JP2013125086A - Pigment dispersion for color filter - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a pigment dispersion for a color filter capable of forming a cured film excellent in contrast, a color composition for a color filter containing the pigment dispersion, and a method for producing the pigment dispersion for a color filter.SOLUTION: Provided are: [1] A pigment dispersion for a color filter that contains a diketopyrrolopyrrole pigment, a pigment dispersant, and an organic solvent such as propylene glycol monomethyl ether acetate, and in which the pigment dispersant is composed of a graft polymer containing a constitutional unit having an amido group in a main chain and containing a constitutional unit derived from methacrylic acid isopropyl in a side chain and a weight ratio [the main chain/the side chain] of the main chain to the side chain in the graft polymer ranges from 30/70 to 49/51; [2] a color composition for a color filter containing the pigment dispersion; and [3] a method for producing the pigment dispersion of [1].

Description

  The present invention relates to a color filter pigment dispersion, a color filter coloring composition containing the same, and a method for producing a color filter pigment dispersion.

  A color filter used in a liquid crystal display device is manufactured by a photolithography method in which a coloring composition obtained by blending a pigment dispersion with a resin or the like is applied to a transparent substrate such as glass, and then exposed, cured, developed, and thermally cured. Yes. The pigment dispersion used here is a non-aqueous pigment dispersion in which a pigment is dispersed in an organic solvent. As a method for producing a non-aqueous pigment dispersion, a production method using a polymer dispersant such as a graft polymer is known. ing.

For example, Patent Document 1 contains a pigment, a pigment dispersion polymer, and an organic solvent for the purpose of improving the storage stability and heat resistance of the pigment dispersion, and the amount of polymer not adsorbed on the pigment is contained in the pigment dispersion. A pigment dispersion for a color filter that is 2% by weight or less is disclosed.
On the other hand, an example in which a graft polymer is used as a pigment dispersant for solvent-based paints is also known. For example, Patent Document 2 includes a graft copolymer obtained by grafting a macromonomer to a polymer main chain for the purpose of improving pigment use efficiency, paint viscosity, and the like. A pigment dispersion composition having a group as a pigment fixing group is disclosed.

JP 2009-161692 A Special table 2003-517063 gazette

In order to obtain a clear image, a colored composition used in the production of a color filter using a photolithography method requires high contrast in the resulting photocured film. However, the diketopyrrolopyrrole pigment used for the red filter has high crystallinity itself and easily aggregates in an organic solvent, so that there is a problem that it is difficult to maintain a fine dispersion state and the contrast is lowered. . In order to improve the contrast, when the amount of the dispersant is increased and the pigment particles are made finer, the viscosity increases due to a large amount of the dispersant, and the amount of the binder component that is a curing component of the color filter coloring composition must be reduced. In other words, the film characteristics of the cured film are deteriorated. Therefore, a pigment dispersion that can provide high contrast without requiring a large amount of dispersant is desired.
It is an object of the present invention to provide a pigment dispersion for a color filter capable of forming a cured film having excellent contrast, a coloring composition for a color filter containing the same, and a method for producing the pigment dispersion for a color filter. And

In the pigment dispersion for a color filter, the present inventors contain a structural unit having an amide group in the main chain, a structural unit derived from isopropyl methacrylate having a high hydrophobicity in the side chain, and a main chain polymer. By adding a graft polymer having a large weight ratio of the side chain polymer as a pigment dispersant, diketopyrrolopyrrole pigment particles are finely stabilized in an organic solvent, and dispersion stability is maintained even under heating conditions when forming a cured film. The present inventors have found that high contrast can be obtained when used for color filters.
That is, the present invention provides the following [1] to [3].
[1] A pigment dispersion for a color filter comprising a diketopyrrolopyrrole pigment, a pigment dispersant, and an organic solvent represented by the following formula (1), the pigment dispersant having an amide group in the main chain It is composed of a graft polymer containing a structural unit and containing a structural unit derived from isopropyl methacrylate in the side chain, and the weight ratio of the main chain to the side chain in the graft polymer [main chain / side chain] is 30/70 to 49/51 pigment dispersion for color filters.

(Wherein R ¹ and R ² each independently represents a hydrogen atom or a hydrocarbon group having 1 to 5 carbon atoms, R ³ represents a hydrogen atom or a methyl group, n represents an average number of added moles, ~ 4.)
[2] A coloring composition for a color filter comprising the pigment dispersion of [1].
[3] A pigment dispersant, a diketopyrrolopyrrole pigment, which is a graft polymer containing a structural unit having an amide group in the main chain and a structural unit derived from isopropyl methacrylate in the side chain, and a formula (1) The method for producing a pigment dispersion according to the above [1], comprising a step (1) of obtaining a pigment dispersion (1) by dispersing a mixture containing an organic solvent.

  According to the present invention, there are provided a pigment dispersion for a color filter capable of forming a cured film having excellent contrast, a coloring composition for a color filter containing the same, and a method for producing the pigment dispersion for a color filter. Can do.

  The pigment dispersion for a color filter of the present invention is a pigment dispersion containing a diketopyrrolopyrrole pigment, a pigment dispersant, and an organic solvent represented by the following formula (1), and the pigment dispersant is a main chain. A graft polymer containing a structural unit having an amide group in the side chain and a structural unit derived from isopropyl methacrylate in the side chain, the weight ratio of the main chain to the side chain in the graft polymer [main chain / side chain] Is 30/70 to 49/51.

（式中、Ｒ¹及びＲ²はそれぞれ独立に、水素原子又は炭素数１〜５の炭化水素基を示し、Ｒ³は水素原子又はメチル基を示し、ｎは平均付加モル数を示し、１〜４である。）

(Wherein R ¹ and R ² each independently represents a hydrogen atom or a hydrocarbon group having 1 to 5 carbon atoms, R ³ represents a hydrogen atom or a methyl group, n represents an average number of added moles, ~ 4.)

The reason why the colored composition for color filter containing the pigment dispersion for color filter of the present invention can form a cured film having excellent contrast is not clear, but is considered as follows.
The pigment dispersion for a color filter of the present invention contains a structural unit having an amide group in the main chain of the graft polymer, which is considered to be adsorbed on the diketopyrrolopyrrole pigment. On the other hand, since the side chain of the graft polymer is a polymer containing a structural unit derived from isopropyl methacrylate, and the organic solvent is an ester organic solvent having an alkylene glycol moiety, the pigment dispersion and the organic solvent are easily solvated, Since the branched structure of isopropyl methacrylate is easy to spread in the solvent, it is considered that the diketopyrrolopyrrole pigment which is easily aggregated can be finely and stably dispersed, and the resulting cured film has excellent contrast.
In particular, since the graft polymer has a larger weight ratio of the side chain than the main chain, it can be more easily spread in the solvent and can be stably dispersed. Such a side chain of the graft polymer maintains a fine dispersion state of the pigment particles without causing the pigment particles to be too close or aggregated even when preparing the cured film. The contrast is considered to be excellent.
Hereafter, each component, process, etc. used for this invention are demonstrated.

