JP5620115B2 - Pigment fine particle dispersion, photocurable composition and color filter using the same, and novel compound used therefor - Google Patents

Description

  The present invention relates to a pigment fine particle dispersion particularly suitable for use as a color material such as a color filter, a photocurable composition and a color filter using the same, and a novel compound used therefor.

  The color filter is required to have high performance and high quality, and attempts have been made to improve the organic pigment used in its production. Specifically, there are demands for a pigment dispersion having excellent storage stability and a color filter coloring pixel portion using the coating film having excellent contrast. In order to respond to such needs, for example, researches to reduce the size of pigment particles to a range of 10 to 100 nm and to stabilize the dispersion are underway. As a result, there is a possibility that a new characteristic that could not be predicted in the past can be effectively drawn out by taking advantage of the effect that is manifested for the first time by the nanometer size. In addition to the above-described color filter applications, for example, paints, printing inks, electrophotographic toners, inkjet inks, and the like are being researched and developed. In particular, the above-described color filter and ink-jet ink are being worked on for higher performance using fine chemical technology, and the results are expected.

Here, regarding the method of dispersing the organic pigment, there are various milling methods (breakdown method) such as bead mill method and salt milling method, and liquid phase method. Patent Documents 1 and 2 disclose that pigment fine particles prepared by a breakdown method are used for ink or the like. Patent Document 1 specifically discloses a pigment derivative in which a group having a triazine residue is introduced into a pigment molecule, and this is applied to a dispersion of breakdown pigment particles to improve viscosity reduction and ink gloss. Propose to do. Patent Document 2 proposes to improve the lightness of red ink by using a pigment derivative having a sulfonic acid group introduced into the pigment molecule.
On the other hand, the liquid phase method is suitable for obtaining fine pigment particles. Specifically, a pigment solution obtained by dissolving a pigment in a good solvent (first solvent) and a poor solvent (second solvent) are mixed to form nano particles. There is a reprecipitation method in which particles are deposited. Recently, it has been proposed to add a predetermined polymer compound or the like as a dispersant to the dispersion obtained by the reprecipitation method (see Patent Documents 3 to 6).

JP 2007-186681 A JP 2000-160084 A International Publication No. WO2006 / 121016 Pamphlet JP 2004-43776 A JP 2007-119586 A JP 2007-23169 A

  An object of the present invention is to provide a pigment fine particle dispersion in which the types of pigment derivatives coexisting with the pigment fine particles are enriched. Another object of the present invention is to provide a pigment fine particle dispersion particularly suitable as a color material for a color filter because the particle size of the pigment fine particles is small, the particle size distribution peak is sharp, and good dispersibility is exhibited. Furthermore, a pigment fine particle dispersion and a photocurable composition that can exhibit practically sufficient contrast and heat resistance when forming a pixel of a color filter, a color filter using the same, and a novel compound used therefor The purpose is to provide.

（式中、Ｑはジケトピロロピロール顔料化合物の残基を表す。Ｒ^１及びＲ^２はそれぞれ独立に水素原子またはアルキル基を表す。ｎは１〜４の整数を表す。Ｐは下記一般式（Ｐ−１）、（Ｐ−２）、（Ｐ−４）、および（Ｐ−５）のいずれかで表される基を表す。）

（式中、Ｒ^３〜Ｒ ^６ 及びＲ ^１０ 〜Ｒ^１７は、各々独立に、水素原子、ハロゲン原子、又は置換基を有してもよいアルキル基、アリール基、もしくはヘテロアリール基、あるいは−Ａ^１−Ｚで表される基である。Ｒ^３及びＲ^４は互いに結合することはない。Ａ^１は単結合又は２価の有機連結基を表す。ＺはＳＯ_３Ｈ又はＣＯ_２Ｈで示される酸性基を表す。Ｚが酸性基である場合、塩を形成していてもよい。＊はＱ−Ｃ（Ｒ^１）（Ｒ^２）−に結合する位置を示す。）
（２）前記顔料微粒子が、該顔料および前記一般式（１）で表される化合物を良溶媒に溶解させた溶解液を、該良溶媒に対して貧溶媒となる媒体と混合して生成させたものであることを特徴とする（１）記載の顔料微粒子分散体。
（３）前記一般式（１）で表される化合物の含有量が、前記顔料１００質量部に対して、１〜１００質量部であることを特徴とする（１）又は（２）に記載の顔料微粒子分散体。
（４）前記顔料微粒子を構成する顔料がジケトピロロピロール顔料、キナクリドン顔料、及びアントラキノン顔料からなる群から選ばれた少なくとも１種であることを特徴とする（１）〜（３）のいずれか１項に記載の顔料微粒子分散体。
（５）さらにポリカプロラクトン構造を有する分散剤を含有することを特徴とする（１）〜（４）のいずれか１項に記載の顔料微粒子分散体。
（６）前記分散剤の使用量が、前記顔料１００質量部に対して、１０〜４００質量部である（５）に記載の顔料微粒子分散体。
（７）前記分散剤の分子量が１，０００〜２，０００，０００である（５）または（６）に記載の顔料微粒子分散体。
（８）前記顔料の微粒子の平均粒径が１００ｎｍ以下である（１）〜（７）のいずれか１項に記載の顔料微粒子分散体。
（９）カラーフィルタ用色材である（１）〜（８）のいずれか１項に記載の顔料微粒子分散体。
（１０）（１）〜（９）のいずれか１項に記載の分散体の成分と重合性化合物とを含有する光硬化性組成物。
（１１）（１０）に記載の光硬化性組成物を硬化させて形成した画素を有してなるカラーフィルタ。
（１２）下記一般式（１）で表される化合物。

（式中、Ｑはジケトピロロピロール顔料化合物の残基を表す。Ｒ^１及びＲ^２はそれぞれ独立に水素原子、またはアルキル基を表す。ｎは１〜４の整数を表す。Ｐは下記一般式（Ｐ−１）、（Ｐ−２）、（Ｐ−４）、および（Ｐ−５）のいずれかで表される基を表す。）

（式中、Ｒ^３〜Ｒ ^６ 及びＲ ^１０ 〜Ｒ^１７は、各々独立に、水素原子、ハロゲン原子、又は置換基を有してもよいアルキル基、アリール基、もしくはヘテロアリール基、あるいは−Ａ^１−Ｚで表される基である。Ｒ^３及びＲ^４は互いに結合することはない。Ａ^１は単結合又は２価の有機連結基を表す。ＺはＳＯ_３Ｈ又はＣＯ_２Ｈで示される酸性基を表す。Ｚが酸性基である場合、塩を形成していてもよい。＊はＱ−Ｃ（Ｒ^１）（Ｒ^２）−に結合する位置を示す。）
The above problems have been solved by the following means.
(1) A pigment fine particle dispersion comprising pigment fine particles and a compound represented by the following general formula (1):

(In the formula, Q represents a residue of a diketopyrrolopyrrole pigment compound. R ¹ and R ² each independently represents a hydrogen atom or an alkyl group. N represents an integer of 1 to 4. P represents the following general formula. (P-1) represents a group represented by any one of (P-2), (P-4), and (P-5) .)

(In the formula, R ³ to R ⁶ and R ¹⁰ to R ¹⁷ are each independently a hydrogen atom, a halogen atom, or an alkyl group, aryl group, or heteroaryl group which may have a substituent, or -A. ¹ is a group represented by ^1- Z, R ³ and R ⁴ are not bonded to each other, A ¹ is a single bond or a divalent organic linking group, and Z is represented by SO ₃ H or CO ₂ H. When Z is an acidic group, it may form a salt. * Indicates a position bonded to QC (R ¹ ) (R ² )-)
(2) The pigment fine particles are formed by mixing a solution in which the pigment and the compound represented by the general formula (1) are dissolved in a good solvent with a medium that is a poor solvent for the good solvent. (1) The pigment fine particle dispersion described in (1) above.
(3) The content of the compound represented by the general formula (1) is 1 to 100 parts by mass with respect to 100 parts by mass of the pigment, as described in (1) or (2) Pigment fine particle dispersion.
(4) The pigment constituting the pigment fine particles is at least one selected from the group consisting of a diketopyrrolopyrrole pigment, a quinacridone pigment, and an anthraquinone pigment, any one of (1) to (3) 2. The pigment fine particle dispersion according to item 1.
(5) The pigment fine particle dispersion according to any one of (1) to (4), further comprising a dispersant having a polycaprolactone structure.
(6) The pigment fine particle dispersion according to (5) , wherein the amount of the dispersant used is 10 to 400 parts by mass with respect to 100 parts by mass of the pigment.
(7) The pigment fine particle dispersion according to (5) or (6), wherein the dispersant has a molecular weight of 1,000 to 2,000,000.
(8) The pigment fine particle dispersion according to any one of (1) to (7), wherein an average particle size of the fine particles of the pigment is 100 nm or less.
( 9 ) The pigment fine particle dispersion according to any one of (1) to ( 8 ) , which is a color material for a color filter.
(10) (1) to component a polymerizable compound and a photocurable composition comprising a dispersion according to any one of (9).
( 11 ) A color filter having pixels formed by curing the photocurable composition according to (10).
( 12 ) A compound represented by the following general formula (1).

