JP5251528B2 - Ink-jet ink set for cloth, ink-jet discharging method and ink-jet anti-dyeing method using the same - Google Patents

Description

  The present invention relates to an ink jet discharging method and an ink jet anti-dyeing method. More specifically, the present invention relates to an ink jet ink set for fabrics that suppresses blurring and has excellent emission properties even on fabrics that have not been subjected to ink jet pretreatment. The present invention relates to an ink jet discharging method and an ink jet resist method.

  The method of adding a base compound to the discharge paste and decolorizing the extractable dye is known in the textile printing field, as described in, for example, dyeing finishing technique, written by Kazuo Shiozawa, Jinshoshokan, etc. Is the way. However, when an aqueous ink containing a base compound is directly ejected onto a cloth that has not been subjected to inkjet pretreatment, an image is formed on the cloth. For this reason, the inkjet pre-processing which usually provided the component which consists of water-soluble high molecular compounds, such as carboxymethylcellulose and sodium alginate, to the fabric has been performed (for example, refer patent document 1). In this method, it is considered that the water-soluble polymer compound in the fabric has acted as an ink-holding component (absorbing layer) to prevent bleeding.

  Unlike the ink jet printing process that can be handled on demand, such a pretreatment for ink jet of a fabric needs to be processed in a certain amount in advance. Therefore, it takes a lot of time and the pretreatment cloth Since it has inventory and processing cost, it has become a big obstacle in spreading inkjet printing more.

  In addition, as described above, by applying a paste to the fabric, it is easy to stay on the fabric surface due to the mechanism that suppresses bleeding by absorbing the ink. There is also a problem of not being dyed.

  As an attempt to eliminate the pretreatment by applying a functional liquid for suppressing bleeding using an ink jet head, a method of performing image bordering with a first ink containing a bleeding inhibitor is disclosed (for example, Patent Documents). 2). In the method described in Patent Document 2, addition of a compound having a property of repelling water with a hydrophobic substance is disclosed as a bleed inhibitor, but it is possible to prevent bleed at the boundary between a white background and an image portion or to have a different specific hue. It is considered that the invention is limited to the prevention of blurring of the boundary. The method described in Patent Document 2 has a problem that it cannot cope with blurring suppression in a printed image having a gradation expression with increased expressive power. Also, it is not suitable for fine line and detail image expression. This is because the print area of the first ink and the print image of the second ink must be accurately matched, but the fabric is easily stretchable and the printing position is very difficult to align. Furthermore, since the first ink itself also bleeds into the fabric, very fine fine lines cannot be drawn in principle.

JP-A-6-116880 JP-A-9-296380

  SUMMARY OF THE INVENTION The present invention has been made in view of the above-mentioned problems, and its object is to suppress the occurrence of bleeding even on a fabric that has not been subjected to inkjet pretreatment, and the inkjet ink for fabric that has excellent emission stability. An object of the present invention is to provide a set and an ink jet discharging method and an ink jet resist method using the set.

  The above object of the present invention is achieved by the following configurations.

  1. An inkjet ink set for fabrics, comprising: a first ink containing water, a liquid humectant, and a water-soluble polymer compound; and a second ink containing water, a base compound, and a water-soluble organic solvent. .

  2. The inkjet ink set for fabric according to 1, wherein the first ink contains a solid moisturizing agent.

  3. The water-soluble polymer compound is polyvinyl pyrrolidone, polyethylene glycol, ethylene oxide propylene oxide copolymer, glycerin polyethylene oxide adduct, glycerin polypropylene adduct, diglycerin polyethylene oxide adduct, and diglycerin polypropylene adduct. And the total amount of the water-soluble polymer compound is 1% by mass or more and less than 10% by mass as a solid content with respect to the total mass of the first ink. The inkjet ink set for cloth according to 1 or 2.

  4). The inkjet ink set for cloth according to any one of 1 to 3, wherein the first ink contains a water-soluble cationic polymer.

  5. The inkjet ink set for fabric according to any one of 1 to 4, wherein the first ink contains an inorganic base, and the inorganic base is a potassium salt.

  6). Using the cloth inkjet ink set according to any one of 1 to 5 above, the first ink is applied to the cloth and then the second ink is applied to the cloth dyed with a removable dye in advance. An ink jet discharging method comprising:

  7). 7. The inkjet discharging method according to 6 above, wherein the first ink is applied while heating the fabric.

  8). The printer used to apply the first ink and the second ink to the fabric is a printer in which the first ink head and the second ink head are arranged on the same carriage, and the printer performs the scan in one scan. 7. The ink jet discharging method as described in 6 above, wherein the first ink and the second ink are applied onto a fabric.

  9. 9. The inkjet discharging method according to 6 or 8, wherein the first ink and the second ink are applied while heating the fabric.

  10. The cloth ink-jet ink set according to any one of 1 to 5 above is applied to a cloth previously provided with a removable dye, and the first ink and the second ink are applied to the cloth. Inkjet dyeing method.

  11. 11. The inkjet dyeing method according to 10 above, wherein the first ink is applied while heating the fabric.

  12 The printer used to apply the first ink and the second ink to the fabric is a printer in which a first ink head and a second ink head are arranged on the same carriage, and the printer performs the scanning in one scan. 11. The ink-jet dyeing method as described in 10 above, wherein the first ink and the second ink are applied onto a fabric.

  13. 13. The inkjet dyeing method according to 10 or 12, wherein the first ink and the second ink are applied while heating the fabric.

  14 6. An ink jet dyeing method comprising: applying a removable dye after applying a first ink and a second ink to a fabric using the ink jet ink set for a fabric according to any one of 1 to 5 above. Method.

  15. 15. The inkjet dyeing method according to 14, wherein the first ink is applied while heating the fabric.

  16. The printer used to apply the first ink and the second ink to the fabric is a printer in which a first ink head and a second ink head are arranged on the same carriage, and in one scan, 15. The inkjet dyeing and resisting method as described in 14 above, wherein the first ink and the second ink are applied onto the fabric.

  17. 17. The inkjet dyeing method according to item 14 or 16, wherein the first ink and the second ink are applied while heating the fabric.

  INDUSTRIAL APPLICABILITY According to the present invention, an ink jet ink set for cloth that suppresses the occurrence of bleeding and is excellent in emission stability even for a cloth that has not been subjected to ink jet pretreatment, and an ink jet discharging method and ink jet antifouling method using the same. Could be provided.

It is a schematic diagram which shows the partial structure of the printer for evaluation used in the Example.

  Hereinafter, embodiments for carrying out the present invention will be described in detail.

  As a result of intensive studies in view of the above problems, the present inventor has found that a first ink containing water, a liquid humectant and a water-soluble polymer compound, and a second ink containing water, a base compound and a water-soluble organic solvent. A method for forming a pattern on a cloth dyed with a removable dye in advance or a cloth previously provided with a removable dye, using an inkjet ink set for cloth characterized by comprising: After applying the first ink and the second ink to the treated fabric, bleeding is generated even on the fabric that has not been subjected to the inkjet pretreatment by using a method of drawing by adding a removable dye. It has been found that an inkjet ink set for fabrics that suppresses and has excellent emission stability, and an inkjet discharging method and an inkjet anti-dyeing method using the same can be realized, It is up that led to the invention.

  Hereinafter, the present invention will be described in more detail.

  First, the configuration of the first ink and the second ink according to the present invention will be described.

