JP2018159073A - Aqueous ink composition, inkjet recording method, and colored body - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an aqueous ink composition which has good storage stability, shows neutral color tones of gray to black, and is excellent in both light resistance and water resistance of a recording image.SOLUTION: An aqueous ink composition contains at least two kinds of coloring agents (I) and (II), and at least one kind of a coloring agent selected from C.I.Direct Orange, where a content of (I) in the total mass of the ink composition is 4 mass% or more and 50 mass% or less with respect to the content of (II), and (I) is a dye represented by the following formula (1) or its salt, and (II) is C.I.Acid Black2. In the formula (1), R, R, R, R, R, Rand Rare each independently a hydrogen atom, a sulfo group and the like; and n represents 0 or 1.SELECTED DRAWING: None

Description

  The present invention relates to an aqueous black ink composition, an ink jet recording method using the same, and a colored body.

  Among various color recording methods, the ink jet recording method, which is one of the representative methods, generates small ink droplets and attaches them to various recording materials (paper, film, fabric, etc.). Recording method. This method has been spreading rapidly in recent years due to the fact that the recording head is not in direct contact with the recording material and is quiet with little noise generation, and is easy to downsize and speed up. Expected.

  With the recent development of inkjet technology, the printing speed in inkjet printing has been remarkably improved, and inkjet recording intended for commercial printing and office use has been proposed. In this case, the printing medium is generally plain paper that does not have an ink receiving layer, and hue, light resistance, and water resistance are the most important issues compared with the inkjet dedicated paper having an ink receiving layer, and the improvement is strong. It is desired.

  Black ink is an important ink used for both monocolor and full color images. However, there are many technical difficulties in developing pigments that are neutral in hue and light color gamut, high in color density, and excellent in fastness. There are few things with sufficient performance. Therefore, generally, a black ink is prepared by mixing a plurality of various pigments. However, when an ink is prepared by mixing a plurality of pigments, problems such as different hues depending on the recording material and particularly large discoloration due to bleeding due to water are more likely to occur than when an ink is prepared with a single pigment.

  For example, Patent Document 1 has been proposed as a black ink in which a dye for color adjustment is further blended with a black dye, but a product that sufficiently satisfies the market demand has not been provided.

  Moreover, the dye represented by following formula (1) described in this specification is described in patent documents 2-5. However, these have not sufficiently satisfied the above problems in terms of hue, light resistance and water resistance.

Japanese Patent No. 3178200 International Publication No. 2006/051850 International Publication No. 2013/035560 JP 2008-69331 A JP 2013-32469 A

  An object of the present invention is to provide a water-based ink composition that has good storage stability, exhibits a neutral gray to black hue, and is excellent in both light resistance and water resistance of a recorded image.

  As a result of intensive studies to solve the above-mentioned problems, the present inventors have found that the above-mentioned problems can be solved by a water-based ink composition having a specific configuration described below, and have completed the present invention.

That is, the present invention relates to the following 1) to 11).
1)
A water-based ink composition containing at least two kinds of colorants (I) and colorant (II), wherein the content of the colorant (I) in the total mass of the water-based ink composition is The water-based ink composition wherein the content of the colorant (II) is 2% by mass or more and 65% by mass or less, and the colorant (I) is a dye represented by the following formula (1) or a salt thereof. .

(In the above formula (1),
R ₁ , R ₂ , R ₅ , R ₆ and R ₇ each independently have a hydrogen atom, a halogen atom, a cyano group, a hydroxy group, a carboxy group, a sulfo group, a sulfamoyl group, a nitro group, or a substituent. Represents a group selected from the group consisting of an alkoxy group which may have a substituent, an alkylsulfonyl group which may have a substituent, an alkyl group, an arylsulfamoylamino group which may have a substituent, and an alkylcarbonylamino group .
R ₃ and R ₄ are each independently selected from the group consisting of a hydrogen atom, a halogen atom, a cyano group, a sulfo group, a carboxy group, a nitro group, an optionally substituted alkoxy group, and an alkyl group. Represents a group.
n represents 0 or 1. )
2)
The colorant (II) is C.I. I. The water-based ink composition as described in 1) above, which is Acid Black 2.
3)
The water-based ink composition according to 1) or 2), which further contains a compound represented by the following formula (2) as a pH adjuster.

(In formula (2), R ₈ , R ₉ and R ₁₀ each independently represent a group selected from the group consisting of a hydrogen atom, an alkyl group, a hydroxyalkyl group, and a hydroxyalkoxyalkyl group.)
4)
Any of 1) to 3) above, wherein the content of the colorant (I) in the total mass of the aqueous ink composition is 2% by mass or more and 50% by mass or less with respect to the content of the colorant (II). The water-based ink composition according to claim 1.
5)
In the above formula 1), in the formula (1), R ₁ is a carboxy group or a sulfo group, R ₂ is a hydrogen atom, R ₆ is a nitro group, a carboxy group, or a sulfo group, and n is 1. The water-based ink composition as described.
6)
In the formula (1), R ₁ and R ₃ are sulfo groups, R ₄ is a hydrogen atom, R ₅ is a hydrogen atom, a carboxy group, or a sulfo group, and R ₆ is a nitro group, a carboxy group, or a sulfo group. a group, R ₇ is a hydrogen atom, n is an aqueous ink composition according to the above 1) is 1.
7)
C. I. The water-based ink composition according to any one of 1) to 6) above, further comprising at least one colorant selected from Direct Orange.
8)
An ink jet recording method in which recording is performed by ejecting droplets of the water-based ink composition according to any one of 1) to 7) according to a recording signal and attaching the droplets to a recording material.
9)
8. The ink jet recording method according to 8) above, wherein the recording material is an information transmission sheet.
10)
A colored body colored with the water-based ink composition according to any one of 1) to 7) above.
11)
An inkjet printer loaded with a container containing the water-based ink composition according to any one of 1) to 7) above.

