JPH09300817A - Reversible thermosensitive recording material - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a reversible thermosensitive recording material capable of forming and erasing an image with a clear contrast, and maintaining stably an image with age under the environment of an everyday life. SOLUTION: The recording material is formed of containing on the carrier an ordinarily achromatic or hypochromic dye precursor and reversible developer causing the dye precursor to undergo reversible color tone variation. For the decoloring accelerator, it contains at least one kind of compounds shown by the formula; wherein each R<1> , R<2> , R<3> , R<4> and R<5> is a monovalent group (each group can contain one or more substituents) selected from among a hydrogen atom, an alkyl group, alkenyl group, a cycloalkyl group, an aralkyl group, an allyl group, a heterocyclic residue moiety, an amino group, and a hydroxyl group, and arbitrary two groups selected from among R<1> , R<2> , R<3> , R<4> and R<5> are coupled each other so as to preferably form an 5- or 6-membered N- containing heterocyclic group.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a reversible thermosensitive recording material capable of forming and erasing an image by controlling thermal energy.

[0002]

2. Description of the Related Art Thermal recording materials are disclosed in JP-B-43-4160.
As disclosed in JP-B-45-14039 and the like, a heat-sensitive recording layer containing on a support an electron-donating, usually colorless or pale-colored dye precursor and an electron-accepting developer as main components. And a leuco dye and a developer react instantaneously by heating with a thermal head, a heating pen, a laser beam, etc. to form an image.

One of the drawbacks of this type of heat-sensitive recording material is that once an image is formed, that portion cannot be erased. Therefore, when further information is added as well as correction, the image is not formed. If the area of the recording portion is fixed without using the portion, the amount of information that can be recorded is limited.

In recent years, a reversible thermosensitive recording material has been devised which is capable of repeating image formation and image erasing for the purpose of improving these drawbacks and expanding the applications of the thermosensitive recording material. For example, JP-A-54-119377 and JP-A-63-39377.
Japanese Patent Application Laid-Open No. 63-41186 discloses a heat-sensitive recording material composed of organic low molecular weight particles dispersed in a resin matrix. This method forms an image by a method of reversibly changing the transparency of a heat-sensitive recording material by heat energy.
This type of recording material has excellent stability, but on the other hand, the contrast between the image-formed area and the image-unformed area is insufficient, which makes it difficult to distinguish the image and has a high residual rate after erasing. It was

Further, in the methods described in JP-A-50-81157 and JP-A-50-105555, since the formed image changes depending on the ambient temperature, the image forming and erasing temperatures fluctuate, and the year round. It was difficult to maintain a stable temperature range for image formation and erasure at room temperature.

Further, Japanese Patent Application Laid-Open No. 59-120492 describes a method of forming and erasing an image by using a hysteresis characteristic of a color-developing component and keeping a recording material in a hysteresis temperature range. This method requires a heating source and a cooling source for image formation and erasing, and the temperature range in which image formation and erasing can be maintained is limited to the hysteresis temperature range, which is disadvantageous for use in daily temperature environments. .

On the other hand, JP-A-2-188293, JP-A-2-188294, and International Publication No. WO90 / 1189.
No. 8 describes a reversible thermosensitive recording medium composed of a combination of a leuco dye and a color-developing and decoloring agent for coloring and decoloring the leuco dye by heating. The color-developing agent is an amphoteric compound having an acidic group for coloring the leuco dye and a basic group for decolorizing the colored leuco dye, and has a coloring effect by an acidic group or a decolorizing effect by a basic group by controlling thermal energy. One is preferentially generated to perform color development and decoloration. However, in this method, it is impossible to completely switch the color development reaction and the color removal reaction only by controlling the thermal energy, and since both reactions occur at a certain ratio at the same time, sufficient color development density cannot be obtained, and the color removal Can not be done completely. Therefore, sufficient image contrast cannot be obtained. Further, the decoloring action of the basic group also acts on the color-developed portion at room temperature, and the phenomenon that the density of the color-developed portion decreases with time cannot be avoided. Further, JP-A-5-124360 describes a reversible thermosensitive recording medium that develops and decolorizes a leuco dye by heating, and an organic phosphoric acid compound, α-
Specific phenol compounds such as hydroxyaliphatic carboxylic acids, fatty acid dicarboxylic acids, and alkylthiophenols having an aliphatic group having 12 or more carbon atoms, alkyloxyphenols, alkylcarbamoylphenols, and gallic acid alkylesters are exemplified. However, this recording material also has drawbacks such as low color density and incomplete decoloring for the above reasons. It was not possible to solve these two problems at the same time by examining various conditions. Further, the temporal stability of the image is not satisfactory in practice. Furthermore, JP-A-5-29406
No. 3, fatty acids, waxes, higher alcohols as decoloring accelerators for improving the erasability of the reversible thermosensitive recording medium,
Various esters of phosphoric acid / benzoic acid / phthalic acid or oxyacid, silicone oils, liquid crystal compounds, surfactants and fatty acid saturated hydrocarbons having 10 or more carbon atoms are disclosed, but their effects are small, The image density was high and it was not practical.

