JP5751436B2 - Thermal transfer recording medium - Google Patents

Description

  The present invention relates to a thermal transfer recording medium used in a thermal transfer type printer, and a heat-resistant slipping layer is provided on one surface of a substrate, and an undercoat layer and a dye layer are provided on the other surface of the substrate. The present invention relates to sequentially formed thermal transfer recording media.

  In general, a thermal transfer recording medium is an ink ribbon called a thermal ribbon, which is used in a thermal transfer type printer, and has a thermal transfer layer on one side of the substrate and heat resistance on the other side of the substrate. A slipping layer (back coat layer) is provided. Here, the thermal transfer layer is a layer of ink that is sublimated (sublimation transfer method) or melted (melt transfer method) by the heat generated in the thermal head of the printer, and transferred to the transfer target side. It is.

  Currently, among the thermal transfer systems, the sublimation transfer system can easily form full-color images with various functions of the printer, so digital camera self-prints, cards such as identification cards, amusement output, etc. Widely used. Along with the diversification of such applications, there is a growing demand for smaller size, higher speed, lower cost, and durability for the obtained printed material. A thermal transfer recording medium having a plurality of thermal transfer layers provided so as not to overlap a protective layer imparting durability has been widely used.

  Under such circumstances, with the diversification and widespread use of applications, there has been a problem that sufficient print density cannot be obtained with the conventional thermal transfer recording medium as the printing speed of the printer further increases. . In order to increase the transfer sensitivity, attempts have been made to improve the transfer sensitivity in printing by reducing the thickness of the thermal transfer recording medium. However, wrinkles due to heat, pressure, etc. may occur during the manufacture of the thermal transfer recording medium or during printing. Or a breakage in some cases.

  In addition, attempts have been made to increase the printing density and transfer sensitivity in printing by increasing the dye / resin (Dye / Binder) ratio in the dye layer of the thermal transfer recording medium. In addition to being up, a part of the dye migrates to the heat-resistant slipping layer of the thermal transfer recording medium during the winding state in the manufacturing process (setback), and when the rewinding is performed, the migrated dye has another color. When the dye layer or the protective layer is re-transferred (backside back) and the contaminated layer is thermally transferred to the transfer target, the hue becomes different from the designated color, or so-called scumming occurs.

  Attempts have also been made to increase the energy at the time of image formation on the printer side, not on the thermal transfer recording medium side, but not only the power consumption increases, but also the life of the thermal head of the printer is shortened. And the transfer target are fused, so that so-called abnormal transfer is likely to occur. On the other hand, when a large amount of a release agent is added to the dye layer or the transfer target in order to prevent abnormal transfer, blurring of the image or background staining may occur.

  In order to solve such a problem, several methods have been proposed. For example, Patent Document 1 proposes a thermal transfer sheet having an adhesive layer containing a polyvinylpyrrolidone resin and a modified polyvinylpyrrolidone resin between a base material and a dye layer.

  Patent Document 2 proposes a thermal transfer sheet having an adhesive layer composed of a thermoplastic resin of polyvinyl pyrrolidone resin or polyvinyl alcohol resin and colloidal inorganic pigment ultrafine particles between a substrate and a dye layer.

  Patent Document 3 proposes a thermal transfer sheet having a base layer composed of a copolymer of vinylpyrrolidone and vinyl acetate and colloidal inorganic pigment ultrafine particles between a base material and a dye layer.

JP-A-2005-231354 JP 2006-150956 A JP 2008-155612 A

  However, when printing is performed with a sublimation transfer type high-speed printer using the thermal transfer recording medium proposed in Patent Document 1, abnormal transfer is not confirmed, including those stored under high temperature and high humidity. Transfer sensitivity in printing is low, does not reach a sufficient level, and poor image quality occurs in high density areas, i.e. hue fluctuation occurs when the image receiving layer of the transfer target is fused to the thermal transfer recording medium. As a result, the so-called “shine”, in which the surface of the printed material is partially matted, could not be sufficiently suppressed. In addition, when printing is performed on the thermal transfer recording medium proposed in Patent Document 2, the transfer sensitivity in the printing is high and reaches a sufficient level, but is abnormally transferred when stored at high temperature and high humidity. Was confirmed, and the shine could not be suppressed sufficiently. In addition, when printing is performed with the thermal transfer recording medium proposed in Patent Document 3, the transfer sensitivity in the printing is high and has reached a sufficient level, including those stored at high temperature and high humidity, Although there was no problem with abnormal transfer, printing unevenness was confirmed, and shine could not be sufficiently suppressed. As described above, in the conventional technology, there is a thermal transfer recording medium that has high transfer sensitivity in printing, does not generate abnormal transfer even when stored at high temperature and high humidity, and can be used for a high-speed printer that sufficiently improves the phenomenon of shine. The situation is not found.