  According to the present invention, it is possible to provide a water-based ink composition having good storage stability, a neutral gray to black hue, and excellent light resistance and water resistance of a recorded image.

  The present invention is described in detail below. In the present specification, “%” and “parts”, including examples and the like, are described on a mass basis unless otherwise specified. In the present specification, “CI” means “color index”.

The colorant (I) is a dye represented by the formula (1) and is a black dye.
In the above formula (1), R ₁ , R ₂ , R ₅ , R ₆ and R ₇ are each independently a hydrogen atom, a halogen atom, a cyano group, a hydroxy group, a carboxy group, a sulfo group, a sulfamoyl group, or a nitro group. , An alkoxy group which may have a substituent, an alkylsulfonyl group which may have a substituent, an alkyl group, an arylsulfamoylamino group which may have a substituent, and an alkylcarbonylamino group Represents a group selected from:
R ₃ and R ₄ are each independently selected from the group consisting of a hydrogen atom, a halogen atom, a cyano group, a sulfo group, a carboxy group, a nitro group, an alkoxy group that may have a substituent, and an alkyl group. Represents a group.

  Examples of the alkoxy group which may have a substituent include an alkoxy group which may have a sulfo group, a C1-C6 alkoxy group which may have a sulfo group is preferable, and has a sulfo group. The C1-C4 alkoxy group which may be sufficient is more preferable.

  Examples of the alkylsulfonyl group that may have a substituent include an alkylsulfonyl group that may have a hydroxy group, a C1-C6 alkylsulfonyl group that may have a hydroxy group is preferable, and a hydroxy group A C1-C4 alkylsulfonyl group which may have a hydrogen atom is more preferable.

As said alkyl group, a linear, branched or cyclic alkyl group is mentioned, A linear or branched thing is preferable and a linear thing is more preferable.
Specific examples thereof include linear C1-C6 alkyl groups such as methyl, ethyl, n-propyl, n-butyl, n-pentyl and n-hexyl; isopropyl, isobutyl, sec-butyl, t-butyl, isopentyl and isohexyl. Branched C1-C6 alkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like cyclic C1-C6 alkyl groups; and the like.

  Examples of the arylsulfamoylamino group which may have a substituent include a phenylsulfamoylamino group which may have a substituent, and a phenylsulfamoylamino group which may have an alkyl group. Groups are preferred. Examples of the alkyl group include the same alkyl groups as those described above including preferable ones.

  Examples of the alkylcarbonylamino group include an alkylcarbonylamino group having the same alkyl group as the alkyl group, including those preferable for the alkyl group.

  As said halogen atom, a chlorine atom, a bromine atom, or an iodine atom is mentioned, A chlorine atom or a bromine atom is preferable, and a chlorine atom is more preferable.

Among the above, as R ₁ and R ₂ ,
At least one is preferably a group other than a hydrogen atom,
More preferably, at least one is a carboxy group, a sulfo group or an unsubstituted alkoxy group, and the other is a hydrogen atom or a sulfo group,
More preferably, one is a sulfo group and the other is a hydrogen atom.
Among these, “one” is preferably R ₁ and “the other” is preferably R ₂ .

Of the above, as R ₅ , R ₆ and R ₇ ,
At least one of them is preferably a group other than a hydrogen atom,
A group in which at least one of them is selected from a carboxy group, a sulfo group, and a nitro group is more preferable,
More preferably, at least one is a hydrogen atom and one of the remaining two is a carboxy group, a sulfo group, or a nitro group, and the other is a hydrogen atom or a nitro group,
It is particularly preferable that at least one is a hydrogen atom and one of the remaining two is a sulfo group and the other is a hydrogen atom or a nitro group.
Of these, “of one of the remaining two” is preferably R ₆ and “the other” is preferably R ₅ .

Among the above, as R ₃ and R ₄ ,
At least one is preferably a group other than a hydrogen atom,
More preferably, at least one is a sulfo group, an alkoxy group which may have a substituent, or an alkyl group, and the other is a hydrogen atom, a sulfo group or an alkyl group,
More preferably, at least one is a sulfo group, the other is a hydrogen atom, or one is an alkoxy group which may have a substituent, and the other is an alkyl group,
One is particularly preferably a sulfo group and the other a hydrogen atom.

In the above formula (1), examples of the substitution position of the nitro group, R _{1 to} R ₇ , and — (SO ₃ H) n group whose substitution positions are not specified include the following positions.

[Substitution positions of R ₁ , nitro group, and R ₂ ]
As for the substitution position of each group on the benzene ring substituted by these, the substitution positions of the following (a) to (c) are exemplified with the substitution position of the azo group bonded to the benzene ring as the first position.
(A) R ₁ is in position 2, the nitro group is in position 4, and R ₂ is in position 5.
(B) R ₁ is 4-position, nitro group is 2-position, and R ₂ is 5-position.
(C) R ₁ is in position 2, the nitro group is in position 5, and R ₂ is in position 4.
Of these, (a) or (b) is preferred, and (a) is more preferred.

