JP2011255522A - Resin for thermal transfer image-receiving sheet - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a resin for a thermal transfer image-receiving sheet, providing the thermal transfer image-receiving sheet having excellent dyeing properties and mold releasability, and to provide the thermal transfer image-receiving sheet including a dye receiving layer containing the same.SOLUTION: The resin for the thermal transfer image-receiving sheet contains a graft polymer composed of a main chain segment (A1) formed of a polyester resin and a side chain segment (A2) formed of an addition polymerization-based resin. The segment (A1) is a polyester resin obtained by condensation-polymerizing an alcohol component containing a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane in an amount of 50 mol% or above, and a carboxylic acid component containing a dodecenylsuccinic compound in an amount of 5-40 mol%.

Description

  The present invention relates to a resin for a thermal transfer image receiving sheet, a thermal transfer image receiving sheet having a dye receiving layer containing the resin, and a method for producing the resin for a thermal transfer image receiving sheet.

  There has been proposed a method of forming a color image on a thermal transfer image-receiving sheet that can be dyed with a sublimation dye, using a sublimation dye as a recording agent and a thermal transfer sheet carried on a substrate. In this method, a thermal head of a printer is used as a heating means, and a dye is transferred to an image receiving sheet by heating to obtain a color image. The image formed in this way is very clear because it uses a dye, and is excellent in transparency. Therefore, it is excellent in reproducibility of intermediate colors and gradation, and a high-quality image can be expected. Therefore, in order to exhibit these performances, a thermal transfer image receiving sheet using a polyester resin has been developed.

Patent Document 1 discloses a dye receiving layer containing a graft polymer comprising an unsaturated copolyester as a trunk and a vinyl copolymer as a branch for the purpose of improving color density, sharpness, image stability, and adhesion to a dye supply material. And a dye-receiving material for thermal sublimation printing comprising a substrate and a support.
In Patent Document 2, alkyl succinic acid and / or alkenyl succinic acid is 5 to 40 mol% and aromatic carboxylic acid is 50 to 90 mol% for the purpose of improving dyeing property and releasability from a transfer sheet. Transfer image receiving using a polyester obtained by condensation polymerization of a carboxylic acid component containing styrene and an alcohol component containing 80 mol% or more of an alkylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane A sheet is disclosed.

JP-A-4-318989 JP 2009-280765 A

Since the printing is performed by coloring the dye from the ink sheet to the thermal transfer image receiving sheet by heating from the thermal head, a high dye dyeing property is required to express the target color. It is said. In addition, there is a problem in that during the coloring, the ink sheet and the thermal transfer image receiving sheet are likely to be fused by heating. Therefore, there is a demand for a thermal transfer image-receiving sheet excellent in high dyeing property and releasability that suppresses fusion with an ink sheet. From the viewpoint of achieving both the dyeability and the releasability, the thermal transfer image receiving sheets described in Patent Documents 1 and 2 still have room for improvement.
The present invention relates to a thermal transfer image-receiving sheet resin capable of providing a thermal transfer image-receiving sheet excellent in dyeability and releasability, a thermal transfer image-receiving sheet having a dye-receiving layer containing the resin, and the production of the thermal transfer image-receiving sheet resin It is an object to provide a method.

The present inventors have considered that the factor affecting the dyeing property and the release property is the state of the dye-receiving layer when heated by the thermal head. As a result, it has been found that dyeing property and releasability can be improved by using a resin containing a segment made of a specific polyester resin and a segment made of an addition polymerization resin for the dye-receiving layer.
That is, the present invention provides the following [1] to [3].
[1] A thermal transfer image-receiving sheet resin comprising a graft polymer composed of a main chain segment (A1) made of a polyester resin and a side chain segment (A2) made of an addition polymerization resin, wherein the segment (A1) is Polyester resin obtained by condensation polymerization of an alcohol component containing 50 mol% or more of a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane and a carboxylic acid component containing 5 to 40 mol% of a dodecenyl succinic acid compound A resin for thermal transfer image receiving sheet.
[2] A thermal transfer image receiving sheet having a dye receiving layer containing the resin for thermal transfer image receiving sheet of [1].
[3] Step (1): an alcohol component containing 50 mol% or more of an alkylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane, 5 to 40 mol% of dodecenyl succinic acid compound, and 5 to 5 of fumaric acid. A step of mixing a polyester resin (a1) obtained by condensation polymerization with a carboxylic acid component containing 30 mol% with an aqueous medium to obtain an aqueous dispersion of the polyester resin (a1); and step (2): step (1) A method for producing a resin for a thermal transfer image receiving sheet, comprising the step of adding an addition-polymerizable monomer (a2) having an aromatic group to the aqueous dispersion obtained in (1) to obtain an aqueous dispersion of a graft polymer.

  The resin for a thermal transfer image receiving sheet of the present invention can provide a thermal transfer image receiving sheet excellent in dyeability and releasability. In addition, the thermal transfer image-receiving sheet having a dye-receiving layer containing the resin can form an image with a high color density in order to achieve both excellent dyeing property and releasability, and heat with the ink sheet at the time of printing. Fusing is difficult to occur.

[Resin for thermal transfer image-receiving sheet]
The resin for thermal transfer image receiving sheets of the present invention is a resin for thermal transfer image receiving sheets containing a graft polymer composed of a main chain segment (A1) made of a polyester resin and a side chain segment (A2) made of an addition polymerization resin. The segment (A1) is composed of an alcohol component containing 50 mol% or more of a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane and a carboxylic acid component containing 5 to 40 mol% of a dodecenyl succinic acid compound. It is a polyester resin obtained by polymerization.

The reason why the thermal transfer image-receiving sheet having the resin for thermal transfer image-receiving sheet of the present invention in the dye-receiving layer is excellent in dyeability and releasability is not clear, but is considered as follows.
The raw material monomer of the segment (A1) comprising the polyester resin of the resin for thermal transfer image receiving sheet of the present invention contains a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane as an alcohol component. Since this compound has two aromatic rings in the molecule, that is, a structure similar to a dye, it has a high affinity with the dye, contributes to the improvement of the dyeing property of the thermal transfer image-receiving sheet, and has a rigid structure. Therefore, it is considered that the resin becomes hard and contributes to the improvement of the releasability of the thermal transfer image receiving sheet.
Further, the segment (A2) made of an addition polymerization resin is considered to contribute to the improvement of the releasability of the thermal transfer image receiving sheet because it has poor affinity with the ink sheet.
Furthermore, by using a dodecenyl succinic acid compound as a raw material monomer of the segment (A1), the segment (A1) having a rigid structure such as a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane is partially obtained. The film can be made flexible and the film forming property can be improved. As a result, it is considered that the releasability is greatly improved, the dye is easily penetrated by flexibility, and the dyeing property can be greatly improved.

  The resin for thermal transfer image-receiving sheets of the present invention contains a graft polymer comprising a main chain segment (A1) made of the above-described polyester resin and a side chain segment (A2) made of an addition polymerization resin. The content of the graft polymer in the resin for thermal transfer image-receiving sheets of the present invention is preferably 80 to 100 mol%, more preferably 90 to 100 mol%, from the viewpoint of improving dyeability and releasability of the thermal transfer image-receiving sheet. More preferably, it is substantially 100 mol%.