As described above, according to the conventional technique, a practical reversible thermosensitive image having a clear image contrast, capable of forming a high-density image and completely erasing, and capable of holding an image which is stable with time in an ordinary environment. The manufacture of recording materials has been difficult. On the other hand, JP-A-6-210954 describes that a recording material excellent in stability over time can be produced by combining a reversible developer with an electron-donating dye precursor. As a result of additional tests, it was necessary to significantly improve the image density, the erasing start temperature, the erasing temperature range, and the like at the time of erasing to make it a practical recording material.

[0009]

SUMMARY OF THE INVENTION It is an object of the present invention to provide a reversible thermosensitive recording material capable of forming an image with good contrast, erasable at a low temperature, having good erasability, and capable of holding an image having good stability over time. It is to be. More specifically, it has excellent stability over time in everyday life, has a lower image density when erasing, and is also capable of erasing uniformly at a lower temperature and in a wider temperature range. Another object is to provide a reversible thermosensitive recording material.

[0010]

DISCLOSURE OF THE INVENTION The inventors of the present invention cause a reversible change in color tone of a dye precursor, which is usually colorless or light-colored, on a support and a difference in cooling rate after heating. In a reversible thermosensitive recording material containing a reversible color developing agent, as a result of diligent studies to obtain a reversible thermosensitive recording material with improved erasability without impairing the temporal stability of the image, the following general formula ( If at least one of the specific compounds represented by 1) is made to coexist, a reversible thermosensitive recording material capable of completely and uniformly erasing an image in a wide low temperature range without impairing stability over time. The present invention has been completed by finding out that the above can be obtained.

[0011]

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In the formula (1), R ¹ , R ² , R ³ , R ⁴ and R
⁵ may be the same or different, each is a hydrogen atom,
A monovalent group selected from the group consisting of an alkyl group, an alkenyl group, a cycloalkyl group, an aralkyl group, an aryl group, a heterocyclic residue, an amino group and a hydroxyl group (each group has one or more substituents). May be done), and R
Any two groups selected from ¹ , R ² , R ³ , R ⁴ and R ⁵ may be linked to each other to form a 5- or 6-membered nitrogen-containing heterocyclic group.

In the compound represented by the general formula (1), R ¹ ,
R ² , R ³ , R ⁴ and R ⁵ are each a hydrogen atom, an alkyl group, an alkenyl group, a cycloalkyl group, an aralkyl group,
It is a monovalent group selected from the group consisting of an aryl group, a heterocyclic residue, an amino group and a hydroxyl group. Among these, a hydrogen atom, an alkyl group, a cycloalkyl group, an aralkyl group, an aryl group and an amino group are preferable. In addition, each group may have one or more substituents. Further R ¹ ,
More preferably, at least one of R ² , R ³ , R ⁴ and R ⁵ is a substituted amino group or a substituted aryl group.
The substituted amino group is particularly preferably one represented by the following general formula (2), and the substituted aryl group is particularly preferably one represented by the following general formula (3). Further, any two groups selected from R ¹ , R ² , R ³ , R ⁴ and R ⁵ may be linked to each other to form a 5- or 6-membered nitrogen-containing heterocyclic group. .

[0014]

[Chemical 6]

In the formula (2), R ⁶ is 2 having 1 to 12 carbon atoms.
A valent hydrocarbon group, R ⁷ is a hydrocarbon group having 1 to 24 carbon atoms, X ¹ is an oxygen or sulfur atom, and h
Represents an integer of 0 or 1.

[0016]

[Chemical 7]

In the formula (3), R ⁸ is a hydrocarbon group having 10 to 22 carbon atoms, X ² is a divalent linking group, and i is 0.
Or an integer of 2.

The erasing accelerator used in the present invention may be a compound having at least two partial structures corresponding to atomic groups obtained by removing one hydrogen atom from the guanidine compound represented by the general formula (1).

Specific examples of the compound represented by the general formula (1) are shown below, but the present invention is not limited thereto. These compounds are used alone or in combination of two or more.

[0020]

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[0021]

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Part of the specific methods for producing these compounds will be illustrated below.

Synthesis Method of Exemplified Compound (2) In a flask equipped with a stirrer and a condenser, octadecanoic hydrazide (3.0 g) and triethylamine (1.1) were added.
g, N, N-dimethylformamide (DMF) 30 ml
, While stirring with heating on an oil bath at 100 ℃, 1,
A solution prepared by dissolving 1.9 g of 3-dimethyl-2-chloroimidazolinium chloride in 5 ml of chloroform was added dropwise. The mixture was heated and stirred for 30 minutes as it was. After cooling the reaction solution to room temperature, the reaction mixture was poured into an ice-cooled 5% sodium hydroxide solution, and the precipitated crystals were filtered off under reduced pressure and washed with pure water. Recrystallization from isopropanol gave 2.5 g of the desired product. Melting point 118.5 [deg.] C.

