Patent Application
20190047299
The present invention relates to an ink-jet printing method.
In ink-jet printing methods, droplets of ink are directly projected onto a printing medium from very fine nozzles and allowed to adhere to the printing medium to form characters or images thereon. The ink-jet printing methods have now been extensively employed not only in printing applications for ordinary consumers but also recently in commercial and industrial printing applications because of easiness of full coloration and adaptability for production of a small number and many kinds of printed materials.
In the commercial and industrial printing applications, for example, there has been proposed a high-speed printing method in which a rolled synthetic resin film is scanned using a stationary printing head of a line printing type.
For example, in Patent Literatures 1 and 2, there have been proposed the ink-jet printing methods in which a high-quality printed material having color images noticeable on a white background is obtained by printing such color images on a surface of a resin sheet or a rolled resin film.
JP 2008-200850A (Patent Literature 1) discloses an ink-jet printing method including the steps of forming a non-white pattern layer on a surface of a transparent film substrate, and then forming a white solid image printing layer on the non-white pattern layer, in which a resolution of the aforementioned non-white pattern layer is higher than a resolution of the white solid image printing layer.
JP 2013-10364A (Patent Literature 2) discloses an ink-jet printing method including the steps of printing a print unit constituted of a white solid image printing layer and a non-white pattern layer on a surface of an elongated transparent film substrate using two liquid ejection means, in which after forming the non-white pattern layer and then drying the non-white pattern layer, the white solid image printing layer is formed on the thus dried non-white pattern layer.
In addition, JP 2014-94495A (Patent Literature 3) discloses an ink-jet printing method that is capable of printing images having excellent rub fastness and excellent peeling resistance, said method including the steps of allowing droplets of a white-based ink composition containing a urethane-based resin to adhere to a printing surface of a soft packaging film to print white-based images thereon, allowing droplets of a color ink composition to adhere to the thus formed white-based images to print color images thereon, and heating the white-based images and the color images at a temperature of higher than 40° C. In Patent Literature 3, as the heating means, there are illustrated forced air heating, radiation heating, electric conduction heating, high-frequency drying and microwave drying.
The present invention relates to an ink-jet printing method using a water-based ink containing a black ink, a chromatic ink and a white ink which each contain a pigment (A), an organic solvent (C) having a boiling point of not lower than 90° C. and lower than 250° C., and water, said method including the following steps 1 to 3:
Step 1: ejecting at least one water-based ink selected from the group consisting of the black ink and the chromatic ink onto a transparent resin printing medium to print an image 1 on the printing medium;
Step 2: ejecting the white ink onto the image 1 obtained in the step 1 to print a white image that covers the image 1 on the printing medium; and
Step 3: heating and drying the resulting printed material from a side of a surface of the printing medium on which the white image obtained in the step 2 is formed, using an infrared heater.
When printing characters or images on a resin printing medium by an ink-jet printing method using a water-based ink, since the resin printing medium is incapable of absorbing water therein unlike a paper printing medium, it is necessary to accelerate drying of the ink to obtain good printed characters or images. When the water-based ink contains an organic solvent having a relatively high boiling point (not lower than 90° C.) in order to obtain good printed characters or images as well as improve ejection properties of the ink, the requirement for accelerating drying of the ink becomes much higher. Furthermore, in high-speed printing using a rolled synthetic resin film in which take-up work of the film is needed, there is an increasing demand for technologies for enhancing a velocity of drying of the ink.
As the technologies for enhancing a velocity of drying of printed materials, an infrared drying system is considered to be effective because this system is capable of drying the printed materials with a high energy immediately after being printed. However, when portions of the printed characters or images which are formed by color inks are irradiated with infrared rays, temperature difference tends to be caused on the surface of the printing medium since infrared absorption amounts of yellow, magenta, cyan and black inks are different from each other. In particular, the portion of the printed characters or images which is formed by the black ink is heated to a higher temperature, so that there tends to occur such a problem that the printing medium suffers from thermal deformation.
Thus, in the ink-jet printing methods described in Patent Literatures 1 to 3, when the infrared drying system is applied thereto in order to enhance a velocity of drying of the printed materials, it is not possible to sufficiently suppress deformation of the resin printing medium and obtain such printed materials that are fully satisfactory when used in practical applications.
The present invention relates to an ink-jet printing method that is capable of obtaining good printed materials that are free of occurrence of color migration and deformation of a printing medium even when printed on a resin printing medium.
Meanwhile, the term “printing” as used herein means a concept that includes printing or typing for printing characters or images, and the term “printed material” as used herein means a concept that includes printed matters or typed materials on which characters or images are printed.
The present inventors have found that according to an inkjet printing method using a specific water-based ink and including a specific step, it is possible to obtain good printed materials that are free of occurrence of color migration and deformation of the printing medium even when printing characters or images on a transparent resin printing medium.
That is, the present invention relates to an ink-jet printing method using a water-based ink containing a black ink, a chromatic ink and a white ink which each contain a pigment (A), an organic solvent (C) having a boiling point of not lower than 90° C. and lower than 250° C., and water, said method including the following steps 1 to 3:
Step 1: ejecting at least one water-based ink selected from the group consisting of the black ink and the chromatic ink onto a transparent resin printing medium to print an image 1 on the printing medium;
Step 2: ejecting the white ink onto the image 1 obtained in the step 1 to print a white image that covers the image 1 on the printing medium; and
Step 3: heating and drying the resulting printed material from a side of a surface of the printing medium on which the white image obtained in the step 2 is formed, using an infrared heater.
According to the present invention, there is provided an ink-jet printing method that is capable of obtaining good printed materials that are free of occurrence of color migration and deformation of a printing medium even when printed on a transparent resin printing medium.
The ink-jet printing method of the present invention is an ink-jet printing method using a water-based ink containing a black ink, a chromatic ink and a white ink which each contain a pigment (A), an organic solvent (C) having a boiling point of not lower than 90° C. and lower than 250° C. (hereinafter also referred to merely as an “organic solvent (C)”), and water, said method including the following steps 1 to 3:
Step 1: ejecting at least one water-based ink selected from the group consisting of the black ink and the chromatic ink onto a transparent resin printing medium to print an image 1 on the printing medium;
Step 2: ejecting the white ink onto the image 1 obtained in the step 1 to print a white image that covers the image 1 on the printing medium; and
Step 3: heating and drying the resulting printed material from a side of a surface of the printing medium on which the white image obtained in the step 2 is formed, using an infrared heater.
According to the ink-jet printing method of the present invention, the image 1 printed by ejecting at least one water-based ink selected from the group consisting of the black ink and the chromatic ink is completely covered with the white ink. As a result, it is considered that since the printed surface of the printing medium is free of occurrence of color unevenness or mottling, the positional variation of infrared absorption amounts on the printed surface is extremely small and therefore no temperature difference on the printed surface upon infrared heating is caused, so that it is possible to quickly dry the resulting printed material without suffering from thermal deformation of the resin printing medium. In addition, in the ink-jet printing method of the present invention, it is considered that by using the organic solvent (C) having a specific boiling point in combination with water, the water-based ink can be improved in wet spreadability on a transparent resin printing medium while suppressing occurrence of color migration of the water-based ink and deformation of the printing medium and maintaining good continuous ejection properties of the ink upon high-speed printing.
The water-based ink used in the present invention (hereinafter also referred to merely as an “ink”) contains a pigment (A), the aforementioned organic solvent (C) and water. Also, the water-based ink may further contain a polymer (B), a surfactant (D) and other components, if required. Meanwhile, the term “water-based” as used in the present specification means that water has a largest content among components of a medium contained in the ink.
The pigment used in the present invention may be any kind of pigment, i.e., may be either an inorganic pigment or an organic pigment.
Specific examples of the inorganic pigment include carbon blacks, metal oxides and the like. The carbon blacks are preferably used as a pigment for black inks. The carbon blacks may include furnace blacks, thermal lamp blacks, acetylene blacks and channel blacks. As a pigment for white inks, there may be used metal oxides such as titanium oxide, zinc oxide, silica, alumina and magnesium oxide, etc. Among these pigments for white inks, preferred is titanium oxide.
Specific examples of the organic pigment include azo pigments, diazo pigments, phthalocyanine pigments, quinacridone pigments, isoindolinone pigments, dioxazine pigments, perylene pigments, perinone pigments, thioindigo pigments, anthraquinone pigments and quinophthalone pigments. The organic pigments are preferably used for chromatic inks. The hue of the organic pigment used in the present invention is not particularly limited, and there may be used any chromatic pigment having a yellow color, a magenta color, a cyan color, a red color, a blue color, an orange color, a green color, etc.