[Substitution positions of R ₃ and R ₄ ]
The substitution position of each group on the benzene ring to which these are substituted is such that R ₃ is the 3-position, with the substitution position of the azo group binding to the benzene ring and binding to the benzene ring having R _{5 to} R ₇ as the 1-position. R ₄ is preferably substituted at the 6-position.

[Substitution positions of R ₅ , R ₆ and R ₇ ]
As for the substitution position of each group on the benzene ring substituted by these, the substitution positions of the following (a) to (c) are exemplified with the substitution position of the azo group bonded to the benzene ring as the first position.
(A) R ₅ is 2nd, R ₆ is 4th, and R ₇ is 5th.
(B) R ₅ is 3rd, R ₆ is 5th, and R ₇ is 4th.
(C) R ₅ is 2nd, R ₆ is 5th, R ₇ is 4th.
(D) R ₅ is 3rd, R ₆ is 4th, and R ₇ is 6th.
Of these, (a) is preferred.

[Substitutional position of — (SO ₃ H) n group]
When the substitution position of the hydroxy group substituted on the naphthalene ring substituted by the — (SO ₃ H) n group is 1-position and the substitution position of the sulfo group whose substitution position is specified is the 3-position, the — (SO ₃ H) n group is Substitution at the 5-position is preferred.

Regarding the dye represented by the above formula (1), each group represented by R ₁ to R ₇ and each group whose substitution position including a nitro group and a “— (SO ₃ H) n group” is not specified As for the substitution position, a combination of preferable ones is more preferable, and a combination of more preferable ones is more preferable. The same applies to combinations of preferable ones and combinations of preferable ones and more preferable ones.

  Specific examples of the compound represented by the above formula (1) are listed in Tables 1 to 3 below. However, the compound represented by the above formula (1) is not limited thereto.

  Among the dyes represented by the above formula (1), dyes represented by the following formula (22), formula (23) or formula (26) are particularly preferred, and among these, formula (22) is most preferred. These dyes are particularly effective for color development, light resistance, ozone resistance and water resistance.

  The dye represented by the above formula (1) can be synthesized by the method described in Patent Document 3, for example.

The dye represented by the above formula (1) may be used as a salt.
Examples of the salt of the dye represented by the above formula (1) include salts formed with inorganic or organic cations. Among them, specific examples of inorganic salts include salts formed with cations of elements of Group 1 or Group 2 of the periodic table of elements, and ammonium salts. Among these, preferred inorganic salts are lithium, sodium, potassium and ammonium salts.
Examples of the organic cation salt include, but are not limited to, salts formed with compounds represented by the following formula (16).

In the above formula (16), Z ₁ , Z ₂ , Z ₃ and Z ₄ each independently represent a hydrogen atom, an alkyl group, a hydroxyalkyl group or a hydroxyalkoxyalkyl group, but Z ₁ , Z ₂ , Z All of ₃ and Z ₄ are not hydrogen atoms.

As the alkyl group of Z ₁ , Z ₂ , Z ₃ and Z _{4 in} the formula (16), a C1-C4 alkyl group is preferable, and specific examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec -Butyl, t-butyl and the like.
Examples of hydroxyalkyl groups include hydroxy-C1-C4 alkyl groups such as hydroxymethyl, hydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl, 4-hydroxybutyl, 3-hydroxybutyl, 2-hydroxybutyl and the like.
Examples of hydroxyalkoxyalkyl groups include hydroxyethoxymethyl, 2-hydroxyethoxyethyl, 3-hydroxyethoxypropyl, 2-hydroxyethoxypropyl, 4-hydroxyethoxybutyl, 3-hydroxyethoxybutyl, 2-hydroxyethoxybutyl, etc. A hydroxy C1-C4 alkoxy-C1-C4 alkyl group is mentioned, Among these, a hydroxyethoxy-C1-C4 alkyl group is preferable. Particularly preferred are hydrogen atoms; methyl; hydroxy-C1-C4 alkyl groups such as hydroxymethyl, hydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl, 4-hydroxybutyl, 3-hydroxybutyl, 2-hydroxybutyl; Hydroxyethoxy-C1-C4 alkyl groups such as hydroxyethoxymethyl, 2-hydroxyethoxyethyl, 3-hydroxyethoxypropyl, 2-hydroxyethoxypropyl, 4-hydroxyethoxybutyl, 3-hydroxyethoxybutyl, 2-hydroxyethoxybutyl, etc. Can be mentioned.

Specific examples of Z ¹ , Z ² , Z ³ and Z ^{4 in} the formula (16) are shown in the following Table 4, but the compound represented by the formula (16) is not limited to these specific examples.

  Preferred examples of the organic cation salt include monoethanolamine salts, diethanolamine salts, triethanolamine salts, monoisopropanolamine salts, diisopropanolamine salts, and triisopropanolamine salts.

The aqueous ink composition contains at least a colorant (II) in addition to the colorant (I). By containing the colorant (II), the black ink has a more neutral hue, and gives a recorded image with excellent light resistance and water resistance. As the colorant (II), a black dye is preferable. I. Acid Black 2 is preferred.

