JP2009084416A - Basic dispersant aid, aqueous dispersion/aggregate/nonaqueous dispersion of organic pigment nanoparticle using the dispersant aid, colored photosensitive resin composition obtained from them, color filter using the composition, and liquid crystal display device - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a basic dispersant aid capable of improving display characteristics of a color filter used in a liquid crystal display device and the like and to provide an organic nanoparticle pigment dispersion obtained by the basic dispersant aid. <P>SOLUTION: The basic dispersant aid is represented by a general formula (1) (wherein A is a heterocyclic group bonded to a coupling group via a nitrogen atom; X is at least 2-20C bivalent coupling group; R<SB>1</SB>and R<SB>2</SB>are each independently a hydrogen atom, an alkyl group, an aralkyl group or an aryl group; R<SB>1</SB>and R<SB>2</SB>may be connected with each other, and further, may form a heterocyclic ring containing an oxygen atom, a nitrogen atom, and/or a sulfur atom; and m is a natural number of 1 or 2). <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to a basic dispersion aid, an aqueous dispersion, an aggregate, and a non-aqueous dispersion of organic pigment nanoparticles using the same, a colored photosensitive resin composition obtained thereby, a color filter and a liquid crystal using the same The present invention relates to a display device.

  As nanotechnology, for example, research for reducing the size of particles to a range of 10 to 100 nm and applying them to various applications has been vigorously advanced. It is intended to bring out new properties that could not be predicted in the past due to the effects that are manifested for the first time by using nanometer size. On the other hand, in the field of organic pigments, for example, research and development of paints, printing inks, electrophotographic toners, inkjet inks, color filters, and the like are underway. In particular, for color filters and inkjet inks, efforts have been made to improve performance using fine chemical technology, and the results are expected.

  Regarding color filters, thinning is desired. As a result, it is possible to achieve high performance such as high pixel count of image-related devices such as liquid crystal display devices, digital cameras, and CCD sensors. In recent years, organic pigments are used in place of dyes as color materials for color filters in consideration of weather resistance, heat resistance, and the like. The thickness of the color filter using the pigment greatly depends on the particle diameter of the pigment. In other words, the development of good pigment fine particles is the key to improving the performance of image-related equipment. Specifically, pigment fine particles having a nanometer size level and monodispersed and stable are required.

Here, regarding the method for refining organic particles, it has been common to use a disperser such as a roll mill, a ball mill, or an attritor. Recently, gas phase methods, liquid phase methods, laser ablation methods, and the like have been studied. Among these, the liquid phase method has attracted attention as a method for producing organic particles having excellent simplicity and productivity. Specifically, a method of depositing nanoparticles by mixing a pigment solution and a poor solvent (see Patent Document 1) and a method of adding a predetermined polymer compound at this time are disclosed (Patent Documents 2 and 2). 4)
JP 2004-91560 A JP 2004-43776 A International Publication No. WO2006 / 121016 Pamphlet JP 2007-119586 A

  An object of the present invention is to provide a basic dispersion aid used in a pigment dispersion that can improve the display characteristics of a color filter such as a liquid crystal display device. In particular, a basic dispersion aid that can increase the contrast of a color filter, increase its production efficiency, and realize good display characteristics in a liquid crystal display device, and aqueous dispersions and aggregates of organic pigment nanoparticles using the same And a non-aqueous dispersion, a colored photosensitive resin composition obtained therefrom, and a color filter and a liquid crystal display device using the same.

（式中、Ａは連結基と窒素原子で結合する複素環基を表す。Ｘは、少なくとも炭素原子数２〜２０の２価の連結基を表す。Ｒ₁及びＲ_２は、それぞれ独立に水素原子、アルキル基、アラルキル基、又はアリール基を表す。Ｒ₁及びＲ₂は互いに連結していてもよく、さらに酸素原子、窒素原子、及び／又は硫黄原子を含む複素環を形成してもよい。ｍは、１又は２の自然数を表す。）
（２）前記塩基性分散助剤が下記一般式（２）で表されることを特徴とする塩基性分散助剤。

（式中、Ａは連結基と窒素原子で結合する複素環基を表す。Ｙは酸素原子又は硫黄原子を表す。ｌは０又は１の整数を表す。ｎは１〜１９の自然数を表す。Ｒ₁及びＲ_２は、それぞれ独立に水素原子、アルキル基、アラルキル基、又はアリール基を表す。Ｒ₁及びＲ₂は互いに連結していてもよく、さらに酸素原子、窒素原子、及び／又は硫黄原子を含む複素環を形成してもよい。ｍは１又は２の自然数を表す。）
（３）水性分散物から媒体を切り換えて得た非水性分散物中で、非水性分散剤とともに有機顔料ナノ粒子に分散性を付与することを特徴とする（１）又は（２）に記載の塩基性分散助剤。
（４）有機顔料ナノ粒子と水と（１）〜（３）のいずれか１項に記載の塩基性分散助剤とを含む水性分散物であって、前記有機顔料ナノ粒子が、良溶媒に有機顔料を溶解させた有機顔料溶液を、前記良溶媒と相溶し前記有機顔料に対する貧溶媒とを混合させ、その混合液中に前記塩基性分散助剤の存在下で前記有機顔料をナノメートルサイズの微粒子として析出させたものであることを特徴とする有機顔料ナノ粒子の水性分散物。
（５）前記有機顔料ナノ粒子の一次粒子の平均粒径が１０〜５００ｎｍであることを特徴とする（４）記載の有機顔料ナノ粒子の水性分散物。
（６）（４）又は（５）に記載の水性分散物のｐＨ変化をさせて、前記有機顔料ナノ粒子を再分散可能な凝集状態とした有機顔料ナノ粒子の凝集体。
（７）（６）に記載の凝集体の凝集を解き非水性媒体中に再分散させた有機顔料ナノ粒子の非水性分散物。
（８）酸性基を有する数平均分子量１０００以上の高分子化合物を少なくとも１種含むことを特徴とする（７）に記載の有機顔料ナノ粒子の非水性分散物。
（９）（７）又は（８）に記載の非水性分散物と、バインダーと、モノマーもしくはオリゴマーと、光重合開始剤もしくは光重合開始剤系とを少なくとも含有させたことを特徴とする着色感光性樹脂組成物。
（１０）（９）に記載の着色感光性樹脂組成物を用いて作製したことを特徴とするカラーフィルタ。
（１１）（１０）に記載のカラーフィルタを備えたことを特徴とする液晶表示装置。 The above problems have been achieved by the following means.
(1) A basic dispersion aid represented by the following general formula (1).

(In the formula, A represents a heterocyclic group bonded to the linking group by a nitrogen atom. X represents a divalent linking group having at least 2 to 20 carbon atoms. R ₁ and R ₂ are each independently hydrogen. Represents an atom, an alkyl group, an aralkyl group, or an aryl group, R ₁ and R ₂ may be linked to each other, and may further form a heterocyclic ring containing an oxygen atom, a nitrogen atom, and / or a sulfur atom; M represents a natural number of 1 or 2.)
(2) The basic dispersion aid is represented by the following general formula (2).

(In the formula, A represents a heterocyclic group bonded to the linking group by a nitrogen atom. Y represents an oxygen atom or a sulfur atom. L represents an integer of 0 or 1. n represents a natural number of 1 to 19.) R ₁ and R ₂ each independently represent a hydrogen atom, an alkyl group, an aralkyl group, or an aryl group, R ₁ and R ₂ may be linked to each other, and further an oxygen atom, a nitrogen atom, and / or sulfur A heterocyclic ring containing an atom may be formed, and m represents a natural number of 1 or 2.)
(3) In the non-aqueous dispersion obtained by switching the medium from the aqueous dispersion, dispersibility is imparted to the organic pigment nanoparticles together with the non-aqueous dispersant, as described in (1) or (2) Basic dispersion aid.
(4) An aqueous dispersion containing organic pigment nanoparticles, water, and the basic dispersion aid according to any one of (1) to (3), wherein the organic pigment nanoparticles are used as a good solvent. An organic pigment solution in which an organic pigment is dissolved is mixed with the good solvent and mixed with a poor solvent for the organic pigment, and the organic pigment is nanometerd in the presence of the basic dispersion aid in the mixture. An aqueous dispersion of organic pigment nanoparticles, characterized in that they are precipitated as fine particles of size.
(5) The organic pigment nanoparticle aqueous dispersion according to (4), wherein an average particle diameter of primary particles of the organic pigment nanoparticles is 10 to 500 nm.
(6) An aggregate of organic pigment nanoparticles in which the pH of the aqueous dispersion according to (4) or (5) is changed to make the organic pigment nanoparticles re-dispersible.
(7) A non-aqueous dispersion of organic pigment nanoparticles in which the aggregates described in (6) have been agglomerated and redispersed in a non-aqueous medium.
(8) The non-aqueous dispersion of organic pigment nanoparticles according to (7), comprising at least one polymer compound having an acidic group and having a number average molecular weight of 1000 or more.
(9) A colored photosensitive composition comprising at least the non-aqueous dispersion according to (7) or (8), a binder, a monomer or an oligomer, and a photopolymerization initiator or a photopolymerization initiator system. Resin composition.
(10) A color filter produced using the colored photosensitive resin composition according to (9).
(11) A liquid crystal display device comprising the color filter according to (10).

The basic dispersion aid of the present invention is excellent in that a color filter produced from a dispersion prepared using the same is made to have a high contrast and its production efficiency is improved, and that good display characteristics can be realized in a liquid crystal display device. Has the effect. Further, the basic dispersion aid of the present invention maintains a good dispersion state of the organic pigment fine particles even when the medium is switched from the aqueous dispersion to the non-aqueous dispersion, and the efficient dispersion of the non-aqueous dispersion having stable dispersibility. Enable production. Furthermore, the color filter produced using this excellent dispersion exhibits the above-mentioned high performance, and is excellent in that it is excellent in blackness and exhibits high image display performance when incorporated in a liquid crystal display device to display an image. Play.

The present invention will be described in detail below.
In the present invention, the organic pigment is not limited in terms of hue. Examples thereof include reel carbonium, dioxazine, aminoanthraquinone, diketopyrrolopyrrole, thioindigo, isoindoline, isoindolinone, pyranthrone or isoviolanthrone compound pigment, or a mixture thereof.
More specifically, for example, C.I. I. Pigment red 190 (C.I. No. 71140), C.I. I. Pigment red 224 (C.I. No. 71127), C.I. I. Perylene compound pigments such as C.I. Pigment Violet 29 (C.I. No. 71129); I. Pigment orange 43 (C.I. No. 71105), or C.I. I. Perinone compound pigments such as C.I. Pigment Red 194 (C.I. No. 71100); I. Pigment violet 19 (C.I. No. 73900), C.I. I. Pigment violet 42, C.I. I. Pigment red 122 (C.I. No. 73915), C.I. I. Pigment red 192, C.I. I. Pigment red 202 (C.I. No. 73907), C.I. I. Pigment Red 207 (C.I. No. 73900, 73906) or C.I. I. Pigment Red 209 (C.I. No. 73905), a quinacridone compound pigment; I. Pigment red 206 (C.I. No. 73900/73920), C.I. I. Pigment orange 48 (C.I. No. 73900/73920), or C.I. I. Quinacridonequinone compound pigments such as CI Pigment Orange 49 (C.I. No. 73900/73920); I. Anthraquinone compound pigments such as C.I. Pigment Yellow 147 (C.I. No. 60645); I. Anthanthrone compound pigments such as CI Pigment Red 168 (C.I. No. 59300); I. Pigment brown 25 (C.I. No. 12510), C.I. I. Pigment violet 32 (C.I. No. 12517), C.I. I. Pigment yellow 180 (C.I. No. 21290), C.I. I. Pigment yellow 181 (C.I. No. 11777), C.I. I. Pigment orange 62 (C.I. No. 11775), or C.I. I. Benzimidazolone compound pigments such as CI Pigment Red 185 (C.I. No. 12516); I. Pigment yellow 93 (C.I. No. 20710), C.I. I. Pigment yellow 94 (C.I. No. 20038), C.I. I. Pigment yellow 95 (C.I. No. 20034), C.I. I. Pigment yellow 128 (C.I. No. 20037), C.I. I. Pigment yellow 166 (C.I. No. 20035), C.I. I. Pigment orange 34 (C.I. No. 21115), C.I. I. Pigment orange 13 (C.I. No. 21110), C.I. I. Pigment orange 31 (C.I. No. 20050), C.I. I. Pigment red 144 (C.I. No. 20735), C.I. I. Pigment red 166 (C.I. No. 20730), C.I. I. Pigment red 220 (C.I. No. 20055), C.I. I. Pigment red 221 (C.I. No. 20065), C.I. I. Pigment red 242 (C.I. No. 20067), C.I. I. Pigment red 248, C.I. I. Pigment red 262, or C.I. I. Disazo condensed compound pigments such as CI Pigment Brown 23 (C.I. No. 20060); I. Pigment yellow 13 (C.I. No. 21100), C.I. I. Pigment yellow 83 (C.I. No. 21108), or C.I. I. Disazo compound pigments such as CI Pigment Yellow 188 (C.I. No. 21094); I. Pigment red 187 (C.I. No. 12486), C.I. I. Pigment red 170 (C.I. No. 12475), C.I. I. Pigment yellow 74 (C.I. No. 11714), C.I. I. Pigment yellow 150 (C.I. No. 48545), C.I. I. Pigment red 48 (C.I. No. 15865), C.I. I. Pigment red 53 (C.I. No. 15585), C.I. I. Pigment orange 64 (C.I. No. 12760), or C.I. I. Azo compound pigments such as CI Pigment Red 247 (C.I. No. 15915), C.I. I. Indanthrone compound pigments such as C.I. Pigment Blue 60 (C.I. No. 69800); I. Pigment green 7 (C.I. No. 74260), C.I. I. Pigment Green 36 (C.I. No. 74265), Pigment Green 37 (C.I. No. 74255), Pigment Blue 16 (C.I. No. 74100), C.I. I. Phthalocyanine compound pigments such as CI Pigment Blue 75 (C.I. No. 74160: 2) or 15 (C.I. No. 74160); I. Pigment blue 56 (C.I. No. 42800), or C.I. I. Pigment Blue 61 (C.I. No. 42765: 1) and the like triarylcarbonium compound pigments, C.I. I. Pigment violet 23 (C.I. No. 51319) or C.I. I. Pigment Violet 37 (C.I. No. 51345) and other dioxazine compound pigments, C.I. I. Aminoanthraquinone compound pigments such as C.I. Pigment Red 177 (C.I. No. 65300); I. Pigment red 254 (C.I. No. 56110), C.I. I. Pigment Red 255 (C.I. No. 561050), C.I. I. Pigment red 264, C.I. I. Pigment red 272 (C.I. No. 561150), C.I. I. Pigment orange 71, or C.I. I. Diketopyrrolopyrrole compound pigments such as C.I. Pigment Orange 73; I. Thioindigo compound pigments such as C.I. Pigment Red 88 (C.I. No. 7313); I. Pigment yellow 139 (C.I. No. 56298), C.I. I. Pigment Orange 66 (C.I. No. 48210), an isoindoline compound pigment such as C.I. I. Pigment yellow 109 (C.I. No. 56284), or C.I. I. Pigment Orange 61 (C.I. No. 11295) and the like, an inindolinone compound pigment such as C.I. I. Pigment Orange 40 (C.I. No. 59700), or C.I. I. Pigment red 216 (C.I. No. 59710) and the like, or C.I. I. And isoviolanthrone compound pigments such as CI Pigment Violet 31 (60010). Among these, quinacridone compound pigments, diketopyrrolopyrrole compound pigments, dioxazine compound pigments, phthalocyanine compound pigments, or azo compound pigments are preferable, and diketopyrrolopyrrole compound pigments, phthalocyanine compound pigments, and dioxazine compound pigments are more preferable.
In the present invention, two or more kinds of organic pigments or solid solutions of organic pigments can be used in combination. Moreover, you may combine with an organic pigment | dye, a polymeric organic material, etc.

  The dispersion aid of the present invention is compatible with an organic pigment solution in which an organic pigment is dissolved in a good solvent (first solvent), the good solvent, and a poor solvent (second It can be used when the organic pigment nanoparticles are precipitated by mixing with a solvent. The combination of the good solvent and the poor solvent preferably has a sufficient difference in the solubility of the organic pigment, and it is necessary to select a preferable one according to the organic pigment. You may choose one.

  The good solvent is not particularly limited as long as it can dissolve the organic pigment to be used and is compatible with or uniformly mixed with the poor solvent. As for the solubility of the organic pigment in a good solvent, the solubility of the organic pigment is preferably 0.2% by mass or more, and more preferably 0.5% by mass or more. Although there is no particular upper limit to the solubility of the organic pigment in the good solvent, it is practical that it is 50% by mass or less in consideration of a commonly used organic pigment. This solubility may be the solubility when dissolved in the presence of an acid or alkali. In addition, the compatibility or uniform mixing property of the good solvent and the poor solvent is preferably 30% by mass or more, more preferably 50% by mass or more, with respect to the poor solvent.

  Examples of the good solvent include an aqueous solvent (for example, water or hydrochloric acid, an aqueous sodium hydroxide solution), an alcohol compound solvent, an amide compound solvent, a ketone compound solvent, an ether compound solvent, an aromatic compound solvent, a carbon disulfide solvent, and a fat. Group compound solvents, nitrile compound solvents, sulfoxide compound solvents, halogen compound solvents, ester compound solvents, ionic liquids, mixed solvents thereof, and the like, aqueous solvents, alcohol compound solvents, ketone compound solvents, ether compound solvents, sulfoxide compounds Solvents, ester compound solvents, amide compound solvents, or mixtures thereof are preferred, aqueous solvents, alcohol compound solvents, ester compound solvents, sulfoxide compound solvents or amide compound solvents are preferred, aqueous solvents, sulfoxide compound solvents or amide compounds. More preferably medium, sulfoxide compound solvent or the amide compound solvent is particularly preferred.

  Examples of the sulfoxide compound solvent include dimethyl sulfoxide, diethyl sulfoxide, hexamethylene sulfoxide, sulfolane and the like. Examples of the amide compound solvent include N, N-dimethylformamide, 1-methyl-2-pyrrolidone, 2-pyrrolidinone, 1,3-dimethyl-2-imidazolidinone, 2-pyrrolidinone, ε-caprolactam, formamide, N -Methylformamide, acetamide, N-methylacetamide, N, N-dimethylacetamide, N-methylpropanamide, hexamethylphosphoric triamide and the like.

