JP2001301327A - Heat sensitive recording body - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a heat sensitive recording body, high in glossiness and excellent in head matching property, color producing density as well as storage stability upon printing while provided with a high-class feeling. SOLUTION: In the heat sensitive recording body consisting of a radiation curing type over coat formed of a heat sensitive color producing layer provided on the substrate of paper, plastic sheet, synthetic paper or the like through the intermediate layer, the intermediate layer contains the copolymer of ethylene/acrylic acid and a specified polyglycerol polyglycidyl ether.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

The present invention relates to a thermosensitive recording medium. More specifically, the present invention relates to a high-grade thermal recording medium having high glossiness and excellent head matching property, color density and storage stability at the time of printing.

[0002]

2. Description of the Related Art Conventionally, a heat-sensitive recording medium for obtaining a recorded image by reacting a colorless or light-colored basic dye with an organic or inorganic colorant by heat is relatively inexpensive, and the apparatus is compact and maintenance-free. Therefore, in the field of facsimile and printers in recent years, the demand for thermal recording media such as POS labels, overhead projectors (OHP), second original drawings such as design drawings, cards and the like has been expanding.

[0003] However, these heat-sensitive recording materials have problems in storage stability (especially, discoloration of a color image due to a plasticizer, oil, or water), and also have disadvantages such as background fogging. As a method for solving this problem, a method of providing an ultraviolet curable resin layer on the thermosensitive coloring layer (Japanese Patent Publication No. 58-35478) or a method of providing an electron beam curable resin layer on the thermosensitive coloring layer via an intermediate layer And the like have been proposed (JP-A-59-26291).

[0004]

However, in the method of providing the radiation-curable resin layer on the heat-sensitive color-forming layer, the radiation-curable resin or a commonly used diluting solvent is used to coat the heat-sensitive color-forming layer. , And it was not practical. Also, with the method of providing a radiation-curable resin layer via an intermediate layer on the heat-sensitive coloring layer, with the recent diversification of heat-sensitive recording methods and higher performance, the hardware of thermal printers, facsimile machines, etc. has made remarkable progress. Adhesion to the thermal head and generation of noise during printing (sticking noise) in high-speed printing by a printer or printing by a video printer
And so on. In order to increase the commercial value of thermal recording media, high gloss products are required in the market,
High-gloss thermosensitive recording media tend to stick to the thermal head especially during printing, so it is easy to make printing noises, make fine scratches on the surface of the colored area, or distorted or shrink the colored image. There was a tendency that it was easy to wear.

[0005] Further, if the smoothness of the intermediate layer is increased to improve the uniformity of the image by providing a radiation-curable resin layer via the intermediate layer, the adhesion of the radiation-curable resin to the overcoat decreases. There is a problem of doing. In addition, in order to obtain a high-gloss thermosensitive recording medium, when forming an overcoat layer, it is common to dilute with a solvent or the like in many cases, but to improve the uniformity of the image, an intermediate layer is generally used. When the coating amount is reduced, the diluting solvent etc. soaks into the heat-sensitive coloring layer during coating, and the background fogging is likely to occur. In addition to this, storage stability such as water resistance and plasticizer resistance, as well as head matching during printing There was also a tendency for the property to worsen. In any case, the object of obtaining a high-grade thermal recording medium having high gloss, excellent head matching, and excellent storage properties such as water resistance and plasticizer resistance has not yet been achieved.

[0006]

Means for Solving the Problems The present inventors have made intensive studies to solve the above-mentioned problems, and as a result, completed the present invention. That is, the present invention provides (1) a heat-sensitive color-developing layer containing a colorless or pale-colored color-forming compound and a color-developing compound capable of causing the color-forming compound to develop color when heated on a support, and an intermediate layer interposed therebetween. In a heat-sensitive recording medium having a radiation-curable overcoat layer formed thereon, the intermediate layer is composed of an ethylene / acrylic acid copolymer and the following formula (1):

[0007]

Embedded image

The present invention also relates to a thermosensitive recording material comprising a compound represented by the formula (1), wherein n represents 1 to 5.

