JP2002274047A - Thermal recording material - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a thermal recording material which has a coloring tone of a moderate black for images, and is excellent in the preservation property such as coloring sensitivity, heat-resistance, moisture-resistance and light- resistance. SOLUTION: This thermal recording material contains a specified black coloring compound, a specified red coloring compound, CVL or benzoyl leuco methylene blue, and a bis(3-allyl-4-hydroxyphenyl)sulfone having an α type crystal form as a color developing compound on a plastic film or a synthetic paper.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat-sensitive recording material, and more particularly to a photographic-like heat-sensitive recording material having a moderate black color tone and excellent color development sensitivity, heat resistance, moisture resistance, and light resistance. .

[0002]

2. Description of the Related Art A heat-sensitive recording material utilizing a colorless or pale-colored color-forming substance and a color-developing substance capable of coloring the color-forming substance when heated is disclosed in JP-B-43-4160 and JP-B-45-1403.
No. 9 etc. and widely used. Generally, a thermosensitive recording material is prepared by separately dispersing a developer such as a leuco dye and a phenolic substance into fine particles separately, then mixing the two, and adding a binder, a sensitizer, a filler, a lubricant, etc. Adds an agent to form a coating solution, and is applied to a support such as paper, film, or synthetic paper. Heating allows the leuco dye and / or the developer to melt and come into contact with the color reaction to form a color reaction record. In general, a sheet-like heat-sensitive recording material is prepared. For color development of such a heat-sensitive recording sheet, a thermal printer or the like having a built-in thermal head is used. Compared with other recording methods, this heat-sensitive recording method is (1) no noise is generated at the time of recording, (2) there is no need for developing and fixing, (3) maintenance-free, and (4)
It is widely used in the facsimile field, computer output, printers such as calculators, recorders for medical measurement, automatic ticket vending machines, heat-sensitive recording labels, etc. .

In recent years, as a means for providing photographic gradation and high-quality images, printout of input images by a video camera or scanner by a video printer or the like having a built-in thermal printer has been increasing. To obtain rich gradation and high quality image quality depends on the technology of hardware, but the color tone and various storability are based on the heat-sensitive recording material itself. Conventionally, heat-sensitive recording materials using bisphenol A, which is a mainstream color developing compound, have a photographic-like image close to black with a moderate color tone, but have the disadvantage of image deterioration during long-term storage. . or,
Bisphenol A has been the subject of recent debate about environmental hormone suspicions, and the thermal recording products industry has been abolished. Bisphenol S and its derivatives are used as a color developing compound having good storability. However, since the color tone is black with a bias toward blue to green, there is no problem in displaying characters, bar codes, etc. Is unsuitable for the image. Various methods have been proposed to improve the color tone without impairing the storability, specifically heat resistance, moisture resistance and light resistance, but none of them have been found to be satisfactory.

[0004]

SUMMARY OF THE INVENTION It is an object of the present invention to overcome the disadvantages of the prior art as described above. That is,
An object of the present invention is to provide a photographic-like heat-sensitive recording material having a moderate black color tone without impairing the storage stability such as heat resistance, moisture resistance and light resistance, and having excellent color sensitivity.

[0005]

The present inventor has made various studies to achieve the above object, and as a result, completed the present invention. That is, the present invention provides (1) a heat-sensitive color-forming layer comprising, as a main component, a colorless or light-colored color-forming compound and a color-developing compound capable of coloring the color-forming compound when heated on a plastic film or synthetic paper. In the recording material, the thermosensitive coloring layer is represented by the following formula (1) as a black-based coloring compound.

[0006]

Embedded image

(In the formula (1), R1 and R2 each independently represent a hydrogen atom, an alkyl group having 6 or less carbon atoms, a cyclohexyl group or a p-tolyl group.)
Formula (2) below as a red color-forming compound

[0008]

Embedded image Is a CV as a blue-based coloring compound.
L or benzoylleucomethylene blue is used as a color developing compound with bis (3-allyl-4-
(2) a compound 1 represented by the formula (1), comprising: (hydroxyphenyl) sulfone;
The heat-sensitive recording material according to claim 1, wherein the compound represented by the formula (2), CVL or benzoylleucomethylene blue is contained in an amount of 0.5 to 20 parts by weight with respect to 00 parts.
About.