The average particle size of the pigment particles in the black ink and chromatic ink is preferably not less than 60 nm and not more than 180 nm from the viewpoint of improving a tinting power and dispersion stability of the resulting ink. The average particle size of the pigment particles in the white ink is preferably not less than 150 nm and not more than 400 nm from the viewpoint of improving hiding power (whiteness) of the resulting white ink.
The pigment used in the present invention may be in the form of at least one pigment selected from the group consisting of a self-dispersible pigment, and particles formed by dispersing a pigment with the polymer (B).
The self-dispersible pigment that may be used in the present invention means a pigment onto a surface of which at least one hydrophilic functional group (including an anionic hydrophilic group such as a carboxy group and a sulfonic group or a cationic hydrophilic group such as a quaternary ammonium group) is bonded either directly or through the other atom group such as an alkanediyl group having 1 to 12 carbon atoms to thereby render the pigment dispersible in an aqueous medium without using a surfactant or a resin. In order to form a pigment into a self-dispersible pigment, for example, a necessary amount of the hydrophilic functional group may be chemically bonded to the surface of the pigment by an ordinary method. Specific examples of commercially available products of the self-dispersible pigment include “CAB-O-JET 200”, “CAB-O-JET 300”, “CAB-O-JET 352K”, “CAB-O-JET 250A”, “CAB-O-JET 260M”, “CAB-O-JET 270Y”, “CAB-O-JET 450A”, “CAB-O-JET 465M”, “CAB-O-JET 470Y” and “CAB-O-JET 480V” available from Cabot Japan K.K.; “BONJET CW-1”, “BONJET CW-2”, etc., available from Orient Chemical Industries Co., Ltd.; “Aqua-Black 162”, etc., available from Tokai Carbon Co., Ltd.; and “SENSIJET BLACK SDP-100”, “SENSIJET BLACK SDP-1000”, “SENSIJET BLACK SDP-2000”, etc., available from SENSIENT INDUSTRIAL COLORS. The self-dispersible pigment is preferably used in the form of a pigment water dispersion prepared by dispersing the pigment in water.
[Particles Formed by Dispersing Pigment with Polymer (B)]
In the present invention, the pigment may be used in the form of particles formed by dispersing the pigment with the polymer (B). Examples of the configuration of the particles formed by dispersing the pigment with the polymer include 1) particles formed by kneading the pigment and the polymer and then dispersing the resulting kneaded material in a medium such as water; 2) particles formed by stirring the pigment and the polymer in a medium such as water to disperse the pigment in the medium such as water; 3) particles formed by mechanically dispersing the polymer raw material and the pigment to polymerize the polymer raw material and then dispersing the pigment in a medium such as water with the resulting polymer; and the like.
Furthermore, from the viewpoint of improving storage stability of the resulting ink, the polymer that is present in the particles formed by dispersing the pigment with the polymer may be crosslinked with a crosslinking agent. Examples of the crosslinking agent include compounds containing two or more functional groups that are capable of reacting with a functional group contained in the polymer. For example, in the case where the polymer contains a carboxy group, as the preferred crosslinking agent, there may be mentioned a polyglycidyl ether compound of a polyhydric alcohol.
In the present invention, from the viewpoint of improving dispersibility of the pigment as well as from the viewpoint of improving fusing properties of printed characters or images, the water-based ink preferably further contains the polymer (B). Examples of the polymer (B) used in the present invention include condensation-based resins such as polyurethanes and polyesters, and vinyl-based polymers such as acrylic resins, styrene-based resins, styrene-acrylic resins, butadiene-based resins, styrene-butadiene-based resins, vinyl chloride-based resins, vinyl acetate-based resins and acrylic-silicone-based resins. Among these polymers, preferred are vinyl-based polymers.
The weight-average molecular weight of the polymer (B) is preferably not less than 10,000, more preferably not less than 20,000, even more preferably not less than 30,000 and further even more preferably not less than 40,000, and is also preferably not more than 2,500,000 and more preferably not more than 1,000,000, from the viewpoint of improving dispersibility of the pigment as well as from the viewpoint of improving fusing properties of printed characters or images.
The polymer (B) used in the present invention may be used as a pigment dispersing polymer (B-1) for dispersing the pigment and a fusing aid polymer (B-2) for improving rub fastness of the resulting printed materials. These polymers (B-1) and (B-2) may be used in combination with each other.
Examples of the pigment dispersing polymer (B-1) for dispersing the pigment used include condensation-based resins such as polyesters and polyurethanes, and vinyl-based polymers, etc. Among these polymers, from the viewpoint of improving dispersion stability of the pigment, preferred are vinyl-based polymers obtained by addition-polymerizing a vinyl monomer (such as vinyl compounds, vinylidene compounds and vinylene compounds). As the pigment dispersing polymer (B-1), there may be used either appropriately synthetized products or commercially available products.
The weight-average molecular weight of the pigment dispersing polymer (B-1) is preferably not less than 20,000, more preferably not less than 30,000 and even more preferably not less than 40,000, and is also preferably not more than 500,000, more preferably not more than 300,000 and even more preferably not more than 200,000, from the viewpoint of improving dispersibility of the pigment.
Examples of the vinyl-based polymers include polyacrylic acids such as “ARON AC-10SL” available from Toagosei Co., Ltd., and styrene-acrylic resins such as “JONCRYL 67”, “JONCRYL 611”, “JONCRYL 678”, “JONCRYL 680”, “JONCRYL 690” and “JONCRYL 819” all available from BASF Japan, Ltd., etc.
The fusing aid polymer (B-2) is preferably used in the form of pigment-free polymer particles. Examples of components of the fusing aid polymer (B-2) include condensation-based resins such as polyurethanes and polyesters, and vinyl-based polymers such as acrylic resins, styrene-based resins, styrene-acrylic resins, butadiene-based resins, styrene-butadiene-based resins, vinyl chloride-based resins, vinyl acetate-based resins and acrylic-silicone-based resins. Among these polymers, from the viewpoint of promoting drying of the resulting ink on a printing substrate and improving rub fastness of the resulting printed materials, preferred are acrylic resins.
In addition, from the viewpoint of enhancing productivity of the water-based ink, the fusing aid polymer (B-2) is preferably used in the form of a dispersion containing polymer particles. As the fusing aid polymer (B-2), there may be used either appropriately synthesized products or commercially available products.
The fusing aid polymer (B-2) may be produced by copolymerizing a mixture of monomers by known polymerization methods. Examples of the preferred polymerization methods include a phase inversion emulsification method, an emulsion polymerization method and a suspension polymerization method, etc. Among these polymerization methods, more preferred is an emulsion polymerization method or a suspension polymerization method, and even more preferred is an emulsion polymerization method.
Examples of commercially available products of the fusing aid polymer (B-2) include acrylic resins such as “Neocryl A1127” (anionic self-crosslinkable aqueous acrylic resin) available from DSM NeoResins, Inc., and “JONCRYL 390” available from BASF Japan, Ltd.; urethane resins such as “WBR-2018” and “WBR-2000U” both available from Taisei Fine Chemical Co., Ltd.; styrene-butadiene resins such as “SR-100” and “SR102” both available from Nippon A & L Inc.; styrene-acrylic resins such as “JONCRYL 7100”, “JONCRYL 7600”, “JONCRYL 537J”, “JONCRYL PDX-7164”, “JONCRYL 538J” and “JONCRYL 780” all available from BASF Japan, Ltd.; and vinyl chloride-based resins such as “VINYBLAN 700” and “VINYBLAN 701” both available from Nissin Chemical Industry Co., Ltd., etc.
The fusing aid polymer (B-2) may be used in the form of particles dispersed in water. The dispersion of the particles of the fusing aid polymer (B-2) serves for forming a film of the resulting ink on a printing substrate and improving fusing properties of the ink.
The weight-average molecular weight of the fusing aid polymer (B-2) used in the present invention is preferably not less than 10,000, more preferably not less than 20,000 and even more preferably not less than 50,000, and is also preferably not more than 2,500,000 and more preferably not more than 1,000,000, from the viewpoint of improving fusing properties of the resulting ink.
In addition, the average particle size of particles of the fusing aid polymer (B-2) in the dispersion containing the particles of the fusing aid polymer (B-2) or in the resulting ink is preferably not less than 10 nm, more preferably not less than 30 nm and even more preferably not less than 50 nm, and is also preferably not more than 300 nm, more preferably not more than 200 nm, even more preferably not more than 150 nm and further even more preferably not more than 130 nm, from the viewpoint of improving storage stability of the resulting ink.