BEST MODE FOR CARRYING OUT THE INVENTION

The present invention will be described in detail. In the present invention, the ethylene / acrylic acid copolymer used for the intermediate layer is
The monomer component is a compound comprising ethylene and acrylic acid, having a molecular weight of usually 100,000 or less and an acid value of about 150.
Further, the polyglycerol polyglycidyl ether represented by the formula (1) is a compound usually consisting of n = 1 to 5. The proportion of the ethylene / acrylic acid copolymer and the compound represented by the formula (1) is usually 1 to 50 parts by weight, preferably 5 to 20 parts by weight, based on 100 parts by weight of the former.

Further, if necessary, a binder, a filler and other various additives used for preparing the following thermosensitive coloring layer of the present invention are used in combination.

The heat-sensitive recording material of the present invention comprises a heat-sensitive coloring layer, an intermediate layer containing an ethylene / acrylic acid copolymer and a compound represented by the formula (1), and a radiation-curable overcoat layer on a support. It is formed in order. In the present invention, the heat-sensitive color-forming layer is mainly composed of a colorless or pale-colored color-forming compound and a color-developing compound capable of causing the color-forming compound to develop a color when heated as a main component. Contains fillers, heat-fusible compounds, and other additives.

In forming the thermosensitive coloring layer in the present invention, the coloring compound is usually 1 to 50% by weight, preferably 5 to 30% by weight, and the coloring compound is usually 0.5 to 80% by weight.
% By weight, preferably 5 to 40% by weight;
90% by weight, a filler and a heat-fusible compound (sensitizer) are each usually 0 to 80% by weight, and other lubricants, surfactants, defoamers, ultraviolet absorbers and the like are each in an arbitrary ratio. Each is used in an amount of 0 to 30% by weight. The weight% is the weight ratio of each component in the thermosensitive coloring layer.

Examples of the coloring compound used in the thermosensitive coloring layer are not particularly limited as long as they are generally used for pressure-sensitive recording paper or thermosensitive recording paper. Specific examples thereof include fluoran compounds, triarylmethane compounds, spiro compounds, diphenylmethane compounds, thiazine compounds, lactam compounds, and fluorene compounds.

Specific examples of fluoran compounds that can be used include, for example, 3-diethylamino-6-methyl-7-anilinofluoran, 3-dibutylamino-6-methyl-
7-anilinofluoran, 3- (N-methyl-N-cyclohexylamino) -6-methyl-7-anilinofluoran, 3- (N-ethyl-N-isopentylamino)-
6-methyl-7-anilinofluoran, 3-isobutylethylamino-6-methyl-7-anilinofluoran,
3- [N-ethyl-N- (3-ethoxypropyl) amino] -6-methyl-7-anilinofluoran, 3- (N
-Ethyl-N-hexylamino) -6-methyl-7-anilinofluoran, 3-dipentylamino-6-methyl-7-anilinofluoran, 3- (N-methyl-N-propylamino) -6 -Methyl-7-anilinofluoran, 3- (N-ethyl-N-tetrahydrofurylamino) -6-methyl-7-anilinofluoran, 3-diethylamino-6-methyl-7- (p-chloroanilino)
Fluoran, 3-diethylamino-6-methyl-7-
(P-fluoroanilino) fluoran, 3- (p-toluidinoethylamino) -6-methyl-7-anilinofluoran, 3-diethylamino-6-methyl-7- (p-
Toluidino) fluoran, 3-diethylamino-7-
(O-chloroanilino) fluoran, 3-dibutylamino-7- (o-chloroanilino) fluoran, 3-diethylamino-7- (o-fluoroanilino) fluoran, 3-dibutylamino-7- (o-fluoroanilino) Fluoran, 3-diethylamino-7- (3,4-
Dichloroanilino) fluorane, 3-pyrrolidino-6
Methyl-7-anilinofluoran, 3-diethylamino-6-chloro-7-ethoxyethylaminofluoran,
3-diethylamino-6-chloro-7-anilinofluoran, 3-diethylamino-7-chlorofluoran, 3
-Diethylamino-6-chloro-7-methylfluoran, 3-diethylamino-7-methylfluoran, 3-
Diethylamino-7-octylaminofluoran, 3-
Diethylamino-7-phenylfluoran, 3- (p-
Toluidinoethylamino) -6-methyl-7-phenethylfluoran and the like.