<First ink>
The first ink according to the present invention is an ink liquid containing a water-soluble polymer compound to suppress bleeding during printing using the second ink, and is applied to the fabric from the inkjet head. . The water viscosity of the water-soluble polymer compound according to the present invention increases as the solid content of the water-soluble polymer compound increases. This high viscosity characteristic is used to prevent bleeding after the second ink has landed on the fabric.

  Although a method of adding a water-soluble polymer compound to the second ink is also conceivable, a large amount of a base compound is added to the second ink, so that a sufficient amount of the water-soluble polymer compound can be stabilized to suppress bleeding. It has been found that it is very difficult to add to the first ink, and it has been found that adding to the first ink is a preferable embodiment, and the present invention has been achieved.

  Hereinafter, each additive which comprises the 1st ink which concerns on this invention is demonstrated.

[Water-soluble polymer compound]
The water-soluble polymer compound added to the first ink according to the present invention is not particularly limited as long as it sufficiently suppresses the bleeding of the second ink and does not inhibit the ink jetting property of the first ink. be able to. In order not to change the texture of the printed matter, it is preferable that the water-soluble polymer compound is easy to remove in the washing step after printing and coloring.

  Examples of water-soluble polymer compounds include polyvinylpyrrolidone, polyethylene glycol, ethylene oxide propylene oxide copolymer, glycerin polyethylene oxide adduct, glycerin polypropylene adduct, diglycerin polyethylene oxide adduct, diglycerin polypropylene addition. Products, carboxymethyl cellulose, methyl cellulose, sodium alginate, polyvinyl alcohol and the like.

  Preferred water-soluble polymer compounds include polyvinylpyrrolidone, polyethylene glycol, ethylene oxide propylene oxide copolymer, polyethylene oxide adduct of glycerin, polypropylene adduct of glycerin, polyethylene oxide adduct of diglycerin, polypropylene of diglycerin. Examples include adducts.

  Since the preferable addition amount of the water-soluble polymer compound varies depending on the molecular weight and the type thereof, it is preferable to appropriately select the optimum conditions.

  Among the above water-soluble polymer compounds, polyvinyl pyrrolidone is a particularly preferable water-soluble polymer compound that can be stably ejected from an inkjet head and has a large blurring suppression effect.

  Polyvinyl pyrrolidone is classified by viscosity characteristic value correlating with molecular weight, and K (Kollidon) 15, 30, 60, etc. can be preferably used. It is effective and preferable. The addition amount to the first ink is preferably in the range of 2 to 20% by mass as the solid content.

  Polyethylene glycol can also be preferably used, and polyethylene glycol having a weight average molecular weight of 600 or more can be preferably used. Furthermore, those having a weight average molecular weight of 1000 or more and 4000 or less are particularly effective because they are effective in suppressing bleeding. The amount of polyethylene glycol added to the first ink is preferably 2-20% by mass.

  Examples of the ethylene oxide / propylene oxide copolymer include those having a structure in which polyethylene oxide is added to the end of polypropylene glycol, those having a structure in which polypropylene oxide is added to the end of polyethylene glycol, and ethylene oxide-propylenoxide. A random copolymer etc. are mentioned.

  As a structure having polyethylene oxide added to the end of polypropylene glycol, ADEKA Corporation's Adeka Pluronic L, P, F series, etc., various ethylene oxide-propylene oxide blend ratio products and various molecular weight products are commercially available. And you can choose from them. Particularly, a water-soluble polypropylene glycol part having a molecular weight of 2000 or less can be preferably used. Specifically, L-62, L-64, F-68, F-88, F-108, L-44, L-34, L-23 (above, manufactured by ADEKA Corporation) can be exemplified. .

  As a structure in which polypropylene oxide is added to the end of polyethylene glycol, it can also be selected from reverse types such as ADEKA Corporation, 17R-2, 17R-3, and 17R-4.

  The amount of ethylene oxide / propylene oxide copolymer added to the first ink is preferably in the range of 2 to 20% by mass.

  As the polyethylene oxide adduct of diglycerin, it can be used by selecting from SC-E series of Sakamoto Pharmaceutical Co., Ltd., for example, SC-E450, SC-E750, SC-E1000, SC-E1500, etc. are preferably used. be able to. The addition amount to the first ink is preferably in the range of 2 to 20% by mass.

  As a polypropylene adduct of diglycerin, it can be used by selecting from SC-P series of Sakamoto Yakuhin Kogyo Co., Ltd., and SC-P400, SC-P750, SC-P1000, etc. can be preferably used. The addition amount to the first ink is preferably in the range of 2 to 20% by mass.

  With respect to the amount of the water-soluble polymer compound added to the first ink, the preferred range mentioned above is less than the lower limit, and a sufficient blur suppression effect cannot be exhibited. If the amount exceeds the upper limit, the inkjet ejection is unstable. It is not preferable.

  These water-soluble polymer compounds may be used alone or in combination of two or more.

[Base compound]
As in the second ink, the first ink according to the present invention is characterized in that a basic compound is added in order to remove the dye. Moreover, an inorganic basic compound and an organic basic compound are added for pH adjustment.

  There are organic bases as basic compounds, but organic base compounds have the disadvantage of many odors, and inorganic base compounds are more preferred.

[Liquid moisturizer]
A liquid humectant is preferably added to the first ink according to the present invention from the viewpoint of suppressing nozzle clogging of the first ink in the inkjet head. This is because the liquid humectant has a function of delaying drying of moisture and delaying precipitation of the first ink content. However, since the liquid humectant has the characteristic that it is easy to cause bleeding of the second ink at the same time, it is easy to determine the type and amount of addition from the viewpoint of both the head clogging prevention effect and the occurrence of bleeding. is there.

  Examples of the liquid humectant applicable to the present invention include ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, glycerin, diglycerin and the like.

  The amount of liquid humectant added to the first ink is preferably selected within the range of 5% by mass or more and less than 40% by mass.

[Solid moisturizer]
It is preferable to add a solid humectant to the first ink according to the present invention. The solid humectant, like the liquid humectant, has the effect of preventing the inorganic base compound from being precipitated by drying and increasing the color density. In particular, the combined use with a liquid humectant is preferable from the viewpoint of improving both the drying prevention effect and the effect of increasing the color density.

  Examples of the solid humectant include water-soluble amides, sulfonamides, urea, urea derivatives and the like, and urea is particularly preferable.

  The solid humectant is preferably used in the first ink in an amount ranging from 2% by mass to less than 15% by mass.

(Water-soluble cationic polymer)
A water-soluble cationic polymer can be added to the first ink according to the present invention. The water-soluble cationic polymer is effective in preventing bleeding of the colorant when a colorant is added to the second ink.

  As the cationic polymer that can be used in the present invention, those that lower the solubility and dispersibility of the colorant by ionic bonding with the colorant and the dispersant in the second ink can be used. By using such a water-soluble cationic polymer, it is possible to prevent bleeding of the colorant by causing aggregation of the colorant and its dispersant after the landing of the second ink. Addition of a compound that suppresses bleeding by a mechanism different from that of the water-soluble polymer compound or inorganic base compound, such as a water-soluble cationic polymer, is a preferable embodiment for suppressing bleeding.

  As the water-soluble cationic polymer, for example, polyallylamine, polydiallylamine, polymethyldiallylamine, polydiallyldimethylammonium chloride and the like can be used. Specific examples thereof include PAA-D41-HCl, PAS-21Cl, PAS-M-1L, PAS-H-1L, PAS-J-81L, etc. sold by Nittobo.

