JP4662416B2 - Ink for inkjet recording on both sides, recording method and recording apparatus - Google Patents

Description

  The present invention relates to a recording liquid suitable for inkjet recording, particularly a recording liquid useful for double-sided image formation on so-called plain paper, and is applied to water-based writing instruments, recorders, and water-based ink compositions for pen plotters.

In recent years, inkjet printers and plotters using inks that use pigments as color materials have been put on the market for the purpose of improving the appropriateness of printing on plain paper in inkjet printers, and machines that support both sides have also been introduced.
However, in order to obtain a high-density image with black ink, an ink having low penetrability to paper is used. Therefore, in order to suppress smearing during double-sided printing, a second drying time is provided after the first side printing. The printing speed was very high for printing on one side, and even though resource saving was possible, the productivity was worse than that for single-sided printing.
Further, when a dye-based penetrable ink is used, an ink jet recording apparatus provided with a drying means such as a heater is disclosed in Japanese Patent Application Laid-Open No. 2004-151620 because there is a large amount of back-through and image quality deterioration.

JP 2001-63019 A

Accordingly, in view of the above prior art, a first object of the present invention is to provide an ink and a recording apparatus that can perform duplex printing at high speed.
A second object of the present invention is to provide an ink and a recording apparatus that are unlikely to deteriorate image quality when performing duplex printing at high speed.

The above-described problem is (1) “a recording ink for use in an ink jet recording apparatus that prints the second surface after printing the first surface of the recording medium, and includes at least one colorant, which is dispersed therein. Or a water - soluble organic solvent containing water and N-hydroxyethylpyrrolidone as a solvent to be dissolved, and at least a surfactant and / or 2-ethyl-1,3-hexanediol that promotes penetration into the recording medium Containing a penetrating organic solvent, the time for which the ink is absorbed by the recording surface after printing on the first side is 5S or less, and the polymer fine particles having methacrylic acid as a constituent monomer are impregnated with a dye or pigment. duplex corresponding inkjet recording ink "which is a colored polymer fine particles obtained by, (2)" the recording apparatus first in transporting the recording medium from the first surface to the second surface Item (1) is a recording apparatus having conveying means that abuts against the surface, and the image density reduction rate with respect to image abrasion resistance after ink absorption of the ink is 0.10 or less. Ink for inkjet recording on both sides ", (3)" The recording ink according to item (2) above, wherein the particle diameter of the colored fine particles is from 10 nm to 300 nm ", (4)" As a surfactant Any of (1) to (3) above, comprising an anionic surfactant, wherein the anionic surfactant is polyoxyethylene alkyl ether acetate or dialkylsulfosuccinate (5) “The recording ink described in the item (1) includes a nonionic surfactant as a surfactant, and acetylene glycol as the nonionic surfactant.” (1) to (1), which contain at least one surfactant selected from a surfactant based on polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, and polyethylene-polypropylene copolymer. (4) The recording ink according to any one of items (1), (6), wherein the recording ink contains an amphoteric surfactant as a surfactant. Ink for recording ”, (7)“ The recording ink according to item (1), wherein the recording ink contains a fluorosurfactant as a surfactant ”, (8) The water-soluble organic solvent of the recording ink described in item (1) is further glycerin, ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, di- Propylene glycol, tripropylene glycol, 1,3-butanediol, 2,3-butanediol, 1,4-butanediol, 1,5-pentanediol, tetraethylene glycol, 1,6-hexanediol, 2-methyl- 2,4-pentanediol, polyethylene glycol, 1,2,4-butanetriol, 1,2,6-hexanetriol, thiodiglycol, 2-pyrrolidone, N-methyl-2-pyrrolidone, 1,3-dimethyl- (9) The recording ink according to any one of (1) to (7) above, which contains at least one water-soluble organic solvent selected from 2-imidazolidinone. ) “The recording ink according to the item (1) of the previous term is characterized in that it further contains an alkyl ether as a permeable solvent. The recording ink according to any one of Items (1) to (8), (10) “The alkyl ether is diethylene glycol monohexyl ether or propylene glycol monohexyl ether”. This is solved by the recording ink described in item (9).
Further, the above problem is that the recording ink according to any one of (11) and (1) to (9) of the present invention is made into fine droplets from a nozzle of 35 μm or less by thermal energy or mechanical energy. The problem is solved by an “ink-jet recording method, wherein the image is formed by flying and adhering to a recording material”.
In addition, the above-described problem is solved by any one of the items (1) to (11) in the recording ink cartridge provided with (12) “recording ink storage portion storing recording ink” of the present invention. This is solved by a recording ink cartridge characterized by the above-mentioned recording ink.
In addition, the above-described problem is (13) “a recording ink containing portion or recording ink cartridge containing recording ink, a head portion or a recording unit for dropletizing and discharging the recording ink by the action of thermal energy. In the ink jet recording apparatus, the recording ink is a recording apparatus according to any one of the items (1) to (11), and (14) “the recording apparatus performs the second operation after the first surface printing. This is solved by the “recording apparatus according to item (13)” including a mechanism that reverses the paper surface so that printing can be performed on the surface, and conveyance means that contacts the printing surface.

According to the present invention, it is possible to provide an ink having excellent duplex compatibility and a recording apparatus and a recording method using the same by increasing the permeability using a pigment and / or colored fine particles and setting the time to 5 seconds or less.
In addition, by controlling the rub resistance of the ink of the present invention, it is possible to reduce abnormal images such as rub stains during double-sided conveyance, so that high-quality images can be obtained even with double-sided printing.

The ink of the present invention uses a surfactant that controls permeability and a penetrating solvent, so that the penetration time into paper is 5 S or less, and pigments and / or dyes or colored resin particles colored with pigments are used as colorants. An ink and a recording apparatus in which the double-sided printing is improved by suppressing bleeding are provided.
Here, the improvement in image quality may be caused by rubbing against the abutting member in the transport path by the paper only by improving the permeability to the paper surface. It became clear that. More specifically, it has been clarified that image quality deterioration during double-sided printing is improved by improving the scratch resistance.

  The ink of the present invention is not only the one using pressure by PZT, the one ejected by a diaphragm deflected by electrostatic force, the drop-on-demand ink jet printer of the foam jet type recording system using film boiling, and the ink is charged and PZT It can be used satisfactorily for any printer of the so-called charge control system that is vibrated with. In particular, even a nozzle having a small nozzle diameter of 20 μm or less can be stably discharged because of its high reliability.

As pigments used in the present invention, organic pigments such as azo, phthalocyanine, anthraquinone, dioxazine, indigo, thioindigo, perylene, isoindolenone, aniline black, azomethine, rhodamine B lake pigment, carbon Examples of the inorganic pigment include iron oxide, titanium oxide, calcium carbonate barium sulfate, aluminum hydroxide, barium yellow, bitumen, cadmium red, chrome yellow, and metal powder.
More specifically, as black pigments, carbon blacks (CI Pigment Black 7) such as furnace black, lamp black, acetylene black, channel black, or copper oxides, iron oxides (C.I. Pigment black 11), metals such as titanium oxide, and organic pigments such as aniline black (CI pigment black 1).