Further, the concentration of the organic pigment solution in which the organic pigment is dissolved in the good solvent is preferably a saturated concentration of the organic pigment with respect to the good solvent in the dissolving condition or a range of about 1/100 of this.
There are no particular limitations on the conditions for preparing the organic pigment solution, and a range from normal pressure to subcritical and supercritical conditions can be selected. The temperature at normal pressure is preferably −10 to 150 ° C., more preferably −5 to 130 ° C., and particularly preferably 0 to 100 ° C.

  The same thing as a good solvent and a poor solvent is not combined, and the solubility with respect to a good solvent should just be sufficiently higher than the solubility with respect to a poor solvent in relation to each organic pigment to employ | adopt. For example, the solubility difference is preferably 0.2% by mass or more, and more preferably 0.5% by mass or more. Although there is no particular upper limit to the difference in solubility between the good solvent and the poor solvent, it is practical that the difference is 50% by mass or less in consideration of a commonly used organic pigment.

  When the organic pigment is uniformly dissolved in a good solvent, it may be dissolved acidic or alkaline. In general, in the case of a pigment having an alkaline and dissociable group in the molecule, alkali is used, and when there is no alkaline and dissociable group and there are many nitrogen atoms in the molecule that are prone to add protons, acidity is used. For example, quinacridone, diketopyrrolopyrrole, disazo condensation compound pigments are alkaline, and phthalocyanine compound pigments are acidic.

In the case of alkaline dissolution, inorganic bases such as lithium hydroxide, sodium hydroxide, potassium hydroxide, calcium hydroxide and barium hydroxide, or organic bases such as trialkylamine, diazabicycloundecene (DBU) and metal alkoxides Of these, it is preferable to use an inorganic base.
The amount of the base to be used is not particularly limited, but in the case of an inorganic base, it is preferably 1.0 to 30 molar equivalents, more preferably 1.0 to 25 molar equivalents relative to the organic pigment. It is particularly preferably 0 to 20 molar equivalents. In the case of an organic base, it is preferably 1.0 to 100 molar equivalents, more preferably 5.0 to 100 molar equivalents, and particularly preferably 20 to 100 molar equivalents with respect to the organic pigment.

When the acid is dissolved, it is preferable to use an inorganic acid such as sulfuric acid, hydrochloric acid, or phosphoric acid, or an organic acid such as acetic acid, trifluoroacetic acid, oxalic acid, methanesulfonic acid, or trifluoromethanesulfonic acid. Is preferable, and sulfuric acid is more preferable.
The amount of the acid to be used is not particularly limited, but an excess amount is often used as compared with the base. Regardless of the inorganic acid and organic acid, the organic pigment is preferably 3 to 500 molar equivalents, more preferably 10 to 500 molar equivalents, and particularly preferably 30 to 200 molar equivalents. .

  When mixing alkali or acid with an organic solvent and using it as a good solvent for organic pigments, a solvent having high solubility in some alkali or acid such as water or lower alcohol in order to completely dissolve the alkali or acid Can be added to the organic solvent. The amount of water or lower alcohol is preferably 50% by mass or less, more preferably 30% by mass or less, based on the total amount of the organic pigment solution. Specifically, water, methanol, ethanol, n-propanol, isopropanol, butyl alcohol, or the like can be used.

  The viscosity of the organic pigment solution is preferably 0.5 to 80.0 mPa · s, and more preferably 1.0 to 50.0 mPa · s.

  Although a poor solvent is not specifically limited, It is preferable that the solubility of an organic pigment is 0.02 mass% or less, and it is more preferable that it is 0.01 mass% or less. Although there is no particular lower limit to the solubility of the organic pigment in the poor solvent, 0.000001% by mass or more is practical in consideration of a commonly used organic pigment. This solubility may be the solubility when dissolved in the presence of an acid or alkali. The preferred range of the compatibility or uniform mixing property between the poor solvent and the good solvent is as described above.

  Examples of the poor solvent include an aqueous solvent (for example, water or hydrochloric acid, an aqueous sodium hydroxide solution), an alcohol compound solvent, a ketone compound solvent, an ether compound solvent, an aromatic compound solvent, a carbon disulfide solvent, an aliphatic compound solvent, Examples thereof include nitrile compound solvents, halogen compound solvents, ester compound solvents, ionic liquids, and mixed solvents thereof, and aqueous solvents, alcohol compound solvents, ketone compound solvents, ether compound solvents, ester compound solvents, or mixtures thereof are preferable. An aqueous solvent, an alcohol compound solvent or an ester compound solvent is more preferable.

Examples of the alcohol compound solvent include methanol, ethanol, isopropyl alcohol, n-propyl alcohol, 1-methoxy-2-propanol, and the like. Examples of the ketone compound solvent include acetone, methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone. Examples of the ether compound solvent include dimethyl ether, diethyl ether, tetrahydrofuran, and the like. Examples of the aromatic compound solvent include benzene and toluene. Examples of the aliphatic compound solvent include hexane. Examples of the nitrile compound solvent include acetonitrile. Examples of the halogen compound solvent include dichloromethane and trichloroethylene. Examples of the ester compound solvent include ethyl acetate, ethyl lactate, 2- (1-methoxy) propyl acetate and the like. The ionic liquids, for example, 1-butyl-3-methylimidazolium and PF ₆ ^-, etc. and salts thereof.

  There are no particular limitations on the conditions of the poor solvent for precipitation of the organic particles, and a range from normal pressure to subcritical and supercritical conditions can be selected. The temperature at normal pressure is preferably −30 to 100 ° C., more preferably −10 to 60 ° C., and particularly preferably 0 to 30 ° C.

  When mixing the organic pigment solution and the poor solvent, either of them may be added and mixed, but it is preferable to jet the organic pigment solution into the poor solvent and mix, and the poor solvent is stirred at that time. It is preferable that the The stirring speed is preferably 100 to 10000 rpm, more preferably 150 to 8000 rpm, and particularly preferably 200 to 6000 rpm. A pump or the like can be used for the addition. At this time, it may be added in the liquid or externally, but the addition in the liquid is more preferable. Further, it is preferable to continuously supply the liquid into the liquid through a supply pipe. The inner diameter of the supply pipe is preferably 0.1 to 200 mm, and more preferably 0.2 to 100 mm. The rate at which the liquid is supplied from the supply pipe is preferably 1 to 10,000 ml / min, more preferably 5 to 5000 ml / min.

By adjusting the Reynolds number when mixing the organic pigment solution and the poor solvent, the particle size of the organic nanoparticles to be formed can be controlled. Here, the Reynolds number is a dimensionless number representing the state of fluid flow and is represented by the following equation.
Re = ρUL / μ Equation (1)
In Equation (1), Re represents the Reynolds number, ρ represents the density [kg / m ³ ] of the organic pigment solution, and U represents the relative velocity [m / s] when the organic pigment solution and the poor solvent meet. L represents the equivalent diameter [m] of the flow path or supply port where the organic pigment solution and the poor solvent meet, and μ represents the viscosity coefficient [Pa · s] of the organic pigment solution.

The equivalent diameter L refers to the diameter of the equivalent circular pipe when assuming an opening diameter of a pipe having an arbitrary cross-sectional shape or a circular pipe equivalent to the flow path. The equivalent diameter L is expressed by the following equation (2), where A is the cross-sectional area of the pipe, p is the wetted length (circumferential length) of the pipe, or p is the outer periphery of the flow path.
L = 4 A / p Formula (2)
It is preferable to form particles by injecting an organic pigment solution into a poor solvent through a pipe. When a circular pipe is used for the pipe, the equivalent diameter matches the diameter of the circular pipe. For example, the equivalent diameter can be adjusted by changing the opening diameter of the liquid supply port. The value of the equivalent diameter L is not particularly limited, but is, for example, the same as the preferable inner diameter of the supply port described above.

  The relative speed U when the good solvent solution and poor solvent of the organic pigment meet is defined by the relative speed in the direction perpendicular to the surface of the part where both meet. That is, for example, when a good solvent solution of an organic pigment is injected into a stationary poor solvent and mixed, the speed of injection from the supply port becomes equal to the relative speed U. Although the value of the relative speed U is not specifically limited, For example, it is preferable to set it as 0.5-100 m / s, and it is more preferable to set it as 1.0-50 m / s.

The density ρ of the organic pigment solution is a value determined by the type of material selected, but is, for example, 0.8 to 2.0 kg / m ³ in the range of the material preferably used in the production method of the present invention. That is practical. Also, the viscosity coefficient μ of the organic pigment solution is a value determined by the material used, the environmental temperature, and the like, but its preferred range is synonymous with the preferred viscosity of the organic pigment solution described above.

  The smaller the Reynolds number (Re) value, the easier it is to form a laminar flow, and the larger the value, the easier it is to form a turbulent flow. For example, the particle size of the organic nanoparticles can be controlled by adjusting the Reynolds number to 60 or more, preferably 100 or more, and more preferably 150 or more. There is no particular upper limit to the number of lay nozzles, but it is preferable because, for example, good organic nanoparticles can be controlled and obtained by adjusting and controlling in the range of 100,000 or less. Or it is good also as conditions which raised Reynolds number so that the average particle diameter of the nanoparticle obtained may be 60 nm or less. At this time, within the above range, it is possible to control and obtain organic nanoparticles having a smaller particle diameter by increasing the Reynolds number.

The mixing ratio of the organic pigment solution and the poor solvent (ratio of good solvent / poor solvent in the organic fine particle precipitate) is preferably 1/50 to 2/3, more preferably 1/40 to 1/2, and 1 / 20 to 3/8 is particularly preferable.
When the organic fine particles are precipitated, the concentration of nanoparticles in the dispersion is not particularly limited, but the organic particles are preferably in the range of 10 to 40000 mg, more preferably in the range of 20 to 30000 mg with respect to 1000 ml of the solvent. Especially preferably, it is the range of 50-25000 mg.
Moreover, the preparation scale at the time of producing | generating a pigment nanoparticle is although it does not specifically limit, It is preferable that the mixing amount of a poor solvent is a 10-2000L preparation scale, and it is more preferable that it is a 50-1000L preparation scale.

  Regarding the particle size of organic particles, there is a method of expressing the average size of the population by quantifying by a measurement method, but as a common use, the mode diameter indicating the maximum value of the distribution, the median value of the integral distribution curve Median diameter, various average diameters (number average, length average, area average, mass average, volume average, etc.), etc. In the present invention, unless otherwise specified, the average particle diameter is the number average. The diameter. The average particle diameter of the pigment nanoparticles (primary particles) is preferably 10 to 500 nm, more preferably 10 to 200 nm, still more preferably 10 to 100 nm, and particularly preferably 20 to 80 nm. . The particles formed by the production method of the present invention may be crystalline particles, amorphous particles, or a mixture thereof.

In the present invention, the ratio (Mv / Mn) of the volume average particle diameter (Mv) and the number average particle diameter (Mn) is used as an index representing the monodispersity of the particles unless otherwise specified. The monodispersity (Mv / Mn) of the organic pigment nanoparticles (primary particles) is preferably 1.0 to 2.0, more preferably 1.0 to 1.8, and 1.0 to A ratio of 1.5 is particularly preferred.
Examples of the method for measuring the particle size of the organic particles include microscopy, mass method, light scattering method, light blocking method, electrical resistance method, acoustic method, and dynamic light scattering method. Particularly preferred. Examples of the microscope used for the microscopy include a scanning electron microscope and a transmission electron microscope. Examples of the particle measuring apparatus by the dynamic light scattering method include Nanotrack UPA-EX150 manufactured by Nikkiso Co., Ltd. and Dynamic Light Scattering Photometer DLS-7000 series manufactured by Otsuka Electronics Co., Ltd.

  In the present invention, in preparing the dispersion by depositing the organic pigment nanoparticles, a dispersant may be contained in at least one of the pigment solution and the poor solvent. At this time, at least the pigment solution may contain a dispersant (in the present invention, the dispersant added to the aqueous dispersion is particularly referred to as an aqueous dispersant and may be distinguished from a non-aqueous dispersant described later). preferable.

The polymer dispersant used as the aqueous dispersant preferably has a mass average molecular weight of 1,000 to 500,000, more preferably 10,000 to 500,000, and more preferably 10,000 to 100. Is particularly preferred.
Specifically, polyvinyl pyrrolidone, polyvinyl alcohol, polyvinyl methyl ether, polyethylene glycol, polypropylene glycol, polyacrylamide, vinyl alcohol-vinyl acetate copolymer, polyvinyl alcohol-partial formalized product, polyvinyl alcohol-partial butyralized product, vinylpyrrolidone- Vinyl acetate copolymer, polyethylene oxide / propylene oxide block copolymer, polyacrylate, polyvinyl sulfate, poly (4-vinylpyridine) salt, polyamide, polyallylamine salt, condensed naphthalenesulfonate, cellulose derivative, starch Derivatives and the like. In addition, natural polymers such as alginate, gelatin, albumin, casein, gum arabic, tongant gum, lignin sulfonate, etc. can be used. Of these, polyvinylpyrrolidone is preferable. These polymer compounds can be used singly or in combination of two or more, or a low molecular weight dispersant may be used in combination. The dispersant used for dispersing the pigment is described in detail on pages 29 to 46 of “Pigment dispersion stabilization and surface treatment technology / evaluation” (Chemical Information Association, issued in December 2001).

  Examples of anionic dispersants (anionic surfactants) include N-acyl-N-alkyl taurine salts, fatty acid salts, alkyl sulfate esters, alkyl benzene sulfonates, alkyl naphthalene sulfonates, dialkyl sulfosuccinates, alkyl phosphorus Examples include acid ester salts, naphthalene sulfonic acid formalin condensate, polyoxyethylene alkyl sulfate ester salts, and the like. Of these, N-acyl-N-alkyltaurine salts are preferred. As the N-acyl-N-alkyltaurine salt, those described in JP-A-3-273067 are preferable. These anionic dispersants can be used alone or in combination of two or more.

  Cationic dispersants (cationic surfactants) include quaternary ammonium salts, alkoxylated polyamines, aliphatic amine polyglycol ethers, aliphatic amines, diamines and polyamines derived from aliphatic amines and fatty alcohols, fatty acids And imidazolines derived from these and salts of these cationic substances. These cationic dispersants can be used alone or in combination of two or more.

The amphoteric dispersant is a dispersant having both an anion group part in the molecule of the anionic dispersant and a cationic group part in the molecule of the cationic dispersant.
Nonionic dispersants (nonionic surfactants) include polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyoxyethylene fatty acid ester, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene alkylamine, Examples thereof include glycerin fatty acid esters. Of these, polyoxyethylene alkylaryl ether is preferable. These nonionic dispersants can be used alone or in combination of two or more.

  In order to further improve the uniform dispersibility and storage stability of the pigment nanoparticles, the content of the dispersant is preferably in the range of 0.1 to 1000 parts by weight, more preferably 100 parts by weight of the pigment. Is in the range of 1 to 500 parts by mass, more preferably in the range of 10 to 300 parts by mass. If the amount is less than 0.1 parts by mass, the dispersion stability of the pigment nanoparticles may not be improved. If the amount is 1000 parts by mass or more, the viscosity tends to increase. Moreover, a dispersing agent may be used independently or may be used in combination of multiple things.

  The basic dispersion aid of the present invention is a method for precipitating organic pigment nanoparticles and preparing a dispersion liquid, controlling the particle size of the pigment particles at the nanoscale level, imparting pH responsiveness, and basic treatment (improving redispersibility). ), The following basic dispersion aid is preferably contained in at least one of the pigment solution and the poor solvent, and more preferably contained in the pigment solution.

  The basic dispersion aid of the present invention is represented by the following general formula (1).

式中、Ａは連結基と窒素原子で結合する複素環基を表す。Ｘは、少なくとも炭素原子数２〜２０の２価の連結基を表す。Ｒ₁及びＲ_２は、それぞれ独立に水素原子、アルキル基、アラルキル基、又はアリール基を表す。Ｒ₁及びＲ₂は互いに連結していてもよく、さらに酸素原子、窒素原子、及び／又は硫黄原子を含む複素環を形成してもよい。ｍは、１又は２の自然数を表す。
Ａとしては、例えば、ピラゾール、イミダゾール、インドール、カルバゾール、５−アミノベンゾイミダゾール、３−アミノアントラキノン、アクリドン、５−アミノベンゾイミダゾロン、５−アミノウラシル、アデニンが挙げられ、好ましくは、５−アミノベンゾイミダゾール、３−アミノアントラキノン、アクリドン、５−アミノベンゾイミダゾロン、５−アミノウラシルが挙げられ、より好ましくは、５−アミノベンゾイミダゾール、３−アミノアントラキノン、５−アミノベンゾイミダゾロン、５−アミノウラシルが挙げられる。
Ｘは、例えば、アルキレン、ポリエチレンオキシド、ポリプロピレンオキシドを含む連結基が挙げられ、好ましくはアルキレンである。

In the formula, A represents a heterocyclic group bonded to the linking group through a nitrogen atom. X represents a divalent linking group having at least 2 to 20 carbon atoms. R ₁ and R ₂ each independently represent a hydrogen atom, an alkyl group, an aralkyl group, or an aryl group. R ₁ and R ₂ may be linked to each other, and may further form a heterocyclic ring containing an oxygen atom, a nitrogen atom, and / or a sulfur atom. m represents a natural number of 1 or 2.
Examples of A include pyrazole, imidazole, indole, carbazole, 5-aminobenzimidazole, 3-aminoanthraquinone, acridone, 5-aminobenzimidazolone, 5-aminouracil, and adenine. Preferably, 5-amino Examples include benzimidazole, 3-aminoanthraquinone, acridone, 5-aminobenzimidazolone, and 5-aminouracil, and more preferably 5-aminobenzimidazole, 3-aminoanthraquinone, 5-aminobenzimidazolone, and 5-amino. Examples include uracil.
X includes, for example, a linking group including alkylene, polyethylene oxide, and polypropylene oxide, and is preferably alkylene.

In R ₁ or R ₂ , the alkyl group includes methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl, pentyl, hexyl, cyclohexyl, heptyl, octyl, 2 -An ethylhexyl group etc. are mentioned, Preferably, they are a methyl group, an ethyl group, a propyl group, an isopropyl group, and n-butyl group, More preferably, they are a methyl group, an ethyl group, and a propyl group.
As the aralkyl group, a benzyl group, 4-chlorobenzyl group, 4-methylbenzyl group, 4-butoxybenzyl group, 4-methoxybenzylmethoxyphenyl group, and 4-hydroxybenzyl group are preferable. Particularly preferred are a benzyl group, a 4-chlorobenzyl group, a 4-methylbenzyl group, and a 4-butoxybenzyl group.
The aryl group is preferably a phenyl group, a 4-chlorophenyl group, a 4-methylphenyl group, a 4-butoxyphenyl group, a 4-methoxyphenyl group, or a 4-hydroxyphenyl group. Particularly preferred are a phenyl group, a 4-chlorophenyl group, a 4-methylphenyl group, and a 4-butoxyphenyl group.