Similarly, tolyl methane compounds include:
For example, 3,3-bis (p-dimethylaminophenyl)-
6-dimethylaminophthalide (alias: crystal violet lactone or CVL), 3,3-bis (p-dimethylaminophenyl) phthalide, 3- (p-dimethylaminophenyl) -3- (1,2-dimethylaminoindole -3-yl) phthalide, 3- (p-dimethylaminophenyl) -3- (2-methylindol-3-yl)
Phthalide, 3- (p-dimethylaminophenyl) -3-
(2-phenylindol-3-yl) phthalide, 3,
3-bis (1,2-dimethylindol-3-yl)-
5-dimethylaminophthalide, 3,3-bis (1,2-
Dimethylindol-3-yl) -6-dimethylaminophthalide, 3,3-bis (9-ethylcarbazole-3)
-Yl) -5-dimethylaminophthalide, 3,3- (2
-Phenylindol-3-yl) -5-dimethylaminophthalide, 3-p-dimethylaminophenyl-3-
(1-methylpyrrol-2-yl) -6-dimethylaminophthalide and the like.

Further, as the spiro compound, for example, 3-
Methylspirodinaphthopyran, 3-ethylspirodinaphthopyran, 3,3′-dichlorospirodinaphthopyran,
3-benzylspirodinaphthopyran, 3-propylspirobenzopyran, 3-methylnaphtho- (3-methoxybenzo) spiropyran, 1,3,3-trimethyl-6-nitro-8'-methoxyspiro (indoline-2,2 '-
Benzopyran) and the like, as diphenylmethane compounds, for example, N-halophenyl-leuco auramine,
4-bis-dimethylaminophenylbenzhydrylbenzyl ether, N-2,4,5-trichlorophenylleucouramine and the like; thiazine compounds such as benzoylleucomethylene blue and p-nitrobenzoylleucomethylene blue; Examples of the fluorene-based compound include rhodamine B anilinolactam and rhodamine B-p-chloroanilinolactam, and examples of the fluorene-based compound include 3,6-bis (dimethylamino) fluorenespiro (9,3 ′)-6. '-Dimethylaminophthalide, 3,6-bis (dimethylamino) fluorenespiro (9,3')-6'-pyrrolidinophthalide,
3-dimethylamino-6-diethylaminofluorenespiro (9,3 ')-6'-pyrrolidinophthalide and the like. These coloring compounds are used alone or in combination.

The color-developing compound is not particularly limited as long as it is generally used in pressure-sensitive recording paper or heat-sensitive recording paper. Specific examples of the color developing compound that can be used include, for example, α-naphthol, β-naphthol, p-octylphenol, 4-t-octylphenol, pt-butylphenol, p-phenylphenol, 1,1-bis (p
-Hydroxyphenyl) propane, 2,2-bis (p-
Hydroxyphenyl) propane (alias: bisphenol A or BPA), 2,2-bis (p-hydroxyphenyl) butane, 1,1-bis (p-hydroxyphenyl)
Cyclohexane, 4,4′-thiobisphenol, 4,
4'-cyclohexylidenediphenol, 2,2'-
(2,5-dibromo-4-hydroxyphenyl) propane, 4,4-isopropylidenebis (2-t-butylphenol), 2,2′-methylenebis (4-chloroenol), 4,4′-dihydroxydiphenylsulfone ,
2,4'-dihydroxydiphenyl sulfone, bis (3
-Allyl-4-hydroxyphenyl) sulfone, 4-hydroxy-4'-methoxydiphenyl sulfone, 4-hydroxy-4'-ethoxydiphenyl sulfone, 4-hydroxy-4'-isopropoxydiphenyl sulfone,
4-hydroxy-4′-butoxydiphenyl sulfone,
Methyl bis (4-hydroxyphenyl) acetate, bis (4
-Hydroxyphenyl) butyl acetate, benzyl bis (4-hydroxyphenyl) acetate, 2,4-dihydroxy-
Phenolic compounds such as 2′-methoxybenzanilide, benzyl p-hydroxybenzoate, ethyl p-hydroxybenzoate, dibenzyl 4-hydroxyphthalate,
Dimethyl 4-hydroxyphthalate, ethyl 5-hydroxyisophthalate, 3,5-di-t-butylsalicylic acid,
Examples thereof include aromatic carboxylic acid derivatives such as 3,5-di-α-methylbenzyl salicylic acid, aromatic carboxylic acids and metal salts thereof.

