WO2020004558A1 - 感熱記録体 - Google Patents
感熱記録体 Download PDFInfo
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- WO2020004558A1 WO2020004558A1 PCT/JP2019/025639 JP2019025639W WO2020004558A1 WO 2020004558 A1 WO2020004558 A1 WO 2020004558A1 JP 2019025639 W JP2019025639 W JP 2019025639W WO 2020004558 A1 WO2020004558 A1 WO 2020004558A1
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- WIPO (PCT)
- Prior art keywords
- undercoat layer
- heat
- mass
- sensitive recording
- recording medium
- Prior art date
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/42—Intermediate, backcoat, or covering layers
- B41M5/44—Intermediate, backcoat, or covering layers characterised by the macromolecular compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/323—Organic colour formers, e.g. leuco dyes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M2205/00—Printing methods or features related to printing methods; Location or type of the layers
- B41M2205/04—Direct thermal recording [DTR]
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M2205/00—Printing methods or features related to printing methods; Location or type of the layers
- B41M2205/38—Intermediate layers; Layers between substrate and imaging layer
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/323—Organic colour formers, e.g. leuco dyes
- B41M5/327—Organic colour formers, e.g. leuco dyes with a lactone or lactam ring
- B41M5/3275—Fluoran compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/333—Colour developing components therefor, e.g. acidic compounds
- B41M5/3333—Non-macromolecular compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/333—Colour developing components therefor, e.g. acidic compounds
- B41M5/3333—Non-macromolecular compounds
- B41M5/3335—Compounds containing phenolic or carboxylic acid groups or metal salts thereof
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/333—Colour developing components therefor, e.g. acidic compounds
- B41M5/3338—Inorganic compounds
Definitions
- the present invention relates to a heat-sensitive recording material utilizing a color-forming reaction between a leuco dye and a color former.
- thermosensitive recording medium that has high image quality without white spots and high sensitivity in a halftone area.
- Patent Document 1 As a method for obtaining a clear recorded image with good dot reproducibility, an elastic layer is provided between the support and the heat-sensitive coloring layer, and the hardness of the heat-sensitive recording material measured by a C hardness tester according to JIS K6301 is 90. The following is proposed (Patent Document 1).
- the object of the present invention is to provide a heat-sensitive recording medium which provides a high-quality and clear printed image with little print missing, and has high sensitivity and excellent halftone print density.
- Patent Document 1 merely proposes to specify the hardness of the thermosensitive recording medium.
- thermosensitive recording medium The present inventors have conducted intensive studies to solve the above-mentioned object, and as a result, provided an undercoat layer containing plastic hollow particles, and set the elastic modulus of the thermosensitive recording medium measured by the nanoindentation method to 200 N / mm 2 or less. As a result, the inventors have found that the above problems can be solved, and have completed the present invention. That is, the present invention relates to the following thermosensitive recording medium.
- Item 1 a heat-sensitive recording material having, in this order, an undercoat layer containing plastic hollow particles and an adhesive, and a heat-sensitive recording layer containing a leuco dye and a color former on a support, A thermosensitive recording medium having an elastic modulus of 200 N / mm 2 or less as measured by a nanoindentation method.
- Item 2 The heat-sensitive recording material according to Item 1, wherein the undercoat layer contains plastic hollow particles having an average particle diameter of 5.0 ⁇ m or more.
- Item 3 The heat-sensitive recording material according to Item 2, wherein the proportion of the hollow plastic particles having an average particle diameter of 5.0 ⁇ m or more contained in the undercoat layer is 50% by mass or less based on the total solid content of the undercoat layer.
- Item 4 The heat-sensitive recording material according to Item 2, wherein the ratio of the hollow plastic particles having an average particle diameter of 5.0 ⁇ m or more contained in the undercoat layer is 30% by mass or less based on the total solid content of the undercoat layer.
- Item 5 The heat-sensitive recording material according to any one of Items 1 to 4, wherein the undercoat layer contains an adhesive having a glass transition temperature of ⁇ 10 ° C. or lower.
- Item 6 The heat-sensitive recording material according to any one of Items 1 to 5, wherein the adhesive contained in the undercoat layer contains latex.
- Item 7 The heat-sensitive recording material according to Item 6, wherein the ratio of the latex contained in the undercoat layer is 25% by mass or more based on the total solid content of the undercoat layer.
- the heat-sensitive recording medium of the present invention provides a high-quality and clear printed image with little print missing (white spots), and has high sensitivity and excellent halftone print density.
- the expression “comprising” includes the concepts of “comprising”, “consisting only of substance”, and “consisting of only”.
- the “average particle diameter” refers to a volume-based median diameter measured by a laser diffraction method. More simply, the particle diameter may be measured from a particle image (SEM image) using an electron microscope, and may be indicated by an average value of 10 particles.
- the present invention is a thermosensitive recording medium having, on a support, an undercoat layer containing plastic hollow particles and an adhesive, and a thermosensitive recording layer containing a leuco dye and a coloring agent in this order,
- the thermosensitive recording material has a modulus of elasticity measured by a nanoindentation method of 200 N / mm 2 or less.
- the support in the present invention is not particularly limited in type, shape, dimensions, and the like.
- high-quality paper acidic paper, neutral paper
- medium-quality paper coated paper, art paper, cast-coated paper, glassine paper
- resin-laminated paper polyolefin-based synthetic paper
- synthetic fiber paper non-woven fabric, synthetic resin film, and the like
- various transparent supports and the like can be appropriately selected and used.
- the thickness of the support is not particularly limited, and is usually about 20 to 200 ⁇ m.