Synthesis Method of Exemplified Compound (7) In a flask equipped with a stirrer and a condenser, 12-thia-
7.3 g of triacotanoic hydrazide, 1.8 g of triethylamine, N, N-dimethylacetamide (DM
A) 120 ml was charged, and a solution obtained by dissolving 3.0 g of 1,3-dimethyl-2-chloroimidazolinium chloride in 20 ml of chloroform was added dropwise while stirring under heating on an oil bath at 90 ° C. The mixture was heated and stirred as it was for 3 hours. After cooling the reaction solution to room temperature, the reaction mixture was poured into an ice-cooled sodium hydrogen carbonate solution, and the precipitated crystals were separated by filtration under reduced pressure and washed with pure water. Recrystallization from acetonitrile gave 7.6 g of the desired product. Melting point 109.8 [deg.] C.

A method for synthesizing the exemplified compound (11). In a flask equipped with a stirrer, 2.6 g of 2- (4- (1,3-dimethylimidazolidylidene) aminophenyl) acetohydrazide, 2.2 g of triethylamine, N, N
-Prepare 30 ml of dimethylformamide (DMF),
3.0 g of octadecanoyl chloride was added dropwise. After stirring for 2 hours as it was, the reaction mixture was poured into an ice-cooled 5% sodium hydroxide solution, and the precipitated crystals were separated by filtration under reduced pressure and washed with pure water and methanol. Recrystallization from isopropanol gave 1.3 g of the desired product. Melting point 24
5.5 ° C.

The amount of the compound represented by the general formula (1) is preferably 0.05% by weight or more and 100% with respect to the dye precursor.
It is the following. If it is less than this range, the effect is not sufficient, and if it exceeds this range, either the heat-resistant storage stability or the decoloring property of the image may be adversely affected.

On the other hand, the reversible developer used in the present invention is preferably an electron-accepting compound, and is not particularly limited as long as it can reversibly change the color tone by heating in the presence of an electron-donating dye precursor. However, those represented by the following general formula (4) gave particularly preferable results in terms of color density and decoloring property. Further, any compound having the same characteristics as the compound of the following general formula (4) can be used in the present invention.
The compound of the general formula (4) is disclosed in JP-A-6-210954.
Japanese Patent Application No. 5-160547, Japanese Patent Application No. 5-25682
5, Japanese Patent Application No. 5-317555, Japanese Patent Application No. 5-3281
No. 01 and Japanese Patent Application No. 6-10310.

[0028]

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In the equation (4), n is an integer of 1 to 3, j, k
And 1 each represent 0 or 1. However, when j is 1,
k represents 1. R ⁹ and R ¹⁰ represent a divalent hydrocarbon group having 1 to 18 carbon atoms, and R ¹¹ represents a hydrocarbon group having 1 to 24 carbon atoms. X ³ represents a divalent group having at least one or more -CONH- bond, X ⁴ represents at least one or more having a divalent group, an oxygen atom or a sulfur atom -CONH- bond.

In the compound represented by the above general formula (4), R
^{Although 9} and R ¹⁰ are divalent hydrocarbon groups having 1 to 18 carbon atoms, they may contain an aromatic ring, or may be an aromatic ring alone. The divalent group having at least one —CONH— bond represented by X ³ and X ⁴ is, for example, amide (—CONH—, —NHCO—) or urea (—NHC).
ONH-), urethane (-NHCOO-, -OCONH
-), Diacylamine (-CONHCO-), diacylhydrazide (-CONHNHCO-), oxalic acid diamide (-NHCOCONH-), acylurea (-CONH)
CONH-, -NHCONHCO-), 3-acylcarbazide ester (-CONHNHCOO-), semicarbazide (-NHCONHNH-, -NHNHCONH)
-), Acyl semicarbazide (-CONHNHCONH
-, - NHCONHNHCO-), diacyl aminomethane (-CONHCH ₂ NHCO-), 1- acylamino-1- Ureidometan (-CONHCH ₂ NHCONH
-, - NHCONHCH ₂ NHCO-), a group such as malonamide (-NHCOCH ₂ CONH-).

The electron-accepting compound represented by the general formula (4) has an ability to develop a color of a leuco dye, and also has a specific decoloring effect, that is, a reversible effect depending on temperature. Incidentally, electron-accepting compounds used in ordinary heat-sensitive recording materials, that is, 2,2-bis (4-hydroxyphenyl) propane, bis (4-hydroxyphenyl)
No such reversible effect is observed with sulfone, benzyl 4-hydroxybenzoate and the like. Specific examples of the electron-accepting compound represented by the general formula (4) are shown below, but the invention is not limited thereto.