(In the formula, Q represents a residue of a diketopyrrolopyrrole pigment compound. R ¹ and R ² each independently represents a hydrogen atom or an alkyl group. N represents an integer of 1 to 4. P represents the following general formula. Represents a group represented by any one of formulas (P-1), (P-2), (P-4), and (P-5) .

(In the formula, R ³ to R ⁶ and R ¹⁰ to R ¹⁷ are each independently a hydrogen atom, a halogen atom, or an alkyl group, aryl group, or heteroaryl group which may have a substituent, or -A. ¹ is a group represented by ^1- Z, R ³ and R ⁴ are not bonded to each other, A ¹ is a single bond or a divalent organic linking group, and Z is represented by SO ₃ H or CO ₂ H. When Z is an acidic group, it may form a salt. * Indicates a position bonded to QC (R ¹ ) (R ² )-)

According to the present invention, there is provided a pigment fine particle dispersion enriched in the types of pigment derivatives that coexist with the pigment fine particles. The pigment fine particle dispersion of the present invention is particularly suitable as a color material for a color filter because the particle size of the pigment fine particles contained therein is small, the particle size distribution peak is sharp, and it exhibits good dispersibility. Yes. Furthermore, the pigment fine particle dispersion and the photocurable composition of the present invention exhibit an excellent effect of exhibiting practically sufficient contrast and heat resistance when forming a pixel of a color filter.
In addition, the compound represented by the general formula (1) of the present invention is useful as a crystal growth inhibitor of a pigment compound or a dispersion aid in a pigment dispersion.

  The pigment fine particle dispersion of the present invention contains pigment fine particles and a compound represented by the general formula (1). According to such a preferred embodiment of the present invention, since the compound represented by the general formula (1) has a specific pigment mother nucleus structure, the mother nucleus strongly adsorbs to the pigment molecule by a strong interaction. Further, since the compound of the present invention has a specific heterocyclic group in the molecule, it is considered that the interaction between the pigment nuclei can be shielded by its high intermolecular force, and the ability to suppress aggregation and association of pigment particles is high. . As a result, for example, when the dispersion is used as a color filter, it is possible to achieve practically sufficient contrast and high heat resistance that can meet the high image reproducibility recently required. Further, although there are unclear points about the mechanism of action, the compound represented by the above general formula (1) is a specific surface state of the build-up fine particles obtained by the reprecipitation method that cannot be obtained by crushing. It acts suitably, and the above effect is exhibited at a higher level by combining these.

[Compound represented by general formula (1)]
The pigment fine particle dispersion of the present invention contains pigment fine particles and a compound represented by the following general formula (1).

Ｑはジケトピロロピロール顔料化合物の残基を表す。

Q represents a residue of a diketopyrrolopyrrole pigment compound .

R ¹ and R ² each independently represents a hydrogen atom or an alkyl group. The alkyl groups for R ¹ and R ² each independently preferably have 1 to 5 carbon atoms, and examples include methylene, ethylene, propylene, isopropylene, butylene, and isobutylene. R ¹ and R ² are preferably both hydrogen atoms.

n represents an integer of 1 to 4, and 1 or 2 is preferable in that the coloring power of the organic dye is maintained.

P represents a group represented by any one of the following general formulas (P-1), (P-2), (P-4), and (P-5) . Formula (P-3) is a reference example.

＊はＱ−Ｃ（Ｒ^１）（Ｒ^２）−に結合する位置を示す。

* Shows the position couple | bonded with QC (R < ¹ >) (R < ² >)-.

R ^{3 to} R ¹⁷ are each independently a hydrogen atom, a halogen atom, or an optionally substituted alkyl group, aryl group, or heteroaryl group, or a group represented by -A ¹ -Z. . R ³ and ^{R 4} which bind to each other have greens. A ¹ represents a single bond or a divalent organic linking group. Z represents an acidic group represented by SO ₃ H or CO ₂ H. When Z is an acidic group, a salt may be formed.

○ About R ^{3 to} R ¹⁷ • Alkyl group: C 1-10 is preferable, and methylene, ethylene, propylene, isopropylene, butylene, isobutylene and the like can be mentioned.
-Aryl group: a phenyl group, a naphthyl group, and an anthracenyl group.
Heteroaryl group: an aryl group having a nitrogen atom, oxygen atom or sulfur atom, and examples include aryl thiazole, aryl oxazole and aryl imidazole groups.
-Substituents that may be present: As optional substituents, alkyl groups, alkoxy groups, methoxy groups, alkoxycarbonyl groups, amide groups, halogen atoms (fluorine atoms, chlorine atoms, bromine atoms, iodine atoms), or cyano Groups and the like. Among these, a methyl group, a methoxy group, or unsubstituted (hydrogen) is preferable.
R ^{1 to} R ¹³ are preferably a hydrogen atom, a methyl group, an ethyl group, a phenyl group, a naphthyl group, -A ¹ -COOH, or -A ¹ -SO ₃ H.
A divalent linking group represented by A ¹ is preferably a substituted or unsubstituted alkylene group or a divalent organic linking group composed of the alkylene group and a hetero atom or a partial structure containing a hetero atom. Here, as an alkylene group, a C1-C10 alkylene group is preferable. Examples of the hetero atom in the partial structure containing a hetero atom include an oxygen atom, a nitrogen atom, and a sulfur atom, and among them, an oxygen atom and a nitrogen atom are preferable. When the alkylene group has a substituent, examples of the substituent include a hydroxy group and a halogen atom. The divalent organic linking group includes a heteroatom or a heteroatom selected from —C (═O) —, —OC (═O) —, and —NHC (═O) — at the end of the above alkylene group. A compound having a partial structure and linked to an adjacent oxygen atom via the heteroatom or a partial structure containing a heteroatom is preferable from the viewpoint of adsorptivity to the pigment. A ¹ is preferably a single bond or a phenyl group.
· Z represents an acidic group represented by SO ₃ H or CO ₂ H. Z is preferably SO ₃ H.
· ^R 3 ^{to R 17} are, in the case of the group represented by ^-A 1 -Z is preferably used in the step of dispersing the pigment. Further, when it is made to coexist with a basic dispersion resin, the dispersion stability is improved.

  The compound represented by the general formula (1) exhibits an adsorptivity with the pigment due to the unique interaction as described above, and when the basic dispersion resin described later is used, it is strongly adsorbed to the pigment molecule. It is considered to play a role. From this viewpoint, in the present invention, it is preferable to use a basic dispersion resin in combination. As described above, the compound represented by the general formula (1) is preferably used as a pigment synergist (dispersant, dispersion aid, crystal growth inhibitor, etc.), and is mainly used in combination with a dispersant as described above. It is preferable to be used as a dispersion resin used.

A compound constituting a group represented by any one of the general formulas (P-1), (P-2), (P-4), and (P-5) that forms the compound represented by the general formula (1) Examples of the compound (the compound introduced at the N-position to become the group) include the following general formulas (p-1), (p-2), (p-4), (p-4 ′), and (p- 5 ). It is preferable to synthesize | combine using the compound represented by either (Hereinafter, these compounds may be named generically and may be called a compound represented by general formula (p).). Formula (p-3) is a reference example.

Specific preferred examples of the compound represented by formula (p) below, the present invention is not to be construed as being limited thereto. However, Formula a1-5 is a reference example.

○ Compound represented by formula (p-1)

○ Compound represented by formula (p-2)

○ Compound represented by formula (p-3)

○ Compounds represented by general formula (p-4) (p-4 ')

○ Compound represented by formula (p-5)

  In the pigment fine particle dispersion of the present invention, the content of the compound represented by the general formula (1) is not particularly limited, but is preferably 1 to 100 parts by mass with respect to 100 parts by mass of the pigment, and 10 to 50 More preferably, it is part by mass. By setting it to the above lower limit value or more, it is possible to stably disperse fine pigment particles having a large surface area, and by setting the upper limit value or less, it is possible to prevent a decrease in color value due to excessive addition of a pigment derivative. In the present invention, two or more compounds represented by the above general formula (1) may be used.

Although the specific example of a compound represented by General formula (1) below is shown, this invention is limited to this and is not interpreted. N in the formula represents an integer of 1 to 4, and m represents an integer of 0 to 2. However, Formula b-12 and b-21 to b-28 are reference examples.