As the organic solvent (C), there may be used those organic solvents having a boiling point of not lower than 90° C. and lower than 250° C. from the viewpoint of suppressing occurrence of color migration of the resulting water-based ink and deformation of the printing medium as well as from the viewpoint of improving continuous ejection properties of the ink upon high-speed printing. The boiling point of the organic solvent (C) is preferably not lower than 130° C., more preferably not lower than 140° C. and even more preferably not lower than 150° C., and is also preferably not higher than 245° C., more preferably not higher than 240° C. and even more preferably not higher than 235° C., from the same viewpoints as described above.
Examples of the organic solvent (C) include a polyhydric alcohol (c-1) and a glycol ether (c-2), etc.
Examples of the aforementioned polyhydric alcohol (c-1) include 1,2-alkanediols such as ethylene glycol (boiling point (b.p.) 197° C.), propylene glycol (b.p. 188° C.), 1,2-butanediol (b.p. 193° C.), 1,2-pentanediol (b.p. 206° C.) and 1,2-hexanediol (b.p. 223° C.), diethylene glycol (b.p. 245° C.), polyethylene glycol, dipropylene glycol (b.p. 232° C.), 1,3-propanediol (b.p. 210° C.), 1,3-butanediol (b.p. 208° C.), 1,4-butanediol (b.p. 230° C.), 3-methyl-1,3-butanediol (b.p. 203° C.), 1,5-pentanediol (b.p. 242° C.), 2-methyl-2,4-pentanediol (b.p. 196° C.), 1,2,6-hexanetriol (b.p. 178° C.), 1,2,4-butanetriol (b.p. 190° C.), 1,2,3-butanetriol (b.p. 175° C.) and petriol (b.p. 216° C.).
Among these polyhydric alcohols, from the viewpoint of improving storage stability and continuous ejection properties of the resulting ink, preferred is at least one polyhydric alcohol selected from the group consisting of alkanediols having not less than 2 and not more than 6 carbon atoms, such as propylene glycol, diethylene glycol and 1,2-hexanediol, and polypropylene glycols having a molecular weight of 500 to 1000, and more preferred is at least one polyhydric alcohol selected from the group consisting of 1,2-alkanediols having not less than 3 and not more than 4 carbon atoms, such as propylene glycol and diethylene glycol, and the aforementioned polypropylene glycols.
(Glycol Ether (c-2))
Specific examples of the glycol ether (c-2) include alkylene glycol monoalkyl ethers and alkylene glycol dialkyl ethers. Among these compounds, from the viewpoint of improving continuous ejection properties of the resulting ink as well as from the viewpoint of obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium, preferred are alkylene glycol monoalkyl ethers. The number of carbon atoms in an alkyl group of the alkylene glycol monoalkyl ethers is preferably not less than 1, more preferably not less than 2 and even more preferably not less than 3, and is also preferably not more than 6 and more preferably not more than 4. The alkyl group of the alkylene glycol monoalkyl ethers may be in the form of either a straight chain or a branched chain.
Specific examples of the alkylene glycol monoalkyl ethers include ethylene glycol ethyl ether (b.p. 136° C.), ethylene glycol isopropyl ether (b.p. 144° C.), ethylene glycol propyl ether (b.p. 151° C.), ethylene glycol butyl ether (b.p. 171° C.), diethylene glycol methyl ether (b.p. 194° C.), diethylene glycol ethyl ether (b.p. 202° C.), diethylene glycol isopropyl ether (b.p. 207° C.), diethylene glycol isobutyl ether (b.p. 230° C.), diethylene glycol butyl ether (b.p. 230° C.), triethylene glycol methyl ether (b.p. 248° C.), dipropylene glycol butyl ether (b.p. 231° C.), dipropylene glycol methyl ether (b.p. 189° C.) and tripropylene glycol methyl ether (b.p. 243° C.).
Of these alkylene glycol monoalkyl ethers, preferred is at least one compound selected from the group consisting of ethylene glycol isopropyl ether, ethylene glycol propyl ether, diethylene glycol methyl ether, diethylene glycol isopropyl ether, diethylene glycol isobutyl ether and diethylene glycol butyl ether, and more preferred is at least one compound selected from the group consisting of ethylene glycol isopropyl ether, diethylene glycol isopropyl ether and diethylene glycol isobutyl ether.
In the present invention, the water-based ink may also contains, in addition to the aforementioned organic solvent (C), those organic solvents that may be usually compounded in the water-based ink, such as the other alcohols, alkyl ethers of the alcohols, glycol ethers, nitrogen-containing heterocyclic compounds such as N-methyl-2-pyrrolidone, amides, amines and sulfur-containing compounds.
For example, 1,6-hexanediol (b.p. 250° C.), triethylene glycol (b.p. 285° C.), tripropylene glycol (b.p. 273° C.), polypropylene glycol (b.p. not lower than 250° C.) and glycerin (b.p. 290° C.), etc., may be used in combination with the aforementioned compound having a boiling point of lower than 250° C.
The water-based ink used in the present invention preferably also contains a surfactant (D) from the viewpoint of improving continuous ejection properties of the ink and obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium. As the surfactant (D), there are preferably used those surfactants containing a silicone-based surfactant (d-1).
The silicone-based surfactant (d-1) is not particularly limited, and any suitable silicone-based surfactant may be appropriately selected and used as the silicone-based surfactant (d-1) according to the objects and applications of the water-based ink. Among these silicone-based surfactants, from the viewpoint of suppressing increase in viscosity of the resulting ink, improving continuous ejection properties of the ink and obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium, a polyether-modified silicone-based surfactant is preferably used.
The polyether-modified silicone-based surfactant is capable of suppressing increase in viscosity of the resulting ink and occurrence of intercolor bleeding between the inks. Therefore, it is considered that the polyether-modified silicone-based surfactant contributes to production of good printed materials that are free of occurrence of color migration upon high-speed printing.
The polyether-modified silicone-based surfactant has such a structure that a hydrocarbon group bonded to a side chain and/or a terminal end of a silicone oil is substituted with a polyether group. Examples of the suitable polyether group of the polyether-modified silicone-based surfactant include a polyethyleneoxy group, a polypropyleneoxy group and a polyalkyleneoxy group formed by addition-bonding an ethyleneoxy group (EO) and a propyleneoxy group (a trimethyleneoxy group or a propane-1,2-diyloxy group; PO) to each other in a block form or a random form. More specifically, as the polyether-modified silicone-based surfactant, there may be used a compound formed by grafting a polyether group to a main chain of a silicone, a compound formed by bonding a silicone and a polyether group to each other in a block form, etc.
The HLB value of the polyether-modified silicone-based surfactant is preferably not less than 3.0, more preferably not less than 4.0 and even more preferably not less than 4.5 from the viewpoint of improving solubility of the polyether-modified silicone-based surfactant in the water-based ink. The term “HLB” as used herein means the value indicating an affinity of the surfactant to water and an oil, and can be calculated according to the following formula by Griffin method. Meanwhile, as the “hydrophilic group contained in surfactant” shown in the following formula, there may be mentioned, for example, a hydroxy group and an ethyleneoxy group.
HLB=20×[(molecular weight of hydrophilic group contained in surfactant)/(molecular weight of surfactant)]
Specific examples of the polyether-modified silicone-based surfactant include “KF” series products available from Shin-Etsu Chemical Industry Co., Ltd., “SILFACE SAG005” available from Nissin Chemical Industry Co., Ltd., and “BYK-348” available from BYK Chemie Japan K.K., etc.
In the present invention, as the surfactant (D), the surfactants other than the polyether-modified silicone-based surfactant may be used in combination therewith. Among the surfactants other than the polyether-modified silicone-based surfactant, from the viewpoint of attaining good applicability to the ink, preferred is a nonionic surfactant.
Examples of the nonionic surfactant include (1) alkyl ethers, alkenyl ethers, alkynyl ethers or aryl ethers of polyoxyalkylenes which are produced by adding ethyleneoxide, propyleneoxide or butyleneoxide (hereinafter collectively referred to as an “alkyleneoxide”) to a saturated or unsaturated, linear or branched higher alcohol having 8 to 22 carbon atoms, a polyhydric alcohol or an aromatic alcohol, (2) esters of a higher alcohol containing a saturated or unsaturated, linear or branched hydrocarbon group having 8 to 22 carbon atoms, and a polyvalent fatty acid, (3) polyoxyalkylene aliphatic amines containing a linear or branched alkyl group or alkenyl group having 8 to 20 carbon atoms, and (4) ester compounds of a higher fatty acid having 8 to 22 carbon atoms and a polyhydric alcohol, or compounds produced by adding an alkyleneoxide to the ester compounds.