(Polyester resin segment (A1))
The segment (A1) constituting the graft polymer contained in the thermal transfer image-receiving sheet resin of the present invention comprises an alcohol component containing 50 mol% or more of a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane, It is a segment made of a polyester resin obtained by condensation polymerization with a carboxylic acid component containing 5 to 40 mol% of a dodecenyl succinic acid compound. The segment (A1) is a main chain in the graft polymer contained in the thermal transfer image-receiving sheet resin of the present invention.

Specifically, the propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane is preferably a compound represented by the following general formula (I).

In the general formula (I), R ¹ O and R ² O are both oxypropylene groups.
x and y correspond to the added mole number of propylene oxide, and are positive numbers. Furthermore, from the viewpoint of reactivity with the carboxylic acid component, the average value of the sum of x and y is preferably 2 to 7, more preferably 2 to 5, and still more preferably 2 to 3.

  The propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane is contained in the alcohol component in an amount of 50 mol% or more, preferably 70, from the viewpoint of improving the dyeability and releasability of the thermal transfer image-receiving sheet. More than mol%, more preferably more than 80 mol%, still more preferably substantially 100 mol%. In the present invention, the propylene oxide adduct means the whole structure in which an oxypropylene group is added to 2,2-bis (4-hydroxyphenyl) propane.

The alcohol component which is a raw material monomer of the segment (A1) can contain other alcohol components together with the propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane.
Specifically, as a raw material monomer derived from the structural unit of segment (A1) (hereinafter, also simply referred to as “raw material monomer of segment (A1)”), an alcohol having a non-aromatic carbon-carbon unsaturated bond For example, unsaturated fatty alcohols can also be used. In the graft polymer contained in the resin for thermal transfer sheets, the carbon-carbon unsaturated bond portion can be a bond portion with the segment (A2). In this case, the unsaturated bond is a saturated bond and Become. Examples of the alcohol having a non-aromatic carbon-carbon unsaturated bond (unsaturated aliphatic alcohol) include allyl alcohol.
Other alcohol components include polyhydric alcohols having two or more hydroxyl groups, such as ethylene glycol, propylene glycol (1,2-propanediol), glycerin, pentaerythritol, trimethylolpropane, 2,2-bis. (4-Hydroxyphenyl) propane, hydrogenated bisphenol A, sorbitol, or their alkylene (2 to 4 carbon) oxide adduct (average number of added moles 1 to 16). Among these, other than propylene oxide adducts of 2,2-bis (4-hydroxyphenyl) propane, alkylene oxide adducts of 2,2-bis (4-hydroxyphenyl) propane can be preferably used, and ethylene oxide addition More preferred. In addition, you may use these alcohol components individually or in combination of 2 or more types.

式中、Ｒ³は、水素原子、炭素数１〜４の炭化水素基であって、同一でも異なってもよい。炭素数１〜４の炭化水素基としては、炭素数１〜４のアルキル基が好ましい。
なかでも染着性及び離型性の向上の観点から、該無水物が好ましく、具体的には前記式（II）で表される化合物が更に好ましい。 Since the segment (A1) is a polyester resin, a carboxylic acid component is used as a raw material monomer in addition to the alcohol component.
In this invention, 5-40 mol% of dodecenyl succinic acid compounds are included as a carboxylic acid component. The “dodecenyl succinic acid compound” in the present invention means dodecenyl succinic acid, and anhydrides and alkyl esters of dodecenyl succinic acid. Dodecenyl succinic acid is a succinic acid substituted with an alkenyl group having 12 carbon atoms, and an anhydride and an alkyl ester of dodecenyl succinic acid can also be used as the carboxylic acid component of the present invention. Specifically, the dodecenyl succinic acid compound used in the present invention is preferably a compound represented by the following formula (II) or (III).

In formula, R < ³ > is a hydrogen atom and a C1-C4 hydrocarbon group, Comprising: You may be same or different. As a C1-C4 hydrocarbon group, a C1-C4 alkyl group is preferable.
Among these, from the viewpoint of improving dyeability and releasability, the anhydride is preferable, and specifically, the compound represented by the formula (II) is more preferable.

  The dodecenyl succinic acid compound is contained in the carboxylic acid component in an amount of 5% or more, preferably 10 mol% or more, more preferably 20 mol% or more, from the viewpoint of improving the film formability of the thermal transfer image-receiving sheet resin. Further, from the viewpoint of appropriately maintaining the hardness of the resin, the carboxylic acid component contains 40% or less, preferably 35 mol% or less, more preferably 30 mol% or less. From the viewpoint of improving the dyeability and releasability of the thermal transfer image-receiving sheet, the carboxylic acid component contains 5 to 40 mol%, preferably 10 to 35 mol%, more preferably 20 to 30 mol%.

The carboxylic acid component which is a raw material monomer of the segment (A1) can contain a carboxylic acid component other than this together with the dodecenyl succinic acid compound.
It is preferable to use a carboxylic acid having a non-aromatic carbon-carbon unsaturated bond for the carboxylic acid component which is a raw material monomer of the segment (A1). The carbon-carbon unsaturated bond portion is preferably a bond portion with the segment (A2) in the resin for thermal transfer sheets of the present invention. In this case, the unsaturated bond is a saturated bond.

  Examples of the carboxylic acid having a non-aromatic carbon-carbon unsaturated bond include unsaturated aliphatic carboxylic acids such as fumaric acid and maleic acid; unsaturated alicyclic carboxylic acids such as tetrahydrophthalic acid; acrylic acid and methacrylic acid Etc. From the viewpoint of reactivity, fumaric acid, maleic acid and tetrahydrophthalic acid are preferable, and fumaric acid is more preferable.

  In the carboxylic acid component, the content of the carboxylic acid having a non-aromatic carbon-carbon unsaturated bond is preferably 5 to 30 mol%, more preferably 7 to 25 mol%, still more preferably 8 to 15 mol%. It is.

Examples of other carboxylic acids include aromatic dicarboxylic acids such as phthalic acid, isophthalic acid, and terephthalic acid; aliphatic dicarboxylic acids such as adipic acid and succinic acid; and alicyclic dicarboxylic acids such as cyclohexanedicarboxylic acids and decalin dicarboxylic acids. And trivalent or higher polyvalent carboxylic acids such as trimellitic acid and pyromellitic acid, anhydrides of these acids, and alkyl (C1 to C3) esters thereof. From the viewpoint of dyeability of the thermal transfer image-receiving sheet, aromatic dicarboxylic acids and alicyclic dicarboxylic acids are preferable, and aromatic dicarboxylic acids are more preferable. Specifically, isophthalic acid is preferable. Further, from the viewpoint of dyeability of the thermal transfer image receiving sheet, aliphatic dicarboxylic acid is preferable, and succinic acid is more preferable. The said carboxylic acid component may be individual or 2 or more types may be contained.
Of the raw material monomers derived from the structural unit of the main chain segment (A1) made of polyester resin, as the raw material monomer having a non-aromatic carbon-carbon unsaturated bond, unsaturated aliphatic carboxylic acid, unsaturated fat One or more selected from cyclic carboxylic acids and unsaturated aliphatic alcohols may be included, but from the viewpoint of reactivity, it is preferable that a carboxylic acid component is present, and it is more preferable that only a carboxylic acid component is present. More preferably, only the acid is present.