A general synthesis method is a method (A) in which a compound represented by the general formula (p), an aldehyde compound or a ketone compound, and an organic dye compound are reacted in a solvent. The other is a method (B) in which an organic dye compound is reacted in a solvent with respect to a compound obtained by reacting the compound represented by the general formula (p) with an aldehyde compound or a ketone compound.
Examples of reacting the phthalimide compound instead of the compound represented by the general formula (p) include the methods described in JP-B-7-110923 and JP-A-2009-57477. The pigment derivative compound of the present invention can be synthesized in the same manner except that the phthalimide compound disclosed herein is changed to the compound represented by the general formula (p). Specifically, after the organic dye compound is stirred with a sulfuric acid solvent, the compound represented by the general formula (p) is reacted with paraformaldehyde, and the compound represented by the general formula (p) is allowed to act on paraformaldehyde. A method of synthesizing an N-hydroxymethyl derivative and reacting it with an organic dye compound in a sulfuric acid solvent. Specific reaction examples are shown in the Examples section below.

  The compound represented by the general formula (1) may be added to the dispersion of pigment fine particles at any stage, and may be added to a good solvent or a poor solvent in the reprecipitation method described below, Alternatively, it may be added after the precipitation of pigment fine particles or after concentration or redispersion. In the present invention, considering a non-aqueous dispersion for a color filter, a dispersant suitable as a photocurable composition for a color filter when the dispersion is concentrated or powdered and then redispersed. In addition, it is preferable to add as a dispersion aid.

  In the notation of a group in the present specification, the notation that does not indicate substitution and non-substitution is meant to include not only a substituent but also a substituent. For example, the expression “alkyl group” includes not only an alkyl group having no substituent (unsubstituted alkyl group) but also an alkyl group having a substituent (substituted alkyl group).

[Organic pigments]
The pigment fine particle dispersion of the present invention contains fine particles of a pigment (hereinafter sometimes referred to as “Pigment A”) together with the compound represented by the general formula (1).
Pigment A is an organic pigment and is not limited in hue. For example, perylene pigment, perinone pigment, quinacridone pigment, quinacridonequinone pigment, anthraquinone pigment, anthanthrone pigment, benzimidazolone pigment, disazo condensation pigment, Disazo pigment, azo pigment, indanthrone pigment, phthalocyanine pigment, triarylcarbonium pigment, dioxazine pigment, aminoanthraquinone pigment, diketopyrrolopyrrole pigment, thioindigo pigment, isoindoline pigment, isoindolinone pigment, pyranthrone pigment, or isoviola Nthrone pigment, or a mixture thereof. Among these, quinacridone pigments, anthraquinone pigments, benzimidazolone pigments, phthalocyanine pigments, azo pigments and dioxazine pigments are preferable, and diketopyrrolopyrrole pigments are more preferable.
In the present invention, the above organic pigments or solid solutions of organic pigments may be used in combination. Alternatively, a composite material combined with other compounds may be used.

  The pigment A may be the same or different from the pigment B, and is preferably structurally similar. The pigment A and the pigment B are the same. It is preferable to use it. Even if the pigment A and the pigment B are different, the pigment fine particle dispersion of the present invention can achieve both desired color purity and high contrast as a color material for a color filter, but is structurally similar. In addition, it is preferable to use the same one because color adjustment is easy.

  In the pigment fine particle dispersion of the present invention, the content of the pigment fine particles is not particularly limited. However, when considering the use as a color material for a color filter, the concentration contained in the pigment fine particle dispersion is 1 to 40% by mass. It is preferable that it is 5-20 mass%.

[Crushing method]
The pigment fine particles used in the present invention may be pigment fine particles prepared by a breakdown method such as a pulverization method. In that case, it can obtain by mixing various solvents, resin, varnish etc. if necessary, and disperse | distributing with a horizontal sand mill, a vertical sand mill, an annular bead mill, an attritor, etc. The specific polymer compound (specific polymer) and other pigment dispersants to be described later may be dispersed after mixing all components. First, the pigment and the specific polymer compound (specific polymer), etc. Alternatively, only the pigment or only the pigment and the pigment dispersant may be dispersed, and then another component may be added and dispersed again.
Also, before dispersing with a horizontal sand mill, vertical sand mill, annular bead mill, attritor, etc., pre-dispersion using a kneader mixer such as a kneader, 3-roll mill, solid dispersion with 2-roll mill, etc., or pigment A synergist having a basic group and / or a dispersant may be treated. Moreover, a disperser and a mixer such as a high speed mixer, a homomixer, a ball mill, a roll mill, a stone mill, and an ultrasonic disperser can be used.

[Reprecipitation method]
In the pigment fine particle dispersion of the present invention, the organic pigment particles to be contained therein include an organic pigment solution in which an organic material is dissolved in a good solvent (hereinafter sometimes referred to as a first solvent), and the good solvent. It is preferably produced by mixing with a solvent that is compatible with the organic pigment and that is a poor solvent (hereinafter sometimes referred to as a second solvent). Hereinafter, this method is sometimes referred to as “reprecipitation method”, and the resulting dispersion containing organic pigment particles is sometimes referred to as “pigment reprecipitation solution”. Further, the reprecipitation method in which the compound represented by the general formula (1) or the dispersant is co-dissolved in the organic pigment solution is distinguished from the reprecipitation method, particularly “coprecipitation method”. There are times.

○ Poor solvent First, the poor solvent for organic pigments will be explained. The poor solvent is not particularly limited as long as it is compatible with or uniformly mixed with a good solvent for dissolving the organic pigment. As a poor solvent, 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 a solubility in the presence of an acid or an alkali. In particular, in the case of a pigment species whose solubility changes remarkably depending on the hydrogen ion concentration (pH), an acid or an alkali may be appropriately mixed with a poor solvent and used. preferable.
The amount of the good solvent dissolved in the poor solvent is preferably 30% by mass or more, and more preferably 50% by mass or more. There is no particular upper limit to the amount of good solvent dissolved in the poor solvent, but it is practical to mix them in an arbitrary ratio.
Examples of the poor solvent include aqueous solvents (for example, water, hydrochloric acid, sodium hydroxide aqueous solution), alcohol compound solvents, ketone compound solvents, ether compound solvents, aromatic compound solvents, carbon disulfide solvents, aliphatic compound solvents, nitrile compounds. Solvents, halogen compound solvents, ester compound solvents, ionic liquids, mixed solvents thereof and the like are included, and aqueous solvents, alcohol compound solvents, ketone compound solvents, ether compound solvents, ester compound solvents, or a mixture thereof are preferable, and aqueous solvents A solvent, an alcohol compound solvent or an ester compound solvent is more preferred.
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, propylene glycol monomethyl ether acetate (MMPGAc), and the like. The ionic liquids, for example, 1-butyl-3-methylimidazolium and PF ₆ ^-, etc. and salts thereof.
The poor solvent may be used by mixing a plurality of solvents, and depending on the system, it may be used by mixing a good solvent. However, in this case, it is necessary to mix within a range that does not hinder the precipitation, refinement, and crystallization of the pigment particles.

○ Good solvent Next, the good solvent which dissolves the organic pigment will be described. The good solvent is not particularly limited as long as it can dissolve the pigment to be used and is compatible with or uniformly mixed with the poor solvent. The solubility of the organic pigment in the good solvent 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, it is practical that the solubility 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. A preferred range of solubility or compatibility between the poor solvent and the good solvent is as described above.
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 or a range of about 1/100 of this in the dissolving conditions. 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.

  In the present invention, the organic pigment can be dissolved in a good solvent 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.

  Bases used for alkaline dissolution are inorganic bases such as lithium hydroxide, sodium hydroxide, potassium hydroxide, calcium hydroxide, or barium hydroxide, or trialkylamine, diazabicycloundecene (DBU), An organic base such as a metal alkoxide is preferable, but an organic base is preferable. The amount of the base used is an amount capable of uniformly dissolving the pigment, and is not particularly limited. However, in the case of an inorganic base, it is preferably 1.0 to 30 molar equivalents, more preferably 1 with respect to the organic pigment. 0.0 to 25 molar equivalents, more preferably 1.0 to 20 molar equivalents. In the case of an organic base, it is preferably 1.0 to 100 molar equivalents, more preferably 1.0 to 50 molar equivalents, and still more preferably 1.0 to 20 molar equivalents relative to the organic pigment.

  The acid used for the acid dissolution is 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, but preferably It is an inorganic acid. Particularly preferred is sulfuric acid. The amount of the acid used is an amount capable of uniformly dissolving the organic pigment, and is not particularly limited, but is often used in an excessive amount as compared with the base. Regardless of the inorganic acid or organic acid, it is preferably 3 to 500 molar equivalents, more preferably 10 to 500 molar equivalents, and further preferably 30 to 200 molar equivalents with respect to the organic pigment.

  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.