  Therefore, in view of the above problems, the present invention has high transfer sensitivity at the time of high-speed printing, that is, it can reduce the dye used for the dye layer, and also has abnormalities in printing even after storage under high temperature and high humidity. Transfer can be prevented, and image quality defects occurring at high density portions, that is, hue variation occurs when the image receiving layer of the transfer target is fused to the thermal transfer recording medium, and as a result, the surface of the print is partially It is an object of the present invention to provide a heat-sensitive transfer recording medium that can reduce the phenomenon of so-called “shininess” that causes matting.

  The heat-sensitive transfer recording medium according to the present invention is a heat-sensitive transfer in which a heat-resistant slipping layer is provided on one surface of a substrate made of a synthetic resin film, and an undercoat layer and a dye layer are provided in this order on the other surface of the substrate. In the recording medium, the undercoat layer contains at least a water-soluble polymer and a vinylpyrrolidone-vinylimidazole copolymer.

  The thermal transfer recording medium of the present invention has high transfer sensitivity at high speed printing, can reduce the amount of dye used in the dye layer, and can prevent abnormal transfer in printing even after storage at high temperature and high humidity. Thus, it is possible to obtain a sufficiently satisfactory print with less so-called “shine” phenomenon.

1 is a side sectional view showing a configuration of a thermal transfer recording medium according to an embodiment of the present invention.

Embodiments of the present invention will be described below with reference to the drawings.
As shown in FIG. 1, the thermal transfer recording medium of one embodiment of the present invention is provided with a heat-resistant slipping layer 40 that imparts slidability with a thermal head on one surface of the substrate 10, and the other of the substrate 10. On this surface, an undercoat layer 20 and a dye layer 30 containing at least a water-soluble polymer and a vinylpyrrolidone-vinylimidazole copolymer are sequentially formed.

  Since the base material 10 is required to have heat resistance and strength not to be softened and deformed by heat pressure in thermal transfer, for example, polyethylene terephthalate, polyethylene naphthalate, polypropylene, cellophane, acetate, polycarbonate, polysulfone, polyimide, polyvinyl alcohol, aromatic A synthetic resin film such as polyamide, aramid, and polystyrene, and paper such as condenser paper and paraffin paper can be used alone or in combination. Among these, a polyethylene terephthalate film is preferable in view of physical properties, workability, cost, and the like.

  In addition, the thickness can be in the range of 2 μm to 50 μm in consideration of operability and workability, but in consideration of handling properties such as transfer suitability and workability, it is about 2 μm to 9 μm. Those are preferred.

  Moreover, in the base material 10, it is also possible to perform an adhesion treatment on the surface on which the heat resistant slipping layer 40 and / or the undercoat layer 20 is formed. As the adhesion treatment, known techniques such as corona treatment, flame treatment, ozone treatment, ultraviolet treatment, radiation treatment, roughening treatment, plasma treatment, primer treatment, etc. can be applied, and these treatments are used in combination. You can also In the present invention, it is effective to improve the adhesion between the substrate and the undercoat layer, and it is preferable to use a primer-treated polyethylene terephthalate film from the viewpoint of cost.

Next, the heat-resistant slipping layer 40 can be handled by a conventionally known layer. For example, a resin serving as a binder, a functional additive that imparts releasability and slipperiness, a filler, a curing agent, a solvent, and the like are blended. Thus, a coating solution for forming a heat resistant slipping layer can be prepared, coated and dried. The coating amount after drying of the heat resistant slipping layer 40 is suitably about 0.10 g / m ² or more and 2.00 g / m ² or less. Here, the coating amount after drying of the heat-resistant slipping layer 40 refers to the amount of solid content remaining after coating and drying the coating solution for forming the heat-resistant slipping layer. Similarly, the coating amount and the coating amount after drying of the dye layer 30 indicate the solid content remaining after the coating liquid is applied and dried.