For example, in the equation (4), j = 0 / k = 0 / l
Examples of the compound of = 0 include 4'-hydroxyhexadecaneanilide, N-octadecyl-4-hydroxybenzamide, N- (4-hydroxyphenyl) -N'-octadecylurea, N- (4-hydroxybenzo) -N '.
-Octadecanohydrazide, N- (3,4-dihydroxyphenyl-N'-octadecyloxamide, etc.,

In the formula (4), the compound in which j = 0 / k = 1 / l = 0 is N- [2- (4-hydroxyphenyl) ethyl] -N'-octadecylurea, N- [3 −
(4-Hydroxyphenyl) propiono] -N'-octadecanohydrazide, N- [3- (4-hydroxyphenyl) propiono] -N'-docosanohydrazide, 1-
[3- (4-hydroxyphenyl) propionyl] amino-1-octadecanoylaminomethane, 1- (4-hydroxyphenylacetyl) -4-octadecyl semicarbazide and the like,

In the formula (4), as the compound having j = 1 / k = 1 / l = 0, N-hexadecyl- (4-hydroxyphenylthio) acetamide and N- [2- (4-hydroxyphenylthio] ) Ethyl] -N'-octadecyl urea, N- (4-hydroxyphenylthio) aceto-N '
-Docosanohydrazide, N- [11- (4-hydroxyphenylthio) undecano] -N'-decanohydrazide, N- [2- (4-hydroxyphenylthio) ethyl] -N'-octadecyloxamide, N -[4- (4
-Hydroxyphenylthio) phenyl] -N'-octadecyloxamide, N- [4- (4-hydroxyphenylthiomethyl) benzo] -N'-docosanohydrazide and the like,

In the formula (4), a compound in which j = 0 / k = 0 / l = 1 is N- (4-hydroxyphenyl)-
3-dodecylthiopropanamide, N- (4-hydroxyphenyl) -N'-3-octadecylthiopropylurea, 4-hydroxy-4'-octadecyloxybenzanilide, 4-hydroxy-4'-dodecylthiobenzanilide, 2- (4-octadecanoylaminophenyl) -4'-hydroxyacetanilide, 2- [4-
(N'-octadecylureido) phenyl] -4'-hydroxyacetanilide and the like,

In the formula (4), a compound in which j = 0 / k = 1 / l = 1 is N- [3- (4-hydroxyphenyl) propiono] -N '-(3-dodecylthiopropiono). ) Hydrazide, N- [3- (3,4-dihydroxyphenyl) propiono] -N '-(11-decylthioundecano) hydrazide and the like,

In the formula (4), the compound in which j = 1 / k = 1 / l = 1 is N- [3- (4-hydroxyphenylthio) propiono] -N '-(3-octadecylthiopropion Ono) hydrazide, N- [11- (3,4,5-
Trihydroxyphenylthio) undecano] -N'-
(11-octadecyl thioundecano) hydrazide and the like.

These reversible developers may be used alone,
Two or more kinds may be used in combination, and the amount of the reversible developer used with respect to the dye precursor is 5 to 5000% by weight, preferably 10 to 3000% by weight.

The electron-donating dye precursor used in the present invention is represented by a known compound generally used for pressure-sensitive recording paper, heat-sensitive recording paper and the like, but is not particularly limited.
Specific examples include the followings, but the present invention is not limited thereto.

(1) Triarylmethane compound 3,3-bis (p-dimethylaminophenyl) -6-dimethylaminophthalide (crystal violet lactone), 3,3-bis (p-dimethylaminophenyl) phthalide, 3- (p-dimethylaminophenyl) -3-
(1,2-dimethylindol-3-yl) phthalide,
3- (p-dimethylaminophenyl) -3- (2-methylindol-3-yl) phthalide, 3- (p-dimethylaminophenyl) -3- (2-phenylindole-
3-yl) phthalide, 3,3-bis (1,2-dimethylindol-3-yl) -5-dimethylaminophthalide, 3,3-bis (1,2-dimethylindole-3-
Yl) -6-dimethylaminophthalide, 3,3-bis (9-ethylcarbazol-3-yl) -5-dimethylaminophthalide, 3,3-bis (2-phenylindol-3-yl) -5 -Dimethylaminophthalide, 3-p
-Dimethylaminophenyl-3- (1-methylpyrrol-2-yl) -6-dimethylaminophthalide and the like.

(2) Diphenylmethane compound 4,4'-bis (dimethylaminophenyl) benzhydrylbenzyl ether, N-chlorophenylleuco auramine, N-2,4,5-trichlorophenyl leuco auramine and the like.