Specific examples of the binder which can be used in the present invention include, for example, methylcellulose, methoxycellulose, hydroxyethylcellulose, carboxymethylcellulose, sodium carboxymethylcellulose, cellulose, polyvinyl alcohol (PVA), carboxyl group-modified polyvinyl alcohol, sulfonic acid group-modified Polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylamide, polyacrylic acid, starch and derivatives thereof, casein, gelatin, water-soluble isoprene rubber, alkali salts of styrene / maleic anhydride copolymer, iso (or diiso) butylene / maleic anhydride Water-soluble ones such as polymer salts, styrene / butadiene (SB) copolymer, carboxylated styrene / butadiene (SB) copolymer, styrene / buta Ene / acrylic acid copolymer,
Polyvinyl acetate, polyvinyl chloride, vinyl chloride / vinyl acetate copolymer, polystyrene, acrylic resin, acrylic / styrene resin, polyacrylate, polyester, polycarbonate, polyurethane, polybutyral, epoxy resin, furan resin, vinyl toluene resin ,
Examples include hydrophobic polymer compounds such as rosin ester resin, composite particles of colloidal silica and acrylic copolymer, and emulsions thereof.

Examples of the fillers usable in the present invention include, for example, aluminum hydroxide, magnesium hydroxide, calcium carbonate, magnesium carbonate, magnesium oxide, aluminum oxide, silicon dioxide, titanium dioxide, talc, clay, kaolin. , Colloidal silica, inorganic fillers such as barium sulfate metal powder and fillers surface-treated with these inorganic fillers, styrene microballs, polystyrene resin beads, acrylic resin beads, urethane resin beads, polycarbonate resin beads, polyolefin resin, benzoguanamine-formalin Condensate resin powder, benzoguanamine-melamine-formalin condensate resin powder, urea-formalin condensate resin powder, epoxy resin powder, polyethylene powder, tetrabromobi Phenol A, decabromodiphenyl oxide, tricresyl phosphate, triethyl phosphate, organic fillers such as aromatic polyesters and the like.

Examples of the heat-fusible compound that can be used in the present invention include waxes such as animal and vegetable waxes and synthetic waxes, higher fatty acids, higher fatty acid amides, higher fatty acid anilides, acetylated aromatic amines, and naphthalene derivatives. , Aromatic ethers, aromatic carboxylic acid derivatives, aromatic sulfonic acid ester derivatives, carbonic or oxalic acid diester derivatives, biphenyl derivatives, terphenyl derivatives, etc., which are solid at ordinary temperature and have a melting point of about 70 ° C. or more Can be. These usually act as sensitizers for increasing color sensitivity.