  The physical properties of the first ink can be adjusted according to the fabric. The viscosity is preferably 3 mPa · s or more and less than 20 mPa · s. The surface tension is preferably 25 mN / m or more and 70 mN / m or less.

  When the first ink is unevenly distributed on the fabric surface and it is desired to enhance the reaction on the surface, the viscosity is preferably 5 mPa · s or more and less than 20 mPa · s, and the surface tension is preferably 35 mN / m or more and less than 70 mN / m.

  When it is desired to penetrate the first ink to the deep part of the fabric, the viscosity is preferably 3 mPa · s or more and less than 12 mPa · s, and the surface tension is preferably 20 mN / m or more and less than 35 mN / m.

  In order to adjust the surface tension and the viscosity, various water-soluble organic solvents can be added. For example, alcohols (eg, methanol, ethanol, propanol, isopropanol, butanol, isobutanol, sec-butanol, t-butanol), polyhydric alcohols (eg, ethylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, propylene glycol) , Dipropylene glycol, polypropylene glycol, butylene glycol, hexanediol, pentanediol, glycerin, hexanetriol, thiodiglycol), amines (eg, ethanolamine, diethanolamine, triethanolamine, N-methyldiethanolamine, N-ethyldiethanolamine) , Morpholine, N-ethylmorpholine, ethylenediamine, diethylenediamine, triethyl Tetramine, tetraethylenepentamine, polyethyleneimine, pentamethyldiethylenetriamine, tetramethylpropylenediamine), amides (eg, formamide, N, N-dimethylformamide, N, N-dimethylacetamide, etc.), heterocycles (eg, 2 -Pyrrolidone, N-methyl-2-pyrrolidone, cyclohexyl pyrrolidone, 2-oxazolidone, 1,3-dimethyl-2-imidazolidinone), sulfoxides (for example, dimethyl sulfoxide) and the like.

  In particular, when it is desired to cause the second ink to penetrate to the deep part of the fabric to develop a color, it is preferable to use the following low surface tension solvent (in the parenthesis, the surface tension of the solvent (mN / m)).

  Examples of the glycol ether include ethylene glycol monoethyl ether (28.2), ethylene glycol monobutyl ether (27.4), diethylene glycol monoethyl ether (31.8), diethylene glycol monobutyl ether (33.6), and triethylene glycol. Examples thereof include monobutyl ether (32.1), propylene glycol monopropyl ether (25.9), dipropylene glycol monomethyl ether (28.8), tripropylene glycol monomethyl ether (30.0) and the like.

  Examples of the 1,2-alkanediol include 1,2-butanediol, 1,2-pentanediol, 1,2-hexanediol (28.1), 1,2-heptanediol, and the like.

  In addition, when it is desired to cause the second ink to penetrate to the deep part of the fabric to develop a color, the following surfactant can be used.

(Surfactant)
In the first ink according to the present invention, various surfactants can be used when it is desired to further penetrate the base compound of the second ink into the deep part of the fabric. The surfactant that can be used in the present invention is not particularly limited, and examples thereof include anionic surfactants such as dialkyl sulfosuccinates, alkyl naphthalene sulfonates, fatty acid salts, polyoxyethylene alkyl ethers, polyoxyethylene alkyl ethers, and polyoxyethylene alkyl ethers. Nonionic surfactants such as oxyethylene alkyl allyl ethers, acetylene glycols, polyoxyethylene / polyoxypropylene block copolymers, and cationic surfactants such as alkylamine salts and quaternary ammonium salts. In particular, an anionic surfactant and a nonionic surfactant can be preferably used.

  In order to further infiltrate the colorant of the second ink into the deep part of the fabric, it is preferable to control the surface tension of the first ink to 20 mN / m or more and 35 mN / m or less, particularly a silicone-based surfactant or a fluorine-based interface. It is preferable to control the surface tension by adding an activator.

<Silicone-based surfactant or fluorine-based surfactant>
The silicone surfactant is preferably a polyether-modified polysiloxane compound, and examples thereof include KF-351A and KF-642 manufactured by Shin-Etsu Chemical Co., and BYK345, BYK347, and BYK348 manufactured by Big Chemie.

  The fluorine-based surfactant means a compound in which a part or all of the fluorine-based surfactant is substituted with a fluorine atom instead of the hydrogen atom bonded to the carbon of the hydrophobic group of the normal surfactant. Of these, those having a perfluoroalkyl group in the molecule are preferred.

  Among the fluorosurfactants, a certain kind is a product name of Megafac F from Dainippon Ink and Chemicals, and a product name of Surflon from Asahi Glass Co., Minnesota Mining and・ Manufacturing Company under the name Fluorad FC, Imperial Chemical Industry under the name Monfloor, and EI DuPont Nemeras & Company Zonyls And the product name Licobet VPF from the company Farbeberke Hoechst.

  Examples of nonionic fluorosurfactants include Megafax 144D manufactured by Dainippon Ink and Surflon S-141 and 145 manufactured by Asahi Glass Co., and amphoteric fluorosurfactants. Examples of the agent include Surflon S-131 and 132 manufactured by Asahi Glass Co., Ltd.

<< Second ink >>
The second ink according to the present invention includes at least a base compound, a water-soluble organic solvent, and water.

[Base compound]
The second ink according to the present invention is characterized in that a base compound is added in order to remove the dye.

  Although there are organic base compounds as the base compounds, many organic base compounds have drawbacks such as odor, and inorganic base compounds are preferred from the viewpoint of the effects of the present invention.

  Examples of the inorganic base compound include lithium hydroxide, sodium hydroxide, potassium hydroxide, lithium carbonate, sodium carbonate, potassium carbonate, ammonium carbonate, sodium bicarbonate, potassium bicarbonate, ammonium bicarbonate, ammonium acetate, lithium acetate, Sodium acetate, potassium acetate, and the like can be used. Furthermore, the inorganic base compound is preferably a potassium salt from the viewpoint of emission stability.

  The amount of the inorganic base compound added to the second ink is preferably in the range of 0.1 molar equivalent / L to 1 molar equivalent / L.

[Non-removable colorant]
The second ink according to the present invention can contain an irremovable colorant as required, and can be colored while reducing and decoloring the detachable dye.

  The addition amount of the non-repellent colorant is preferably 3% by mass or more and less than 20% by mass, and more preferably 5% by mass or more and less than 15% by mass.

  As the non-repellent colorant that can be used in the present invention, a dye having a structure that is difficult to be decomposed is used among the dye types corresponding to the types of fibers to be colored. In general, structures that are susceptible to degradation are structures in which the molecule contains an ester group or a skill amide group that is susceptible to degradation under basic conditions. Refers to a molecular structure having no partial structure. Reactive dyes are used in the case of cellulose fibers, and disperse dyes are used in the case of polyester fibers. The pigment is used regardless of the type of fiber.

(Water-soluble organic solvent)
The 2nd ink which concerns on this invention can contain the water-soluble organic solvent shown below as a specific example.

  Alcohols (for example, methanol, ethanol, propanol, isopropanol, butanol, isobutanol, sec-butanol, t-butanol), polyhydric alcohols (for example, ethylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, propylene glycol, di-) Propylene glycol, polypropylene glycol, butylene glycol, hexanediol, pentanediol, glycerin, hexanetriol, thiodiglycol), amines (eg, ethanolamine, diethanolamine, triethanolamine, N-methyldiethanolamine, N-ethyldiethanolamine, morpholine) , N-ethylmorpholine, ethylenediamine, diethylenediamine, triethylenetet Amine, tetraethylenepentamine, polyethyleneimine, pentamethyldiethylenetriamine, tetramethylpropylenediamine), amides (eg, formamide, N, N-dimethylformamide, N, N-dimethylacetamide, etc.), heterocyclic rings (eg, 2 -Pyrrolidone, N-methyl-2-pyrrolidone, cyclohexyl pyrrolidone, 2-oxazolidone, 1,3-dimethyl-2-imidazolidinone), sulfoxides (for example, dimethyl sulfoxide) and the like.