- the density of the support is not particularly limited, and is preferably about 0.60 to 0.85 g / cm 3 .
- the thermal recording medium of the present invention has an undercoat layer containing plastic hollow particles and an adhesive between the support and the thermal recording layer. Thereby, the recording sensitivity can be increased. In addition, the presence of the hollow plastic particles improves the cushioning properties, so that the printed image becomes clearer and the halftone print density can be increased.
- the plastic hollow particles conventionally known ones, for example, a polymer having a crosslinked structure in the film material, for example, an acrylic resin (for example, an acrylic resin having acrylonitrile as a component), a styrene resin, a vinylidene chloride resin And the like having a hollow ratio of about 50 to 99%.
- the hollow ratio is a value obtained by the following equation (d / D) ⁇ 100.
- d indicates the inner diameter of the hollow plastic particles
- D indicates the outer diameter of the hollow plastic particles.
- the average particle size of the plastic hollow particles is preferably 5.0 ⁇ m or more, more preferably 6 ⁇ m or more, and even more preferably 6 to 9 ⁇ m.
- the content ratio of the hollow plastic particles can be selected from a wide range, but generally it is preferably about 2 to 90% by mass of the total solid content of the undercoat layer.
- the content ratio of the hollow plastic particles having an average particle size of 5.0 ⁇ m or more can be selected from a wide range, but is generally preferably 50% by mass or less, more preferably 30% by mass or less, of the total solid content of the undercoat layer. And more preferably 10 to 30% by mass.
- the sensitivity of the undercoat layer can be increased by setting the content ratio of the hollow plastic particles having an average particle diameter of 5.0 ⁇ m or more to 50% by mass or less.
- plastic hollow particles having an average particle diameter of 5.0 ⁇ m or more When plastic hollow particles having an average particle diameter of 5.0 ⁇ m or more are used, it is preferable to use them in combination with plastic hollow particles having an average particle diameter of less than 5.0 ⁇ m.
- the mass ratio of the plastic hollow particles having an average particle diameter of 5.0 ⁇ m or more to the plastic hollow particles having an average particle diameter of less than 5.0 ⁇ m in the undercoat layer is preferably in the range of 10/50 to 50/10, and more preferably 15/45 to 50/50. A range of 45/15 is more preferred.
- the undercoat layer may also contain oil-absorbing pigments having an oil absorption of 70 ml / 100 g or more, especially about 80 to 150 ml / 100 g, and / or thermally expandable particles.
- oil-absorbing pigments having an oil absorption of 70 ml / 100 g or more, especially about 80 to 150 ml / 100 g, and / or thermally expandable particles.
- the oil absorption is a value determined according to the method described in JIS K5101.
- oil absorbing pigments can be used, and specific examples thereof include inorganic pigments such as calcined kaolin, amorphous silica, light calcium carbonate, and talc.
- the average particle size of the primary particles of these oil-absorbing pigments is preferably about 0.01 to 5 ⁇ m, particularly preferably about 0.02 to 3 ⁇ m.
- the content ratio of the oil-absorbing pigment can be selected from a wide range, it is generally preferably about 2 to 95% by mass, more preferably about 5 to 90% by mass of the total solid content of the undercoat layer.
- the undercoat layer is generally formed by mixing and stirring plastic hollow particles, an oil-absorbing pigment, an adhesive, an auxiliary agent, and the like with water as a medium, and applying and drying a coating liquid for an undercoat layer on a support.
- the coating amount of the undercoat layer coating liquid is not particularly limited, is preferably about 2 ⁇ 20g / m 2 by dry weight, about 2 ⁇ 12g / m 2 is more preferable.
- the adhesive can be appropriately selected from those usable for the heat-sensitive recording layer.
- examples include oxidized starch, starch-vinyl acetate graft copolymer, carboxymethylated cellulose, polyvinyl alcohol, latex, and the like, with latex being preferred.
- the latex is not particularly restricted but includes, for example, polyvinyl acetate, polyurethane, styrene-butadiene copolymer, styrene-butadiene-acrylonitrile copolymer, acrylonitrile-butadiene copolymer, polyacrylic acid, polyacrylic acid ester, chloride Vinyl-vinyl acetate copolymer, polybutyl methacrylate, ethylene-vinyl acetate copolymer, silylated urethane, acryl-silicon composite, acryl-silicon-urethane composite, urea resin, melamine resin, amide resin, polyurethane resin And other water-insoluble polymers.
- polyvinyl acetate polyurethane
- styrene-butadiene copolymer styrene-butadiene-acrylonitrile copolymer
- acrylonitrile-butadiene copolymer polyacrylic acid,
- the content ratio of the latex can be selected in a wide range, it is generally preferably 10% by mass or more, more preferably 25% by mass or more, and more preferably 25 to 40% by mass of the total solid content of the undercoat layer. By setting the content ratio of the latex to 10% by mass or more, the cushioning property of the undercoat layer can be further enhanced, so that the elastic modulus of the thermosensitive recording medium can be reduced.
- the glass transition temperature (Tg) of the adhesive is not particularly limited, but is preferably 5 ° C or lower, more preferably -10 ° C or lower, and even more preferably -40 to -20 ° C.
- Tg glass transition temperature
- the cushioning property of the undercoat layer can be further enhanced, so that the elastic modulus of the thermosensitive recording medium can be reduced.
- the content ratio of the adhesive can be selected in a wide range, it is generally preferably about 5 to 40% by mass based on the total solid content of the undercoat layer.
- the heat-sensitive recording layer of the heat-sensitive recording medium of the present invention may contain various known colorless or light-colored leuco dyes. Specific examples of such a leuco dye are shown below.