Examples of the heterocyclic group formed by connecting R ₁ and R ₂ to each other include imidazole and morpholine.
m represents a natural number of 1 or 2, preferably 1 in terms of particle shape control, and 2 in terms of pH control and dispersibility improvement.

  The basic dispersion aid is preferably one represented by the following general formula (2).

式中、Ａは連結基と窒素原子で結合する複素環基を表す。Ｙは酸素原子又は硫黄原子を表す。ｌは０又は１の整数を表す。ｎは１〜１９の自然数を表す。Ｒ₁及びＲ_２は、それぞれ独立に水素原子、アルキル基、アラルキル基、又はアリール基を表す。Ｒ₁及びＲ₂は互いに連結していてもよく、さらに酸素原子、窒素原子、及び／又は硫黄原子を含む複素環を形成してもよい。ｍは１又は２の自然数を表す。
式中、Ａ及びｍの好ましい範囲は上記一般式（１）と同じである。
Ｙがなす基としては、カルボニル基又はチオカルボニル基が好ましく、カルボニル基であることがより好ましい。
ｌは、０又は１の整数を表すが、合成上の理由から、Ａの複素環基の構造により、適宜選ばれる。

In the formula, A represents a heterocyclic group bonded to the linking group through a nitrogen atom. Y represents an oxygen atom or a sulfur atom. l represents an integer of 0 or 1. n represents a natural number of 1 to 19. R ₁ and R ₂ each independently represent a hydrogen atom, an alkyl group, an aralkyl group, or an aryl group. R ₁ and R ₂ may be linked to each other, and may further form a heterocyclic ring containing an oxygen atom, a nitrogen atom, and / or a sulfur atom. m represents a natural number of 1 or 2.
In the formula, preferred ranges of A and m are the same as those in the general formula (1).
The group formed by Y is preferably a carbonyl group or a thiocarbonyl group, and more preferably a carbonyl group.
l represents an integer of 0 or 1, and is appropriately selected depending on the structure of the heterocyclic group of A for the reasons of synthesis.

n is preferably 4 to 19, more preferably 6 to 17, and particularly preferably 8 to 15.
Hereinafter, although the specific compound represented by General formula (1) or (2) is shown, this invention is not limited to these.

水性分散物における塩基性分散助剤の添加量としては、顔料１００質量部に対して、０．１質量部〜１０００質量部が好ましく、５質量部〜５００質量部がより好ましく、１０質量部〜３００質量部が特に好ましい。添加量が少なすぎると、後述の単離のための凝集が不十分になる。多すぎると過度な凝集が生じてしまい、後述の再分散が困難になる。

The addition amount of the basic dispersion aid in the aqueous dispersion is preferably from 0.1 parts by weight to 1000 parts by weight, more preferably from 5 parts by weight to 500 parts by weight, with respect to 100 parts by weight of the pigment. 300 parts by mass is particularly preferred. When the addition amount is too small, aggregation for isolation described later becomes insufficient. If the amount is too large, excessive agglomeration occurs and redispersion described later becomes difficult.

In the present invention, the organic pigment nanoparticles can be aggregated so as to be easily isolated by neutralizing the aqueous dispersion of the organic pigment nanoparticles.
When the good solvent is acidic, the aqueous dispersion of organic pigment nanoparticles is also acidic, and when the good solvent is basic, the aqueous dispersion is also basic. The basic dispersion aid in the present invention is most effective when the aqueous dispersion is acidic.
At this time, the basic dispersion aid coats around the organic pigment nanoparticles in a protonated state, but as a base to be added, the protons are neutralized, around the organic pigment nanoparticles, It is necessary to produce a basic basic auxiliary. Therefore, it is necessary to appropriately select the basicity and the amount added to neutralize the protonated state of the neutral basic assistant.
Examples of the base to be added include inorganic bases such as lithium hydroxide, sodium hydroxide, potassium hydroxide, calcium hydroxide, and barium hydroxide, or organic substances such as trialkylamine, diazabicycloundecene (DBU), and metal alkoxide. Although it is a base, an inorganic base is preferable from the viewpoint of ease of removal and cost. When neutralizing with these, it is preferable to neutralize to pH7 or more as a whole system, More preferably, it is pH9 or more.
In the present invention, under acidic conditions, the basic dispersion aid having the above basic group is protonated and has a positive charge, whereby particles repel each other and tend to disperse. By neutralizing, the positive charge is extinguished, the repulsive force between the particles is lost, and aggregation occurs.
In addition, since the basic dispersion aid in the present invention has a basic group, it strongly interacts with a non-aqueous dispersant having an acidic group, which will be described later, thereby improving dispersibility and improving contrast. The basic dispersion aid covers the periphery of the pigment particles, and the pigment particle surface can be in a state of being basic-treated. As a result, the pigment particles and the non-aqueous dispersant having an acidic group are strongly bonded by an acid-base interaction, and the dispersibility of the pigment particles by the non-aqueous dispersant having the acidic group can be improved.
Since nanoparticles that tend to disperse are originally small in size, even if an attempt is made to isolate them by filter filtration or centrifugal filtration as they are, they are slipped through or clogged, and it takes an enormous amount of time for isolation. However, isolation is greatly improved by forming large aggregates by pH control as described above. In the present invention, the range of pH change is not particularly limited, but the range of pH change is preferably 7 to 12, and more preferably 9 to 12. The direction of pH change is not particularly limited, but it is preferable to change from the (low) pH side to the (high) pH side, that is, to change in the alkaline direction.
As an aggregate, it is preferable that an average particle diameter is 10,000 nm or more, and a larger one is more preferable. If the thickness is less than 10,000 nm, it takes a long time to isolate the aggregate, and even if it is attempted to filter off, it passes through the filter paper or filter, or is clogged.

In the present invention, the organic pigment nanoparticles can be aggregated (soft agglomerated) to such an extent that they can be redispersed so that the organic pigment nanoparticles can be easily isolated by changing the pH of the aqueous dispersion of the organic pigment nanoparticles. . Here, soft agglomeration is an agglomeration that is weak enough to be redispersed as necessary, and the soft agglomerates are sometimes called flocs. In this way, for example, organic pigment fine particles precipitated in an aqueous dispersion composition can be quickly separated by filtration or the like. Then, the separated soft agglomerates can be re-dispersed in an organic solvent suitable for the production of a color filter, and an organic solvent-based dispersion composition can be efficiently obtained. That is, when the mixed solvent of the good solvent and the poor solvent is an aqueous solvent, the dispersion medium (continuous phase) can be switched by efficiently replacing it with a third solvent made of an organic solvent. The average particle diameter of the aggregate is not particularly limited, but is preferably 10 to 5000 μm, more preferably 100 to 5000 μm in consideration of the filterability described above.
In order to re-disperse the above-mentioned soft-aggregated particles, a normal dispersion method may be insufficient. The basic dispersion aid acts on the formation of such soft agglomerates (floc) and this redispersion, and even once soft agglomeration can be rapidly redispersed, and a good dispersion state can be realized. Therefore, good fine dispersibility (characteristic that achieves uniform and fine particle size) and dispersion stability (uniform and fine particle size can be maintained for a long time) when deposited in a mixture of good and poor solvents Characteristic) is maintained even after switching the medium to the final solvent suitable for the color filter and redispersing it, and can achieve high performance in the color filter. Moreover, the acidic dispersion aid can achieve high performance in the color filter and the liquid crystal display device without interfering with the optical characteristics of the color filter.

Hereinafter, a method for isolating the aggregated organic pigment nanoparticles will be described.
First, the aggregated liquid may be allowed to stand for 0.5 to 2 hours before isolation. Since the aggregate settles quickly, the supernatant can be removed by decanting or sucking, and the isolation of the aggregate is further facilitated. Further, by performing centrifugation instead of standing, faster aggregate sedimentation is possible, and the time can be shortened.
As an isolation method, various filtration methods are possible, and examples thereof include ultrafiltration, centrifugal separation, and filtration with a filter paper or a filter.
In the case of ultrafiltration, for example, a method used for desalting / concentration of a silver halide emulsion can be applied. Research Disclosure No. 10208 (1972), no. 13 122 (1975) and no. 16 351 (1977) is known. The pressure difference and flow rate that are important as operating conditions can be selected with reference to the characteristic curve described in Haruhiko Oya's “Membrane Utilization Technology Handbook”, Koshobo Publishing (1978), p275. In order to process the particles, it is necessary to find an optimum condition in order to suppress the aggregation of particles. There are two methods for replenishing the solvent that is lost due to membrane permeation: a constant volume method in which the solvent is continuously added and a batch method in which the solvent is intermittently added, but the desalting time is relatively short. The formula is preferred. As the solvent to be replenished, pure water obtained by ion exchange or distillation is used. However, a dispersant, a poor solvent for the dispersant may be mixed in pure water, or directly into the organic nanoparticle dispersion. It may be added.
For the filter filtration, for example, an apparatus such as pressure filtration can be used. Examples of preferable filters include filter paper, nanofilters, and ultrafilters.
The centrifuge used for concentration of the organic nanoparticles by centrifugation may be any device as long as it can precipitate the organic nanoparticles in the organic nanoparticle dispersion (or the organic nanoparticle concentrated extract). As a centrifuge, for example, in addition to a general-purpose device, a device with a skimming function (a function of sucking the supernatant layer during rotation and discharging it out of the system) or continuous centrifugation for continuously discharging solid matter Machine.
Centrifugation conditions are preferably 50 to 10000, more preferably 100 to 8000, and particularly preferably 150 to 6000 in terms of centrifugal force (a value representing how many times the gravitational acceleration is applied). Although the temperature at the time of centrifugation is based on the solvent seed | species of a dispersion liquid, -10-80 degreeC is preferable, -5-70 degreeC is more preferable, 0-60 degreeC is especially preferable.
The isolated aggregate can be washed for the purposes of desalting, dehydration, and removal of excess dispersant. The washing operation may be subjected to ultrafiltration, centrifugal separation, filtration with a filter paper or a filter, and the washing liquid may be added and washed as it is. Once the aggregate is taken out and reslurried in the washing liquid, ultrafiltration, centrifugation, You may isolate by filtration with a filter paper or a filter, and you may perform washing | cleaning combining them.
In addition, the washing can be performed not only after the isolation as described above but also before the isolation. This is achieved by allowing the agglomerated nanopigment particle dispersion to stand, removing the supernatant, adding a washing liquid, and reslurry. After reslurry, the slurry is allowed to stand, and the supernatant is removed and filtered, or may be filtered as it is. When washing is performed before isolation, the aggregates are always wet, so that not only the washing efficiency is increased, but also redispersion described later becomes easier.
The washing liquid is not particularly limited as long as it can achieve desalting, dehydration, removal of excess dispersant / flocculant, and specifically an aqueous solvent (for example, water, hydrochloric acid, aqueous sodium hydroxide), Alcohol compound solvent, amide compound solvent, ketone compound solvent, ether compound solvent, aromatic compound solvent, carbon disulfide solvent, aliphatic compound solvent, nitrile compound solvent, sulfoxide compound solvent, halogen compound solvent, ester compound solvent, ionic liquid , And mixed solvents thereof are preferable, and aqueous solvents, alcohol compound solvents, ketone compound solvents, ether compound solvents, nitrile compound solvents, sulfoxide compound solvents, ester compound solvents, amide compound solvents, or a mixture thereof are preferable, and particularly aqueous. Solvent, alcohol compound solvent, ester compound solution , Nitrile compound solvent.
The washed agglomerates can be re-dispersed as described below, or can be re-dispersed after being wetted with a re-dispersing solvent (described later), or dried and taken out as a powder of organic nanoparticle dispersion. Dispersion may be performed.

  In the production method of the present invention, the organic pigment nanoparticles isolated as described above can be re-dispersed in a non-aqueous medium to obtain a non-aqueous dispersion. It is preferable to disperse in an organic solvent at 180 ° C. or higher and lower than 300 ° C. In the present invention, “boiling point” means a boiling point at 1 atm unless otherwise specified. Hereinafter, this organic solvent may be referred to as a “high boiling point organic solvent”. At this time, the organic pigment nanoparticles are usually dispersed in the above-mentioned mixed solvent of the good solvent and the poor solvent in the deposited state, and it is preferable to replace the mixed solvent and the high boiling organic solvent. Here, the total amount of the solvent may be substituted, but it is usually difficult to replace the entire amount, and in the present invention, when the solvent is replaced, the main solvent may be replaced. The content of the pigment in the non-aqueous dispersion of the present invention is not particularly limited, but is preferably 10 to 20% by mass, and more preferably 5 to 15% by mass. The content of the basic dispersion aid contained in the non-aqueous dispersion of the present invention is not particularly limited, but it is practical that 0.05 to 5% by mass is contained.

  The solvent replacement may be performed by any procedure, for example, as follows. First, the solvent content of the dispersion containing the precipitated fine particles is reduced or removed (hereinafter, this operation may be referred to as “concentration / removal”). As a result, a concentrated liquid or paste of organic pigment nanoparticles is formed once, or a powder of organic pigment nanoparticles is formed. A predetermined high-boiling organic solvent can be added thereto to form a dispersion in which pigment nanoparticles are dispersed in the organic solvent. In the present invention, when dispersed in a high-boiling organic solvent, it means that the high-boiling organic solvent accounts for the majority (exceeding 50% by mass) in the solvent content excluding the solid content in the dispersion. And it is preferable that a high boiling point organic solvent is 70 mass% or more.

  In the present invention, it is possible to directly replace the high boiling point organic solvent after the particles are precipitated, but before replacing the solvent with the high boiling point organic solvent, the first solvent is replaced with a third solvent described later. Then, it is also preferable to reduce or remove the third solvent and replace it with the high boiling point solvent. That is, a mixed solvent of a good solvent (first solvent) and a poor solvent (second solvent) is first substituted with a third solvent (first substitution), and then the third solvent is substituted with a predetermined high boiling point organic solvent ( (Second substitution) It is preferable to carry out two-stage solvent substitution. In the present invention, the “dispersion” refers to a composition in which predetermined fine particles are dispersed, and the form thereof is not particularly limited, and is a liquid composition (dispersion), a paste-like composition, and a solid composition. Used to mean including things.

The organic solvent having a boiling point of 150 ° C. or higher can be selected from the following solvents: glycol ether compounds such as diethylene glycol monomethyl ether, glycol ester compounds such as diethylene glycol monomethyl ether acetate or propylene glycol diacetate. , Aliphatic carboxylic acid compounds such as butyric acid or their anhydrides, butyl butyrate, aliphatic or aromatic ester compounds such as propyl benzoate, dicarboxylic acid diester compounds such as diethyl malonate, methyl 3-methoxypropionate Alkoxycarboxylate compounds such as ethyl acetoacetate; halogenated carboxylic acid compounds such as chloroacetic acid and dichloroacetic acid; lauryl alcohol, phenol Alcohol compounds or phenolic compounds; ether compounds such as anisole; alkoxy alcohol compounds such as 3-methoxybutanol; glycol oligomer compounds such as diethylene glycol and tripropylene glycol; amino alcohol compounds such as triethanolamine; 3 Alkoxy alcohol ester compounds such as methoxybutyl acetate; ketone compounds such as dibutyl ketone; morpholine compounds such as N-phenylmorpholine; aliphatic or aromatic amine compounds such as 1-octylamine, dicyclohexylamine, aniline.
Especially, in this invention, it is preferable to use a glycol ether compound, a glycol ester compound, or a carboxylic acid ester compound.

  Specific examples of the organic solvent having a boiling point of 150 ° C. or higher include ethylene glycol monobutyl ether acetate, diethylene glycol monobutyl ether acetate, diethylene glycol monoethyl ether acetate, 1,3-butylene glycol diacetate, diethylene glycol dibutyl ether, diethylene glycol monoethyl ether, and tripropylene. Examples include glycol n-butyl ether, diethyl adipate, dibutyl oxalate, dimethyl malonate, diethyl malonate, dimethyl succinate, and diethyl succinate.

An organic solvent having a boiling point of 150 ° C. or more may be used alone or in combination with a solvent usually used for preparing a pigment dispersion such as 3-methoxybutyl acetate or propylene glycol monomethyl ether acetate (PGMEA).
Further, the organic solvent having a boiling point of 150 ° C. or higher may be used alone, but may be composed of a plurality of types.

  The addition amount of the organic solvent having a boiling point of 150 ° C. or higher is not particularly limited, but is preferably 50 to 300,000 parts by mass and more preferably 500 to 1000 parts by mass with respect to 100 parts by mass of the pigment nanoparticles.

  The mode of concentration / removal when replacing the solvent is not particularly limited. For example, an extraction solvent is added to and mixed with the pigment nanoparticle dispersion, and the pigment nanoparticles are concentrated and extracted into the extraction solvent phase. A mode in which a concentrated nanoparticle solution is used, a mode in which pigment nanoparticles are precipitated and concentrated by centrifugation, a mode in which desalting and concentration is performed by ultrafiltration, a mode in which spray drying is used, and a solvent is sublimated by vacuum freeze drying and concentrated. Examples include an embodiment, an embodiment in which the solvent is dried and concentrated by heating or reduced pressure, an embodiment in which they are combined, an embodiment in which the solvent is concentrated by centrifugation, an embodiment using spray drying, and a solvent is dried by heating or reduced pressure. The aspect which concentrates is preferable.

  The extraction solvent used for the concentration extraction is not particularly limited, but it is not substantially mixed with the dispersion solvent (for example, aqueous solvent) of the pigment nanoparticle dispersion (in the present invention, it is not compatible) The dissolution amount is preferably 50% by mass or less, more preferably 30% by mass or less, and there is no particular lower limit to this dissolution amount, but it is 1% by mass or more considering the solubility of ordinary solvents. It is practical.) A solvent that forms an interface when allowed to stand after mixing is preferable. In addition, this extraction solvent is a solvent that generates weak aggregation (floc that can be redispersed without applying high shearing force such as milling or high-speed stirring) in which the pigment nanoparticles can be redispersed in the extraction solvent. Is preferred. In such a state, the dispersion of a dispersion solvent such as water can be easily removed by filter filtration or the like while the target pigment nanoparticles are wetted with the extraction solvent without causing strong aggregation that changes the particle size. This is preferable. The extraction solvent is preferably an ester compound solvent, an alcohol compound solvent, an aromatic compound solvent, or an aliphatic compound solvent, more preferably an ester compound solvent, an aromatic compound solvent, or an aliphatic compound solvent, and particularly preferably an ester compound solvent.