[Pigment dispersant]
The pigment dispersant used in the present invention contains a structural unit having an amide group in the main chain and is derived from isopropyl methacrylate in the side chain from the viewpoint of improving the adsorptivity to the organic pigment and the contrast of the resulting cured film. A graft polymer containing the structural unit of
The weight ratio of the main chain to the side chain in the graft polymer [main chain / side chain] is 30/70 to 49/51 from the viewpoint of improving the contrast of the resulting cured film, and 31/69 to 45 / 55 is preferable, 32/68 to 41/59 is more preferable, and 34/66 to 40/60 is still more preferable.
The weight average molecular weight of the graft polymer is preferably 5,000 to 500,000, more preferably 30,000 to 200,000, and still more preferably, from the viewpoint of adsorptivity to the pigment, and thus the contrast of the cured film. Is 40,000 to 100,000, more preferably 60,000 to 90,000. The number average molecular weight of the graft polymer is preferably 3,000 to 300,000, more preferably 5,000 to 13,000, and still more preferably 10,000 to 12,000, from the viewpoint of maintaining contrast even after heating. 000.

The number average molecular weight of the main chain of the graft polymer is preferably from 500 to 50,000, more preferably from 1,000 to 20,000, from the viewpoint of adsorptivity to the pigment, and hence the contrast of the cured film. Preferably, it is 2,500 to 5,000. Moreover, the weight average molecular weight of the main chain is preferably 1,500 to 150,000, more preferably 5,000 to 50,000, and still more preferably 10,000 to 15,000 from the same viewpoint.
The number average molecular weight of the side chain of the graft polymer is preferably 500 to 20,000, more preferably 1,000 to 8,000, and more preferably 1,000 to 8,000, from the viewpoint of solubility in a solvent, and thus the contrast of the cured film. Preferably it is 1,500-3,000. Further, from the same viewpoint, the weight average molecular weight of the side chain is preferably 1,000 to 50,000, more preferably 2,000 to 20,000, and further preferably 2,500 to 5,000.
In addition, the measurement of a weight average molecular weight and a number average molecular weight can be performed by the method of an Example description.

<Monomer that is a constituent unit of the main chain of the graft polymer>
As the monomer that is a constituent unit of the main chain of the graft polymer, a vinyl monomer containing an amide group is preferably contained from the viewpoint of adsorptivity to the pigment.
Specific examples of the vinyl monomer containing an amide group include (meth) acrylamides and vinylpyrrolidones.
(Meth) acrylamides include (meth) acrylamide, N, N-dialkyl (meth) acrylamide (the alkyl group preferably has 1 to 8 carbon atoms, more preferably 1 to 4 carbon atoms), and N-alkyl (meta). ) Acrylamide (the alkyl group preferably has 1 to 8 carbon atoms, more preferably 1 to 4 carbon atoms), N, N-dialkyl (the alkyl group preferably has 1 to 8 carbon atoms, more preferably 1 to 4 carbon atoms) Aminoalkyl (the alkyl group preferably has 1 to 6 carbon atoms) (meth) acrylamide, (meth) acrylamide 2-methylpropylsulfonic acid, morpholino (meth) acrylamide, piperidino (meth) acrylamide, N-methyl-2-pyrrolidyl (Meth) acrylamide, N, N-methylphenyl (meth) acrylamide and the like can be mentioned.
Examples of vinyl pyrrolidones include N-vinyl-2-pyrrolidone.

Among these vinyl monomers containing an amide group, vinylpyrrolidones are preferable and N-vinylpyrrolidone is more preferable from the viewpoint of adsorptivity to organic pigments.
The content of the structural unit derived from the vinyl monomer containing the amide group in all the structural units of the main chain is preferably 25 to 60% by weight, more preferably 30 to 55% by weight from the viewpoint of promoting adsorption to the organic pigment. %, More preferably 35 to 50% by weight.
The content of the structural unit derived from the vinyl monomer containing an amide group in all the structural units of the graft polymer is from the viewpoint of adsorptivity to the organic pigment, and from the viewpoint of suppression of viscosity increase and optimization of the dispersed particle size Preferably it is 1-30 weight%, More preferably, it is 5-25 weight%, More preferably, it is 10-23 weight%.

As the monomer that is a constituent unit of the main chain of the graft polymer, it is preferable to use a vinyl monomer further containing a hydroxyl group from the viewpoint of promoting adsorption to the pigment.
Examples of the vinyl monomer containing a hydroxyl group include (meth) acrylic acid hydroxyalkyl such as 2-hydroxyethyl (meth) acrylate; glycerin mono (meth) acrylate; (meth) acrylic acid poly (meth) acrylate such as polyethylene glycol Examples include alkylene glycol.
Among these vinyl monomers containing a hydroxyl group, hydroxyalkyl (meth) acrylate is preferable and 2-hydroxyethyl (meth) acrylate is more preferable from the viewpoint of adsorptivity to the pigment.
The content of the structural unit derived from the vinyl monomer containing a hydroxyl group in all the structural units of the main chain is preferably 20 to 50% by weight, more preferably 25 to 45% by weight, from the viewpoint of promoting adsorption to the pigment. More preferably, it is 30 to 40% by weight.
The content of the structural unit derived from the vinyl monomer containing a hydroxyl group in all the structural units of the graft polymer is preferably from the viewpoint of adsorptivity to the pigment, and from the viewpoint of suppressing the increase in viscosity and optimizing the dispersed particle size. It is 2 to 30% by weight, more preferably 5 to 20% by weight, still more preferably 7 to 18% by weight.

<Monomer that is a structural unit of the side chain of the graft polymer>
From the viewpoint of enhancing the dispersibility of the pigment in the organic solvent, the monomer that is a constituent unit of the side chain of the graft polymer contains isopropyl methacrylate.
The content of the structural unit derived from isopropyl methacrylate in the side chain of the graft polymer is preferably 50 to 100% by weight, more preferably 80 to 100% by weight, still more preferably, based on all the structural units in the side chain. It is 90 to 100% by weight, still more preferably substantially 100% by weight.
The side chain of the graft polymer may contain a monomer copolymerizable with isopropyl methacrylate as long as the effects of the present invention are not impaired.
Monomers that can be copolymerized with isopropyl methacrylate include (meth) acrylic acid esters, and (meth) acrylic acid esters include methyl (meth) acrylate, ethyl (meth) acrylate, and (meth) acrylic acid. (Meth) acrylates such as stearyl; benzyl (meth) acrylate; isobornyl (meth) acrylate; 2-hydroxyethyl (meth) acrylate; glycerol mono (meth) acrylate; perfluorooctylethyl (meth) acrylate ; (Meth) acrylic acid methoxypolyethylene glycol and the like. Among these, alkyl (meth) acrylate and / or benzyl (meth) acrylate having an alkyl group having 1 to 3 carbon atoms are preferred, and methyl (meth) acrylate and / or benzyl (meth) acrylate are more preferred. Preferably, benzyl (meth) acrylate is more preferable.
Said (meth) acrylic acid ester can be used individually or in combination of 2 or more types.

<Production of graft polymer>
As a method for producing a graft polymer, (i) a method of copolymerizing a monomer that is a constituent unit of a main chain and a macromonomer that constitutes a side chain (macromonomer method); and (ii) a polymer that constitutes a main chain; Although there is a method of coupling reaction with a polymer constituting the side chain (coupling method), (ii) the coupling method is preferable from the viewpoint of fine stabilization of the organic pigment.