[Water-soluble polymer compound]
The second ink according to the present invention may contain a water-soluble polymer compound for the purpose of suppressing bleeding.

  When an appropriate water-soluble polymer compound is added, the degree of dry thickening immediately after landing of the ink is increased, the fluidity is lowered, and bleeding is suppressed.

  However, if a basic compound and a water-soluble polymer compound are added at a high concentration, precipitation may occur and injection stability may be significantly deteriorated. The type and amount of the water-soluble polymer compound must be carefully selected. is there.

  Examples of water-soluble polymer compounds that can be added to the second ink include polyvinyl pyrrolidone, polyethylene glycol, ethylene oxide propylene oxide copolymer, glycerin polyethylene oxide adduct, glycerin polypropylene adduct, and diglycerin polyethylene oxide addition. Products, diglycerin polypropylene adducts, acrylic copolymer resins, and the like can be preferably used.

  Among them, the acrylic copolymer resin is preferable because it has a relatively small influence on the injection property and can be added in an amount necessary for expressing the effect of suppressing bleeding.

  As acrylic copolymer resin, what copolymerized the hydrophobic monomer and the hydrophilic monomer can be used preferably.

  Examples of hydrophobic monomers include acrylic acid esters (such as n-butyl acrylate, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate), methacrylic acid esters (such as ethyl methacrylate, butyl methacrylate, glycidyl methacrylate), styrene. Etc.

  Examples of the hydrophilic monomer include acrylic acid, methacrylic acid, acrylamide, and the like, and those having an acidic group such as acrylic acid can preferably be those neutralized with a base compound after polymerization.

  As the molecular weight of these resins, those having an average molecular weight of 3000 to 30000 can be used. Preferably, 7000 to 20000 can be used.

  Resin having a Tg of about -30 ° C to 100 ° C can be used. Preferably, about -10 degreeC to 80 degreeC can be used. As the acid value of the resin, an acid value of about 90 mgKOH / g to 200 mgKOH / g can be particularly preferably used. As the polymerization method, it is preferable to use solution polymerization.

  The acidic group derived from the acidic monomer of the resin is preferably partially or completely neutralized with the basic compound component. As the neutralizing base compound in this case, alkali metal-containing basic compounds such as sodium hydroxide and potassium hydroxide, and amines (for example, ammonia, alkanolamine, alkylamine, etc.) can be used.

  In particular, neutralization with amines having a boiling point of less than 200 ° C. is preferable from the viewpoint of suppressing bleeding. In particular, those neutralized with ammonia are preferred.

  When the water-soluble polymer compound is added to the second ink, it is necessary that the polymer compound component is easily removed in the washing step after the heating step after the aqueous ink is discharged to form an image on the fabric. . If a large amount of the polymer compound component remains, it is not preferable because the touch and texture become hard. As the polymer compound component, those having high solubility in dyed water or detergent are preferable.

  Furthermore, it is necessary to exist stably in the second ink, and to cause little occurrence of precipitation and change in physical properties such as viscosity under various storage environments.

  Even when the water-based ink is dried in the vicinity of the ejection opening of the head, it can be easily removed by re-dissolving, re-swelling, or re-dispersing with the water-based ink or the cleaning liquid, and maintenance is easy.

  The amount added to the second ink is preferably in the range of 1% by mass to 10% by mass, although it depends on the type and molecular weight of the polymer compound.

  The second ink according to the present invention can control the surface tension of the ink in order to penetrate deeply into a thick fabric and develop a color without unevenness.

  In this case, the surface tension is preferably controlled in the range of 20 mN / m to 35 mN / m. If it is less than 20 mN / m, the bleeding increases. If it is greater than 35 mN / m, the effect of penetrating to the deep part and coloring uniformly will be insufficient.

  As a method of adjusting the surface tension of the second ink within the above range, it can be adjusted by using an appropriate amount of a low surface tension solvent and an appropriate amount of a surfactant. In particular, it is preferable to adjust by using appropriate amounts of both a low surface tension solvent and a surfactant.

[Low surface tension solvent]
The low surface tension solvent preferably contains 10 to 30% by mass of a solvent having a surface tension of 25 to 40 mN / m. More preferably, it is an embodiment containing 10 to 30% by mass of a solvent having a surface tension of 25 to 35 mN / m.

  Examples of the solvent having a surface tension of 25 to 40 mN / m include water-soluble organic solvents such as glycol ether and 1,2-alkanediol.

  The solvent may be contained alone in an amount of 10 to 30% by mass, or a plurality thereof may be used and the total amount thereof may be contained in an amount of 10 to 30% by mass.

  The method for measuring surface tension is described in general interface chemistry and colloid chemistry reference books. For example, New Experimental Chemistry Course Vol. 18 (Interface and Colloid), The Chemical Society of Japan, Maruzen Co., Ltd. Issue: P.A. 68-117 can be referred to, and specifically, it can be determined by using a ring method (Dunoi method) or a vertical plate method (Wilhelmy method).

  The surface tension was measured using a surface tension meter CBVP type A-3 (Kyowa Science Co., Ltd.).

  Specific water-soluble organic solvents and surface tension values are shown below (the numerical values in parentheses are mN / m).

  Examples of glycol ethers include ethylene glycol monoethyl ether (28.2), ethylene glycol monobutyl ether (27.4), diethylene glycol monoethyl ether (31.8), diethylene glycol monobutyl ether (33.6), and triethylene glycol monobutyl ether. (32.1), propylene glycol monopropyl ether (25.9), dipropylene glycol monomethyl ether (28.8), tripropylene glycol monomethyl ether (30.0) and the like.

  Examples of the 1,2-alkanediol include 1,2-butanediol, 1,2-pentanediol, 1,2-hexanediol (28.1), 1,2-heptanediol, and the like.

[Surfactant]
Various surfactants can be used in the second ink according to the present invention. The surfactant that can be used in the present invention is not particularly limited, but examples thereof include anionic surfactants such as dialkyl sulfosuccinates, alkyl naphthalene sulfonates, fatty acid salts, polyoxyethylene alkyl ethers, polyoxy Nonionic surfactants such as ethylene alkylallyl ethers, acetylene glycols, polyoxyethylene / polyoxypropylene block copolymers, and cationic surfactants such as alkylamine salts and quaternary ammonium salts. In particular, an anionic surfactant and a nonionic surfactant can be preferably used.

  In order to control the surface tension of the water-based ink according to the present invention to 20 mN / m or more and 35 mN / m or less, it is particularly preferable to contain a silicone surfactant or a fluorine surfactant.

  In the second ink according to the present invention, the surface tension of the second ink is preferably controlled to 20 mN / m or more and 35 mN / m or less in order to further penetrate the base compound into the deep part of the fabric. It is preferable to add a surfactant or a fluorosurfactant to control the desired surface tension.

<Silicone-based surfactant or fluorine-based surfactant>
The silicone surfactant is preferably a polyether-modified polysiloxane compound, and examples thereof include KF-351A and KF-642 manufactured by Shin-Etsu Chemical Co., and BYK345, BYK347, and BYK348 manufactured by Big Chemie.