  Examples of the ester compound solvent include 2- (1-methoxy) propyl acetate, ethyl acetate, and ethyl lactate. Examples of the alcohol compound solvent include n-butanol and isobutanol. Examples of the aromatic compound solvent include benzene, toluene, xylene and the like. Examples of the aliphatic compound solvent include n-hexane and cyclohexane. Further, the extraction solvent may be a pure solvent based on the above preferred solvent or a mixed solvent composed of a plurality of solvents.

The amount of the extraction solvent is not particularly limited as long as the pigment nanoparticles can be extracted, but is preferably smaller than the pigment nanoparticle dispersion in consideration of concentration and extraction. When this is represented by volume ratio, when the pigment nanoparticle dispersion liquid is 100, the extraction solvent to be added is preferably in the range of 1 to 100, more preferably in the range of 10 to 90, and 20 to 80. The range of is particularly preferable. If it is too much, it will take a lot of time for concentration, and if it is too little, extraction will be insufficient and nanoparticles will remain in the dispersion solvent.
After adding the extraction solvent, it is preferable to stir and mix so as to be in sufficient contact with the dispersion. A normal method can be used for stirring and mixing. Although there is no restriction | limiting in particular in the temperature when adding and mixing an extraction solvent, It is preferable that it is 1-100 degreeC, and it is more preferable that it is 5-60 degreeC. Any device may be used for adding and mixing the extraction solvent as long as each step can be preferably performed. For example, a separation funnel type device can be used.

  The methods described above can be used for ultrafiltration, filter filtration, and centrifugation.

  Freeze drying is not particularly limited, and any method may be adopted as long as it is a normal method. For example, a refrigerant direct expansion method, an overlapping refrigeration method, a heat medium circulation method, a triple heat exchange method, and an indirect heating freezing method can be mentioned, but preferably a refrigerant direct expansion method, an indirect heating freezing method, more preferably an indirect heating freezing method. It is good to use. In any method, it is preferable to perform freeze-drying after preliminary freezing. The pre-freezing conditions are not particularly limited, but it is necessary that the sample to be freeze-dried is completely frozen.

  Indirect heating freezing equipment includes small freeze dryer, FTS freeze dryer, LYOVAC freeze dryer, experimental freeze dryer, research freeze dryer, triple heat exchange vacuum freeze dryer, monocooling freeze dryer , HULL freeze dryers, preferably small freeze dryers, laboratory freeze dryers, research freeze dryers, monocooling freeze dryers, more preferably small freeze dryers, monocooling freeze dryers Should be used.

  Although the temperature of freeze-drying is not specifically limited, For example, it is -190--4 degreeC, Preferably it is -120--20 degreeC, More preferably, it is about -80--60 degreeC. The pressure of lyophilization is not particularly limited, and can be appropriately selected by those skilled in the art. For example, the pressure may be 0.1 to 35 Pa, preferably 1 to 15 Pa, and more preferably about 5 to 10 Pa. The freeze-drying time is, for example, about 2 to 48 hours, preferably about 6 to 36 hours, and more preferably about 16 to 26 hours. However, these conditions can be appropriately selected by those skilled in the art. Regarding the freeze-drying method, for example, Formulation Machine Technology Handbook: Formulation Machine Technology Study Group, Jinshokan, p. 120-129 (September 2000); Vacuum Handbook: Japan Vacuum Technology Co., Ltd., Ohm, p. 328-331 (1992); Journal of the Research Group on Freezing and Drying: Koji Ito et al. 15, p. 82 (1965) or the like.

The drying under reduced pressure is not particularly limited as long as the solvent can be evaporated. For example, a general-purpose vacuum dryer and a rotary pump, an apparatus that can be heated and reduced in pressure while stirring the liquid, and an apparatus that can be continuously dried by passing the liquid through a heated and reduced pressure tube.
The heating and drying temperature is preferably 30 to 230 ° C, more preferably 35 to 200 ° C, and particularly preferably 40 to 180 ° C. The pressure during decompression is preferably 100 to 100,000 Pa, more preferably 300 to 90,000 Pa, and particularly preferably 500 to 80,000 Pa.
Moreover, you may dry by the following aspects. For example, as dryers using hot air, shelf dryers, band dryers, stirring dryers, fluidized bed dryers, spray dryers, air dryers, etc., dryers using heat conduction are drum dryers, multiple dryers, etc. A tube dryer, a cylindrical dryer or the like is preferably used. Depending on the solvent composition, a freeze dryer or an infrared dryer can be used.
Among these means, a spray dryer (for example, COC-12 manufactured by Okawara Chemical Co., Ltd.) and a fluidized bed dryer (for example, (( Nara Machinery Seisakusho MSD-100) is particularly preferably used. In addition, a plurality of drying means may be used in combination to prepare a pigment powder with a small amount of residual solvent. For example, a pigment dispersion pre-concentrated with a cylindrical dryer is completely dried with a drum dryer. Processes such as obtaining powder can be used.
The drying conditions are not particularly limited as long as the solvent can be evaporated and materials such as pigments and dispersants are not denatured. Further, for the purpose of increasing the drying speed, it is possible to combine means such as depressurization, stirring and mixing and multi-stage depending on the type of dryer.

The amount to reduce or remove the solvent content is not particularly limited, but in an embodiment in which the solvent content is reduced, it is preferable to remove 50% by mass or more of the total solvent content, and more preferably 75% by mass or more. In the aspect of removing the solvent, it is preferable to remove 80% by mass or more of the total solvent, and more preferably 90% by mass or more.
When the solvent content is reduced by the concentration / removal step, the water content in the remaining dispersion is not particularly limited, but is preferably 0.01 to 3% by mass, preferably 0.01 to 1% by mass. It is more preferable. At this time, for example, it is preferable to remove the solvent component by the above-described drying method or the like to obtain a powder of pigment nanoparticles, for example, the solid content is preferably 50 to 100% by mass, and 70 to 100% by mass More preferably. The concentration / removal step may be performed a plurality of times.

In the present invention, it is preferable to redisperse the organic particles in an aggregated state by the concentration / removal step. The organic particles contained in the organic particle liquid may be aggregated by isolation and solvent replacement. Aggregate intentionally because rapid filter filtration is possible. In order to obtain a good dispersion state again in such a case, flocs aggregated to such an extent that they can be redispersed are preferable.
Further, in order to disperse the above-mentioned aggregated particles, a normal dispersion method may be insufficient. Even in the case of organic particles in such an agglomerated state, in the present invention, the organic particles are suitably redispersed by incorporating a predetermined dispersant in the non-aqueous dispersion together with the above basic dispersion aid. be able to. At this time, the dispersant added to form a non-aqueous dispersion is sometimes called a non-aqueous dispersion.

As the non-aqueous dispersant, a polymer compound having a mass average molecular weight of 1000 or more is preferably used, and a polymer compound represented by the following general formula (1) is more preferably used.

In the general formula (1), A ¹ is an acidic group, a basic group having a nitrogen atom, a urea group, a urethane group, a group having a coordinating oxygen atom, a hydrocarbon group having 4 or more carbon atoms, or an alkoxysilyl group. , A monovalent organic group having a group selected from an epoxy group, an isocyanate group and a hydroxyl group, or a monovalent organic group containing an organic dye structure or a heterocyclic ring which may have a substituent. The n A ¹ may be the same or different.
Specifically, A ¹ is not particularly limited, and examples of the “monovalent organic group having an acidic group” include a carboxylic acid group, a sulfonic acid group, a monosulfate group, a phosphoric acid group, Examples thereof include monovalent organic groups having a monophosphate ester group, a boric acid group, and the like. Examples of the “monovalent organic group having a basic group having a nitrogen atom” include, for example, a monovalent organic group having an amino group (—NH ₂ ), a substituted imino group (—NHR ⁸ , —NR ⁹ R). ¹⁰ ) having a monovalent organic group (wherein R ⁸ , R ⁹ , and R ¹⁰ are each independently an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, or a carbon number) A monovalent organic group having a guanidyl group represented by the following general formula (a1) [in the general formula (a1), R ^a1 and R ^a2 are each independently carbon; It represents an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, or an aralkyl group having 7 to 30 carbon atoms. A monovalent organic group having an amidinyl group represented by the following general formula (a2) [in the general formula (a2), R ^a3 and R ^a4 are each independently an alkyl group having 1 to 20 carbon atoms, carbon An aryl group having 6 to 20 carbon atoms or an aralkyl group having 7 to 30 carbon atoms is represented. And the like.

As the “monovalent organic group having a urea group”, for example, —NHCONHR ¹⁵ (where R ¹⁵ is a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, Or an aralkyl group having 7 to 30 carbon atoms).
Examples of the “monovalent organic group having a urethane group” include —NHCOOR ¹⁶ , —OCONHR ¹⁷ (wherein R ¹⁶ and R ¹⁷ are each independently an alkyl group having 1 to 20 carbon atoms, 6 carbon atoms). Or an aryl group having 20 or less or an aralkyl group having 7 to 30 carbon atoms).
Examples of the “monovalent organic group having a“ group having a coordinating oxygen atom ”” include a group having an acetylacetonato group and a group having a crown ether.
Examples of the “monovalent organic group having a hydrocarbon group having 4 or more carbon atoms” include an alkyl group having 4 or more carbon atoms (for example, octyl group, dodecyl group, etc.) and an aryl group having 6 or more carbon atoms (for example, phenyl Group, a naphthyl group, etc.), an aralkyl group having 7 or more carbon atoms (for example, a benzyl group) and the like. At this time, there is no upper limit to the number of carbon atoms, but it is preferably 30 or less. Examples of the “monovalent organic group having an alkoxysilyl group” include groups having a trimethoxysilyl group, a triethoxysilyl group, and the like.
Examples of the “monovalent organic group having an epoxy group” include a group having a glycidyl group.
Examples of the “monovalent organic group having an isocyanate group” include a 3-isocyanatopropyl group.
Examples of the “monovalent organic group having a hydroxyl group” include a 3-hydroxypropyl group.

A ¹ is preferably an acidic group, a basic group having a nitrogen atom, a urea group, or a monovalent organic group having a hydrocarbon group having 4 or more carbon atoms.

  Further, the organic dye structure or the heterocyclic ring is not particularly limited. More specifically, examples of the organic dye structure include phthalocyanine compounds, insoluble azo compounds, azo lake compounds, anthraquinone compounds, quinacridone compounds, dioxazine compounds, Examples include diketopyrrolopyrrole compounds, anthrapyridine compounds, ansanthrone compounds, indanthrone compounds, flavanthrone compounds, perinone compounds, perylene compounds, and thioindigo compounds. Examples of the heterocyclic ring include thiophene, furan, xanthene, pyrrole, pyrroline, pyrrolidine, dioxolane, pyrazole, pyrazoline, pyrazolidine, imidazole, oxazole, thiazole, oxadiazole, triazole, thiadiazole, pyran, pyridine, piperidine, dioxane, Examples include morpholine, pyridazine, pyrimidine, piperazine, triazine, trithiane, isoindoline, isoindolinone, benzimidazolone, succinimide, phthalimide, naphthalimide, hydantoin, indole, quinoline, carbazole, acridine, acridone, and anthraquinone.

  The organic dye structure or the heterocyclic ring may have a substituent T. Examples of the substituent T include alkyl groups having 1 to 20 carbon atoms such as a methyl group and an ethyl group, a phenyl group, and a naphthyl group. Aryl groups having 6 to 16 carbon atoms such as groups, acyloxy groups having 1 to 6 carbon atoms such as acetoxy groups, alkoxy groups having 1 to 6 carbon atoms such as methoxy groups and ethoxy groups, halogen atoms such as chlorine and bromine, C2-C7 alkoxycarbonyl groups such as methoxycarbonyl group, ethoxycarbonyl group and cyclohexyloxycarbonyl group, carbonate groups such as cyano group and t-butyl carbonate, hydroxyl group, amino group, carboxyl group, sulfonamide group, N -A sulfonylamide group etc. are mentioned.

Also, the A ¹ can be represented by the following general formula (4).

In the general formula (4), B ¹ is an acidic group, a basic group having a nitrogen atom, a urea group, a urethane group, a group having a coordinating oxygen atom, a hydrocarbon group having 4 or more carbon atoms, or an alkoxysilyl group. Represents an organic dye structure or a heterocyclic ring optionally having a substituent selected from an epoxy group, an isocyanate group, and a hydroxyl group, and R ¹⁸ represents a single bond or an a1-valent organic or inorganic linking group. . a1 represents 1 to 5, a1 amino ^{B 1} represents may be the same or different. Preferred embodiments of the group represented by the general formula (4) has the same meaning as the A ^1.

R ¹⁸ represents a single bond or an a1 + 1 valent linking group, and a1 represents 1 to 5. The linking group R ¹⁸ is a group consisting of 1 to 100 carbon atoms, 0 to 10 nitrogen atoms, 0 to 50 oxygen atoms, 1 to 200 hydrogen atoms, and 0 to 20 sulfur atoms. And may be unsubstituted or may further have a substituent. R ¹⁸ is preferably an organic linking group.

Specific examples of R ¹⁸ include the following structural units or groups formed by combining the structural units. The linking group R ¹⁸ may have the substituent T.

In the general formula (1), R ¹ represents an (m + n) -valent linking group. m + n satisfies 3-10.
Examples of the (m + n) -valent linking group represented by R ¹ include 1 to 100 carbon atoms, 0 to 10 nitrogen atoms, 0 to 50 oxygen atoms, 1 to 200 hydrogen atoms, and A group consisting of 0 to 20 sulfur atoms is included, which may be unsubstituted or may further have a substituent. R ¹ is preferably an organic linking group.

Specific examples of R ¹ include groups (which may form a ring structure) configured by combining the groups (t-1) to (t-34) or a plurality thereof. . If the linking group R ¹ described above has a substituent, examples of the substituent include the substituent T can be mentioned.

R ² represents a single bond or a divalent linking group. R ² includes a group consisting of 1 to 100 carbon atoms, 0 to 10 nitrogen atoms, 0 to 50 oxygen atoms, 1 to 200 hydrogen atoms, and 0 to 20 sulfur atoms. It may be unsubstituted or may further have a substituent.
Specific examples of R ² include groups formed by combining the groups of t-3 to 5, 7 to 18, 22 to 26, 32, and 34, or a plurality thereof. R ² preferably has a sulfur atom at the position of connection with R ¹ . When R ² has a substituent, examples of the substituent include the substituent T.

In said general formula (1), m represents 1-8. As m, 1-5 are preferable, 1-3 are more preferable, and 1-2 are especially preferable.
Moreover, n represents 2-9. n is preferably 2 to 8, more preferably 2 to 7, and particularly preferably 3 to 6.

In the general formula (1), P ¹ represents a polymer compound residue (polymer skeleton) and can be appropriately selected from ordinary polymers.
Among polymers, in order to constitute a polymer skeleton, a vinyl monomer polymer or copolymer, ester compound polymer, ether compound polymer, urethane compound polymer, amide compound polymer, epoxy compound polymer, silicone compound polymer, and these Modified product or copolymer [for example, polyether / polyurethane copolymer, copolymer of polyether / vinyl monomer, etc. (any of random copolymer, block copolymer, graft copolymer) May be included). Is preferably selected from the group consisting of vinyl monomer polymers or copolymers, ester compound polymers, ether compound polymers, urethane compound polymers, and modified products or copolymers thereof. At least one kind is more preferable, and a polymer or copolymer of vinyl monomers is particularly preferable.
Furthermore, the polymer is preferably soluble in an organic solvent. If the affinity with the organic solvent is low, for example, when used as a pigment dispersant, the affinity with the dispersion medium is weakened, and it may not be possible to secure a sufficient adsorption layer for stabilizing the dispersion.
Also, P ¹ preferably has a sulfur atom in the coupling position with R ^1.

  Among the polymer compounds represented by the general formula (1), the polymer compound represented by the following general formula (2) is more preferable.

In the general formula (2), A ² has the same meaning as A ¹ in the general formula (1), the same applies its specific preferred embodiment. A ² may have a substituent, and examples thereof include the substituent T.

In the general formula (2), R ³ represents a (x + y) -valent linking group. R ³ has the same meaning as R ¹ , and the preferred range is also the same. At this time, R ³ is an x + y-valent linking group, and the value of x and its preferred range are the same as n in the general formula (1), the value of y and its preferred range are the same as m, and x + y The value of and the preferred range thereof are the same as m + n.

The linking group represented by R ³ is preferably an organic linking group, and preferred specific examples of the organic linking group are shown below. However, the present invention is not limited to these.

  Among the above, from the viewpoint of availability of raw materials, ease of synthesis, and solubility in various solvents, the above (r-1), (r-2), (r-10), (r-11), ( The groups of r-16) and (r-17) are preferred.

Further, when the above R ³ has a substituent, the substituent T can be cited as the substituent.

In the general formula (2), R ⁴ and R ⁵ each independently represents a single bond or a divalent linking group.
The “divalent linking group” represented by R ⁴ and R ⁵ is a linear, branched, or cyclic alkylene group, arylene group, or aralkylene group, which may have a substituent, — O -, - S -, - C (= O) -, - N (R 19) -, - SO -, - SO 2 -, - CO 2 -, or _{^{-N (R 20) SO 2 -}} , or they A divalent group in which two or more groups are combined is preferable (the R ¹⁹ and R ²⁰ each independently represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms). Of these, an organic linking group is preferred.

As R ⁴ , a linear or branched alkylene group or aralkylene group, —O—, —C (═O) —, —N (R ¹⁹ ) —, —SO ₂ —, —CO ₂ —, or — N (R ²⁰ ) SO ₂ — or a divalent group in which two or more of these groups are combined is more preferable. —N (R ¹⁹ ) —, —CO ₂ —, or a divalent group in which two or more of these groups are combined is particularly preferable.

R ⁵ is a single bond, straight chain or branched alkylene group, aralkylene group, —O—, —C (═O) —, —N (R ¹⁹ ) —, —SO ₂ —, —CO _2. —, Or —N (R ²⁰ ) SO ₂ —, or a divalent group in which two or more of these groups are combined is more preferable. O) —, —N (R ¹⁹ ) —, —CO ₂ —, or a divalent group in which two or more of these groups are combined is particularly preferable.

Moreover, when said R < ⁴ >, R < ⁵ > has a substituent, the said substituent T is mentioned as this substituent.

P ² in the general formula (2) represents a polymer skeleton and can be appropriately selected from ordinary polymers and the like. The preferred embodiment of the polymer, has the same meaning as P ¹ in Formula (1), the same applies to its preferred embodiment.