Examples of commercially available products of the nonionic surfactant include “SURFYNOL” series products available from Nissin Chemical Industry Co., Ltd., and Air Products & Chemicals, Inc., “ACETYLENOL” series products available from Kawaken Fine Chemicals Co., Ltd., and “EMULGEN 120” (polyoxyethylene lauryl ether) available from Kao Corporation.
The contents of the respective components in the water-based ink used in the present invention as well as various properties of the water-based ink are as follows.
The content of the pigment (A) in the black or chromatic water-based ink is preferably not less than 2.0% by mass, more preferably not less than 4.0% by mass and even more preferably not less than 6.0% by mass from the viewpoint of enhancing optical density of the water-based ink printed. Also, the content of the pigment (A) in the black or chromatic water-based ink is preferably not more than 30.0% by mass, more preferably not more than 20% by mass, even more preferably not more than 15% by mass and further even more preferably not more than 10.0% by mass from the viewpoint of reducing viscosity of the water-based ink upon volatilization of the solvent therefrom as well as from the viewpoint of improving continuous ejection properties of the water-based ink and obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium.
The content of the pigment (A) in the white water-based ink is preferably not less than 4.0% by mass, more preferably not less than 6.0% by mass and even more preferably not less than 8.0% by mass, and is also preferably not more than 40% by mass, more preferably not more than 30% by mass, even more preferably not more than 20% by mass and further even more preferably not more than 15% by mass, from the viewpoint of completely covering the image 1 printed by the black and chromatic inks with the white ink to thereby eliminate color unevenness or mottling of the printed surface and prevent occurrence of thermal deformation of the resin printing medium.
The content of the polymer (B) in the black or chromatic water-based ink is preferably not less than 1.0% by mass, more preferably not less than 2.0% by mass and even more preferably not less than 3.0% by mass, and is also preferably not more than 20% by mass, more preferably not more than 13% by mass and even more preferably not more than 8.0% by mass, from the viewpoint of improving fusing properties of the water-based ink. The content of the polymer (B) in the black or chromatic water-based ink as used herein means a total content of the pigment dispersing polymer (B-1) of the pigment-containing polymer particles and the fusing aid polymer (B-2). Furthermore, when using a crosslinking agent, the content of the polymer (B) in the water-based ink means a total content of these polymers and the crosslinking agent.
In addition, in the case where the polymer (B) is used as the pigment dispersing polymer (B-1), the content of the pigment dispersing polymer (B-1) in the black or chromatic water-based ink is preferably not less than 0.01% by mass, more preferably not less than 0.05% by mass and even more preferably not less than 0.1% by mass, and is also preferably not more than 10% by mass, more preferably not more than 7.0% by mass and even more preferably not more than 5.0% by mass, from the viewpoint of improving fusing properties of the water-based ink.
Furthermore, in the case where the polymer (B) is used as the fusing aid polymer (B-2) in the ink, the content of the fusing aid polymer (B-2) in the black or chromatic water-based ink is preferably not less than 0.9% by mass, more preferably not less than 1.0% by mass and even more preferably not less than 1.2% by mass, and is also preferably not more than 10% by mass, more preferably not more than 6.0% by mass and even more preferably not more than 3.0% by mass, from the viewpoint of improving fusing properties of the water-based ink.
The content of the polymer (B) in the white water-based ink is preferably not less than 1.0% by mass, more preferably not less than 2.0% by mass and even more preferably not less than 3.0% by mass, and is also preferably not more than 20% by mass, more preferably not more than 13% by mass and even more preferably not more than 8.0% by mass, from the viewpoint of improving fusing properties of the water-based ink. The content of the polymer (B) in the white water-based ink as used herein means a total content of the pigment dispersing polymer (B-1) of the pigment-containing polymer particles and the fusing aid polymer (B-2). Furthermore, when using a crosslinking agent, the content of the polymer (B) in the white water-based ink means a total content of these polymers and the crosslinking agent.
In addition, in the case where the polymer (B) is used as the pigment dispersing polymer (B-1), the content of the pigment dispersing polymer (B-1) in the white water-based ink is preferably not less than 0.01% by mass, more preferably not less than 0.05% by mass and even more preferably not less than 0.1% by mass, and is also preferably not more than 10% by mass, more preferably not more than 7.0% by mass and even more preferably not more than 5.0% by mass, from the viewpoint of improving fusing properties of the water-based ink.
Furthermore, in the case where the polymer (B) is used as the fusing aid polymer (B-2) in the ink, the content of the fusing aid polymer (B-2) in the white water-based ink is preferably not less than 0.9% by mass, more preferably not less than 1.0% by mass and even more preferably not less than 1.2% by mass, and is also preferably not more than 10% by mass, more preferably not more than 6.0% by mass and even more preferably not more than 3.0% by mass, from the viewpoint of improving fusing properties of the water-based ink.
The content of the organic solvent (C) in the black or chromatic water-based ink is preferably not less than 15% by mass, more preferably not less than 20% by mass and even more preferably not less than 25% by mass, and is also preferably not more than 45% by mass, more preferably not more than 40% by mass and even more preferably not more than 35% by mass, from the viewpoint of improving continuous ejection properties of the water-based ink.
The content of the polyhydric alcohol (c-1) in the black or chromatic water-based ink is preferably not less than 10% by mass, more preferably not less than 15% by mass and even more preferably not less than 20% by mass, and is also preferably not more than 45% by mass, more preferably not more than 40% by mass and even more preferably not more than 35% by mass, from the viewpoint of improving storage stability and continuous ejection properties of the water-based ink.
The content of the glycol ether (c-2) in the black or chromatic water-based ink is preferably not less than 1% by mass, more preferably not less than 2% by mass and even more preferably not less than 3% by mass, and is also preferably not more than 15% by mass, more preferably not more than 12% by mass and even more preferably not more than 8% by mass, from the viewpoint of improving storage stability and continuous ejection properties of the water-based ink.
The content of a high-boiling organic solvent having a boiling point of not lower than 250° C. in the black or chromatic water-based ink used in the present invention is preferably not more than 5% by mass, more preferably not more than 4% by mass and even more preferably not more than 3% by mass from the viewpoint of imparting adequate drying properties to the water-based ink and inhibiting occurrence of color migration, upon high-speed printing.
The content of the organic solvent (C) in the white water-based ink is preferably not less than 15% by mass, more preferably not less than 20% by mass and even more preferably not less than 25% by mass, and is also preferably not more than 45% by mass, more preferably not more than 40% by mass and even more preferably not more than 35% by mass, from the viewpoint of improving continuous ejection properties of the water-based ink.
The content of the polyhydric alcohol (c-1) in the white water-based ink is preferably not less than 10% by mass, more preferably not less than 15% by mass and even more preferably not less than 20% by mass, and is also preferably not more than 45% by mass, more preferably not more than 40% by mass and even more preferably not more than 35% by mass, from the viewpoint of improving storage stability and continuous ejection properties of the water-based ink.
The content of the glycol ether (c-2) in the white water-based ink is preferably not less than 1% by mass, more preferably not less than 2% by mass and even more preferably not less than 3% by mass, and is also preferably not more than 15% by mass, more preferably not more than 12% by mass and even more preferably not more than 8% by mass, from the viewpoint of improving storage stability and continuous ejection properties of the water-based ink.
The content of a high-boiling organic solvent having a boiling point of not lower than 250° C. in the white water-based ink used in the present invention is preferably not more than 5% by mass, more preferably not more than 4% by mass and even more preferably not more than 3% by mass from the viewpoint of imparting adequate drying properties to the water-based ink and inhibiting occurrence of color migration, upon high-speed printing.
The total content of the surfactant (D) in the black or chromatic water-based ink is preferably not less than 0.01% by mass, more preferably not less than 0.05% by mass and even more preferably not less than 0.1% by mass, and is also preferably not more than 3.0% by mass, more preferably not more than 2.0% by mass and even more preferably not more than 1.0% by mass, from the viewpoint of suppressing increase in viscosity of the water-based ink and improving continuous ejection properties of the water-based ink as well as from the viewpoint of obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium.
The total content of the surfactant (D) in the white water-based ink is preferably not less than 0.01% by mass, more preferably not less than 0.05% by mass and even more preferably not less than 0.1% by mass, and is also preferably not more than 3.0% by mass, more preferably not more than 2.0% by mass and even more preferably not more than 1.0% by mass, from the viewpoint of suppressing increase in viscosity of the water-based ink and improving continuous ejection properties of the water-based ink as well as from the viewpoint of obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium.