  As an example of the heat resistant slipping layer, the binder resin may be polyvinyl butyral resin, polyvinyl acetoacetal resin, polyester resin, vinyl chloride-vinyl acetate copolymer, polyether resin, polybutadiene resin, acrylic polyol, polyurethane acrylate, polyester. Examples thereof include acrylate, polyether acrylate, epoxy acrylate, nitrocellulose resin, cellulose acetate resin, polyamide resin, polyimide resin, polyamideimide resin, and polycarbonate resin.

  Functional additives include natural waxes such as animal waxes and plant waxes, synthetic hydrocarbon waxes, aliphatic alcohols and acid waxes, fatty acid esters and glycerite waxes, synthetic ketone waxes, amine and amide waxes , Synthetic waxes such as chlorinated hydrocarbon wax and alpha-olefin wax, higher fatty acid esters such as butyl stearate and ethyl oleate, sodium stearate, zinc stearate, calcium stearate, potassium stearate, magnesium stearate, etc. Surfactants such as higher fatty acid metal salts, long chain alkyl phosphate esters, polyoxyalkylene alkyl aryl ether phosphate esters or phosphate esters such as polyoxyalkylene alkyl ether phosphate esters, etc. Rukoto can.

  As fillers, talc, silica, magnesium oxide, zinc oxide, calcium carbonate, magnesium carbonate, kaolin, clay, silicone particles, polyethylene resin particles, polypropylene resin particles, polystyrene resin particles, polymethyl methacrylate resin particles, polyurethane resin particles, etc. Can be mentioned.

  Examples of the curing agent include isocyanates such as tolylene diisocyanate, triphenylmethane triisocyanate, tetramethylxylene diisocyanate, and derivatives thereof, but are not particularly limited.

  Next, the undercoat layer 20 includes at least a water-soluble polymer and a vinyl pyrrolidone-vinyl imidazole copolymer, and the water-soluble polymer and the vinyl pyrrolidone-vinyl imidazole copolymer are blended to form an undercoat layer. It is formed by preparing a coating solution, coating and drying.

  In the undercoat layer 20, the water-soluble polymer and the vinylpyrrolidone-vinylimidazole copolymer are essential components. In particular, the water-soluble polymer and the vinylpyrrolidone-vinylimidazole copolymer are the main components of the undercoat layer 20. Preferably there is.

Here, the main component means that other components may be added in addition to the water-soluble polymer and the vinylpyrrolidone-vinylimidazole copolymer, as long as the effects of the present invention are not impaired. The total of the functional polymer and the vinyl pyrrolidone-vinyl imidazole copolymer is included in an amount exceeding 50% by mass as viewed from the whole when the undercoat layer is formed, but is preferably 80% by mass or more.

  Examples of water-soluble polymers include polyvinyl alcohol, polyvinyl pyrrolidone, starch, gelatin, methyl cellulose, ethyl cellulose, carboxymethyl cellulose, sodium alginate and the like. Among these, polyvinyl alcohol and polyvinyl pyrrolidone are preferable, and polyvinyl alcohol is more preferable. The polyvinyl alcohol here is generally obtained by saponifying polyvinyl acetate, and so-called partially saponified polyvinyl alcohol in which several tens percent of acetic acid groups remain, so that only a few percent of acetic acid groups remain. It includes up to fully saponified polyvinyl alcohol and is not particularly limited.

  The vinyl pyrrolidone-vinyl imidazole copolymer is a copolymer of an N-vinyl pyrrolidone monomer and a vinyl imidazole which is a vinyl polymerizable monomer. The form of copolymerization is not limited to any of random copolymerization, block copolymerization, and graft copolymerization. Here, the N-vinyl pyrrolidone-based monomer refers to N-vinyl pyrrolidone (N-vinyl-2-pyrrolidone, N-vinyl-4-pyrrolidone, etc.) and derivatives thereof. Examples of those having a substituent on the pyrrolidone ring such as vinyl-3-methylpyrrolidone, N-vinyl-5-methylpyrrolidone, N-vinyl-3-benzylpyrrolidone, N-vinyl-3,3,5-trimethylpyrrolidone However, it is not particularly limited.