- leuco dyes include, for example, 3,3-bis (p-dimethylaminophenyl) -6-dimethylaminophthalide, 3- (4-diethylamino-2-methylphenyl) -3- (4-dimethylamino Blue-forming dyes such as phenyl) -6-dimethylaminophthalide and fluoran, 3- (N-ethyl-Np-tolyl) amino-7-N-methylanilinofluoran, 3-diethylamino-7-ani Green coloring dyes such as linofluoran, 3-diethylamino-7-dibenzylaminofluoran, rhodamine B-anilinolactam, 3,6-bis (diethylamino) fluoran- ⁇ -anilinolactam, 3-cyclohexylamino- 6-chlorofluorane, 3-diethylamino-6-methyl-7-chlorofluorane, 3-dieththy
- the content ratio of the leuco dye is not particularly limited, and is preferably about 3 to 30% by mass, more preferably about 5 to 25% by mass, and still more preferably about 7 to 20% by mass based on the total solid content of the heat-sensitive recording layer. .
- the content is 3% by mass or more, the coloring ability can be enhanced, and the printing density can be improved.
- Heat resistance can be improved by setting the content to 30% by mass or less.
- the coloring agent include, for example, 4-tert-butylphenol, 4-acetylphenol, 4-tert-octylphenol, 4,4′-sec-butylidenediphenol, 4-phenylphenol, 4,4′-dihydroxy Diphenylmethane, 4,4'-isopropylidenediphenol, 4,4'-cyclohexylidenediphenyl, 4,4'-cyclohexylidenediphenol, 1,1-bis (4-hydroxyphenyl) -ethane, 1,1- Bis (4-hydroxyphenyl) -1-phenylethane, 4,4′-bis (p-tolylsulfonylaminocarbonylamino) diphenylmethane, 1,1-bis (4-hydroxyphenyl) cyclohexane, 2,2′-bis [ 4- (4-hydroxyphenyl) phenoxy] diethyl ether, 4,4′- Hydroxydiphenyl sulfide, 4,4'-thiobis (3-methyl)
- n an integer of 1 to 6.
- the content of the color former is not particularly limited and may be adjusted according to the leuco dye to be used.
- the content is preferably 0.5 parts by mass or more, more preferably 0.8 part by mass with respect to 1 part by mass of the leuco dye.
- the above is more preferable, 1 part by mass or more is further preferable, 1.2 parts by mass or more is further preferable, and 1.5 parts by mass or more is particularly preferable.
- the content of the coloring agent is preferably 10 parts by mass or less, more preferably 5 parts by mass or less, still more preferably 4 parts by mass or less, particularly preferably 3.5 parts by mass or less, based on 1 part by mass of the leuco dye. .
- the content is 0.5 parts by mass or more, recording performance can be improved.
- the content is 10 parts by mass or less, background fog in a high-temperature environment can be effectively suppressed.
- a preservability improver can be further contained in the heat-sensitive recording layer, mainly in order to further improve the preservability of the color image.
- a preservative improver include 1,1,3-tris (2-methyl-4-hydroxy-5-cyclohexylphenyl) butane, 1,1,3-tris (2-methyl-4-hydroxy -5-tert-butylphenyl) butane, 1,1-bis (2-methyl-4-hydroxy-5-tert-butylphenyl) butane, 4,4 '-[1,4-phenylenebis (1-methylethylidene) )] Phenol compounds such as bisphenol and 4,4 '-[1,3-phenylenebis (1-methylethylidene)] bisphenol; 4-benzyloxyphenyl-4'-(2-methyl-2,3-epoxypropyloxy ) Phenylsulfone, 4- (2-methyl-1,2-epoxyethyl) dipheny
- a preservability improver When a preservability improver is used, its use amount may be an amount effective for improving the preservability. Usually, it is preferably about 1 to 30% by mass based on the total solid content of the heat-sensitive recording layer, and is preferably 5 to 30% by mass. About 20% by mass is more preferable.
- a sensitizer may be contained in the heat-sensitive recording layer in the present invention. Thereby, the recording sensitivity can be increased.
- the sensitizer include stearic acid amide, methoxycarbonyl-N-stearic acid benzamide, N-benzoylstearic acid amide, N-eicosanoic acid amide, ethylenebisstearic acid amide, behenic acid amide, methylenebisstearic acid amide, N-methylol stearamide, dibenzyl terephthalate, dimethyl terephthalate, dioctyl terephthalate, diphenyl sulfone, benzyl p-benzyloxybenzoate, phenyl 1-hydroxy-2-naphthoate, 2-naphthyl benzyl ether, m-terphenyl , P-benzylbiphenyl, di-p-chlorobenzyl oxalate, di-p-methylbenz
- the content of the sensitizer may be an amount effective for sensitization, and is usually preferably about 2 to 40% by mass, more preferably about 5 to 25% by mass, based on the total solids of the heat-sensitive recording layer. preferable.
- thermosensitive recording layer a fine pigment having a high whiteness and an average particle diameter of 10 ⁇ m or less can be contained in the thermosensitive recording layer.
- inorganic pigments such as calcium carbonate, magnesium carbonate, kaolin, clay, talc, calcined clay, silica, diatomaceous earth, synthetic aluminum silicate, zinc oxide, titanium oxide, aluminum hydroxide, barium sulfate, surface-treated calcium carbonate, and silica
- organic pigments such as urea-formalin resin, styrene-methacrylic acid copolymer resin, and polystyrene resin.