  The main chain segment (A1) made of a polyester resin is preferably a linear polyester from the viewpoint of dyeability of the thermal transfer image receiving sheet. Therefore, it is preferable that the raw material monomer from which the structural unit of the segment (A1) is derived does not substantially contain a trihydric or higher polyhydric alcohol such as glycerin or trimethylolpropane and a trivalent or higher polyvalent carboxylic acid.

From the viewpoint of releasability and storage stability of the thermal transfer image-receiving sheet, the acid value of the segment (A1) is 5 to 40 mgKOH / g, preferably 5 to 35 mgKOH / g, more preferably 5 to 30 mgKOH / g. More preferably, it is 10-20 mgKOH / g. The segment (A1) has an amount of carboxy groups in the above range, and the segment (A1) made of a polyester resin having a rigid structure with poor dispersibility and the segment (A2) made of an addition polymerization resin are uniformly dispersed in the liquid. As a result, it is considered that the surface of the dye receiving layer becomes smooth and contributes to the improvement of dyeing property and releasability.
Moreover, from the viewpoint of film forming properties when used in the dye-receiving layer, the number average molecular weight of the segment (A1) is preferably 1,000 to 10,000, more preferably 2,000 to 8,000.

(Addition polymerization resin segment (A2))
The segment (A2) constituting the graft polymer contained in the thermal transfer image-receiving sheet resin of the present invention is an addition comprising a structural unit derived from an addition polymerizable monomer (a2) (hereinafter also referred to as “monomer (a2)”). It is a polymerization resin segment. The segment (A2) is a side chain in the graft polymer contained in the thermal transfer image-receiving sheet resin of the present invention.
Examples of the addition polymerizable monomer (a2) used in the present invention include styrene, methylstyrene, α-methylstyrene, β-methylstyrene, t-butylstyrene, chlorostyrene, chloromethylstyrene, methoxystyrene, styrenesulfonic acid or the like. Styrenes such as salts; (meth) acrylic acid esters such as alkyl (meth) acrylate (C1-18), benzyl (meth) acrylate, dimethylaminoethyl (meth) acrylate; polyethylene, propylene, butadiene, etc. Olefins such as vinyl chloride; vinyl esters such as vinyl acetate and vinyl propionate; vinyl ethers such as vinyl methyl ether; vinylidene halides such as vinylidene chloride; N-vinyl compounds such as N-vinyl pyrrolidone; Is mentioned.
Among these, styrenes and (meth) acrylic acid esters are preferable, addition polymerizable monomers having an aromatic group are more preferable, and styrene, methylstyrene, benzyl methacrylate, and benzyl acrylate are still more preferable. Among these, styrene is particularly preferable from the viewpoint of the raw material price of the monomer, the releasability of the thermal transfer image-receiving sheet, and the storage stability.
The content of the structural unit derived from the addition-polymerizable monomer having an aromatic group is preferably 70% by weight or more, more preferably 85% by weight in the segment (A2) from the viewpoint of releasability of the thermal transfer image-receiving sheet. More preferably, it is substantially 100% by weight. A segment made of an addition-polymerizable monomer having an aromatic group has low compatibility with the resin, so that the releasability of the thermal transfer image-receiving sheet is improved.

  The weight ratio of the total amount of unsaturated aliphatic carboxylic acid, unsaturated alicyclic carboxylic acid and unsaturated aliphatic alcohol among the raw material monomers of segment (A2) and segment (A1) [segment (A2) / segment ( The total of the above-mentioned components having an unsaturated group of A1) is preferably from 1/1 to 15/1, more preferably from 1/1 to 10/1, from the viewpoint of dyeability and releasability of the thermal transfer image-receiving sheet. Is more preferably 2/1 to 5/1.

The weight ratio [segment (A1) / segment (A2)] of the segment (A1) and the segment (A2) constituting the graft polymer contained in the resin for the thermal transfer image-receiving sheet of the present invention is the dyeing property of the thermal transfer image-receiving sheet. From a viewpoint of improvement, Preferably it is 55 / 45-95 / 5, More preferably, it is 65 / 35-95 / 5, More preferably, it is 75 / 25-95 / 5, More preferably, it is 85 / 15-95 / 5.
It is considered that the presence of more segment (A1) than segment (A2) can sufficiently exhibit the dyeing property derived from the molecular structure of segment (A1) while forming a fine phase separation structure. It is done.

  Further, from the viewpoint of releasability and storage stability of the thermal transfer image receiving sheet, the softening point of the resin for thermal transfer image receiving sheet of the present invention is preferably 80 to 165 ° C. From the same viewpoint, the acid value of the resin is preferably 5 to 40 mgKOH / g, more preferably 5 to 35 mgKOH / g, and still more preferably 10 to 35 mgKOH / g.

[Method for producing resin for thermal transfer image-receiving sheet]
As a method for producing the resin for thermal transfer image-receiving sheets of the present invention, an alcohol component containing 50 mol% or more of propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane and 5 to 40 mol% of dodecenyl succinic acid compound are used. Polyester resin (a1) (hereinafter also referred to as resin (a1)) having a non-aromatic carbon-carbon unsaturated bond is prepared by condensation polymerization with the carboxylic acid component contained, and the polyester resin (a1) A method of addition polymerization of the addition polymerizable monomer (a2) in the presence is preferred.

(Polyester resin (a1))
Resin (a1) is a polycondensation of an alcohol component containing 50 mol% or more of a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane and a carboxylic acid component containing 5 to 40 mol% of a dodecenyl succinic acid compound. It is a polyester resin obtained. The resin (a1) preferably has a non-aromatic carbon-carbon unsaturated bond. The “non-aromatic carbon-carbon unsaturated bond” is derived from the unsaturated aliphatic carboxylic acid, unsaturated alicyclic carboxylic acid, and unsaturated aliphatic alcohol described above.

Resin (a1) has, as a raw material component, an alcohol component containing 50 mol% or more of a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane and a carboxylic acid component containing 5 to 40 mol% of dodecenyl succinic acid compound. Is obtained.
Here, the propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane and the dodecenyl succinic acid compound are the same as the polyester resin segment (A1), and the preferred structure and the preferred content are also the same. is there.

As an alcohol component which is a raw material component of the resin (a1), other alcohol components can be used together with a propylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane. The resin (a1) has a non-aromatic carbon-carbon unsaturated bond, and an alcohol having a non-aromatic carbon-carbon unsaturated bond can be used. Examples of the alcohol having a non-aromatic carbon-carbon unsaturated bond include unsaturated aliphatic alcohols such as allyl alcohol.
Other alcohols are the same as those in the segment (A1) made of the polyester resin. You may use alcohol individually or in combination of 2 or more types.