In the above, the waxes include, for example, wood wax, carnauba wax, shellac, paraffin, montan wax, oxidized paraffin, polyethylene wax,
Polyethylene oxide and the like are higher fatty acids such as stearic acid and behenic acid, and higher fatty acid amides are stearic acid amide, oleic acid amide and N
-Methyl stearamide, erucamide, methylol behenamide, methylol stearamide,
Methylenebisstearic acid amide, ethylenebisstearic acid amide, etc., as higher fatty acid anilide, for example, stearic acid anilide, linoleic acid anilide, etc. For example, 1-benzyloxynaphthalene, 2-benzyloxynaphthalene, 1-hydroxynaphthoic acid phenyl ester and the like,
Examples of the aromatic ether include 1,2-diphenoxyethane, 1,4-diphenoxyethane, 1,2-bis (3-methylphenoxy) ethane, and 1,2-bis (4-
Methoxyphenoxy) ethane, 1,2-bis (3,4-
Dimethylphenyl) ethane, 1-phenoxy-2- (4
-Chlorophenoxy) ethane, 1-phenoxy-2-
(4-methoxyphenoxy) ethane and the like; and aromatic carboxylic acid derivatives such as p-hydroxybenzoic acid benzyl ester, p-benzyloxybenzoic acid benzyl ester and terephthalic acid dibenzyl ester; and aromatic sulfonic acid ester derivatives Examples thereof include p-toluenesulfonic acid phenyl ester, phenylmesitylenesulfonate, 4-methylphenylmesitylenesulfonate, and the like, and examples of carbonic acid or oxalic acid diester derivatives include, for example, diphenyl carbonate, dibenzyl oxalate, dioxalate ( 4-methylbenzyl) ester, oxalic acid di (4-chlorobenzyl) ester and the like include biphenyl derivatives such as p-benzylbiphenyl and p-benzylbiphenyl.
-Allyloxybiphenyl and the like, and terphenyl derivatives include, for example, m-terphenyl and the like.

In addition, tetrafluoride resin, stearic acid-modified silicone oil, aspartic acid ester derivative, Famex A-1212 (manufactured by Ajinomoto Co.), polyethylene wax, carnauba wax, zinc stearate, etc.
Magnesium stearate, aluminum stearate, calcium stearate, amide stearate,
Straight chain C such as polyoxyethylene stearamide, polyoxyethylene sorbite stearic ester, etc.
Various lubricants such as a compound having a long-chain alkyl group of 16 to C18, a surfactant, an antifoaming agent, an external light absorbing agent and the like are added as necessary.

Using the above materials, for example, the following method
Therefore, the thermosensitive coloring layer in the present invention is prepared. That is,
First, a color-forming compound and a color-developing compound are respectively
Separately with binder or other additives as needed
Both ball mills, attritors, sand mills, etc.
After crushing and dispersing (when crushing and dispersing
Usually uses water as the medium), and mix to form a thermosensitive coloring layer.
Prepare cloth liquid and support paper, plastic sheet, synthetic paper, etc.
Usually 1 to 20 g / m2 on dry weight ^Twobecome
Coating with a bar coater, blade coater, etc.
(The ratio of the coloring compound to the developing compound is usually the dry weight ratio.
2: 1 to 1:10), dried and provided with a thermosensitive coloring layer
Obtained support.

Next, an ethylene / acrylic acid copolymer and a compound represented by the formula (1) or, if necessary, a binder, a filler and other additives are used in combination to form a coating liquid for forming an intermediate layer. The solid content weight is 0.5 to 5 g on the thermosensitive coloring layer.
/ M ² and dried to form an intermediate layer.

In the heat-sensitive recording medium of the present invention, a radiation-curable overcoat layer is provided on the thus formed intermediate layer. The radiation-curable overcoat layer is usually composed of a monofunctional or polyfunctional monomer or oligomer as a main component, and if necessary, the above-mentioned filler, lubricant, surfactant, defoaming agent, ultraviolet absorber, further polymer, Contains additives such as a leveling agent, a radical reactive silicone macromer, an antioxidant, a polymerization inhibitor, an antistatic agent, and a fluorescent dye. In the case of curing with ultraviolet rays, the composition contains a photopolymerization initiator and, if necessary, a photopolymerization accelerator. In forming the overcoat layer in the present invention, a monofunctional or polyfunctional monomer or oligomer is 20 to 100% by weight,
0.1 to 50% by weight of a filler or a lubricant, if necessary,
In addition, a surfactant, an antifoaming agent, an ultraviolet absorber and the like are each used at an arbitrary ratio, for example, 0 to 30% by weight, respectively. In the case of ultraviolet curing, the polymerization initiator and the accelerator are each used in an amount of 0.1.
1 to 15% by weight is contained.