(Production of graft polymer by coupling method)
The polymer constituting the main chain used for the coupling reaction preferably contains a structural unit derived from a vinyl monomer containing a reactive functional group. The polymer can be obtained by copolymerizing a mixture of monomers that are constituent units of the main chain.
Examples of the vinyl monomer containing a reactive functional group include monomers containing an epoxy group, an isocyanate group, a carboxy group, a phosphoric acid group, a sulfonic acid group, and an amino group. Is preferable, (meth) acrylic acid esters containing a glycidyl group are preferable, and glycidyl (meth) acrylate is more preferable.
When the polymer constituting the main chain used for the coupling reaction contains an epoxy group as a reactive functional group, the epoxy value of the main chain is 45 to 125 mgKOH / g from the viewpoint of reactivity with the side chain and the like. Preferably, 55 to 115 mgKOH / g is more preferable, and 65 to 105 mgKOH / g is still more preferable.
The epoxy value can be measured by the method described in the examples.

The polymer constituting the side chain used in the coupling reaction is preferably polyisopropyl methacrylate having a reactive functional group that reacts with the reactive functional group of the polymer constituting the main chain at one end.
When the reactive functional group of the polymer constituting the main chain is an epoxy group, one end of the polymer constituting the side chain is preferably a carboxy group or an amino group.
The polymer constituting the side chain used for the coupling reaction is preferably obtained by solution polymerization using, for example, a polymerization initiator or chain transfer agent containing a carboxy group or amino group which is a reactive functional group.
The coupling reaction between the polymer constituting the side chain and the polymer constituting the main chain may be performed under the condition that each reactive functional group sufficiently reacts, but each polymer is dissolved in an organic solvent in the presence of a catalyst. It is preferable to carry out.
Examples of the catalyst include quaternary ammonium salts such as quaternary ammonium halides, tertiary amines such as triethylamine, alkali metal hydroxides, inorganic acids, sulfonic acids, carboxylic acids, solid acids, solid bases, and the like. . In these, a quaternary ammonium halide is more preferable and tetrabutylammonium bromide is still more preferable.
As the graft polymer, a polymer obtained by polymerization or a coupling reaction may be used as it is, but it is preferable to use it after purification in order to improve dispersion stability by removing unreacted monomers and the like.

[Diketopyrrolopyrrole pigment]
The diketopyrrolopyrrole pigment (hereinafter also simply referred to as “pigment”) used in the present invention is not particularly limited as long as it is suitably used for a color filter.
Specifically, C.I represented by the following formula (2). I. Pigment red 254, C.I. I. Pigment red 255, C.I. I. Pigment red 264, C.I. I. Pigment red 272, C.I. I. And CI Pigment Orange 71.

In Formula (2), X ¹ and X ² each independently represent a hydrogen atom or a halogen atom, and Y ¹ and Y ² each independently represent a hydrogen atom, a methyl group, a —CN group, or a phenyl group. or an -SO ₃ H group. The halogen atom is preferably a fluorine atom or a chlorine atom.
Among these, from the viewpoint of more effectively expressing the effects of the present invention, C.I. I. Pigment Red 254 is preferred.
Suitable examples of commercially available diketopyrrolopyrrole pigments include BASF Corporation C.I. I. Pigment Red 254, trade names "Irgaphor Red B-CF", "Igaphor Red BK-CF", "Irgaphor Red BT-CF", "Irgazin DPP Red BO", "Irgazin DPP Red BL", "Cromophtal DPP Red BP" , “Cromophtal DPP Red BOC” and the like.
The diketopyrrolopyrrole pigment represented by the general formula (2) reacts, for example, benzonitrile or halogenated benzonitrile with a halogenated acetate such as bromoacetate in the presence of a reducing agent such as zinc powder. Or the resulting compound can be further sulfonated.
From the viewpoint of improving the brightness Y value, it is desirable to use a finely-pulverized product having an average primary particle diameter of preferably 100 nm or less, more preferably 20 to 60 nm. The average primary particle diameter of the pigment can be obtained by directly measuring the size of the primary particles from an electron micrograph. Specifically, the short axis diameter and the long axis diameter of each primary particle are measured, and the average value thereof is defined as the particle diameter of the particle. For 100 or more particles, the volume of each particle is expressed as one side of the particle diameter. The volume average particle diameter is obtained by approximating to the cube as described above, and this is used as the average primary particle diameter.
The above diketopyrrolopyrrole pigments can be used alone or in combination of two or more.

[Organic solvent]
In the present invention, an organic solvent represented by the following formula (1) is used.

In the formula, each of R ¹ and R ² independently represents a hydrogen atom or a hydrocarbon group having 1 to 5 carbon atoms, R ³ represents a hydrogen atom or a methyl group, and n is an average added mole number of 1 to 4. is there.
As the organic solvent, a high-boiling organic solvent having a boiling point at 1 atm of 100 ° C. or higher, preferably 110 ° C. to 300 ° C., more preferably 120 to 280 ° C., still more preferably 130 to 260 ° C. is preferable.
The organic solvent has a viscosity at 25 ° C. of 0.8 to 5.0 mPa · s and 0.9 to 4.0 mPa · s from the viewpoint of improving the contrast of the cured film using the pigment dispersion. Is preferable, and it is still more preferable that it is 1.0-3.5 mPa * s.

Preferred examples of the organic solvent include alkylene glycol monoalkyl ether acetate, polyalkylene glycol monoalkyl ether acetate, and alkylene glycol monoalkyl ether propionate. Specific examples thereof include ethylene glycol monomethyl ether acetate and ethylene glycol monoethyl ether acetate. , Ethylene glycol monomethyl ether propionate, ethylene glycol monoethyl ether propionate, propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, propylene glycol monomethyl ether propionate, propylene glycol monoethyl ether propionate, diethylene glycol monomethyl Ether ace Over DOO, diethylene glycol monobutyl ether acetate and the like.
Among these, from the viewpoint of dispersibility of the diketopyrrolopyrrole pigment, propylene glycol monomethyl ether acetate (PGMEA, boiling point: 146 ° C., viscosity at 25 ° C .: 1.1 mPa · s, SP value: 8.73) Diethylene glycol monobutyl ether acetate (BCA, boiling point: 247 ° C., viscosity at 25 ° C .: 3.1 mPa · s, SP value: 8.94) is preferred, and propylene glycol monomethyl ether acetate (PGMEA) is more preferred.

[Method for producing pigment dispersion]
Although there is no restriction | limiting in particular in the manufacturing method of the pigment dispersion for color filters of this invention, It is preferable to have the following process (1) from a viewpoint of obtaining the cured film excellent in contrast.
Step (1): A pigment dispersant which is a graft polymer containing a structural unit having an amide group in the main chain and a structural unit derived from isopropyl methacrylate in the side chain (hereinafter also simply referred to as “pigment dispersant”) , A step of dispersing a mixture containing a diketopyrrolopyrrole pigment and an organic solvent represented by formula (1) (hereinafter also simply referred to as “mixture”) to obtain a pigment dispersion (1). From the viewpoint of improving contrast, it is more preferable to further include the following step (2).
Step (2): A step of obtaining a pigment dispersion (2) by removing at least part of the pigment dispersant not adsorbed to the pigment from the pigment dispersion (1) obtained in the step (1).