As the carboxylic acid component which is a raw material component of the resin (a1), other carboxylic acid components can be used together with the dodecenyl succinic acid compound. The resin (a1) has a non-aromatic carbon-carbon unsaturated bond, and a carboxylic acid having a non-aromatic carbon-carbon unsaturated bond is used as a carboxylic acid component as a raw material component of the polyester. It can be preferably used.
The carboxylic acid having a non-aromatic carbon-carbon unsaturated bond is the same as in the case of the polyester resin segment (A1), the preferred structure and the preferred content are the same, and fumaric acid is more preferred. .
In the carboxylic acid component, the content of the carboxylic acid having a non-aromatic carbon-carbon unsaturated bond is preferably 5 to 30 mol%, more preferably 7 to 25 mol%, still more preferably 8 to 15 mol%. It is.
The other carboxylic acid is the same as in the case of the segment (A1) made of the polyester resin, and the same structure and preferable content are the same. Succinic acid and isophthalic acid are preferable, and isophthalic acid is more preferable. Carboxylic acids may be used alone or in combination of two or more.

The polyester resin (a1) is produced, for example, by subjecting the alcohol component and the carboxylic acid component to condensation polymerization at a temperature of 180 to 250 ° C. in an inert gas atmosphere, if necessary, using an esterification catalyst. be able to.
From the viewpoint of releasability of the thermal transfer image-receiving sheet, the polyester preferably has a sharp molecular weight distribution, and is preferably subjected to condensation polymerization using an esterification catalyst. Examples of the esterification catalyst include metal compounds such as tin catalyst, titanium catalyst, antimony trioxide, zinc acetate, and germanium dioxide. From the viewpoint of the reaction efficiency of the esterification reaction in the synthesis of the polyester, a tin catalyst is preferable. As the tin catalyst, dibutyltin oxide, tin dioctylate, salts thereof and the like are preferably used.
In the present invention, since a carboxylic acid having a non-aromatic carbon-carbon unsaturated bond is used, it is preferable to use a radical polymerization inhibitor. As the radical polymerization inhibitor, 4-t-butylcatechol and the like are preferable.

From the viewpoint of releasability and storage stability of the thermal transfer image-receiving sheet, the softening point of the resin (a1) is preferably 70 to 165 ° C, and the glass transition temperature is preferably 35 to 85 ° C. From the viewpoint of releasability and storage stability of the thermal transfer image-receiving sheet, the acid value of the resin (a1) is preferably 5 to 40 mgKOH / g, more preferably 5 to 35 mgKOH / g, still more preferably 5 to 30 mgKOH / g. g, more preferably 10 to 20 mg KOH / g.
The glass transition temperature, softening point, and acid value can all be obtained by appropriately adjusting the type of monomer used, the blending ratio, the temperature of condensation polymerization, and the reaction time.
Moreover, from the viewpoint of film forming properties when used in the dye-receiving layer, the number average molecular weight of the resin (a1) is preferably 1,000 to 10,000, more preferably 2,000 to 8,000.

(Addition polymerizable monomer (a2))
The addition polymerizable monomer (a2) used in the present invention is as described above, and the addition polymerizable monomer having an aromatic group is preferably 55% by weight or more, more preferably 70% by weight or more, more preferably 85% by weight. %, More preferably 90% by weight or more, and still more preferably substantially 100% by weight. The addition polymerizable monomer having an aromatic group is preferably styrene, benzyl methacrylate or benzyl acrylate. Among these, styrene is preferable from the viewpoint of the raw material price of the monomer, the releasability of the thermal transfer image-receiving sheet, and the storage stability.

(Method for producing resin for thermal transfer image receiving sheet)
The resin for thermal transfer image receiving sheets of the present invention can be obtained by a method of polymerizing the addition polymerizable monomer (a2) in the presence of the resin (a1). The polymerization method is not limited, and examples thereof include a method in which the resin (a1) and the monomer (a2) are directly mixed and polymerized, a method in which the resin (a1) and the monomer (a2) are dissolved in an organic solvent, and the like. It is done. The thermal transfer image-receiving sheet resin of the present invention is preferably obtained by a method having the following steps (1) and (2).
Step (1): A step of mixing the polyester resin (a1) with an aqueous medium to obtain an aqueous dispersion of the polyester resin (a1).
Step (2): A step of adding the addition polymerizable monomer (a2) to the aqueous dispersion obtained in the step (1) and polymerizing it to obtain an aqueous dispersion of a resin for a thermal transfer image-receiving sheet.

<Step (1)>
Step (1) is a step of mixing the polyester resin (a1) with an aqueous medium to obtain an aqueous dispersion of the polyester resin (a1).
The aqueous medium in which the polyester resin (a1) is dispersed is a water-based medium, that is, a medium having a water content of 50% by weight or more. From the viewpoint of environmental safety, the content of water in the aqueous medium is preferably 80% by weight or more, more preferably 90% by weight or more, and still more preferably 100% by weight. Components other than water include alcohol solvents such as methanol, ethanol, isopropanol and butanol; ketone solvents such as acetone, methyl ethyl ketone, diethyl ketone, dipropyl ketone, methyl isobutyl ketone and methyl isopropyl ketone; ether solvents such as tetrahydrofuran And an organic solvent that dissolves in water.

As a method of dispersing the polyester resin (a1) in the aqueous medium, the polyester resin (a1) is dissolved in a ketone solvent, a neutralizing agent described later is added to ionize the carboxyl group of the polyester resin (a1), Next, a method of adding water to invert the phase to an aqueous system, preferably a method of adding water and then distilling off the ketone solvent to invert to an aqueous system.
More specifically, for example, a reactor equipped with a stirrer, a reflux condenser, a thermometer, a dropping funnel and a nitrogen gas introduction pipe is prepared, and the neutralizing agent is added to the polyester resin (a1) dissolved in the ketone solvent. Etc. to ionize the carboxyl group (unnecessary if already ionized), then add water and phase invert to aqueous system, preferably add water and then distill away ketone solvent to phase in aqueous system To do.
The dissolving operation of the polyester resin (a1) in the ketone solvent and the subsequent addition of the neutralizing agent are usually performed at a temperature not higher than the boiling point of the ketone solvent. Examples of the water used include deionized water.

  As the ketone solvent, those mentioned above can be used, and methyl ethyl ketone is preferable from the viewpoint of the solubility of the polyester resin (a1) and the ease of distilling off the solvent.

  Examples of the neutralizing agent include aqueous alkaline solutions such as aqueous ammonia and sodium hydroxide; allylamine, isopropylamine, diisopropylamine, ethylamine, diethylamine, triethylamine, 2-ethylhexylamine, tri-n-octylamine, t-butylamine, sec-butylamine, propylamine, methylaminopropylamine, dimethylaminopropylamine, n-propanolamine, butanolamine, 5-amino-4-octanol, monoethanolamine, N, N-dimethylethanolamine, isopropanolamine, neopen Examples include amines such as tanolamine, diglycolamine, ethylenediamine, and piperazine. The amount of the neutralizing agent used may be an amount that can neutralize at least the acid value of the polyester resin (a1).

<Step (2)>
In the step (2), the addition-polymerizable monomer (a2) is added to the aqueous dispersion obtained in the step (1) and polymerized to form an aqueous dispersion of a thermal transfer image-receiving sheet resin (hereinafter referred to as an aqueous dispersion (A). It is a process of obtaining also.
First, the addition polymerizable monomer (a2) is added to the aqueous dispersion of the polyester resin (a1). The addition amount is a weight ratio of the polyester resin (a1) and the addition polymerizable monomer (a2) [polyester resin (a1) / addition polymerizable monomer (a2)], preferably 55/45 to 95/5, more preferably 65/35 to 95/5, more preferably 75/25 to 95/5, and still more preferably 85/15 to 95/5.
Moreover, you may add water etc. further from the point of the efficiency of stirring.

