WO2012053512A1 - Composé azoïque hydrosoluble ou sel de celui-ci, composition d'encre et corps coloré - Google Patents

Composé azoïque hydrosoluble ou sel de celui-ci, composition d'encre et corps coloré Download PDF

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Publication number
WO2012053512A1
WO2012053512A1 PCT/JP2011/073938 JP2011073938W WO2012053512A1 WO 2012053512 A1 WO2012053512 A1 WO 2012053512A1 JP 2011073938 W JP2011073938 W JP 2011073938W WO 2012053512 A1 WO2012053512 A1 WO 2012053512A1
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water
ink
formula
salt
ink composition
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PCT/JP2011/073938
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English (en)
Japanese (ja)
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陵太郎 森田
梶浦　典子
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日本化薬株式会社
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Priority to JP2012539733A priority Critical patent/JPWO2012053512A1/ja
Publication of WO2012053512A1 publication Critical patent/WO2012053512A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/30—Inkjet printing inks
    • C09D11/32—Inkjet printing inks characterised by colouring agents
    • C09D11/328—Inkjet printing inks characterised by colouring agents characterised by dyes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
    • C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
    • C09B43/16—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues

Definitions

  • the present invention relates to a water-soluble disazo compound or a salt thereof, an ink composition containing the same, and a colored body colored with these.
  • ink ejection methods have been developed as recording methods using an ink jet printer, which is one of the representative methods. These all generate ink droplets and attach them to various recording materials (paper, film, fabric, etc.) for recording. In this method, since the recording head and the recording material are not in direct contact with each other, no noise is generated and the method is quiet. In addition, since it has the characteristics that it is easy to downsize, speed up, and colorize, it has been rapidly spreading in recent years and is expected to grow greatly in the future. Conventionally, inks such as fountain pens and felt pens, and inks for ink-jet recording have been used in which water-soluble pigments (dyes) are dissolved in an aqueous medium.
  • inks such as fountain pens and felt pens, and inks for ink-jet recording have been used in which water-soluble pigments (dyes) are dissolved in an aqueous medium.
  • a water-soluble organic solvent is added to these water-based inks in order to prevent clogging of ink at a pen tip or an ink discharge nozzle.
  • These inks give a recorded image of sufficient density, do not cause clogging of the pen tip and nozzles, have good drying properties on the recording material, have little bleeding, and have excellent storage stability. Such performance is required.
  • Ink jet nozzle clogging occurs when the water in the ink evaporates in the vicinity of the nozzle before other solvents and additives, and the pigment solidifies and precipitates when the composition state is low in water and high in solvents and additives.
  • the very important required performances is that solids are not easily deposited even when the moisture content in the ink is low. For this reason, high solubility in solvents and additives is one of the properties required for pigments.
  • a method for eliminating nozzle clogging a method using a dye having a high printing density is known. By using a pigment having a high printing density, the pigment content in the ink can be reduced while maintaining the conventional printing density. This not only makes it difficult to precipitate the dye, but is also advantageous in terms of cost, and development of a dye having a high printing density is desired.
  • the color area that can be expressed in a single color or mixed color becomes narrow, and the range of the color area that is desired to be expressed may be insufficient. For this reason, development of highly saturated pigments and inks containing them is desired.
  • the ink performance is required to be stable for long-term storage, high in recorded image density, and excellent in fastness such as water resistance, moisture resistance, light resistance and gas resistance. It is done.
  • the gas resistance means that a gas having an oxidizing action (also referred to as an oxidizing gas) existing in the air reacts with a dye (dye) of a recorded image on the recording material or in the recording material to record.
  • ozone gas is considered to be a main causative substance that promotes the discoloration and fading phenomenon of ink jet recorded images. Since this discoloration phenomenon is characteristic of ink jet recorded images, improvement of ozone gas resistance is an important technical problem in this field.
  • inkjet printers have the advantage that the type of recording paper is not limited, and the price of the printer itself is low, and the spread is particularly widespread in small to medium-sized office environments such as small offices and home offices (SOHO).
  • SOHO small offices and home offices
  • pigment ink does not dissolve in water-based ink, it does not enter a solution state, but is a dispersed ink. Therefore, when this is used for ink jet recording, there are problems with the stability of the ink itself and the nozzles of the recording head. Problems such as clogging occur.
  • pigment ink when pigment ink is used, there is often a problem in abrasion resistance. In the case of a dye ink, such a problem is considered to be relatively difficult to occur.
  • the water resistance is extremely inferior to that of a pigment ink, and an improvement to the problem is strongly desired.
  • dye ink tends to cause a problem that a dye attached to the surface of plain paper by ink jet recording penetrates more quickly toward the back side of the paper, resulting in a decrease in color density.
  • the ink receiving layer As one method for obtaining a photographic image-recorded inkjet image, there is a method of providing an ink receiving layer on the surface of a recording material.
  • the ink receiving layer provided for such a purpose often contains a porous white inorganic substance in order to speed up drying of the ink and to reduce bleeding of the pigment with high image quality.