The content of water in the black or chromatic water-based ink is preferably not less than 10% by mass, more preferably not less than 12% by mass and even more preferably not less than 15% by mass, and is also preferably not more than 50% by mass, more preferably not more than 40% by mass and even more preferably not more than 30% by mass, from the viewpoint of improving continuous ejection properties and storage stability of the water-based ink as well as from the viewpoint of obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium.
The content of water in the white water-based ink is preferably not less than 10% by mass, more preferably not less than 12% by mass and even more preferably not less than 15% by mass, and is also preferably not more than 50% by mass, more preferably not more than 40% by mass and even more preferably not more than 30% by mass, from the viewpoint of improving continuous ejection properties and storage stability of the water-based ink as well as from the viewpoint of obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium.
The water-based ink used in the present invention may also contain, in addition to the aforementioned components, various ordinary additives such as a humectant, a wetting agent, a penetrant, a defoaming agent, an antiseptic agent, a mildew-proof agent and a rust preventive.
In the case where the water-based ink is in the form of a black ink or a chromatic ink, the average particle size of the particles contained in the water-based ink is preferably not less than 40 nm, more preferably not less than 60 nm and even more preferably not less than 80 nm, and is also preferably not more than 200 nm, more preferably not more than 180 nm, even more preferably not more than 150 nm and further even more preferably not more than 120 nm, from the viewpoint of improving storage stability and ejection properties of the water-based ink.
In the case where the water-based ink is in the form of a white ink, the average particle size of the particles contained in the white water-based ink is preferably not less than 100 nm, more preferably not less than 150 nm and even more preferably not less than 200 nm, and is also preferably not more than 400 nm, more preferably not more than 350 nm, even more preferably not more than 300 nm and further even more preferably not more than 280 nm, from the viewpoint of covering the image 1 printed by a black ink and/or a chromatic ink with the white ink.
In the case where the water-based ink is in the form of a black ink or a chromatic ink, the static surface tension of the water-based ink as measured at 20° C. is preferably not less than 22 mN/m, more preferably not less than 24 mN/m and even more preferably not less than 25 mN/m, and is also preferably not more than 45 mN/m, more preferably not more than 40 mN/m and even more preferably not more than 35 mN/m, from the viewpoint of improving ejection durability of the water-based ink.
In the case where the water-based ink is in the form of a white ink, the static surface tension of the water-based ink as measured at 20° C. is preferably not less than 22 mN/m, more preferably not less than 24 mN/m and even more preferably not less than 25 mN/m, and is also preferably not more than 45 mN/m, more preferably not more than 40 mN/m and even more preferably not more than 35 mN/m, from the viewpoint of improving ejection durability of the water-based ink.
In the case where the water-based ink is in the form of a black ink or a chromatic ink, the viscosity of the water-based ink as measured at 32° C. is preferably not less than 2.0 mPa·s, more preferably not less than 3.0 mPa·s and even more preferably not less than 5.0 mPa·s, and is also preferably not more than 12 mPa·s, more preferably not more than 9.0 mPa·s and even more preferably not more than 7.0 mPa·s, from the viewpoint of improving continuous ejection properties of the water-based ink.
In the case where the water-based ink is in the form of a white ink, the viscosity of the water-based ink as measured at 32° C. is preferably not less than 2.0 mPa·s, more preferably not less than 3.0 mPa·s and even more preferably not less than 5.0 mPa·s, and is also preferably not more than 12 mPa·s, more preferably not more than 9.0 mPa·s and even more preferably not more than 7.0 mPa·s, from the viewpoint of improving continuous ejection properties of the water-based ink.
In the case where the water-based ink is in the form of a black ink or a chromatic ink, the pH value of the water-based ink is preferably not less than 7.0, more preferably not less than 8.0, even more preferably not less than 8.5 and further even more preferably not less than 8.7 from the viewpoint of improving storage stability and continuous ejection properties of the water-based ink as well as from the viewpoint of obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium, and is also preferably not more than 11.0 and more preferably not more than 10.0 from the viewpoint of improving resistance of members to the water-based ink and suppressing skin irritation.
In the case where the water-based ink is in the form of a white ink, the pH value of the water-based ink is preferably not less than 7.0, more preferably not less than 8.0, even more preferably not less than 8.5 and further even more preferably not less than 8.7 from the viewpoint of improving storage stability and continuous ejection properties of the water-based ink as well as from the viewpoint of obtaining good printed materials that are free of occurrence of color migration or deformation of the printing medium, and is also preferably not more than 11.0 and more preferably not more than 10.0 from the viewpoint of improving resistance of members to the water-based ink and suppressing skin irritation.
Meanwhile, the average particle size, static surface tension, viscosity and pH value of the water-based ink may be measured by the methods described in Examples below.
The ink-jet printing method of the present invention includes the following steps 1 to 3 for printing characters or images on a printing medium:
Step 1; ejecting at least one water-based ink selected from the group consisting of the black ink and the chromatic ink onto a transparent resin printing medium to print an image 1 on the printing medium;
Step 2: ejecting the white ink onto the image 1 obtained in the step 1 to print a white image that covers the image 1 on the printing medium; and
Step 3: heating and drying the resulting printed material from a side of a surface of the printing medium on which the white image obtained in the step 2 is formed, using an infrared heater.
The step 1 is the step of ejecting at least one water-based ink selected from the group consisting of the black ink and the chromatic ink onto the transparent resin printing medium to print an image 1 on the printing medium.
The transparent resin printing medium used in the present invention may be in the form of either a sheet of paper or a rolled paper. However, from the viewpoint of enhancing productivity of printed materials, among them, preferred is a rolled printing medium. The transparent resin printing medium as used herein means a resin printing medium having transparency enough to recognize the printed characters or images from a surface of the printing medium opposed to the surface thereof on which the characters or images are printed.
As the transparent resin printing medium, there may be mentioned a transparent synthetic resin film. Examples of the transparent synthetic resin film as the transparent resin printing medium include a polyester film, a polyvinyl chloride film, a polypropylene film, a polyethylene film, a nylon film, etc. These films may be in the form of any of a biaxially stretched film, a monoaxially stretched film and a non-stretched film. Among these films, preferred are a polyester film and a stretched polypropylene film, and more preferred are a polyester film such as a polyethylene terephthalate film subjected to a surface treatment such as a corona discharge treatment, and a biaxially stretched polypropylene film.
Examples of commercially available products of the transparent synthetic resin film include “LUMIRROR T60” (polyethylene terephthalate) available from Toray Industries, Inc., “TAIKO FE2001” (corona-treated polyethylene terephthalate) available from Futamura Chemical Co, Ltd., “PVC80B P” (polyvinyl chloride) available from Lintec Corporation, “KINATH KEE 70CA” (polyethylene) available from Lintec Corporation, “YUPO SG90 PAT1” (polypropylene) available from Lintec Corporation and “BONYL RX” (nylon) available from Kohjin Film & Chemicals Co., Ltd., etc.
In the present invention, there may be used any types of printing heads including a serial-type printing head and a line-type printing head, but the line-type printing head is preferably used in the present invention. The line-type printing head is a printing head of an elongated shape having a length near a width of the printing medium. In the ink-jet printing apparatus using the line-type printing head, while keeping the printing head in a stationery state and moving the printing medium along a transporting direction thereof, droplets of the ink are ejected from openings of nozzles of the printing head in association with the movement of the printing medium, whereby it is possible to allow the ink droplets to adhere onto the printing medium to print characters or images, etc., thereon.
The ink droplets are preferably ejected by a piezoelectric method. In the piezoelectric method, the ink droplets are ejected from a number of nozzles communicated with respective pressure chambers by vibrating a wall surface of the respective pressure chambers by means of a piezoelectric element. Meanwhile, in the present invention, there may also be used a thermal method for ejecting the ink droplets.
The voltage applied to the printing head is preferably not less than 5 V, more preferably not less than 10 V and even more preferably not less than 15 V, and is also preferably not more than 40 V, more preferably not more than 35 V and even more preferably not more than 30 V, from the viewpoint of conducting the high-speed printing with a high efficiency, etc.
The drive frequency of the printing head is preferably not less than 10 kHz, more preferably not less than 15 kHz and even more preferably not less than 18 kHz, and is also preferably not more than 80 kHz, more preferably not more than 70 kHz and even more preferably not more than 60 kHz, from the viewpoint of conducting the high-speed printing with a high efficiency, etc. The amount of the ink droplets ejected is preferably not less than 0.5 pL, more preferably not less than 1.0 pL, even more preferably not less than 1.5 pL and further even more preferably not less than 1.8 pL, and is also preferably not more than 30 pL, more preferably not more than 20 pL and even more preferably not more than 10 pL, as calculated per one ink droplet ejected, from the viewpoint of maintaining accuracy of impact positions of the ink droplets and improving quality of printed characters or images.