Next, the addition polymerizable monomer (a2) is polymerized in the presence of the polyester resin (a1).
In the polymerization, a known radical polymerization initiator, a crosslinking agent and the like are added as necessary. As the radical polymerization initiator, a water-soluble radical polymerization initiator is preferably used, and a persulfate is more preferably used.
The polymerization reaction is advanced by heating a mixed solution containing the polyester resin (a1) and the addition polymerizable monomer (a2). The polymerization temperature depends on the type of polymerization initiator used, but for example, when sodium persulfate is used, it is preferably 60 to 100 ° C., more preferably 70 to 90, from the viewpoint of efficiently performing the polymerization reaction. ° C.

The glass transition temperature of the graft polymer (A) in the aqueous dispersion (A) obtained as described above is preferably from the viewpoint of storage stability, storage stability of the thermal transfer image-receiving sheet, and dyeability. 40-80 degreeC, More preferably, it is 50-80 degreeC, More preferably, it is 60-80 degreeC. The softening point of the graft polymer (A) is preferably 80 to 250 ° C, more preferably 120 to 220 ° C.
The solid content concentration of the aqueous dispersion (A) is preferably 20 to 40% by weight, more preferably 25 to 40% by weight, and still more preferably 30 to 40% by weight, from the viewpoint of the dispersibility and productivity of the resin particles. It is. The pH of the aqueous dispersion (A) at 25 ° C. is preferably 5 to 10, more preferably 6 to 9, and still more preferably 7 to 9 from the viewpoint of storage stability of the aqueous dispersion (A). is there.

  The volume median particle size (D50) of the resin particles in the aqueous dispersion (A) is preferably 20 to 1000 nm, more preferably 50 to 800 nm, and still more preferably, from the viewpoint of film forming properties when obtaining a thermal transfer image-receiving sheet. Is 80-500 nm. Here, “volume median particle size (D50)” means a particle size at which the cumulative volume frequency calculated by the volume fraction is 50% when calculated from the smaller particle size. The measuring method is as described in the examples.

[Thermal transfer image-receiving sheet]
The thermal transfer image receiving sheet of the present invention has a dye receiving layer containing the resin for thermal transfer image receiving sheet on a substrate.

(Base material)
Examples of the base material include synthetic paper (polyolefin, polystyrene, etc.), fine paper, art paper, coated paper, cast coated paper, wallpaper, backing paper, synthetic resin or emulsion-impregnated paper, synthetic rubber latex-impregnated paper, synthetic resin Various resin films or sheets such as internal paper, paperboard, cellulose fiber paper, polyolefin, polyvinyl chloride, polyethylene terephthalate, polystyrene, polymethacrylate, polycarbonate, etc. can be used. A white opaque film formed by adding an agent or a foamed foam sheet can also be used. Moreover, the laminated body which combined the said base material can also be used.
The thickness of these base materials can be about 10 to 300 μm, for example. From the viewpoint of improving the adhesion to the dye-receiving layer, it is preferable that the surface of the substrate is subjected to primer treatment or corona discharge treatment.

(Dye-receiving layer)
The dye receiving layer in the thermal transfer image receiving sheet of the present invention contains the resin for thermal transfer image receiving sheet of the present invention.
The dye-receiving layer is manufactured using a coating liquid form obtained by dissolving a resin in an organic solvent, or a coating liquid form containing a resin dispersion liquid obtained by dispersing each resin in an organic solvent or water. From the viewpoint of environmental safety and the like, the latter is preferable, and it is more preferable to manufacture by performing the following steps (3) to (4).
Step (3): A step of preparing a dye-receiving layer coating solution containing an aqueous dispersion of the thermal transfer image-receiving sheet resin obtained in the step (2).
Step (4): A step of providing a dye receiving layer using the dye receiving layer coating solution obtained in the step (3).

<Step (3)>
Step (3) is a step of preparing a dye-receiving layer coating solution containing an aqueous dispersion of the thermal transfer image-receiving sheet resin obtained in step (2).
The dye-receiving layer coating solution preferably contains a film-forming agent. Examples of the film forming agent include butyl carbitol acetate, diethyl carbitol, gelatin and the like. From the viewpoint of the strength and releasability of the dye receiving layer, gelatin is preferred.
From the viewpoint of uniformly dissolving the film-forming agent, it is preferable to previously dissolve the film-forming agent in water. The aqueous dispersion of the thermal transfer image-receiving sheet resin and the aqueous solution of the film-forming agent are mixed and stirred. It is preferable to obtain a coating solution. A ball mill etc. are mentioned as an agitator used suitably. In order to uniformly mix the film-forming agent in a dissolved state, the stirring temperature is preferably 30 to 60 ° C, more preferably 40 to 50 ° C.

The dye-receiving layer coating solution preferably contains a release agent from the viewpoint of further improving the releasability of the thermal transfer image-receiving sheet during thermal transfer. As the release agent, for example, a dispersible or water-soluble modified silicone oil can be appropriately used. These release agents can be contained in the dye-receiving layer coating solution in an amount of 0.1 to 20 parts by weight, preferably 0.5 to 10 parts by weight, based on 100 parts by weight of the resin. As a commercially available release agent, “KF-615A” (trade name) manufactured by Shin-Etsu Chemical Co., Ltd. can be preferably used.
In order to uniformly disperse or dissolve the release agent, it is preferable to use a stirrer such as a ball mill, and the dispersion or dissolution temperature is preferably 20 to 40 ° C.
The dye receiving layer coating solution further contains pigments and fillers such as titanium oxide, zinc oxide, kaolin clay, and calcium carbonate from the viewpoint of improving the whiteness of the dye receiving layer and increasing the sharpness of the transferred image. can do. From the viewpoint of the whiteness of the thermal transfer image-receiving sheet of the present invention, these pigments and fillers can be contained in an amount of 0.1 to 20 parts by weight with respect to 100 parts by weight of the resin in the dye-receiving layer coating solution. The dye-receiving layer coating solution may further contain other additives such as a catalyst and a curing agent, if necessary.
The dye-receiving layer coating solution may contain other resins than the thermal transfer image-receiving sheet resin of the present invention as long as the effects of the present invention are not impaired. Specific examples of the other resin include a vinyl chloride polymer, a vinyl chloride vinyl acetate copolymer, a vinyl chloride acrylic copolymer, and a polyurethane. The dyeing property and light resistance of the thermal transfer image-receiving sheet, and the resin dispersion From the viewpoint of dispersibility, a vinyl chloride acrylic copolymer is preferred.
These other resins can also be contained in the dye-receiving layer coating solution by dissolving them in an organic solvent together with the thermal transfer image-receiving sheet resin of the present invention during the resin production process. In addition, the resin dispersion can be added to the aqueous dispersion of the resin for thermal transfer image-receiving sheet and mixed to be contained in the dye-receiving layer coating liquid.