The pigment for color ink is for yellow ink and C.I. I. Pigment Yellow 1 (Fast Yellow G), 3, 12 (Disazo Yellow AAA), 13, 14, 17, 23, 24, 34, 35, 37, 42 (Yellow Iron Oxide), 53, 55, 74, 81, 83 (Disazo Yellow HR), 95, 97, 98, 100, 101, 104, 108, 109, 110, 117, 120, 128, 138, 150, 153,
For magenta and C.I. I. Pigment Red 1, 2, 3, 5, 17, 22 (Brilliant First Scarlet), 23, 31, 38, 48: 2 (Permanent Red 2B (Ba)), 48: 2 (Permanent Red 2B (Ca)), 48 : 3 (Permanent Red 2B (Sr)), 48: 4 (Permanent Red 2B (Mn)), 49: 1, 52: 2, 53: 1, 57: 1 (Brilliant Carmine 6B), 60: 1, 63: 1, 63: 2, 64: 1, 81 (Rhodamine 6G Lake), 83, 88, 92, 101 (Bengara), 104, 105, 106, 108 (Cadmium Red), 112, 114, 122 (Dimethylquinacridone), 123, 146, 149, 166, 168, 170, 172, 177, 178, 179, 185, 190, 193, 209, 2 19,
For cyan, C.I. I. Pigment Blue 1, 2, 15 (copper phthalocyanine blue R), 15: 1, 15: 2, 15: 3 (phthalocyanine blue G), 15: 4, 15: 6 (phthalocyanine blue E), 16, 17: 1, 56, 60, 63; etc. can be used.

  In addition, the following pigments can be used alone or in combination for red, green, and blue as intermediate colors.

  C. I. Pigment red 177, 194, 224, C.I. I. Pigment orange 43, C.I. I. Pigment violet 3, 19, 23, 37, C.I. I. Pigment Green 7, 36.

As black, carbon black is carbon black produced by the furnace method and the channel method, the primary particles are 15 nm to 40 nm, the specific surface area by the BET adsorption method is 50 to 300 m ² / g, and the DBP oil absorption is 40 to 150 ml. / 100 g, those having a volatile content of 0.5 to 10% and a pH of 2 to 9 are used, and acidic carbon black having a pH of 6 or less is particularly preferred at a high concentration. Further, carbon black treated with hypochlorous acid, carbon black treated with a sulfonating agent, and carbon black treated with a diazonium compound and introduced with an anionic dissociation group such as sulfonic acid or carboxylic acid are more preferable. As a yellow pigment, C.I. I pigment yellow 74, 128, and 138 are preferable. As magenta pigments, quinacridone C.I. I. Pigment Red 122 and 209 are preferable. Cyan is a phthalocyanine compound C.I. I. Pigment Blue 15: 3, aluminum coordination phthalocyanine, and metal-free phthalocyanine are preferable. Among these color organic pigments, pigments into which a sulfonic acid group or a carboxylic acid group has been introduced by surface treatment are further excellent in dispersion stability, and those capable of obtaining dispersion stability without a dispersant can be suitably used as self-dispersing pigments. . Also, pigments encapsulated on the surface, pigments grafted with a polymer, and the like can be made into highly reliable inks with excellent dispersion stability.

<Reference Example 1>
Carbon black treated with hypochlorous acid 1
After mixing 300 g of commercially available acidic carbon black having a pH of 2.5 (trade name Monarch 1300, manufactured by Cabot Corporation) with 1000 ml of water, 450 g of sodium hypochlorite (effective chlorine concentration: 12%) was added dropwise, and 100 to 105 ° C. For 8 hours. To this solution, 100 g of sodium hypochlorite (effective chlorine concentration 12%) was further added and dispersed for 3 hours with a horizontal disperser. The resulting slurry was diluted 10 times with water, pH was adjusted with lithium hydroxide, desalted and concentrated with an ultrafiltration membrane to a conductivity of 0.2 mS / cm, and a carbon black dispersion having a pigment concentration of 15% It was. Coarse particles were removed by centrifugation and further filtered through a 1 micron nylon filter to obtain a carbon black dispersion 1. The total content of Fe, Ca and Si was 100 ppm or less as measured by ICP. The chlorine ion concentration was also set to 10 ppm or less. The average particle size (D50%) measured by Microtrac UPA was 95 nm.

<Reference Example 2>
Carbon black 2 treated with sulfonating agent
150 g of a commercially available carbon black pigment (“Printex # 85” manufactured by Degussa) was mixed well in 400 ml of sulfolane, finely dispersed with a bead mill, 15 g of amidosulfuric acid was added, and the mixture was stirred at 140 to 150 ° C. for 10 hours. The obtained slurry is put into 1000 ml of ion-exchanged water, and a surface-treated carbon black wet cake is obtained by a centrifuge at 12000 rpm. This carbon black wet cake was redispersed in 2000 ml of ion exchange water, pH was adjusted with lithium hydroxide, and desalted and concentrated with an ultrafiltration membrane to obtain a carbon black dispersion having a pigment concentration of 10% by weight. This was filtered through a 1 micron nylon filter to obtain a carbon black solution 2. The total content of Fe, Ca and Si was 100 ppm or less as measured by ICP. The sulfate ion concentration was also 100 ppm or less. The average particle size was 80 nm.

<Reference Example 3>
Carbon black dispersion 3 treated with diazo compound
100 g of carbon black having a surface area of 230 m ² / g and a DBP oil absorption of 70 ml / 100 g and 34 g of p-amino-N-benzoic acid are mixed and dispersed in 750 g of water, and 16 g of nitric acid is added dropwise thereto and stirred at 70 ° C. did. After 5 minutes, a solution of 11 g of sodium nitrite dissolved in 50 g of water was added, and the mixture was further stirred for 1 hour. The resulting slurry was diluted 10 times and centrifuged to remove coarse particles, the pH was adjusted with diethanolamine to pH 8-9, desalted and concentrated with an ultrafiltration membrane, and a carbon black dispersion with a pigment concentration of 15%. did. This was made into carbon black dispersion 3 with a polypropylene 0.5 μm filter. The total content of Fe, Ca and Si was 100 ppm or less as measured by ICP. The nitrate ion concentration was 10 ppm or less. The average particle size was 99 nm.