<Step (1)>
There is no particular limitation on the dispersion method in the step (1), and the target pigment dispersion (1) may be obtained by dispersing the mixture once. However, after the mixture is predispersed, the main dispersion is further performed. Is preferable from the viewpoint of obtaining a finer and more uniform pigment dispersion (1).

(Preliminary dispersion)
In the preliminary dispersion in step (1), the pigment dispersant, the diketopyrrolopyrrole pigment, and all the components of the organic solvent represented by the formula (1) may be mixed and dispersed at one time. It is preferable that a premixture is prepared by premixing the organic solvent represented by the formula (1), a pigment is mixed in the premixture obtained, and dispersed to obtain a final mixture.
In the preliminary dispersion step, the ratio of the pigment in the pigment dispersion is preferably 3% by weight or more from the viewpoint of obtaining good colorability, and preferably 3 to 30% by weight from the viewpoint of obtaining good colorability and viscosity. 5 to 20% by weight is more preferable.
In the preliminary dispersion step, the content of the pigment dispersant in the pigment dispersion is preferably 2 to 15% by weight from the viewpoint of lowering the viscosity of the dispersion and obtaining a cured film excellent in contrast. Weight percent is more preferred.
In the preliminary dispersion step, the weight ratio of the pigment dispersant to the pigment (pigment dispersant / pigment) is 0.4 from the viewpoint of adhering a necessary amount of the pigment dispersant to the pigment and thus improving the contrast of the obtained cured film. It is -1.6, It is preferable to set it as 0.6-1.4, and it is more preferable to set it as 0.8-1.2.
The content of the organic solvent in the preliminary dispersion step is preferably 20 to 90% by weight and more preferably 40 to 85% by weight from the viewpoint of uniform dispersion.
The dispersion time in the preliminary dispersion step is not particularly limited, but is preferably 0.1 to 10 hours, more preferably 0.5 to 4 hours, and still more preferably 1 to 3 hours.

There is no particular limitation on the mixing disperser used in the preliminary dispersion, and various known dispersers can be used. Examples thereof include high-speed stirring and mixing devices such as homomixers, kneaders such as roll mills, kneaders and extruders, high-pressure dispersers such as high-pressure homogenizers, media-type dispersers such as paint shakers and bead mills. These devices can be used in combination.
Among these, from the viewpoint of uniformly mixing the organic pigment in the organic solvent, a high-speed stirring and mixing device such as a homomixer, and a media type dispersing machine such as a paint shaker or a bead mill are more preferable.
In the case of using a media type disperser, the material of the media used in the preliminary dispersion step is preferably a ceramic material such as zirconia or titania, a polymer material such as polyethylene or nylon, a metal, or the like, and zirconia is preferable from the viewpoint of wear. In addition, the diameter of the media is preferably 0.1 to 0.5 mm, more preferably 0.1 to 0.4 mm, from the viewpoint of crushing the aggregated particles in the organic pigment.

(Distributed)
This dispersion is a step of dispersing the preliminary dispersion obtained in the preliminary dispersion, and is performed to further refine the mixture obtained in the preliminary dispersion step. From the viewpoint of miniaturizing the organic pigment, It is preferable to use a media-type disperser, and the above-described high-pressure disperser may be used in combination.
As the material of the media used in this dispersion step, ceramics such as zirconia and titania, polymer materials such as polyethylene and nylon, metals and the like are preferable, and zirconia is preferable from the viewpoint of wear. Further, the diameter of the medium is preferably 0.15 mm or less, more preferably 0.1 mm or less, further preferably 0.07 mm or less from the viewpoint of making the organic pigment finer, and from the viewpoint of separating the media from the pigment, 0. 0.003 mm or more is more preferable, and 0.01 mm or more is even more preferable.
From the above viewpoint, the media diameter used in this dispersion step is preferably 0.003 to 0.1 mm, and more preferably 0.01 to 0.07 mm.
As the media type disperser used in this dispersion step, a paint shaker, a bead mill or the like is preferable. As a commercially available media type disperser, Ultra Apex Mill (trade name, manufactured by Kotobuki Industries Co., Ltd.), Pico Mill (Asada Tekko Co., Ltd.) Company name, product name) and the like.
From the viewpoint of storage stability of the resulting pigment dispersion, it is preferable to maintain the temperature during dispersion at 10 to 35 ° C, more preferably 15 to 30 ° C, and still more preferably 18 to 27 ° C.
The dispersion time of this dispersion is preferably 2 to 200 hours and more preferably 3 to 50 hours from the viewpoint of sufficiently miniaturizing the organic pigment.

In this dispersion step, the ratio of the diketopyrrolopyrrole pigment in the pigment dispersion, the content of the pigment dispersant in the pigment dispersion, the weight ratio of the pigment dispersant to the pigment [pigment dispersant / pigment], the content of the organic solvent The amount is the same as in the preliminary dispersion step.
The viscosity of the pigment dispersion is preferably 1 to 100 mPa · s (20 ° C), more preferably 1 to 80 mPa · s (20 ° C), and still more preferably 1 to 50 mPa · s (20 ° C). The viscosity can be adjusted by adjusting the power of the disperser and the mixing ratio of the diketopyrrolopyrrole pigment, the pigment dispersant, and the organic solvent.

<Step (2)>
Step (2) is a step of obtaining the pigment dispersion (2) by removing at least part of the pigment dispersant not adsorbed to the pigment from the pigment dispersion (1) obtained in the step (1).
However, the weight ratio of the pigment dispersant to the pigment [pigment dispersant / pigment] is 0.2 to 0.5 in the step (2).
A method for removing at least a part of the pigment dispersant is not particularly limited, but a method using a centrifugal treatment or a filtration treatment is preferable.

(Centrifuge separation)
Specific examples of the centrifugation treatment include the following methods.
First, the pigment dispersion (1) obtained in the step (1) is centrifuged using a centrifuge, separated into a liquid and a solid, and the liquid is removed to recover the solid.
Next, since the pigment dispersant that has not been adsorbed to the pigment exists in the organic solvent, by removing all or part of the upper layer portion (supernatant liquid) during or after centrifugation, the unadsorbed pigment dispersant is removed. The pigment dispersant can be removed appropriately. In addition, the recovered solid content is mainly composed of particles in which the pigment dispersant is adsorbed to the pigment, and becomes a slurry or cake after centrifugation and remains on the side wall or bottom of the centrifuge. It can be recovered.
The liquid content is removed to recover the solid content, and the total amount of the dispersant not adsorbed on the pigment is adjusted to 2% by weight or less, whereby the storage stability of the resulting pigment dispersion (2) and the cured film obtained The contrast can be greatly improved.

The centrifuge that can be used is not particularly limited, but for example, a sedimentation tube type centrifuge, a basket type centrifuge, and the like are preferable. Examples of the sedimentation tube centrifuge include Hitachi Koki Co., Ltd. and himac CP56G. Non-porous wall-type centrifuges include KBS type and Tanabe Wiltech Co., Ltd. manufactured by Kansai Centrifugal Machinery Co., Ltd. S-type centrifuge manufactured by the company etc. are mentioned.
There is no particular limitation on the operation method of the centrifuge. (I) a continuous type in which the separation liquid layer is discharged while supplying the pigment dispersion (1); and (ii) after the supply of the pigment dispersion (1), the liquid layer is discharged when the separation liquid layer is formed. Any of the batch operation methods may be used.
The centrifugal acceleration in the centrifugal separation treatment is preferably 5,000 to 50,000 G, more preferably 10, from the viewpoint of reducing the amount of the pigment dispersant not adsorbed to the organic pigment contained in the pigment dispersion (1). 000-30,000G.