(3) Xanthene compound Rhodamine B anilinolactam, Rhodamine B p-chloroanilinolactam, 3-diethylamino-7-dibenzylaminofluorane, 3-diethylamino-7-octylaminofluorane, 3- Diethylamino-7-phenylfluorane, 3-diethylamino-7-chlorofluorane, 3-diethylamino-6-chloro-7-methylfluorane, 3-diethylamino-7- (3,4-dichloroanilino) fluorane, 3 -Diethylamino-7
-(2-chloroanilino) fluoran,

3-Diethylamino-6-methyl-7-anilinofluorane, 3- (N-ethyl-N-tolyl) amino-6-methyl-7-anilinofluorane, 3-piperidino-6-methyl- 7-anilinofluoran, 3-
(N-ethyl-N-tolyl) amino-6-methyl-7-
Phenethylfluoran, 3-diethylamino-7- (4
-Nitroanilino) fluoran, 3-dibutylamino-
6-methyl-7-anilinofluoran, 3- (N-methyl-N-propyl) amino-6-methyl-7-anilinofluoran, 3- (N-ethyl-N-isoamyl) amino-6 Methyl-7-anilinofluoran, 3- (N-
Methyl-N-cyclohexyl) amino-6-methyl-7
-Anilinofluorane, 3- (N-ethyl-N-tetrahydrofuryl) amino-6-methyl-7-anilinofluorane and the like.

(4) Thiazine Compounds Benzoyl leuco methylene blue, p-nitrobenzoyl leuco methylene blue and the like.

(5) Spiro compound 3-methylspirodinaphthopyran, 3-ethylspirodinaphthopyran, 3,3'-dichlorospirodinaphthopyran, 3-benzylspirodinaphthopyran, 3-methylnaphtho- (3 -Methoxybenzo) spiropyran, 3-propylspirobenzopyran and the like.

The above dye precursors may be used alone or in combination of two or more.

As a specific example of the method for producing the reversible thermosensitive recording material of the present invention, a dye precursor and a reversible developer are used as main components, and further, the decoloring accelerator of the present invention is added and supported. Examples thereof include a method of coating on the body to form a reversible thermosensitive recording layer.

The coating solution for containing the dye precursor, the reversible color developer and the compound of the present invention in the reversible thermosensitive recording layer is prepared by dissolving each compound in a solvent or dispersing it in a dispersion medium and then mixing them. Method, a method of dissolving each compound in a solvent or dispersing in a dispersion medium, a method of heating and dissolving each compound to homogenize and then cooling, and dissolving in a solvent or dispersed in a dispersion medium. , There is no particular designation.
If necessary, a dispersing aid may be used for dispersion.
When water is used as the dispersion medium, examples of the dispersion aid include water-soluble polymers such as polyvinyl alcohol and various surfactants. Further, a water-soluble organic solvent such as ethanol may be mixed. When an organic solvent represented by hydrocarbons is used as the dispersion medium, lecithin, phosphoric acid esters or the like may be used as the dispersant.

It is also possible to add a binder to the reversible thermosensitive recording layer for the purpose of improving the strength of the reversible thermosensitive recording layer. Specific examples of the binder include starches, hydroxyethyl cellulose, methyl cellulose, carboxymethyl cellulose, gelatin, casein, polyvinyl alcohol, modified polyvinyl alcohol, sodium polyacrylate, acrylic acid amide / acrylic acid ester copolymer, acrylic acid amide / acrylic. Water-soluble polymer such as acid ester / methacrylic acid terpolymer, alkali salt of styrene / maleic anhydride copolymer, alkali salt of ethylene / maleic anhydride copolymer, polyvinyl acetate, polyurethane, polyacrylic acid Ester, styrene / butadiene copolymer, acrylonitrile / butadiene copolymer, methyl acrylate / butadiene copolymer, ethylene / vinyl acetate copolymer, ethylene / vinyl chloride copolymer, polyvinyl chloride, ethylene Vinylidene chloride copolymers, such as latex of polyvinylidene chloride and the like but not particularly limited thereto.

A thermal solvent may be contained in the reversible thermosensitive recording layer as an additive for controlling the color developing sensitivity of the reversible thermosensitive recording layer. These compounds are 60 ° C-2
Those having a melting point of 00 ° C are preferable, and particularly 80 ° C to 1
The compound with a melting point of 80 ° C. gave good results. In addition to these, sensitizers used in general thermal recording paper can be used. Examples of these compounds include waxes such as N-hydroxymethylstearic acid amide, behenic acid amide, stearic acid amide, and palmitic acid amide, 2-
Naphthol derivatives such as benzyloxynaphthalene, p-
Biphenyl derivatives such as benzylbiphenyl and 4-allyloxybiphenyl, 1,2-bis (3-methylphenoxy) ethane, 2,2'-bis (4-methoxyphenoxy) diethyl ether, bis (4-methoxyphenyl)
Examples thereof include polyether compounds such as ethers, carbonic acid such as diphenyl carbonate, dibenzyl oxalate, oxalic acid bis (p-methylbenzyl) ester, and oxalic acid diester derivatives. Two or more kinds of them can be added in combination.