[0009]

BEST MODE FOR CARRYING OUT THE INVENTION As the alkyl group having 6 or less carbon atoms in R1 and R2 of the formula (1), for example, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-
Butyl group, sec-butyl group, t-butyl group, n-pentyl (amyl) group, isopentyl (isoamyl) group, n
-Hexyl group and the like. Specific examples of the color-forming compound represented by the formula (1) include, for example, 3-diethylamino-6-methyl-7-anilinofluoran, 3-dibutylamino-6-methyl-7-anilinofluoran, Dipentylamino-6-methyl-7-anilinofluoran, 3- (N-methyl-N-propylamino) -6-methyl-7-anilinofluoran, 3- (N-isobutyl-N-ethylamino) -6-methyl-7-anilinofluoran, 3- (N-ethyl-N-isopentylamino)
-6-methyl-7-anilinofluoran, 3- (N-ethyl-N-hexylamino) -6-methyl-7-anilinofluoran, 3- (N-methyl-N-cyclohexylamino) -6 -Methyl-7-anilinofluoran, 3-
(N-ethyl-N-p-tolylamino) -6-methyl-
7-anilinofluoran and the like are used, and these are used alone or in combination.

The bis (3-allyl-4-hydroxyphenyl) sulfone having an α-type crystal form used in the present invention is described in JP-A-11-29549, and its physical properties are Cu-Kα radiation. The diffraction angle (2θ) [°] 7.2 and 2
A crystalline form characterized by an X-ray diffractogram with a peak at 2.0 and a differential scanning calorimeter (Differenti)
It is a bis (3-allyl-4-hydroxyphenyl) sulfone having a melting point of 149 ° C. or higher at an extrapolation melting temperature (Te) in an al scanning calorimeter.

The heat-sensitive recording material of the present invention comprises a compound represented by the formula (1), a compound represented by the formula (2), CVL (crystal violet lactone) or benzoyl leucomethylene blue, and bis (3) having an α-type crystal form. -Allyl-4-hydroxyphenyl) sulfone is used as a main component, and binders and other fillers, if necessary, sensitizers (heat-fusible compounds), and other additives as described below are used. Can be obtained by providing as a layer on a plastic film or synthetic paper a mixture prepared by mixing.

The component ratio of the heat-sensitive coloring layer of the present invention is expressed by the following formula (1).
Is usually 1 to 50% by weight, preferably 5 to 50% by weight.
To 30% by weight of the compound represented by the formula (2) (CAS N
o. 26567-23-7), CVL (crystal violet lactone) or leucomethylene blue is usually 0.05 to 5% by weight, preferably 0.2 to 2% by weight, respectively, bis (3- Allyl-4-hydroxyphenyl) sulfone is usually 1 to 60% by weight,
Preferably 10 to 40% by weight, binder 1 to 60% by weight, filler and sensitizer (heat-fusible compound) are each 0 to 7%.
0% by weight, other lubricants, surfactants and the like are each used in an arbitrary ratio, for example, usually 0 to 20% by weight, respectively (% by weight is the weight ratio of each component in the thermosensitive coloring layer).

In order to form a thermosensitive coloring layer having a medium black color tone and excellent image storability, a more preferred embodiment is such that, in the above-mentioned compositions, the respective amounts used are expressed by the formula ( The compound represented by the formula (2), CVL (crystal violet lactone) or benzoyl leucomethylene blue is usually 0.5 to 20 parts each, preferably 2 to 10 parts each, based on 100 parts of the compound represented by 1).
The bis (3-allyl-4-hydroxyphenyl) sulfone having the α-form crystal form is used usually in a weight ratio of 1 to 60 parts, preferably 10 to 40 parts. When the amount of the compound represented by the formula (2), CVL (crystal violet lactone) or benzoyl leucomethylene blue exceeds the above-mentioned amount ratio, there is no problem with the color tone, but the storage stability such as heat resistance, moisture resistance and light resistance is lowered. Cause. In the heat-sensitive recording material of the present invention, a color-forming compound or a color-developing compound other than the main components other than the present invention may be used in combination.

The plastic film or synthetic paper used as a support in the present invention is, for example, a thermoplastic polymer film such as polyethylene, polypropylene or polystyrene, the same film containing an inorganic pigment, or the same film containing a void (hollow). Etc. are used. These films or synthetic papers have a surface wetting tension of 35 dyn / cm or more because of the need to provide a thermosensitive coloring layer as a support.
It is preferably at least 40 dyn / cm, more preferably 50 dyn / cm.
Dyn / cm or more is preferred. Therefore, for a film having a low wetting tension, a film having the above wetting tension can be obtained by applying a corona discharge treatment or applying a surfactant or the above-mentioned intermediate layer, and the coating property between the film and the thermosensitive coloring layer can be obtained. And the adhesiveness can be increased.