  The fluorine-based surfactant means a compound in which a part or all of the fluorine-based surfactant is substituted with a fluorine atom instead of the hydrogen atom bonded to the carbon of the hydrophobic group of the normal surfactant. Of these, those having a perfluoroalkyl group in the molecule are preferred.

  Among the fluorine-based surfactants, certain types are traded under the trade name Megafac F from Dainippon Ink & Chemicals, and Surflon from Asahi Glass, Minnesota Mining and Under the trade name Fluorad FC from Manufacturing Company, under the trade name Monflor from Imperial Chemical Industry, and Zonyls from EI Dupont Nemeras & Company. It is commercially available under the trade name and also under the trade name Licobet VPF from Farbeberke Hoechst.

  Examples of nonionic fluorosurfactants include Megafax 144D manufactured by Dainippon Ink and Surflon S-141 and 145 manufactured by Asahi Glass Co., and amphoteric fluorosurfactants. Examples of the agent include Surflon S-131 and 132 manufactured by Asahi Glass Co., Ltd.

[Other additives]
A pH adjuster and a solid humectant can be added to the second ink as necessary.

<< Fabric >>
As a fabric used for this invention, it can use for the fabric which consists of all fibers, such as a cellulose fiber, a protein fiber, and a polyester fiber. In addition, ink-jet pretreatment for absorbing ink is not necessary for the fabric, but general pretreatment used in usual dyeing processes such as hair baking, desizing, refining, and bleaching can be performed.

<< Inkjet discharging method, Inkjet dyeing method >>
The first ink and the second ink according to the present invention are applied directly from the inkjet head to the fabric. The order of applying the first ink and the second ink can be arbitrarily selected. A method of applying the first ink to the fabric and then applying the second ink, a method of applying the second ink, and then applying the first ink, or a method of applying the first ink and the second ink simultaneously can be selected.

  Further, in the ink jet discharging method and the ink jet resisting method according to the present invention, the fabric can be colored in advance or later using a removable dye called background dyeing. Any method such as a method or a dyeing method may be used.

[Removable dye]
The removable dye used in the present invention refers to a dye that is susceptible to decomposing action, and is a dye having a partial structure that decomposes under basic conditions such as an ester group or an amide group. Generally, it is an azo dye such as thiazole azo, quinolone azo, or imino. Generally, depending on the type of fiber, such as a reactive dye for cellulose fibers and a disperse dye for polyester fibers, the type of dye is properly used, but the presence or absence of a reducing action is not dependent on such a classification method.

[Method for Applying First Ink and Second Ink to Fabric]
The method of applying the first ink to the fabric and then applying the second ink is the most preferable method for suppressing bleeding. Specifically, the head for the first ink is provided on the upstream side in the fabric conveyance direction. In this method, a head for the second ink is arranged on the downstream side, and the first ink and then the second ink are sequentially printed. In this method, there is room for the first ink to permeate into the fabric and further to dry, so that the bleeding is least likely to occur during image recording with the subsequent second ink.

  In order to promote drying of the first ink, it is preferable to provide a drying zone between the head position for the first ink and the head position for the second ink from the viewpoint of suppressing bleeding.

  A method of simultaneously applying the first ink and the second ink is also preferable because it has the advantage of reducing the apparatus size. A plurality of heads can be arranged on one carriage, and a first ink head and a second ink head can be mounted therein and applied simultaneously.

  The application region of the first ink can be arbitrarily selected. The first ink can be applied to the entire area of the fabric, or can be applied only to a specific area. The first ink suppresses bleeding of the image, and basically may be applied only to the image portion to which the second ink is applied. This has the merit of reducing the consumption of the first ink and lowering the production cost. Further, it is preferable to avoid applying the first ink to a white background because it may lead to contamination of the white background. Further, it is also a preferable form that the amount of the first ink is increased or decreased according to the amount of the second ink applied. In this case, it is preferable to increase the first ink application amount as the ink amount increases.

More specifically, the first ink is not applied to a portion where the second ink is not substantially applied, and the first ink is applied to an area where the total amount of the second ink is greater than 20 ml / m ² for each pixel area. ink minimum 12 ml / ^{m 2} is applied to, the second ink application amount is 20 ml / ^{m 2} less than in the region, applying the first ink in the range of 4 ml / ^{m 2} of 20 ml / ^{m 2} in response to the second ink This is a preferred embodiment.

  The amount of the first ink applied can be increased or decreased depending on the type and concentration of the water-soluble polymer compound in the first ink.

The first ink application amount, be 40 ml / ^{m 2} applied from 10 ml / ^{m 2} with respect to the fabric, from the viewpoint of bleed suppression. Of course, the amount of the first ink applied can be determined at an arbitrary ratio according to the amount of the second ink applied, and the first ink may not be applied to the white background where the second ink is not applied.

  The first ink can be supplied from one or more heads. In particular, it is preferable to supply from a plurality of heads from the viewpoint that unevenness is hardly generated in the applied amount of the first ink.

  When the first ink is applied from a plurality of heads, a plurality of types of first inks may be introduced and applied to each head.

[Fabric heating]
In the ink jet discharging method or ink jet resist method of the present invention, the first ink and the second ink can be applied by heating the fabric. As a heating method, for example, a heater can be arranged around the lower part of the platen and heated to an arbitrary temperature.

  By heating when the first ink is applied, the permeability of the first ink can be controlled. In particular, heating is preferable when it is desired to leave the first ink component near the surface. Also, the drying of the first ink is accelerated, which is preferable from the viewpoint of suppressing bleeding.

  The fabric surface temperature can be heated in the range of 35 ° C to 70 ° C.

  By heating at the time of applying the second ink, it is possible to suppress bleeding and control permeation. The fabric surface temperature can be heated in the range of 35 ° C to 70 ° C.

[Dry]
In the case where the second ink is applied after the first ink is applied, drying is preferably performed after the first ink is applied. In particular, it is particularly preferable to provide a drying zone and evaporate the moisture and the volatile solvent applied by the first ink.

  As a drying method, there are a method of contacting a heated member from the back surface or the front surface, a method of irradiating with an infrared heater, and the like. In these methods, it is preferable to use a blower together to further increase the drying efficiency.

  The pre-dried fabric is preferably subjected to steaming. The conditions may be determined in consideration of the type of fabric and the like, but in an environment with a humidity of 50 to 100% (more preferably 80 to 100%) and a temperature of 90 to 120 ° C (preferably 95 to 105 ° C). 3 to 120 minutes (preferably 5 to 40 minutes). Further, after that, it is preferable to wash with warm water containing a surfactant (preferably a nonionic surfactant). The printed fabric subjected to such post-processing has excellent color development and fastness, and less water-based ink bleeding.

  EXAMPLES Hereinafter, the present invention will be specifically described with reference to examples, but the present invention is not limited thereto. In addition, although the display of "part" or "%" is used in an Example, unless otherwise indicated, "part by mass" or "mass%" is represented.

Example 1
<Preparation of ink set>
[Preparation of first ink]
(Preparation of the first ink 1)
The following additives were added, mixed and dissolved, and then filtered through a 0.8 μm membrane filter to prepare the first ink 1.

Water-soluble polymer compound: polyvinylpyrrolidone (PVP (K15), manufactured by Tokyo Chemical Industry Co., Ltd.)
6% by mass
Liquid humectant: 20% by mass of propylene glycol (PG)
Liquid humectant: Glycerin (Gly) 5% by mass
Solid moisturizer: urea 10% by mass
Water-soluble cationic polymer: diallylamine (DAA) 1% by mass
Ion exchange water was added to finish 100% by mass.