(Redistribution processing)
Furthermore, in the case of a centrifugal separation treatment, an organic solvent can be added to the solid content obtained by the centrifugal separation treatment and redispersed. As the organic solvent, the organic solvent can be used.
The redispersion treatment aims to crush and stabilize the pigment aggregate. As the pigment is atomized, the surface area and surface energy increase, and the pigment starts to reagglomerate in an attempt to reduce the surface energy, so that the pigment is further crushed and the pigment particles are stabilized. It is preferable to perform redispersion processing.
The redispersion method is not particularly limited, and the redispersion method can be mixed and dispersed using a dispersing machine such as the paint shaker or the high-pressure homogenizer.
Further, it can be redispersed using an ultrasonic homogenizer or the like.
Examples of commercially available high-power ultrasonic homogenizers include SILENTSON UT-204 manufactured by Sharp Corporation, ultrasonic homogenizers US-300T manufactured by Nippon Seiki Seisakusho, US-1200T, RUS-1200T, MUS-1200T, An ultrasonic processor UIP series manufactured by Heelscher is listed. Using these ultrasonic irradiation apparatuses, it is possible to finely disperse preferably at a frequency of 25 kHz or less.
Examples of the ultrasonic irradiation method include a batch method in which stirring means such as an agitator, a magnetic stirrer, and a disper are used in combination, and a flow method in which the dispersion is sent at a constant flow rate in a chamber equipped with an ultrasonic irradiation unit. An ultrasonic homogenizer may be used in combination with the above-described paint shaker, high-pressure homogenizer, or the like.
High-quality pigment in which the amount of pigment dispersant not adsorbed on the pigment is reduced by redispersing the premixture obtained by adding the organic solvent to the solid content obtained by centrifugal separation in this step by ultrasonic irradiation treatment, etc. A dispersion can be produced efficiently.

(Filtration treatment)
The filtration method is not particularly limited, but one or more types of filtration selected from microfiltration membranes (MF membranes), ultrafiltration membranes (UF membranes), reverse osmosis membranes (RO membranes), and nanofiltration (NF) membranes. A filtration method using a membrane is preferred. By this filtration treatment, the pigment particles and the pigment dispersant adsorbed thereto are left in the pigment dispersion (mother liquor), and at least a part of the pigment dispersant not adsorbed on the pigment can be separated and removed from the mother liquor.
There are no particular restrictions on the filtration method, and either a full-volume filtration method or a cross-flow filtration method may be used, but from the viewpoint of preventing the suspended substances in the supplied pigment dispersion from depositing on the membrane surface, etc. The method is preferred.
As the pore size of the filtration membrane to be used, pore size regions such as microfiltration membranes, ultrafiltration membranes, reverse osmosis membranes, and nanofiltration membranes can be used. The pore diameter of the filtration membrane is preferably 1 to 50 nm, more preferably 2 to 30 nm, and still more preferably 3 to 20 nm.
The filtration membrane used is not particularly limited as long as it does not deteriorate due to the organic solvent. For example, cellulose film, 304 and 316 stainless steel film, bleached cotton film, polysulfone (PS) film, polypropylene (PP) film, polyethersulfone (PES) film, polyethylene terephthalate (PET) film, polyvinylidene fluoride (PVDF) A filtration membrane made mainly of various materials such as a membrane, a polytetrafluoroethylene (PTFE) membrane, and a ceramic membrane can be used.
Examples of the filter membrane type include a depth type (thickness filtration type) that traps foreign matters inside the filter medium, and a surface type (surface filtration type) that traps foreign substances on the surface of the filter medium.
Filtration treatment is performed under pressure or reduced pressure. The shape of the membrane includes a hollow fiber type, a tube type, a flat plate type, a monolith type, and the like. As a method of flowing the dispersion, an internal pressure filtration method or an external pressure filtration method is used. The method may be used.
As the filtration treatment, a cross flow filtration method using an ultrafiltration membrane is more preferable. Further, a diafiltration method that performs filtration while adding an organic solvent is also preferable.

  In step (2), at least a part of the pigment dispersant not adsorbed on the pigment is removed, but the amount of the pigment dispersant not adsorbed on the organic pigment in the pigment dispersion depends on the storage stability and the cured film obtained. From the viewpoint of obtaining a pigment dispersion for a color filter excellent in contrast, it is preferably 2% by weight or less, more preferably 1.5% by weight or less, still more preferably 1% by weight or less, and ideally an unadsorbed pigment. Preferably no dispersant is present.

[Pigment dispersion for color filter]
The pigment dispersion for a color filter obtained by the production method of the present invention includes a pigment dispersant that is the graft polymer, a diketopyrrolopyrrole pigment, and an organic solvent represented by the formula (1).
The proportion of the diketopyrrolopyrrole pigment in the pigment dispersion is preferably 3% by weight or more from the viewpoint of obtaining good colorability, and preferably 3 to 30% by weight from the viewpoint of obtaining good colorability and viscosity. -20% by weight is more preferred.
The weight ratio of the pigment dispersant to the pigment in the pigment dispersion [pigment dispersant / pigment] is 0.2 to 1.5, preferably 0.3 to 1.2, from the viewpoint of improving contrast. .4 to 1.0 is more preferable.
The content of the organic solvent in the pigment dispersion is preferably 20 to 90% by weight, and more preferably 40 to 85% by weight from the viewpoint of good colorability and low viscosity of the dispersion.

The volume median particle size (D50) of the organic pigment in the pigment dispersion is preferably 80 nm or less, more preferably 20 to 70 nm, and still more preferably 20 to 60 nm in order to obtain a good contrast as a color filter color material. .
The volume median particle size (D50) means a particle size at which the cumulative volume frequency calculated by the volume fraction becomes 50% by accumulation from the small particle size side. The volume median particle size (D50) was determined by diluting the pigment dispersion immediately after production with propylene glycol monomethyl ether acetate (PGMEA) 300 times, and using a particle size analyzer (ZETASIZER Nano-ZS, manufactured by Sysmex Corporation). As the measurement conditions, for example, in the case of a diketopyrrolopyrrole pigment, pigment particle refractive index: 1.51, pigment density: 1.45 g / cm ³ , PGMEA refractive index: 1.400, PGMEA viscosity: 1.3 cps are input. And it can measure at 20 degreeC.
The viscosity (20 ° C.) at a solid content of 12% by weight of the pigment dispersion obtained by the production method of the present invention is preferably 1 to 200 mPa · s, and preferably 1 to 100 mPa · s in order to obtain a favorable viscosity as a color material for a color filter. -S is more preferable.