Examples of monofunctional monomers that can be used include:
For example, styrene, vinyl acetate, vinyl monomers such as N-vinylpyrrolidone, epoxy (meth) acrylate,
Oligomers such as saturated polyester / styrene, polyethylene (meth) acrylate, polyether (meth) acrylate, silicon (meth) acrylate, polybutadiene (meth) acrylate, polyene / thiol, polystyrylethyl (meth) acrylate, and polyamide (meth) acrylate Styrene, vinyl acetate, vinyl monomers such as N-vinyl pyrrolidone, N, N-dimethylaminomethyl (meth) acrylate, N, N-dimethylaminoethyl (meth) acrylate, N, N-diethylaminoethyl (meth) acrylate, Butyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2
-Ethylhexyl (meth) acrylate, hydroxybutyl (meth) acrylate, n-hexyl acrylate, cyclohexyl acrylate, n-decyl acrylate, isobornyl (meth) acrylate, dicyclopentanyloxyethyl (meth) acrylate, phenoxyethyl (meth) acrylate Phenoxy polyethylene glycol (meth) acrylate, nonylphenoxyethyl (meth) acrylate, lauryl (meth) acrylate, phenylglycidyl ether (meth) acrylate, acryloyl morpholine, etc.

Similarly, examples of the polyfunctional monomer include ethylene glycol diacrylate, polyethylene glycol diacrylate, polypropylene glycol diacrylate, neopentyl glycol diacrylate, tripropylene glycol diacrylate, and di (alkylene oxide adduct of bisphenol A). (Meth) acrylate, tetraethylene glycol diacrylate, neopentyl glycol diacrylate hydroxypivalate, 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, 1,12-dodecanediol di (Meth) acrylate, 1,14-tetradecanediol di (meth) acrylate, 1,16-hexadecanediol di (meth)
Bifunctional monomers such as acrylate, 1,20-eicosanediol di (meth) acrylate, isopentyldiol di (meth) acrylate, 3-ethyl-1,8-octanediol di (meth) acrylate, and trimethylolpropanetri (Meth) acrylate, trimethyloloctanetri (meth) acrylate, trimethylolpropanepolyethoxytri (meth) acrylate,
Trimethylolpropane polypropoxytri (meth) acrylate, trimethylolpropanepolyethoxypolypropoxytri (meth) acrylate, tris [(meth) acryloyloxyethyl] isocyanurate, pentaerythritol tri (meth) acrylate, pentaerythritol polyethoxytetra (Meth) acrylate, pentaerythritol polypropoxytetra (meth) acrylate, pentaerythritol tetra (meth) acrylate, ditrimethylolpropanetetra (meth) acrylate, dipentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, Dipentaerythritol hexa (meth) acrylate, caprolactone-modified tris [(meth) acryloyloxye Le], and 3 or more functional monomers, such as isocyanurate.

Examples of oligomers include, for example, epoxy (meth) acrylate, urethane (meth) acrylate, saturated polyester / styrene, polyethylene (meth) acrylate, polyether (meth) acrylate, silicone (meth) acrylate, polybutadiene (meth) ) Acrylate, polyene / thiol, polystyrylethyl (meth) acrylate, polyamide (meth)
Acrylate and the like.

The radiation-curable resin composition used in the present invention may or may not be cured with an electron beam. However, when it is cured with an ultraviolet ray, a photopolymerization initiator may be used.
A photopolymerization accelerator is used. As the photopolymerization initiator, for example, acetophenone, benzophenone, benzoin ether, chloroacetophenone, diethoxyacetophenone, hydroxyacetophenone, α-aminoacetophenone, benzylmethylketal, thioxanthone, α-
Acyl oxime esters, acyl phosphine oxides, glyoxy esters, 3-ketocoumarin, 2-ethylanthraquinone, camphorquinone, benzyl and the like can be mentioned. N-methyldiethanolamine, triethanolamine, diethanolamine, isoamyl P-dimethylaminobenzoate as a photopolymerization accelerator,
Amine compounds such as N, N-diethyl-P-aminobenzonitrile, phosphorus compounds such as tri-n-butylphosphine, chlorine compounds such as hexachloroethane, and Michler's ketone are used alone or in combination of two or more. be able to.