  The vinyl pyrrolidone-vinyl imidazole copolymer is considered to have been compensated by the vinyl imidazole component for the poor heat resistance and moisture resistance of the water-soluble polymer component and the vinyl pyrrolidone component. The adhesiveness between the material and the dye layer is high, so that abnormal transfer in printing can be prevented, and the function of reducing the shine in the high density portion during high-speed printing can be exhibited. Here, in the vinylpyrrolidone-vinylimidazole copolymer, the polymerization ratio of vinylpyrrolidone and vinylimidazole is preferably (vinylpyrrolidone) / (vinylimidazole) = 8/2 to 2/8 in a molar ratio. In some cases, the above functions can be sufficiently exhibited.

  The mixing ratio of the water-soluble polymer to the vinylpyrrolidone-vinylimidazole copolymer is (water-soluble polymer) / (vinylpyrrolidone-vinylimidazole copolymer) = 8/2 to 2/8 on a mass basis. It is preferable. Further, when considering the transfer sensitivity at the time of high-speed printing and the adhesion to the substrate or the dye layer, it is preferably 7/3 to 3/7. By satisfying this range, the transfer sensitivity during high-speed printing is higher, high-density prints with less shine are obtained, and there is no abnormal transfer in printing even after storage under high temperature and high humidity. A sufficiently satisfactory print can be obtained.

  In addition, the undercoat layer 20 may contain known additives such as an isocyanate compound, a silane coupling agent, a dispersant, a viscosity modifier, and a stabilizer as long as the performance is not impaired.

The coating amount of the undercoat layer 20 after drying is not generally limited, but is preferably in the range of 0.10 g / m ² or more and 0.30 g / m ² or less. If it is less than 0.10 g / m ² , the transfer sensitivity at the time of high-speed printing is insufficient due to deterioration at the time of laminating the dye layer, and there is a concern that the adhesion to the substrate or the dye layer has a problem. On the other hand, if it exceeds 0.30 g / m ² , the sensitivity of the thermal transfer recording medium itself is affected, and there is a fear that the transfer sensitivity at the time of high-speed printing is insufficient.

Next, the dye layer 30 can be a conventionally known one. For example, the dye layer 30 is formed by preparing a coating solution for forming a dye layer by blending a heat-transferable dye, a binder, a solvent, and the like, and applying and drying the coating solution. The An appropriate coating amount of the dye layer 30 after drying is about 0.70 g / m ² . The dye layer can be composed of a single layer of one color, or a plurality of dye layers containing dyes having different hues can be repeatedly formed on the same surface of the same substrate in the surface order.

  The heat transferable dye in the dye layer is not particularly limited as long as it is a dye that melts, diffuses, or sublimates and transfers due to heat. For example, the yellow component includes solvent yellow 56, 16, 30, 93, 33, Disperse Yellow 201, 231, 33 and the like. Examples of the magenta component include C.I. I. Disperse thread 60, C.I. I. Disperse violet 26, C.I. I. Solvent Red 27, or C.I. I. Solvent Red 19 etc. can be mentioned. As the cyan component, C.I. I. Disperse Blue 354, C.I. I. Solvent Blue 63, C.I. I. Solvent Blue 36, or C.I. I. Disperse Blue 24 and the like. As a black ink dye, it is common to perform color matching by combining the above dyes.

  As the binder contained in the dye layer 30, any conventionally known resin binder can be used, and is not particularly limited, but cellulose-based materials such as ethyl cellulose, hydroxyethyl cellulose, ethyl hydroxy cellulose, hydroxypropyl cellulose, methyl cellulose, and cellulose acetate Examples thereof include vinyl resins such as resins, polyvinyl alcohol, polyvinyl acetate, polyvinyl butyral, polyvinyl acetal, polyvinyl pyrrolidone, and polyacrylamide, polyester resins, styrene-acrylonitrile copolymer resins, and phenoxy resins.