C. I. Acid Black2 can be easily obtained. When this is used for ink jet recording, it is preferable to remove inorganic impurities mixed in when it is generally obtained as a commercial product by a refining operation. Examples of such a purification operation include a purification method using a reverse osmosis membrane; or a purification method in which the dye base is stirred in a mixed solvent of alcohol such as methanol and water, separated by filtration, and dried. Examples of inorganic impurities include chlorides (for example, sodium chloride) and sulfides (for example, sodium sulfate) of Group 1 and / or Group 2 elements of the periodic table of elements. When purification is performed, the total content of inorganic impurities in the total mass of the ink composition is preferably 100 ppm or less, and more preferably 50 ppm or less. The lower limit may be equal to or lower than the detection limit of the detection device, that is, 0%.

In order to obtain the effects of the present invention with the aqueous ink composition, the content of the colorant (II) and the content of the colorant (II) in the total mass of the ink composition are extremely important. . That is, the content of the colorant (I) is usually from 2% to 65%, preferably from 4% to 60%, more preferably from 4% to 50% with respect to the content of the colorant (II). is there. These contents are calculated by rounding off the first decimal place.
If it exceeds this range, the effect of the present invention cannot be obtained, or the effect is significantly reduced.

  The ink of the present invention may further contain a toning dye in order to obtain a desired hue. The dye for toning is preferably a reactive dye, an acid dye or a direct dye, more preferably a direct dye, from the viewpoint of dyeability on a recording material.

  Specific examples of reactive dyes for toning include C.I. I. Yellow dyes such as Reactive Yellow 2, 3, 18, 81, 84, 85, 95, 99, 102; I. Orange dyes such as Reactive Orange 5, 9, 12, 13, 35, 45, 99; I. Brown dyes such as Reactive Brown 2, 8, 9, 17, 33; I. Reactive Red 3, 3: 1, 4, 13, 24, 29, 31, 33, 125, 151, 206, 218, 226, 245, and the like.

  Specific examples of the acid dye for toning include C.I. I. Acid Yellow 1, 3, 11, 17, 18, 19, 23, 25, 36, 38, 40, 40: 1, 42, 44, 49, 59, 59: 1, 61, 65, 72, 73, 79, Yellow dyes such as 99, 104, 110, 159, 169, 176, 184, 193, 200, 204, 207, 215, 219, 219: 1, 220, 230, 232, 235, 241, 242, 246; C. I. Acid Orange 3, 7, 8, 10, 19, 24, 51, 56, 67, 74, 80, 86, 87, 88, 89, 94, 95, 107, 108, 116, 122, 127, 140, 142, Orange dyes such as 144, 149, 152, 156, 162, 166, 168; I. Acid Brown 2, 4, 13, 14, 19, 28, 44, 123, 224, 226, 227, 248, 282, 283, 289, 294, 297, 298, 301, 355, 357, 413, etc. A dye; I. Acid Red 1, 6, 8, 9, 13, 18, 27, 35, 37, 52, 54, 57, 73, 82, 88, 97, 97: 1, 106, 111, 114, 118, 119, 127, 131, 138, 143, 145, 151, 183, 195, 198, 211, 215, 217, 225, 226, 249, 251, 254, 256, 257, 260, 261, 264, 265, 266, 274, 276, 277, 289, 296, 299, 315, 318, 336, 337, 357, 359, 361, 362, 364, 366, 399, 407, 415, and the like;

  Specific examples of direct dyes for toning include C.I. I. Direct Yellow 8, 11, 12, 21, 28, 33, 39, 44, 49, 50, 85, 86, 87, 88, 89, 98, 100, 110, 132, 142, 144, 146, etc. A dye; I. Orange dyes such as Direct Orange 17, 26, 39, 102; I. Direct Red 2, 4, 6, 9, 17, 23, 26, 28, 31, 39, 54, 55, 57, 62, 63, 64, 65, 68, 72, 75, 76, 79, 80, 81, 83 83: 1, 84, 89, 92, 95, 99, 111, 141, 173, 180, 184, 207, 211, 212, 214, 218, 221, 223, 224, 225, 226, 227, 232, 233 , 240, 241, 242, 243, 247, etc .;

  Of these dyes, C.I. I. Direct Yellow 86, 132, 142, C.I. I. Direct Orange 17, 39, C.I. I. Direct Red 80, 84, 227, C.I. I. Direct Brown 106, 125, 195, C.I. I. When one or more kinds of dyes selected from Acid Red 249, 254 are contained, the print density obtained with the aqueous ink composition is more suitable because it produces a higher color. Among these, C.I. I. Orange dyes selected from Direct Orange are preferred.

When the aqueous ink composition contains the pH adjusting agent represented by the above formula (2), it is possible to provide a stable ink that suppresses fluctuations in pH over a long period of time and does not cause changes in physical properties. This effect is an effect that cannot be obtained when an inorganic compound such as a hydroxide (for example, sodium hydroxide) of a group 1 element of the periodic table of elements is used. For this reason, when providing the said stable water-based ink composition, it is preferable that this water-based ink composition further contains the pH adjuster represented by Formula (2).
The pH range after the adjustment is usually pH 7 or higher, preferably 7 to 12, more preferably 7 to 10.

In formula (2), as the alkyl group, hydroxyalkyl group, and hydroxyalkoxyalkyl group in R ₈ , R _9, and R ₁₀ , each of Z ₁ , Z ₂ , Z _3, and Z ₄ in formula (16) And the same groups including those preferred and the like.
Among these, R ₈ , R ₉ and R ₁₀ are preferably a hydrogen atom, an alkyl group or a hydroxyalkyl group, and specific examples thereof include, for example, a hydrogen atom, a methyl group, an ethyl group, a hydroxymethyl group and a hydroxyethyl group. Groups and the like.