○ Mixing conditions There are no particular restrictions on the use conditions of the poor solvent when preparing the organic particles, that is, when the organic particles are deposited and formed, 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.
The mixing ratio of the pigment solution and the poor solvent (ratio of good solvent / poor solvent in the reprecipitation liquid) is preferably 1/50 to 1/1, more preferably 1/40 to 1/1, and more preferably 1/10 to 10 in volume ratio. 1/1 is particularly preferred. This may be the same as or different from the volume flow ratio of the pigment solution and the poor solvent in the flow reactor. For example, when the mixing ratio is 1/2, the following method can be taken as a specific example.
(I) The volume flow ratio between the good solvent and the poor solvent is halved. (Ii) The solvent obtained by mixing the good solvent in advance with the ratio of (good solvent / poor solvent volume ratio) = (¼). Using A, the volume flow ratio of the pigment solution and the solvent A is set to 1/5. In this case, the amount obtained by adding the good solvent in the pigment solution and the good solvent in the solvent A is 1 + 1 = 2, while the amount of the poor solvent in the solvent A is 4. The mixing ratio is 1/2. The pigment concentration in the pigment reprecipitation liquid is not particularly limited as long as the pigment particles can be generated, but the pigment particles should be in the range of 10 to 40,000 mg per 1000 ml of the reprecipitation liquid. Is preferable, more preferably in the range of 20 to 30000 mg, and particularly preferably in the range of 40 to 25000 mg.

  In the present invention, it is preferable to rapidly mix the pigment solution and the poor solvent, and a means for promoting mixing is particularly preferable in this part. As one of the methods, mixing is promoted by turbulent mixing field, for example, a method of causing a high-speed fluid to flow in a counterflow state and colliding in a narrow space can be considered. However, the mixing mode is not limited to turbulent flow control. For example, as shown in Japanese Patent Laid-Open No. 2006-104448, fluids are brought into contact with each other in a laminar flow state at the intersection of Y-shaped flow paths. A method of mixing by molecular diffusion is also conceivable.

In the present invention, whether the fluid flow state is turbulent or laminar is determined by the tube Reynolds number. That is, the pipe representative length (referred to as a representative diameter in the present invention) is D [m], the linear flow velocity of the flowing liquid is u [m / s] (definition will be described later), and the density and viscosity of the liquid are ρ [kg], respectively. / M ³ ], η [Pa · s], the tube Reynolds number Re [−] is Re = Duρ / η
Defined by In the present invention, it is assumed that a state where Re is 1000 or more is turbulent flow, a state where 100 or more and less than 1000 is a transition region, and a state where Re is less than 100 is laminar flow.
The representative length D of the above equation is a physical property of the tube that has the most influence on the flow in the tube. In the case of a cylindrical tube, its diameter is defined. Otherwise, it is defined by the following equation.
D = 4A / p
Here, A [m ² ] is the cross-sectional area of the flow path, and p [m] is the length (immersion side length) of the portion where the fluid contacts the wall in the flow path.
Using this D, the aforementioned linear flow velocity u is defined as follows.
u = Q / {(D / 2) ² × π}
Here, Q is the volume flow rate [m ³ ] of the fluid flowing through the flow path that defines the linear flow velocity. The representative diameter when the diameter or cross-sectional shape is changed in the middle of the flow path depends on the cross-sectional shape after the change. The linear flow velocity and the Reynolds number may be obtained according to the representative diameter.
In the present invention, the flow state of the mixing field is important, but it is difficult to appropriately measure the state of the mixing field. Therefore, when both of the following two conditions are satisfied, the state of the mixing field is controlled by turbulent flow. Estimated.
(I) From the tube Reynolds number Re immediately before mixing of each fluid to be mixed, at least the flow state in one flow path connected to the mixing field is regarded as turbulent flow.
(Ii) From the tube Reynolds number Re immediately after mixing of the fluid after mixing, the flow state immediately after mixing is regarded as turbulent flow.

  In the above particle formation step, it is preferable to adjust the representative diameter, flow rate, etc. of the reactor so that the average particle diameter of the precipitated pigment particles falls within a desired range. In the reactor used in this embodiment, the flow rate of each flow path can be made relatively large, and the mixing state of the mixing field created at this time is considered suitable for pigment particle formation. The linear flow rates of the pigment solution and the poor solvent in each raw material supply channel of the reactor are preferably 1 to 30 m / s.

[Dispersant used for reprecipitation]
In the present invention, when the pigment is dissolved in a good solvent, both the pigment dispersant and the pigment derivative may be dissolved together. In the organic solvent, a polymer dispersant is preferably used as the dispersant from the viewpoint of ensuring dispersibility by a repulsive action utilizing the entropy repulsive force of the molecular chain. The particle surface can also be modified by using pigment derivatives, and in particular, the interaction force with other dispersants can be improved, or the solubility and crystal form of the particles can be controlled. Pigment derivatives are also preferably used.

  As a dispersant that can be used, for example, a low molecular or high molecular dispersant of anionic, cationic, amphoteric, nonionic or pigment derivative can be used. The molecular weight of the polymer dispersant can be used without limitation as long as it can be uniformly dissolved in a solution, but preferably has a molecular weight of 1,000 to 2,000,000, and 5,000 to 1,000,000. 000 is more preferable, 10,000 to 500,000 is more preferable, and 10,000 to 100,000 is particularly preferable. Examples of the polymer dispersant include those exemplified in the dispersants A and B described later.

  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. 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. These nonionic dispersants can be used alone or in combination of two or more.

  A pigment derivative type dispersant is derived from an organic pigment as a parent substance, and is obtained by a pigmentation reaction of a pigment derivative type dispersant produced by chemically modifying the parent structure or a chemically modified pigment precursor. Defined as a pigment derivative type dispersant. For example, a sugar-containing pigment derivative-type dispersant, a piperidyl-containing pigment derivative-type dispersant, a naphthalene or perylene-derived pigment derivative-type dispersant, a pigment derivative-type dispersant having a functional group linked to a pigment parent structure via a methylene group, Pigment parent structure chemically modified with polymer, pigment derivative type dispersant having sulfonic acid group, pigment derivative type dispersant having sulfonamide group, pigment derivative type dispersant having ether group, carboxylic acid group, carboxylic acid ester And pigment derivative type dispersants having a group or a carboxamide group.

[Pigment fine particles]
Regarding the particle size of fine particles, there is a method of expressing the average size of the population by quantifying by a measurement method, but it is often used that the mode diameter indicating the maximum value of the distribution, the median value of the integral distribution curve There are corresponding median diameters, 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 diameter. Say. The average particle size of the fine particles (primary particles) in the dispersion of the present invention is preferably 100 nm or less, more preferably 75 nm or less, and particularly preferably 50 nm or less. The fine particles in the dispersion of the present invention may be a single crystal, a polycrystal or an aggregate of that size, or may contain these.

  In the present invention, the ratio (Mv / Mn) of the volume average particle diameter (Mv) to the number average particle diameter (Mn) is used as an index representing the uniformity (monodispersity) of the particles, unless otherwise specified. The monodispersity of the organic nanoparticles (primary particles) of the present invention (in the present invention, monodispersity refers to the degree of uniform particle size), that is, Mv / Mn is 1.0 to 2.0. It is preferably 1.0 to 1.8, more preferably 1.0 to 1.5.

  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 based on the dynamic light scattering method include Nikkiso's Nanotrac UPA-EX150, Otsuka Electronics' dynamic light scattering photometer DLS-7000 series (both are trade names), and the like. In the present invention, the value relating to the particle diameter means a value measured by the method employed in the examples unless otherwise specified.

  The fine particles in the dispersion of the present invention preferably have a crystallinity of 65% or more in the dispersion medium, but this crystallinity is preferably 80 to 100%, and 90 to 100%. More preferably. The crystallite size of the fine particles in the dispersion of the present invention is not particularly limited, but is preferably 20 to 500 angstroms, and more preferably 20 to 200 angstroms. In the present invention, the crystallinity and crystallite diameter are values measured as follows unless otherwise specified.

(Evaluation of crystallinity)
As a typical index of crystallinity, the method of obtaining α crystallinity is that the peak intensity I _α and β-type crystal at 28 ± 0.5 °, which is a characteristic Bragg angle (2θ) of _α- type crystal. calculated by the following formula from the peak intensity I _beta characteristic 27 ° the Bragg angle (2 [Theta]) of.
(Α crystallinity) = (I _α ) / (I _α + I _β )
The peak intensity I _α of 28 ± 0.5 ° which is the characteristic Bragg angle (2θ) of the _α- type crystal and the peak intensity I _β of 27 ° which is the characteristic Bragg angle (2θ) of the β-type crystal are as follows: So ask. The background is removed from the diffraction pattern obtained by the X-ray diffraction measurement as follows. A straight line in contact with the vicinity of 23 ° on the low angle side and the vicinity of 30 ° on the high angle side of the Bragg angle of the α-type crystal was drawn, and this straight line was removed as a background. The peak intensities I _α and I _β are obtained from the diffraction pattern from which the background is removed, and the α crystallinity is calculated by the above formula.