<Reference Example 4>
Carbon black dispersion 4 treated with diazo compound
Example 1-Preparation of Carbon Black Product A solution of about 75 ° C. containing 2 liters of water and 43 g of sulfanilic acid was stirred into 202 g of carbon black having a surface area of 230 m ² / g and 70 ml / 100 g of DBPA. Added. The mixture was cooled to room temperature with stirring and 26.2 g of concentrated nitric acid was added. A 20.5 g solution of sodium nitrite in water was added. 4-Sulfobenzenediazonium hydroxide inner salt was prepared and reacted with carbon black. The dispersion was stirred until the generated foaming stopped. The obtained slurry is diluted, adjusted to pH 8 with lithium hydroxide to remove coarse particles by centrifugation, and subsequently desalted and concentrated with an ultrafiltration membrane to disperse carbon black with a pigment concentration of 15%. Liquid. This was filtered through a polypropylene 1 μm filter to obtain a carbon black dispersion 4. The total content of Fe, Ca and Si was 100 ppm or less as measured by ICP. The nitrate ion concentration was 50 ppm or less. The average particle size was 95 nm.

<Reference Example 5>
Surface pigmented color pigment dispersion (yellow dispersion 1, magenta dispersion 1, cyan dispersion 1)
As a yellow pigment, C.I. I. Pigment Yellow 128 was subjected to low-temperature plasma treatment to prepare a pigment into which a carboxylic acid group was introduced. A dispersion of this in ion-exchanged water was desalted and concentrated with an ultrafiltration membrane to obtain a yellow pigment dispersion 1 having a pigment concentration of 15%. The average particle diameter was 70 nm, and the total content of Fe, Ca and Si was 100 ppm or less.
Similarly, CI pigment magenta 122 was used as a magenta pigment to prepare a magenta pigment dispersion 1 having a pigment concentration of 15%. The total content of average particles 60 nm and Fe, Ca, Si was 100 ppm or less.
Similarly, C.I. I. Cyan Pigment Dispersion Liquid 1 having a pigment concentration of 15% was prepared using Pigment Cyan 15: 3. The average particle diameter was 80 nm, and the total content of Fe, Ca and Si was 100 ppm or less.

In the present invention, a pigment dispersion using a pigment dispersant can also be used.
As a pigment dispersant, it is a hydrophilic polymer. In natural systems, vegetable polymers such as gum arabic, tragan gum, guar gum, karaya gum, locust bean gum, arabinogalactone, pectin, quince seed starch, alginic acid, carrageenan, agar, etc. Seaweed polymers, animal polymers such as gelatin, casein, albumin and collagen, microbial polymers such as xanthene gum and dextran, and semisynthetic systems such as methylcellulose, ethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, etc. Fiber polymers, starch polymers such as sodium starch glycolate and sodium starch phosphate, and seaweed polymers such as sodium alginate and propylene glycol alginate Pure synthetic systems include vinyl polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, and polyvinyl methyl ether, non-crosslinked polyacrylamide, polyacrylic acid and alkali metal salts thereof, acrylic resins such as water-soluble styrene acrylic resins, and water-soluble styrene malees. Acid resin, water-soluble vinyl naphthalene acrylic resin, water-soluble vinyl naphthalene maleic resin, polyvinyl pyrrolidone, polyvinyl alcohol, alkali metal salt of β-naphthalene sulfonic acid formalin condensate, cationic functional group such as quaternary ammonium and amino group Examples thereof include a polymer compound having a salt in the side chain and a natural polymer compound such as shellac.
In particular, a polymer dispersing agent is preferably introduced with a carboxylic acid group such as a homopolymer of acrylic acid, methacrylic acid or styrene acrylic acid or a copolymer of monomers having other hydrophilic groups.
When a surfactant is used, anionic surfactants such as polyoxyethylene alkyl ether phosphates and polyoxyethylene alkyl ether acetates, and nonionic surfactants such as nonylphenyl ether can also be used.

<Reference Example 6>
Dispersant pigment dispersion (surfactant dispersion: yellow dispersion 2, magenta dispersion 2, cyan dispersion 2, polymer dispersion: yellow dispersion 3, magenta dispersion 3, cyan dispersion 3)
Yellow pigment: C.I. I. Pigment yellow 128, magenta pigment: C.I. I. Pigment Red 122
Cyan pigment: C.I. I. Pigment Blue 15: 3
Dispersant A: Nonionic surfactant “Emulgen 913” manufactured by Kao Corporation), HLB 15.5
Dispersant B: Acrylic resin aqueous solution “John Crill 611” (ammonia neutralized, solid content 20%) manufactured by Johnson Polymer Co., Ltd., acid value 57

1. Salt milling refinement process A 1-gallon kneader made of stainless steel (manufactured by Inoue Seisakusho) was charged with 250 parts of the pigment, 2500 parts of sodium chloride and 200 parts of diethylene glycol and kneaded for 3 hours. Next, this mixture is poured into 2.5 liters of warm water, heated to about 80 ° C. and stirred with a high speed mixer for about 1 hour to form a slurry, and then filtered and washed repeatedly 5 times to remove sodium chloride and The solvent was removed and a dried pigment was obtained.
2. Surface treatment step To a paint conditioner, 20 parts of a pigment, 5 parts of a dispersant A and B below (in terms of solid content) and water were added, and the total amount was made 100 parts and dispersed for 3 hours. The obtained aqueous pigment dispersion was centrifuged at 15000 rpm for 6 hours.
To 20 parts of the surface-treated pigment, 0.1 part of 30% ammonia water and 79.9 parts of purified water were added and redispersed with a paint conditioner to prepare a pigment concentrate. For the pigments that were not surface-treated, add 5 parts (solid content) of dispersant C (prescription 1) or dispersant B (formulation 2) and purified water to 20 parts of pigment, and paint as 100 parts in total. The ink was dispersed with a conditioner and purified with a reverse osmosis membrane to prepare a concentrated recording liquid for inkjet. The concentrated solution was filtered through a 1 μm nylon filter, and then filtered through a 0.5 μm polypyropylene filter to obtain a working dispersion.
Each content of Fe, Ca, and Si was 100 ppm or less.
The average particle size of the dispersion here is yellow dispersion 2: 93 nm, yellow dispersion 3: 80 nm.
Magenta dispersion 2: 60 nm Magenta dispersion 2: 56 nm
Cyan dispersion 2: 90 nm Cyan dispersion 3: 87 nm

In the present invention, fine particles colored with dyes and pigments are used as coloring materials to improve fixing properties and color development on plain paper, and aggregation and the like occur when water-soluble calixarene of the following formula is contained. A colored fine particle recording liquid that is difficult to obtain can be obtained. As the colored fine particles, those in which the fine particles are made of a polymer and those made of inorganic fine particles such as silica and alumina can be used. For the purpose of imparting gloss, it is preferable to use polymer fine particles.
In particular, it is preferable to use an acrylic or polyester-based fine particle impregnated with a dye / pigment, that is, a colored polymer fine particle in which the dye / pigment is present in the surface layer, inside, or entirely. More specifically, colored fine particles produced by the method disclosed in JP-A-2000-53898 can be mentioned. One example according to this is shown below.