  • discoloration due to ozone gas is noticeable.
  • With the recent spread of digital cameras and color printers there are increasing opportunities to print images obtained with digital cameras and the like as photographic image quality at home, so the above-mentioned color change of recorded images due to oxidizing gas is regarded as a problem. .
  • yellow dyes Compared to the other three primary colors, magenta and cyan, yellow dyes have been proposed that have good resistance to oxidizing gas as well as light resistance. However, yellow dyes and yellow inks for inkjet recording that sufficiently satisfy the high sharpness and various fastnesses required by the market have not been obtained yet.
  • Examples of known yellow pigments for inkjet which are excellent in water solubility and sharpness include C.I. I. (Color index) Direct yellow 132 is exemplified.
  • Patent Document 1 discloses a yellow anionic azo compound having light resistance and water fastness.
  • Patent Document 2 discloses a yellow water-soluble azo compound that is highly soluble in water and has moisture resistance, ozone gas resistance, and light resistance.
  • Patent Document 3 discloses a yellow water-soluble azo compound that is highly soluble in water, has moisture resistance, ozone gas resistance, and light resistance, and is particularly excellent in fastness such as water resistance on plain paper. ing.
  • the present invention relates to a water-soluble yellow dye (compound) having high solubility in water and excellent in chroma, ozone resistance and water resistance of recorded images, and various recordings containing the same, particularly yellow ink for inkjet recording.
  • the purpose is to provide a composition.
  • the present invention 1) A water-soluble azo compound represented by the following formula (1) or a salt thereof, (In the formula, Q represents a halogen atom, x represents an integer of 2 to 4, and the group A represents an amino group represented by any one of the following formulas (2) to (5).) (In formula (2), y represents an integer of 1 to 5) (In the formula (4), m represents 1 or 2.) (In formula (5), n represents an integer of 0 to 2, and Z represents a hydrogen atom, a carboxy group, or a sulfo group.)
  • the water-soluble azo compound of the present invention represented by the above formula (1) or a salt thereof has a high solubility in water, and for example, in the process of producing the ink composition of the present invention containing the compound or a salt thereof, It has the characteristic that the filterability with respect to a membrane filter is favorable.
  • an image recorded by the ink composition of the present invention containing the compound of the present invention is excellent in saturation, ozone resistance, and water resistance as compared with those using conventional compounds.
  • the water-soluble azo compound of the present invention represented by the formula (1) or a salt thereof, and the ink composition containing the same are extremely useful for various recording ink applications, particularly ink jet recording ink applications. It is.
  • the water-soluble azo compound of the present invention represented by the above formula (1) or a salt thereof is a water-soluble yellow dye.
  • acidic functional groups such as sulfo groups and carboxy groups are represented in the form of free acids.
  • the present invention includes both the water-soluble azo compound represented by the formula (1) or a salt of the compound, but it is complicated to always describe both of them as “compound or salt thereof”. It is. Therefore, unless otherwise specified, for convenience, the “water-soluble azo compound of the present invention or a salt thereof” including both the “water-soluble azo compound of the present invention” will be simply described as “the (water-soluble azo) compound of the present invention”.
  • the compound of the present invention is represented by the above formula (1).
  • Q represents a halogen atom.
  • the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
  • a fluorine atom or a chlorine atom is preferable, and a chlorine atom is particularly preferable.
  • x represents an integer of 2 to 4, preferably 3.
  • the group A represents an amino group represented by any one of the above formulas (2) to (5).
  • y in Formula (2) represents an integer of 1 to 5, preferably 1 or 2, and more preferably 1.
  • m represents 1 or 2, preferably 2.
  • Z represents a hydrogen atom, a carboxy group, or a sulfo group, preferably a sulfo group.
  • n represents an integer of 0 to 2, and is preferably 1.
  • the group A is preferably an amino group represented by the above formula (2) or (3), and more preferably an amino group represented by the above formula (2).
  • the compound of the present invention represented by the above formula (1) can be produced, for example, as follows.
  • Q, group A, Z, m, n, x, and y used appropriately in the following formulas (AA) to (F) are the formulas (1), (2), (4), (5), respectively.
  • Represents the same meaning as in A compound represented by the following formula (AA) obtained using a commercially available 2-amino-4-halogenophenol as a raw material is converted into methyl- ⁇ -sulfone represented by the following formula (B) using sodium bisulfite and formalin. Convert to acid derivative.
  • 3-amino-4-chlorobenzoic acid represented by the following formula (C) is diazotized by a conventional method to obtain the methyl- ⁇ -sulfonic acid derivative represented by the following formula (B)
  • a coupling reaction is carried out at a reaction temperature of 0 to 15 ° C. and a pH of 2 to 4, followed by a hydrolysis reaction at a reaction temperature of 80 to 95 ° C. and a pH of 10.5 to 11.5. Is obtained.
  • This synthesis is a method according to the method described in JP-A-2004-75719.