Specific examples of combinations of R ₈ , R ₉ and R ₁₀ of the preferred compound as the formula (2) are shown in Table 5 below.

The water-based ink composition may appropriately contain a water-soluble organic solvent and an ink preparation agent as necessary within a range that does not impair the effects of the present invention.
The surface tension of the aqueous ink composition is usually 25 to 70 mN / m, preferably 25 to 60 mN / m.
The viscosity of the water-based ink composition is usually 30 mPa · s or less, preferably 20 mPa · s or less.

Examples of the water-soluble organic solvent include C1-C4 alkanols such as methanol, ethanol, propanol, isopropanol, butanol, isobutanol, sec-butanol and tert-butanol; N, N-dimethylformamide or N, N-dimethylacetamide Carboxylic acid amides; lactams such as 2-pyrrolidone and N-methylpyrrolidin-2-one; cyclics such as 1,3-dimethylimidazolidin-2-one and 1,3-dimethylhexahydropyrimido-2-one Ureas; ketones or keto alcohols such as acetone, methyl ethyl ketone, 2-methyl-2-hydroxypentan-4-one; cyclic ethers such as tetrahydrofuran, dioxane; ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol 1,2-bu C2-C6 such as lenglycol, 1,4-butylene glycol, 1,6-hexylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol, thiodiglycol, dithiodiglycol Monomer, oligomer or polyalkylene glycol or thioglycol having an alkylene unit; polyol (triol) such as glycerin, hexane-1,2,6-triol; ethylene glycol monomethyl ether or ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol mono Ethyl ether, diethylene glycol monobutyl ether butyl carbitol or triethylene C1-C4 alkyl ethers of polyhydric alcohols such as recall monomethyl ether or triethylene glycol monoethyl ether; .gamma.-butyrolactone, or dimethyl sulfoxide and the like.
Among these water-soluble organic solvents, 2-pyrrolidone, isopropyl alcohol, glycerin, diglycerin, butyl carbitol, ethylene glycol, diethylene glycol, and propylene glycol are preferable, and 2-pyrrolidone, isopropyl alcohol, glycerin, and butyl carbitol are more preferable. . These organic solvents may be used alone or in combination of two or more.

  The content of the water-soluble organic solvent is usually 0 to 50%, preferably 10 to 50%, more preferably 25 to 50% with respect to the total mass of the water-based ink composition.

  Examples of the ink preparation agent include antiseptic / antifungal agents, pH adjusting agents, chelating reagents, rust preventive agents, water-soluble ultraviolet absorbers, water-soluble polymer compounds, dye solubilizers, antioxidants, and surfactants. It is done.

  Examples of the antifungal agent include sodium dehydroacetate, sodium benzoate, sodium pyridinethione-1-oxide, p-hydroxybenzoic acid ethyl ester, 1,2-benzisothiazolin-3-one and salts thereof. When it contains an antifungal agent, it is preferably used in an amount of 0.02 to 1% based on the total mass of the aqueous ink composition.

  Examples of the preservative include organic sulfur, organic nitrogen sulfur, organic halogen, haloallylsulfone, iodopropargyl, N-haloalkylthio, (double) nitrile, pyridine, 8-oxyquinoline, Benzothiazole, isothiazoline, dithiol, pyridine oxyd, nitropropane, organotin, phenol, quaternary ammonium salt, triazine, thiazine, anilide, adamantane, dithiocarbamate, brominated indanone , Benzyl bromacetate compounds, inorganic salt compounds and the like. An example of the organic halogen compound is sodium pentachlorophenol. As a pyridine oxydide-type compound, 2-pyridinethiol-1-oxide sodium is mentioned, for example. An example of the inorganic salt compound is anhydrous sodium acetate. Examples of isothiazoline compounds include 1,2-benzisothiazolin-3-one, 2-n-octyl-4-isothiazolin-3-one, 5-chloro-2-methyl-4-isothiazolin-3-one, 5- Chloro-2-methyl-4-isothiazolin-3-one magnesium chloride, 5-chloro-2-methyl-4-isothiazolin-3-one calcium chloride, 2-methyl-4-isothiazolin-3-one calcium chloride and the like It is done. Other antiseptic / antifungal agents include sodium sorbate, sodium benzoate and the like.

As the pH adjuster, any substance can be used as long as it can control the pH of the ink within a range of, for example, 5 to 11 without adversely affecting the prepared ink. Examples include alkanolamines such as diethanolamine, triethanolamine, N-methyldiethanolamine, alkali metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide, ammonium hydroxide (ammonia), or lithium carbonate. And alkali metal carbonates such as sodium carbonate, sodium hydrogen carbonate and potassium carbonate, and inorganic bases such as potassium acetate, sodium silicate and disodium phosphate.
In these, the pH adjuster represented by the said Formula (2) is preferable.

  Examples of chelating reagents include sodium ethylenediaminetetraacetate, sodium nitrilotriacetate, sodium hydroxyethylethylenediaminetriacetate, sodium diethylenetriaminepentaacetate, sodium uracil diacetate, and the like.

  Examples of the rust inhibitor include acidic sulfite, sodium thiosulfate, ammonium thioglycolate, diisopropylammonium nitrite, pentaerythritol tetranitrate, and dicyclohexylammonium nitrite.