Among the polymer compounds represented by the general formula (2), in particular, R ³ represents the specific examples (r-1), (r-2), (r-10), (r-11), (r -16) or (r-17), wherein R ⁴ is a single bond, linear or branched, alkylene group or aralkylene group, —O—, —C (═O) —, —N (R ¹⁹ ) -, or -CO 2 _-, or a divalent organic group formed by combining two or more of these groups, R ⁵ is a single bond, an ethylene group, a propylene group, or the following general formula (s-a) or A linking group represented by (sb), wherein P ² is a polymer or copolymer of a vinyl monomer, an ester compound polymer, an ether compound polymer, a urethane polymer, or a modified product thereof, y Is a polymer compound in which x is 1 to 2 and x is 3 to 6. There. In the following groups, R ²¹ represents a hydrogen atom or a methyl group, and l represents 1 or 2.

  The polymer compound preferably has a mass average molecular weight of 1000 or more, more preferably 3000 to 100,000 in terms of mass average molecular weight, still more preferably 5000 to 80000, and particularly preferably 7000 to 60000. . When the mass average molecular weight is within the above range, the effects of the multiple functional groups introduced at the polymer ends are sufficiently exhibited, and the performance of adsorbing to a solid surface, micelle forming ability, and surface activity is excellent. Good dispersibility and dispersion stability can be achieved.

  Specific examples of the compound represented by the general formula (1) are shown below. However, the present invention is not limited to these specific examples.

The polymer compound represented by the general formula (1) or (2) can be synthesized, for example, by the following methods.
1. A polymer in which a functional group selected from a carboxyl group, a hydroxyl group, an amino group and the like is introduced at the terminal, an acid halide having a plurality of functional groups (A ¹ or A ² in the general formula), or a plurality of functional groups ( A method in which an alkyl halide having A ¹ or A ^{2 in the} general formula, or an isocyanate having a plurality of functional groups (A ¹ or A ² in the general formula) is polymerized.
2. A method in which a polymer having a carbon-carbon double bond introduced at a terminal and a mercaptan having a plurality of functional groups (A ¹ or A ² in the general formula) are subjected to a Michael addition reaction.
3. A method in which a polymer in which a carbon-carbon double bond is introduced at a terminal and a mercaptan having a plurality of functional groups (A ¹ or A ² in the above general formula) are reacted in the presence of a radical generator.
4). A method of reacting a polymer in which a plurality of mercaptans are introduced at the terminal and a functional group into which a carbon-carbon double bond is introduced (A ¹ or A ² in the above general formula) in the presence of a radical generator.
5). A method of radical polymerization of a vinyl monomer using a mercaptan compound having a plurality of functional groups (A ¹ or A ² in the above general formula) as a chain transfer agent.
Of these, 2, 3, 4, 5 are preferable, 3, 4, 5 are more preferable, and 5 is particularly preferable because of ease of synthesis. As for these synthesis methods, the contents described in paragraphs 0184 to 0216 of Japanese Patent Application No. 2006-129714 can be referred to.

In addition, as a polymer compound having a molecular weight of 1000 or more, a polymer compound having the following acidic group (hereinafter, this compound may be referred to as “acidic group-containing polymer compound”) may be used. It is preferably a polymer compound having a group, and (A) at least one repeating unit derived from a compound having a carboxyl group and (B) at least one repeating unit derived from a compound having a carboxylic ester group. More preferred are copolymer compounds containing seeds.
The repeating unit derived from the compound (A) having a carboxyl group is preferably a repeating unit represented by the following general formula (I), preferably a repeating unit derived from acrylic acid or methacrylic acid. More preferably, the repeating unit derived from the compound (B) having a carboxylic acid ester group is preferably a repeating unit represented by the following general formula (II), and represented by the following general formula (IV). A repeating unit is more preferable, and a repeating unit derived from benzyl acrylate, benzyl methacrylate, phenethyl acrylate, phenethyl methacrylate, 3-phenylpropyl acrylate, or 3-phenylpropyl methacrylate is particularly preferable.

In the formula, R ₁ represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms. R ₂ represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms. R ₃ represents a group represented by the following general formula (III). R ₄ represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a hydroxy group, a hydroxyalkyl group having 1 to 5 carbon atoms, or an aryl group having 6 to 20 carbon atoms. R ₅ and R ₆ each represent a hydrogen atom or an alkyl group having 1 to 5 carbon atoms. i represents the number of 1-5. R ₇ represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms. R ₈ represents a group represented by the following general formula (V). R ₉ represents an alkyl group having 2 to 5 carbon atoms or an aryl group having 6 to 20 carbon atoms. R ₁₀ and R ₁₁ represent a hydrogen atom or an alkyl group having 1 to 5 carbon atoms. j represents a number from 1 to 5;

Further, in terms of the polymerization ratio of the repeating unit derived from the compound having (A) a carboxyl group and the repeating unit derived from the compound having the (B) carboxylic ester group, all of the repeating units (A) can be obtained. The quantity ratio% to the number of repeating units is preferably 3 to 40, more preferably 5 to 35.
In the production method of the present invention, the molecular weight means a mass average molecular weight unless otherwise specified. Examples of molecular weight measurement methods include chromatography, viscosity, light scattering, sedimentation rate, etc. In the present invention, unless otherwise specified, polystyrene measured by gel permeation chromatography (carrier: tetrahydrofuran). The converted mass average molecular weight is used.

The polymer compound may be water-soluble or oil-soluble, and may be water-soluble and oil-soluble.
The polymer compound may be added in a solution in an aqueous solvent or an organic solvent, in a solid state, or a combination thereof. As a method of adding a solution dissolved in a solvent, for example, a method of adding to an aggregated organic particle liquid in a state dissolved in a solvent similar to the solvent of the aggregated organic particle liquid, compatible with the solvent of the aggregated organic particle liquid, The method of adding in the state melt | dissolved in a different solvent is mentioned. The concentration of the polymer compound when added in a solution dissolved in a solvent is not particularly limited, but is preferably 1 to 70% by mass, more preferably 2 to 65% by mass, and particularly preferably 3 to 60% by mass.

  The polymer compound may be added at any time during or after the precipitation of pigment nanoparticles, during or after concentration, when or after the dispersion of aggregated organic particles after concentration, or after the completion of these steps. It may be added, or may be added in a plurality of times. In particular, in the present invention, it is preferable to add a polymer compound having a mass average molecular weight of 1000 or more at the same time as the third solvent described later. The polymer compound is mixed with the third solvent, and the mixture is concentrated. More preferably, it is added to the pigment nanoparticle liquid. The addition amount of the polymer compound is preferably 0.1 to 1000 parts by mass, more preferably 5 to 500 parts by mass, and more preferably 10 to 300 parts by mass with respect to 100 parts by mass of the pigment. Particularly preferred.

  In addition to the above compounds, the polymer compound having a molecular weight of 1000 or more, for example, polyvinylpyrrolidone, polyvinyl alcohol, polyvinyl methyl ether, polyethylene oxide, polyethylene glycol, polypropylene glycol, polyacrylamide, vinyl alcohol-vinyl acetate copolymer, polyvinyl alcohol -Partially formalized product, polyvinyl alcohol-partially butyralized product, vinylpyrrolidone-vinyl acetate copolymer, polyethylene oxide / propylene oxide block copolymer, polyamide, cellulose derivative, starch derivative and the like. In addition, natural polymer compounds such as alginate, gelatin, albumin, casein, gum arabic, tonganto gum and lignin sulfonate can also be used. Examples of the polymer compound having an acidic group include polyvinyl sulfate and condensed naphthalene sulfonic acid.

Examples of the polymer compound having a carboxyl group include polyacrylic acid, polymethacrylic acid, and cellulose derivatives having a carboxyl group in the side chain. A copolymer compound containing (A) at least one repeating unit derived from a compound having a carboxyl group and (B) at least one repeating unit derived from a compound having a carboxylic ester group is disclosed in 59-44615, JP-B 54-34327, JP-B 58-12577, JP-B 54-25957, JP-A 59-53836, and JP-A 59-71048. Examples thereof include methacrylic acid copolymers, acrylic acid copolymers, itaconic acid copolymers, crotonic acid copolymers, maleic acid copolymers, and partially esterified maleic acid copolymers. Further, as particularly preferred examples, acrylic acid-acrylic acid ester copolymers, methacrylic acid-acrylic acid ester copolymers, acrylic acid-methacrylic acid ester copolymers, methacrylic acid-described in US Pat. No. 4,139,391 are described. Examples include methacrylic acid ester copolymers, and multi-component copolymers of acrylic acid or methacrylic acid, acrylic acid ester or methacrylic acid ester, and other vinyl compounds.
Examples of vinyl compounds include styrene or substituted styrene (eg, vinyl toluene, vinyl ethyl benzene), vinyl naphthalene or substituted vinyl naphthalene, acrylamide, methacrylamide, acrylonitrile, methacrylonitrile, and the like, and styrene is preferred.

  Only one type of polymer compound having a molecular weight of 1000 or more may be used, or two or more types may be used in combination, or a compound having a molecular weight of less than 1000 may be used in combination.

  In the method for producing pigment nanoparticles of the present invention, it is preferable to contain a third solvent after the pigment nanoparticles are deposited. Although the kind of 3rd solvent is not specifically limited, It is preferable that it is an organic solvent, for example, an ester compound solvent, an alcohol compound solvent, an aromatic compound solvent, an aliphatic compound solvent, a ketone compound solvent is preferable, an ester compound solvent, a ketone Compound solvents are particularly preferred. In the present invention, a solvent different from both the first solvent and the second solvent, which finally becomes a desired dispersion medium (continuous phase) in the meaning including the third solvent and the fourth solvent described later, is a generic term. This is referred to as “third solvent”.

  Examples of the ester compound solvent include 2- (1-methoxy) propyl acetate, ethyl acetate, and ethyl lactate. Examples of the alcohol compound solvent include methanol, ethanol, n-butanol, isobutanol and the like. Examples of the aromatic compound solvent include benzene, toluene, xylene and the like. Examples of the aliphatic compound solvent include n-hexane and cyclohexane. Examples of the ketone compound solvent include methyl ethyl ketone, acetone, and cyclohexanone.

  Of these, ethyl lactate, ethyl acetate, acetone, and ethanol are preferable, and ethyl lactate is more preferable. These may be used alone or in combination of two or more. Note that the good solvent (first solvent), the poor solvent (second solvent), the third solvent, and the high-boiling organic solvent are not the same as each other.

The timing of adding the third solvent is not particularly limited as long as it is after the precipitation of the pigment nanoparticles, but it is preferable that the pigment nanoparticles are precipitated, concentrated and removed, and then added thereto. As described above, it is preferable that after the first concentration / removal step, the third solvent is added and the solvent content is reduced / removed again by the second concentration / removal step. After that, it is preferable to add a predetermined high boiling point organic solvent.
The amount of the third solvent added is not particularly limited, but is preferably 100 to 300,000 parts by mass and more preferably 500 to 1000 parts by mass with respect to 100 parts by mass of the pigment nanoparticles.

If necessary, the organic pigment nanoparticles in an aggregated state can be finely dispersed (in the present invention, the fine dispersion means that the particles in the dispersion are aggregated to increase the degree of dispersion).
The aggregated organic pigment nanoparticles described above are preferably obtained as flocs aggregated to such an extent that they can be redispersed in order to enable rapid filter filtration and obtain a good dispersion state again.
For this reason, the degree of dispersion using a normal dispersion method is insufficient for micronization, and a method with higher micronization efficiency is required.
As a method for finely dispersing such an aggregate of nanoparticles, for example, a dispersion method using ultrasonic waves or a method of applying physical energy can be used.
The ultrasonic irradiation device used preferably has a function capable of applying an ultrasonic wave of 10 kHz or higher, and examples thereof include an ultrasonic homogenizer and an ultrasonic cleaner. When the liquid temperature rises during ultrasonic irradiation, thermal aggregation of the nanoparticles occurs, so the liquid temperature is preferably 1 to 100 ° C, more preferably 5 to 60 ° C. The temperature control method can be performed by controlling the dispersion temperature, controlling the temperature of the temperature adjusting layer that controls the temperature of the dispersion, or the like.
There are no particular restrictions on the disperser used to disperse the concentrated organic nanoparticles by applying physical energy, for example, kneader, roll mill, atrider, super mill, dissolver, homomixer, sand mill, etc. Machine. In addition, a high-pressure dispersion method and a dispersion method using fine particle beads are also preferable.
As a preferred method for producing the organic nanoparticle dispersion, the viscosity at 25 ° C. after kneading and dispersing the colorant with the resin component is 10,000 mPa · s or higher, desirably 100,000 mPa · s or higher. The method of kneading and dispersing as described above, and then adding a solvent and finely dispersing so that the viscosity after the fine dispersion treatment is 1,000 mPa · s or less, desirably 100 mPa · s or less, is relatively low. .
The machines used in the redispersion treatment are two rolls, three rolls, ball mills, tron mills, dispersers, kneaders, kneaders, homogenizers, blenders, single- and twin-screw extruders, etc., which disperse while giving a strong shearing force. . Next, a solvent was added, and mainly a vertical or horizontal sand grinder, pin mill, slit mill, ultrasonic disperser, high pressure disperser, etc. were used, and it was made of glass having a particle diameter of 0.1 to 1 mm, zirconia, etc. Fine dispersion with beads. Furthermore, precise dispersion treatment can be performed using fine particle beads of 0.1 mm or less.
It is also possible to disperse the main pigment and the complementary pigment separately, and then mix the dispersions of the two to add further dispersion treatment, or to disperse the main pigment and the complementary pigment together.
For details on dispersion, see T.W. C. It is also described in “Paint Flow and Pigment Dispersion” by Patton (published by John Wiley and Sons, 1964), and this method may be used.
The pigment nanoparticles can be used, for example, in a dispersed state in a vehicle. The vehicle refers to a portion of a medium in which a pigment is dispersed when it is in a liquid state, a portion that is liquid and binds to the pigment to harden a coating film (binder). And a component (organic solvent) to be dissolved and diluted.
The pigment nanoparticle concentration of the pigment nanoparticle dispersion composition after redispersion is appropriately determined according to the purpose, but preferably the pigment nanoparticle content is 2 to 30% by mass with respect to the total amount of the dispersion composition. More preferably, it is 4-20 mass%, and it is especially preferable that it is 5-15 mass%. In the case of dispersing in the vehicle as described above, the amount of the binder and the dissolved dilution component is appropriately determined depending on the type of the organic pigment, etc. Preferably, it is 3-20 mass%, More preferably, it is 5-15 mass%. It is preferable that a dissolution dilution component is 5-80 mass%, and it is more preferable that it is 10-70 mass%.
In the organic nanoparticle dispersion composition, the re-dispersed organic nanoparticles (primary particles) can be finely dispersed particles, and the particle size can be preferably 10 to 1000 nm, and 10 to 500 nm. More preferably, 10-50 nm is especially preferable. Further, the Mv / Mn of the re-dispersed particles is preferably 1.0 to 2.0, more preferably 1.0 to 1.8, and 1.0 to 1.5. Is particularly preferred.
According to the production method of the present invention, for example, pigment particles contained in an organic pigment nanoparticle dispersion composition or a colored photosensitive resin composition to be described later have a minute particle size of nanometer size (for example, 10 to 100 nm). Nevertheless, it can be concentrated and redispersed. For this reason, when used in a color filter, the optical density is high, the uniformity of the filter surface is excellent, the contrast is high, and the noise of the image can be reduced.
Furthermore, since the organic pigment nanoparticles contained in the organic pigment nanoparticle dispersion composition and the colored photosensitive composition can be finely dispersed in a highly uniform manner, a high color density can be achieved with a thin film thickness. For example, a thin layer such as a color filter can be formed.
In addition, in an organic pigment nanoparticle dispersion composition and a colored photosensitive resin composition, by including a pigment exhibiting a clear color tone and high coloring power, for example, as an image forming material for producing a color proof or a color filter Are better.
Furthermore, for an alkaline developer used for exposure / development in the formation of a colored image, an organic nanoparticle dispersion composition, a colored photosensitive resin composition, a binder (binder) that is soluble in an alkaline aqueous solution It can be used and can meet environmental requirements.
In addition, an organic solvent having an appropriate drying property can be used as the solvent (pigment dispersion medium) used in the organic pigment nanoparticle dispersion composition and the colored photosensitive resin composition. Can be satisfied.

  The colored photosensitive resin composition of the present invention comprises a dispersion of the organic pigment nanoparticles, a binder, a monomer or an oligomer, and a photopolymerization initiator or photopolymerization initiator system. Hereinafter, each component of the colored photosensitive resin composition will be described.

  The procedure for preparing organic pigment nanoparticles and dispersions thereof has already been described in detail. The content of the pigment nanoparticles is 3 to 90% by mass with respect to the total solid content in the colored photosensitive resin composition (in the present invention, the total solid content refers to the total composition excluding the organic solvent). Preferably, 20-80 mass% is more preferable, and 25-60 mass% is further more preferable. If this amount is too large, the viscosity of the dispersion increases, which may cause problems in production suitability. If the amount is too small, the coloring power is not sufficient. The pigment nanoparticles functioning as a colorant (pigment particles) preferably have a particle size of 0.1 μm or less, particularly 0.08 μm or less. Moreover, you may use it in combination with a normal pigment for toning. As the pigment, those described above can be used.

  The monomer or oligomer is preferably a polyfunctional monomer that has two or more ethylenically unsaturated double bonds and undergoes addition polymerization upon irradiation with light. Examples of such monomers and oligomers include compounds having at least one addition-polymerizable ethylenically unsaturated group in the molecule and having a boiling point of 100 ° C. or higher at normal pressure. Examples include monofunctional acrylates and monofunctional methacrylates such as dipentaerythritol hexa (meth) acrylate, polyethylene glycol mono (meth) acrylate, polypropylene glycol mono (meth) acrylate and phenoxyethyl (meth) acrylate; polyethylene glycol di ( (Meth) acrylate, polypropylene glycol di (meth) acrylate, trimethylolethane triacrylate, trimethylolpropane tri (meth) acrylate, trimethylolpropane diacrylate, neopentyl glycol di (meth) acrylate, pentaerythritol tetra (meth) acrylate, Pentaerythritol tri (meth) acrylate, dipentaerythritol hexa (meth) acrylate, dipenta Rithritol penta (meth) acrylate, hexanediol di (meth) acrylate, trimethylolpropane tri (acryloyloxypropyl) ether, tri (acryloyloxyethyl) isocyanurate, tri (acryloyloxyethyl) cyanurate, glycerin tri (meth) acrylate And polyfunctional acrylates and polyfunctional methacrylates such as those obtained by adding ethylene oxide or propylene oxide to a polyfunctional alcohol such as trimethylolpropane or glycerin and then (meth) acrylated. Further, as described in JP-A-10-62986, general formulas (1) and (2), a compound obtained by adding ethylene oxide or propylene oxide to a polyfunctional alcohol and then (meth) acrylated is also suitable. As mentioned.