  • the chlorine atom on the triazine ring in the obtained compound represented by the above formula (E) is represented by the following formulas (F) to (I) under the reaction temperature of 75 to 90 ° C. and pH of 7 to 9.
  • the compound of the present invention represented by the above formula (1) can be obtained by substituting with an amine.
  • amine represented by the above formula (F) examples include glycine, ⁇ -alanine, 4-aminobutyric acid, 5-aminovaleric acid, 6-aminohexanoic acid and the like.
  • the amine represented by the above formula (G) can be easily obtained as a commercial product as iminodiacetic acid.
  • Specific examples of the amine of the above formula (H) include aspartic acid and glutamic acid.
  • Examples of the amine represented by the above formula (I) include aniline, benzylamine, phenethylamine, 4-aminomethylbenzenesulfonic acid, 4-aminomethylbenzoic acid, 2-aminobenzenesulfonic acid, 3-aminobenzenesulfonic acid, 4 Specific examples include aminobenzenesulfonic acid, 2-aminobenzoic acid, 3-aminobenzoic acid, 4-aminobenzoic acid and the like.
  • the compound represented by the above formula (1) exists also as a free acid or a salt thereof.
  • the salt of the compound represented by the formula (1) include salts with inorganic or organic cations.
  • Specific examples of the inorganic cation salt include alkali metal salts such as lithium salts, sodium salts, potassium salts and the like; and ammonium salts (NH 4 + ).
  • Examples of organic cation salts include, but are not limited to, quaternary ammonium salts represented by the following formula (7).
  • Z 1 to Z 4 each independently represents a hydrogen atom, a C1-C4 alkyl group, a hydroxy C1-C4 alkyl group, or a hydroxy C1-C4 alkoxy C1-C4 alkyl group, and Z 1 -Z At least one of 4 is a group other than a hydrogen atom.
  • examples of the C1-C4 alkyl group in Z 1 to Z 4 include methyl, ethyl and the like.
  • examples of the hydroxy C1-C4 alkyl group include hydroxymethyl, hydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl, 4-hydroxybutyl, 3-hydroxybutyl, 2-hydroxybutyl and the like.
  • examples of the hydroxy C1-C4 alkoxy C1-C4 alkyl group include hydroxyethoxymethyl, 2-hydroxyethoxyethyl, 3- (hydroxyethoxy) propyl, 3- (hydroxyethoxy) butyl, 2- (hydroxyethoxy ) Butyl and the like.
  • alkali metal salts such as sodium, potassium and lithium
  • organic quaternary ammonium salts such as monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine and triisopropanolamine salts
  • Ammonium salt and the like.
  • lithium salts, sodium salts, and ammonium salts are more preferable.
  • the salt or free acid of the compound represented by the above formula (1) can be easily obtained by the following method or the like.
  • the reaction solution after completion of the final step or the aqueous solution containing the salt of the compound represented by the formula (1) for example, acetone or C1-C4 alcohol
  • a method of adding a water-soluble organic solvent, a method of salting out by adding sodium chloride, and the like for example, acetone or C1-C4 alcohol
  • a potassium salt, a lithium salt, an ammonium salt, a quaternary ammonium salt, and the like corresponding to each added compound can be obtained.
  • a mixed salt of lithium salt and sodium salt, etc .; and a mixture of lithium salt, sodium salt, and ammonium salt Salts and the like can also be prepared.
  • the salt of the compound represented by the above formula (1) may change the physical properties such as solubility or the ink performance when used as an ink depending on the type of the salt. For this reason, it is also preferable to select the type of salt according to the intended ink performance.
  • the compound of the present invention represented by the above formula (1) can be isolated as a solid free acid by adding a mineral acid such as hydrochloric acid, and the resulting free acid solid can be isolated with water or, for example, By washing with acidic water such as hydrochloric acid water, inorganic salts (inorganic impurities) contained as impurities, such as sodium chloride and sodium sulfate, can be removed.
  • acidic water such as hydrochloric acid water
  • inorganic salts inorganic impurities contained as impurities, such as sodium chloride and sodium sulfate
  • Examples of the inorganic base include alkali metal hydroxides such as lithium hydroxide, sodium hydroxide, and potassium hydroxide; alkali metal carbonates such as lithium carbonate, sodium carbonate, and potassium carbonate; ammonium hydroxide (ammonia water); Etc.
  • Examples of the organic base include, for example, organic amines corresponding to the quaternary ammonium represented by the above formula (7), for example, alkanolamines such as diethanolamine and triethanolamine, but are not limited thereto. .
  • the compound of the present invention is suitable for dyeing natural and synthetic fiber materials or blended products, and also for producing inks for writing and ink jet recording.
  • the reaction solution after completion of the final step in the synthesis reaction of the compound of the present invention represented by the above formula (1) can be directly used for the production of the ink composition of the present invention.
  • the reaction solution or the like is dried by the above-described method or a spray drying method to isolate the compound, the obtained compound can be processed into an ink composition.