<Reference Example 7>
In a sealable reaction vessel equipped with a stirring blade, a cooling pipe, and a nitrogen gas introduction pipe, 20 parts by weight of methyl ethyl ketone as a polymerization solvent and an initial charge monomer and a polymerization chain transfer agent having the following composition as a polymerizable unsaturated monomer were charged, Gas replacement was performed sufficiently.
Methyl methacrylate, monomer 12.8 parts by weight 2-hydroxyethyl methacrylate, monomer 1.2 parts by weight Methacrylic acid, monomer 2.9 parts by weight Silicone macromer (FM-0711 manufactured by Chisso Corporation) 2 parts by weight Styrene acrylonitrile Macromer (AN-6, manufactured by Toagosei Co., Ltd.) 1 part by weight Mercaptoethanol (polymerization chain transfer agent) 0.3 part by weight In a nitrogen atmosphere, the temperature of the mixture in the reaction vessel was increased to 65 ° C. with stirring. Separately, the following dropped monomer monomer and polymerization chain transfer agent, 60 parts of methyl ethyl ketone, and 0.2 part of 2,2′-azobis (2,4-dimethylvaleronitrile) are mixed and sufficiently purged with nitrogen. The obtained mixed solution was gradually dropped into the reaction vessel over 3 hours.
Methyl methacrylate, monomer 51 parts by weight 2-hydroxyethyl methacrylate, monomer 4.2 parts by weight Methacrylic acid, monomer 11 parts by weight Silicone macromer (FM-0711 manufactured by Chisso Corporation) 8 parts by weight Styrene acrylonitrile macromer (Toa Gosei) AN-6) 4 parts by weight Mercaptoethanol (polymerization chain transfer agent) 1.2 parts by weight 2,2′-azobis (2,4-dimethylvaleronitrile) 0. 2 hours after the completion of dropping. A solution in which 1 part by weight was dissolved in 5 parts by weight of methyl ethyl ketone was added, and further aged at 65 ° C. for 2 hours and at 70 ° C. for 2 hours to obtain a vinyl polymer solution.
A part of the obtained vinyl polymer solution was isolated by drying at 105 ° C. for 2 hours under reduced pressure to completely remove the solvent. The weight average molecular weight was about 10,000 and Tg was 180 ° C.
25 g of toluene and 5 g of anthraquinone dye are completely dissolved in 5 g of the vinyl polymer obtained by drying the vinyl polymer solution obtained above under reduced pressure, and 2 g of an aqueous sodium hydroxide solution is added to the vinyl polymer solution. Some acidic groups were neutralized. Subsequently, after adding 300 g of ion-exchange water and stirring, it emulsified for 30 minutes using Nanomaker TM (made by Nanomizer) which is an emulsifier. The obtained emulsion was completely removed by removing toluene at 60 ° C. under reduced pressure, further concentrating by removing a part of water, and removing impurities such as monomers with an ultrafiltration membrane, and purified disperse dye A magenta dispersion liquid 4 (average particle diameter: 98 nm, solid content concentration: 10%) of vinyl polymer fine particles impregnated with styrene was obtained.
In the same manner, the dye is added to C.I. I. Disperse Yellow 118 as Yellow Dispersion 4 (average particle size: 98 nm, solid content concentration: 10%), C.I. I. Blue dispersion 4 (average particle size; 98 nm, solid content concentration: 10%) was obtained as Disperse Blue 36.

  In the present invention, wettability to recording paper can be improved by using a surfactant. Preferred surfactants include interfacial polyoxyethylene alkyl ether acetates, dialkyl sulfosuccinates, polyoxyethylene alkyl ethers, polyoxyethylene alkyl phenyl ethers, polyoxyethylene polyoxypropylene block copolymers, and acetylene glycol surfactants. Agents. More specifically, as the anionic surfactant, polyoxyethylene alkyl ether acetate (II) and / or dialkylsulfosuccinic acid (III) having a branched alkyl chain having 5 to 7 carbon chains can be used. The properties of plain paper are also improved and the colorant can be dissolved and dispersed stably.

Ｒ_５、Ｒ_６：炭素数５〜７の分岐したアルキル基
Ｍ：アルカリ金属イオン、第４級アンモニウム、第４級ホスホニウム、
アルカノールアミン

R _{5, R 6:} branched alkyl group having 5-7 carbon atoms M: an alkali metal ion, quaternary ammonium, quaternary phosphonium,
Alkanolamine

Further, by using lithium ions, quaternary ammonium and quaternary phosphonium represented by the following general formula as counter ions of the surfactant of the present invention, the surfactant exhibits excellent dissolution stability.
Preferred nonionic surfactants include those represented by general formula (IV) which are polyoxyethylene alkylphenyl ethers and general formula (V) which are acetylene glycol surfactants. By using these together, penetrability can be mentioned as a further synergistic effect, and this makes it possible to obtain ink with reduced blurring at the color boundary and less blurring of characters.

Ｒは分岐しても良い６〜１４の炭素鎖
ｋ：５〜１２

R may be branched 6-14 carbon chain k: 5-12

ｐ、ｑは０〜４０

p and q are 0 to 40

Ink storage stability can be obtained by setting the pH of the ink to 6 or more, and many copy papers and sticky notes used in the office have a pH of 5 to 6, and these recordings are possible. The ink is ejected from a fine ejection port of 9 to 60 μm on paper, and is ejected as a droplet having a weight of 2 ng to 50 ng at a rate of 5 to 20 m / s, and the adhesion amount in a single color is 1.5 g / m ² to 30 g / m ^2. As described above, it is possible to provide a recording method for forming a high-quality, high-resolution recorded image by recording on a so-called plain paper having a sizing degree of 3 seconds or more according to the JIS P-8122 test method. However, when the pH is 9 or more, the active agent (III) is likely to change its physical properties due to decomposition during storage, and therefore the pH is preferably 6 to 9 when (III) is used.

  The amount of addition of (II), (III), (IV), (V) that can be used in the present invention is between 0.05 to 10% by weight, and the desired penetrability for the ink properties required by the printer system. It is possible to give Here, if it is 0.05% or less, bleeding occurs at the boundary between the two-color overlapping portions in any case, and if it is added in an amount of 10% by weight or more, the compound itself may easily precipitate at a low temperature, resulting in poor reliability.

Next, the surfactants (II) and (III) used in the present invention are specifically shown in free acid form.