(Preparation of first inks 2 to 19)
First inks 2 to 19 were prepared in the same manner as in the preparation of the first ink 1 except that the composition of each additive was changed as shown in Table 1.

  The details of each additive described in abbreviations in Table 1 are as follows. Moreover, the numerical value of Table 1 represents the mass%.

<Water-soluble polymer compound>
PVP15: Polyvinylpyrrolidone K15, manufactured by Tokyo Chemical Industry Co., Ltd. PVP30: Polyvinylpyrrolidone K30, manufactured by Tokyo Chemical Industry Co., Ltd. PEG: Polyethylene glycol, Mw600, manufactured by Kanto Chemical Co., Ltd. : SC-E450, polyethylene oxide adduct of diglycerin, Sakamoto Pharmaceutical Co., Ltd. P450: SC-P450, polypropylene oxide adduct of diglycerin, Sakamoto Pharmaceutical Co., Ltd. Gly450: Glycerin (EO) 450, ethylene of glycerin Oxide adduct, ethylene oxide molecular weight 450
HEC: Hydroxyethyl cellulose CMC: Carboxymethyl cellulose <Liquid humectant>
PG: Propylene glycol, manufactured by Kanto Chemical Co. Gly: Glycerin, manufactured by Kanto Chemical Co. <Solid moisturizer>
* 1: Dimethylurea <Water-soluble cationic polymer>
DAA: diallylamine, PAS-21Cl, Nittobo DMAA: dimethyldiallylamine, PAS-M-1L, Nittobo AMAC: diallyldimethylammonium chloride, PAS-H-1L, Nittobo [Preparation of second ink ]
(Preparation of the second ink 1)
The following additives were added, mixed, and dissolved, followed by filtration through a 0.8 μm membrane filter to prepare the second ink 1.

Water-soluble organic solvent: ethylene glycol (EG) 10% by mass
Water-soluble organic solvent: Propylene glycol (PG) 25% by mass
Base compound: 5% by mass of potassium carbonate
Ion exchange water was added to finish 100% by mass.

(Preparation of the second ink 2)
The following additives were added, mixed and dissolved, and then filtered through a 0.8 μm membrane filter to prepare the second ink 2.

Water-soluble organic solvent: ethylene glycol (EG) 10% by mass
Water-soluble organic solvent: Propylene glycol (PG) 25% by mass
Base compound: 5% by mass of potassium carbonate
Dispersion A 50% by mass
Ion exchange water was added to finish 100% by mass.

<Preparation of dispersion A>
C. I. Disperse Red 283 10% by mass
BYK-190 Big Chemie (active ingredient 40%) 12.5% by mass
Propylene glycol (PG) 25% by mass
Glycerin (Gly) 10% by mass
Olfine E1010 (acetylene glycol-based activator, manufactured by Shin-Etsu Chemical Co., Ltd.)
0.5% by mass
Ion exchange water was added to finish 100% by mass.

  After the above additives were added and mixed, bead mill dispersion was performed using a MiniCer disperser manufactured by Ashizawa Finetech. Dispersion was performed using 0.5 mm zirconia beads at a peripheral speed of 12 m / s. Dispersion was terminated when the average particle size by light scattering method reached 150 nm, and dispersion A was obtained.

(Preparation of second inks 3 to 5)
The second ink 3 was prepared in the same manner as in the preparation of the second ink 1 except that the same amount of sodium carbonate, potassium hydroxide, and sodium hydroxide was used instead of potassium carbonate (5% by mass) as the base compound. ~ 5 were prepared.

[Preparation of ink sets 1 to 26]
Ink sets 1 to 26 were prepared by combining the prepared first inks 1 to 19 and second inks 1 to 5 as shown in Table 2.

<< Production of Fabric: Production of Polyester Test Cloth B >>
After pre-processing for ink jet (applying a paste) to a polyester desin cloth 91 g / m ² (color dyeing company), using a TP-V manufactured by Konicaminolta and the following disperse ink for background dyeing as a printing ink jet printer After printing, polyester test cloth A was obtained by drying at 80 ° C. for 5 minutes. Next, the polyester test cloth A was subjected to the following fixing treatment A to obtain a polyester test cloth B.

(Preparation of disperse ink for ground dyeing)
The following additives were added, mixed, and dissolved, followed by filtration through a 0.8 μm membrane filter to prepare a ground dye dispersed ink.

Dispersion B 50% by mass
Propylene glycol (PG) 25% by mass
Glycerin (Gly) 10% by mass
Olfine E1010 (supra) 0.5% by mass
Ion exchange water was added to finish 100% by mass.

<Preparation of dispersion B>
C. I. Disperse Blue 139 10% by mass
BYK-190 Big Chemie (active ingredient 40%) 12.5% by mass
Propylene glycol (PG) 25% by mass
Glycerin (Gly) 10% by mass
Olfine E1010 (supra) 0.5% by mass
Ion exchange water was added to finish 100% by mass.

  After the above additives were added and mixed, bead mill dispersion was performed using a MiniCer disperser manufactured by Ashizawa Finetech. Dispersion was performed using 0.5 mm zirconia beads at a peripheral speed of 12 m / s. Dispersion was terminated when the average particle size by light scattering method reached 150 nm, and dispersion B was obtained.

(Fixing treatment A)
The polyester test cloth A was subjected to a color development treatment at 170 ° C. for 10 minutes using an HT steamer. Thereafter, as washing treatment, washing with water for 10 minutes, washing with 50 ° C. hot water for 10 minutes, using a commercially available reducing detergent, washing at 80 ° C. for 5 minutes, washing with 50 ° C. hot water for 10 minutes, and washing with water for 10 minutes were performed. Thereafter, drying was performed at a temperature of 50 ° C. until there was no water.

<Creating a print>
(Evaluation printer)
Of the carriage of the first head 1 on which the four heads of the evaluation printer shown in FIG. 1 are mounted, two heads are filled with the first ink described in Table 2. Next, of the carriage of the second head 2 mounted with six heads, two heads described in Table 2 were filled in two heads.

(Print)
Polyester test cloth B, which is the fabric produced above, was set in the printer for evaluation shown in FIG. The conveyed fabric was uniformly applied to the entire surface of the fabric under the condition of 9 ml / m ² from each of the two heads constituting the first head 1. Next, among the six heads constituting the second head 2, image recording was performed by applying the second ink from two heads. As a recorded image, a solid image of 10 cm × 10 cm of the second ink was printed. This image has a 100% duty and a second ink application amount of about 11 ml / m ² .

  In addition, a drying zone was provided between the first head 1 and the second head 2, and the fabric was heated to 55 ° C. by the heater H2 (4) to dry the first ink applied on the fabric.

  Furthermore, at the time of recording the first ink and the second ink, the fabric was heated to 40 ° C. using platen heaters H1 (3) and H3 (5) provided at the bottom of the fabric. However, the heater H1 (3) was not used in the production of the print sample 23, and the heater H1 (3) and the heater H3 (5) were not used in the production of the print sample 24.

(Post-processing)
After the fabric was printed according to the above method, it was dried at 80 ° C. for 5 minutes. Next, in the same manner as the fixing method A used in the preparation of the polyester test cloth B described above, fixing treatment was performed, and print samples 1 to 26 were obtained.