  • the compound represented by the above formula (1) is mixed with water or a mixed solution (also referred to as an aqueous medium) of water and a water-soluble organic solvent (an organic solvent that can be mixed with water). It is dissolved and an ink preparation agent is added if necessary.
  • a metal cation chloride contained as an impurity such as sodium chloride
  • sulfate such as sodium sulfate
  • Is preferred when this ink composition is used as an ink for an ink jet printer, a metal cation chloride contained as an impurity, such as sodium chloride; sulfate, such as sodium sulfate; Is preferred.
  • the total content of sodium chloride and sodium sulfate is about 1% by mass or less with respect to the total mass of the compound represented by the formula (1), and the lower limit is 0% by mass, that is, the detection instrument. It may be below the detection limit.
  • Examples of a method for producing a compound having a small amount of inorganic impurities include a method using a known reverse osmosis membrane; a dry product or a wet cake of the compound of the present invention, for example, acetone or C1-C4 alcohol (for example, methanol, ethanol, isopropanol, etc.)
  • a water-soluble organic solvent such as
  • a water-containing water-soluble organic solvent a suspension purification or crystallization method; and the like, and desalting treatment may be performed by these methods.
  • the compound represented by the formula (1) is usually 0.1 to 20% by mass, preferably 1 to 10% by mass, more preferably 2 to 2% by mass in the total mass of the ink composition. 8% by mass is contained.
  • the ink composition of the present invention is prepared using water as a medium, and may optionally contain a water-soluble organic solvent and an ink preparation agent as long as the effects of the present invention are not impaired.
  • the water-soluble organic solvent dissolves the dye; prevents the composition from drying (maintains a wet state); adjusts the viscosity of the composition; promotes penetration of the dye into the recording material; adjusts the surface tension of the composition;
  • the ink composition of the present invention is preferably contained.
  • ink preparation agent examples include antiseptic / antifungal agents, pH adjusting agents, chelating reagents, rust preventive agents, ultraviolet absorbers, viscosity adjusting agents, dye dissolving agents, antifading agents, surface tension adjusting agents, antifoaming agents, etc.
  • Known additives may be mentioned.
  • the content of the water-soluble organic solvent is 0 to 60% by mass, preferably 10 to 50% by mass, and the ink preparation agent is 0 to 20% by mass, preferably 0%, based on the total mass of the ink composition of the present invention. It is preferable to use up to 15% by mass.
  • the balance other than the compound represented by the above formula (1), the water-soluble organic solvent, and the ink preparation agent is water.
  • water-soluble organic solvent examples include C1-C4 alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol and tert-butanol; N, N-dimethylformamide, N Amides such as N-dimethylacetamide; 2-pyrrolidone, N-methyl-2-pyrrolidone, hydroxyethyl-2-pyrrolidone, 1,3-dimethylimidazolidin-2-one, 1,3-dimethylhexahydropyrimido Heterocyclic ketones such as -2-one; ketones or ketoalcohols such as acetone, methyl ethyl ketone, 2-methyl-2-hydroxypentan-4-one; cyclic ethers such as tetrahydrofuran, dioxane; ethylene glycol, 1,2- or 1,3-propylene glycol, 1,2 Or mono having a
  • the water-soluble organic solvent includes substances that are solid at room temperature, such as trimethylolpropane.
  • the substance or the like shows water solubility, and an aqueous solution containing the substance or the like shows the same properties as the water-soluble organic solvent and can be used with the expectation of the same effect. Therefore, in this specification, for the sake of convenience, such a solid substance is included in the category of a water-soluble organic solvent as long as it can be used in expectation of the same effect as described above.
  • water-soluble organic solvent examples include isopropanol, glycerin, mono-, di- or triethylene glycol, dipropylene glycol, 2-pyrrolidone, hydroxyethyl-2-pyrrolidone, N-methyl-2-pyrrolidone, trimethylolpropane, And butyl carbitol, more preferably isopropanol, glycerin, diethylene glycol, 2-pyrrolidone, N-methyl-2-pyrrolidone, and butyl carbitol. These water-soluble organic solvents are used alone or in combination.
  • antiseptic / antifungal agent examples include organic sulfur, organic nitrogen sulfur, organic halogen, haloallylsulfone, iodopropargyl, N-haloalkylthio, benzothiazole, nitrile, pyridine, 8-oxyquinoline, isothiazoline, dithiol, pyridine oxide, nitropropane, organotin, phenol, quaternary ammonium salt, triazine, thiadiazine, anilide, adamantane, dithiocarbamate, bromo Indanone compound, benzyl bromacetate compound, inorganic salt compound and the like can be mentioned.
  • An example of the organic halogen compound is sodium pentachlorophenol.
  • Examples of pyridine oxide compounds include sodium 2-pyridinethiol-1-oxide.
  • Examples of the isothiazoline compounds include 1,2-benzisothiazolin-3-one, 2-n-octyl-4-isothiazolin-3-one, 5-chloro-2-methyl-4-isothiazoline-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, etc. Can be mentioned.