  Here, the blending ratio of the dye and the binder in the dye layer 30 is preferably (dye) / (binder) = 10/100 to 300/100 on a mass basis. This is because when the ratio of (dye) / (binder) is less than 10/100, the amount of dye is too small and the color development sensitivity becomes insufficient, and a good thermal transfer image cannot be obtained, and this ratio is 300/100. If it exceeds the upper limit, the solubility of the dye in the binder is extremely lowered, so that when it becomes a thermal transfer recording medium, the storage stability is deteriorated and the dye is likely to precipitate. The dye layer may contain known additives such as an isocyanate compound, a silane coupling agent, a dispersant, a viscosity modifier, and a stabilizer as long as the performance is not impaired.

  The heat-resistant slip layer 40, the undercoat layer 20, and the dye layer 30 can be formed by applying and drying by a conventionally known application method. Examples of the application method include a gravure coating method, a screen printing method, a spray coating method, and a reverse roll coating method.

  Below, the material used for each Example and each comparative example of this invention is shown. In the text, “part” is based on mass unless otherwise specified.

<Preparation of substrate with heat-resistant slip layer>
As a base material, use a polyethylene terephthalate film with 4.5 μm single-sided easy-adhesion treatment, and apply a heat-resistant slipping layer coating solution of the following composition to the non-adhesive-treated surface by gravure coating method, After apply | coating so that it might be set to 0.90 g / m < ² > and drying at 100 degreeC for 1 minute, the base material with a heat resistant slipping layer was obtained by aging for 1 week in a 40 degreeC environment.

<Heat resistant slipping layer coating solution>
Acrylic polyol resin 12.5 parts Polyoxyalkylene alkyl ether / phosphate ester 2.5 parts Talc 6.0 parts 2,6-tolylene diisocyanate prepolymer 4.0 parts Toluene 50.0 parts Methyl ethyl ketone 20.0 parts Ethyl acetate 5.0 parts

Example 1
The undercoat layer coating solution-1 having the following composition was applied to the easy-adhesion treated surface of the substrate with a heat-resistant slip layer by a gravure coating method so that the coating amount after drying was 0.20 g / m ² . The undercoat layer was formed by drying at 100 ° C. for 2 minutes. Subsequently, a dye layer coating solution having the following composition is applied on the undercoat layer by a gravure coating method so that the coating amount after drying is 0.70 g / m ² and dried at 90 ° C. for 1 minute. Thus, a dye layer was formed, and the thermal transfer recording medium of Example 1 was obtained.

<Undercoat layer coating solution-1>
Polyvinylpyrrolidone 1.0 part Vinylpyrrolidone-vinylimidazole copolymer 4.0 parts
[Copolymerization ratio (molar ratio): 3/7]
Pure water 76.0 parts Isopropyl alcohol 19.0 parts

<Dye layer coating solution>
C. I. Solvent Blue 636.0 parts Polyvinyl acetal resin 4.0 parts Toluene 45.0 parts Methyl ethyl ketone 45.0 parts

(Example 2)
In the thermal transfer recording medium produced in Example 1, the thermal recording transfer medium of Example 2 was obtained in the same manner as in Example 1 except that the undercoat layer was changed to the undercoat layer coating liquid-2 of the following composition. .

<Undercoat layer coating solution-2>
Polyvinyl alcohol 1.0 part Vinylpyrrolidone-vinylimidazole copolymer 4.0 parts
[Copolymerization ratio (molar ratio): 1/1]
Pure water 76.0 parts Isopropyl alcohol 19.0 parts

(Example 3)
In the thermal transfer recording medium produced in Example 1, the thermal recording transfer medium of Example 3 was obtained in the same manner as in Example 1, except that the undercoat layer was changed to the undercoat layer coating solution-3 of the following composition. .

<Undercoat layer coating solution-3>
Polyvinyl alcohol 3.5 parts Vinylpyrrolidone-vinylimidazole copolymer 1.5 parts
[Copolymerization ratio (molar ratio): 1/1]
Pure water 76.0 parts Isopropyl alcohol 19.0 parts

Example 4
In the thermal transfer recording medium produced in Example 1, the thermal recording transfer medium of Example 4 was obtained in the same manner as in Example 1, except that the undercoat layer was changed to the undercoat layer coating solution-4 of the following composition. .