(Measurement of crystallite diameter)
X-ray diffraction analysis using Cu-Kα1 line is performed. Thereafter, in the range of 2θ = 4 deg to 70 deg, the half width of the peak showing the maximum intensity or the peak showing a sufficiently large intensity that can be separated from the adjacent peak is measured. Calculate:
D = K × λ / (β × cos θ): Scherrer equation [D: crystallite diameter (Å, crystallite size), λ: measured X-ray wavelength (Å), β: diffraction line due to crystal size Spread (radian), θ: Bragg angle of diffraction line (radian), K: constant (differing between β and D constants)]
In general, it is known that K = 0.9 when a half width β1 / 2 is used for β. Also, since the wavelength of the Cu-Kα1 line is 1.54050 mm, the crystallite diameter D in the present invention is calculated based on the following formula:
D = 0.9 × 1.54050 / (β1 / 2 × cos θ)
Here, when the peak of the spectrum obtained by the measurement is broad and the half width of the peak cannot be determined, it is estimated that the crystallite diameter is less than 20 mm or is in an amorphous state (amorphous).

[Concentration and redispersion]
○ Concentration of dispersion The process of removing the solvent from the mixed liquid after the organic pigment fine particles are deposited is not particularly limited. For example, a method of filtering with a filter or the like, a method of precipitating and concentrating the organic pigment fine particles by centrifugation. Etc. As the filter filtration device, for example, a device such as reduced pressure or pressure filtration can be used. Examples of preferable filters include filter paper, nanofilters, and ultrafilters. Any device may be used as the centrifuge as long as the water-insoluble compound fine particles can be precipitated. For example, in addition to a general-purpose device, a device having a skimming function (a function of sucking a supernatant layer during rotation and discharging it out of the system), a continuous centrifuge that continuously discharges solid matter, and the like can be given. 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. In addition, as a solvent removal step, a method of concentrating the solvent by sublimation by vacuum freeze-drying, a method of drying and concentrating the solvent by heating or decompression, a method combining them, or the like can also be used.

Re-dispersion Organic pigment fine particles can be used, for example, in a dispersed state in a vehicle. The vehicle refers to a portion of a medium in which an organic pigment is dispersed when in a liquid state, and is a portion that is liquid and binds to the water-insoluble compound to harden a coating film (binder). And a component (organic solvent) for dissolving and diluting it. In the present invention, the polymer compound used for fine particle formation and / or the organic pigment dispersant used for redispersion are collectively referred to as a binder.

  The fine particle concentration of the dispersion of fine particles after redispersion is appropriately determined according to the purpose, but preferably the fine particles are 2 to 30% by mass, and 4 to 20% by mass with respect to the total amount of the dispersion. It is more preferable that the content is 5 to 15% by 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 water-insoluble compound, but the binder may be 1 to 30% by mass with respect to the total amount of the dispersion. 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%.

  The organic pigment fine particles can be re-dispersed in the same organic solvent used in the poor solvent liquid, and the organic pigment fine particles can be dispersed in the same organic solvent as the poor solvent without adding another dispersant. It is preferable that the aggregated state is spontaneously solved and dispersed in the medium, and this property is referred to as “can self-disperse” or “have self-dispersibility”. However, in order to further improve the redispersibility in the present invention, a pigment dispersant or the like may be added during redispersion of the fine particles. From this point of view, aggregates that are difficult to redisperse may be distinguished from soft agglomerates that can be redispersed or loosely reaggregated (flocculate). As for the aggregation form and the like of these fine particles, reference can be made to Journal of the Imaging Society of Japan, “Organic Pigment Refinement and Dispersion Technology”, Takashi Deno, Vol. 45, No. 5, 2006, pages 12-21.

  As a method for redispersing fine particles in such a soft aggregated state (agglomerate), 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 limitations on the disperser used when dispersing the pigment nanoparticles by applying physical energy, for example, dispersers such as kneaders, roll mills, atriders, super mills, dissolvers, homomixers, and sand mills. Can be mentioned. Further, a high-pressure dispersion method and a dispersion method using fine particle beads are also preferable.

[Polymer dispersant]
In the present invention, it is preferable to remove the aqueous solvent content of the dispersion prepared by the reprecipitation method as described above. It is preferable not to have a drying step after the step of removing the aqueous phase. At this time, for the purpose of further improving the dispersibility of the pigment, a dispersant such as a specific pigment dispersant or surfactant may be added as long as the effects of the present invention are not impaired. The dispersant used here may be used in the reprecipitation method described above, and may coexist at the time of precipitation of pigment fine particles, for example. In the present invention, polymer compounds are mainly exemplified as the following dispersants. However, in the present invention, when it is referred to as molecular weight, it means mass average molecular weight unless otherwise specified, and molecular weight and dispersity are values measured by the following measuring methods.

[Method for measuring molecular weight and dispersity of polymer compound]
The molecular weight and degree of dispersion are measured using GPC (gel filtration chromatography) unless otherwise specified. The gel packed in the column used in the GPC method is preferably a gel having an aromatic compound as a repeating unit, and examples thereof include a gel made of a styrene-divinylbenzene copolymer. It is preferable to use 2 to 6 columns connected together. Examples of the solvent used include ether solvents such as tetrahydrofuran and amide solvents such as N-methylpyrrolidinone, but ether solvents such as tetrahydrofuran are preferred. The measurement is preferably performed at a solvent flow rate in the range of 0.1 to 2 mL / min, and most preferably in the range of 0.5 to 1.5 mL / min. By performing the measurement within this range, the apparatus is not loaded and the measurement can be performed more efficiently. The measurement temperature is preferably 10 to 50 ° C, most preferably 20 to 40 ° C.

Specific conditions for molecular weight measurement are shown below.
Apparatus: HLC-8220GPC (manufactured by Tosoh Corporation)
Detector: Differential refractometer (RI detector)
Pre-column: TSKGUARDCOLUMN MP (XL)
6mm x 40mm (manufactured by Tosoh Corporation)
Sample side column: The following two columns are directly connected (all manufactured by Tosoh Corporation)
・ TSK-GEL Multipore-HXL-M 7.8 mm x 300 mm
Reference side column: Same as sample side column Temperature chamber temperature: 40 ° C
Moving bed: tetrahydrofuran Sample-side moving bed flow rate: 1.0 mL / min Reference-side moving bed flow rate: 0.3 mL / min Sample concentration: 0.1% by weight
Sample injection volume: 100 μL
Data collection time: 16 minutes to 46 minutes after sample injection Sampling pitch: 300 msec

○ Dispersant A
For the purpose of further improving the dispersibility of the processed pigment, a dispersant such as a pigment dispersant or a surfactant can be added to the pigment dispersion of the present invention. Dispersants (pigment dispersants) include polymer dispersants [for example, polyamidoamines and salts thereof, polycarboxylic acids and salts thereof, high molecular weight unsaturated acid esters, modified polyurethanes, modified polyesters, modified poly (meth) acrylates, (Meth) acrylic copolymer, naphthalenesulfonic acid formalin condensate], polyoxyethylene alkyl phosphate ester, polyoxyethylene alkyl amine, alkanol amine, pigment derivative and the like. The polymer dispersant can be further classified into a linear polymer, a terminal-modified polymer, a graft polymer, and a block polymer according to the structure.

  The polymer dispersant is adsorbed on the surface of the pigment and acts to prevent reaggregation. Therefore, a terminal-modified polymer, a graft polymer and a block polymer having an anchor site to the pigment surface can be mentioned as preferred structures. On the other hand, the pigment derivative has an effect of promoting the adsorption of the polymer dispersant by modifying the pigment surface. The polymer dispersant acts to adsorb on the surface of the pigment and prevent reaggregation in the dispersion step. For this reason, a block polymer, a graft polymer, and a terminal-modified polymer having an anchor site to the pigment surface can be cited as preferred structures. On the other hand, the pigment derivative has an effect of promoting the adsorption of the polymer dispersant by modifying the pigment surface.

-Graft type polymer The graft type polymer is not particularly limited, but is a compound obtained by reacting a polyalkyleneimine and a polyester compound described in JP-A-54-37082, JP-A-61-174939, etc. Preferable examples include a compound in which the amino group of the side chain of polyallylamine described in JP-A-9-169821 is modified with polyester, a polyester polyol-added polyurethane described in JP-A-60-166318, and the like. As described in Kaihei 9-171253, Macromonomer Chemistry and Industry (IPC Publishing Department, 1989), etc., a graft-type polymer having a polymerizable oligomer (hereinafter referred to as a macromonomer) as a copolymerization component. Can also be mentioned. Moreover, the graft | grafting type | mold polymer which has an organic pigment | dye part of Unexamined-Japanese-Patent No. 2003-238837 is preferable at the point of adsorb | sucking to a pigment and giving favorable dispersibility. Suitable examples of the branch of the graft polymer include polystyrene, polyethylene oxide, polypropylene oxide, poly (meth) acrylic acid ester, polycaprolactone, and the like, but a graft polymer having a polycaprolactone chain is more preferable. Commercially available products of the graft-type polymer include Solsperse 24000, 28000, 32000, 38500, 39000, 35000 (above Lubrizol), Disperbyk-161, -171, -174 (above BYK). Chemie), etc. [all trade names].