As the support of the reversible thermosensitive recording material of the present invention, paper, various non-woven fabrics, woven fabrics, synthetic resin films such as polyethylene terephthalate and polypropylene, paper laminated with synthetic resins such as polyethylene and polypropylene,
Synthetic paper, metal foil, glass, etc., or a composite sheet in which these are combined can be optionally used according to the purpose, but is not limited to these and any opaque, semi-transparent or transparent indicator can be used. In order to make the background appear white or another specific color, a white pigment, a colored dye or a bubble may be contained in or on the support. In particular, when the hydrophilicity of the support is small and it is difficult to apply the reversible thermosensitive recording layer when an aqueous liquid is applied to films or the like, the same hydrophilic treatment as that used for the hydrophilic treatment of the surface by corona discharge or the binder is used. A treatment such as coating the surface of the support with a functional polymer is also effective.

The layer structure of the reversible thermosensitive recording material of the present invention may be only a reversible thermosensitive recording layer. If necessary, a protective layer may be provided on the reversible thermosensitive recording layer, or an intermediate layer containing one or more of water-soluble polymer, white or colored dye / pigment, and hollow particles between the reversible thermosensitive recording layer and the support. It can also be provided. In this case, the protective layer and / or the intermediate layer may be composed of two or three or more layers. The reversible thermosensitive recording layer may also be a multi-layered structure having two or more layers by containing each component one by one or changing the compounding ratio for each layer. Further, a material capable of electrically, optically, and magnetically recording information in the reversible thermosensitive recording layer and / or on the surface opposite to the surface on which another layer and / or the reversible thermosensitive recording layer is provided. May be included. Further, a back coat layer may be provided on the surface opposite to the surface on which the reversible thermosensitive recording layer is provided for the purpose of preventing blocking, curling and charging.

The method for forming the reversible thermosensitive recording material of the present invention by laminating each layer in the present invention on a support is not particularly limited, and it can be formed by a conventional method. For example, a smearing device such as an air knife coater, a blade coater, a bar coater, a curtain coater, and the like, various printing machines by a system such as lithographic, letterpress, intaglio, flexo, gravure, screen, and hot melt can be used. In addition to the usual drying process, UV irradiation and
Each layer can be held by EB irradiation.

For the reversible thermosensitive recording layer, a method of mixing respective dispersions obtained by finely pulverizing each component, coating and drying on a support, and mixing respective solutions obtained by dissolving each component in a solvent are mixed. It can be obtained by a method of coating and drying on a support. Drying conditions vary depending on a dispersion medium or solvent such as water. In addition, there is a method in which the components are mixed and heated to melt a fusible component, and the mixture is heated and applied.

Further, the reversible thermosensitive recording layer and / or the protective layer and / or the intermediate layer include diatomaceous earth, talc, kaolin, calcined kaolin, calcium carbonate, magnesium carbonate, titanium oxide, zinc oxide, silicon oxide and hydroxide. In addition to pigments such as aluminum and urea-formalin resin, zinc stearate, higher fatty acid metal salts such as calcium stearate, paraffin, oxidized paraffin, polyethylene, polyethylene oxide, stearic acid amide, and the like for the purpose of preventing head wear and sticking. Waxes such as castor wax may also be contained in addition to a dispersant such as sodium dioctylsulfosuccinate, a surfactant, and a fluorescent dye.

Next, a method of coloring and decoloring the reversible thermosensitive recording material of the present invention will be described. In order to develop the color, rapid cooling after heating may occur, and heating with a thermal head, laser light or the like is suitable. Also, if heated and slowly cooled, the color disappears. It can be erased by using radiant heat from a thermal head, a heat roll, a heat stamp, high frequency heating, hot air, an electric heater and a light source such as a tungsten lamp and a halogen lamp. Is.

[0057]

The mechanism of image formation and erasing of the heat-sensitive recording material of the present invention is not clear, but it is considered as follows. When a colorless or light-colored dye precursor is heated together with an electron-accepting compound such as a phenolic compound, electron transfer from the dye precursor to the electron-accepting compound occurs to develop a color. At this time, it is considered that the electron-accepting compound molecule exists in the extremely close vicinity of the dye molecule that has developed color. When the electron-accepting compound molecule is separated from the dye molecule which has developed color, the dye molecule which has developed color receives electrons again and becomes a state of a dye precursor before color development. It is considered that the present invention changes the distance between the molecule of the electron-accepting compound and the molecule of the dye by heating to perform coloring and decoloring.

More specifically, many electron-accepting compounds, which have hitherto been called reversible color developers, have a fatty chain in their structure, and therefore, the phase of the dye precursor molecule and that of the dye molecule that has formed color are changed. It is considered that the solubility is low and that they hardly dissolve in the solidified state. Further, in the state where the dye precursor molecule and the reversible developer molecule can freely move like the heating and melting state, the dye precursor molecule and the reversible developer molecule are melted to each other at a certain ratio to be in a colored state. Therefore, when the colored mixture in the molten state is slowly cooled, the reversible developer molecules and the dye molecules are not dissolved with each other but phase-separated and the color is erased as the temperature is lowered. In particular, the electron-accepting compound represented by the formula 7 of the present invention contains a bond having a hydrogen bonding ability such as an amide bond in the molecule, and therefore, if it is rapidly crystallized by an intermolecular hydrogen bond. Conceivable. On the other hand, when cooling is performed rapidly, the solidified state is obtained before the phase separation, that is, in the state of the color development, so that the color development state is fixed and the color development state is stably maintained after the solidification.