<Undercoat layer coating solution-4>
Polyvinyl alcohol 1.5 parts Vinylpyrrolidone-vinylimidazole copolymer 3.5 parts
[Copolymerization ratio (molar ratio): 1/1]
Pure water 76.0 parts Isopropyl alcohol 19.0 parts

(Example 5)
In the heat-sensitive transfer recording medium produced in Example 1, the example was applied in the same manner as in Example 1 except that the undercoat layer was applied and dried so that the coating amount after drying was 0.05 g / m ^2. No. 5 thermal recording transfer medium was obtained.

(Example 6)
In the heat-sensitive transfer recording medium produced in Example 1, the Example was applied in the same manner as in Example 1 except that the undercoat layer was applied and dried so that the coating amount after drying was 0.35 g / m ^2. No. 6 thermal recording transfer medium was obtained.

(Comparative Example 1)
After forming the undercoat layer on the easy-adhesion treated surface of the substrate with a heat-resistant slipping layer, the same dye layer coating solution as in Example 1 is dried on the easy-adhesive treated surface by a gravure coating method. The coating amount was 0.70 g / m ² and dried at 90 ° C. for 1 minute to form a dye layer, whereby the thermal transfer recording medium of Comparative Example 1 was obtained.

(Comparative Example 2)
In the thermal transfer recording medium produced in Example 1, the thermal recording transfer medium of Comparative Example 2 was obtained in the same manner as in Example 1 except that the undercoat layer was changed to the undercoat layer coating solution-5 of the following composition. .

<Undercoat layer coating solution-5>
Polyvinylpyrrolidone 5.0 parts Pure water 76.0 parts Isopropyl alcohol 19.0 parts

(Comparative Example 3)
In the thermal transfer recording medium produced in Example 1, the thermal recording transfer medium of Comparative Example 3 was obtained in the same manner as in Example 1 except that the undercoat layer was changed to the undercoat layer coating solution-6 of the following composition. .

<Undercoat layer coating solution-6>
Polyvinyl alcohol 2.5 parts Polyvinylimidazole 2.5 parts Pure water 76.0 parts Isopropyl alcohol 19.0 parts

(Comparative Example 4)
In the thermal transfer recording medium produced in Example 1, the thermal recording transfer medium of Comparative Example 4 was obtained in the same manner as in Example 1 except that the undercoat layer was changed to the undercoat layer coating solution-7 of the following composition. .

<Undercoat layer coating solution-7>
Vinylpyrrolidone-vinylimidazole copolymer 5.0 parts
[Copolymerization ratio (molar ratio): 1/1]
Pure water 76.0 parts Isopropyl alcohol 19.0 parts

(Comparative Example 5)
In the thermal transfer recording medium produced in Example 1, the thermal recording transfer medium of Comparative Example 5 was obtained in the same manner as in Example 1 except that the undercoating layer was changed to the undercoating layer coating solution-8 of the following composition. .

<Undercoat layer coating solution-8>
0.7 parts of vinylpyrrolidone-vinyl acetate copolymer
[Copolymerization ratio (molar ratio): 7/3]
Alumina sol 28.0 parts Pure water 23.4 parts Isopropyl alcohol 47.9 parts

<Preparation of transfer object>
As a base material, a white foamed polyethylene terephthalate film of 188 μm is used, and an image-receiving layer coating solution having the following composition is applied to one surface thereof by a gravure coating method so that the coating amount after drying is 5.0 g / m ^2. By applying and drying, a transfer object for thermal transfer was produced.