- the content ratio of the pigment is preferably an amount that does not lower the coloring density, that is, 50% by mass or less based on the total solid content of the thermosensitive coloring layer.
- An adhesive is used as another component material constituting the heat-sensitive recording layer, and further, a crosslinking agent, a wax, a metal soap, a water-proofing agent, a dispersant, a colored dye, a fluorescent dye, and the like can be used as necessary.
- any of a water-soluble adhesive and a water-dispersible adhesive can be used.
- the water-soluble adhesive include polyvinyl alcohol, carboxy-modified polyvinyl alcohol, acetoacetyl-modified polyvinyl alcohol, diacetone-modified polyvinyl alcohol, modified polyvinyl alcohol such as silicon-modified polyvinyl alcohol, starch and derivatives thereof, methoxycellulose, carboxymethylcellulose, and hydroxy.
- Cellulose derivatives such as ethylcellulose, hydroxypropylmethylcellulose, methylcellulose and ethylcellulose, sodium polyacrylate, polyvinylpyrrolidone, polyamide, diisobutylene-maleic anhydride copolymer salt, styrene-acrylic acid copolymer salt, styrene-maleic anhydride copolymer Polymer salt, ethylene-maleic anhydride copolymer salt, acrylamide-acrylate copolymer, acrylic Amides - acrylic acid ester - methacrylic acid copolymer, polyacrylamide, sodium alginate, gelatin, casein, gum arabic, and the like.
- water-dispersible adhesive examples include polyvinyl acetate, polyurethane, styrene-butadiene copolymer, styrene-butadiene-acrylonitrile copolymer, acrylonitrile-butadiene copolymer, polyacrylic acid, polyacrylate, vinyl chloride-acetic acid.
- Water such as vinyl copolymer, polybutyl methacrylate, ethylene-vinyl acetate copolymer, silylated urethane, acryl-silicon complex, and acryl-silicon-urethane complex, urea resin, melamine resin, amide resin, polyurethane resin, etc.
- Latexes of insoluble polymers and the like can be mentioned. These can be used alone or in combination of two or more. At least one of these is blended in an amount of preferably about 5 to 50% by mass, more preferably about 10 to 40% by mass, based on the total solid content of the heat-sensitive recording layer.
- a crosslinking agent for curing the adhesive of the heat-sensitive recording layer or another layer can be contained in the heat-sensitive recording layer.
- the crosslinking agent include aldehyde compounds such as glyoxal, polyamine compounds such as polyethyleneimine, epoxy compounds, polyamide resins, melamine resins, glyoxylates, dimethylol urea compounds, aziridine compounds, and blocked isocyanate compounds; ammonium persulfate.
- inorganic compounds such as ferric chloride, magnesium chloride, sodium tetraborate and potassium tetraborate; boric acid, boric acid triesters, boron-based polymers, hydrazide compounds, and glyoxylates. These may be used alone or in combination of two or more.
- the amount of the crosslinking agent used is preferably in the range of about 1 to 10 parts by mass with respect to 100 parts by mass of the total solid content of the heat-sensitive recording layer. Thereby, the water resistance of the heat-sensitive recording layer can be improved.
- waxes such as paraffin wax, carnauba wax, microcrystalline wax, polyolefin wax, and polyethylene wax; for example, higher fatty acid amides such as stearamide, ethylenebisstearic acid amide, higher fatty acid esters, and derivatives thereof. Can be mentioned.
- the metal soap examples include higher fatty acid polyvalent metal salts such as zinc stearate, aluminum stearate, calcium stearate, and zinc oleate. If necessary, various auxiliaries such as an oil repellent, a defoaming agent and a viscosity modifier can be added to the heat-sensitive recording layer as long as the effects of the present invention are not impaired.
- the heat-sensitive recording layer is generally composed of water as a dispersion medium, and a ball mill, a co-ball mill, an attritor, a vertical and horizontal sand mill, or a leuco dye and a color former, if necessary, together or separately with a sensitizer and a storage stability improver.
- a water-soluble synthetic polymer compound such as polyacrylamide, polyvinylpyrrolidone, polyvinyl alcohol, methylcellulose, styrene-maleic anhydride copolymer salt, and other surfactants, and a dispersion liquid.
- a coating solution for a heat-sensitive recording layer prepared by mixing a pigment, an adhesive, an auxiliary agent and the like as necessary is applied. After that, it is dried and formed on the undercoat layer.
- the coating amount of the heat-sensitive recording layer is not particularly limited, is preferably about 1 ⁇ 12g / m 2 of the coating amount after drying, more preferably 2 ⁇ 10g / m 2, more preferably 2.5 ⁇ 8g / m 2 And 3 to 5.5 g / m 2 are particularly preferred.
- the heat-sensitive recording layer can be formed in two or more layers as necessary, and the composition and the coating amount of each layer may be the same or different.
- a protective layer may be provided on the heat-sensitive recording layer as needed.
- the protective layer preferably contains a pigment and an adhesive.
- the protective layer preferably contains a lubricant such as polyolefin wax or zinc stearate, and may also contain an ultraviolet absorber. Further, by providing a protective layer having gloss, the added value of the product can be increased.
- the adhesive contained in the protective layer is not particularly limited, and any of a water-soluble adhesive and a water-dispersible adhesive can be used.
- the adhesive can be appropriately selected from those that can be used for the heat-sensitive recording layer.
- the protective layer is generally formed on the heat-sensitive recording layer by applying a protective layer coating solution prepared by mixing water, a dispersion medium, a pigment, an adhesive, and, if necessary, an auxiliary agent, and then drying. Is done.