Further, urethane acrylates described in JP-B-48-41708, JP-B-50-6034 and JP-A-51-37193; JP-A-48-64183, JP-B-49-43191 And polyester acrylates described in Japanese Patent Publication No. 52-30490; polyfunctional acrylates and methacrylates such as epoxy acrylates which are reaction products of epoxy resin and (meth) acrylic acid.
Among these, trimethylolpropane tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol hexa (meth) acrylate, and dipentaerythritol penta (meth) acrylate are preferable.
In addition, “polymerizable compound B” described in JP-A-11-133600 can also be mentioned as a preferable example.

  Monomers or oligomers may be used alone or in admixture of two or more. The content of the colored photosensitive resin composition with respect to the total solid content is generally 5 to 50% by mass, and 10 to 40% by mass. Is preferred. If this amount is too large, it becomes difficult to control the developability, which causes a problem in production suitability. If the amount is too small, the curing power at the time of exposure is insufficient.

  As the binder, a binder having an acidic group is preferable, and it can be added at the time of preparing the inkjet ink for color filter or the colored photosensitive resin composition, but when producing the pigment nanoparticle dispersion composition, or pigment nanoparticle It is also preferable to add at the time of formation. It is also possible to add a binder to both or one of the poor solvent for adding the organic pigment solution and the organic pigment solution to form pigment nanoparticles. Alternatively, it is also preferable to add the binder solution in a separate system when forming the pigment nanoparticles.

  The binder is preferably an alkali-soluble polymer having a polar group such as a carboxylic acid group or a carboxylic acid group in the side chain. Examples thereof include JP-A-59-44615, JP-B-54-34327, JP-B-58-12577, JP-B-54-25957, JP-A-59-53836, and JP-A-57-36. A methacrylic acid copolymer, an acrylic acid copolymer, an itaconic acid copolymer, a crotonic acid copolymer, a maleic acid copolymer, a partially esterified maleic acid copolymer as described in JP-A-59-71048 Etc. Moreover, the cellulose derivative which has a carboxylic acid group, carboxylate, etc. in a side chain can also be mentioned, In addition to this, what added the cyclic acid anhydride to the polymer which has a hydroxyl group can also be used preferably. As particularly preferred examples, copolymers of benzyl (meth) acrylate and (meth) acrylic acid described in US Pat. No. 4,139,391, benzyl (meth) acrylate and (meth) acrylic acid are used. And multi-component copolymers with other monomers.

  The binder may be used singly or may be used in the state of a composition used in combination with a normal film-forming polymer, and the addition amount relative to 100 parts by mass of pigment nanoparticles is generally 10 to 200 parts by mass. And 25-100 mass parts is preferable.

  In addition, in order to improve the crosslinking efficiency, a polymerizable group may be included in the side chain, and a UV curable resin, a thermosetting resin, or the like is also useful. Furthermore, as the binder resin, an organic high molecular polymer having a water-soluble atomic group in a part of the side chain can be used.

  As a photopolymerization initiator or a photopolymerization initiator system (in the present invention, a photopolymerization initiator system refers to a mixture that exhibits a photopolymerization initiation function by a combination of a plurality of compounds), US Pat. No. 2,367,660 Vicinal polyketaldonyl compounds disclosed in US Pat. No. 2,448,828, acyloin ether compounds described in US Pat. No. 2,448,828, α-hydrocarbon-substituted fragrances described in US Pat. No. 2,722,512 Group acyloin compounds, polynuclear quinone compounds described in US Pat. Nos. 3,046,127 and 2,951,758, combinations of triarylimidazole dimers described in US Pat. No. 3,549,367 and p-amino ketones, Benzothiazole compounds and trihalomethyl-s-triazines described in Japanese Patent No. 51-48516 Compound, trihalomethyl are described in U.S. Patent No. 4239850 - triazine compounds include U.S. Patent trihalomethyl oxadiazole compounds described in No. 4,212,976 specification or the like. In particular, trihalomethyl-s-triazine, trihalomethyloxadiazole, and triarylimidazole dimer are preferable.

  In addition, “polymerization initiator C” described in JP-A-11-133600, oxime-based compounds such as 1-phenyl-1,2-propanedione-2- (o-ethoxycarbonyl) oxime, O— Benzoyl-4 '-(benzmercapto) benzoyl-hexyl-ketoxime, 2,4,6-trimethylphenylcarbonyl-diphenyl phosphonyl oxide, hexafluorophospho-trialkylphenyl phosphonium salt and the like may be mentioned as suitable ones. it can.

The photopolymerization initiator or the photopolymerization initiator system may be used alone or in combination of two or more, but it is particularly preferable to use two or more. When at least two kinds of photopolymerization initiators are used, display characteristics, particularly display unevenness, can be reduced.
The content of the photopolymerization initiator or the photopolymerization initiator system with respect to the total solid content of the colored photosensitive resin composition is generally 0.5 to 20% by mass, and preferably 1 to 15% by mass. If this amount is too large, the sensitivity becomes too high and control becomes difficult. If the amount is too small, the exposure sensitivity becomes too low.

  In the colored photosensitive resin composition, in addition to the above components, an organic solvent for preparing a resin composition (fourth solvent) may be further used. Examples of the organic solvent include, but are not limited to, esters, ethers, and ketones. Among these solvents, methyl 3-ethoxypropionate, ethyl 3-ethoxypropionate, ethyl cellosolve acetate, ethyl lactate, butyl acetate, methyl 3-methoxypropionate, 2-heptanone, cyclohexanone, ethyl carbitol acetate, butyl carbitol Acetate, propylene glycol methyl ether acetate and the like are preferably used as the solvent. These solvents may be used alone or in combination of two or more. The high-boiling organic solvent can be used as the fourth solvent. For example, a solvent having a boiling point of 180 ° C. to 250 ° C. can be used if necessary. As for content of a 4th solvent, 10-95 mass% is preferable with respect to the resin composition whole quantity.

  Moreover, it is preferable to contain an appropriate surfactant in the colored photosensitive resin composition. Suitable surfactants include those disclosed in JP-A Nos. 2003-337424 and 11-133600. The content of the surfactant is preferably 5% by mass or less with respect to the total amount of the resin composition.

  The colored photosensitive resin composition preferably contains a thermal polymerization inhibitor. Examples of the thermal polymerization inhibitor include hydroquinone, hydroquinone monomethyl ether, p-methoxyphenol, di-t-butyl-p-cresol, pyrogallol, t-butylcatechol, benzoquinone, 4,4′-thiobis (3-methyl). -6-t-butylphenol), 2,2'-methylenebis (4-methyl-6-t-butylphenol), 2-mercaptobenzimidazole, phenothiazine and the like. The content of the thermal polymerization inhibitor is preferably 1% by mass or less based on the total amount of the resin composition.

In addition to the colorant (pigment), a colorant (dye or pigment) can be added to the colored photosensitive resin composition as necessary. In the case of using a pigment among the colorants, it is desirable that the pigment is uniformly dispersed in the colored photosensitive resin composition. Therefore, the particle diameter is preferably 0.1 μm or less, particularly 0.08 μm or less.
Specific examples of the dye or pigment include the colorant described in JP-A-2005-17716 [0038] to [0040] and JP-A-2005-361447 [0068] to [0072]. And the colorants described in JP-A-2005-17521 [0080] to [0088] can be suitably used. The content of the auxiliary dye or pigment is preferably 5% by mass or less based on the total amount of the resin composition.

The colored photosensitive resin composition may contain an ultraviolet absorber as necessary. Examples of the ultraviolet absorber include salicylate-based, benzophenone-based, benzotriazole-based, cyanoacrylate-based, nickel chelate-based, hindered amine-based compounds and the like in addition to the compounds described in JP-A-5-72724.
As for content of a ultraviolet absorber, 5 mass% or less is preferable with respect to the resin composition whole quantity.

  Further, in the colored photosensitive resin composition, in addition to the above additives, “adhesion aid” described in JP-A-11-133600, other additives, and the like can be contained.

The color filter of the present invention is excellent in contrast. In the present invention, the contrast represents the ratio of the amount of transmitted light between two polarizing plates when the polarization axis is parallel and when it is vertical (“1990 Seventh Color Optical Conference, 512-color display 10.4. "Refer to" Color TFT for size TFT-LCD, Ueki, Koseki, Fukunaga, Yamanaka "etc.).
The high contrast of the color filter means that the bright and dark discrimination when combined with the liquid crystal can be increased, and this is a very important performance in order to replace the liquid crystal display with a CRT.

  When the color filter of the present invention is used for a television, the chromaticities of all the single colors of red (R), green (G), and blue (B) by the F10 light source are the values shown in the table below ( Hereinafter, in the present invention, the difference (ΔE) from the “target chromaticity”) is preferably in the range of 5 or less, more preferably 3 or less, and particularly preferably 2 or less.

------------------------
xy Y
------------------------
R 0.656 0.336 21.4
G 0.293 0.634 52.1
B 0.146 0.088 6.90
------------------------

In the present invention, the chromaticity is measured with a microspectrophotometer (manufactured by Olympus Optical Co., Ltd .; OSP100 or 200), calculated as a result of the F10 light source field of view of 2 degrees, and expressed as an xyY value in the xyz color system. Further, the difference from the target chromaticity is represented by a color difference of the La ^* b ^* color system.

  The liquid crystal display device provided with the color filter of the present invention has a high contrast and excellent descriptive power such as black spots, and is particularly preferably a VA system. It can also be suitably used as a large-screen liquid crystal display device such as a notebook personal computer display or a television monitor. The color filter of the present invention can be used for a CCD device and exhibits excellent performance.

  EXAMPLES Hereinafter, although this invention is demonstrated in more detail based on an Example, this invention is limited to this and is not interpreted.

(Synthesis example) Synthesis of basic dispersion aid

ブロモウンデカン酸（１０．０質量部）に塩化チオニル（２０．０質量部）を添加し、１時間過熱還流した後、過剰の塩化チオニルを減圧留去した。これを、５−アミノベンズイミダゾロン（７．０質量部）とトリエチルアミン（３．８質量部）を溶解させたＮＭＰ（和光純薬工業社製）（１００質量部）溶液に滴下し、１００℃で１時間加熱した。水（２００質量部）を加え、析出した固体をろ取し、水、メタノールで洗浄することにより、Ａ−１前駆体（１２．６質量部）を収率８３％で得た。Ａ−１前駆体（５質量部）をＮＭＰ（４０質量部）に溶解させ、これに５０％ジメチルアミン水溶液（２０質量部）添加し、１００℃で３時間過熱した。メタノール（１００質量部）を添加し、析出した固体をろ取し、メタノールで洗浄することにより、例示化合物Ａ−１（３．５質量部）を収率７８％で得た（ｍ．ｐ．＞３００℃）。
^１Ｈ ＮＭＲ（３００ＭＨｚ，ＤＭＳＯ−ｄ_６）δ１．２（ｓ，１２Ｈ），１．２−１．４（ｍ，２Ｈ），１．５−１．６（ｍ，２Ｈ），２．０（ｓ，６Ｈ），２．１（ｔ，２Ｈ），２．２（ｔ，２Ｈ），６．８（ｄ，１Ｈ），７．０（ｄ，１Ｈ），７．４（ｓ，１Ｈ），９．６（ｓ，１Ｈ），１０．４（ｓ，１Ｈ），１０．５（ｓ，１Ｈ）．

Thionyl chloride (20.0 parts by mass) was added to bromoundecanoic acid (10.0 parts by mass), and the mixture was heated to reflux for 1 hour, and then excess thionyl chloride was distilled off under reduced pressure. This was dropped into an NMP (manufactured by Wako Pure Chemical Industries, Ltd.) (100 parts by mass) solution in which 5-aminobenzimidazolone (7.0 parts by mass) and triethylamine (3.8 parts by mass) were dissolved, and 100 ° C. For 1 hour. Water (200 parts by mass) was added, and the precipitated solid was collected by filtration and washed with water and methanol to obtain an A-1 precursor (12.6 parts by mass) in a yield of 83%. The A-1 precursor (5 parts by mass) was dissolved in NMP (40 parts by mass), 50% dimethylamine aqueous solution (20 parts by mass) was added thereto, and the mixture was heated at 100 ° C. for 3 hours. Methanol (100 parts by mass) was added, and the precipitated solid was collected by filtration and washed with methanol to obtain Exemplified Compound A-1 (3.5 parts by mass) in a yield of 78% (mp). > 300 ° C.).
¹ H NMR (300 MHz, DMSO-d ₆ ) δ 1.2 (s, 12H), 1.2-1.4 (m, 2H), 1.5-1.6 (m, 2H), 2.0 ( s, 6H), 2.1 (t, 2H), 2.2 (t, 2H), 6.8 (d, 1H), 7.0 (d, 1H), 7.4 (s, 1H), 9.6 (s, 1H), 10.4 (s, 1H), 10.5 (s, 1H).

前記例示化合物Ａ−１の合成と同様にして合成したＡ−１前駆体（３質量部）をＮＭＰ（２４質量部）に溶解させ、これにモルホリン（６．５質量部）添加し、１００℃で４．５時間過熱した。メタノール（１００質量部）を添加し、析出した固体をろ取し、メタノールで洗浄することにより、例示化合物Ａ−２（２．６質量部）を収率８６％で得た（ｍ．ｐ．＞３００℃）。
^１Ｈ ＮＭＲ（３００ＭＨｚ，ＤＭＳＯ−ｄ_６）δ１．２（ｓ，１２Ｈ），１．３−１．４（ｍ，２Ｈ），１．５−１．６（ｍ，２Ｈ），２．２−２．３（ｍ，８Ｈ），３．５（ｔ，４Ｈ），６．８（ｄ，１Ｈ），７．０（ｄ，１Ｈ），７．４（ｓ，１Ｈ），９．６（ｓ，１Ｈ），１０．４（ｓ，１Ｈ），１０．５（ｓ，１Ｈ）．

The A-1 precursor (3 parts by mass) synthesized in the same manner as in the synthesis of the exemplified compound A-1 was dissolved in NMP (24 parts by mass), and morpholine (6.5 parts by mass) was added to the A-1 precursor. Overheated for 4.5 hours. Methanol (100 parts by mass) was added, and the precipitated solid was collected by filtration and washed with methanol to obtain Exemplified Compound A-2 (2.6 parts by mass) in a yield of 86% (mp. > 300 ° C.).
¹ H NMR (300 MHz, DMSO-d ₆ ) δ 1.2 (s, 12H), 1.3-1.4 (m, 2H), 1.5-1.6 (m, 2H), 2.2- 2.3 (m, 8H), 3.5 (t, 4H), 6.8 (d, 1H), 7.0 (d, 1H), 7.4 (s, 1H), 9.6 (s , 1H), 10.4 (s, 1H), 10.5 (s, 1H).

前記例示化合物Ａ−１の合成と同様にして合成したＡ−１前駆体（３質量部）をＮＭＰ（２４質量部）に溶解させ、これにイミダゾール（５．１質量部）添加し、１００℃で６．５時間過熱した。アセトニトリル（２００質量部）を添加し、析出した固体をろ取し、アセトニトリルで洗浄し、例示化合物Ａ−３（２．３質量部）を収率８０％で得た（ｍ．ｐ．２７６−２７８℃）。
^１Ｈ ＮＭＲ（３００ＭＨｚ，ＤＭＳＯ−ｄ_６）δ１．２（ｓ，１２Ｈ），１．５−１．６（ｍ，２Ｈ），１．６−１．７（ｍ，２Ｈ），３．９（ｔ，２Ｈ），６．８（ｄ，１Ｈ），６．９−７．０（ｍ，２Ｈ），７．２（ｓ，１Ｈ），７．４（ｓ，１Ｈ），７．８（ｓ，１Ｈ），９．７（ｓ，１Ｈ），１０．４（ｓ，１Ｈ），１０．５（ｓ，１Ｈ）．

The A-1 precursor (3 parts by mass) synthesized in the same manner as in the synthesis of the exemplary compound A-1 was dissolved in NMP (24 parts by mass), and imidazole (5.1 parts by mass) was added thereto, and then 100 ° C. For 6.5 hours. Acetonitrile (200 parts by mass) was added, and the precipitated solid was collected by filtration and washed with acetonitrile to obtain Exemplified Compound A-3 (2.3 parts by mass) in a yield of 80% (mp 276-). 278 ° C).
¹ H NMR (300 MHz, DMSO-d ₆ ) δ 1.2 (s, 12H), 1.5-1.6 (m, 2H), 1.6-1.7 (m, 2H), 3.9 ( t, 2H), 6.8 (d, 1H), 6.9-7.0 (m, 2H), 7.2 (s, 1H), 7.4 (s, 1H), 7.8 (s , 1H), 9.7 (s, 1H), 10.4 (s, 1H), 10.5 (s, 1H).

ブロモヘキサン酸（７．４質量部）に塩化チオニル（２０．０質量部）を添加し、１時間過熱還流した後、過剰の塩化チオニルを減圧留去した。これを、５−アミノベンズイミダゾロン（７．０質量部）とトリエチルアミン（３．８質量部）を溶解させたＮＭＰ（１００質量部）溶液に滴下し、１００℃で１時間加熱した。水（２００質量部）を加え、析出した固体をろ取し、水で洗浄することにより、Ａ−４前駆体（１２．０質量部）を収率８８％で得た。Ａ−４前駆体（５質量部）をＮＭＰ（４６質量部）に溶解させ、これに５０％ジメチルアミン水溶液（２２質量部）添加し、１００℃で３時間過熱した。アセトニトリル（１００質量部）を添加し、析出した固体をろ取し、アセトニトリルで洗浄することにより、例示化合物Ａ−４（３．４質量部）を収率８５％で得た（ｍ．ｐ．＞３００℃）。
^１Ｈ ＮＭＲ（３００ＭＨｚ，ＤＭＳＯ−ｄ_６）δ１．２−１．３（ｍ，２Ｈ），１．３−１．４（ｍ，２Ｈ），１．５−１．６（ｍ，２Ｈ），２．０（ｓ，６Ｈ），２．１（ｔ，２Ｈ），２．２（ｔ，２Ｈ），６．８（ｄ，１Ｈ），７．０（ｄ，１Ｈ），７．４（ｓ，１Ｈ），９．７（ｓ，１Ｈ），１０．４（ｓ，１Ｈ），１０．５（ｓ，１Ｈ）．

Thionyl chloride (20.0 parts by mass) was added to bromohexanoic acid (7.4 parts by mass), and the mixture was heated to reflux for 1 hour, and then excess thionyl chloride was distilled off under reduced pressure. This was added dropwise to an NMP (100 parts by mass) solution in which 5-aminobenzimidazolone (7.0 parts by mass) and triethylamine (3.8 parts by mass) were dissolved, and heated at 100 ° C. for 1 hour. Water (200 parts by mass) was added, and the precipitated solid was collected by filtration and washed with water to obtain an A-4 precursor (12.0 parts by mass) in a yield of 88%. The A-4 precursor (5 parts by mass) was dissolved in NMP (46 parts by mass), 50% dimethylamine aqueous solution (22 parts by mass) was added thereto, and the mixture was heated at 100 ° C. for 3 hours. Acetonitrile (100 parts by mass) was added, and the precipitated solid was collected by filtration and washed with acetonitrile to obtain Exemplified Compound A-4 (3.4 parts by mass) in a yield of 85% (mp. > 300 ° C.).
¹ H NMR (300 MHz, DMSO-d ₆ ) δ 1.2-1.3 (m, 2H), 1.3-1.4 (m, 2H), 1.5-1.6 (m, 2H), 2.0 (s, 6H), 2.1 (t, 2H), 2.2 (t, 2H), 6.8 (d, 1H), 7.0 (d, 1H), 7.4 (s , 1H), 9.7 (s, 1H), 10.4 (s, 1H), 10.5 (s, 1H).