The radiation-curable resin composition used in the present invention may contain liquid paraffin, paraffin wax, polyethylene wax, synthetic wax, vegetable oil, animal oil, sorbitan ester, polyoxyethylene sorbite fatty acid ester, Glycerin fatty acid esters can be added. In addition, acrylic copolymer, silicone oil, silicone oil modified with alkyl group, amino group, epoxy group, fluorine group, carboxyl group, hydroxyl group, mercapto group, fluorine surfactant, polymer, leveling agent, radical reactivity Silicone macromers, defoamers, ultraviolet absorbers, antioxidants, polymerization inhibitors, antistatic agents, fluorescent dyes and the like can be added.

The radiation-curable resin composition used in the present invention can be obtained by uniformly mixing the above components. The radiation-curable resin composition thus obtained is applied on the intermediate layer by a conventional roll coater, bar coater, gravure coater, flexo coater, screen printing machine or the like by a method known per se, and diluted with a solvent or the like. In this case, after coating and drying, the coating film is cured by irradiating ultraviolet rays or electron beams. The coating amount of the overcoat layer is not particularly limited. However, if the dry weight is too small, the object of the present invention cannot be achieved.If the dry weight is too large, the recording sensitivity of the thermosensitive recording medium may decrease, or the coating weight may decrease. Usually, the dry weight is preferably 0.5
It is good to apply in the range of ^{20 to 20} g / m ² , more preferably 1 to 10 g / m ² . Examples of the radiation irradiation device include an electron beam acceleration device having an energy of 100 to 500 eV and an ultraviolet irradiation device having a xenon lamp, a high-pressure mercury lamp, and a metal halide lamp as a light source. The amount of light, the arrangement of the light source, and the like are determined depending on the device used. When a high-pressure mercury lamp is used, 80 to 120 W /
transfer speed of 20-60
It is preferable to cure by irradiating 1 to 4 times at m / min.

In a thermosensitive recording medium having a radiation-curable overcoat layer formed on a thermosensitive coloring layer via an intermediate layer, the intermediate layer is composed of an ethylene / acrylic acid copolymer and a compound represented by the formula (1). The heat-sensitive recording medium of the present invention, which contains, has higher gloss than the conventionally known ones, and is excellent in head matching and storage stability during printing.

[0033]

EXAMPLES The present invention will be described more specifically with reference to examples, but the present invention is not limited to these examples. In the examples, "parts" indicates parts by weight.

Example 1 (Formation of heat-sensitive recording layer) A mixture having the following composition was pulverized and dispersed using a sand grinder so that the average particle size became 2 μm or less, to prepare solutions [A] and [B], respectively. did. [A] solution: 3-dibutylamino-6-methyl-7-anilinofluoran 25 parts 25% PVA aqueous solution 20 parts water 55 parts [B] solution: bis (3-allyl-4hydroxyphenyl) sulfone 25 parts 25 % PVA aqueous solution 20 parts Water 55 parts

Next, the respective preparations were mixed at the following ratios to prepare a coating solution for the thermosensitive coloring layer. The coating solution was applied to a high-quality paper having a basis weight of 50 g / m ² so that the weight when dried was 8 g / m ^2, and dried. Thus, a thermosensitive coloring layer was obtained. [A] liquid 8 parts [B] liquid 16 parts 50% calcium carbonate dispersion 10 parts 50% carboxylated styrene / butadiene copolymer latex 6 parts water 20 parts

(Formation of Intermediate Layer) Next, as a coating solution for the intermediate layer, the following preparation solution was applied onto the thermosensitive coloring layer so that the weight when dried was 2 g / m ^2, and the intermediate layer was dried. Formed. 30% ethylene / acrylic acid copolymer (molecular weight = about 100,000, acid value = 156) 100 parts of aqueous ammonium solution 5 parts of a compound of formula (1) where n = about 3, epoxy equivalent = 183