The printing head resolution is preferably not less than 400 dpi (dot/inch), more preferably not less than 500 dpi and even more preferably not less than 550 dpi.
From the viewpoint of reducing viscosity of the water-based ink and improving continuous ejection properties of the water-based ink, the inside temperature of the printing head, preferably a line-type printing head, upon the printing, is preferably controlled to not lower than 20° C., more preferably not lower than 25° C. and even more preferably not lower than 30° C., and is also preferably controlled to not higher than 45° C., more preferably not higher than 40° C. and even more preferably not higher than 38° C.
The temperature of the surface of the printing medium opposed to an ink-ejection region of the printing head, preferably the line-type printing head, is preferably controlled to not lower than 25° C., more preferably not lower than 30° C. and even more preferably not lower than 35° C., and is also preferably controlled to not higher than 65° C., more preferably not higher than 60° C. and even more preferably not higher than 55° C. Also, the aforementioned temperature of the surface of the printing medium is preferably controlled to not lower than 35° C. and more preferably not lower than 40° C. from the viewpoint of accelerating fusing and solidification of the water-based ink on the printing medium.
The transportation speed of the printing medium is preferably not less than 3 m/min, more preferably not less than 10 m/min, even more preferably not less than 20 m/min, further even more preferably not less than 30 m/min and still further even more preferably not less than 40 m/min from the viewpoint of enhancing productivity of printed materials. The transportation speed of the printing medium means a velocity of movement of the printing medium in the direction along which the printing medium is moved upon the printing. In the present invention, the transportation speed of the printing medium upon printing is also referred to as a “printing speed”.
After ejecting the black ink and/or the chromatic ink onto the printing medium in the step 1 to print the image 1 thereon, the black ink and/or the chromatic ink thus ejected are preferably fused/cured on the printing medium with fusing/curing means so as to prevent droplets of the respective inks from suffering from intercolor bleeding therebetween even when the inks are successively ejected from the next printing heads.
The term “fusing” as used herein means a concept including both penetration of the inks impacted onto the printing medium into fibers of paper thereof and drying of the inks from the surface of the printing medium, and also indicates such a condition that the ink impacted on the surface of the printing medium is no longer present in the form of droplets thereon. In addition, the term “curing” as used herein means such a condition that the ink droplets impacted onto the printing medium are solidified so that the ink is fixed onto the surface of the printing medium.
Examples of the fusing/curing means include an apparatus capable of applying a thermal energy to the inks on the printing medium, such as a heater, a hot-air fan, etc.
The step 2 is the step of ejecting the white ink onto the image 1 obtained in the step 1 to print a white image that covers the image 1 on the printing medium.
In the step 2, the white ink is ejected onto the image 1 formed by at least one water-based ink selected from the group consisting of the black ink and the chromatic ink to cover and hide the image 1 therewith, so that the image 1 may be printed with a background formed by the white ink (more specifically, such a condition that the image 1 can be recognized from a rear surface of the printing medium). By conducting the step 2, color unevenness or mottling of the inks on the printed surface can be eliminated, so that even when heating the resulting printed material by an infrared heater in the step 3, the positional variation of infrared absorption amounts on the printed surface becomes extremely small, so that it is possible to prevent occurrence of thermal deformation of the resin printing medium.
The temperature of the surface of the printing medium onto which the white ink is ejected is preferably not lower than 25° C., more preferably not lower than 30° C. and even more preferably not lower than 35° C., and is also preferably not higher than 65° C., more preferably not higher than 60° C. and even more preferably not higher than 55° C. In addition, the temperature of the surface of the printing medium is preferably not lower than 35° C. and more preferably not lower than 40° C. from the viewpoint of accelerating fusing and solidification of the water-based ink on the printing medium. The printing medium may be heated or cooled in order to control the temperature of the surface of the printing medium. Examples of the heating means used include an apparatus capable of applying a thermal energy to the inks on the printing medium, such as a heater, a hot-air fan, etc.
The step 3 is the step of heating and drying the resulting printed material from a side of a surface of the printing medium on which the white image obtained in the step 2 is formed, using an infrared heater.
The infrared heater may be a heating element provided with a composite oxide film containing Si, Fe, Zr, Ti, Mn, etc., which is deposited on a surface of quartz glass, ceramics, etc.
As the infrared radiation, there is preferably used near infrared radiation through mid-infrared radiation. Examples of the infrared heater include a short-wave infrared heater, a carbon infrared heater, a medium-wave infrared heater and the like. Among these infrared heaters, from the viewpoint of heating and drying the surface of the printing medium on which the white image is formed, for a short period of time with high productivity of printed materials, preferred is a short-wave infrared heater or a carbon infrared heater, and more preferred is a short-wave infrared heater.
The distance between the infrared heater and the resin printing medium is preferably not less than 100 mm and more preferably not less than 130 mm, and is also preferably not more than 200 mm and more preferably not more than 170 mm.
The irradiation conditions of the short-wave infrared heater include a rated voltage of 220 V, an output of 3000 to 5000 W, a coil temperature of 1400 to 2500° C. and a maximum energy wavelength of about 1.1 to about 1.7 μm.
The irradiation energy density of the short-wave infrared radiation is preferably not less than 40 kw/m2, more preferably not less than 45 kw/m2, even more preferably not less than 50 kw/m2, further even more preferably not less than 60 kw/m2, still further even more preferably not less than 70 kw/m2 and still further even more preferably not less than 80 kw/m2 from the viewpoint of fully drying the white image.
The irradiation time of the short-wave infrared radiation is preferably not less than 0.2 second, more preferably not less than 0.5 second, even more preferably not less than 0.8 second, further even more preferably not less than 1.0 second and still further even more preferably not less than 1.2 seconds from the viewpoint of fully drying the white image, and is also preferably not more than 8 seconds, more preferably not more than 5 seconds, even more preferably not more than 4 seconds and further even more preferably not more than 3 seconds from the viewpoint of enhancing productivity of the resulting printed material.
Examples of commercially available products of the short-wave infrared heater include “ZKC” series products available from Heraeus K.K., etc.
Next, the ink-jet printing apparatus suitably used in the ink-jet printing method of the present invention is explained by referring to
The ink-jet printing apparatus 10 includes a plurality of printing heads 12K, 12C, 12M, 12Y and 12W, a preheater section 22, a plurality of fusing/curing means 20, an under heater section 26 and an afterheater section 24 constructed of an infrared heater.
The printing medium 16 is formed of a rolled transparent synthetic resin film, and wound around a take-up core 32 from one end side thereof. The printing medium 16 wound off from the take-up core 32 is transported via the preheater section 22, a turning roller 42, the printing heads 12K, 12C, 12M, 12Y and 12W, the fusing/curing means 20, the under heater section 26 and a turning roller 44, and then wound around a take-up core 34.
The preheater section 22 is in the form of a heater for preliminarily heating the printing medium 16. Examples of the heater constituting the preheater section 22 include a surface heater and a hot air heater.
The printing heads 12K, 12C, 12M and 12Y are operated and used in the step 1 of the method of the present invention for ejecting predetermined amounts of the black ink (K), the cyan ink (C), the magenta ink (M) and the yellow ink (Y), respectively, onto a front surface side of the printing medium 16 to thereby print an image 1 thereon. The printing heads are each preferably in the form of a line-type printing head in which a plurality of printing nozzles are arranged in line. The color inks are ejected from the respective printing heads while transporting the printing medium 16, so that the colored image 1 can be formed on the printing medium 16. Meanwhile, in
The fusing/curing means 20 are respectively disposed between adjacent two of the printing heads 12K, 12C, 12M, 12Y and 12W to fuse and cure the black ink (K), the cyan ink (C), the magenta ink (M) and the yellow ink (Y), respectively, which have been ejected onto the surface of the printing medium 16. Examples of the fusing/curing means 20 include an apparatus capable of applying a thermal energy to the inks on the printing medium, such as a heater, a hot-air fan, etc.
The under heater section 26 serves as a heating device for heating the printing medium 16 from a rear surface side of the printing medium 16. The under heater section 26 may be, for example, constructed of a heater of a hot water type or a heater of a thermoelectric type having a stainless steel or ceramic plate.
The afterheater section 24 is disposed on a downstream side of the printing head 12W such that the surface of the white image obtained in the step 2 is heated and dried to rapidly fuse and cure the white ink (W). The afterheater section 24 is constructed of an infrared heater.