- the coating amount of the protective layer coating liquid is not particularly limited, and is preferably about 0.3 to 15 g / m 2 , more preferably about 0.3 to 10 g / m 2 , and preferably 0.5 to 8 g / m 2 in terms of dry weight. About 2 is more preferred, about 1 to 8 g / m 2 is particularly preferred, and about 1 to 5 g / m 2 is even more preferred.
- the protective layer can be formed in two or more layers as necessary, and the composition and the coating amount of each layer may be the same or different.
- the heat-sensitive recording material in order to increase the added value of the heat-sensitive recording material, can be further processed to obtain a heat-sensitive recording material having higher functions.
- an adhesive paper, a rewet adhesive paper, a delayed tack paper, or the like can be obtained by applying a coating process using an adhesive, a rewetting adhesive, a delayed tack type adhesive, or the like to the back surface.
- a recording paper capable of performing double-sided recording can be provided by using the back surface thereof and imparting functions as thermal transfer paper, ink jet recording paper, carbonless paper, electrostatic recording paper, zeographic paper, and the like.
- a double-sided thermosensitive recording medium can also be used.
- a back layer can be provided for suppressing penetration of oil and plasticizer from the back surface of the thermosensitive recording medium, and for curl control and antistatic.
- the elastic modulus of the thermosensitive recording medium of the present invention measured by the nanoindentation method is 200 N / mm 2 or less.
- the measurement of the elastic modulus by the nanoindentation method can be performed by a known method, and for example, can be performed according to the method described in Examples.
- the measurement of the elastic modulus is performed from the outermost surface on the opposite side of the support of the thermal recording medium.
- Examples of the method for forming each of the above layers on the support include an air knife method, a blade method, a gravure method, a roll coater method, a spray method, a dip method, a bar method, a curtain method, a slot die method, a slide die method, and an extrusion method. Any of the known coating methods may be used. Each coating solution may be applied and dried one layer at a time to form each layer, or the same coating solution may be applied in two or more layers. Further, simultaneous multi-layer coating in which two or more layers are simultaneously coated may be performed. Also, after any layers have been formed or after all layers have been formed, a smoothing process can be performed using a known method such as a super calender or a soft calender.
- Example 1 (1) Preparation of Coating Solution for Undercoat Layer 154 parts of plastic hollow particles A (trade name: 461WE20, D50: 20 ⁇ m, manufactured by Akzo Nobel, solid content concentration: 13.0%), and hollow plastic particles B (trade name: Lowpike SN) -1055, 162 parts, D50: 1.0 ⁇ m, solid content concentration 26.5%, manufactured by Dow Chemical Co., Ltd., styrene / butadiene latex (trade name: Nalstar SR-116, manufactured by Japan A & L Co., Ltd., solid content concentration 50.
- plastic hollow particles A trade name: 461WE20, D50: 20 ⁇ m, manufactured by Akzo Nobel, solid content concentration: 13.0%
- hollow plastic particles B trade name: Lowpike SN
- styrene / butadiene latex trade name: Nalstar SR-116, manufactured by Japan A & L Co., Ltd., solid content concentration 50.
- Sensitizer Dispersion 40 parts of di-p-methylbenzyl oxalate (trade name: HS-3520, manufactured by DIC) and polyvinyl alcohol (polymerization degree 500, saponification degree 88%) 40 parts of a 10% aqueous solution and 20 parts of water are mixed, and the median diameter becomes 1.0 ⁇ m by a laser diffraction particle size analyzer SALD2200 (manufactured by Shimadzu Corporation) using a sand mill (manufactured by IMEX Co., Ltd., sand grinder). This was crushed to obtain a sensitizer dispersion liquid (liquid C).
- Example 2 A thermosensitive recording medium was obtained in the same manner as in Example 1, except that 308 parts of the hollow particles A and 162 parts of the hollow particles B were used in preparing the coating liquid for the undercoat layer.
- the ratio of the hollow plastic particles having an average particle diameter of 5.0 ⁇ m or more contained in the undercoat layer was 40% by mass.
- Example 3 In the preparation of the coating liquid for the undercoat layer in Example 1, 63 parts of styrene / butadiene latex was used in 32 parts, and modified starch (trade name: Petrocoat C-8, manufactured by Nisseki Chemical Co., solid content concentration: 30%) 53 A heat-sensitive recording material was obtained in the same manner as in Example 1 except that parts were added.
- modified starch trade name: Petrocoat C-8, manufactured by Nisseki Chemical Co., solid content concentration: 30%
- Example 4 Except that 63 parts of styrene / butadiene latex was used in the preparation of the undercoat layer coating liquid of Example 1 and 67 parts of trade name: L-1571 (manufactured by Asahi Kasei Corporation, solid content concentration: 48%, Tg: 3 ° C.) In the same manner as in Example 1, a thermosensitive recording medium was obtained.
- L-1571 manufactured by Asahi Kasei Corporation, solid content concentration: 48%, Tg: 3 ° C.
- Example 5 In preparing the undercoat layer coating liquid of Example 1, 63 parts of styrene / butadiene-based latex was changed to 33 parts of trade name: L-1571 (manufactured by Asahi Kasei Corporation, solid content concentration: 48%, Tg: 3 ° C.), and modified starch was used. (Trade name: Petrocoat C-8, manufactured by Nisse Chemical Co., Ltd., solid content concentration: 30%) A heat-sensitive recording material was obtained in the same manner as in Example 1 except that 53 parts was added.