The color-forming compound which can be used in combination in the present invention is not particularly limited as long as it is generally used for pressure-sensitive recording paper or heat-sensitive recording paper. Specific examples include, for example, fluoran compounds, triarylmethane compounds,
Examples include spiro compounds, diphenylmethane compounds, thiazine compounds, lactam compounds, and fluorene compounds.

Specific examples of the fluoran compound include, for example, 3- [N-ethyl-N- (3-ethoxypropyl) amino] -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-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) fluoran, 3-pyrrolidino-6-methyl-
7-anilinofluoran, 3-diethylamino-6-chloro-7-ethoxyethylaminofluoran, 3-diethylamino-6-chloro-7-anilinofluoran, 3
-Diethylamino-6-chloro-7-methylfluoran, 3- (p-toluidinoethylamino) -7-methylfluoran, 3-diethylamino-7-methylfluoran, 3-diethylamino-7-octylaminofluor Oran, 3-diethylamino-7-phenylfluoran, 3
-(P-Toluidinoethylamino) -6-methyl-7-
Phenethylfluoran and the like.

Specific examples of the triarylmethane compound include, for example, 3,3-bis (p-dimethylaminophenyl) phthalide and 3- (p-dimethylaminophenyl)-
3- (1,2-dimethylaminoindol-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-ethylcarbazol-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, specific examples of the spiro compound include, for example, 3-methylspirodinaphthopyran, 3-ethylspirodinaphthopyran, 3,3'-dichlorospirodinaphthopyran, 3-benzylcipirodinaphthopyran, -Propylspirobenzopyran, 3-methylnaphtho- (3-methoxybenzo) spiropyran, 1,3,3-trimethyl-6-nitro-8'-methoxyspiro (indoline-
2,2′-benzopyran) and the like are specific examples of diphenylmethane-based compounds, for example, N-halophenyl-leuco auramine, 4,4-bis-dimethylaminophenylbenzhydryl benzyl ether, N-2,4,5 -Specific examples of thiazine compounds include, for example, p-nitrobenzoylleucomethylene blue and the like, and specific examples of lactam compounds include, for example, rhodamine B anilinolactam and rhodamine B-p-chloride. Anilinolactam and the like are specific examples of the fluorene-based compound, for example, 3,6-bis (dimethylamino) fluorenespiro (9,3 ′)-6-′dimethylaminophthalide, 3,6-bis (dimethylamino) Fluorenespiro (9,3 ')-6'-pyrrolidinophthalide, 3-dimethyla Roh-6-diethylamino-fluorene-spiro (9,3 ') - 6'-like pyrrolidinopyridine phthalide can be mentioned. These color-forming compounds are used alone or in combination of two or more.

In the present invention, the color-developing compound which can be used in combination with the color-developing compound represented by the formula (3) is not particularly limited as long as it is generally used in pressure-sensitive recording paper or heat-sensitive recording paper. Examples include phenol compounds, aromatic carboxylic acid derivatives having a phenolic hydroxyl group, aromatic carboxylic acids and metal salts thereof.

Specific examples of the phenol compounds include, for example, α-naphthol, β-naphthol, p-octylphenol, 4-t-octylphenol, p-t-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-chlorophenol), 4,4'-dihydroxydiphenylsulfone, 2,4'-dihydroxydiphenylsulfone, -Hydroxy-4'-methoxydiphenylsulfone, 4-hydroxy-4'-ethoxydiphenylsulfone, 4-hydroxy-4'-isopropoxydiphenylsulfone, 4-hydroxy-4'-butoxydiphenylsulfone and the like.

Specific examples of the aromatic carboxylic acid derivative or aromatic carboxylic acid include methyl bis (4-hydroxyphenyl) acetate, butyl bis (4-hydroxyphenyl) acetate, benzyl bis (4-hydroxyphenyl) acetate, Phenolic compounds such as 2,4-dihydroxy-2′-methoxybenzanilide, benzyl p-hydroxybenzoate, ethyl p-hydroxybenzoate,
Dibenzyl hydroxyphthalate, dimethyl 4-hydroxyphthalate, ethyl 5-hydroxyisophthalate, 3,
Examples thereof include aromatic carboxylic acid derivatives such as 5-di-t-butylsalicylic acid and 3,5-di-α-methylbenzylsalicylic acid, aromatic carboxylic acids and metal salts thereof.