Terminal-modified polymer Examples of the terminal-modified polymer are described in JP-A-9-77994, JP-A-2002-273191, JP-A-2007-277514, JP-A-2007-140487, and the like. And a polymer having a functional group at the terminal of the polymer.

-Block-type polymer Although it does not specifically limit as a block-type polymer, The block-type polymer which consists of a pigment adsorption block and a block which is not adsorbed to a pigment is mentioned. Although it does not restrict | limit especially as a monomer which comprises a pigment adsorption block, For example, the monomer which has a functional group which can adsorb | suck to a pigment is mentioned. Specific examples include a monomer having an organic dye structure or a heterocyclic structure, a monomer having an acidic group, and a monomer having a basic nitrogen atom. Examples of the monomer having an organic dye structure or a heterocyclic structure include organic dye skeletons and maleimide derivatives described in JP-A No. 2003-238837. Commercially available products can be used as the block polymer. As specific examples, Disperbyk-2000, -2001 (above BYK Chemie), EFKA4330, 4340 (above EFKA), etc. [all trade names] can be mentioned.

  The amount of the dispersant A used in the dispersion is not particularly limited, but is preferably 10 to 400 parts by weight with respect to 100 parts by weight of the pigment, for example, considering use as a color material with the color filter. More preferably, it is -200 mass parts.

  Moreover, in the range which does not impair the effect of this embodiment, you may use another high molecular compound simultaneously with the above-mentioned specific copolymer as needed. As other polymer compounds, natural resins, modified natural resins, synthetic resins, synthetic resins modified with natural resins, and the like are used. The natural resin is typically rosin, and the modified natural resin includes rosin derivatives, fiber derivatives, rubber derivatives, protein derivatives and oligomers thereof. Examples of the synthetic resin include an epoxy resin, an acrylic resin, a maleic acid resin, a butyral resin, a polyester resin, a melamine resin, a phenol resin, and a polyurethane resin. Examples of synthetic resins modified with natural resins include rosin-modified maleic acid resins and rosin-modified phenolic resins. Synthetic resins include polyamidoamine and its salt, polycarboxylic acid and its salt, high molecular weight unsaturated acid ester, polyurethane, polyester, poly (meth) acrylate, (meth) acrylic copolymer, naphthalenesulfonic acid formalin condensate Is mentioned.

[Photocurable composition]
The photocurable composition contains a dispersion of the pigment fine particles, a photopolymerizable compound, and a photopolymerization initiator, and preferably further contains an alkali-soluble resin. The organic pigment fine particles and the method for producing the dispersion have already been described in detail. The content of fine particles in the photocurable composition is preferably 3 to 90% by mass with respect to the total solid content (in the present invention, the total solid content refers to the total composition excluding the organic solvent), and 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. Moreover, you may use it in combination with a normal pigment for toning. As the pigment, those described above can be used.

  The photopolymerizable compound (hereinafter sometimes referred to as a polymerizable monomer or a polymerizable oligomer) is a polyfunctional monomer that has two or more ethylenically unsaturated double bonds and undergoes addition polymerization upon irradiation with light. Is preferred. Examples of such a photopolymerizable compound 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 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, di Pentaerythritol hexa (meth) acrylate, dipentaerythritol penta (meth) acrylate, hexane All di (meth) acrylate, trimethylolpropane tri (acryloyloxypropyl) ether, tri (acryloyloxyethyl) isocyanurate, tri (acryloyloxyethyl) cyanurate, glycerin tri (meth) acrylate; multifunctional such as trimethylolpropane and glycerin Polyfunctional acrylates and polyfunctional methacrylates such as those obtained by adding ethylene oxide or propylene oxide to alcohol and then (meth) acrylated can be mentioned. 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.

  The photopolymerizable compound may be used alone or in combination of two or more. The content of the photocurable 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 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), U.S. 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, 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 photocurable 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.

  The alkali-soluble resin can be added at the time of preparing a photocurable composition or an ink-jet ink for a color filter, but it is also preferably added at the time of producing the fine particle dispersion or at the time of forming fine particles. It is also possible to add the alkali-soluble resin to both or one of the poor solvents for adding the water-insoluble compound solution and the water-insoluble compound solution to form fine particles of the water-insoluble compound. Alternatively, it is also preferable to add an alkali-soluble resin solution when forming fine particles of a water-insoluble compound in a separate system.

  As the alkali-soluble resin, a binder having an acidic group is preferable, and an alkali-soluble polymer having a polar group such as a carboxylic acid group or a carboxylic acid group in the side chain is preferable. 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 alkali-soluble resin may be used alone or in the form of a composition used in combination with a normal film-forming polymer. The amount of water-insoluble compound added to 100 parts by mass of the fine particles is 10 to 200 masses. Part is general, and 25-100 mass parts is preferable.

  In addition, in order to improve the crosslinking efficiency, the side chain of the alkali-soluble resin may have a polymerizable group, and a UV curable resin, a thermosetting resin, or the like is also useful. Furthermore, as the alkali-soluble resin, a resin having a water-soluble atomic group in a part of the side chain can be used. As for content of an organic solvent, 10-95 mass% is preferable with respect to photocurable composition whole quantity. In addition, an appropriate surfactant, a thermal polymerization inhibitor, an ultraviolet absorber, an adhesion aid, other additives, and the like can be contained in the photocurable composition.

The photocurable composition can be made into an inkjet ink by adjusting the composition appropriately. In addition to the color filter, the inkjet ink may be a normal inkjet ink such as for printing. Among them, the inkjet ink for the color filter is preferable.
The ink-jet ink is not particularly limited as long as it contains the water-insoluble compound fine particles, and preferably contains the water-insoluble compound fine particles in a medium containing a polymerizable monomer and / or a polymerizable oligomer. Here, as the polymerizable monomer and / or polymerizable oligomer, those described above for the photocurable composition can be used.
At this time, the ink characteristics used at the time of ejection, the ink spraying method, the ink jet head form, the pattern shape of the color filter, and the formation method thereof are disclosed in JP 2008-138194 A and the preferred range. It is the same.

  The components contained in the coating film using the photocurable composition are the same as those already described. Further, the properties of the coating film using the photocurable composition and the coating method on the substrate are the same as those disclosed in Japanese Patent Application Laid-Open No. 2008-138194 and preferable ranges.

[Color filter]
The pixel of the color filter of the present invention is preferably formed using the above-described pigment fine particle dispersion or a redispersion in which the solvent is switched, and is preferably 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 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, which is a very important performance in order to replace the liquid crystal display with a CRT.

  When the color filter is used for a television, the chromaticity 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 referred to as “this”). In the 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.

x y 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.

  A liquid crystal display device provided with a color filter has a high contrast and is excellent in descriptive power such as black spots, and the VA method is particularly preferable. 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 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. In the examples, “part” and “%” are based on mass unless otherwise specified.

(Synthesis Example) Example of Compound Invention (Synthesis Example 1) Synthesis of Compound bb-11 PR255 (trade name: Cromophthal DPP Coral Red C, manufactured by Ciba Specialty Chemicals) 11.5 g of sulfuric acid: 230 g (Wako Pure Chemicals) The reaction solution was kept at 20 ° C. or lower. Next, 3.9 g of maleimide was added, and then the reaction solution was heated to 30 ° C., 1.4 g of paraformaldehyde (manufactured by Tokyo Chemical Industry Co., Ltd.) was added, and reacted at 30 ° C. for 2 hours. The obtained reaction solution was reprecipitated in 1 L of ice water and filtered to obtain a water paste. Furthermore, 9.6g of compounds bb-11 (compound contained in the previous exemplary compound b-11) was obtained by washing with water and methanol and drying by heating at 50 ° C. As a result of NMR analysis of this compound, it was PR255: bb-11 = 34: 66, and a 397 peak was confirmed by MS.

(Synthesis example 2) Synthesis | combination of compound bb-11 'Maleimide: 31g was dripped at the place which put water 240mL into 29g and was stirred uniformly, and it was made to react at 100 degreeC for 3 hours. The reaction product was filtered and washed with water to obtain 21 g of N-hydroxymaleimide.
In a separate flask, PR255: 11.5 g was dissolved in sulfuric acid: 230 g, and the reaction solution was kept at 20 ° C. or lower. Next, after adding 5.1 g of N-hydroxymaleimide synthesized previously, the reaction solution was heated to 30 ° C. and reacted at 30 ° C. for 2 hours. The obtained reaction solution was reprecipitated in 1 L of ice water and filtered to obtain a water paste. Furthermore, 9.1g of compounds bb-11 '(compound contained in the previous exemplary compound b-11) were obtained by washing with water and methanol and drying by heating at 50 ° C. As a result of NMR analysis of this compound, it was PR255: bb-11 ′ = 22: 78, and a 397 peak was confirmed by MS.