  • antiseptic / antifungal agents include sodium acetate, sodium sorbate, sodium benzoate and the like; and trade names Proxel RTM GXL (S) and Proxel RTM XL-2 (S) manufactured by Arch Chemical Co., Each is listed. In the present specification, the superscript “RTM” means a registered trademark.
  • any substance can be used as long as it can control the pH of the ink in the range of 6.0 to 11.0 for the purpose of improving the storage stability of the ink.
  • alkanolamines such as diethanolamine and triethanolamine
  • hydroxides of alkali metals such as lithium hydroxide, sodium hydroxide and potassium hydroxide
  • ammonium hydroxides or alkali metals such as lithium carbonate, sodium carbonate and potassium carbonate And carbonates
  • aminosulfonic acids such as taurine; and the like.
  • chelating reagent examples include disodium ethylenediaminetetraacetate, sodium nitrilotriacetate, sodium hydroxyethylethylenediaminetriacetate, sodium diethylenetriaminepentaacetate, sodium uracil diacetate, and the like.
  • rust preventive agent examples include acidic sulfite, sodium thiosulfate, ammonium thioglycolate, diisopropylammonium nitrite, pentaerythritol tetranitrate, dicyclohexylammonium nitrite and the like.
  • the ultraviolet absorber examples include benzophenone compounds, benzotriazole compounds, cinnamic acid compounds, triazine compounds, and stilbene compounds.
  • a compound that absorbs ultraviolet rays such as a benzoxazole-based compound and emits fluorescence, a so-called fluorescent whitening agent, and the like can also be used.
  • examples of the viscosity modifier include water-soluble polymer compounds in addition to water-soluble organic solvents, and examples thereof include polyvinyl alcohol, cellulose derivatives, polyamines, and polyimines.
  • dye solubilizer examples include urea, ⁇ -caprolactam, ethylene carbonate, and the like. Of these, urea is preferably used.
  • the anti-fading agent is used for the purpose of improving image storage stability.
  • various organic and metal complex antifading agents can be used.
  • organic anti-fading agents include hydroquinones, alkoxyphenols, dialkoxyphenols, phenols, anilines, amines, indanes, chromans, alkoxyanilines, heterocycles, etc. Includes nickel complexes and zinc complexes.
  • Examples of the surface tension adjusting agent include surfactants, and examples include anionic surfactants, amphoteric surfactants, cationic surfactants, and nonionic surfactants.
  • anionic surfactants include alkyl sulfocarboxylates, ⁇ -olefin sulfonates, polyoxyethylene alkyl ether acetates, N-acyl amino acids and salts thereof, N-acyl methyl taurate, alkyl sulfate polyoxyalkyl ethers 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, alkylaryl sulfonate, diethylsulfosuccinate Salts, diethylhexylsulfosuccinate, 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. Etc.
  • Nonionic surfactants include ethers such as polyoxyethylene nonylphenyl ether, polyoxyethylene octylphenyl ether, polyoxyethylene dodecylphenyl ether, polyoxyethylene oleyl ether, polyoxyethylene lauryl ether, polyoxyethylene alkyl ether; Ester systems such as polyoxyethylene oleate, polyoxyethylene distearate, sorbitan laurate, sorbitan monostearate, sorbitan monooleate, sorbitan sesquioleate, polyoxyethylene monooleate, polyoxyethylene stearate; 2,4,7,9-tetramethyl-5-decyne-4,7-diol, 3,6-dimethyl-4-octyne-3,6-diol, 3,5-dimethyl -1-hexyne-3-acetylene glycol (alcohol) -based ol; Nissin Chemical Industry Co., Ltd. trade name Surfynol
  • antifoaming agents include highly oxidized oils, glycerin fatty acid esters, fluorines, and silicone compounds.
  • the surface tension of the ink composition of the present invention is usually 25 to 70 mN / m, more preferably 25 to 60 mN / m, and the viscosity is preferably 30 mPa ⁇ s or less, more preferably 20 mPa ⁇ s or less. .
  • the ink composition of the present invention there is no particular limitation on the order of dissolving each agent such as an additive.
  • the water used for preparing the ink composition is preferably water with few impurities such as ion exchange water and distilled water. Further, 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.
  • fine filtration may be performed using a membrane filter or the like to remove impurities in the ink composition.
  • the pore size of the filter used for microfiltration is usually 1 ⁇ m to 0.1 ⁇ m, preferably 0.8 ⁇ m to 0.1 ⁇ m.
  • the ink composition containing the compound of the present invention is suitable for use in printing, copying, marking, writing, drafting, stamping, or recording (printing), particularly inkjet recording.
  • the ink composition of the present invention is less likely to precipitate solids even when dried in the vicinity of the nozzles of the recording head of an ink jet printer, and for this reason, the recording head is also less likely to block.
  • the ink jet recording method of the present invention As a method for recording on a recording material by the ink jet recording method of the present invention, the following method may be mentioned. That is, a container filled with the ink composition of the present invention is loaded into a predetermined position of an ink jet printer, the ink composition of the present invention is used as ink, and ink droplets of the ink are ejected according to a recording signal to be recorded. This is a method for recording on a material.