Specific examples of the binder that can be used include, for example, methylcellulose, methoxycellulose, hydroxyethylcellulose, carboxymethylcellulose, sodium carboxymethylcellulose, cellulose, polyvinyl alcohol (PVA), carboxyl group-modified polyvinyl alcohol, sulfonic acid group-modified polyvinyl alcohol, Polyvinylpyrrolidone, polyacrylamide, polyacrylic acid, starch and derivatives thereof, casein, gelatin, aqueous isoprene rubber, alkali salts of styrene / maleic anhydride copolymers, iso (or diiso) butylene / maleic anhydride copolymer salts, etc. Water-soluble or styrene / butadiene (SB) copolymer, carboxylated styrene / butadiene (SB) copolymer, styrene / butadiene / acrylic Acid-based 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, rosin ester resin,
Examples include hydrophobic polymer compounds such as composite particles of colloidal silica and an acrylic copolymer, and emulsions thereof.

Other additives used as needed include, for example, fillers, heat-fusible compounds (sensitizers) and the like. Specific examples of the filler include calcium carbonate, magnesium carbonate, magnesium oxide, silica, white carbon, talc, clay, alumina, magnesium hydroxide, aluminum hydroxide, aluminum oxide, barium sulfate, polystyrene resin, acrylic resin, polyolefin resin, Benzoguanamine resin, melamine resin, urea-formalin resin and the like can be mentioned.

Specific examples of the heat-fusible compound 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, naphthalene derivatives, and aromatic ethers. , Aromatic carboxylic acid derivatives, aromatic sulfonic acid ester derivatives, carbonic acid or oxalic acid diester derivatives,
Biphenyl derivatives, terphenyls, and the like that are solid at room temperature and have a melting point of about 70 ° C. or more can be used.

Specific examples of waxes include wood wax, carnauba wax, shellac, paraffin, montan wax, acid or paraffin, polyethylene wax, polyethylene oxide and the like, and higher fatty acids such as stearic acid and behenic acid. Examples of the higher fatty acid amide include stearic acid amide, oleic acid amide, N-methylstearic acid amide, erucic acid amide, methylolbehenic acid amide, methylolstearic acid amide, methylenebisstearic acid amide, and ethylenebisstearic acid amide. The higher fatty acid anilide includes, for example, stearic acid anilide and linoleic acid anilide, and the acetylated aromatic amine includes, for example, acetotoluide.

Specific examples of the naphthalene derivative include:
For example, 1-benzyloxynaphthalene, 2-benzyloxynaphthalene, 1-hydroxynaphthoic acid phenyl ester and the like are specific examples of aromatic ethers, for example, 1,2-diphenoxyethane, 1,4-diphenoxyethane, , 2-bis (3-methylphenoxy) ethane,
1,2-bis (4-methoxyphenoxy) ethane, 1,
2-bis (3,4-dimethylphenyl) ethane, 1-phenoxy-2- (4-chlorophenoxy) ethane, 1-
Specific examples of aromatic carboxylic acid derivatives include phenoxy-2- (4-methoxyphenoxy) ethane and the like, for example, benzyl p-hydroxybenzoate, benzyl p-benzyloxybenzoate, dibenzyl terephthalate and the like. However, specific examples of the aromatic sulfonic acid ester derivative include, for example, p-toluenesulfonic acid phenyl ester, phenyl mesitylene sulfonate,
Specific examples of carbonic acid or oxalic acid diester derivatives include, for example, diphenyl carbonate, dibenzyl oxalate, di (4-methylbenzyl) oxalate, and di (4-methyl oxalate).
Chlorobenzyl) ester and the like, specific examples of the biphenyl derivative include, for example, p-benzylbiphenyl and p-allyloxybiphenyl, and specific examples of the terphenyl derivative include, for example, m-terphenyl.

Other lubricants such as zinc stearate, calcium stearate and aluminum stearate, various surfactants, defoamers, ultraviolet absorbers and the like are added as required.