The decolorization promoting compound represented by the general formula (1) used in the present invention has a basic guanidino group. It is generally known that a heat-sensitive recording material using an electron-donating dye precursor has a printed image erased by contact with a basic compound such as amine. That is, since the decolorization accelerator used in the present invention has a guanidino group having a strongly basic and decolorizing action in the molecule, the phase of the electron-donating dye precursor and the electron-accepting reversible color developing agent is It is considered that the decoloring phenomenon is accelerated at the time of separation.

[0060]

EXAMPLES Next, the method of the present invention will be described in more detail by way of examples. Parts and percentages in the examples are on a weight basis.

Example 1 (A) Preparation of a reversible heat-sensitive coating solution 40 parts of 3-diethylamino-6-methyl-7-anilinofluoran was added to a 2.5% aqueous solution of polyvinyl alcohol 90
The resulting mixture was pulverized with a paint conditioner to obtain a dye precursor dispersion (Solution A). Then 3- (4-hydroxyphenyl) propanoyl-docosanoic hydrazide 2
100 parts of 1.25% polyvinyl alcohol aqueous solution 400
A reversible developer dispersion liquid (B liquid) was pulverized together with the above parts using a paint conditioner. Furthermore, magnesium carbonate 20
And 47 parts of a 0.2% aqueous polyvinyl alcohol solution were pulverized in the same manner (liquid C). Further, 10 parts of (1,3-dimethylimidazolidylidene) -octadecanoic hydrazide was pulverized together with 40 parts of a 1.25% polyvinyl alcohol aqueous solution in a paint conditioner to prepare a decolorization accelerator dispersion (D
Liquid). After mixing these four kinds of dispersion liquids A, B, C and D, a 10% aqueous solution of polyvinyl alcohol 17
0 part and 350 parts of water were added and mixed well to prepare a reversible heat-sensitive coating liquid.

(B) Preparation of reversible heat-sensitive recording material The reversible heat-sensitive coating liquid prepared in (A) was applied onto a polyethylene terephthalate (PET) sheet to give a solid content of 2.6 g /
After coating and drying so as to have a m ² of 5%, an aqueous 5% polyvinyl alcohol solution was coated and dried so as to have a solid content of 2 g / m ^2, and processed by a super calender to obtain a reversible thermosensitive recording material.

Example 2 Instead of the (1,3-dimethylimidazolidylidene) -octadecanoichydrazide of the liquid D used in Example 1, (1,3-dimethylimidazolylidene) -docosanoic hydrazide was used. A reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that it was used.

Example 3 Instead of (1,3-dimethylimidazolidylidene) -octadecanoichydrazide of the liquid D used in Example 1, (1,3-dimethylimidazolidylidene) -hexadecanoichydrazide was used. A reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that was used.

Example 4 Instead of (1,3-dimethylimidazolidylidene) -octadecanoichydrazide of the liquid D used in Example 1, (1,3-dimethylimidazolylidene) -tetradecanoic hydrazide was used. A reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that was used.

Example 5 Instead of (1,3-dimethylimidazolidylidene) -octadecanoic hydrazide of the liquid D used in Example 1, (1,3-dimethylimidazolidylidene) -12-thia-docosa was used. A reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that Ick hydrazide was used.

Example 6 Instead of (1,3-dimethylimidazolidylidene) -octadecanoichydrazide of the liquid D used in Example 1, (1,3-dimethylimidazolidylidene) -4-thia-
A reversible thermosensitive recording material was obtained in the same manner as in Example 1 except that docosanoic hydrazide was used.

Comparative Example 1 A reversible thermosensitive recording material was prepared in the same manner as in Example 1 except that ((1,3-dimethylimidazolidylidene) -octadecanoic hydrazide of the liquid D used in Example 1 was omitted. Got

Comparative Example 2 The same procedure as in Example 1 was carried out except that stearic acid amide was used in place of (1,3-dimethylimidazolidylidene) -octadecanoic hydrazide in the liquid D used in Example 1. A reversible thermosensitive recording material was obtained.

Test 1 (Color density = Thermal response) The thermal recording materials obtained in Examples 1 to 7 and Comparative Examples 1 and 2 were applied to a thermal facsimile printing tester manufactured by Okura Electric Co. with a Kyocera print head KJT-256-8MGF1. TH-PMD
Was applied under the condition of an applied voltage of 26 V for an applied pulse of 1.1 milliseconds, and the density of the obtained color image was measured using a densitometer Macbeth RD918. The results are shown in Table 1.