  • Some inkjet printers use, for example, a piezo method using mechanical vibration; a bubble jet (registered trademark) method using bubbles generated by heating; and the like.
  • the ink jet recording method of the present invention can be used by any method.
  • ink composition of the present invention can also be used as such an ink set. Further, the ink composition of the present invention may be used for one of the ink sets, and a known ink (composition) may be used for the other.
  • the ink composition of the present invention may be a yellow ink composition containing the compound of the present invention and a known yellow dye for the purpose of fine-tuning the hue within a range that does not impair the effects obtained by the present invention.
  • the compound of the present invention can be used in combination with a magenta dye or a cyan dye for the purpose of toning inks of other colors, such as black ink, or for preparing red ink or green ink.
  • the ink composition of the present invention can be used in combination with inks of various colors such as magenta, cyan, and, if necessary, green, blue (or violet), red, and black. .
  • each color ink may be filled in each container, and these containers may be loaded into a predetermined position of the ink jet printer and used for ink jet recording.
  • Examples of the recording material used in the inkjet recording method of the present invention include information transmission sheets such as paper and film, fibers and fabrics (cellulose, nylon, wool, etc.), leather, base materials for color filters, and the like.
  • a transmission sheet is preferred.
  • the information transmission sheet is not particularly limited, and a plain paper as well as a surface-treated sheet, specifically, a paper, synthetic paper, a substrate such as a film provided with an ink receiving layer, or the like is used.
  • the ink receiving layer is a layer having an action such as absorbing ink and accelerating its drying.
  • the ink receiving layer is formed by, for example, a method of impregnating or coating the base material with a cationic polymer; inorganic fine particles capable of absorbing the pigment in the ink, together with a hydrophilic polymer such as polyvinyl alcohol or polyvinylpyrrolidone, on the surface of the base material. It is provided by the method of coating; Examples of the material of the inorganic fine particles that can absorb the pigment in the ink include porous silica, alumina sol, special ceramics, and the like.
  • the information transmission sheet having such an ink receiving layer is usually called an inkjet exclusive paper, an inkjet exclusive film, a glossy paper, a glossy film or the like.
  • Typical examples of commercially available information transmission sheets having an ink receiving layer are Canon Inc., trade name Professional Photo Paper, Canon Photographic Paper / Glossy Pro [Platinum Grade], and Glossy Gold; Seiko Epson ( Product name Photo Paper Krispia (high gloss), Photo Paper (Gloss); Nihon Hewlett-Packard Co., Ltd. Product Name Advanced Photo Paper (Gloss); Fuji Film Co., Ltd. Pro; manufactured by Brother Industries, Ltd., trade name: photographic glossy paper BP71G; Also, plain paper means paper that is not particularly provided with an ink receiving layer, and many different types are commercially available depending on the application.
  • plain paper As Typical plain papers, double-sided plain plain paper (manufactured by Seiko Epson Corporation); PB PAPER GF-500 (manufactured by Canon Inc.); Multipurse Paper, All-in-one Printing Paper ( Hewlett Packard).
  • plain paper copy (PPC) paper or the like whose use is not limited to ink jet recording is also plain paper.
  • the colored body of the present invention comprises (a) the water-soluble azo compound of the present invention; (b) the ink composition of the present invention containing the compound; or (c) the invention containing the compound and a water-soluble organic solvent.
  • the substance to be colored is not particularly limited, and examples thereof include, but are not limited to, the recording material described above.
  • the above-mentioned recording material is colored.
  • the coloring method for the substance is not particularly limited, and examples thereof include a printing method such as a dip dyeing method, a textile printing method, and screen printing, and the ink jet recording method of the present invention.
  • the ink jet recording method of the present invention is preferable.
  • a colored body colored by the ink jet recording method of the present invention is preferable.
  • the water-soluble azo compound of the present invention represented by the above formula (1) is excellent in solubility in water or a water-soluble organic solvent. Moreover, it has the characteristic that the filterability with respect to a membrane filter, for example in the process of manufacturing the ink composition of this invention is favorable.
  • the ink composition of the present invention is very clear on a recording material such as plain paper and an information transmission sheet having an ink receiving layer, has a high saturation and printing density, and is capable of producing a yellow recorded image of an ideal hue. give. Therefore, it is also possible to faithfully reproduce a photographic color image on paper.
  • the ink composition of the present invention has very good storage stability without solid deposition, physical property change, hue change, etc. after long-term storage.
  • the ink composition of the present invention uses a continuous ink jet printer, and is used physically even when the ink is recirculated at a relatively long time interval or intermittently used by an on-demand ink jet printer. No change in properties.
  • the image recorded on the information transmission sheet having the ink receiving layer by the 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 resistance to light.
  • the water-soluble azo compound of the present invention represented by the formula (1) and the ink composition of the present invention containing the compound are extremely useful for various recording ink applications, particularly for ink jet recording ink applications. is there.