The heat-sensitive recording material of the present invention is prepared using the above-mentioned materials by, for example, the following method. That is, first, a compound represented by the formula (1), a compound represented by the formula (2), CVL or benzoylleucomethylene blue, and bis (3-allyl-4-hydroxyphenyl) sulfone having an α-form crystal form are prepared by a conventional method. Ball mill, each with binder or other additives as needed
After pulverizing and dispersing with a disperser such as an attritor or sand mill, mix to prepare a coating solution for the thermosensitive coloring layer, and then dry it on a smooth surface of plastic film or synthetic paper (the coated surface is subjected to corona treatment in advance). 1 to 20 g / m _{2 in} weight
The heat-sensitive recording material of the present invention is obtained by coating and drying with a bar coater, a blade coater or the like.

If necessary, an intermediate layer may be provided between the thermosensitive coloring layer and the support, or an overcoat layer may be provided on the thermosensitive coloring layer. The intermediate layer and the overcoat layer are pulverized and dispersed in the same manner as in the preparation of the thermosensitive coloring layer coating solution together with a binder or other additives as necessary, to obtain an intermediate layer coating solution or a protective layer coating solution, and then dried. It is applied so that the weight at the time is usually 0.1 to 20 g / m ₂ .

On a plastic film or synthetic paper, a specific ratio of the compound represented by the formula (1), the compound represented by the formula (2), a CVL or benzoyl leuco methyl blue coloring compound and a bis (3 -Allyl-
The heat-sensitive recording material of the present invention provided with a heat-sensitive coloring layer mixture containing (4-hydroxyphenyl) sulfone has a moderate black color tone for use in images, and has color-forming sensitivity, heat resistance, moisture resistance, and light resistance. Excellent preservability such as properties.

[0031]

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

Example 1 (Formation of thermosensitive coloring layer) A mixture having the following composition was pulverized and dispersed using a sand grinder so that the average particle size became 1 μm or less, and the solutions [A], [B] and [ C]
A liquid [D] was prepared. [A] solution: 3-dibutylamino-6-methyl-7-anilinofluoran (compound represented by formula (1)) 25 parts 25% PVA aqueous solution 20 parts water 55 parts [B] solution: CVL 25 parts 25 % PVA aqueous solution 20 parts Water 55 parts [C] Solution: Compound represented by formula (2) 25 parts 25% PVA aqueous solution 20 parts Water 55 parts [D] Solution: α-type crystal bis (3-allyl-4-) (Hydroxyphenyl) sulfone (X-ray powder diffraction angle (2θ) by Cu-Kα ray [線] 7.2, 14.5, 16.3, 18.0, 20.0, 21.0, 22.0, 24) 7.7 and 29.0. DSC (Te) = 155.5 ° C.) 25 parts 25% PVA aqueous solution 20 parts Water 55 parts Then, each prepared solution was mixed at the following ratio to form a thermosensitive coloring layer. A coating solution is prepared, and synthetic paper YUPO FPG-80 (trademark) Name: the weight of the dry onto Oji-Yuka Synthetic Paper Co., Ltd.) is 7 g / m ₂ so as applied to obtain a thermosensitive coloring layer was dried. [A] liquid 24 parts [B] liquid 1 part [C] liquid 2 parts [D] liquid 48 parts 20% stearic acid amide dispersion 15 parts 40% styrene / acrylic ester copolymer emulsion 15 parts

(Formation of Protective Layer) Further, a protective layer coating solution having the following ratio was applied onto the thermosensitive coloring layer so that the dry weight was 3 g / m _2, and dried to form a protective layer. The heat-sensitive recording material of the present invention is obtained. 40% styrene / acrylate copolymer emulsion 20 parts 5% bentonite dispersion 40 parts 30% zinc stearate dispersion 3 parts

Example 2 Instead of 3-dibutylamino-6-methyl-7-anilinofluoran of Example 1, 3-dipentylamino-6
Example 1 Using Methyl-7-anilinofluoran
To obtain the heat-sensitive recording material of the present invention.

Example 3 In place of 3-dibutylamino-6-methyl-7-anilinofluoran of Example 1, 3- (N-ethyl-N-isopentylamino) -6-methyl-7-anilino The heat-sensitive recording material of the present invention is obtained in the same manner as in Example 1 using fluoran.

Example 4 A heat-sensitive recording material of the present invention is obtained in the same manner as in Example 1 except that benzoylleucomethylene blue is used in place of CVL of Example 1.