<Process (4)>
Step (4) is a step of providing a dye receiving layer using the dye receiving layer coating solution obtained in step (3).
The dye-receiving layer in the thermal transfer image-receiving sheet of the present invention is obtained by applying and drying a coating solution on one surface of a substrate, and for example, using a gravure printing method, a screen printing method, or a gravure plate It is preferable to apply by a reverse roll coating method or the like. In addition, when an intermediate layer is provided between the substrate and the dye-receiving layer as described later, the intermediate layer coating solution and the dye-receiving layer coating solution are applied in layers and dried on one surface of the substrate. An intermediate layer and a dye-receiving layer can also be provided.
The thickness of the dye receiving layer to be formed is generally 1 to 50 μm, and preferably 3 to 15 μm from the viewpoint of image quality and productivity. The solid content after drying is preferably 3 to 15 g per 1 m ^{2 of} the dye receiving layer.

(Middle layer)
The thermal transfer image-receiving sheet of the present invention preferably has an intermediate layer between the substrate and the dye-receiving layer, and the intermediate layer more preferably contains a water-soluble polymer and hollow particles.
<Water-soluble polymer>
The water-soluble polymer is used as a binder for fixing the hollow particles, and examples thereof include gelatin, polyvinyl alcohol, polyvinyl pyrrolidone and the like. Among these, the gelation temperature of the aqueous solution near room temperature of 10 to 30 ° C. From the viewpoint of thermal properties of having gelatin, gelatin is preferable. The viscosity (60 degreeC) measured by JISK6503-2001 from the viewpoint of the mold release property and film forming property of a thermal transfer image receiving sheet, Preferably it is 2.5-6.0 mPa * s, More preferably, it is 3. 0 to 5.5 mPa · s.
The content of the water-soluble polymer in the intermediate layer is preferably 1 to 75% by weight, more preferably 1 to 50% by weight of the entire intermediate layer.
The water-soluble polymer contained in the intermediate layer is preferably crosslinked with a crosslinking agent such as aldehydes, epoxies, vinyl sulfones, triazines, and carbodiimides.

<Hollow particles>
The hollow particles contained in the intermediate layer are not particularly limited as long as they are polymer particles having pores at least partially. For example, 1) Non-foamed hollow particles in which the water present inside the particle partition walls formed of resin evaporates outside the particles after coating and drying, and the inside of the particles becomes hollow. 2) Low boiling point such as butane and pentane 3) Hollow polymer particles in which the low-boiling liquid inside the particles expands to become hollow by heating the particles coated with the resin, 3) Hollow polymer particles obtained by heating and foaming the above 2) in advance, 4) Resin particles And hollow particles formed by neutralizing at least a part of the acidic groups contained in the polymer forming the. In the present invention, those obtained by the method 1) or 3) can be preferably used from the viewpoints of the dyeability of the thermal transfer image-receiving sheet and the adhesion between the intermediate layer and the dye-receiving layer.

  The material constituting the hollow particles is not particularly limited, and various known materials used in the methods 1) to 3), such as polyacrylic acid, polyacrylic acid ester, styrene-acrylic copolymer, Acrylic resins such as a mixture thereof, polystyrene, polyvinylidene chloride, polyacrylonitrile, vinylidene chloride-acrylonitrile copolymer, and the like can be used. In the present invention, a styrene-acrylic copolymer, a vinylidene chloride-acrylonitrile copolymer, and the like are preferably used from the viewpoints of dyeability of the thermal transfer image-receiving sheet and adhesion between the intermediate layer and the dye-receiving layer.

The shape of the hollow particles is not particularly limited, and may be any shape other than spherical as well as spherical, but in the present invention, from the viewpoint of adhesion between the intermediate layer and the dye-receiving layer, it is substantially spherical. It is preferable that
The volume median particle size (D50) of the hollow particles is preferably 0.1 to 5 μm, more preferably 0.3 to 3 μm, and still more preferably 0, from the viewpoint of adhesion between the intermediate layer and the dye-receiving layer. .3 to 1 μm. This value can be measured with a field emission scanning electron microscope (manufactured by Hitachi, Ltd., trade name: S-4800 type).

In the present invention, the hollow particles having a solid concentration of preferably 10 to 40% by weight, more preferably 15 to 35% by weight are used.
The hollow particles preferably have an insoluble content of methyl ethyl ketone (MEK) of 70% by weight or less, more preferably 10 from the viewpoints of dyeability of the thermal transfer image-receiving sheet and adhesion between the intermediate layer and the dye-receiving layer. It is -70 weight%, More preferably, it is 30-70 weight%. In the present invention, “MEK insoluble matter” is defined as the weight ratio of the insoluble hollow particle component of the hollow particles when 2.0 parts by weight of the hollow particles are dissolved in 95 parts by weight of MEK at 25 ° C. It is what is done.
The MEK insoluble content of the hollow particles can be adjusted, for example, by controlling the degree of crosslinking of the resin constituting the hollow particles.

In the present invention, the hollow particles are preferably used as a dispersion in an aqueous medium. Examples of commercially available hollow particles that can be preferably used include “Nipol MH8101” manufactured by Nippon Zeon Co., Ltd. and “SX8782” manufactured by JSR Corporation. (D) "etc. (all are trade names).
The intermediate layer preferably has a weight ratio of the hollow particles to the water-soluble polymer (hollow particles / water-soluble polymer) of 30 from the viewpoint of dyeing property and adhesion between the intermediate layer and the dye-receiving layer. / 70 to 90/10, more preferably 40/60 to 80/20, still more preferably 50/50 to 80/20.

The intermediate layer may contain pigments and fillers such as titanium oxide, zinc oxide, kaolin clay, calcium carbonate, fine powder silica from the viewpoint of improving the whiteness of the intermediate layer and increasing the clarity of the transferred image. it can. These pigments and fillers are preferably 0.1 to 20 parts by weight, more preferably 0.1 to 20 parts by weight with respect to 100 parts by weight of the water-soluble polymer in the intermediate layer from the viewpoint of the whiteness of the thermal transfer image-receiving sheet. 10 parts by weight can be contained.
If necessary, the intermediate layer may further contain additives such as a film-forming aid such as glycol ethers, a mold release agent, a curing agent, and a catalyst.

The intermediate layer is formed on at least one surface of the base material of the thermal transfer image-receiving sheet by dispersing or dissolving a water-soluble polymer and various additives used as necessary in an organic solvent or water, and applying and drying. be able to.
The thickness of the intermediate layer is preferably 10 to 100 μm, more preferably 20 to 50 μm, from the viewpoint of cushioning properties and heat insulating properties. In addition, the solid content after drying is preferably 7 to 70 g / m ² per 1 m ² of the intermediate layer.
The intermediate layer is prepared by, for example, dissolving water-soluble polymer containing gelatin, hollow particles, and additives used as necessary in water on at least one surface of the base material of the thermal transfer image-receiving sheet or dispersing in water. The coating liquid obtained in this manner can be applied and dried by, for example, a gravure printing method, a screen printing method, a reverse roll coating method using a gravure plate, or the like.

[Transfer sheet]
The transfer sheet (ink ribbon) used when performing thermal transfer using the thermal transfer image receiving sheet of the present invention is usually obtained by receiving a dye layer containing a sublimation dye on paper or a polyester film, and receiving the dye. A laminate layer composed of a protective layer or the like to be transferred onto the image is provided, and any transfer sheet can be used.
Examples of sublimable dyes that can be suitably used for the thermal transfer image-receiving sheet of the present invention include pyridoneazo series, dicyanostyryl series, quinophthalone series, merocyanine series for yellow dyes; benzeneazo series, pyrazolone azomethine series, isothiazole series for magenta dyes, Pyrazolotriazole series: As cyan dyes, anthraquinone series, cyanomethylene series, indophenol series, and indonaphthol series are listed.