ブロモウンデカン酸（１０．０質量部）に塩化チオニル（２０．０質量部）を添加し、１時間過熱還流した後、過剰の塩化チオニルを減圧留去した。これを、２−アミノベンズイミダゾール（５．０質量部）とトリエチルアミン（３．８質量部）を溶解させたＮＭＰ（１００質量部）溶液に滴下し、１００℃で３時間加熱した。水（２００質量部）を加え、析出した固体をろ取し、水で洗浄することにより、Ａ−５前駆体（１１．５質量部）を収率８０％で得た。Ａ−５前駆体（５質量部）をＮＭＰ（４３質量部）に溶解させ、これに５０％ジメチルアミン水溶液（２１質量部）添加し、１００℃で３.５時間過熱した。水（１００質量部）を添加し、析出した固体をろ取し、水で洗浄することにより、例示化合物Ａ−５（４．０質量部）を収率８８％で得た（ｍ．ｐ．１３７−１３９℃）。
^１Ｈ ＮＭＲ（３００ＭＨｚ，ＤＭＳＯ−ｄ_６）δ１．２−１．４（ｍ，１４Ｈ），１．５−１．６（ｍ，２Ｈ），２．０（ｓ，６Ｈ），２．１（ｔ，２Ｈ），２．４（ｔ，２Ｈ），６．８（ｄ，１Ｈ），７．０−７．１（ｍ，２Ｈ），７．４−７．５（ｍ，２Ｈ）．

Thionyl chloride (20.0 parts by mass) was added to bromoundecanoic acid (10.0 parts by mass), and the mixture was heated to reflux for 1 hour, and then excess thionyl chloride was distilled off under reduced pressure. This was added dropwise to an NMP (100 parts by mass) solution in which 2-aminobenzimidazole (5.0 parts by mass) and triethylamine (3.8 parts by mass) were dissolved, and heated at 100 ° C. for 3 hours. Water (200 parts by mass) was added, and the precipitated solid was collected by filtration and washed with water to obtain an A-5 precursor (11.5 parts by mass) in a yield of 80%. The A-5 precursor (5 parts by mass) was dissolved in NMP (43 parts by mass), 50% dimethylamine aqueous solution (21 parts by mass) was added thereto, and the mixture was heated at 100 ° C. for 3.5 hours. Water (100 parts by mass) was added, and the precipitated solid was collected by filtration and washed with water to obtain Exemplified Compound A-5 (4.0 parts by mass) in a yield of 88% (mp. 137-139 ° C).
¹ H NMR (300 MHz, DMSO-d ₆ ) δ 1.2-1.4 (m, 14H), 1.5-1.6 (m, 2H), 2.0 (s, 6H), 2.1 ( t, 2H), 2.4 (t, 2H), 6.8 (d, 1H), 7.0-7.1 (m, 2H), 7.4-7.5 (m, 2H).

ブロモウンデカン酸（１０．０質量部）に塩化チオニル（２０．０質量部）を添加し、１時間過熱還流した後、過剰の塩化チオニルを減圧留去した。これを、３−アミノアントラキノン（８．４質量部）とトリエチルアミン（３．８質量部）を溶解させたＮＭＰ（１００質量部）溶液に滴下し、１００℃で３時間加熱した。水（２００質量部）を加え、析出した固体をろ取し、水で洗浄することにより、Ａ−６前駆体（１５．０質量部）を収率８５％で得た。Ａ−６前駆体（５質量部）をＮＭＰ（３５質量部）に溶解させ、これに５０％ジメチルアミン水溶液（１７質量部）添加し、１００℃で６.５時間過熱した。アセトニトリル−水１：１溶液（１００質量部）を添加し、析出した固体をろ取し、アセトニトリル−水１：１溶液で洗浄することにより、例示化合物Ａ−６（３．８質量部）を収率８２％で得た（ｍ．ｐ．１７６−１７８℃）。
^１Ｈ ＮＭＲ（３００ＭＨｚ，ＤＭＳＯ−ｄ_６）δ１．２−１．３（ｍ，１４Ｈ），１．６−１．７（ｍ，２Ｈ），２．０（ｓ，６Ｈ），２．１（ｔ，２Ｈ），２．４（ｔ，２Ｈ），７．８−７．９（ｍ，２Ｈ），８．０−８．２（ｍ，４Ｈ），８．４（ｓ，１Ｈ），１０．５（ｓ，１Ｈ）．

Thionyl chloride (20.0 parts by mass) was added to bromoundecanoic acid (10.0 parts by mass), and the mixture was heated to reflux for 1 hour, and then excess thionyl chloride was distilled off under reduced pressure. This was added dropwise to an NMP (100 parts by mass) solution in which 3-aminoanthraquinone (8.4 parts by mass) and triethylamine (3.8 parts by mass) were dissolved, and heated at 100 ° C. for 3 hours. Water (200 parts by mass) was added, and the precipitated solid was collected by filtration and washed with water to obtain an A-6 precursor (15.0 parts by mass) in a yield of 85%. The A-6 precursor (5 parts by mass) was dissolved in NMP (35 parts by mass), 50% dimethylamine aqueous solution (17 parts by mass) was added thereto, and the mixture was heated at 100 ° C. for 6.5 hours. An acetonitrile-water 1: 1 solution (100 parts by mass) was added, and the precipitated solid was collected by filtration and washed with an acetonitrile-water 1: 1 solution, whereby Exemplified Compound A-6 (3.8 parts by mass) was obtained. Yield was 82% (mp 176-178 ° C).
¹ H NMR (300 MHz, DMSO-d ₆ ) δ 1.2-1.3 (m, 14H), 1.6-1.7 (m, 2H), 2.0 (s, 6H), 2.1 ( t, 2H), 2.4 (t, 2H), 7.8-7.9 (m, 2H), 8.0-8.2 (m, 4H), 8.4 (s, 1H), 10 .5 (s, 1H).

ブロモウンデカン酸（１０．０質量部）に塩化チオニル（２０．０質量部）を添加し、１時間過熱還流した後、過剰の塩化チオニルを減圧留去した。これを、５−アミノウラシル（４．８質量部）とトリエチルアミン（３．８質量部）を溶解させたＮＭＰ（１００質量部）溶液に滴下し、１００℃で３時間加熱した。水（２００質量部）を加え、析出した固体をろ取し、水で洗浄することにより、Ａ−７前駆体（１１．８質量部）を収率８４％で得た。Ａ−７前駆体（５質量部）をＮＭＰ（４４質量部）に溶解させ、これに５０％ジメチルアミン水溶液（２１質量部）添加し、１００℃で４時間過熱した。アセトニトリル（１００質量部）を添加し、析出した固体をろ取し、アセトニトリルで洗浄することにより、例示化合物Ａ−７（３．０質量部）を収率６６％で得た（ｂ．ｐ．１８３−１８５℃）。
^１Ｈ ＮＭＲ（３００ＭＨｚ，ＤＭＳＯ−ｄ_６）δ１．２（ｓ，１２Ｈ），１．３−１．４（ｍ，２Ｈ），１．４−１．５（ｍ，２Ｈ），２．０（ｓ，６Ｈ），２．１（ｔ，２Ｈ），２．３（ｔ，２Ｈ），８．０（ｓ，１Ｈ），９．０（ｓ，１Ｈ）．

Thionyl chloride (20.0 parts by mass) was added to bromoundecanoic acid (10.0 parts by mass), and the mixture was heated to reflux for 1 hour, and then excess thionyl chloride was distilled off under reduced pressure. This was added dropwise to an NMP (100 parts by mass) solution in which 5-aminouracil (4.8 parts by mass) and triethylamine (3.8 parts by mass) were dissolved, and heated at 100 ° C. for 3 hours. Water (200 parts by mass) was added, and the precipitated solid was collected by filtration and washed with water to obtain an A-7 precursor (11.8 parts by mass) in a yield of 84%. A-7 precursor (5 parts by mass) was dissolved in NMP (44 parts by mass), 50% dimethylamine aqueous solution (21 parts by mass) was added thereto, and the mixture was heated at 100 ° C. for 4 hours. Acetonitrile (100 parts by mass) was added, and the precipitated solid was collected by filtration and washed with acetonitrile to obtain Exemplified Compound A-7 (3.0 parts by mass) in a yield of 66% (bp). 183-185 ° C).
¹ H NMR (300 MHz, DMSO-d ₆ ) δ 1.2 (s, 12H), 1.3-1.4 (m, 2H), 1.4-1.5 (m, 2H), 2.0 ( s, 6H), 2.1 (t, 2H), 2.3 (t, 2H), 8.0 (s, 1H), 9.0 (s, 1H).

<Example 1-1>
While heating 1000 parts by volume of methanesulfonic acid (Wako Pure Chemical Industries, Ltd.) to 80 ° C., the pigment C.I. I. Pigment Violet 23 (manufactured by Clariant, Hostaperm Violet RL-NF) 45 parts by mass and Exemplified Compound A-1 (Tokyo Chemical Industry Co., Ltd., 4.5 parts by mass) were added to prepare pigment solution A.
Separately from this, 4000 parts by mass of water was prepared as a poor solvent.
Here, the temperature of the solution was controlled at 25 ° C., and the pigment solution A at 80 ° C. was added to the poor solvent stirred at 500 rpm by a GK-0222-10 type Lamond Stirrer (trade name, manufactured by Fujisawa Pharmaceutical Co., Ltd.) Infusion was performed using a 500-type large capacity non-pulsating flow pump (trade name, manufactured by Nippon Seimitsu Chemical Co., Ltd.). The pigment solution A has a flow path diameter and supply port diameter of 2.2 mm, and the supply port is placed in a poor solvent, and 220 ml is injected at a flow rate of 200 ml / min to form organic pigment particles. A was prepared. The particle diameter of this pigment dispersion was measured using Nanotrack UPA-EX150 manufactured by Nikkiso Co., Ltd.
The pH of this pigment dispersion was measured with a pH test paper (manufactured by ADVANTEC) and found to be 1. This was neutralized by adding a 48% aqueous sodium hydroxide solution until the pH reached 9. The resulting aggregate was observed with an optical microscope.
The above-mentioned aggregate was filtered off with a filter paper (manufactured by ADVANTEC, No. 2), and the time required for filtration at this time was measured. The filtered organic nano pigment was washed with water (300 parts by mass).
A solution obtained by adding 80 parts by mass of non-aqueous dispersant C-1 (Exemplary Polymer Compound C-1) to 300 parts by mass of ethyl lactate is added to the pigment nanoparticle concentrated paste, and stirred at 1500 rpm for 60 minutes with a dissolver. Thereafter, 25 parts by mass of ethyl acetate was added, and further stirred with a dissolver at 500 rpm for 10 minutes to obtain pigment nanoparticle ethyl lactate dispersion A. The organic pigment powder A of the present invention was obtained by removing the pigment nanoparticle ethyl lactate dispersion A with an evaporator.

Using the organic pigment powder A, a pigment dispersion composition A having the following composition was prepared.
1 part by weight of the organic pigment powder A 4 parts by weight of 1,3 butylene glycol diacetate The pigment dispersion composition A having the above composition was used with a motor mill M-50 (manufactured by Eiger Japan) and zirconia beads having a diameter of 0.65 mm. For 1 hour at a peripheral speed of 9 m / s.
The following evaluation was performed about the obtained pigment dispersion composition. The results are shown in Table 1.
(1) Average particle diameter of organic nanoparticle aqueous dispersion The number average particle diameter was measured using Nanotrack UPA-EX150 manufactured by Nikkiso Co., Ltd.
(2) Diameter of aggregates The aggregates were observed with an optical microscope, and the diameters of the aggregates were measured with reference to a separately observed monosashi. As for the diameter of the aggregate here, the length from end to end of the aggregate was measured, and the longest length was defined as the diameter. The agglomerates herein are those in which nanoparticles, which are primary particles that cannot be seen with the naked eye, gather more and grow to secondary particles.
(3) Filtration time Filtration time per 1 g of pigment was measured by filtering under reduced pressure with an aspirator using Nutsche and filter paper (Advantech Co., No. 2 (trade name)) having a diameter of 9 cm.
(4) Contrast Evaluation Each of the obtained pigment dispersion compositions A to F was applied on a glass substrate so as to have a thickness of 2 μm, thereby preparing a sample. As a backlight unit, a three-wavelength cold cathode tube light source (FWL18EX-N manufactured by Toshiba Lighting & Technology Co., Ltd.) with a diffusion plate installed was used, and two polarizing plates (polarizing plates HLC2-2518 manufactured by Sanritsu Co., Ltd.) were used. ), The amount of transmitted light when the polarization axis is parallel and vertical is measured, and the ratio is defined as the contrast (“1990 Seventh Color Optical Conference, 512-color display 10. 4 ”size TFT-LCD color filter, planting, Koseki, Fukunaga, Yamanaka etc.). Two polarizing plates, a sample, and a color luminance meter are installed at a position 13 mm from the backlight, a polarizing plate at a position 40 mm to 60 mm, a cylinder 11 mm in diameter and 20 mm in length, and light transmitted through this. Was measured on a color luminance meter installed at a position of 400 mm through a polarizing plate installed at a position of 100 mm. The measurement angle of the color luminance meter was set to 2 °. The amount of light of the backlight was set so that the luminance when the two polarizing plates were installed in parallel Nicol was 1280 cd / m ² without the sample being installed.

<Example 1-2>
The said exemplary compound A-1 of Example 1 was changed into exemplary compound A-6, and operation similar to Example 1-1 was performed. The obtained organic nanoparticle non-aqueous dispersion is also referred to as pigment dispersion composition B. Table 1 shows the results of the same evaluation test as in Example 1-1 for the pigment dispersion composition B.

<Example 1-3>
Example Compound A-1 of Example 1 was changed to Example Compound A-7, and the same operation as Example 1-1 was performed. The obtained organic nanoparticle non-aqueous dispersion is also referred to as pigment dispersion composition C. Table 1 shows the results of the same evaluation test as in Example 1-1 for the pigment dispersion composition B.

<Example 1-4>
Polyvinylpyrrolidone (K-25, trade name, manufactured by Wako Pure Chemical Industries, 90 parts by mass) is added together with the exemplified compound A-1 of Example 1, and the same operation as in Example 1-1 is performed. It was. The obtained organic nanoparticle non-aqueous dispersion is also referred to as pigment dispersion composition B. Table 1 shows the results of the same evaluation test as in Example 1-1 for the pigment dispersion composition D.

<Comparative Example 1-1>
Instead of the polymer compound A-1 of Example 1, polyvinyl pyrrolidone (K-25, trade name, manufactured by Wako Pure Chemical Industries, Ltd., 90 parts by mass) was added, and instead of the polymer compound C-1. The same operation as in Example 1 was performed except that a methacrylic acid / benzyl methacrylate copolymer was used. The obtained organic nanoparticle non-aqueous dispersion is also referred to as pigment dispersion composition E. Table 1 shows the results of the same evaluation test as in Example 1-1 for the pigment dispersion composition E.

<Reference Example 1-1>
An aqueous pigment dispersion was prepared in the same manner as in Example 1-1, and isolation was performed without performing pH operation, whereby Dispersion Composition F was obtained. The filtration time at this time was evaluated. The results are shown in Table 1.

[Table 1]
---------------------------------------
Pigment dispersion Primary particle size Aggregate Filtration time Contrast composition (nm) diameter (per 1g pigment)
---------------------------------------
A 31 500μm or more 3 minutes 15000
B 33 500 μm or more 2 minutes 16000
C 34 500 μm or more 3 minutes 15200
D 28 500 μm or more 5 minutes 16500
E 36 5 μm or less 15 minutes 11000
F 31 1 hour
---------------------------------------
As shown in Table 1, according to the basic dispersion aid of the present invention, high contrast is achieved in a non-aqueous dispersion in which fine particles are aggregated once in an aqueous dispersion and re-dispersed by switching the medium to an organic solvent. Moreover, it can be seen that the filterability is good, the isolation time is greatly reduced, and the characteristics and productivity of the desired dispersion and color filter are remarkably improved.

<Example 2>
Hereinafter, a method for producing a colored photosensitive resin composition and a color filter will be described.
[Formation of black (K) image]
The alkali-free glass substrate was cleaned with a UV cleaning apparatus, then brush-cleaned with a cleaning agent, and further ultrasonically cleaned with ultrapure water. The substrate was heat-treated at 120 ° C. for 3 minutes to stabilize the surface state.
After cooling the substrate and adjusting the temperature to 23 ° C., the composition described in Table 2 below is applied on a glass substrate coater (manufactured by FS Asia Co., Ltd., trade name: MH-1600) having a slit-like nozzle. A colored photosensitive resin composition K1 was applied. Subsequently, a part of the solvent was dried by VCD (vacuum drying apparatus; manufactured by Tokyo Ohka Kogyo Co., Ltd.) for 30 seconds to eliminate the fluidity of the coating layer, and then pre-baked at 120 ° C. for 3 minutes to obtain a film thickness of A 4 μm photosensitive resin layer K1 was obtained.