[Coloring composition for color filter]
The coloring composition for a color filter of the present invention contains the pigment dispersion for a color filter obtained by the above production method, and is represented by a graft polymer that is a pigment dispersant, a diketopyrrolopyrrole pigment, and the formula (1). In addition to the organic solvent, a binder component or the like can be contained.
Examples of the binder component include a binder component containing an ionizing radiation curable component.
The binder component containing an ionizing radiation curable component contains an alkali-soluble resin, a polyfunctional monomer, a photopolymerization initiator activated by ionizing radiation, and further a polyfunctional oligomer, a monofunctional monomer, a sensitizer, etc. Can be blended.
The content of the binder component in the colored composition comprising the ionizing radiation curable component is preferably 20 to 80% by weight in the effective component excluding the solvent, and the content of the photopolymerization initiator is in the effective component excluding the solvent. 0.2 to 20% by weight is preferred.

  As the alkali-soluble resin, those generally used for negative resists can be used, and those having solubility in an alkaline aqueous solution, that is, 1 wt.% At 20 ° C. in a 0.05 wt% tetramethylammonium hydroxide aqueous solution. % Is not particularly limited as long as it can dissolve at least%. For example, methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, n-butyl (meth) acrylate, sec-butyl (meth) acrylate, isobutyl (meth) acrylate, tert-butyl (meth) acrylate, n-pentyl (meth) acrylate, n-hexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, n-octyl (meth) acrylate, n-decyl (meth) acrylate, benzyl ( One or more selected from (meth) acrylate, styrene, γ-methylstyrene, N-vinyl-2-pyrrolidone, glycidyl (meth) acrylate, and the like, (meth) acrylic acid, itaconic acid, crotonic acid, maleic acid, Fumaric acid, vinyl vinegar Copolymers consisting of one or more selected from among these anhydrides, polymers obtained by adding an ethylenically unsaturated compound, and the like, further having a glycidyl group or a hydroxyl group in the copolymer. Among these, a polymer having an ethylenically unsaturated bond obtained by adding an ethylenically unsaturated compound having a glycidyl group or a hydroxyl group to a copolymer is polymerized with a polyfunctional monomer described later at the time of exposure. This is particularly suitable in that the colored layer becomes more stable.

In addition, the alkali-soluble resin is preferably a copolymer of (meth) acrylic acid ester and (meth) acrylic acid from the viewpoint of maintaining the dispersion of the pigment in the cured film and improving the contrast. A copolymer of methyl acrylate or benzyl (meth) acrylate and (meth) acrylic acid is more preferred, and a copolymer of benzyl (meth) acrylate and (meth) acrylic acid is more preferred. This is because the isopropyl methacrylate part contained in the side chain of the graft polymer, which is a pigment dispersant, has a high affinity with (meth) acrylic acid ester and can maintain the dispersion of the pigment even when an alkali-soluble resin is blended. Because it is. The copolymerization ratio (molar ratio) of (meth) acrylic acid ester and (meth) acrylic acid is preferably 97/3 to 50/50, and more preferably 95/5 to 70/30.
The weight average molecular weight of the alkali-soluble resin is preferably 5,000 to 50,000.

As polyfunctional monomers, (meth) acrylic acid esters (for example, dipentaerythritol hexaacrylate) having two or more ethylenically unsaturated double bonds, urethane (meth) acrylates, (meth) acrylic acid amides, allyl compounds And vinyl esters. The content of the polyfunctional monomer in the pigment dispersion of the present invention is preferably 10 to 60% by weight in the effective component excluding the solvent.
Examples of the photopolymerization initiator include aromatic ketones, lophine dimers, benzoin, benzoin ethers, polyhalogens and the like. For example, a combination of 4,4′-bis (diethylamino) benzophenone and 2- (o-chlorophenyl) -4,5-diphenylimidazole dimer, 4- [pN, N-di (ethoxycarbonylmethyl) -2, 6-di (trichloromethyl) -s-triazine], 2-methyl-4 ′-(methylthio) -2-morpholinopropiophenone is preferred.
The above-mentioned alkali-soluble resins, polyfunctional monomers, photopolymerization initiators, polyfunctional oligomers, monofunctional monomers, additives such as sensitizers, and the like can be used alone or in combination of two or more. .

  In the following production examples, examples and comparative examples, “parts” and “%” are “parts by weight” and “% by weight” unless otherwise specified. The molecular weight of the graft polymer, the epoxy value, the acid value, and the contrast of the cured film were evaluated by the following methods.

(1) Measurement of number average molecular weight and weight average molecular weight of graft polymer, etc. Eluent obtained by dissolving phosphoric acid and lithium bromide in N, N-dimethylformamide so as to have concentrations of 60 mmol / L and 50 mmol / L, respectively. N, N-dimethylformamide in a gel chromatography method [GPC apparatus (HLC-8120GPC) manufactured by Tosoh Corporation, column (TSK-GEL, α-M × 2), manufactured by Tosoh Corporation, flow rate: 1 mL / min] 0.1 ml of a polymer solution diluted to 0.3 wt% was injected and measured. Polystyrene was used as a standard substance.

(2) Measurement of epoxy value at the time of production of graft polymer This refers to a value obtained by adding hydrochloric acid to a polymer solution and expressing the amount consumed by chlorohydrin in mg of potassium hydroxide.
(3) Measurement of acid value of graft polymer It was measured according to JIS K0070.

(4) Evaluation of contrast (measurement of contrast ratio of cured film)
Pigment dispersions obtained in Examples and Comparative Examples, dipentaerythritol hexaacrylate (polyfunctional monomer: Nippon Kayaku Co., Ltd., DPHA), 2-methyl-4 ′-(methylthio) -2-morpholinopropiophenone (Photopolymerization initiator: Wako Pure Chemical Industries, Ltd.) 0.035 parts and PGMEA 0.474 parts were mixed until uniform to obtain a colored composition. The pigment, graft polymer, and DPHA were blended so as to satisfy the following formula.
Pigment / (graft polymer + DPHA) = 0.45
The obtained colored composition was applied onto a glass substrate with a spin coater, then allowed to stand for 6 minutes on a horizontal base, and dried on a hot plate at 80 ° C. for 3 minutes. Subsequently, 60 mJ / cm < ² > of ultraviolet rays were irradiated to the obtained coating film using the ultraviolet fiber spot irradiation apparatus (Mortex Co., Ltd. make, MUV-202U), and the cured film was obtained. The contrast ratio of the cured film was measured with a contrast ratio measuring instrument (CT-1 manufactured by Aisaka Electric Co., Ltd.). Then, post-baking was performed for 90 minutes at 230 degreeC using oven (the product made by ADVANTEC, DRC433FA). After the post-baking, the contrast ratio of the cured film was measured again.
The larger the contrast ratio value, the better the contrast.