  Examples of the water-soluble ultraviolet absorber include sulfonated benzophenone compounds, benzotriazole compounds, salicylic acid compounds, cinnamic acid compounds, and triazine compounds.

  Examples of the water-soluble polymer compound include polyvinyl alcohol, cellulose derivatives, polyamines and polyimines.

  Examples of the dye solubilizer include ε-caprolactam, ethylene carbonate, urea and the like. Among these, urea is preferable.

  As the antioxidant, for example, various organic and metal complex antifading agents can be used. Examples of the organic anti-fading agent include hydroquinones, alkoxyphenols, dialkoxyphenols, phenols, anilines, amines, indanes, chromans, alkoxyanilines, and heterocyclic rings.

Examples of the surfactant include known surfactants such as anions, cations, and nonions.
Examples of anionic surfactants include alkyl sulfonates, alkyl carboxylates, α-olefin sulfonates, polyoxyethylene alkyl ether acetates, N-acyl amino acids and salts thereof, N-acyl methyl taurate, alkyl sulfate poly Oxyalkyl ether sulfate, alkyl sulfate polyoxyethylene alkyl ether phosphate, rosin acid soap, castor oil sulfate ester, lauryl alcohol sulfate ester, alkylphenol type phosphate ester, alkyl type phosphate ester, alkyl allyl sulfone hydrochloride, diethyl sulfo Examples thereof include oxalate, diethylhexylsilsulfosuccinate, dioctylsulfosuccinate and the like.
Examples of the cationic surfactant include 2-vinylpyridine derivatives and poly-4-vinylpyridine derivatives. Amphoteric surfactants include lauryldimethylaminoacetic acid betaine, 2-alkyl-N-carboxymethyl-N-hydroxyethylimidazolinium betaine, coconut oil fatty acid amidopropyldimethylaminoacetic acid betaine, polyoctylpolyaminoethylglycine and other imidazoline derivatives. Can be mentioned.
Nonionic surfactants include polyoxyethylene nonyl phenyl ether, polyoxyethylene octyl phenyl ether, polyoxyethylene dodecyl phenyl ether, polyoxyethylene oleyl ether, polyoxyethylene lauryl ether, polyoxyethylene alkyl ether, polyoxyallylalkyl. Ethers such as alkyl ethers, polyoxyethylene oleic acid, polyoxyethylene oleate, polyoxyethylene distearate, sorbitan laurate, sorbitan monostearate, sorbitan monooleate, sorbitan sesquioleate, polyoxyethylene monooleate Esters, polyoxyethylene stearate, 2,4,7,9-tetramethyl-5-decyne-4,7-di Acetylene glycol (alcohol) systems such as 3,6-dimethyl-4-octyne-3,6-diol and 3,5-dimethyl-1-hexyne-3ol (for example, Surfynol 104 manufactured by Nisshin Chemical Co., Ltd.) , 105, 82, 420, 440, 465, Olphine STG, etc.).
Of these, Surfynol 420, 440 and 465 are preferred.

In the production of the water-based ink composition, there is no particular limitation on the order of dissolving each additive such as a colorant, a water-soluble organic solvent, and an ink adjusting agent.
The water used for the preparation of the ink composition is preferably water with few inorganic impurities such as ion exchange water and distilled water.
In addition, if necessary, after the ink composition is prepared, fine filtration may be performed using a membrane filter or the like to remove impurities in the ink composition. In particular, when the ink composition is used for ink jet recording, it is preferable to perform microfiltration. The pore size of the filter used for microfiltration is usually 1 μm to 0.1 μm, preferably 0.8 μm to 0.1 μm.

  The aqueous ink composition can be used in various fields. For example, it can be used for writing, water-based printing, information recording, and the like, and is particularly preferably used for inkjet recording.

  When performing the ink jet recording, an ink jet printer is generally used. There is no restriction | limiting in particular about the ink nozzle etc. with which the inkjet printer is provided, According to the objective, it can select suitably. For example, a charge control method that ejects ink using electrostatic attraction force; a drop-on-demand method (pressure pulse method) that uses the vibration pressure of a piezo element; Acoustic ink jet method that discharges ink using pressure; a known ink jet recording method such as thermal ink jet that heats ink to form bubbles and uses the generated pressure, for example, bubble jet (registered trademark) method; be able to. The ink jet recording method is a method in which a large amount of ink having a small colorant content called a photo ink is ejected in a small volume; a plurality of inks having substantially the same hue and different colorant contents are used. A method of improving image quality; or a method of using a color ink and a colorless and transparent ink in combination;

The ink jet recording method is a method of performing recording by ejecting droplets of the water-based ink composition in accordance with a recording signal and attaching them to a recording material.
By using the above water-based ink composition as a black ink and combining it with each ink composition such as magenta, cyan, yellow, green, blue (or violet), and red (or orange) as necessary, full color It is also possible to obtain a recorded image. In this case, the ink composition of each color can be poured into each container, and the container can be loaded into a predetermined position of the ink jet printer and used for ink jet recording in the same manner as the container containing the aqueous ink composition. it can.