The ink of the present invention uses water as a liquid medium. In order to make the ink have desired physical properties, to prevent drying of the ink, and to improve the dissolution stability of the compound of the present invention, etc. For the purpose, the following water-soluble organic solvents can be used.
Ethylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, polypropylene glycol, 1,3-purpandiol, 1,3-butanediol, 1,4 butanediol, 1,5 pentanediol, 1,6 hexanediol, glycerol, Polyhydric alcohols such as 1,2,6-hexanetriol, 1,2,4-butanetriol, 1,2,3-butanetriol, petriol, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether , Polyethylene alcohol such as diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, tetraethylene glycol monomethyl ether, propylene glycol monoethyl ether Alkyl ethers, polyhydric alcohol aryl ethers such as ethylene glycol monophenyl ether, ethylene glycol monobenzyl ether; N-methyl-2-pyrrolidone, N-hydroxyethyl-2-pyrrolidone, 2-pyrrolidone, 1,3 -Nitrogen-containing heterocyclic compounds such as dimethylimidazolidinone and ε-caprolactam; amides such as formamide, N-methylformamide, formamide, N, N-dimethylformamide; monoethanolamine, diethanolamine, triethanolamine, monoethylamine, Examples thereof include amines such as diethylamine and triethylamine, sulfur-containing compounds such as dimethyl sulfoxide, sulfolane and thiodiethanol, propylene carbonate, ethylene carbonate, and γ-butyrolactone. These solvents are used alone or in combination with water.

Among these, particularly preferred are diethylene glycol, thiodiethanol, polyethylene glycol 200 to 600, triethylene glycol, glycerol, 1,2,6-hexanetriol, 1,2,4-butanetriol, petriol, 1, With 3-butanediol, 2,3-butanediol, 1,4-butanediol, 1,5-pentanediol, N-methyl-2-pyrrolidone, N-hydroxyethylpyrrolidone, 2-pyrrolidone, 1,3 dimethylimidazolidinone By using these compounds, excellent effects can be obtained for the high solubility of the present compound and the prevention of poor jetting characteristics due to water evaporation.
In the present invention, a pyrrolidone derivative such as N-hydroxyethyl 2-pyrrolidone is particularly preferable for obtaining the dispersion stability of the colorant.

  In addition to the surfactants (II) to (V) of the present invention, penetrants added for the purpose of adjusting the surface tension include diethylene glycol monophenyl ether, ethylene glycol monophenyl ether, ethylene glycol monoallyl ether, diethylene glycol mono Alkyl and aryl ethers of polyhydric alcohols such as phenyl ether, diethylene glycol monobutyl ether, propylene glycol monobutyl ether, triethylene glycol monobutyl ether, tetraethylene glycol chlorophenyl ether, 2-ethyl-1,3-hexanediol, 2,2,4 -Diols such as trimethyl-1,3-pentanediol, 2,2dimethyl-1,3-propanediol, and polyoxyethylene polyoxypropylene block copolymers Fluorine-based surfactants, lower alcohols such as ethanol and 2-propanol can be mentioned. Particularly preferred are diethylene glycol monobutyl ether as polyhydric alcohol alkyl ether, and 2-ethyl-1,3-hexane as diol having 6 or more carbon atoms. Diol and 2,2,4-trimethyl 1,3-pentanediol. Diols are preferred because they are less likely to cause aggregation of water-insoluble colorants. The addition amount depends on the kind and desired physical properties, but is 0.1 to 20% by weight, preferably 0.5 to 10% by weight. If it is less than the lower limit, the permeability is insufficient, and if it is more than the upper limit, the particle formation characteristics are adversely affected. In addition, the addition of these improves the wettability of the ink jet head member and the recording device, improves the filling properties, and makes it difficult for recording defects to occur due to bubbles.

The ink physical properties in the present invention can be appropriately adjusted by the system. Here, the surface tension of the ink is an index indicating the permeability to paper, and the measurement of the dynamic surface tension in a short time of 1 second or less after the surface is formed corresponds to the permeability of the ink. Different from static surface tension measured at saturation time. Any measuring method can be used as long as it can measure a dynamic surface tension of 1 second or less by a conventionally known method described in JP-A-63-312372. The value of the surface tension is preferably 50 mN / m or less, more preferably 40 mN / m or less, whereby excellent drying properties can be obtained. On the other hand, from the viewpoint of ink ejection stability, if the dynamic surface tension is too low, the particle formation tends to be unstable. The dynamic surface tension that can be stably discharged is preferably 40 mN / m or more in 1 msec.
The viscosity range is appropriately selected from 1 mPa · s to 10 mPa · s depending on the discharge method.

  The pigment particle diameter range in the ink is preferably 10 nm to 300 nm, and the average particle diameter is preferably 60 nm to 120 nm. Both the solid content in the ink is 1 to 25% by weight and the water content is in the range of 25 to 93% by weight, more preferably in the range of 50 to 80% by weight.

In addition to the colorant and solvent, conventionally known additives can be added to the ink of the present invention.
For example, as a preservative and antifungal agent, sodium dehydroacetate, sodium sorbate, sodium 2-pyridinethiol-1-oxide, sodium benzoate, sodium pentachlorophenol, isothiazoline and the like can be used in the present invention.
As the other pH adjusting agent, any substance can be used as long as the pH can be adjusted to 7 or more without adversely affecting the ink to be prepared.
Examples thereof include amines such as diethanolamine and triethanolamine, hydroxides of alkali metal elements such as lithium hydroxide and sodium hydroxide, ammonium hydroxide, quaternary ammonium hydroxide, quaternary phosphonium hydroxide, Examples thereof include alkali metal carbonates such as lithium carbonate, sodium carbonate, and potassium carbonate.
Examples of the chelating reagent include sodium ethylenediaminetetraacetate, sodium nitrilotriacetate, sodium hydroxyethylethylenediaminetriacetate, sodium diethylenetriaminepentaacetate, sodium uramil diacetate, and the like.
Examples of the rust preventive include acidic sulfite, sodium thiosulfate, ammonium thiodiglycolate, diisopropyl ammonium nitrite, pentaerythritol tetranitrate, dicyclohexyl ammonium nitrite and the like.
In addition, a water-soluble ultraviolet absorber and a water-soluble infrared absorber can be added depending on the purpose.
In addition, a dye can be used together as necessary. As this preferable dye, those having excellent water resistance and light resistance, which are classified into acid dyes, direct dyes, basic dyes, reactive dyes and food dyes in the color index, are used.

Next, an example of the ink jet recording apparatus of the present invention suitable for recording using the above-described aqueous pigment ink of the present invention will be described below.
FIG. 1 is a schematic configuration diagram of a mechanism unit showing an example of an ink jet recording apparatus according to a first embodiment of the present invention.
The ink jet recording apparatus includes a carriage movable in the main scanning direction inside the recording apparatus main body (1), a recording head composed of an ink jet head mounted on the carriage, an ink cartridge for supplying ink to the recording head, and the like. A paper feed cassette (or a paper feed tray) that accommodates the printing mechanism (2) and the like and can stack a large number of sheets (3) from the front side in the lower part of the apparatus main body (1) (4). In addition, a manual feed tray (5) is detachably mounted on the front side, and is set on the paper fed from the paper feed cassette (4) or the manual feed tray (5). The paper (3) is taken in, and after a required image is recorded by the printing mechanism (2), it is discharged to a paper discharge tray (6) mounted on the rear side. An upper cover (7) is attached to the upper part so as to be opened and closed.