Test 2 (Image erasability) The heat-sensitive recording materials obtained in Examples 1 to 6 and Comparative Examples 1 and 2 were applied to the Okura Denki 5 heat-facsimile printing tester with Kyocera print head KJT-256-8MGF1. TH-PM
D was applied with an applied pulse of 1.1 milliseconds for an applied voltage of 26 V, and this was printed at 100 ° C. using a heat stamp.
After heating for 1 second, the concentration was measured in the same manner as in Test 1. The results are shown in Table 1.

Test 3 (Decoloring start temperature) The thermal recording materials obtained in Examples 1 to 6 and Comparative Examples 1 and 2 were heat-sensitive facsimile printing tester TH-manufactured by Okura Electric Co. with a print head KJT-256-8MGF1 manufactured by Kyocera. PMD
Was printed under the conditions of an applied voltage of 26 V with an applied pulse of 1.1 milliseconds, and this was heated from 60 ° C. to 150 ° C. at 10 ° C. intervals at a total of 10 locations for 1 second each, and then tested. Each concentration was measured in the same manner as in 1. The heating temperature at which the optical density of the printed image was lower than 0.15 was defined as the decolorization start temperature. The results are shown in Table 1.

Test 4 (Change in Color Density with Time = Image Stability) The thermal recording materials obtained in Examples 1 to 6 and Comparative Examples 1 and 2 were heat-sensitive facsimiles manufactured by Okura Electric Co. with a print head KJT-256-8MGF1 manufactured by Kyocera. Printing tester TH-PMD
Printing was performed under the conditions of an applied voltage of 26 V with an applied pulse of 1.1 milliseconds, and stored for 24 hours in an atmosphere of a temperature of 50 ° C. and a relative humidity of 10%. The density was measured, and the image residual ratio was calculated by the following formula 1. The results are shown in Table 1.

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A = (C / B) × 100 A: Image residual ratio (%) B: Image density before test C: Image density after test

[0075]

[Table 1]

[0076]

INDUSTRIAL APPLICABILITY As shown in Table 1, a reversible thermosensitive material containing a normally colorless to light-colored dye precursor and a reversible developer which causes the dye precursor to reversibly change its color tone by heating. By containing the compound represented by the general formula (1) in the recording material, an image can be formed / erased with a clear contrast, and a more stable image can be retained over time in the environment of everyday life. A reversible thermosensitive recording material could be obtained.

Claims (5)

[Claims] 1. A reversible method comprising a dye precursor which is usually colorless or light-colored on a support and a reversible developer which causes the dye precursor to undergo reversible color tone change due to a difference in cooling rate after heating. A reversible thermosensitive recording material, characterized in that it contains at least one guanidine compound represented by the following general formula (1) as a decolorization accelerator. Embedded image (In the formula (1), R ¹ , R ² , R ³ , R ⁴ and R ⁵ may be the same or different and each represents a hydrogen atom, an alkyl group, an alkenyl group, a cycloalkyl group, an aralkyl group,
A monovalent group selected from the group consisting of an aryl group, a heterocyclic residue, an amino group and a hydroxyl group (each group may have one or more substituents), and R ¹ and R ² , R
Any two groups selected from ³ , R ⁴ and R ⁵ may be linked to each other to form a 5- or 6-membered nitrogen-containing heterocyclic group. ) 2. The decolorization accelerator is a compound having at least two partial structures corresponding to atomic groups obtained by removing one hydrogen atom from the guanidine compound represented by the general formula (1). The reversible thermosensitive recording material according to claim 1. 3. R ¹ , R ² , R ³ and R ^{4 of the} above general formula (1).
2. The reversible thermosensitive recording material according to claim 1, wherein at least one of R ⁵ and R ⁵ is a substituted amino group, and the substituted amino group is a substituted amino group represented by the following general formula (2). Embedded image (In the formula (2), R ⁶ is a divalent hydrocarbon group having 1 to 12 carbon atoms, R ⁷ is a hydrocarbon group having 1 to 24 carbon atoms, X ¹ is an oxygen or sulfur atom, h is 0 or 1
Represents the integer. ) 4. R ¹ , R ² , R ³ and R ^{4 of the} above general formula (1).
And at least one of R ⁵ is a substituted aryl group,
The reversible thermosensitive recording material according to claim 1, wherein the substituted aryl group is a substituted aryl group represented by the following general formula (3). Embedded image (In the formula (3), R ⁸ is a hydrocarbon group having 10 to 22 carbon atoms, X ² is a divalent linking group, and i represents 0 or an integer of 2.) 5. The reversible thermosensitive recording material according to claim 1, wherein the reversible developer is a compound represented by the following general formula (4). Embedded image (In the formula (4), n is an integer of 1 to 3, j, k and l each represent 0 or 1, provided that when j is 1, k represents 1. R ⁹ and R ¹⁰ are carbon atoms. 1 to 18 divalent hydrocarbon group, R ¹¹ is .X ³ representing a hydrocarbon group having 1 to 24 carbon atoms
Represents a divalent linking group having at least one or more -CONH- bond, X ⁴ represents at least one or more having a divalent group, or an oxygen atom or a sulfur atom -CONH- bond. )