<Image-receiving layer coating solution>
Vinyl chloride-vinyl acetate-vinyl alcohol copolymer 19.5 parts Amino-modified silicone oil 0.5 part Toluene 40.0 parts Methyl ethyl ketone 40.0 parts

<Evaluation of adhesion of dye layer at room temperature>
With respect to the thermal transfer recording media of Examples 1 to 6 and Comparative Examples 1 to 5, a cellophane tape having a width of 18 mm and a length of 150 mm was pasted on the dye layer of the thermal transfer recording medium stored at room temperature, and immediately thereafter. Table 1 shows the results of evaluation by examining the presence or absence of the dye layer adhering to the cellophane tape when peeled off.
The evaluation was performed according to the following criteria.
○: Adhesion of the dye layer is not recognized Δ: Adhesion of the dye layer is recognized very slightly ×: Adhesion of the dye layer is observed on the entire surface

<Evaluation of adhesion of dye layer after storage at high temperature and high humidity>
Regarding the thermal transfer recording media of Examples 1 to 6 and Comparative Examples 1 to 5, the dye layers of the thermal transfer recording media stored for 72 hours at 40 ° C. and 90% RH and then stored for 24 hours at room temperature. Table 1 shows the results of evaluation by examining the presence or absence of the dye layer adhering to the cellophane tape side when a cellophane tape having a width of 18 mm and a length of 150 mm is applied to the top and then immediately peeled off. The evaluation was performed according to the same standard as the above evaluation at normal temperature.

<Print evaluation>
Regarding the thermal transfer recording media of Examples 1 to 6 and Comparative Examples 1 to 5, the thermal transfer recording media stored at room temperature and after being stored in a 40 ° C. 90% RH environment for 72 hours, further 24 at normal temperature. Table 1 shows the results of evaluating the maximum reflection density, the presence / absence of abnormal transfer, and the shine by performing solid printing with a thermal simulator using a heat-sensitive transfer recording medium and a transfer medium that have been stored for a long time. Note that the maximum reflection density is a value obtained by measuring a printed portion where no shine is confirmed with X-Rite 528.
The printing conditions are as follows.
Printing environment: 23 ° C, 50% RH
Applied voltage: 29V
Line cycle: 0.7msec
Print density: 300 dpi sub-scan 300 dpi main scan

<Abnormal transcription evaluation>
The abnormal transcription was evaluated according to the following criteria.
○: Abnormal transfer to the transfer object is not observed Δ: Abnormal transfer to the transfer object is very slight ×: Abnormal transfer to the transfer object is observed on the entire surface

<Electricity evaluation>
Moreover, the evaluation of shine was performed according to the following criteria.
◯: shine is not recognized Δ: shine is partially recognized
X: Tekari is clearly recognized.

From the results shown in Table 1, the feeling of Examples 1 to 6 in which an undercoat layer formed by applying and drying a coating solution containing a water-soluble polymer and a vinylpyrrolidone-vinylimidazole copolymer as main components was provided. It was found that the thermal transfer recording medium clearly has a higher transfer sensitivity during high-speed printing than the thermal transfer recording medium of Comparative Example 1 in which no undercoat layer is provided. It was also found that there is no practical problem with the adhesion of the dye layer during normal temperature storage and high temperature / high humidity storage, abnormal transfer during printing, and shine caused in high density areas. Among them, the heat-sensitive transfer recording media of Examples 1 and 2 showed that polyvinyl alcohol is more preferable as the water-soluble polymer from the maximum reflection density of the room temperature storage product and the high temperature / high humidity storage product. In addition, the thermal recording medium of Example 2 and the thermal transfer recording media of Examples 3 and 4 show that the water-soluble polymer and the vinylpyrrolidone-vinylimidazole copolymer are obtained from the results of shine in normal temperature storage and high temperature / high humidity storage. It was found that the content ratio of is more preferably a water-soluble polymer / vinylpyrrolidone-vinylimidazole copolymer = 7/3 to 3/7 in terms of a solid content mass ratio. Further, the thermal transfer recording medium of Example 5 has a coating amount of the undercoat layer of less than 0.10 g / m ^{2 as} compared with the thermal transfer recording medium of Example 4, so that after storage at a somewhat high temperature and high humidity. It was found that the adhesiveness of the lipstick was lowered, and that the effect of shine was somewhat lowered. In addition, the thermal transfer recording medium of Example 6 is less than the thermal transfer recording medium of Example 4 because the coating amount of the undercoat layer is more than 0.30 g / m ² , so that the effect of the transfer sensitivity is reduced. I found out.

