WO2017111097A1 - 熱転写シート - Google Patents
熱転写シート Download PDFInfo
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- WO2017111097A1 WO2017111097A1 PCT/JP2016/088509 JP2016088509W WO2017111097A1 WO 2017111097 A1 WO2017111097 A1 WO 2017111097A1 JP 2016088509 W JP2016088509 W JP 2016088509W WO 2017111097 A1 WO2017111097 A1 WO 2017111097A1
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- layer
- thermal transfer
- transfer sheet
- transfer
- acrylate
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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
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/14—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
- B32B37/26—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer which influences the bonding during the lamination process, e.g. release layers or pressure equalising layers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/06—Interconnection of layers permitting easy separation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/315—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by selective application of heat to a heat sensitive printing or impression-transfer material
- B41J2/32—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by selective application of heat to a heat sensitive printing or impression-transfer material using thermal heads
- B41J2/325—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by selective application of heat to a heat sensitive printing or impression-transfer material using thermal heads by selective transfer of ink from ink carrier, e.g. from ink ribbon or sheet
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J31/00—Ink ribbons; Renovating or testing ink ribbons
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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
- B41M5/36—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using a polymeric layer, which may be particulate and which is deformed or structurally changed with modification of its' properties, e.g. of its' optical hydrophobic-hydrophilic, solubility or permeability properties
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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
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/38207—Contact thermal transfer or sublimation processes characterised by aspects not provided for in groups B41M5/385 - B41M5/395
- B41M5/38214—Structural details, e.g. multilayer systems
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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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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1802—C2-(meth)acrylate, e.g. ethyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
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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
- B41M2205/06—Printing methods or features related to printing methods; Location or type of the layers relating to melt (thermal) mass transfer
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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
- B41M2205/10—Post-imaging transfer of imaged layer; transfer of the whole imaged layer
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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
- B41M2205/30—Thermal donors, e.g. thermal ribbons
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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
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/38257—Contact thermal transfer or sublimation processes characterised by the use of an intermediate receptor
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/0027—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using protective coatings or layers by lamination or by fusion of the coatings or layers
Definitions
- the present invention relates to a thermal transfer sheet.
- thermal transfer sheets for transferring a transfer layer onto a transfer medium are known.
- a thermal transfer sheet provided with a receiving layer as a transfer layer on one surface of a substrate (sometimes referred to as an intermediate transfer medium)
- a thermal transfer sheet sometimes called a protective layer transfer sheet
- a protective layer sometimes called a release layer
- a thermal transfer sheet in which these configurations are appropriately combined for example, a transfer layer having a stacked configuration in which a release layer and a receiving layer are stacked in this order from the substrate side on one surface of the substrate.
- Heat transfer ink sheet and a hot-melt ink layer on the same surface of the substrate Mamoruso the like thermal transfer sheet provided sequentially surfaces are known.
- the transfer layer of these thermal transfer sheets is transferred onto the transfer target by superimposing the transfer target and the thermal transfer sheet and heating the other surface of the substrate with a heating means such as a thermal head or a heating roll. .
- Transfer of the transfer layer onto the transfer medium is performed by applying energy to the thermal transfer sheet while the transfer medium and the transfer layer of the thermal transfer sheet are in close contact, and transferring the transfer layer onto the transfer medium. This is done by peeling the transfer layer that has been transferred onto the body from the thermal transfer sheet.
- the thermal transfer sheet used when transferring the transfer layer onto the transfer target is not only applied when the energy applied to the thermal transfer sheet is high when transferring the transfer layer onto the transfer target, Even when the applied energy is low, that is, regardless of the amount of energy applied to the thermal transfer sheet when transferring the transfer layer onto the transfer target, in other words, in a wide energy range, It is desirable that the releasability when peeling only the transfer layer transferred above from the thermal transfer sheet (hereinafter referred to as the releasability of the transfer layer) is good. However, at present, the peelability of the transfer layer cannot be satisfied in a wide energy region, and there remains room for improvement in this respect.
- thermo transfer sheet even when the energy to be applied to the thermal transfer sheet is increased when the transfer layer is transferred onto the transfer target, various types may occur between the transfer target and the thermal transfer sheet. It is a main object to provide a thermal transfer sheet that can solve the above problem.