(Formation of Overcoat Layer) Next, the following composition was applied onto the intermediate layer so that the dry coating amount was 3 g / m ^2, and an ultraviolet irradiation apparatus (GS ASE) equipped with a high-pressure mercury lamp of 80 W / cm was used. -20; manufactured by Nippon Battery Co., Ltd.) and cured by irradiating twice at a conveyor speed of 40 m / min to obtain a thermosensitive recording medium of the present invention. Dipentaerythritol hexaacrylate 35 parts EO-modified bisphenol A diacrylate (KAYARAD R-551; manufactured by Nippon Kayaku) 6 parts 1,4-butanediol diacrylate 12 parts Calcium carbonate 40 parts Photoinitiator (Irgacure 184; Ciba Geigy) 7 copies

Example 2 A 30% ethylene / acrylic acid copolymer alkanolamine salt aqueous solution was used in place of the 30% ethylene / acrylic acid copolymer ammonium aqueous solution of Example 1 in the same manner as in Example 1. A thermosensitive recording medium of the present invention was obtained.

Example 3 The procedure of Example 1 was repeated, except that a 25% aqueous solution of ethylene / acrylic acid copolymer sodium salt was used instead of the 30% aqueous solution of ethylene / acrylic acid copolymer ammonium used in Example 1. The thermosensitive recording medium of the invention was obtained.

Example 4 In the same manner as in Example 1 except that the compound of the formula (1) of Example 1 was replaced with a compound of the formula (1) having n = 2 and an epoxy equivalent of 173, the present invention was carried out. A thermosensitive recording medium was obtained. Table 1 shows the quality performance of the thermosensitive recording medium of the present invention obtained as described above.

Table 1 Quality Performance Table 1) 2) 3) 4) 5) Gloss Coloring Density Water Resistance Plasticizer Head Matching Example 1 84 2.03 ○ / ○ 2.03 ○ / ○ / ○ Example 2 84 2.02 ／/ ○ 2.02 ○ / ○ / ○ Example 3 82 2.00 ／/ ○ 2.00 ／/ ○ / ○ Example 4 82 2.01 ／/ ○ 2.02 ／/ ○ / ○

1) Glossiness The 60-degree specular glossiness of the thermosensitive recording medium was measured according to JIS Z8741. Gloss checker IG-320 for measurement
(Manufactured by Horiba, Ltd.) was used. 2) Color density A commercially available video graphic printer (UP-860;
Print image (color print) by Sony Corporation
Then, the colored print portion is placed in a Macbeth reflection densitometer (RD-914).
Type). 3) Water resistance After the heat-sensitive recording medium was immersed in tap water for 24 hours, the surface was rubbed with a finger, and peeling of the uncolored printed portion / colored printed portion was observed. ○--No peeling. △---There is little peeling. × --- There is peeling. 4) Plasticizer resistance A value measured by a Macbeth reflection densitometer on the same side of the thermosensitive recording medium after superimposed on a commercially available plastic eraser on the color printing surface under a load of 0.0198 MPa (200 g / cm ² ) at room temperature for 24 hours. . 5) Head Matching Color printing sound at the time of printing / scratch on the surface of the thermal recording medium / adhesion to the thermal head was determined. ○---None. △ −−− Slight. × −−−

As is clear from the table, the heat-sensitive recording material of the present invention has a high glossiness and is excellent in color density, storage property and head matching property.

[0044]

According to the present invention, in a heat-sensitive recording medium having a radiation-curable overcoat layer formed on a heat-sensitive coloring layer, gloss is provided by providing an intermediate layer containing an ethylene / acrylic acid copolymer and a specific polyglycerol polyglycidyl ether. An object of the present invention is to provide a thermosensitive recording medium which has high performance and is excellent in head matching property, color developing property and storage stability at the time of printing.

Claims (1)

[Claims] 1. A radiation-curable layer comprising a colorless or pale-colored color-forming compound and a color-developing compound capable of causing the color-forming compound to develop color when heated on a support. In the thermosensitive recording medium having the overcoat layer formed of the above, the intermediate layer is composed of an ethylene / acrylic acid copolymer and the following formula (1): (Wherein n represents 1 to 5 in the formula (1)).