  In contrast, in the thermal transfer recording medium of Comparative Example 2, as compared with the thermal transfer recording medium of Example 1, as a result of providing the undercoat layer with only the water-soluble polymer polyvinyl pyrrolidone, high temperature and high humidity were obtained. It has been found that there is a problem with the adhesiveness of the dye layer during storage, and at the same time, there is a problem with shine. Further, in the thermal transfer recording medium of Comparative Example 3, as compared with the thermal transfer recording medium of Example 1, as a result of providing the undercoat layer with a mixture of polyvinyl alcohol and polyimidazole which are water-soluble polymers, Although an increase in the maximum reflection density was confirmed, it was found that it had the same problem as the thermal transfer recording medium of Comparative Example 2. Further, in the thermal transfer recording medium of Comparative Example 4, as compared with the thermal transfer recording medium of Example 1, as a result of providing the undercoat layer only with the vinylpyrrolidone-vinylimidazole copolymer, the sensitivity of Comparative Examples 2 and 3 was obtained. Although some improvement was confirmed with respect to the adhesion and shine of the dye layer in the high-temperature and high-humidity storage confirmed with the thermal transfer recording medium, it was not sufficient, and the maximum reflection density was found to be somewhat inferior. Further, in the thermal transfer recording medium of Comparative Example 5, as compared with the thermal transfer recording medium of Example 1, the subbing layer was provided with a mixture of vinylpyrrolidone-vinyl acetate copolymer and alumina sol.・ Although the adhesion of the dye layer and the maximum reflection density are in the range where there is no practical problem in both high humidity storage, it has been found that there is a problem with shine in high temperature and high humidity storage products.

  The thermal transfer recording medium obtained by the above-described embodiment of the present invention can be used in a sublimation transfer type printer, and various colors can be easily formed in full color along with the high speed and high functionality of the printer. It can be used widely for camera self-prints, cards such as identification cards, and amusement output.

DESCRIPTION OF SYMBOLS 10 ... Base material, 20 ... Undercoat layer, 30 ... Dye layer, 40 ... Heat-resistant slipping layer.

Claims (8)

In a thermal transfer recording medium in which a heat-resistant slipping layer is provided on one surface of a substrate made of a synthetic resin film, and an undercoat layer and a dye layer are provided in this order on the other surface of the substrate,
The thermal transfer recording medium, wherein the undercoat layer contains at least a water-soluble polymer and a vinylpyrrolidone-vinylimidazole copolymer.   The base material comprising the synthetic resin film is any one of polyethylene terephthalate, polyethylene naphthalate, polypropylene, cellophane, acetate, polycarbonate, polysulfone, polyimide, polyvinyl alcohol, aromatic polyamide, aramid, and polystyrene. Item 2. The thermal transfer recording medium according to Item 1.   2. The thermal transfer recording medium according to claim 1, wherein the thickness of the substrate made of the synthetic resin film is 2 μm or more and 50 μm or less. The thermal transfer recording medium according to claim 1, wherein the coating amount of the heat resistant slipping layer after drying is from 0.10 g / m ^{2 to} 2.00 g / m ² .   2. The thermal transfer recording medium according to claim 1, wherein the water-soluble polymer is any one of polyvinyl alcohol, polyvinyl pyrrolidone, starch, gelatin, methyl cellulose, ethyl cellulose, carboxymethyl cellulose, and sodium alginate. The thermal transfer recording medium according to claim 1, wherein the coating amount of the dye layer after drying is 0.70 g / m ² .   The binder of the dye layer is ethyl cellulose, hydroxyethyl cellulose, ethyl hydroxy cellulose, hydroxypropyl cellulose, methyl cellulose, cellulose acetate, polyvinyl alcohol, polyvinyl acetate, polyvinyl butyral, polyvinyl acetal, polyvinyl pyrrolidone, polyacrylamide, polyester resin, styrene-acrylonitrile. The thermal transfer recording medium according to claim 1, wherein the thermal transfer recording medium is a polymerization resin or a phenoxy resin.   2. The thermal transfer recording medium according to claim 1, wherein a mixing ratio of the dye and the binder in the dye layer is (dye) / (binder) = 10/100 to 300/100 on a mass basis.

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