- Example 6 In the preparation of the undercoat layer coating liquid of Example 1, the procedure was the same as that of Example 1 except that 154 parts of the hollow particles A were changed to 200 parts of the hollow particles C (D50: 7.5 ⁇ m, solid content concentration 10.0%). A thermosensitive recording medium was obtained. The ratio of the hollow plastic particles having an average particle diameter of 5.0 ⁇ m or more contained in the undercoat layer was 20% by mass.
- Example 7 In preparing the coating liquid for the undercoat layer in Example 1, 154 parts of the plastic hollow particles A were replaced with plastic hollow particles D (trade name: Matsumoto Microsphere F Series, manufactured by Matsumoto Yushi Co., Ltd., D50: 3.5 ⁇ m, solid content concentration: 13.0). %) was 485 parts, and a thermosensitive recording medium was obtained in the same manner as in Example 1, except that 162 parts of the plastic hollow particles B were 0 parts.
- plastic hollow particles D trade name: Matsumoto Microsphere F Series, manufactured by Matsumoto Yushi Co., Ltd., D50: 3.5 ⁇ m, solid content concentration: 13.0.
- thermosensitive recording medium was obtained in the same manner as in Example 1 except that 154 parts were used.
- thermosensitive recording medium was obtained in the same manner as in Example 1 except that 154 parts of the plastic hollow particles A were changed to 0 parts and 162 parts of the plastic hollow particles B were changed to 238 parts in preparation of the coating liquid for the undercoat layer.
- a bar code was recorded using a label printer (trade name: L-2000, manufactured by Ishida), and the recorded image quality was visually observed and evaluated according to the following criteria.
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Abstract
Description
該感熱記録体のナノインデンテーション法によって測定された弾性率が、200N/mm2以下である
感熱記録体。
項2:前記下塗り層中に、平均粒子径が5.0μm以上のプラスチック中空粒子を含有する、項1に記載の感熱記録体。
項3:前記下塗り層中に含有される平均粒子径が5.0μm以上のプラスチック中空粒子の割合が、下塗り層の全固形量中50質量%以下である、項2に記載の感熱記録体。
項4:前記下塗り層中に含有される平均粒子径が5.0μm以上のプラスチック中空粒子の割合が、下塗り層の全固形量中30質量%以下である、項2に記載の感熱記録体。
項5:前記下塗り層中に、ガラス転移温度が-10℃以下の接着剤を含有する、項1~4のいずれか一項に記載の感熱記録体。
項6:前記下塗り層中に含有される接着剤がラテックスを含む、項1~5のいずれか一項に記載の感熱記録体。
項7:前記下塗り層に含有されるラテックスの割合が、下塗り層の全固形量中25質量%以上である、項6に記載の感熱記録体。
該感熱記録体のナノインデンテーション法によって測定された弾性率が、200N/mm2以下である
ことを特徴とする。
本発明における支持体は、種類、形状、寸法等に格別の限定はなく、例えば、上質紙(酸性紙、中性紙)、中質紙、コート紙、アート紙、キャストコート紙、グラシン紙、樹脂ラミネート紙、ポリオレフィン系合成紙、合成繊維紙、不織布、合成樹脂フィルム等の他、各種透明支持体等の中から適宜選択して使用することができる。支持体の厚みは特に制限されず、通常、20~200μm程度である。また、支持体の密度は特に制限されず、0.60~0.85g/cm3程度が好ましい。
本発明の感熱記録体では、支持体と感熱記録層との間に、プラスチック中空粒子及び接着剤を含有する下塗り層を有する。これにより記録感度を高めることができる。また、プラスチック中空粒子の存在によりクッション性が向上することで、印字画像がより鮮明になり、中間調印字濃度を高めることができる。
本発明の感熱記録体における感熱記録層には、無色又は淡色の各種公知のロイコ染料を含有させることができる。そのようなロイコ染料の具体例を以下に挙げる。
感熱記録体では、感熱記録層上に必要に応じて保護層を備えることもできる。保護層は、顔料及び接着剤を含有することが好ましい。更に保護層には、サーマルヘッドに対するスティッキングを防止する目的で、ポリオレフィンワックス、ステアリン酸亜鉛のような滑剤を含有させることが好ましく、紫外線吸収剤を含有させることもできる。また、光沢を有する保護層を設けることにより、製品の付加価値を高めることもできる。