(Synthesis example 3) Synthesis | combination of compound bb-27 PR202: 15g was dissolved in sulfuric acid: 300g, and the reaction liquid was hold | maintained at 60 degreeC. Next, 3.3 g of methylimidazole was added, then 1.4 g of paraformaldehyde was added, and the mixture was allowed to react at 60 ° C. for 2 hours. The obtained reaction solution was reprecipitated in 1 L of ice water and filtered to obtain a water paste. Furthermore, after washing with water and methanol, 12 g of Compound bb-27 (compound contained in the above exemplified Compound b-27) was obtained by drying by heating at 50 ° C. As a result of NMR analysis of this compound, it was PR202: bb-27 = 18: 82, and a peak of 474 was confirmed by MS.

(Synthesis Example 4) Synthesis of Compound bb-23 As in Synthesis Example 3, except that PR202: 15 g was changed to PR122: 13.6 g and methylimidazole: 3.3 g was changed to dimethylhydantoin: 5.2 g. Compound bb-23 (compound contained in the above exemplified compound b-23) was synthesized. According to NMR analysis, this compound was PR122: bb-23 = 20: 80, and a peak of 480 was confirmed by MS.

(Synthesis Example 5) Synthesis of Compound bb-28 Compound bb-28 (Previous Exemplified Compound b-28) was prepared in the same manner as Synthesis Example 3 except that 3.3 g of methylimidazole was changed to 12 g of aminobenzimidazolinone. Compound) was synthesized. According to NMR analysis, this compound was PR202: bb-28 = 37: 63, and a peak of 541 was confirmed by MS.

Synthesis Example 6 Synthesis of Compound bb-15 Isatin: 5.0 g was dissolved in 94 g of sulfuric acid and stirred in an ice-water bath. To this was added dropwise 7 mL of fuming sulfuric acid, and the mixture was stirred at room temperature for about 10 minutes, and then reacted at 70 ° C. for 5 hours. The reaction solution is cooled to 20 ° C. or less, PR255: 10 g is added, and further dissolved in sulfuric acid: 106 g. Paraformaldehyde: 1.2 g was added and reacted at 30 ° C. for 2 hours. The obtained reaction solution was reprecipitated in 1 L of ice water and filtered to obtain a water paste. Furthermore, 16g of compound bb-15 (compound contained in previous exemplary compound b-15) was obtained by washing with water and methanol and drying by heating at 50 ° C. As a result of NMR analysis of this compound, it was PR255: bb-15 = 35: 65, and a peak of 527 was confirmed by MS.

(Example I)
[ Preparation of organic pigment nanoparticle dispersion]
Dimethyl sulfoxide (manufactured by Wako Pure Chemical Industries, Ltd.) is used as a good solvent, and pigment C.I. I. 50 g of Pigment Red 254 (IRGAZIN DPP RED BO, trade name, manufactured by Ciba Specialty Chemicals Co., Ltd.) was dispersed, and 52.3 g of a 25% methanol solution of tetramethylammonium hydroxide was added dropwise thereto. The obtained exemplary compound bb-11 was added to prepare a pigment solution. As a result of measuring the viscosity of this pigment solution using Viscomate VM-10A-L (trade name, manufactured by CBC Materials), the viscosity when the liquid temperature of the pigment solution was 24.5 ° C. was 14.3 mPa · s. Separately, 1000 ml of propylene glycol monomethyl ether acetate containing 19 g of 1 mol / l hydrochloric acid aqueous solution (manufactured by Wako Pure Chemical Industries, Ltd.) was prepared as a poor solvent.
Here, the temperature of the solution was controlled at 10 ° C., and the pigment solution was added to 1000 ml of a poor solvent stirred at 500 rpm with a GK-0222-10 type Lamond Stirrer (trade name, manufactured by Fujisawa Pharmaceutical Co., Ltd.). By using a non-pulsating pump (trade name, manufactured by Nippon Seimitsu Chemical Co., Ltd.), 100 ml of liquid pigment having a flow path diameter of 1.1 mm is injected at a flow rate of 400 ml / min. To prepare a dispersion (dispersion 1) of crystalline organic pigment nanoparticles. The organic pigment nanoparticle dispersion (dispersion 101a) was temperature-controlled at 5 ° C. and stirred for 2 hours.

[Preparation of organic pigment powder]
The organic pigment nanoparticle dispersion liquid (dispersion 101a) prepared by the above procedure was subjected to H-112 type (trade name, manufactured by Kokusan Co., Ltd.) centrifugal filter and P89C type (trade name, manufactured by Shikishima Canvas Co., Ltd.). ) Using a filter cloth, the mixture was concentrated at 5000 rpm for 90 minutes, and then 1100 g of ion-exchanged water was added and mixed, followed by centrifugal filtration in the same manner. Again, 1100 g of ion-exchanged water was added and mixed, followed by centrifugal filtration. The obtained organic pigment nanoparticle concentrated paste 101b was recovered.
The organic pigment nanoparticle concentrated paste was dried in an oven at 100 ° C. for 2 hours to obtain an organic pigment powder 101c having an average particle size of 25 nm.

[Preparation of organic pigment dispersion composition]
The organic pigment powder was pulverized to 180 μm or less with a mortar, and then it was made into an organic pigment dispersion composition 101d having the following composition, which was uniformly stirred and mixed.
9.7 g of the organic pigment powder 101c
Pigment derivative 1 2.0 g
Exemplified compound bb-11 2.3 g
Dispersant resin 1 11.3 g
Propylene glycol monomethyl ether acetate
24.7g

Substituting compound added to Pigment solution of Exemplified Compound bb-11, prepared except that were changed as shown in Table 1, in the same manner as in Example 1, a pigment dispersion liquid (dispersion 102d~104d, c11d) did. Furthermore, a pace, a powder, and an organic pigment dispersion composition (dispersions 102 to 104, c11) were prepared using the respective dispersion samples. For dispersion c11, it means that the following pigment derivative 1 was used instead of bb-11.

  Each sample of the obtained pigment dispersion composition was evaluated at the end. The results are summarized in Table 1. In addition, when it carried out similarly to Example 1 without using an additive compound and prepared the pigment dispersion composition and performed the same measurement evaluation, performance was in each item with respect to the Example using this. Confirmed that it was inferior.

  Dispersion compositions 102-104, c11 are reference examples

(Example II)
< Production of processed pigment>
Pigment C.I. I. Pigment Red 254 (IRGAZIN DPP RED BO, trade name, manufactured by Ciba Specialty Chemicals Co., Ltd.) 50 g, sodium chloride 500 g, and diethylene glycol 100 g were charged into a stainless steel 1 gallon kneader (Inoue Co., Ltd.) for 9 hours. Kneaded. Next, this mixture is poured into about 3 liters of water, stirred for about 1 hour with a high speed mixer, filtered, washed with water to remove sodium chloride and solvent (diethylene glycol), and dried to obtain each processed pigment 201a. It was.

[Preparation of organic pigment dispersion composition]
The organic pigment powder was pulverized to 180 μm or less with a mortar, and then the organic pigment dispersion composition 201b having the following composition was obtained and uniformly stirred and mixed.
9.7 g of the organic pigment powder 201a
Pigment derivative 1 4.3g
Dispersant resin 1 11.3 g
Propylene glycol monomethyl ether acetate
24.7g
Example Compound bb-11 3.5 g

  The organic pigment dispersion composition 201b having the above composition was subjected to sand grinder mill BSG-01 (trade name, manufactured by AIMEX) using zirconia beads having a diameter of 0.5 mm for 1 hour at 1500 rpm, and then zirconia beads having a diameter of 0.05 mm. And dispersed at 2500 rpm for 2 hours to obtain an organic pigment dispersion composition 201.

Substituting compound added to Pigment solution of Exemplified Compound bb-11, except that were changed as shown in Table 2, in the same manner as in Example 1, a pigment dispersion liquid (dispersion 202B～205b) was prepared. Furthermore, paste, powder, and an organic pigment dispersion composition (dispersions 202 to 205) were prepared using the respective dispersion samples.

  Each sample of the obtained pigment dispersion composition was evaluated at the end. The results are summarized in Table 2. In addition, when it carried out similarly to Example 1 without using an additive compound and prepared the pigment dispersion composition and performed the same measurement evaluation, performance was in each item with respect to the Example using this. Confirmed that it was inferior.

  Dispersion compositions 203-205 are reference examples.