The colored body means a substance colored with the water-based ink composition, and is preferably a substance colored by the inkjet recording method.
The substance is not particularly limited as long as it can be colored by the aqueous ink composition. Among such substances, recording materials such as information transmission sheets such as paper and film; fibers and fabrics (cellulose, nylon, wool, etc.); leather; base materials for color filters;
Examples of the information transmission sheet include those that have been surface-treated, specifically, those in which an ink receiving layer is provided on a substrate such as paper, synthetic paper, and film, and those in which an ink receiving layer is not particularly provided. It is done. The ink receiving layer is formed by, for example, impregnating or coating the base material with a cationic polymer; a porous white inorganic material capable of absorbing a colorant in an aqueous ink composition such as porous silica, alumina sol, or special ceramics; It is provided by coating the surface of the substrate together with a hydrophilic polymer such as alcohol or polyvinylpyrrolidone; Those provided with such an ink receiving layer are usually called ink jet dedicated paper (film), glossy paper (film) and the like. Specific examples thereof include, for example, Pictrico manufactured by Asahi Glass Co., Ltd .; professional photo paper manufactured by Canon Inc., super photo paper, matte photo paper, glossy gold, platinum grade; photographic paper manufactured by Seiko Epson Corporation ( Glossy), photo matte paper, photographic paper Crispier (high gloss); Premium Plus Photo Paper, Premium Glossy Film, Photo Paper, Advanced Photo Paper manufactured by Hewlett-Packard Japan; Photo-like QP manufactured by Konica Corporation; Examples include painting photo finishing Pro; manufactured by FUJIFILM Corporation.
On the other hand, examples of the information transmission sheet that is not particularly provided with an ink receiving layer include plain paper, high-quality paper, and coated paper. Many types of plain paper are commercially available depending on the application. Examples of commercially available plain paper include: Double-sided fine plain paper manufactured by Seiko Epson Corporation; Color plain paper manufactured by Canon Inc .; Multipurpose Paper, All-in-One Printing manufactured by Hewlett Packard Co., Ltd. Paper; Matte paper for inkjet manufactured by Mitsubishi Paper Industries, Ltd., trade name DL-9084; Premium multi-purpose paper 4024 manufactured by Xerox Corporation; and the like. In addition, PPC (plain paper copy) paper and the like are plain paper.

The aqueous ink composition is very clear on the recording material, has high saturation and printing density, and gives a black recorded image with an ideal hue. Further, the aqueous black ink composition of the present invention has very good storage stability without solid precipitation, physical property change, hue change and the like after long-term storage.
The aqueous black ink composition of the present invention is used for inkjet recording and writing instruments, and even when used as an inkjet ink, solid precipitation due to drying of the ink composition near the nozzle is very unlikely to occur. ) Is not blocked. In addition, the aqueous black ink composition of the present invention uses a continuous ink jet printer, and when the ink is recirculated at a relatively long time interval or used intermittently by an on-demand ink jet printer, Does not cause changes in physical properties.
Furthermore, the image recorded with the water-based black ink composition of the present invention has various fastness properties such as water resistance, moisture resistance, ozone gas resistance, abrasion resistance, and light resistance, particularly light resistance and water resistance.
In addition, the recording material has excellent long-term storage stability, and particularly excellent in light resistance and water resistance together with the hue on plain paper. In addition, it is excellent in color developability such as saturation, brightness, and print density, color rendering, and sensor-compatible characteristics in the near infrared light region.

  EXAMPLES The present invention will be described more specifically with reference to examples. However, the present invention is not limited to the examples. Moreover, in each structural formula of the compound obtained in the Example, acidic functional groups, such as a sulfo group, were described in the form of a free acid.

[(A) Synthesis of Colorant (I)] [Synthesis Examples 1 to 3] According to the method described in Patent Document 3, the colorant represented by the following formula (22), formula (23) and formula (26) (I) was synthesized respectively.

[(B) Preparation of aqueous ink composition]
[Examples 1-5 and Comparative Examples 1-6]
Each component described in Table 6 below was mixed and stirred for about 1 hour to obtain a solution, followed by filtration with a 0.45 μm membrane filter (trade name cellulose acetate filter paper manufactured by Advantech) for evaluation tests. A water-based ink composition was prepared. In addition, the numerical value of each component in the following Table 6 means “part”.

Moreover, the abbreviations in Table 6 below have the following meanings.
(I): Colorant (I).
(II): Colorant (II).
AB2: C.I. I. Acid Black2.
DO39: C.I. I. Direct Orange 39.
GLY: Glycerin.
2-PY: 2-pyrrolidone.
IPA: isopropyl alcohol.
BCA: Butyl carbitol.
SF440: Surfynol 440.
TEA: triethanolamine.

[(C) Inkjet recording]
The water-based ink compositions prepared in each Example and Comparative Example were subjected to inkjet recording on the following plain papers 1 and 2 using an inkjet printer manufactured by EPSON Co., Ltd., trade name PX105.
Plain paper 1: Premium Multipurpose Paper 4024 manufactured by Xerox Co., Ltd.
Plain paper 2: manufactured by Mitsubishi Paper Industries Co., Ltd., inkjet mat paper, trade name DL-9084.
During ink jet recording, an image pattern is created so that six levels of gradations of 100%, 80%, 60%, 40%, 20%, and 10% density can be obtained, and a dark black to light black gradation recorded matter. Got. The following evaluation tests were carried out using this as a test piece.

[(D) Colorimeter and colorimetric conditions]
When color measurement was necessary in the following evaluation tests, color measurement was performed using the following colorimeter and color measurement conditions.
Colorimeter:
Product name SpectroEye manufactured by GRETAG-MACBETH.
Colorimetric conditions:
The density standard is ANSI A, the viewing angle is 2 °, and the light source is D50.