本発明では、感熱記録体の付加価値を高めるために、これに更に加工を施し、より高い機能を付与した感熱記録体とすることができる。例えば、裏面に粘着剤、再湿接着剤、ディレードタック型の粘着剤等による塗布加工を施すことにより粘着紙、再湿接着紙、ディレードタック紙などとすることができる。また、裏面を利用して、これに熱転写用紙、インクジェット記録用紙、ノーカーボン用紙、静電記録用紙、ゼオグラフィー用紙などとしての機能を付与し、両面記録が可能な記録紙とすることもできる。もちろん、両面感熱記録体とすることもできる。また、感熱記録体裏面からの油及び可塑剤の浸透を抑制したり、カールコントロール及び帯電防止のためにバック層を設けることもできる。
本発明の感熱記録体のナノインデンテーション法によって測定された弾性率は、200N/mm2以下である。このように弾性率を200N/mm2以下とすることにより、印字欠けが少なく、印字画像がより鮮明になり、中間調印字濃度を高めることができる。ナノインデンテーション法による弾性率の測定は、公知の方法により行うことができ、例えば、実施例に記載の方法に即して実施することができる。弾性率の測定は、感熱記録体の支持体の反対側の最表面から行う。
(1)下塗り層用塗液の調製
プラスチック中空粒子A(商品名:461WE20、D50:20μm、アクゾノーベル社製、固形分濃度13.0%)154部、プラスチック中空粒子B(商品名:ローペイクSN-1055、ダウ・ケミカル社製、D50:1.0μm、固形分濃度26.5%)162部、スチレン・ブタジエン系ラテックス(商品名:ナルスターSR-116、日本A&L社製、固形分濃度50.5%、Tg:-28℃)63部、及びカルボキシメチルセルロース(商品名:セロゲンAGガム、第一工業製薬社製)2部を混合攪拌して、下塗り層用塗液を得た。
3-ジ-(n-ブチル)アミノ-6-メチル-7-アニリノフルオラン40部、ポリビニルアルコール(重合度500、鹸化度88%)の10%水溶液40部、及び水20部を混合し、サンドミル(アイメックス社製、サンドグラインダー)を用いて、レーザー回折式粒径測定器SALD2200(島津製作所社製)によるメジアン径が0.5μmになるまで粉砕してロイコ染料分散液(A液)を得た。
4-ヒドロキシ-4’-イソプロポキシジフェニルスルホン(日本曹達社製、D8)40部、ポリビニルアルコール(重合度500、鹸化度88%)の10%水溶液40部、及び水20部を混合し、サンドミル(アイメックス社製、サンドグラインダー)を用いて、レーザー回折式粒径測定器SALD2200(島津製作所社製)によるメジアン径が1.0μmになるまで粉砕して呈色剤分散液(B液)を得た。
シュウ酸ジ-p-メチルベンジルエステル(商品名:HS-3520、DIC社製)40部、ポリビニルアルコール(重合度500、鹸化度88%)の10%水溶液40部、及び水20部を混合し、サンドミル(アイメックス社製、サンドグラインダー)を用いて、レーザー回折式粒径測定器SALD2200(島津製作所社製)によるメジアン径が1.0μmになるまで粉砕して増感剤分散液(C液)を得た。
A液29.5部、B液59.1部、C液45.5部、完全鹸化ポリビニルアルコール(商品名:PVA110、鹸化度:99モル%、平均重合度:1000、クラレ社製)の10%水溶液45部、ブタジエン系共重合体ラテックス(商品名:L-1571、旭化成社製、固形分濃度48%)9.4部、軽質炭酸カルシウム(商品名:Brilliant-15、白石工業社製)25.1部、パラフィンワックス(商品名:ハイドリンL-700、中京油脂社製、固形分濃度30%)11.7部、アジピン酸ジヒドラジド(大塚化学社製)2部、及び水120部からなる組成物を混合撹拌して感熱記録層用塗液を得た。
アセトアセチル変性ポリビニルアルコール(商品名:ゴーセネックスZ-200、鹸化度:99.4モル%、平均重合度:1000、変性度:5モル%、日本合成化学工業社製)の10%水溶液300部、カオリン(商品名:HYDRAGLOSS90、KaMin LLC社製)63部、ポリエチレンワックス(商品名:ケミパールW-400、三井化学社製、固形分濃度40%)0.5部、及び水114.5部からなる組成物を混合撹拌して保護層用塗液を得た。
坪量60g/m2の上質紙の片面上に、下塗り層用塗液、感熱記録層用塗液、及び保護層記録用塗液を乾燥後の塗布量がそれぞれ3.0g/m2、4.0g/m2、2.0g/m2となるように塗布・乾燥して、下塗り層、感熱記録層、及び保護層を順次形成した後、スーパーカレンダーで表面を平滑化して感熱記録体を得た。下塗り層中に含有される平均粒子径が5.0μm以上のプラスチック中空粒子の割合は、20質量%であった。
実施例1の下塗り層用塗液の調製において、中空粒子A154部を308部とし、中空粒子B162部を87部とした以外は、実施例1と同様にして感熱記録体を得た。下塗り層中に含有される平均粒子径が5.0μm以上のプラスチック中空粒子の割合は、40質量%であった。
実施例1の下塗り層用塗液の調製において、スチレン・ブタジエン系ラテックス63部を32部とし、変性デンプン(商品名:ペトロコートC-8、日澱化学社製、固形分濃度30%)53部を加えた以外は、実施例1と同様にして感熱記録体を得た。
実施例1の下塗り層用塗液の調製において、スチレン・ブタジエン系ラテックス63部を、商品名:L-1571(旭化成社製、固形分濃度48%、Tg:3℃)67部とした以外は、実施例1と同様にして感熱記録体を得た。
実施例1の下塗り層用塗液の調製において、スチレン・ブタジエン系ラテックス63部を、商品名:L-1571(旭化成社製、固形分濃度48%、Tg:3℃)33部とし、変性デンプン(商品名:ペトロコートC-8、日澱化学社製、固形分濃度30%)53部を加えた以外は、実施例1と同様にして感熱記録体を得た。
実施例1の下塗り層用塗液の調製において、中空粒子A154部を中空粒子C(D50:7.5μm、固形分濃度10.0%)200部とした以外は、実施例1と同様にして感熱記録体を得た。下塗り層中に含有される平均粒子径が5.0μm以上のプラスチック中空粒子の割合は、20質量%であった。
実施例1の下塗り層用塗液の調製において、プラスチック中空粒子A154部をプラスチック中空粒子D(商品名マツモトマイクロスフェアーFシリーズ、松本油脂社製、D50:3.5μm、固形分濃度13.0%)485部とし、プラスチック中空粒子B162部を0部とした以外は、実施例1と同様にして感熱記録体を得た。
実施例1の下塗り層用塗液の調製において、プラスチック中空粒子Aをプラスチック中空粒子D(商品名マツモトマイクロスフェアーFシリーズ、松本油脂社製、D50:3.5μm、固形分濃度13.0%)154部とした以外は、実施例1と同様にして感熱記録体を得た。
実施例1の下塗り層用塗液の調製において、プラスチック中空粒子A154部を0部とし、プラスチック中空粒子B162部を238部とした以外は、実施例1と同様にして感熱記録体を得た。