The printing mechanism (2) slides the carriage (13) in the main scanning direction (perpendicular to the paper surface in FIG. 1) with a main guide rod (11) and a sub guide rod (12) horizontally mounted on left and right side plates (not shown). The carriage (13) comprises an inkjet head having nozzles that discharge ink droplets of yellow (Y), cyan (C), magenta (M), and black (Bk) on the lower surface side of the carriage (13). The recording head (14) is mounted with the ink droplet ejection direction downward, and each ink tank (ink cartridge) (15) for supplying ink of each color to the recording head (14) is provided above the carriage (13). Is installed in a replaceable manner. The ink cartridge (15) is held on the carriage (13) by the cartridge pressing lever (16).
Here, the recording head (14) may be one in which a plurality of heads for ejecting ink droplets of each color are arranged in the main scanning direction, or one head having nozzles for ejecting ink droplets of each color. The one used may be used. Also, the recording head (14) is one that discharges ink droplets by pressurizing ink by displacing the diaphragm by an electromechanical transducer such as a piezoelectric element and changing the volume in the liquid chamber, and is disposed in the liquid chamber. By generating a bubble by film boiling by the generated heating resistor and pressurizing ink in the liquid chamber to discharge ink droplets, using a diaphragm that forms the wall surface of the liquid chamber and an electrode facing it, electrostatic force between the two In this case, it is possible to use one that displaces the diaphragm and ejects ink droplets.

On the other hand, in order to convey the sheet (3) in the sub-scanning direction with respect to the printing position by the recording head (14), the sheet (3) is statically placed between the conveyance roller (21) and the conveyance driven roller (22). A conveying belt (23) that is electroadsorbed and conveyed is stretched and disposed, and a printing receiving member (24) is provided at a position facing the recording head (14) across the conveying belt (23). . The transport roller (21) is provided with a leading end roller (25) for defining the feed angle of the paper (3) pressed through the transport belt (23).
Here, it is preferable that the transport roller (21) has a diameter that ensures sheet adhesion at the time of double-sided printing and does not perform curvature separation, for example, φ30 mm or more. In addition, the conveyance driven roller (22) has a diameter of 16 mm or less so that the sheet can be separated in curvature. Furthermore, the conveyance belt (23) is made of a medium resistance member having a volume resistance of 10 ⁸ to 10 ¹¹ Ω, thereby preventing charge-up associated with the conveyance of the sheet and ensuring the conveyance.

On the other hand, in order to feed the paper (3) from the paper feed cassette (4) onto the transport belt (23), the paper feed roller (26) and the friction pad ( 27) and a guide member (29) for guiding the fed paper (3) to an intermediate roller (28) disposed in contact with the conveying roller (21). The paper feed cassette (4) has a bottom plate (32) on the cassette body (31) and an extended bottom portion (33) that forms a sheet placing surface together with the bottom plate (32), and the mounting position of the extended bottom portion (33). By changing the length, it is possible to select the length of the sheet placement surface, and it is possible to use a large size sheet exceeding the cassette body (31). Further, an end fence (34) for regulating the rear end of the sheet is attached to the extended bottom (33) so as to be movable in the length direction without any step.
Further, in order to feed the paper (3) from the manual feed tray (5) to the conveyor belt (23), a pickup roller (35) for picking up the paper (3) of the manual feed tray (5) and the paper (3) are fed. A feed roller (36) for feeding, a feed roller (37), and a guide member (38) for guiding the paper (3) to the intermediate roller (28) are provided.
Then, the paper (3) for which printing has been completed is discharged to the paper discharge tray (6), and at the time of double-sided printing, the paper (3) for which single-sided printing has been completed is sent to the paper discharge tray (6), and again the apparatus Guide members (41), (42), (43) for guiding the paper (3) for feeding into the main body (1), a branching claw (44) for switching between paper discharge and refeed, A paper discharge roller (45) capable of rotating forward and reverse for feeding paper (3) to the paper discharge tray (6) and re-feeding, and a paper discharge roller (46) driven by the paper discharge roller (45) are provided. Provided.
The guide member (42) is integrally formed with a guide portion (42a) for feeding the paper (3) to the transport belt (23) in order to refeed the paper (3). A conveyance roller driven roller (47) for feeding the paper (3) to the intermediate roller (28) by following the conveyance roller (21) for conveying the paper (3) to be re-fed along the line 42a) is provided. Further, a paper passage sensor (48) for detecting the passage of the paper (3) is provided in the transport path by the guide member (41).

Examples of the present invention and comparative examples are shown below.
Example 1
The mixture was mixed using the following composition and allowed to stand for 1 day. The pH was adjusted to 9 with the compound of specific example (I-1), and the mixture was filtered through a 0.5 μm polypropylene filter to obtain black ink 1.
Carbon dispersion 1
8% by weight as the solid content in the ink
Resin emulsion 5% by weight
0.1% by weight of compound of specific example (I-1)
Glycerol 15% by weight
5% by weight of N-hydroxyethylpyrrolidone
2-ethyl-1,3-hexanediol 1% by weight
Activator of specific example (II-2) 1% by weight
Sodium dehydroacetate 0.2% by weight
High pure water (10 MΩ) Remaining The concentration of the dispersion and the dye is the concentration of the solid colorant in the ink.

(Example 2)
A black ink 2 was prepared in the same manner as in Example 1 except that the following composition was used, and adjusted to pH 8.8 with lithium hydroxide.
Carbon dispersion 2 7% by weight
3% by weight of resin particles
1,2,6-hexanetriol 8% by weight
1,5-pentanediol 10% by weight
2-ethyl-1,3-hexanediol 1.5% by weight
2-pyrrolidone 8% by weight
Activator of specific example (II-3) 1.0% by weight
Active agent of specific example (III-1) 1.2% by weight
Specific example (I-3) 25% aqueous solution 0.8% by weight
Urea 5% by weight
2-pyridinethiol-1-oxide sodium 0.2% by weight
High purity water (10MΩ)

(Example 3)
A black ink 3 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 9.5 with lithium hydroxide.
Carbon dispersion 3 8% by weight
Diethylene glycol 15% by weight
Glycerol 5% by weight
2-ethyl-1,3-hexanediol 2% by weight
2-pyrrolidone 2% by weight
Styrene acrylic acid polymer 1.5% by weight
1% by weight of (II-2) surfactant
(VI) activator R: C ₉ H ₁₉ k: 12 1% by weight
Specific example (I-3) 25% aqueous solution 0.1% by weight
Sodium dehydroacetate 0.2% by weight
Ion exchange water