Synthesis Example 1 (Main chain: Synthesis of poly (glycidyl methacrylate, 2-hydroxyethyl methacrylate, N-vinylpyrrolidone) (a1))
15. N-vinyl-2-pyrrolidone (hereinafter referred to as “VP”) 100 g, glycidyl methacrylate (hereinafter referred to as “GMA”) in a separable flask equipped with a reflux condenser, a thermometer, a nitrogen introduction tube and a stirring device. 2 g, 2-hydroxyethyl methacrylate (hereinafter referred to as “HEMA”) 24.0 g, mercaptoethanol (hereinafter referred to as “ME”) 3.0 g, and ethanol 194.7 g were charged, and nitrogen substitution was performed. While stirring at 77 ° C., 2,2′-azobis (2,4-dimethylvaleronitrile) (manufactured by Wako Pure Chemical Industries, Ltd., product name: V-65) in 25.1 g of ethanol. A solution in which 3.9 g) was dissolved was added.
While stirring at 77 ° C., a solution in which VP 150.0 g, GMA 76.2 g, HEMA 120.2 g, V-65 6.4 g, ethanol 445.3 g, and ME 6.7 g were mixed dropwise over 90 minutes. .
Next, a solution in which 96.1 g of VP, 60.9 g of GMA, 96.1 g of HEMA, 2.6 g of V-65, 167 g of ethanol, and 3.1 g of ME were added dropwise over 3 hours. After stirring for 1 hour, a solution in which 0.6 g of V-65 was dissolved in 19.2 g of ethanol was added. After further stirring for 1 hour, a solution prepared by dissolving 0.6 g of V-65 in 19.2 g of ethanol was added. After further stirring for 1 hour, the mixture was cooled and poly (glycidyl methacrylate / 2-hydroxyethyl methacrylate / N-vinylpyrrolidone) (a1) (content of structural unit derived from 2-hydroxyethyl methacrylate 32.5%, An ethanol solution having a content of structural units derived from N-vinylpyrrolidone of 46.9%) was obtained.
The number average molecular weight of (a1) was 3600, the weight average molecular weight was 13900, the epoxy value was 84 mgKOH / g, and the solid content of the solution was 43.3%.

Synthesis Example 2 (Side Chain: Synthesis of Single Terminal Carboxylic Acid Type Polyisopropyl Methacrylate (b1))
In a separable flask equipped with a reflux condenser, a thermometer, a nitrogen inlet tube and a stirrer, 100 g of isopropyl methacrylate (hereinafter referred to as “i-PrMA”), 3-mercaptopropionic acid (chain transfer agent, hereinafter referred to as “MPA”). )) And 5.3 g of propylene glycol monomethyl ether acetate (hereinafter referred to as “PGMEA”), and after purging with nitrogen, stirring at 78 ° C., i-PrMA 400 g, MPA 21.2 g, PGMEA 200 g, V A mixture of -65 and 4 g was added dropwise over 3 hours. Thereafter, the mixture was stirred for 1 hour, heated to 82 ° C., a mixed solution in which 4 g of V-65, 2 g of MPA, and 200 g of PGMEA were added, and stirred for 2 hours. After cooling, a PGMEA solution of one-terminal carboxylic acid type polyisopropyl methacrylate (b1) was obtained. The number average molecular weight was 2000, the weight average molecular weight was 3400, the acid value was 29.9 mgKOH / g, and the solid content of the solution was 52.7%.

Synthesis Example 3 (Side Chain: Synthesis of Single-Terminated Carboxylic Acid Type Polymethyl Methacrylate (b2))
A PGMEA solution of one-terminal carboxylic acid type polymethyl methacrylate (b2) in the same manner as in Synthesis Example 2 except that methyl methacrylate (hereinafter referred to as “MMA”) is used instead of i-PrMA in Synthesis Example 2. Got. The number average molecular weight of the obtained polymer was 1,800, the weight average molecular weight was 3,200, the acid value was 38.1 mgKOH / g, and the solid content of the solution was 53.8%.

Synthesis Example 4 (Side Chain: Synthesis of Single-Terminated Carboxylic Acid Type Poly (n-butyl methacrylate) (b3))
One-terminal carboxylic acid-type poly (n-butyl methacrylate) was synthesized in the same manner as in Synthesis Example 2 except that in Synthesis Example 2, it was changed to n-butyl methacrylate (hereinafter referred to as “n-BMA”) instead of i-PrMA. A PGMEA solution of (b3) was obtained. The number average molecular weight of the obtained polymer was 2100, the weight average molecular weight was 3800, the acid value was 30.0 mgKOH / g, and the solid content of the solution was 53.0%.

Production Example 1 (Production of Graft Polymer (A-1) by Coupling Reaction of Epoxy Group and Carboxylic Acid)
In a separable flask equipped with a reflux condenser, a thermometer, and a stirrer, 100 g of the solution (a1) obtained in Synthesis Example 1 (solid content 43.3 g) and 167 of the solution (b1) obtained in Synthesis Example 2 were obtained. 0.0 g (solid content 88.0 g), PGMEA 43.3 g, and tetrabutylammonium bromide (catalyst, hereinafter referred to as “TBAB”) 3.3 g were charged and stirred at 85 ° C. for 3 hours. The reaction rate was 98%.
After cooling, ethanol was removed with an evaporator (bath temperature 63 ° C., pressure 92 kPa) to obtain a PGMEA solution of graft polymer (A-1 ′).
In order to remove the low molecular weight component in the graft polymer, the obtained (A-1 ′) was dissolved with acetone so as to become a 10% solution, and 10% of the graft polymer was added to a 5 L polybeaker containing 4.5 L of hexane. The solution was added dropwise over 2 hours. After completion of dropping, the mixture was allowed to stand for 30 minutes, and then suction filtered with a filtration device. What could not be filtered was collected and dissolved again with acetone to a 10% solution. Thereafter, a 10% solution of (A-1 ′) was dropped into a 5 L polybeaker containing 4.5 L of distilled water over 2 hours. After completion of dropping, the mixture was allowed to stand for 30 minutes, and then suction filtered with a filtration device. The material that could not be filtered was recovered, dissolved in PGMEA, and the evaporator (bath temperature 63 ° C., pressure 92 kPa) was used to remove acetone and water, and the graft polymer obtained by the coupling reaction of epoxy group and carboxylic acid ( A-1) (Content of structural unit derived from isopropyl methacrylate in side chain: 100%, Content of structural unit derived from 2-hydroxyethyl methacrylate in polymer: 10.7%, Configuration derived from N-vinylpyrrolidone A unit content of 15.4% by weight) was obtained. The number average molecular weight of the polymer (A-1) was 14,000, the weight average molecular weight was 69000, and the solid content of the polymer solution was 33%.

Production Example 2 (Production of Graft Polymer (A-2))
In Production Example 1, graft polymer (A-2) was prepared in the same manner as in Production Example 1 except that (b1) the amount of solution added was 139.7 g (solid content: 73.6 g) and the amount of TBAB added was changed to 1.4 g. (Content of structural unit derived from isopropyl methacrylate in side chain: content of structural unit derived from 2-hydroxyethyl methacrylate in polymer: 12.0%, content of structural unit derived from N-vinylpyrrolidone 17.4% by weight). In addition, solid content of the obtained polymer (A-2) solution was 32%.
Production Example 3 (Production of Graft Polymer (A-3))
In Production Example 1, graft polymer (A-3) was prepared in the same manner as in Production Example 1 except that (b1) the solution addition amount was 100.3 g (solid content 52.9 g) and the TBAB addition amount was 1.1 g. (Content of structural unit derived from isopropyl methacrylate in side chain: content of structural unit derived from 2-hydroxyethyl methacrylate in polymer: 14.6%, content of structural unit derived from N-vinylpyrrolidone 21.2% by weight). In addition, solid content of the obtained polymer (A-3) solution was 22%.