<< Evaluation of Printed Sample >>
Each of the produced print samples was subjected to the following evaluations.

(Evaluation of smear resistance)
The periphery of the solid image of each of the prepared print samples was visually observed, and the bleeding resistance was evaluated according to the following criteria.

5: No blurring is observed in the peripheral area of the image 4: Slight blurring is observed in the peripheral area of the image, but the quality is good 3: Slight blurring is observed in the peripheral area of the image, but practical use 2: acceptable quality 2: Obvious blurring is observed at the periphery of the image, which is a problem in practical use 1: Vigorous blurring is observed at the periphery of the image; Yes (Evaluation of unevenness resistance)
The density uniformity of the solid image of each of the prepared print samples was visually observed, and unevenness resistance was evaluated according to the following criteria.

5: No unevenness is observed in the solid image 4: Unevenness is not confirmed in the solid image part, but the left and right edges are different in density 3: Uneven noticeable unevenness is observed in the solid image part 2 : Occurrence of obvious unevenness in the solid image portion is observed in several places 1: Very large unevenness in the solid image portion The results obtained as described above are shown in Table 2.

  As is clear from the results shown in Table 2, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to blurring and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

Example 2
<Preparation of ink set>
Ink set 1 and ink set 23 prepared in Example 1 were used.

<< Fabric >>
The polyester test cloth B produced in Example 1 was used as the cloth.

<Creating a print>
In the print creation method described in the first embodiment, the first ink and the second ink constituting the ink set 1 and the ink set 23 are filled with two of the six heads of the second head, and the first ink is filled in the two heads. Then, print samples 27 to 29 were obtained in the same manner except that two heads were filled with the second ink and the first ink and the second ink were simultaneously ejected onto the fabric.

<< Evaluation of Printed Sample >>
Each of the created print samples was evaluated for bleeding resistance and unevenness resistance in the same manner as described in Example 1, and the results obtained are shown in Table 3.

  As is clear from the results shown in Table 3, the printed matter produced by simultaneously ejecting the first ink and the second ink having the configuration defined in the present invention is more resistant to bleeding of the formed image than the comparative example. It can be seen that high-quality printed matter is obtained with excellent unevenness resistance.

Example 3
<Preparation of ink set>
Ink sets 1, 2, 23 and 24 prepared in Example 1 were used.

<< Production of Fabric: Production of Triacetate Test Cloth B >>
Triacetate test cloth A was obtained in the same manner as in the preparation of polyester test cloth A described in Example 1, using triacetate feather double (color dyeing company). Next, the triacetate test cloth B was obtained by performing the following fixing treatment B on the triacetate test cloth A.

<Fixing treatment B>
Using an HT steamer, color development was performed at 170 ° C. for 10 minutes. Thereafter, as washing treatment, washing with water for 10 minutes, washing with 50 ° C. hot water for 10 minutes, using a commercially available reducing detergent, washing at 80 ° C. for 5 minutes, washing with 50 ° C. hot water for 10 minutes, and washing with water for 10 minutes were performed. Thereafter, drying was performed at a temperature of 50 ° C. until there was no water.

<Creating a print>
In the same manner as described in Example 1, images were recorded on the fabric to obtain print samples 30 to 33. However, the post-process was performed according to the following method.

(Post-process)
The fabric was printed and then dried at 80 ° C. for 5 minutes. Next, the fixing process B was performed.

<< Evaluation of Printed Sample >>
Each of the created print samples was evaluated for bleeding resistance and unevenness resistance in the same manner as in the method described in Example 1, and the obtained results are shown in Table 4.

  As is apparent from the results shown in Table 4, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to bleeding and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

Example 4
<Preparation of ink set>
Ink sets 1, 2, 23 and 24 prepared in Example 1 were used.

<< Production of Fabric: Production of Diacetate Test Cloth B >>
A diacetate test cloth A was obtained in the same manner as in the preparation of the polyester test cloth A described in Example 1, using diacetate feather double (color dyeing company). Next, the following fixing treatment C was applied to the diacetate test cloth A to prepare a diacetate test cloth B.

<Fixing treatment C>
Color development was performed for 30 minutes at 100 ° C. using a rocket steamer. Thereafter, as washing treatment, washing with water for 10 minutes, washing with 50 ° C. hot water for 10 minutes, using a commercially available reducing detergent, washing at 80 ° C. for 5 minutes, washing with 50 ° C. hot water for 10 minutes, and washing with water for 10 minutes were performed. Thereafter, drying was performed at a temperature of 50 ° C. until there was no water.

<Creating a print>
In the same manner as in the method described in Example 1, images were recorded on the fabric, and print samples 34 to 37 were obtained. However, the post-process was performed according to the following method.

(Post-process)
The fabric was printed and then dried at 80 ° C. for 5 minutes. Next, the fixing process C was performed.

<< Evaluation of Printed Sample >>
Each of the created print samples was evaluated for bleeding resistance and unevenness resistance in the same manner as described in Example 1, and the obtained results are shown in Table 5.

  As is apparent from the results shown in Table 5, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to blurring and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

Example 5
<Preparation of ink set>
Ink sets 1, 2, 23 and 24 prepared in Example 1 were used.

<< Production of Fabric: Production of Polyester Test Cloth A >>
After pre-processing for ink jet (applying a paste) to a polyester desin cloth 91 g / m ² (color dyeing company), using a TP-V manufactured by Konicaminolta and the following disperse ink for background dyeing as a printing ink jet printer After printing, polyester test cloth A was obtained by drying at 80 ° C. for 5 minutes.

<Creating a print>
In the same manner as in the method described in Example 1, images were recorded on the fabric with the configuration described in Table 6 to obtain print samples 38 to 43. However, in the production of the print sample 40, the heater H1 (3) was not used, and in the production of the print sample 41, the heater H1 (3) and the heater H3 (5) were not used.

<< Evaluation of Printed Sample >>
Each of the created print samples was evaluated for bleeding resistance and unevenness resistance in the same manner as in the method described in Example 1, and the obtained results are shown in Table 6.

  As is apparent from the results shown in Table 6, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to blurring and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

Example 6
<Creation of print sample>
In the method for preparing the print sample described in Example 2, print samples 44 to 46 were obtained in the same manner except that the polyester test cloth A prepared in Example 5 was used instead of the polyester test cloth B. .

<< Evaluation of Printed Sample >>
For each of the prepared print samples, the bleeding resistance and unevenness resistance were evaluated in the same manner as in the method described in Example 1, and the obtained results are shown in Table 7.

  As is apparent from the results shown in Table 7, the printed matter produced by simultaneously ejecting the first ink and the second ink having the configuration defined in the present invention is more resistant to bleeding of the formed image than the comparative example. It can be seen that high-quality printed matter is obtained with excellent unevenness resistance.

Example 7
<Creation of print sample>
In the method for preparing a print sample described in Example 3, the same procedure was used except that the following triacetate test cloth A was used instead of the triacetate test cloth B, and the fixing process B was used instead of the fixing process A. Samples 47-50 were obtained.

(Production of Fabric: Production of Triacetate Test Fabric A)
After performing pretreatment for inkjet (gluing of paste) to Triacetate Hane duplex (color dyeing company), using TP-V made by Konamicolta and the above-mentioned disperse dye ink for ground dyeing, at 80 ° C. Triacetate test cloth A was obtained by drying for 5 minutes.

<< Evaluation of Printed Sample >>
For each of the prepared print samples, the bleeding resistance and unevenness resistance were evaluated in the same manner as in the method described in Example 1, and the obtained results are shown in Table 8.