エリオニクス社製ナノインデンテーションENT-2100を用い、荷重0.7mN(圧子:球状圧子φ100μm、バネ補正なし、保持時間1000msec、分割数500、ステップ間隔30msec、ポアソン比 溶融石英0.17)にて弾性率(単位:N/mm2)を測定した。
感熱記録評価機(商品名:TH-PMD、大倉電機社製)を用い、印加エネルギー:0.16mJ/dotの中間調エネルギー領域にて各感熱記録体を記録し、得られた印字部をマクベス濃度計(RD-914、マクベス社製)のビジュアルモードで測定した。数値が大きい程、印字の濃度が濃いことを示しており、記録濃度については、実用上、0.90以上であることが好ましい。
感熱記録評価機(商品名:TH-PMD、大倉電機社製)を用い、印加エネルギー:0.24mJ/dotの高エネルギー領域にて各感熱記録体を記録し、得られた印字部をマクベス濃度計(RD-914、マクベス社製)のビジュアルモードで測定した。数値が大きい程、印字の濃度が濃いことを示しており、記録濃度については、実用上、1.30以上であることが好ましい。
ラベルプリンタ(商品名:L-2000、イシダ社製)を用いてバーコードを記録し、その記録画質を目視で観察し、下記の基準で評価した。
◎:印字欠けがほとんどなく、記録濃度が均一である。
○:わずかに印字欠けがみられる。
△:印字欠けがあり、印字濃度にバラつきがあるものの実使用上問題なし。
×:印字欠けが多くあり、実使用上問題あり。
Claims (7)
- 支持体上に、プラスチック中空粒子及び接着剤を含有する下塗り層と、ロイコ染料及び呈色剤を含有する感熱記録層とをこの順に有する感熱記録体であって、
該感熱記録体のナノインデンテーション法によって測定された弾性率が、200N/mm2以下である
感熱記録体。 - 前記下塗り層中に、平均粒子径が5.0μm以上のプラスチック中空粒子を含有する、請求項1に記載の感熱記録体。
- 前記下塗り層中に含有される平均粒子径が5.0μm以上のプラスチック中空粒子の割合が、下塗り層の全固形量中50質量%以下である、請求項2に記載の感熱記録体。
- 前記下塗り層中に含有される平均粒子径が5.0μm以上のプラスチック中空粒子の割合が、下塗り層の全固形量中30質量%以下である、請求項2に記載の感熱記録体。
- 前記下塗り層中に、ガラス転移温度が-10℃以下の接着剤を含有する、請求項1~4のいずれか一項に記載の感熱記録体。
- 前記下塗り層中に含有される接着剤がラテックスを含む、請求項1~5のいずれか一項に記載の感熱記録体。
- 前記下塗り層に含有されるラテックスの割合が、下塗り層の全固形量中25質量%以上である、請求項6に記載の感熱記録体。
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WO2022085657A1 (ja) * | 2020-10-20 | 2022-04-28 | 王子ホールディングス株式会社 | 感熱記録体 |
CN115515796A (zh) * | 2020-04-23 | 2022-12-23 | 王子控股株式会社 | 热敏记录体 |
WO2023195511A1 (ja) * | 2022-04-07 | 2023-10-12 | 王子ホールディングス株式会社 | 感熱記録体 |
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JP6384368B2 (ja) * | 2015-03-10 | 2018-09-05 | 王子ホールディングス株式会社 | 感熱記録体 |
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2019
- 2019-06-27 KR KR1020217001366A patent/KR20210025595A/ko not_active Application Discontinuation
- 2019-06-27 EP EP19826708.0A patent/EP3815919A4/en active Pending
- 2019-06-27 BR BR112020026497-0A patent/BR112020026497A2/pt unknown
- 2019-06-27 WO PCT/JP2019/025639 patent/WO2020004558A1/ja active Application Filing
- 2019-06-27 CN CN201980043793.6A patent/CN112334319B/zh active Active
- 2019-06-27 US US17/256,437 patent/US11993095B2/en active Active
- 2019-06-27 JP JP2020527639A patent/JP7127684B2/ja active Active
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CN115515796A (zh) * | 2020-04-23 | 2022-12-23 | 王子控股株式会社 | 热敏记录体 |
WO2022085657A1 (ja) * | 2020-10-20 | 2022-04-28 | 王子ホールディングス株式会社 | 感熱記録体 |
JP7491181B2 (ja) | 2020-10-20 | 2024-05-28 | 王子ホールディングス株式会社 | 感熱記録体 |
WO2023195511A1 (ja) * | 2022-04-07 | 2023-10-12 | 王子ホールディングス株式会社 | 感熱記録体 |
Also Published As
Publication number | Publication date |
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BR112020026497A2 (pt) | 2021-03-23 |
CN112334319B (zh) | 2023-02-10 |
JPWO2020004558A1 (ja) | 2021-07-15 |
KR20210025595A (ko) | 2021-03-09 |
EP3815919A4 (en) | 2022-03-23 |
US11993095B2 (en) | 2024-05-28 |
JP7127684B2 (ja) | 2022-08-30 |
US20210268821A1 (en) | 2021-09-02 |
EP3815919A1 (en) | 2021-05-05 |
CN112334319A (zh) | 2021-02-05 |
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