[Table 2]
----------------------------------
Composition component K content (parts by mass)
----------------------------------
K pigment dispersion 1 (carbon black) 25
Propylene glycol monomethyl ether acetate 8.0
Methyl ethyl ketone 53
Binder 2 9.1
Hydroquinone monomethyl ether 0.002
DPHA solution 4.2
Polymerization initiator A 0.16
Surfactant 1 0.044
----------------------------------
In a proximity type exposure machine (manufactured by Hitachi High-Tech Electronics Engineering Co., Ltd.) having an ultra-high pressure mercury lamp, with the substrate and mask (quartz exposure mask having an image pattern) standing vertically, the exposure mask surface and the mask The distance between the photosensitive resin layers was set to 200 μm, and pattern exposure was performed at an exposure amount of 300 mJ / cm ² .
Next, after spraying pure water with a shower nozzle to uniformly wet the surface of the photosensitive resin layer K1, a KOH developer (KOH, containing nonionic surfactant, trade name: CDK-1, (Fujifilm Electronics Materials Co., Ltd.) was subjected to shower development at 23 ° C. for 80 seconds and a flat nozzle pressure of 0.04 MPa to obtain a patterning image. Subsequently, ultrapure water was sprayed at a pressure of 9.8 MPa with an ultrahigh pressure washing nozzle to remove the residue, and a black (K) image K was obtained. Subsequently, heat treatment was performed at 220 ° C. for 30 minutes.

[Formation of red (R) pixels]
A heat-treated pixel R was formed in the same process as the formation of the black (K) image using a colored photosensitive resin composition R1 having a composition shown in Table 3 below on the substrate on which the image K was formed. The film thickness of the photosensitive resin layer R1 and the coating amount of pigments (CIPR 254 and CIPR 177) are shown below.
Photosensitive resin film thickness (μm) 1.60
Pigment coating amount (g / m ² ) 1.00
C. I. P. R. 254 coating amount (g / m ² ) 0.70
C. I. P. R. 177 coating amount (g / m ² ) 0.30

[Table 3]
----------------------------------
Composition component Content (parts by mass)
----------------------------------
R pigment dispersion 1 (C.I.P.R254) 35
R pigment dispersion 2 (C.I.P.R177) 6.8
Propylene glycol monomethyl ether acetate 7.6
Methyl ethyl ketone 37
Binder 1 0.7
DPHA solution 3.8
Polymerization initiator B 0.12
Polymerization initiator A 0.05
Phenothiazine 0.01
Surfactant 1 0.06
----------------------------------
[Formation of green (G) pixels]
Using the colored photosensitive resin composition G1 having the composition shown in Table 4 below on the substrate on which the image K and the pixel R are formed, the heat-treated pixel G is formed in the same process as the formation of the black (K) image. Formed. The film thickness of the photosensitive resin layer G1 and the coating amounts of pigments (CIPG36 and CIPY150) are shown below.
Photosensitive resin film thickness (μm) 1.60
Pigment application amount (g / m ² ) 1.92
C. I. P. G. 36 coating amount (g / m ² ) 1.34
C. I. P. Y. 150 coating amount (g / m ² ) 0.58

[Table 4]
------------------------------
Composition component Content (parts by mass)
------------------------------
G pigment dispersion 1 (C.I.P.G36) 28
Y pigment dispersion 1 (C.I.P.Y150) 15
Propylene glycol monomethyl ether acetate 29
Methyl ethyl ketone 26
Cyclohexanone 1.3
Binder 2 2.5
DPHA solution 3.5
Polymerization initiator B 0.12
Polymerization initiator A 0.05
Phenothiazine 0.01
Surfactant 1 0.07
------------------------------

[Formation of blue (B) pixels]
Using the colored photosensitive resin composition B1 having the composition shown in Table 5 below on the substrate on which the image K, the pixel R, and the pixel G are formed, heat treatment is performed in the same process as the formation of the black (K) image. Pixel B was formed, and the target color filter A was obtained.
The film thickness of the photosensitive resin layer B1 and the coating amount of pigments (CIPB15: 6 and CIPVV23) are shown below.
Photosensitive resin film thickness (μm) 1.60
Pigment application amount (g / m ² ) 0.75
C. I. P. B. 15: 6 coating amount (g / m ² ) 0.45
C. I. P. V. 23 coating amount (g / m ² ) 0.30

[Table 5]
--------------------------------
Composition component Content (parts by mass)
--------------------------------
B pigment dispersion 1 (C.I.P.B.15: 6) 15.0
V Pigment Dispersion Composition 1 (C.I.P.V.23) 7.5
Propylene glycol monomethyl ether acetate 28
Methyl ethyl ketone 26
Binder 3 17
DPHA solution 4.0
Polymerization initiator B 0.17
Phenothiazine 0.02
Surfactant 1 0.06
--------------------------------
Here, the preparation of the colored photosensitive resin compositions K1, R1, G1, and B1 described in Tables 2 to 5 will be described in more detail.
The colored photosensitive resin composition K1 is first weighed in K pigment dispersion 1 and propylene glycol monomethyl ether acetate in the amounts shown in Table 2, mixed at a temperature of 24 ° C. (± 2 ° C.), and stirred at 150 rpm for 10 minutes. Then, methyl ethyl ketone, binder 2, hydroquinone monomethyl ether, DPHA solution, polymerization initiator (2,4-bis (trichloromethyl) -6- [4 '-(N, N-bisethoxycarbonyl) in the amounts shown in Table 2 Methyl) amino-3′-bromophenyl] -s-triazine) and surfactant 1 are weighed out and added in this order at a temperature of 25 ° C. (± 2 ° C.) and at a temperature of 40 ° C. (± 2 ° C.) at 150 rpm. Obtained by stirring for 30 minutes.
In addition, the composition was shown below about the following component among the compositions of Table 2.
<K pigment dispersion 1>
・ Carbon black (trade name: Nipex 35, manufactured by Degussa Japan Co., Ltd.)
13.1 parts by mass / pigment dispersant A (the following compound C-1 synthesized according to JP 2000-239554 A) 0.65 parts by mass (refer to JP 2000-239554 A)
・ Polymer (benzyl methacrylate / methacrylic acid = 72/28 molar ratio
Random copolymer of, molecular weight 37,000) 6.72 parts by mass / propylene glycol monomethyl ether acetate 79.53 parts by mass <Surfactant 1>
(Megafuck F-780-F (Dainippon Ink Chemical Co., Ltd.))
_{· C 6 F 13 CH 2 CH} 2 OCOCH = CH 2: 40 parts by weight and _{H (OCH (CH 3) CH} 2) 7 OCOCH = CH 2: 55 parts by mass of _{H (OCH 2 CH 2) 7} OCOCH = CH 2 : Copolymer with 5 parts by mass (molecular weight 30,000)
30 parts by mass <Binder 2>
・ Polymer (benzyl methacrylate / methacrylic acid = 78/22 molar ratio
Random copolymer of, molecular weight 38,000) 27 parts by mass / propylene glycol monomethyl ether acetate 73 parts by mass <DPHA solution>
Dipentaerythritol hexaacrylate (containing polymerization inhibitor MEHQ 500 ppm, manufactured by Nippon Kayaku Co., Ltd., trade name: KAYARAD DPHA) 76 parts by mass Propylene glycol monomethyl ether acetate 24 parts by mass The colored photosensitive resin composition R1 is: First, Pigment Dispersion 1, R Pigment Dispersion 2, and Propylene Glycol Monomethyl Ether Acetate in the amounts shown in Table 3 are weighed, mixed at a temperature of 24 ° C. (± 2 ° C.) and stirred at 150 rpm for 10 minutes, 3, methyl ethyl ketone, binder 1, DPHA solution, 2-trichloromethyl-5- (p-styrylstyryl) -1,3,4-oxadiazole, 2,4-bis (trichloromethyl) -6- [4 ′-(N, N-bisethoxycarbonylmethyl) amino-3′-bromopheny ] -S-triazine and phenothiazine were weighed out, added in this order at a temperature of 24 ° C. (± 2 ° C.), stirred at 150 rpm for 30 minutes, and then the surfactant 1 in the amount shown in Table 3 was weighed out, It was obtained by adding at 24 ° C. (± 2 ° C.), stirring at 30 rpm for 5 minutes, and filtering through nylon mesh # 200.
In addition, among the compositions described in Table 3, the pigment dispersions 1 and 2 were prepared using the method described in Example 1 of International Publication No. WO2006 / 121016 pamphlet so that the composition became the following parts by mass. Each was prepared.

<R pigment dispersion 1>
C. I. P. R. 254 (Product name: Irgaphor Red BT-CF Ciba Specialty Chemicals Co., Ltd.)
10 parts by mass-pigment dispersant A 1 part by mass-polymer (benzyl methacrylate / methacrylic acid = 72/28 molar ratio
Random copolymer, molecular weight 30,000)
10 parts by mass-79 parts by mass of propylene glycol monomethyl ether acetate-polymer (benzyl methacrylate / methacrylic acid = 72/28 molar ratio
Random copolymer, molecular weight 30,000)
15 parts by mass ・ Propylene glycol monomethyl ether acetate 62.5 parts by mass

＜バインダー１＞
・ポリマー（ベンジルメタクリレート／メタクリル酸／メチルメタクリレート
＝３８／２５／３７モル比のランダム共重合物、分子量４万）２７質量部
・プロピレングリコールモノメチルエーテルアセテート ７３質量部

<Binder 1>
-27 parts by mass of polymer (benzyl methacrylate / methacrylic acid / methyl methacrylate = random copolymer of 38/25/37 molar ratio, molecular weight 40,000)-73 parts by mass of propylene glycol monomethyl ether acetate

<R pigment dispersion 2>
・ C. I. P. R. 177 (trade name: Chromophthal Red A2B, manufactured by Ciba Specialty Chemicals Co., Ltd.) 22.5 parts by mass / polymer (benzyl methacrylate / methacrylic acid = 72/28 molar ratio)
Random copolymer, molecular weight 30,000)
15 parts by mass ・ Propylene glycol monomethyl ether acetate 62.5 parts by mass

The colored photosensitive resin composition G1 was first weighed in the amounts of G pigment dispersion 1, Y pigment dispersion 1, and propylene glycol monomethyl ether acetate in the amounts shown in Table 3, and mixed at a temperature of 24 ° C. (± 2 ° C.). Stir at 150 rpm for 10 minutes, then methyl ethyl ketone, cyclohexanone, binder 2, DPHA solution, 2-trichloromethyl-5- (p-styrylstyryl) -1,3,4-oxadiazole in the amounts listed in Table 3. 2,4-bis (trichloromethyl) -6- [4 ′-(N, N-bisethoxycarbonylmethyl) amino-3′-bromophenyl] -s-triazine and phenothiazine were weighed out and the temperature was 24 ° C. (± 2 ° C) in this order and stirred at 150 rpm for 30 minutes. Further, the amount of surfactant 1 shown in Table 3 was weighed, and the temperature was 24 ° C (± 2 ° C). Was added and stirred for 5 minutes at 30 rpm, it was obtained by filtering with a nylon mesh # 200.
In addition, among the compositions described in Table 6, “trade name: GT-2” manufactured by FUJIFILM Electronics Materials Co., Ltd. was used as the G pigment dispersion 1. As the Y pigment dispersion 1, “trade name: CF erotic-EX3393” manufactured by Mikuni Dye Co., Ltd. was used.
The colored photosensitive resin composition B1 is first weighed in the amounts of B pigment dispersion 1, B pigment dispersion 2, and propylene glycol monomethyl ether acetate shown in Table 5 and mixed at a temperature of 24 ° C. (± 2 ° C.). Stirred at 150 rpm for 10 minutes, then methyl ethyl ketone, binder 3, DPHA solution, 2-trichloromethyl-5- (p-styrylstyryl) -1,3,4-oxadiazole in the amounts listed in Table 2-5, The phenothiazine was weighed out and added in this order at a temperature of 25 ° C. (± 2 ° C.), stirred at a temperature of 40 ° C. (± 2 ° C.) at 150 rpm for 30 minutes, and the surfactants in the amounts shown in Table 2-5 1 was weighed out, added at a temperature of 24 ° C. (± 2 ° C.), stirred at 30 rpm for 5 minutes, and filtered through nylon mesh # 200.
Of the compositions shown in Table 5, “Brand Name: CF Bull-EX3357” manufactured by Mikuni Color Co., Ltd. was used as the B pigment dispersion 1. As the pigment dispersion composition 1, the pigment dispersion composition A described above was used.
The composition of the binder 3 is as follows.
<Binder 3>
・ Polymer (Random copolymer of benzyl methacrylate / methacrylic acid / methyl methacrylate = 36/22/42 molar ratio, molecular weight 37,000) 27 parts by mass Propylene glycol monomethyl ether acetate 73 parts by mass

The color filter A was produced as described above. Color filters B to E were prepared in the same manner as color filter A, except that pigment dispersion composition A used as V pigment dispersion composition 1 in color filter A was replaced with B to E, respectively.
Table 6 shows the results of measuring the contrast in the same manner as the contrast measurement for each color filter.

[Table 6]
------------------------
Contrast Remarks ------------------------
Color filter A 14300 Invention color filter B 14900 Invention color filter C 15000 Invention color filter D 15800 Invention color filter E 9200 Comparative example ------------------- ------
From the above results, the color filters of the present invention were all good color filters with high contrast.

<Example 3>
A liquid crystal display device was prepared using the color filters A to E, and the display characteristics were evaluated.
(Formation of ITO electrode)
The glass substrate on which the color filter is formed is put into a sputtering apparatus, and 1300 mm thick ITO (Indium Tin Oxide) is vacuum-deposited on the entire surface at 100 ° C., and then annealed at 240 ° C. for 90 minutes to crystallize the ITO and make the ITO transparent An electrode was formed.
(Spacer formation)
A spacer was formed on the ITO transparent electrode produced above by the same method as the spacer forming method described in [Example 1] of JP-A-2004-240335.
(Formation of liquid crystal alignment control protrusions)
A liquid crystal alignment control protrusion was formed on the ITO transparent electrode on which the spacer was formed, using the following positive photosensitive resin layer coating solution.
However, the following methods were used for exposure, development, and baking.
A proximity exposure machine (manufactured by Hitachi High-Tech Electronics Engineering Co., Ltd.) is arranged so that the predetermined photomask is at a distance of 100 μm from the surface of the photosensitive resin layer, and the irradiation energy is 150 mJ / Proximity exposure was performed at cm ² .
Subsequently, a 2.38% tetramethylammonium hydroxide aqueous solution was developed by spraying it on a substrate at 33 ° C. for 30 seconds in a shower type developing device. In this way, by removing the unnecessary portion (exposed portion) of the photosensitive resin layer by developing and removing the liquid crystal, the liquid crystal alignment control protrusions made of the photosensitive resin layer patterned into a desired shape are formed on the color filter side substrate. A display device substrate was obtained.
Next, the liquid crystal display device substrate on which the liquid crystal alignment control protrusions were formed was baked at 230 ° C. for 30 minutes to form cured liquid crystal alignment control protrusions on the liquid crystal display device substrate.
<Positive photosensitive resin layer coating solution formulation>
・ Positive resist solution (FH-2413F manufactured by FUJIFILM Electronics Materials Co., Ltd.): 53.3 parts by mass ・ Methyl ethyl ketone: 46.7 parts by mass ・ Megafac F-780F (Dainippon Ink Chemical Co., Ltd.) Made)
: 0.04 part by mass An alignment film made of polyimide was further provided on the liquid crystal display device substrate obtained above.
After that, an epoxy resin sealant is printed at a position corresponding to a black matrix outer frame provided around the pixel group of the color filter, and MVA mode liquid crystal is dropped and bonded to the counter substrate. The bonded substrate was heat treated to cure the sealant. A polarizing plate HLC2-2518 manufactured by Sanritsu Co., Ltd. was attached to both surfaces of the liquid crystal cell thus obtained. Next, a backlight of a three-wavelength cold-cathode tube light source (FWL18EX-N manufactured by Toshiba Lighting & Technology Co., Ltd.) was constructed and placed on the back side of the liquid crystal cell provided with the polarizing plate to obtain a liquid crystal display device. .
It was confirmed that the liquid crystal display device using the color filter of the present invention was excellent in blackness and blue descriptive power and showed good display characteristics as compared with the liquid crystal display device using the color filter of the comparative example.

Claims (11)

A basic dispersion aid represented by the following general formula (1).

(In the formula, A represents a heterocyclic group bonded to the linking group by a nitrogen atom. X represents a divalent linking group having at least 2 to 20 carbon atoms. R ₁ and R ₂ are each independently hydrogen. Represents an atom, an alkyl group, an aralkyl group, or an aryl group, R ₁ and R ₂ may be linked to each other, and may further form a heterocyclic ring containing an oxygen atom, a nitrogen atom, and / or a sulfur atom; M represents a natural number of 1 or 2.) The basic dispersion aid is represented by the following general formula (2).

(In the formula, A represents a heterocyclic group bonded to the linking group by a nitrogen atom. Y represents an oxygen atom or a sulfur atom. L represents an integer of 0 or 1. n represents a natural number of 1 to 19.) R ₁ and R ₂ each independently represent a hydrogen atom, an alkyl group, an aralkyl group, or an aryl group, R ₁ and R ₂ may be linked to each other, and further an oxygen atom, a nitrogen atom, and / or sulfur A heterocyclic ring containing an atom may be formed, and m represents a natural number of 1 or 2.)   The basic dispersion aid according to claim 1 or 2, which imparts dispersibility to the organic pigment nanoparticles together with the non-aqueous dispersant in a non-aqueous dispersion obtained by switching the medium from the aqueous dispersion. .   An aqueous dispersion comprising organic pigment nanoparticles, water, and the basic dispersion aid according to any one of claims 1 to 3, wherein the organic pigment nanoparticles dissolve the organic pigment in a good solvent. The organic pigment solution is mixed with the good solvent and mixed with a poor solvent for the organic pigment, and the organic pigment is precipitated in the mixture as nanometer-sized fine particles in the presence of the basic dispersion aid. An aqueous dispersion of organic pigment nanoparticles, characterized in that   5. The aqueous dispersion of organic pigment nanoparticles according to claim 4, wherein the average particle diameter of primary particles of the organic pigment nanoparticles is 10 to 500 nm.   An aggregate of organic pigment nanoparticles in which the pH of the aqueous dispersion according to claim 4 or 5 is changed so that the organic pigment nanoparticles are in an aggregated state capable of being redispersed.   A non-aqueous dispersion of organic pigment nanoparticles in which the agglomerates of claim 6 have been agglomerated and redispersed in a non-aqueous medium.   The non-aqueous dispersion of organic pigment nanoparticles according to claim 7, comprising at least one polymer compound having an acidic group and having a number average molecular weight of 1000 or more.   A colored photosensitive resin composition comprising at least the non-aqueous dispersion according to claim 7, a binder, a monomer or an oligomer, and a photopolymerization initiator or a photopolymerization initiator system.   A color filter produced using the colored photosensitive resin composition according to claim 9.   A liquid crystal display device comprising the color filter according to claim 10.