Production Example 4 (Production of Graft Polymer (A-4))
In Production Example 1, purified graft polymer (A-4) was prepared in the same manner as in Production Example 1 except that (b1) the amount of solution added was 202.0 g (solid content 106.5 g) and the amount of TBAB added was 4.0 g. ) In addition, solid content of the obtained polymer (A-4) solution was 28%.
Production Example 5 (Production of graft polymer (B))
In Production Example 1, instead of the solution (b1) obtained in Synthesis Example 2, the solution (b2) obtained in Synthesis Example 3 (136.8 g (solid content: 73.6 g)) and the TBAB addition amount were changed to 4.0 g. A graft polymer (B) was obtained in the same manner as in Production Example 1 except that. In addition, solid content of the obtained polymer (B) solution was 28%.
Production Example 6 (Production of graft polymer (C))
In Production Example 1, the procedure was the same as Production Example 1 except that the solution (b2) obtained in Synthesis Example 3 was replaced with 163.6 g (solid content 88.0 g) instead of the solution (b1) obtained in Synthesis Example 2. Thus, a graft polymer (C) was obtained. In addition, solid content of the obtained polymer (C) solution was 27%.
Production Example 7 (Production of graft polymer (D))
In Production Example 1, the same procedure as in Production Example 1 was conducted except that the solution (b3) obtained in Synthesis Example 4 was replaced with 138.9 g (solid content: 73.6 g) instead of the solution (b1) obtained in Synthesis Example 2. Thus, a graft polymer (D) was obtained. In addition, solid content of the obtained polymer (D) solution was 30%.

Example 1 (Preparation of pigment dispersion (1))
(Step (1): Production of pigment dispersion)
89.5 g of PGMEA, 45.5 g of the graft polymer (A-1) solution obtained in Production Example 1 (effective amount 15 g), diketopyrrolopyrrole pigment (manufactured by BASF Corporation, CI Pigment Red 254, trade name “ IRGAPHOR RED BK-CF ”, average primary particle size 30 nm (catalog value) 15.0 g, and further 0.3 mmφ zirconia beads 300 g were put in a 500 ml plastic container and stirred at 25-30 ° C. for 3 hours in a paint shaker. The zirconia beads were removed to obtain a preliminary dispersion.
Next, 100 g of this preliminary dispersion and 200 g of 0.05φ zirconia beads were placed in a 250 ml plastic container and stirred for 24 hours at 25 to 30 ° C. with a paint shaker to remove the zirconia beads, thereby obtaining a pigment dispersion.
(Step (2): Removal of graft polymer (A-1) [pigment dispersant]) not adsorbed to the pigment)
40 g of the obtained pigment dispersion was diluted with 80 g of PGMEA and centrifuged for 12 hours under the conditions of 26323 G using a centrifuge (manufactured by Hitachi Koki Co., Ltd., Himac CP56G). Got.
31 g of PGMEA is added to 9 g of the obtained sediment, and redispersion treatment is performed by ultrasonic irradiation using an ultrasonic cleaner (manufactured by Sharp Corporation, SILENTSONIC UT-204) to obtain a pigment dispersion (1). It was.
The evaluation results of the obtained pigment dispersion (1) are shown in Table 1.

Examples 2-3 and Comparative Examples 1-4 (Preparation of pigment dispersions (2)-(7))
In Example 1, instead of the graft polymer (A-1) solution and 89.5 g of PGMEA, in Example 2, the graft polymer (A-2) solution 46.9 g (effective amount 15 g) and PGMEA 88.1 g, Examples 3 was 68.2 g (effective portion 15 g) of the graft polymer (A-3) solution and 66.8 g of PGMEA, and Comparative Example 1 was 53.6 g (effective portion 15 g) of the graft polymer (A-4) solution and 81.4 g of PGMEA. In Comparative Example 2, the graft polymer (B) solution 53.6 g (solid content 15 g) and PGMEA 81.4 g, and in Comparative Example 3, the graft polymer (C) solution 55.6 g (solid content 15 g) and PGMEA 79.4 g, comparative example In Example 4, except for using 50.0 g of the graft polymer (D) solution and 85.0 g of PGMEA, the pigment dispersion ( 2) to (7) were obtained. The evaluation results of the obtained pigment dispersions (2) to (7) are shown in Table 1.

From Table 1, the colored compositions containing the pigment dispersions obtained in Examples 1 to 3 were cured with better contrast than the colored compositions containing the pigment dispersions obtained in Comparative Examples 1 to 4. It can be seen that a film can be formed.
When the contrast is different by about 100 in this evaluation, the amount of light transmitted through the cured film is greatly different, so that the difference in the vividness of the image quality when the liquid crystal display device is obtained can be clearly seen.

Claims (12)

A pigment dispersion for a color filter comprising a diketopyrrolopyrrole pigment, a pigment dispersant, and an organic solvent represented by the following formula (1), wherein the pigment dispersant comprises a structural unit having an amide group in the main chain. And a weight ratio [main chain / side chain] of the main chain to the side chain in the graft polymer is 30/70 to 49/51. A pigment dispersion for a color filter.

(Wherein R ¹ and R ² each independently represents a hydrogen atom or a hydrocarbon group having 1 to 5 carbon atoms, R ³ represents a hydrogen atom or a methyl group, n represents an average number of added moles, 1 to 4)   The pigment dispersion for a color filter according to claim 1, wherein the graft polymer has a weight-average molecular weight in terms of polystyrene of 40,000 to 80,000.   The pigment dispersion for a color filter according to claim 1 or 2, wherein the side chain polymer of the graft polymer has a polystyrene-equivalent weight average molecular weight of 1,500 to 30,000.   The pigment dispersion for a color filter according to any one of claims 1 to 3, wherein the graft polymer has a hydroxyl group.   The pigment dispersion for a color filter according to any one of claims 1 to 4, wherein the organic solvent represented by the formula (1) is propylene glycol monomethyl ether acetate.   The pigment dispersion for a color filter according to any one of claims 1 to 5, wherein the structural unit having an amide group is derived from vinylpyrrolidone.   The graft polymer is obtained by a coupling reaction between a polymer containing a structural unit having an amide group and a polymer containing a structural unit derived from isopropyl methacrylate. Pigment dispersion for color filters.   The coloring composition for color filters containing the pigment dispersion in any one of Claims 1-7.   Furthermore, the coloring composition for color filters of Claim 8 containing alkali-soluble resin which is a copolymer of (meth) acrylic acid ester and (meth) acrylic acid.   A pigment dispersant, a diketopyrrolopyrrole pigment, which is a graft polymer containing a structural unit having an amide group in the main chain and a structural unit derived from isopropyl methacrylate in the side chain, and an organic compound represented by the formula (1) The manufacturing method of the pigment dispersion in any one of Claims 1-9 which has the process (1) which disperse | distributes the mixture containing a solvent and obtains a pigment dispersion (1).   The method includes a step (2) of obtaining at least a part of the pigment dispersant not adsorbed to the pigment to obtain the pigment dispersion (2) from the pigment dispersion (1) obtained in the step (1). 10. A method for producing a color filter pigment dispersion as described in 10.   The coloring composition for color filters containing the pigment dispersion obtained by the method of Claim 10 or 11.