[(E) Hue evaluation test]
Of the test pieces of the examples and comparative examples obtained in the above “(C) Inkjet recording”, L *, a *, b * of the gradation portion of 100% density in the test piece using plain paper 1 The chroma C * value was calculated using the following formula.
C * = (a * ² + b * ² ) ^1/2
In addition, obtained C * is a preferable black hue, so that it is close to 0, and it evaluated it on the basis of the following four steps. In this standard, “B” or more is a normal practical black hue.
A: C * is less than 3.0.
B: C * is 3.0 or more and less than 4.0.
C: C * is 4.0 or more and less than 7.0.
D: C * is 7.0 or more.
The results are shown in Table 7 below.

[(F) Light resistance test]
Of the test pieces obtained in “(C) Inkjet recording” and the test pieces of Comparative Examples, test pieces using plain paper 1 were prepared, and then air-dried for 24 hours. The test piece after drying was set in a xenon weatherometer XL75 (manufactured by Suga Test Instruments Co., Ltd.) and irradiated for 72 hours at a temperature of 24 ° C., a humidity of 60% RH, and 100 kLux. After the completion of irradiation, each test piece was measured for color difference (ΔE) before and after the test. In addition, the smaller the obtained color difference ΔE means that there is less discoloration due to light, and the light resistance is excellent.
A: ΔE is less than 3.0.
B: ΔE is 3.0 or more and less than 5.0.
C: ΔE is 5.0 or more and less than 8.0.
D: ΔE is 8.0 or more.
The results are shown in Table 7 below.

[(G) Water resistance test]
Of the test pieces obtained in “(C) Inkjet recording” and the test pieces of Comparative Examples, test pieces using plain paper 2 were prepared, and then air-dried for 24 hours. The test piece after drying was immersed in ion-exchanged water for 10 minutes, and then the test piece was slowly taken out from water and dried by natural drying for 24 hours. The color of this test piece was measured, and the residual rate (%) of the Dk value before and after the test was calculated. In addition, the one where the obtained residual rate (%) is large means that there is little fading by water, and shows that it is excellent in water resistance.
A: The residual rate after the test is 95% or more.
B: The residual rate after the test is 93% or more and less than 95%.
C: The residual ratio after the test is 90 or more and less than 93%.
D: Residual rate after test is less than 90%.
The results are shown in Table 7 below.

  As is clear from the results of Table 7, it was revealed that each example gave an achromatic and high-quality black image. Furthermore, it is confirmed that each comparative example is excellent in light resistance and water resistance, and the content of the colorant (I) with respect to the colorant (II) is extremely important for improving light resistance and water resistance. Became clear.

  Since the water-based ink composition of the present invention is excellent in hue, light resistance and water resistance, it is very suitably used for various recording applications, particularly inkjet recording.

Claims (8)

At least two kinds of colorants (I) and colorant (II), and C.I. I. An aqueous ink composition containing at least one colorant selected from Direct Orange, wherein the content of the colorant (I) in the total mass of the aqueous ink composition is that of the colorant (II) The colorant (I) is a dye represented by the following formula (1) or a salt thereof, and the colorant (II) is C.I. I. An aqueous ink composition that is Acid Black 2.
(In the above formula (1),
R ₁ , R ₂ , R ₅ , R ₆ and R ₇ each independently have a hydrogen atom, a halogen atom, a cyano group, a hydroxy group, a carboxy group, a sulfo group, a sulfamoyl group, a nitro group, or a substituent. Represents a group selected from the group consisting of an alkoxy group which may have a substituent, an alkylsulfonyl group which may have a substituent, an alkyl group, an arylsulfamoylamino group which may have a substituent, and an alkylcarbonylamino group .
R ₃ and R ₄ are each independently selected from the group consisting of a hydrogen atom, a halogen atom, a cyano group, a sulfo group, a carboxy group, a nitro group, an optionally substituted alkoxy group, and an alkyl group. Represents a group.
n represents 0 or 1. ) The aqueous ink composition according to claim 1, further comprising a compound represented by the following formula (2) as a pH adjuster.
(In formula (2), R ₈ , R ₉ and R ₁₀ each independently represent a group selected from the group consisting of a hydrogen atom, an alkyl group, a hydroxyalkyl group, and a hydroxyalkoxyalkyl group.) In the formula (1), R ₁ is a carboxy group or a sulfo group, R ₂ is a hydrogen atom, R ₆ is a nitro group, a carboxy group, or a sulfo group, and n is 1. The water-based ink composition as described. In the formula (1), R ₁ and R ₃ are sulfo groups, R ₄ is a hydrogen atom, R ₅ is a hydrogen atom, a carboxy group, or a sulfo group, and R ₆ is a nitro group, a carboxy group, or a sulfo group. The water-based ink composition according to claim 1, which is a group, R ₇ is a hydrogen atom, and n is 1.   An ink jet recording method for performing recording by ejecting droplets of the water-based ink composition according to any one of claims 1 to 4 in accordance with a recording signal and attaching the droplets to a recording material.   The ink jet recording method according to claim 5, wherein the recording material is an information transmission sheet.   The colored body to which the water-based ink composition as described in any one of Claims 1-4 adhered.   An inkjet printer having a container containing the water-based ink composition according to claim 1.