As shown in
The container 50 has such an open-bottomed box shape as to cover the heaters 54. The heaters 54 are suspended by clamps 56 within the container 50 such that the heaters are respectively located near an opening 51 of the container 50. The clamps 56 support the heaters 54 at opposite ends thereof. The container 50 is provided on an upper surface thereof with a fan 52 for ventilating an inside of the container.
Meanwhile, although the two heaters 54 of a cylindrical tubular shape are shown in
In the following Production Examples, Examples and Comparative Examples, the “part(s)” and “%” indicate “part(s) by mass” and “% by mass”, respectively, unless otherwise specified.
The weight-average molecular weight of the polymer was measured by gel permeation chromatography [GPC apparatus: “HLC-8120GPC” available from Tosoh Corporation; columns: “TSK-GEL, α-M”×2 available from Tosoh Corporation; flow rate: 1 mL/min)] using a solution prepared by dissolving phosphoric acid and lithium bromide in N,N-dimethyl formamide such that the concentrations of phosphoric acid and lithium bromide in the solution were 60 mmol/L and 50 mmol/L, respectively, as an eluent, and using a monodisperse polystyrene having a known molecular weight as a reference standard substance.
The particles were subjected to cumulant analysis using a laser particle analyzing system “ELS-8000” available from Otsuka Electrics Co., Ltd., to measure an average particle size thereof. The above measurement was conducted under the conditions including a temperature of 25° C., an angle between incident light and detector of 90° and a cumulative number of 100 times, and a refractive index of water (1.333) was input to the analyzing system as a refractive index of the dispersing medium. The measurement was also conducted by adjusting a concentration of the dispersion to be measured to 5×10−3% by mass in terms of a solid content thereof.
Sodium sulfate dried to constant weight in a desiccator was weighed in an amount of 10.0 g and charged into a 30 mL polypropylene container (ϕ: 40 mm; height: 30 mm), and about 1.0 g of a sample to be measured was added to the container. The contents of the container were mixed with each other and then accurately weighed. The resulting mixture was maintained in the container at 105° C. for 2 hours to remove volatile components therefrom, and further allowed to stand in a desiccator for 15 minutes to measure a mass thereof. The mass of the sample after removing the volatile components therefrom was regarded as a mass of solids therein. The solid content of the sample was calculated by dividing the mass of the solids by the mass of the sample initially added.
The viscosity of the water-based ink was measured at 32° C. using an E-type viscometer “TV-25” (equipped with a standard cone rotor (1°34′×R24); rotating speed: 50 rpm) available from Toki Sangyo Co., Ltd.
A platinum plate was dipped in 5 g of the water-based ink filled in a cylindrical polyethylene container (3.6 cm in diameter×1.2 cm in depth), and the static surface tension of the water-based ink was measured at 20° C. using a surface tension meter “CBVP-Z” (tradename) available from Kyowa Interface Science Co., Ltd.
The pH value of the water-based ink was measured at 25° C. using a bench-top pH meter “F-71” available from Horiba Ltd., equipped with a pH electrode “6337-10D” available from Horiba Ltd.
Sixteen (16) parts of methacrylic acid available from Wako Pure Chemical Industries, Ltd., 44 parts of styrene available from Wako Pure Chemical Industries, Ltd., 30 parts of a styrene macromonomer “AS-6S” (number-average molecular weight: 6,000; solid content: 50%) available from Toagosei Co., Ltd., and 25 parts of methoxypolyethylene glycol methacrylate “BLEMMER PME-200” available from NOF Corporation were mixed with each other to prepare 115 parts of a monomer mixture solution.
Eighteen (18) parts of methyl ethyl ketone and 0.03 part of 2-mercaptoethanol as a chain transfer agent as well as 10% (11.5 parts) of the monomer mixture solution prepared above were charged into a reaction vessel and mixed with each other, and then an inside atmosphere of the reaction vessel was fully replaced with a nitrogen gas.
Separately, a mixed solution prepared by mixing remaining 90% (103.5 parts) of the monomer mixture solution, 0.27 part of the aforementioned chain transfer agent, 42 parts of methyl ethyl ketone and 3 parts of 2,2′-azobis(2,4-dimethylvaleronitrile) “V-65” as a polymerization initiator available from Wako Pure Chemical Industries, Ltd., was charged into a dropping funnel. In a nitrogen atmosphere, the mixed solution in the reaction vessel was heated to 75° C. while stirring, and then the mixed solution in the dropping funnel was added dropwise thereinto over 3 hours. After the elapse of 2 hours from completion of the dropwise addition while maintaining the resulting mixed solution at a temperature of 75° C., a solution prepared by dissolving 3 parts of the aforementioned polymerization initiator in 5 parts of methyl ethyl ketone was added to the mixed solution, and the resulting reaction solution was further aged at 75° C. for 2 hours and at 80° C. for 2 hours, followed by further adding 50 parts of methyl ethyl ketone thereto, thereby obtaining a solution of a pigment dispersing polymer (having a weight-average molecular weight of 50,000). The solid content of the thus obtained pigment dispersing polymer solution was 45% by mass.
Added into a solution prepared by dissolving 95.2 parts of the pigment dispersing polymer solution obtained in Production Example 1 in 53.9 parts of methyl ethyl ketone were 15.0 parts of a 5N sodium hydroxide aqueous solution and 0.5 part of a 25% ammonia aqueous solution both acting as a neutralizing agent as well as 341.3 parts of ion-exchanged water. Then, 100 parts of C.I. Pigment Black 7 (P.B. 7) as a carbon black pigment available from Cabot Japan K.K., was further added to the resulting mixture to prepare a pigment mixed solution. The degree of neutralization of the polymer in the thus prepared pigment mixed solution was 78.8 mol %. The pigment mixed solution was mixed at 20° C. for 1 hour using a disper blade operated at 7000 rpm. The resulting dispersion was dispersed under a pressure of 180 MPa using a Microfluidizer “High-Pressure Homogenizer M-140K” available from Microfluidics Corporation by passing the dispersion through the device 15 times.
The thus obtained dispersion of the black pigment-containing polymer particles was held at 60° C. under reduced pressure to remove methyl ethyl ketone therefrom, followed by further removing a part of water therefrom. The resulting dispersion was subjected to centrifugal separation, and a liquid layer portion separated therefrom was filtered through a filter “Minisart Syringe Filter” (pore diameter: 5 μm; material: cellulose acetate) available from Sartorius Inc., to remove coarse particles therefrom, thereby obtaining a water dispersion of the black pigment-containing polymer particles. The solid content of the thus obtained water dispersion was 25% by mass.
Then, 0.45 part of an epoxy crosslinking agent “DENACOL EX 321L” (tradename; trimethylolpropane polyglycidyl ether; epoxy equivalent: 130) available from Nagase ChemteX Corporation and 15.23 parts of ion-exchanged water were added to 100 parts of the resulting water dispersion of the black pigment-containing polymer particles, and the resulting mixture was subjected to heat treatment at 70° C. for 3 hours while stirring. After cooling the mixture to room temperature, a liquid layer portion separated therefrom was filtered through a filter “Minisart Syringe Filter” (pore diameter: 5 μm; material; cellulose acetate) available from Sartorius Inc., to remove coarse particles therefrom, thereby obtaining a water dispersion of the black pigment-containing polymer particles (solid content: 22% by mass). The average particle size of the black pigment-containing polymer particles in the resulting water dispersion was 100 nm. The results are shown in Table 1.
A 5 L plastic container was charged with 2500 g of a polyacrylic acid dispersant “ARON AC-10SL” (solid content; 40%) available from Toagosei Co., Ltd., and 3.57 g of ion-exchanged water, and then while cooling the thus filled container in an ice bath and stirring the resulting solution therein at 100 rpm, 1666.43 g of a 5N sodium hydroxide aqueous solution was slowly added thereto to neutralize the polymer. The aqueous solution obtained by the neutralization was mixed with ion-exchanged water to adjust a solid content of the solution to 20%, thereby obtaining a neutralized aqueous solution of the polyacrylic acid dispersant.
Then, a 2 L plastic container was charged with 30.0 g of the thus obtained neutralized aqueous solution of the polyacrylic acid dispersant, 300 g of C.I. Pigment White 6 (P.W. 6; titanium oxide “CR80”) available from ISHIHARA SANGYO KAISHA, LTD., and 306 g of water. Then, 1000 g of zirconia beads were added to the container, and the contents of the container were dispersed for 8 hours using a bench top-type pot mill pedestal available from AS ONE Corporation. Thereafter, the resulting dispersion was filtered through a metal mesh to remove the zirconia beads from the resulting dispersion, and then ion-exchanged water was added to the dispersion to adjust a solid content thereof to a desired value, thereby obtaining a water dispersion of white pigment-containing polymer particles (solid content: 30% by mass). The average particle size of the white pigment in the resulting water dispersion was 270 nm. The results are shown in Table 1.