Example 4
A yellow ink 1 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 9.5 with lithium hydroxide.
Yellow dispersion 1 5.0% by weight
Ethylene glycol 5% by weight
Glycerol 2% by weight
1,5-pentanediol 8% by weight
2-pyrrolidone 2% by weight
2-ethyl 1,3-hexanediol 2% by weight
1% by weight of polyoxyethylene polyoxyethylene block copolymer
1% by weight of activator of specific example (II-4)
Activator of specific example (V) p, q = 20 0.8% by weight
Specific example (I-4) 25% aqueous solution 2% by weight
Urea 5% by weight
Sodium benzoate 0.2% by weight
Ion exchange water

Magenta ink 1 was prepared by adjusting the pH to 9.1 with lithium hydroxide in the same manner as in Example 1 except that the following composition was used.
Magenta dispersion 1 5.0% by weight
Ethylene glycol 5% by weight
Glycerol 15% by weight
2-pyrrolidone 2% by weight
2, ethyl-1,3 hexanediol 2% by weight
1% by weight of polyoxyethylene polyoxyethylene block copolymer
1% by weight of activator of specific example (II-4)
Activator of specific example (V) p, q = 20 0.8% by weight
Specific example (I-4) 25% aqueous solution 2% by weight
Urea 5% by weight
Sodium benzoate 0.2% by weight
Ion exchange water

Cyan dispersion 1 5% by weight
0.1% by weight of compound of specific example (I-1)
Glycerol 15% by weight
5% by weight of N-hydroxyethylpyrrolidone
2-ethyl-1,3-hexanediol 1% by weight
Activator of specific example (II-2) 1% by weight
Sodium dehydroacetate 0.2% by weight
High purity water (10MΩ)

(Example 5)
A yellow ink 2 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 7.8 with sodium hydroxide.
Yellow dispersion 2 10% by weight
Triethylene glycol 5% by weight
Petriol 10% by weight
N-methyl-2-pyrrolidone 5% by weight
Diethylene glycol monohexyl ether 2% by weight
Specific example (I-5) 0.4% by weight
Specific Example (IV) Activator R: C ₁₀ H ₂₁ K: 7 1 wt%
Specific example (I-2) 25% aqueous solution 1.5% by weight
Hydroxyethylurea 5% by weight
2-pyridinethiol-1-oxide sodium 0.2% by weight
Ion exchange water

Magenta dispersion 2 10% by weight
Triethylene glycol 5% by weight
Petriol 10% by weight
N-methyl-2-pyrrolidone 5% by weight
Diethylene glycol monohexyl ether 2% by weight
Specific example (I-5) 0.4% by weight
Activator of specific example (IV) R: C ₁₀ H ₂₁ K: 7 1% by weight
Specific example (I-2) 25% aqueous solution 1.0% by weight
Hydroxyethylurea 5% by weight
2-pyridinethiol-1-oxide sodium 0.2% by weight
Remaining amount of ion-exchanged water Cyan dispersion 2 10% by weight
Triethylene glycol 5% by weight
Petriol 10% by weight
N-methyl-2-pyrrolidone 5% by weight
Diethylene glycol monohexyl ether 2% by weight
Specific example (I-5) 1% by weight
Activator of specific example (V) R: C ₁₀ H ₂₁ K: 7 1% by weight
Specific example (I-2) 25% aqueous solution 1.0% by weight
Hydroxyethylurea 5% by weight
2-pyridinethiol-1-oxide sodium 0.2% by weight
Ion exchange water

(Example 6)
A yellow ink 3 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 8 with lithium hydroxide.
Yellow dispersion 3 8% by weight
2-pyrrolidone 8% by weight
Glycerol 7% by weight
1,3-butanediol 3% by weight
Activator of specific example (II-1) 0.3% by weight
(IV) Activator p + q = 15 0.5% by weight
(IV) Activator p + q = 0 0.5% by weight
Specific example (I-7) 25% aqueous solution 2% by weight
Hydroxyethylurea 5% by weight
Sodium dehydroacetate 0.2% by weight
Ion exchange water

Magenta ink 3 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 8 with lithium hydroxide.
Magenta dispersion 3 6% by weight
2-pyrrolidone 8% by weight
Glycerol 7% by weight
1,3 butanediol 3% by weight
Active agent of specific example (I-1) 0.3% by weight
(IV) Activator p + q = 15 0.5% by weight
(IV) Activator p + q = 0 0.5% by weight
Specific example (I-7) 25% aqueous solution 2% by weight
Hydroxyethylurea 5% by weight
Sodium dehydroacetate 0.2% by weight
Ion exchange water

A cyan ink 3 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 8 with lithium hydroxide.
Cyan dispersion 3 8% by weight
2-pyrrolidone 8% by weight
Glycerol 7% by weight
1,3 butanediol 3% by weight
Active agent of specific example (II-1) 0.3% by weight
Tetramethylammonium nitrate (conductivity adjusting agent) 0.4% by weight
(IV) Activator p + q = 15 0.5% by weight
(IV) Activator p + q = 0 0.5% by weight
Specific example (I-7) 25% aqueous solution 2% by weight
Hydroxyethylurea 5% by weight
Sodium dehydroacetate 0.2% by weight
Ion exchange water

(Example 7)
A yellow ink 4 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 9.5 with lithium hydroxide.
Yellow dispersion 4 8% by weight
Ethylene glycol 5% by weight
Glycerol 2% by weight
1,3-propanediol 8% by weight
2-pyrrolidone 2% by weight
1% by weight of polyoxyethylene polyoxyethylene block copolymer
Activator of specific example (II-4) 0.5% by weight
Specific example (I-4) 25% aqueous solution 2% by weight
Urea 5% by weight
Sodium benzoate 0.2% by weight
Ion exchange water

Magenta ink 4 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 9.1 with lithium hydroxide.
Magenta dispersion 4 8% by weight
Ethylene glycol 5% by weight
Glycerol 15% by weight
2-pyrrolidone 2% by weight
1% by weight of polyoxyethylene polyoxyethylene block copolymer
Activator of specific example (II-4) 0.3% by weight
Activator of specific example (V) p, q = 20 0.2% by weight
Specific example (I-4) 25% aqueous solution 2% by weight
Urea 5% by weight
Sodium benzoate 0.2% by weight
Ion exchange water

A cyan ink 4 was prepared in the same manner as in Example 1 except that the following composition was used, and the pH was adjusted to 8.4 with lithium hydroxide.
Cyan dispersion 4 5% by weight
0.1% by weight of compound of specific example (I-1)
Glycerol 15% by weight
5% by weight of N-hydroxyethylpyrrolidone
2-ethyl-1,3-hexanediol 1% by weight
Activator of specific example (II-2) 1% by weight
Sodium dehydroacetate 0.2% by weight
High purity water (10MΩ)

(Comparative Example 1-3)
A black ink 4-6 was produced in the same manner except that the surfactant and 2-ethyl-1,3-hexanediol were removed from the ink of Example 1-3.