Comparative Example 1 A mixture having the following composition was pulverized and dispersed using a sand grinder so that the average particle size became 1 μm or less, to prepare liquids [H]. [H] solution: bisphenol A 25 parts 25% PVA aqueous solution 20 parts water 55 parts Then, instead of the thermosensitive coloring layer coating solution of Example 1, a thermosensitive coloring layer coating solution having the following ratio was used. Similarly, a heat-sensitive recording material for comparison is obtained. [A] solution 24 parts [H] solution 48 parts 20% stearic acid amide dispersion 15 parts 40% styrene / acrylic ester copolymer emulsion 15 parts

Comparative Example 2 A comparative thermosensitive recording material was obtained by using bisphenol S (4,4'-dihydroxydiphenyl sulfone) instead of bisphenol A of Comparative Example 1. Tables 1 and 2 show the quality performance of the heat-sensitive recording material of the present invention and the heat-sensitive recording material for comparison obtained as described above.

Table 1 Quality Performance Table Background 1) Color density 2) Color tone 3) Heat resistance 4) Moisture resistance 5) Light resistance 6) Example 1 0.03 1.65 4-5 1.65 1.45 4- 5 Example 2 0.02 1.65 4-5 1.64 1.44 4-5 Example 3 0.03 1.67 4-5 1.67 1.47 4-5 Example 4 0.03 1 .64 4-5 1.64 1.46 4-5 Comparative Example 1 0.03 1.55 Standard 1.60 0.98 4 Comparative Example 2 0.03 1.50 1-2 1.50 1.40 3

1) Background The uncolored portion of the prepared sample was measured with a Macbeth reflection densitometer RD-9.
A value measured with a type 14 (Macbeth reflection density). 2) Color density Density of the prepared sample was measured using a commercially available video printer (Sony Corporation).
VIDEO GRAPHIC PRINTER), a solid black image was printed, and the image density was measured with a Macbeth reflection densitometer RD-914 (reflection density). 3) Color Tone The color tone of the sample at a Macbeth reflection density of about 0.9 was determined using a gray scale (JIS L 0804) with the image color tone of Comparative Example 1 (using bisphenol A) as a standard. Judgment: no color difference: from "5" to 0.
Color tone difference every 5 steps: Performed in the range of "1". 4) Heat resistance Macbeth reflection density of the image portion of the sample after being left in a thermostat at 60 ° C. for 24 hours. 5) Moisture resistance The Macbeth reflection density of the image portion of the sample after being left in a humidity chamber at 60 ° C. and a relative humidity of 90% for 24 hours. 6) Light fastness The unprinted portion of the sample was taken under a fluorescent lamp of 5,000 lux under 100
Discoloration before and after time irradiation is represented by gray scale (JIS L 0
804). The judgment value is the same as in the color tone judgment, without discoloration: discoloration from "5" in 0.5 steps:
Performed within the range of “1”.

As is clear from Table 1, the color image of the heat-sensitive recording material of the present invention by a video printer shows the same color tone as that of the heat-sensitive recording material using bisphenol A, and the background, color density and heat resistance, moisture resistance, light resistance, etc. It has excellent storage stability.

[0042]

According to the present invention, a heat-sensitive recording material having a medium black color tone for images and having excellent storage stability such as color sensitivity, heat resistance, moisture resistance, and light resistance was obtained.

Claims (2)

[Claims] 1. A thermosensitive recording material comprising a plastic film or synthetic paper provided with a thermosensitive coloring layer mainly composed of a colorless or pale-colored coloring compound and a coloring compound capable of coloring the coloring compound when heated. The thermosensitive coloring layer is represented by the following formula (1) as a black coloring compound. (In the formula (1), R1 and R2 each independently represent a hydrogen atom, an alkyl group having 6 or less carbon atoms, a cyclohexyl group, or a p-
Represents a tolyl group. The compound represented by the following formula (2) is represented by the following formula (2): Is a CV as a blue-based coloring compound.
L or benzoylleucomethylene blue is used as a color developing compound with bis (3-allyl-4-
(Hydroxyphenyl) sulfone. 2. A compound represented by the formula (2), CVL or benzoylleucomethylene blue in a weight ratio of 0.5 to 20 parts with respect to 100 parts of the compound represented by the formula (1). Item 1. The heat-sensitive recording material according to Item 1.