  • Example 1 (Process 1) 17.2 parts of 3-amino-4-chlorobenzoic acid were dissolved in 200 parts of water while adjusting the pH to 6 with sodium hydroxide, and then 7.2 parts of sodium nitrite was added. This solution was added dropwise to 200 parts of 5% hydrochloric acid at 0 to 10 ° C. over 30 minutes, followed by stirring at 10 ° C. or lower for 1 hour to carry out diazotization reaction to prepare a diazo reaction liquid.
  • reaction solution was cooled to 20 to 25 ° C., 800 parts of acetone was added to the reaction solution, and the mixture was stirred at 20 to 25 ° C. for 1 hour.
  • the precipitated solid was separated by filtration to obtain 50.0 parts of a wet cake.
  • This wet cake was dried with a hot air dryer at 80 ° C. to obtain 13.5 parts of a sodium salt ( ⁇ max: 412.5 nm) of the water-soluble azo compound of the present invention represented by the following formula (9).
  • Example 2 In the same manner as in Example 1 except that 26.5 parts of ⁇ -alanine was used instead of 22.5 parts of glycine in Example 1 (Step 2), the water-soluble solution of the present invention represented by the following formula (10) was used. 14.0 parts ( ⁇ max: 413.0 nm) of a sodium salt of a functional azo compound was obtained.
  • Example 3 The water-solubility of the present invention represented by the following formula (11) is obtained in the same manner as in Example 1 except that 40.0 parts of iminodiacetic acid is used instead of 22.5 parts of glycine in Example 1 (Step 2). 14.5 parts ( ⁇ max: 412.5 nm) of a sodium salt of an azo compound was obtained.
  • Example 4 The water-soluble azo compound of the present invention represented by the following formula (12) was obtained in the same manner as in Example 1 except that 44.1 parts of glutamic acid was used instead of 22.5 parts of glycine in Example 1 (Step 2). 14.5 parts ( ⁇ max: 419.0 nm) of a sodium salt of the compound was obtained.
  • Example 5 It is represented by the following formula (13) in the same manner as in Example 1 except that 56.1 parts of 4-aminomethylbenzenesulfonic acid is used instead of 22.5 parts of glycine in Example 1 (Step 2). 14.5 parts ( ⁇ max: 403.5 nm) of the sodium salt of the water-soluble azo compound of the present invention was obtained.
  • Example 6 to 10 (A) Preparation of ink
  • the ink composition of the present invention was obtained by mixing to obtain a solution.
  • the obtained ink composition was filtered through a 0.45 ⁇ m membrane filter to remove impurities, and a test ink was prepared.
  • the pH of the test ink was in the range of 8.0 to 9.5.
  • surfactant trade name Surfinol RTM 104PG50 manufactured by Nissin Chemical Co., Ltd. was used.
  • Preparation of each ink using the compounds obtained in Examples 1 to 5 is referred to as Examples 6 to 10, respectively.
  • Comparative Example 1 Comparative inks were prepared in the same manner as in Examples 6 to 10 except that the compound described in Example 26 of Patent Document 1 was used instead of the compound of the present invention obtained in each Example. This ink preparation is referred to as Comparative Example 1.
  • the structural formula of the compound used in Comparative Example 1 is shown in the following formula (14).
  • Comparative Example 2 Comparative inks were prepared in the same manner as in Examples 6 to 10 except that the coloring matter described in Example 2 of Patent Document 2 was used instead of the compound of the present invention obtained in each Example. This ink preparation is referred to as Comparative Example 2.
  • the structural formula of the compound used in Comparative Example 2 is shown in the following formula (15).
  • Comparative Example 3 Comparative inks were prepared in the same manner as in Examples 6 to 10 except that the dye described in Example 5 of Patent Document 3 was used instead of the compound of the present invention obtained in each Example. This ink preparation is referred to as Comparative Example 3.
  • the structural formula of the compound used in Comparative Example 3 is shown in the following formula (16).
  • Plain paper 1 manufactured by Canon Inc.
  • Plain paper 2 manufactured by Hewlett-Packard Co., Ltd.
  • Plain paper 3 manufactured by Hewlett-Packard Company
  • the reflection density was measured for the portion where the reflection density D value of the recorded matter before the test was closest to 1.0.
  • a colorimetry system (trade name: SpectroEye RTM , manufactured by X-rite) was used. Colorimetry was performed under the conditions of DIN, a viewing angle of 2 degrees, and a light source D65 as a density standard.
  • Various test methods for recorded images and evaluation methods for test results are described below.
  • Comparative Example 1 and Comparative Example 2 showed inferior results to Examples 6 to 10 in saturation.
  • Comparative Example 2 and Comparative Example 3 showed extremely inferior results to Examples 6 to 10 in ozone resistance.
  • Comparative Example 1 showed good ozone resistance, but was inferior to each example in saturation on glossy paper, and extremely inferior to each example in water resistance.
  • Comparative Example 2 the water resistance was good, but the saturation on glossy paper and the ozone resistance test showed results inferior to those of the Examples.