(Comparative Example 4)
An ink was prepared in the same manner except that the penetrating solvent and the surfactant were removed from the ink of Example 4.

(Comparative Example 5)
An ink was prepared in the same manner except that the penetrating solvent and the surfactant were removed from the ink of Example 5.

(Comparative Example 6)
An ink was prepared in the same manner except that the surfactant was removed from the ink of Example 6. "

Next, the following tests were carried out as a four-color ink set using the inks of Examples 1 to 7 and Comparative Examples 1 to 4.
1) Sharpness of image Thermal ink jet nozzle diameter of 18 μm, 300 dpi nozzle with 600 dpi pitch and laminated PZT used for pressurization of liquid chamber flow channel nozzle diameter of 28 μm, 200 dpi pitch with 300 nozzles Printing is performed with an inkjet printer that has 300 nozzles for each color using an electrostatic printer and an electrostatic actuator for pressurization of the liquid chamber flow path, and the two-color overlap boundary, image blur, color tone, and density are integrated visually Judgment. In addition, color development during OHP projection was also evaluated.
Printing paper is commercially available recycled paper, high-quality paper and bond paper, glossy film with water-soluble resin layer absorption layer, OHP sheet <rank in sensory evaluation>
Regardless of the type of paper, the blur of the boundary between the two colors overlaps, the image density is high,
High color reproducibility 5
Somewhat low image density as above 4
Color boundary blur is small, but unevenness of secondary colors is observed depending on the paper type 3
Color boundary bleeding occurs depending on the paper type 2
The image density is low and the sharpness is inferior 1

2) Penetration time Evaluate the penetration time for the following 5 papers by applying filter paper after paper discharge, and the average time is 1 second or less.
From 1 second to 5 seconds 2
From 5 seconds to 10 seconds 1
Ricoh PPC paper type 6200 type 6000 (70W)
NBS RICOH My Recycle Paper Xerox 4024 Paper Canon PB Paper

3) Image fixing property Using a cotton cloth on a Toyo Seiki clock meter, rubbing the solid image part 10 times, and confirming the image density reduction rate and the cotton cloth stain.
No decrease in density and no cotton cloth stains 3
There is a slight dirt on the cotton fabric without a decrease in concentration 2
Concentration drop and cotton cloth stains are large 1

It is a schematic block diagram of the mechanism part which shows an example of the inkjet recording device which concerns on 1st Embodiment in this invention.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Recording device main body 2 Printing mechanism part 3 Paper 4 Paper feed cassette 5 Manual feed tray 6 Paper discharge tray 7 Upper cover 11 Main guide rod 12 Subordinate guide rod 13 Carriage 14 Recording head 15 Ink tank (ink cartridge)
16 Presser lever 21 Conveying roller 22 Conveying driven roller 23 Conveying belt 24 Printing receiving member 25 End roller 26 Feeding roller 27 Friction pad 28 Intermediate roller 29 Guide member 31 Cassette body 32 Bottom plate 33 Extension bottom 34 End fence 35 Pickup roller 36 Feed Roller 37 Feed roller 38 Guide member 41 Guide member 42 Guide member 42a Guide portion 43 Guide member 44 Separating claw 45 Paper discharge roller 46 Paper discharge roller 47 Followed roller 48 Passing sensor 49
51
52
53
54

Claims (14)

A recording ink for use in an ink jet recording apparatus that prints a second surface after printing a first surface of a recording medium , comprising at least one colorant, water and N-hydroxy as a solvent for dispersing or dissolving the colorant A water-soluble organic solvent containing ethylpyrrolidone, containing at least a surfactant that promotes penetration into the recording material and / or a penetrating organic solvent consisting of 2-ethyl-1,3-hexanediol ; The time for ink to be absorbed on the recording surface after printing on one surface is 5S or less, and the colorant is colored polymer fine particles obtained by impregnating polymer fine particles containing methacrylic acid as a constituent monomer with a dye or pigment. Ink for inkjet recording that supports both sides. When the recording apparatus transports a recording medium from the first surface to the second surface, the recording apparatus has a conveying unit that comes into contact with the first surface, and the image density decreases with respect to the image scratch resistance after the ink is absorbed by the ink. The ink for two-sided ink jet recording according to claim 1, wherein the rate is 0.10 or less. The recording ink according to claim 2, wherein the colored fine particles have a particle diameter of 10 nm to 300 nm. The recording according to any one of claims 1 to 3, wherein the surfactant contains an anionic surfactant, and the anionic surfactant is polyoxyethylene alkyl ether acetate or dialkyl sulfosuccinate. For ink. The recording ink according to claim 1 comprises a nonionic surfactant as a surfactant, and an acetylene glycol surfactant, polyoxyethylene alkyl ether, polyoxyethylene alkylphenyl ether, polyethylene as the nonionic surfactant. 5. The recording ink according to claim 1, comprising at least one surfactant selected from polypropylene copolymers. The recording ink according to claim 1, wherein the recording ink contains an amphoteric surfactant as a surfactant. The recording ink according to claim 1, wherein the recording ink contains a fluorosurfactant as a surfactant. The water-soluble organic solvent of the recording ink according to claim 1 , further comprising glycerin, ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, 1,3-butanediol, 2,3 -Butanediol, 1,4-butanediol, 1,5-pentanediol, tetraethylene glycol, 1,6-hexanediol, 2-methyl-2,4-pentanediol, polyethylene glycol, 1,2,4-butane At least one water-soluble organic solvent selected from triol, 1,2,6-hexanetriol, thiodiglycol, 2-pyrrolidone, N-methyl-2-pyrrolidone, 1,3-dimethyl-2-imidazolidinone 8. A composition comprising: The recording ink according to any one of the above. The recording ink according to any one of claims 1 to 8, wherein the recording ink according to claim 1 further contains an alkyl ether as a permeable solvent. The recording ink according to claim 9, wherein the alkyl ether is diethylene glycol monohexyl ether or propylene glycol monohexyl ether. An image is formed by causing the recording ink according to any one of claims 1 to 9 to fly as fine droplets from a nozzle of 35 μm or less by thermal energy or mechanical energy and adhere to a recording material. Inkjet recording method. 12. A recording ink cartridge comprising a recording ink container containing recording ink, wherein the recording ink is the recording ink according to any one of claims 1 to 11. In an ink jet recording apparatus comprising a recording ink containing portion or recording ink cartridge containing recording ink, a head portion or a recording unit for dropping and discharging the recording ink by the action of thermal energy, the recording ink The recording apparatus according to claim 1. 14. The recording apparatus according to claim 13, further comprising a transport unit that has a mechanism for reversing the paper surface so that printing can be performed on the second surface after printing on the first surface, and that contacts the printing surface.

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