  As is clear from the results shown in Table 8, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to blurring and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

Example 8
<Creation of print sample>
In the method for preparing a print sample described in Example 4, the cloth was replaced with the diacetate test cloth B, the following diacetate test cloth A was used, and the fixing process C was used instead of the fixing process A. Print samples 51 to 54 were obtained.

(Production of Fabric: Production of Diacetate Test Fabric A)
After performing pre-treatment for inkjet (gluing of paste) to Diacetate Haedo (color dyeing company), solid printing was performed using TP-V manufactured by Konamicolta and the above-mentioned acidic ink for ground dyeing, and then 80 The diacetate test cloth A was obtained by drying at 5 ° C. for 5 minutes.

<< Evaluation of Printed Sample >>
For each of the prepared print samples, bleeding resistance and unevenness resistance were evaluated in the same manner as in the method described in Example 1, and the obtained results are shown in Table 9.

  As is apparent from the results shown in Table 9, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to blurring and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

Example 9
<Preparation of ink set>
Ink sets 1, 2, 23 and 24 prepared in Example 1 were used.

<< Production of Fabric: Production of Polyester Untreated Fabric >>
As a polyester untreated cloth, a polyester decine cloth 91 g / m ² (color dye company) was used as it was.

<Creation of print sample>
An image was recorded on the fabric in the same manner as described in Example 1, and then solid printing was performed using TP-V manufactured by Konicaminolta and the disperse dye ink for background dyeing.

  Subsequently, after drying at 80 degreeC for 5 minute (s), the said fixation process A was given and the print samples 55-60 were obtained.

<< Evaluation of Printed Sample >>
Each of the created print samples was evaluated for bleeding resistance and unevenness resistance in the same manner as in the method described in Example 1, and the obtained results are shown in Table 10.

  As is apparent from the results shown in Table 10, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to blurring and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

Example 10
<Preparation of ink set>
Ink sets 1 and 23 prepared in Example 1 were used.

<< Production of Fabric: Production of Polyester Untreated Fabric >>
As a polyester untreated cloth, a polyester decine cloth 91 g / m ² (color dye company) was used as it was.

<Creation of print sample>
After printing in the same manner as described in Example 2, solid printing was performed using TP-V manufactured by Konicaminolta and the above-mentioned disperse dye ink for ground dyeing.

  Subsequently, after drying at 80 degreeC for 5 minute (s), the said fixation process A was given and the print samples 61-63 were obtained.

<< Evaluation of Printed Sample >>
Each of the created print samples was evaluated for bleeding resistance and unevenness resistance in the same manner as described in Example 1, and the obtained results are shown in Table 11.

  As is apparent from the results shown in Table 11, the printed matter produced by simultaneously ejecting the first ink and the second ink having the configuration defined in the present invention is more resistant to bleeding of the formed image than the comparative example. It can be seen that high-quality printed matter is obtained with excellent unevenness resistance.

Example 11
<Preparation of ink set>
Ink sets 1, 2, 23 and 24 prepared in Example 1 were used.

<Creation of print sample>
In the method for preparing a print sample described in Example 9, the cloth is replaced with an untreated polyester cloth, and the triacetate untreated cloth is used as it is with triacetate feather double (Color Dye Co., Ltd.). Print samples 64-67 were obtained in the same manner except that B was used.

<< Evaluation of Printed Sample >>
For each of the prepared print samples, bleeding resistance and unevenness resistance were evaluated in the same manner as in the method described in Example 1, and the obtained results are shown in Table 12.

  As is clear from the results shown in Table 12, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to blurring and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

Example 12
<Preparation of ink set>
Ink sets 1, 2, 23 and 24 prepared in Example 1 were used.

<Creation of print sample>
In the method for preparing a print sample described in Example 9, the fabric is replaced with an untreated polyester fabric, and the diacetate untreated fabric is used as it is with diacetate feather double (Color Dye Co., Ltd.). Print samples 68 to 71 were obtained in the same manner except that the fixing process C was used.

<< Evaluation of Printed Sample >>
Each of the created print samples was evaluated for bleeding resistance and unevenness resistance in the same manner as in the method described in Example 1, and the obtained results are shown in Table 13.

  As is apparent from the results shown in Table 13, the printed matter produced using the first ink and the second ink having the configuration defined in the present invention is more resistant to blurring and unevenness of the formed image than the comparative example. It can be seen that high quality prints can be obtained.

1 First head 2 Second head 3 Heater H1
4 Heater H2
5 Heater H3
6, 7 Roller

Claims (17)

  An inkjet ink set for fabrics, comprising: a first ink containing water, a liquid humectant, and a water-soluble polymer compound; and a second ink containing water, a base compound, and a water-soluble organic solvent. .   The inkjet ink set for cloth according to claim 1, wherein the first ink contains a solid humectant.   The water-soluble polymer compound is polyvinyl pyrrolidone, polyethylene glycol, ethylene oxide propylene oxide copolymer, glycerin polyethylene oxide adduct, glycerin polypropylene adduct, diglycerin polyethylene oxide adduct, and diglycerin polypropylene adduct. The total amount of the water-soluble polymer compound is 1% by mass or more and less than 10% by mass as a solid content with respect to the total mass of the first ink. Item 3. An inkjet ink set for fabric according to Item 1 or 2.   The inkjet ink set for cloth according to any one of claims 1 to 3, wherein the first ink contains a water-soluble cationic polymer.   The inkjet ink set for cloth according to any one of claims 1 to 4, wherein the first ink contains an inorganic base, and the inorganic base is a potassium salt.   A cloth ink-jet ink set according to any one of claims 1 to 5 is applied to a cloth dyed with a removable dye in advance, and the second ink is applied after the first ink is applied to the cloth. An ink jet discharging method, characterized by comprising:   The inkjet discharging method according to claim 6, wherein the first ink is applied while heating the fabric.   The printer used to apply the first ink and the second ink to the fabric is a printer in which the first ink head and the second ink head are arranged on the same carriage, and the printer performs the scan in one scan. The ink jet discharging method according to claim 6, wherein the first ink and the second ink are applied onto a fabric.   The inkjet discharging method according to claim 6 or 8, wherein the first ink and the second ink are applied while heating the fabric.   A first ink and a second ink are applied to the cloth, which has been previously provided with a removable dye, using the cloth inkjet ink set according to any one of claims 1 to 5. Inkjet dyeing method.   The inkjet dyeing method according to claim 10, wherein the first ink is applied while the fabric is heated.   The printer used to apply the first ink and the second ink to the fabric is a printer in which a first ink head and a second ink head are arranged on the same carriage, and the printer performs the scanning in one scan. The ink-jet dyeing method according to claim 10, wherein the first ink and the second ink are applied onto a fabric.   The inkjet dyeing method according to claim 10 or 12, wherein the first ink and the second ink are applied while heating the fabric.   6. An ink jet protection according to claim 1, wherein after the first ink and the second ink are applied to the fabric, a removable dye is applied using the fabric inkjet ink set according to any one of claims 1 to 5. Dyeing method.   The inkjet dyeing method according to claim 14, wherein the first ink is applied while heating the fabric.   The printer used to apply the first ink and the second ink to the fabric is a printer in which a first ink head and a second ink head are arranged on the same carriage, and in one scan, The ink-jet dyeing method according to claim 14, wherein the first ink and the second ink are applied onto the fabric.   The inkjet dyeing method according to claim 14 or 16, wherein the first ink and the second ink are applied while heating the fabric.

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