A 1000 mL separable flask was charged with 145 parts of methyl methacrylate available from Wako Pure Chemical Industries, Ltd., 50 parts of 2-ethylhexyl acrylate available from Wako Pure Chemical Industries, Ltd., 5 parts of methacrylic acid available from Wako Pure Chemical Industries, Ltd., 18.5 parts of “LATEMUL E118B” (emulsifier; active ingredient content: 26%) available from Kao Corporation, 96 parts of ion-exchanged water and potassium persulfate available from Wako Pure Chemical Industries, Ltd., and the content of the flask were stirred using an agitation blade (300 rpm), thereby obtaining a monomer emulsion.
A reaction vessel was charged with 4.6 parts of “LATEMUL E118B”, 186 parts of ion-exchanged water and 0.08 part of potassium persulfate, and an inside atmosphere of the reaction vessel was fully replaced with a nitrogen gas. In a nitrogen atmosphere, the contents of the reaction vessel were heated to 80° C. while stirring with an agitation blade (200 rpm), and then the aforementioned monomer emulsion was charged into a dropping funnel and added dropwise into the reaction vessel over 3 hours to allow the monomer emulsion to react with the contents of the reaction vessel. The concentration of the fusing aid polymer particles as solid components in the resulting water dispersion of the fusing aid polymer particles was 41.6% by weight, and the average particle size of the fusing aid polymer particles was 100 nm.
A mixed solution was prepared by mixing 508.9 g of the water dispersion of the black pigment-containing polymer particles (solid content: 22.0% by mass) obtained in Production Example 2, 48.3 g of the water dispersion of the fusing aid polymer particles (solid content: 41.6% by weight) produced in Production Example 4, 44.0 g of diethylene glycol monoisobutyl ether (b.p. 230° C.), 286.0 g of propylene glycol (b.p. 188° C.), 5.5 g of a silicone-based surfactant “KF-6011” (polyether-modified silicone; HLB: 14.5) available from Shin-Etsu Chemical Industry Co., Ltd., and 207.3 g of ion-exchanged water with each other. The resulting mixed solution was filtered through a filter “Minisart Syringe Filter” (pore diameter: 5.0 μm; material: cellulose acetate) available from Sartorius Inc., thereby obtaining a black water-based ink. Various properties of the resulting black water-based ink are shown in Table 2.
A mixed solution was prepared by mixing 374.2 g of the water dispersion of the white pigment-containing polymer particles (solid content: 30.0% by mass) obtained in Production Example 3, 132.3 g of the water dispersion of the fusing aid polymer particles (solid content: 41.6% by weight) produced in Production Example 4, 44.0 g of diethylene glycol monoisobutyl ether (b.p. 230° C.), 286.0 g of propylene glycol (b.p. 188° C.), 5.5 g of a silicone-based surfactant “KF-6011” (polyether-modified silicone) available from Shin-Etsu Chemical Industry Co., Ltd., and 235.3 g of ion-exchanged water with each other. The resulting mixed solution was filtered through a filter “Minisart Syringe Filter” (pore diameter: 5.0 μm; material: cellulose acetate) available from Sartorius Inc., thereby obtaining a white water-based ink. Various properties of the resulting white water-based ink are shown in Table 2.
Using the respective water-based inks, characters or images were printed onto a corona discharge-treated PET “TAIKO Polyethylene Terephthalate Film FE2001” available from Futamura Chemical Co, Ltd., by the following ink-jet printing method to thereby obtain a printed material.
Under the environmental conditions of a temperature of 25±1° C. and a relative humidity of 30±5%, the water-based inks were loaded into a print evaluation apparatus available from Trytech Co., Ltd., equipped with line-type ink-jet printing heads “KJ4B-HD06MHG-STDV” (piezoelectric type) available from Kyocera Corporation. At this time, the line-type printing head loaded with the black ink and the line-type printing head loaded with the white ink were disposed such that they were spaced at a distance of 55 cm apart from each other in the print evaluation apparatus.
An A4-size film heater available from Kawai Corporation was fixedly mounted to a transportation table for transporting the corona discharge-treated PET as the printing medium so as to heat and dry the surface of the printing medium immediately after being printed.
The operating conditions of the print evaluation apparatus were set to a head applied voltage of 26 V, a drive frequency of 20 kHz, an ejected ink droplet amount of 5 pL, a head temperature of 32° C., a head resolution of 600 dpi, a number of ink shots for flashing before being ejected of 200 shots and a negative pressure of −4.0 kPa, and the printing medium was fixed on the film heater (at which the temperature of the surface of the printing medium was 50° C.) such that the longitudinal direction of the printing medium was aligned with a transporting direction thereof.
Then, a printing command was transmitted to the print evaluation apparatus, and the printing medium was transported at a transportation speed of 50 m/min to print a 100% Duty solid image of the black ink having a size of 5 cm×5 cm, followed by printing a 100% Duty solid image of the white ink having a size of 6 cm×6 cm on the printing medium so as to cover a whole surface of the solid image of the black ink with the white image, thereby obtaining a printed material.
The resulting printed material was dried by irradiating the printed material with infrared rays at an energy density of 100 kw/m2 for 2.0 seconds using a short-wave infrared heater “ZKC4800/600G” available from Heraeus K.K., thereby obtaining a final printed material.
The occurrence of color migration and deformation of the resulting final printed material were evaluated according the following evaluation ratings. The results are shown in Table 3.
A: No color migration occurred when rubbing the surface of the resulting printed material with fingers.
B: Slight color migration occurred when rubbing the surface of the resulting printed material with fingers, but there were present no significant problems even when used in practical applications.
C: Much color migration occurred when rubbing the surface of the resulting printed material with fingers, and the printed material got wet on its surface and therefore suffered from problems when used in practical applications.
A: No deformation such as distortion of the resulting printed material was recognized when visually observed.
B: Slight deformation such as distortion of the resulting printed material was recognized when visually observed, but there were present no significant problems even when used in practical applications.
C: Large deformation such as distortion of the resulting printed material was recognized when visually observed, and there were present significant problems when used in practical applications.
The same procedure as in Example 1 was repeated except that the irradiation conditions of the short-wave infrared heater were changed as shown in Table 3. The results are shown in Table 3.
The same procedure as in Example 1 was repeated except that only the 100% Duty solid image of the black ink having a size of 5 cm×5 cm was printed on the printing medium. The results are shown in Table 3.
The same procedure as in Example 1 was repeated except that no short-wave infrared heater was used. The results are shown in Table 3.
The same procedure as in Example 1 was repeated except that the short-wave infrared heater was replaced with a carbon infrared heater “ZKC6000/1000G” available from Heraeus K.K., and the drying procedure was conducted by irradiating infrared rays at an energy density of 100 kw/m2 for 2.0 seconds using the carbon infrared heater, thereby obtaining a printed material. Then, as a result of evaluating the thus obtained printed material by the same method as in Example 1, it was confirmed that occurrence of color migration and deformation of the printed material were rated as Rank A with respect to both of the black ink and the white ink.
The same procedure as in Example 1 was repeated except that the short-wave infrared heater was replaced with a mid-infrared heater “CSG4250/1700” available from Heraeus K.K., and the drying procedure was conducted by irradiating infrared rays at an energy density of 60 kw/m2 for 2.0 seconds using the mid-infrared heater, thereby obtaining a printed material (at which the temperature of the surface of the printing medium was 55° C.). Then, as a result of evaluating the thus obtained printed material by the same method as in Example 1, it was confirmed that occurrence of color migration was rated as Rank B with respect to both of the black ink and the white ink, and deformation of the printed material was rated as Rank A with respect to both of the black ink and the white ink.
From Table 3, it was confirmed that the printing methods used in Examples 1 to 3 were excellent in drying properties of the inks upon high-speed printing and were free of occurrence of color migration and deformation of the printed material as compared to the printing methods used in Comparative Examples 1 and 2.
Furthermore, from the comparison of Examples 1 to 3 with Examples 4 and 5, it was confirmed that the short-wave infrared heater and the carbon infrared heater were excellent in heating performance for the printed material among the short-wave infrared heater, the carbon infrared heater and the mid-infrared heater, and from the viewpoint of enhancing productivity of the printed material, etc., the short-wave infrared heater was more preferred.
According to the ink-jet printing method of the present invention, it is possible to obtain good printed materials that are free of occurrence of color migration and deformation of a printing medium even when printed on a transparent resin printing medium.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2016-025354 | Feb 2016 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2017/003869 | 2/2/2017 | WO | 00 |