  • Comparative Example 3 had good chroma and water resistance, but was inferior to each example in ozone resistance.
  • each example showed excellent results in all the tests of chroma, ozone resistance and water resistance of the recorded matter. Therefore, it can be seen that the water-soluble azo compound of the present invention and the ink composition of the present invention containing the compound have a clear hue and are excellent in ozone resistance and water resistance.
  • the water-soluble azo compound of the present invention which is a yellow pigment and the yellow ink composition of the present invention containing the same give a recorded image with high saturation. In addition to this, it is excellent in various fastness properties such as ozone resistance. Therefore, the compound and the ink composition containing the compound are very useful for various recording applications, particularly for inkjet recording applications.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Ink Jet Recording Methods And Recording Media Thereof (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Ink Jet (AREA)

Abstract

L'invention concerne un pigment (composé) jaune qui présente une solubilité élevée dans l'eau, et qui est excellent en termes de saturation des couleurs des images enregistrées, de résistance à l'ozone, et de résistance à l'eau ; et une composition d'encre jaune contenant le pigment jaune pour divers enregistrements, en particulier l'enregistrement à jet d'encre. Une composition d'encre qui présente : une saturation et une tonalité appropriés à l'enregistrement à jet d'encre ; diverses propriétés de solidité des couleurs élevée, en particulier une résistance à l'ozone élevée des enregistrements ; et une excellente stabilité en conservation, etc. des images enregistrées, est obtenue en utilisant un composé azoïque hydrosoluble représenté par la formule (1) ou son sel, et une composition d'encre le contenant. En outre, dans la formule (1), Q représente un atome d'halogène, x représente un nombre entier de 2 à 4, un groupe A représente un groupe amino représenté par l'une quelconque des formules (2) à (5). Dans la formule (2), y représente un nombre entier de 1 à 5. Dans la formule (4), m représente 1 ou 2. Dans la formule (5), n représente un nombre entier de 0 à 2, et z représente un atome d'hydrogène, un groupe carboxy ou un groupe sulfo.
PCT/JP2011/073938 2010-10-22 2011-10-18 Composé azoïque hydrosoluble ou sel de celui-ci, composition d'encre et corps coloré WO2012053512A1 (fr)

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Cited By (1)

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JP2018076488A (ja) * 2016-10-31 2018-05-17 日本化薬株式会社 アゾ化合物又はその塩、及びインク

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WO2007049366A1 (fr) * 2005-10-25 2007-05-03 Nippon Kayaku Kabushiki Kaisha Compose azoique hydrosoluble, composition d’encre et materiau colore
WO2009066412A1 (fr) * 2007-11-20 2009-05-28 Nippon Kayaku Kabushiki Kaisha Composé azoïque hydrosoluble ou sel de celui-ci, composition d'encre et corps coloré
WO2010125903A1 (fr) * 2009-04-28 2010-11-04 日本化薬株式会社 Composé azoïque hydrosoluble ou son sel, composition d'encre et article coloré
WO2010146994A1 (fr) * 2009-06-17 2010-12-23 日本化薬株式会社 Composé azoïque hydrosoluble ou sel de celui-ci, composition d'encre et corps coloré
JP2011105798A (ja) * 2009-11-13 2011-06-02 Nippon Kayaku Co Ltd 水溶性アゾ化合物又はその塩、インク組成物及び着色体
WO2011086966A1 (fr) * 2010-01-15 2011-07-21 日本化薬株式会社 Composé azoïque hydrosoluble ou sels de celui-ci, composition d'encre et corps coloré

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007049366A1 (fr) * 2005-10-25 2007-05-03 Nippon Kayaku Kabushiki Kaisha Compose azoique hydrosoluble, composition d’encre et materiau colore
WO2009066412A1 (fr) * 2007-11-20 2009-05-28 Nippon Kayaku Kabushiki Kaisha Composé azoïque hydrosoluble ou sel de celui-ci, composition d'encre et corps coloré
WO2010125903A1 (fr) * 2009-04-28 2010-11-04 日本化薬株式会社 Composé azoïque hydrosoluble ou son sel, composition d'encre et article coloré
WO2010146994A1 (fr) * 2009-06-17 2010-12-23 日本化薬株式会社 Composé azoïque hydrosoluble ou sel de celui-ci, composition d'encre et corps coloré
JP2011105798A (ja) * 2009-11-13 2011-06-02 Nippon Kayaku Co Ltd 水溶性アゾ化合物又はその塩、インク組成物及び着色体
WO2011086966A1 (fr) * 2010-01-15 2011-07-21 日本化薬株式会社 Composé azoïque hydrosoluble ou sels de celui-ci, composition d'encre et corps coloré

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2018076488A (ja) * 2016-10-31 2018-05-17 日本化薬株式会社 アゾ化合物又はその塩、及びインク
JP7005271B2 (ja) 2016-10-31 2022-02-10 日本化薬株式会社 アゾ化合物又はその塩、及びインク

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