(Example III, Comparative Example III)
Example 1
<Production of processed pigment>
Pigment C.I. I. Pigment Red 254 (IRGAZIN DPP RED BO, trade name, manufactured by Ciba Specialty Chemicals Co., Ltd.) 50 g, sodium chloride 500 g, and diethylene glycol 100 g were charged into a stainless steel 1 gallon kneader (Inoue Co., Ltd.) for 9 hours. Kneaded. Next, this mixture is poured into about 3 liters of water, stirred for about 1 hour with a high speed mixer, filtered, washed with water to remove sodium chloride and solvent (diethylene glycol), and dried to obtain each processed pigment 301a. It was.

[Preparation of organic pigment dispersion composition]
The organic pigment powder was pulverized to 180 μm or less with a mortar, and then it was made into an organic pigment dispersion composition 301b having the following composition, which was uniformly stirred and mixed.
9.7 g of the organic pigment powder 301a
4.3 g of the compound bb-15
Dispersant resin 1 11.3 g
Propylene glycol monomethyl ether acetate
24.7g
Pigment derivative 2 2.0g

  The organic pigment dispersion composition 301b having the above composition was subjected to sand grinder mill BSG-01 (trade name, manufactured by AIMEX) using zirconia beads having a diameter of 0.5 mm for 1 hour at 1500 rpm, and then zirconia beads having a diameter of 0.05 mm. And dispersed at 2500 rpm for 2 hours to obtain an organic pigment dispersion composition 301.

(Reference Example 1)
A pigment dispersion c31b was prepared in the same manner as in Example 1 except that the compound added to the pigment solution was changed to the exemplified compound bb-15 and changed as shown in Table 3 below. Further, pastes, powders and organic pigment dispersion compositions were prepared using the respective dispersion samples.

  Each sample of the obtained pigment dispersion composition was evaluated at the end. The results are summarized in Table 3. In addition, when it carried out similarly to Example 1 without using an additive compound and prepared the pigment dispersion composition and performed the same measurement evaluation, performance was in each item with respect to the Example using this. Confirmed that it was inferior.

[Evaluation of pigment dispersion composition]

○ Measurement of particle size distribution of pigment fine particles, number average primary particle size (Dp) The particle size distribution of pigment particles contained in the dispersion was measured under the following conditions, and the ratio P and number of particles having a particle size of 20 nm to 30 nm. The average primary particle size Dp was calculated.
・ TEM imaging equipment: Hitachi, H-7650 electron microscope (trade name)
Accelerating voltage: 110 kV
(A tomographic observation was performed, and a surface with little overlap between particles was extracted from the 3D reconstruction data to obtain a projected area of the particles.)
Image measuring device: KS-400 (trade name) manufactured by Carl Zeiss
(The TEM image of 5000 pigment particles selected at random was measured, the equivalent circle diameter was calculated from the projected area, and the above ratios P and Dp were calculated.)

○ Measurement Evaluation of Viscosity For the obtained pigment dispersion composition, pigment dispersion immediately after dispersion was performed using an E-type viscometer (manufactured by Toki Sangyo Co., Ltd., RE-85L [trade name], measurement temperature 25 ° C.). The viscosity η1 of the composition and the viscosity η2 of the pigment dispersion composition after one week at room temperature after dispersion were measured, and the degree of thickening was evaluated. Here, the low viscosity indicates that the increase in viscosity due to the dispersant is suppressed, and the dispersibility and dispersion stability of the pigment are good.

○ Measurement and evaluation of contrast The obtained pigment dispersion composition was applied onto a glass substrate, and a sample was prepared so that the thickness of the coating film after drying was 1 µm. This sample was placed between two polarizing plates, the amount of transmitted light was measured when the polarization axis was parallel and when the polarization axis was parallel, and the ratio was taken as contrast. 512 color display 10.4 “size TFT-LCD color filter, garden plant, Koseki, Fukunaga, Yamanaka”). Here, a high contrast indicates that the pigment is uniformly dispersed in a highly refined state, and thus the transmittance, that is, the coloring power is high.

[Evaluation of colored photosensitive composition and color filter]
The produced colored photosensitive composition and colored filter substrate (color filter) were evaluated as follows. The results are summarized in the above table.

○ Contrast of color filter (CF) A polarizing plate is placed on the coloring pattern of the color filter, and the coloring pattern is sandwiched between them. The luminance when the polarizing plate is parallel and the luminance when the polarizing plate is orthogonal are BM-5 (trade name) manufactured by Topcon Corporation. The value obtained by dividing the parallel brightness by the orthogonal brightness (= the parallel brightness / the orthogonal brightness) was used as an index for evaluating the contrast. Larger values indicate higher contrast.

○ Evaluation of CR heat resistance The produced color filter was forcibly heated in an oven at 250 ° C for 1 hour, and the contrast retention before and after the treatment was evaluated.

○ Evaluation of compound heat resistance When the compounds shown in the examples were forcibly heat-treated in an oven at 250 ° C. for 1 hour and HPLC was measured before and after the treatment, (m, n) = (0, 1) When the compound residual ratio exceeded 80%, it was evaluated as O, 80 to 20% as Δ, and 20% to 0% as x.

  According to the results shown in the above table, the pixel of the color filter manufactured using the dispersion using the compound represented by the general formula (1) of the present invention has high heat resistance as well as contrast, and high-quality image-related equipment. It can be seen that when it is used in the present invention, it exhibits practically superior performance and durability. In addition, the pixel of the color filter of the present invention is excellent in black color (no light leakage and black appears deep and dark when the illumination light from the backlight is blocked to display black) and the color is extremely good. It was.

Claims (12)

A pigment fine particle dispersion comprising pigment fine particles and a compound represented by the following general formula (1):

(In the formula, Q represents a residue of a diketopyrrolopyrrole pigment compound. R ¹ and R ² each independently represents a hydrogen atom or an alkyl group. N represents an integer of 1 to 4. P represents the following general formula. (P-1) represents a group represented by any one of (P-2), (P-4), and (P-5) .)

(In the formula, R ³ to R ⁶ and R ¹⁰ to R ¹⁷ are each independently a hydrogen atom, a halogen atom, or an alkyl group, aryl group, or heteroaryl group which may have a substituent, or -A. ¹ is a group represented by ^1- Z, R ³ and R ⁴ are not bonded to each other, A ¹ is a single bond or a divalent organic linking group, and Z is represented by SO ₃ H or CO ₂ H. When Z is an acidic group, it may form a salt. * Indicates a position bonded to QC (R ¹ ) (R ² )-) The pigment fine particles are produced by mixing a solution obtained by dissolving the pigment and the compound represented by the general formula (1) in a good solvent with a medium that becomes a poor solvent for the good solvent. The pigment fine particle dispersion according to claim 1, wherein The pigment fine particle dispersion according to claim 1 or 2 , wherein the content of the compound represented by the general formula (1) is 1 to 100 parts by mass with respect to 100 parts by mass of the pigment.   The pigment constituting the pigment fine particles is at least one selected from the group consisting of diketopyrrolopyrrole pigments, quinacridone pigments, and anthraquinone pigments, according to any one of claims 1 to 3. Pigment fine particle dispersion.   The pigment fine particle dispersion according to any one of claims 1 to 4, further comprising a dispersant having a polycaprolactone structure. The pigment fine particle dispersion according to claim 5 , wherein the amount of the dispersant used is 10 to 400 parts by mass with respect to 100 parts by mass of the pigment.   The pigment fine particle dispersion according to claim 5 or 6, wherein the dispersant has a molecular weight of 1,000 to 2,000,000.   The pigment fine particle dispersion according to any one of claims 1 to 7, wherein an average particle diameter of the fine particles of the pigment is 100 nm or less. It is a color material for color filters, The pigment fine particle dispersion of any one of Claims 1-8 . The photocurable composition containing the component of the dispersion of any one of Claims 1-9, and a polymeric compound. A color filter having pixels formed by curing the photocurable composition according to claim 10 . A compound represented by the following general formula (1).

(In the formula, Q represents a residue of a diketopyrrolopyrrole pigment compound. R ¹ and R ² each independently represents a hydrogen atom or an alkyl group. N represents an integer of 1 to 4. P represents the following general formula. Represents a group represented by any one of formulas (P-1), (P-2), (P-4), and (P-5) .

(In the formula, R ³ to R ⁶ and R ¹⁰ to R ¹⁷ are each independently a hydrogen atom, a halogen atom, or an alkyl group, aryl group, or heteroaryl group which may have a substituent, or -A. ¹ is a group represented by ^1- Z, R ³ and R ⁴ are not bonded to each other, A ¹ is a single bond or a divalent organic linking group, and Z is represented by SO ₃ H or CO ₂ H. When Z is an acidic group, it may form a salt. * Indicates a position bonded to QC (R ¹ ) (R ² )-)