As the means for applying thermal energy at the time of thermal transfer, any given means can be used. For example, by controlling the recording time with a recording device such as a thermal printer, a thermal energy of about 5 to 100 mJ / mm ² is obtained. It can be done by giving.

Production Examples 1 to 3, 5 and 6
(Production of polyester resin (a1) ac, e and f)
The raw material monomer of polyester resin (a1) excluding fumaric acid shown in Table 1 and tin (II) dioctylate are placed in a four-necked flask equipped with a thermometer, a stainless stir bar, a flow-down condenser, and a nitrogen inlet tube. The mixture was reacted in a mantle heater at 200 ° C. for 6 hours under a nitrogen atmosphere, further depressurized, and reacted for 1 hour under a pressure of 8.3 kPa. Next, fumaric acid and 4-t-butylcatechol were added at 210 ° C. and reacted for 5 hours, then the pressure was reduced, and the softening point measured according to ASTM D36-86 under a pressure of 20 kPa reached the temperature shown in Table 1. It was made to react until it reached | attained, and polyester resin (a1) ac, e, and f were obtained.

Production Example 4
(Production of polyester resin (a1) d)
The raw material monomer of polyester resin (a1) excluding fumaric acid shown in Table 1 and tin (II) dioctylate are placed in a four-necked flask equipped with a thermometer, a stainless stir bar, a flow-down condenser, and a nitrogen inlet tube. The mixture was reacted in a mantle heater at 235 ° C. for 5 hours under a nitrogen atmosphere, further depressurized, and reacted for 1 hour under a pressure of 8.3 kPa. Next, fumaric acid and 4-t-butylcatechol were added at 210 ° C. and reacted for 5 hours, then the pressure was reduced, and the softening point measured according to ASTM D36-86 under a pressure of 20 kPa reached the temperature shown in Table 1. It was made to react until it reached | attained and polyester resin (a1) d was obtained.

Production Examples 7 and 8
(Production of polyester resin (a1) g and h)
A four-neck equipped with a thermometer, a stainless steel stir bar, a flow-down condenser, and a nitrogen inlet tube with raw material monomers of polyester resin (a1) excluding succinic acid and fumaric acid shown in Table 1 and tin (II) dioctylate Place in a flask, react in a mantle heater at 235 ° C for 5 hours in a nitrogen atmosphere, add succinic acid at 190 ° C for 3 hours, further reduce pressure, and react for 1 hour at 8.3 kPa pressure did. Next, fumaric acid and 4-t-butylcatechol were added at 210 ° C. and reacted for 5 hours, then the pressure was reduced, and the softening point measured according to ASTM D36-86 under a pressure of 20 kPa reached the temperature shown in Table 1. It was made to react until it reached | attained, and polyester resin (a1) g and h were obtained.

  The physical properties of the obtained polyester resins (a1) a to h were measured by the following methods. The results are shown in Table 1.

[Softening point of resin]
Using a flow tester (manufactured by Shimadzu Corporation, trade name: CFT-500D), a 1 g sample was heated at a heating rate of 6 ° C./min. Extruded from a 1 mm nozzle. The amount of flow tester drop by the flow tester was plotted against the temperature, and the temperature at which half the sample flowed out was taken as the softening point.

[Glass transition temperature of resin]
Using a differential scanning calorimeter (manufactured by Perkin Elmer, trade name: Pyris 6 DSC), the temperature was raised to 200 ° C., and the sample cooled to 0 ° C. at a temperature lowering rate of 10 ° C./min was heated at a rate of 10 ° C. The temperature was raised in minutes, and the temperature at the intersection of the baseline extension line below the maximum peak temperature of endotherm and the tangent showing the maximum slope from the peak rising portion to the peak apex was defined as the glass transition temperature.

[Acid value of resin]
The measurement solvent was measured according to JIS K0070, except that the mixed solvent of ethanol and ether was changed to a mixed solvent of acetone and toluene (acetone: toluene = 1: 1 (volume ratio)).

[Number average molecular weight of resin]
The molecular weight distribution was measured by gel permeation chromatography and the number average molecular weight was calculated by the following method.
(1) Preparation of sample solution The resin was dissolved in chloroform so that the concentration was 0.5 g / 100 ml. Subsequently, this solution was filtered using a fluororesin filter having a pore size of 2 μm (manufactured by Sumitomo Electric Industries, Ltd., trade name: FP-200) to remove insoluble components to obtain a sample solution.
(2) Molecular weight measurement Tetrahydrofuran was flowed as a dissolution liquid at a flow rate of 1 ml / min, and the column was stabilized in a constant temperature bath at 40 ° C. Measurement was performed by injecting 100 μl of the sample solution. The number average molecular weight of the sample was calculated based on a calibration curve prepared in advance. The calibration curves are several types of monodisperse polystyrene (monodisperse polystyrene manufactured by Tosoh Corporation; 2.63 × 10 ³ , 2.06 × 10 ⁴ , 1.02 × 10 ⁵ (weight average molecular weight), manufactured by GL Sciences Inc. Of monodisperse polystyrene; 2.10 × 10 ³ , 7.00 × 10 ³ , 5.04 × 10 ⁴ (weight average molecular weight)) were used as standard samples.
Measuring device: CO-8010 (trade name, manufactured by Tosoh Corporation)
Analytical column: GMHXL + G3000HXL (both trade names, manufactured by Tosoh Corporation)

Production Examples 9-16
(Production of aqueous dispersions (i) to (viii) of polyester resin (a1): Step (1))
Polyester resins (a1) a to h were added in a four-necked flask equipped with a nitrogen inlet tube, a reflux condenser, a stirrer, and a thermocouple in the types and amounts shown in Table 2, and dissolved in methyl ethyl ketone at 25 ° C. . Next, 25% aqueous ammonia was added, deionized water was added with stirring, and methyl ethyl ketone was distilled off at 60 ° C. under reduced pressure. After cooling to room temperature, the mixture was filtered through a 200-mesh wire mesh to obtain aqueous dispersions (i) to (viii) of the polyester resin (a1).
Each physical property of the obtained aqueous dispersions (i) to (viii) was measured by the following method. The results are shown in Table 2.

[Volume Median Particle Size (D50) of Resin Particles in Aqueous Dispersion]
Using a laser diffraction particle size measuring machine (Horiba, Ltd., trade name: LA-920), add an aqueous dispersion of each resin and distilled water to the measurement cell, and at a concentration where the absorbance is in an appropriate range, Volume median particle size (D50) was measured.

[Solid content concentration of aqueous dispersion]
Using an infrared moisture meter (trade name: FD-230, manufactured by Kett Scientific Laboratory Co., Ltd.), 5 g of an aqueous dispersion was measured at a drying temperature of 150 ° C. and a measurement mode 96 (monitoring time 2.5 minutes / variation width 0.05%). ) And the wet base moisture (% by weight) of the aqueous dispersion was measured. The solid content concentration was calculated according to the following formula.
Solid content concentration (% by weight) = 100-M
M: wet base moisture of aqueous dispersion (% by weight) = [(W−W ₀ ) / W] × 100
W: Sample weight before measurement (initial sample weight)
W ₀ : Sample weight after measurement (absolute dry weight)

[PH of aqueous dispersion]
It measured at 25 degreeC with the pH meter (The product name: HM-20P by Toa DKK Corporation).

