine points of each test piece with a spectrocolorimeter [X-rite938 available from X-Rite, Inc.], and the average of the results of measurement was defined as an image density. The image density was evaluated according to the following criteria, and the results are shown in Tables 2-1 to 2-3, 3-1 to 3-3 and 4. A higher image density indicates higher color developability.
An image density of 1.3 or more indicates that the ink is at a practical level.
The inks for evaluation (R-15) and (R-25) were printed on a black plain cotton broadcloth [black cotton: 100% by mass] with a modified machine of an inkjet printer PX-G930 available from Seiko Epson Corporation, and were dried at 160° C. for 10 minutes to prepare test pieces (21 cm×28 cm) of the black plain cotton broadcloth having the pigment and the polyurethane resin applied thereonto.
The image density was determined based on the L* value, and the L* was measured in nine points of each test piece with a spectrocolorimeter [X-rite938 available from X-Rite, Inc.], and the average of the results of measurement was used. The L* was evaluated according to the following criteria, and the results are shown in Tables 2-3 and 3-3. A higher L* indicates higher color developability.
For the filtration properties after heating, an ink was left to stand for 5 days in a circulating dryer at a temperature set to 60° C., the ink was suctioned using a water flow aspirator (maximum degree of vacuum: about 24 mmHg) to filter the ink under reduced pressure.
The filters have a prefilter (ϕ47 mm, 100 sheets, AP2504700/2-3055-07) and an MF-Millipore membrane (cellulose-mixed ester, hydrophilicity, 8.0 μμmt, ϕ47 mm, white). The filtration properties were evaluated as a weight of the ink which can be passed.
The criteria for evaluation are shown as below. The results are shown in Tables 2-1 to 2-3, 3-1 to 3-3 and 4.
The inks prepared above were each mounted on a modified machine of an inkjet printer PX-G930 available from Seiko Epson Corporation. A solid image was continuously printed with a resolution of 1440*720 dpi to evaluate uneven streaks. The criteria for evaluation are as shown below. The results are shown in Tables 2-1 to 2-3, 3-1 to 3-3 and 4.
The inks for evaluation (R-1) to (R-27) have high initial dispersibility, high storage stability, and high rub resistance. The inks for evaluation (R-1) to (R-27) also demonstrate high color developability in cotton fabrics not pre-treated. Comparative inks (R′-1) and (R′-2) without a quaternary ammonium compound had insufficient color developability (Comparative Examples 1 and 2). In Comparative ink (R′-3) without a quaternary ammonium compound, particles were aggregated under a basic condition, and the ink had insufficient initial dispersibility and storage stability (Comparative Example 3). Comparative ink (R′-4), which contained the quaternary ammonium compound (a1) in the polyurethane resin in a weight proportion of 7.9% by weight relative to the total weight of the active hydrogen atom-containing component (A) and the organic polyisocyanate component (B), had insufficient initial dispersibility of ink, storage stability of ink, color developability (Comparative Example 4).
The aqueous pigment dispersion according to the present invention has high initial dispersion stability and high storage stability, and demonstrating high color developability in particularly fabrics not pre-treated, and therefore is useful as an aqueous pigment dispersion for preparing an inkjet ink composition for printing in cotton fabrics.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2022-059138 | Mar 2022 | JP | national |