Production Examples 17-25
(Production of aqueous dispersions (I) to (IX) of resin for thermal transfer image-receiving sheet: Step (2))
A polyester dispersion, deionized water, and addition polymerizability in the types and amounts shown in Table 3 are added to a 2-liter four-necked flask equipped with a nitrogen inlet tube, reflux condenser, dropping funnel, stirrer, and thermocouple. The monomer (a2) styrene was charged and stirred for 30 minutes. Under a nitrogen stream, sodium persulfate was added and reacted at 80 ° C. for 6 hours. After cooling to room temperature, the mixture was filtered through a 200-mesh wire mesh to obtain aqueous dispersions (I) to (IX) of resins for thermal transfer image-receiving sheets. In addition, as for the compounding amount of each material, the weight ratio between the polyester resin segment (A1) and the addition polymerization resin segment (A2) in the resin for thermal transfer image-receiving sheet in the obtained aqueous dispersion is as shown in Table 3. Was decided.
The physical properties of the obtained aqueous dispersions (I) to (IX) of the obtained resin for thermal transfer image-receiving sheet were measured by the method described above. The results are shown in Table 3.

Examples 1-6 and Comparative Examples 1-4
(Manufacture of thermal transfer image-receiving sheet; steps (3) and (4))
First, the composition and blending amount shown in Table 4 were mixed at 45 ° C. to prepare an intermediate layer coating solution. This coating solution was applied to synthetic paper (manufactured by YUPO Corporation, trade name: YUPO FGS-250, thickness 250 μm, basis weight 200 g / m ² ) with a wire bar so that it would be 20.0 g / m ² after drying. And it was made to dry at 25 degreeC for 5 minutes, and the intermediate | middle layer coating sheet was obtained.
In the preparation of the intermediate layer, the following styrene acrylic copolymer was used as the hollow particles, and the following gelatin was used as the binder.
Styrene acrylic copolymer (manufactured by Nippon Zeon Co., Ltd., trade name: Nipol MH8101, hollow rate = 50%, solid content = 26% by weight)
Gelatin (made by Nitta Gelatin Co., Ltd., trade name: G0723K, viscosity 4.4 mPa · s)

Next, it mixed at 25 degreeC by the composition and compounding quantity shown in Table 4, and produced coating liquid A1-J1 for dye receptive layers. The aqueous dispersion of the thermal transfer image-receiving sheet resin used for preparing the dye-receiving layer coating liquid was adjusted to a solid content concentration of 30% by weight. For the preparation of the dye receiving layer, the following gelatin was used as a film-forming agent, and the following polyether-modified silicone was used as a mold release agent.
Gelatin (made by Nitta Gelatin Co., Ltd., trade name: G0723K, viscosity 4.4 mPa · s)
Polyether-modified silicone (manufactured by Shin-Etsu Chemical Co., Ltd., trade name: KF-615A)
Each of the dye-receiving layer coating solutions is applied to the intermediate layer-coated sheet by a wire bar so as to be 5.0 g / m ² and dried at 50 ° C. for 2 minutes to obtain a thermal transfer image-receiving sheet. It was.

<Evaluation>
(Dyeing property)
A black (K) gradation pattern (L value was changed from 0 to 255 in increments of 15 using a commercially available sublimation printer (trade name, MEGAPICEL III, manufactured by Altec Co., Ltd.) on the produced thermal transfer image-receiving sheet. .6 cm square image), and the transfer color density at the high density print (18th gradation (L = 0: highest density)) is measured with a Gretag densitometer (manufactured by GRETAG-MACBETH). Sex was evaluated. The greater the concentration value, the better the dyeing property. The results are shown in Table 4.

(Releasability)
From the peeling sound between the ink ribbon and the thermal transfer image-receiving sheet at the time of gradation pattern printing, the releasability (thermal fusing property) was evaluated according to the following criteria. The results are shown in Table 4.
AA: There is no abnormal noise and can be peeled.
A: Although there is a slight noise, it can be peeled off.
B: Although there is a clear abnormal noise, it can be peeled off.
C: It is heat-sealed, peeling is difficult, and chipping is observed in the image.
D: It is heat-sealed and cannot be peeled off.

  As is clear from Table 4, the thermal transfer image receiving sheets of Examples 1 to 6 have a high maximum density at the time of high density printing and excellent dyeability as compared with the thermal transfer image receiving sheets of Comparative Examples 1 to 4. It can be seen that the ink ribbon and the image receiving sheet are excellent in releasability without heat-sealing during continuous black solid printing.

  The thermal transfer image receiving sheet of the present invention is excellent in both dyeing property and releasability, and can be suitably used as a thermal transfer image receiving sheet.

Claims (8)

  A thermal transfer image-receiving sheet resin comprising a graft polymer composed of a main chain segment (A1) made of a polyester resin and a side chain segment (A2) made of an addition polymerization resin, wherein the segment (A1) is 2, 2 -A polyester resin obtained by polycondensation of an alcohol component containing 50 mol% or more of a propylene oxide adduct of bis (4-hydroxyphenyl) propane and a carboxylic acid component containing 5 to 40 mol% of a dodecenyl succinic acid compound, Resin for thermal transfer image receiving sheet. The resin for thermal transfer image receiving sheets according to claim 1, wherein the dodecenyl succinic acid compound is represented by the following formula (II) or (III).

(In the formula, R ³ is a hydrogen atom or a hydrocarbon group having 1 to 4 carbon atoms, which may be the same or different.)   The resin for thermal transfer image receiving sheets according to claim 1 or 2, wherein the carboxylic acid component contains isophthalic acid and / or succinic acid.   The resin for thermal transfer image receiving sheets according to any one of claims 1 to 3, wherein the carboxylic acid component contains fumaric acid.   Resin for thermal transfer image receiving sheets in any one of Claims 1-4 whose segment (A1) is linear polyester.   The resin for thermal transfer image-receiving sheets according to any one of claims 1 to 5, wherein the segment (A2) contains 70% by weight or more of a structural unit derived from an addition polymerizable monomer having an aromatic group.   The thermal transfer image receiving sheet which has a dye receiving layer containing the resin for thermal transfer image receiving sheets in any one of Claims 1-6. Step (1): an alcohol component containing 50 mol% or more of an alkylene oxide adduct of 2,2-bis (4-hydroxyphenyl) propane, 5 to 40 mol% of dodecenyl succinic acid compound, and 5 to 30 mol% of fumaric acid A step of mixing an aqueous medium with a polyester resin (a1) obtained by polycondensation with a carboxylic acid component, and an aqueous dispersion of the polyester resin (a1); and step (2): obtained in step (1) A method for producing a resin for a thermal transfer image-receiving sheet, comprising the step of adding an addition-polymerizable monomer (a2) having an aromatic group to the obtained aqueous dispersion and polymerizing it to obtain an aqueous dispersion of a graft polymer.