- a thermal transfer sheet for solving the above problems is a thermal transfer sheet in which a transfer layer is positioned on one surface of a base material, and the thermal transfer sheet includes the thermal transfer sheet and a transfer target. And measuring the tensile strength of the thermal transfer sheet transported along the transport path located between the heating means and the thermal transfer sheet take-up means. Measurement means, and a printer having a peeling means positioned between the heating means and the measurement means, under the conditions of printing power of 0.15 W / dot and thermal transfer sheet conveyance speed of 84.6 mm / sec. While transferring the transfer layer onto the transfer body, the transfer layer transferred onto the transfer body is peeled off from the constituent member in contact with the transfer layer of the thermal transfer sheet. The tensile strength measured by the measuring means is 0.1 N / cm or less.
- a thermal transfer sheet for solving the above-described problem is a thermal transfer sheet in which a transfer layer is positioned on one surface of a substrate, and the transfer layer includes one or two or more transfer layers.
- the layer located closest to the substrate is (A): (1) isobutyl (meth) acrylate homopolymer, or (2) isobutyl ( A copolymer having a copolymerization ratio of (meth) acrylate of 30% or more in molar ratio, and (B): a copolymer of methyl (meth) acrylate and ethyl (meth) acrylate, or both.
- the copolymerization ratio of the methyl (meth) acrylate in the copolymer (B) is 60% or more and 90% or less in terms of a molar ratio, and the copolymerization ratio of the ethyl (meth) acrylate is a molar ratio. 10% or less If the copolymerization ratio of the methyl (meth) acrylate in the copolymer (B) is 80% or more in terms of molar ratio, the copolymer has a weight average molecular weight (Mw). Is less than 15000.
- the thermal transfer sheet is formed by superimposing the thermal transfer sheet and a transfer target, a thermal transfer sheet supply unit, a heating unit, a thermal transfer sheet winding unit, the heating unit and the thermal transfer sheet winding unit, A printer having measuring means for measuring the tensile strength of a thermal transfer sheet transported along a transport path and positioned between and a peeling means positioned between the heating means and the measuring means.
- the transfer layer was transferred onto the transfer member while transferring the transfer layer onto the transfer member under conditions of a printing power of 0.15 W / dot and a thermal transfer sheet conveyance speed of 84.6 mm / sec.
- a thermal transfer sheet for solving the above-described problem is a thermal transfer sheet in which a transfer layer is provided on one surface of a substrate, and the transfer layer includes one or more transfer layers.
- the layer located closest to the substrate is (1) a homopolymer of isobutyl (meth) acrylate, or (2) isobutyl (meth) acrylate.
- the copolymer has a copolymerization ratio of 30% or more in terms of molar ratio.
- a thermal transfer sheet for solving the above-described problem is a thermal transfer sheet in which a transfer layer is provided on one surface of a substrate, and the transfer layer includes one or more transfer layers.
- the layer located closest to the substrate contains a copolymer of methyl (meth) acrylate and ethyl (meth) acrylate, and the copolymer
- the copolymerization ratio of the methyl (meth) acrylate in the polymer is 60% or more and 90% or less in molar ratio
- the copolymerization ratio of the ethyl (meth) acrylate is 10% or more and 40% or less in molar ratio.
- the weight average molecular weight (Mw) of the copolymer is 15000 or less, If the copolymerization ratio of the methyl (meth) acrylate in the serial copolymer is less than 80% by molar ratio, weight average molecular weight of the copolymer (Mw) of the polymer is characterized by at 45000 or less.
- the thermal transfer sheet according to the embodiment of the present disclosure solves various problems that may occur between the transfer target and the thermal transfer sheet even when the energy applied to the thermal transfer sheet is increased. be able to.
- thermal transfer sheet In describing the thermal transfer sheet according to the embodiment of the present disclosure, first, problems that may occur when the transfer layer of the thermal transfer sheet is transferred onto the transfer target will be described.
- One of the problems that may occur when transferring the transfer layer of the thermal transfer sheet onto the transfer target is thermal fusion between the transfer target and the thermal transfer sheet.
- the heat fusion between the transfer target and the thermal transfer sheet referred to in the present specification means that the transfer target and the thermal transfer sheet are overlapped, and energy is applied from the thermal transfer sheet side by a heating means such as a thermal head.
- the constituent members of the thermal transfer sheet that should remain on the thermal transfer sheet side
- it means a phenomenon in which only the transfer layer transferred onto the transfer body cannot be peeled off from the thermal transfer sheet because it is integrated with the transfer layer transferred onto the transfer body.
- the substrate and the transfer layer can be separated to such an extent that the transfer layer transferred onto the transfer target cannot be peeled off from the substrate.
- the phenomenon of unifying means that the transfer layer transferred onto the transfer target cannot be peeled off from the substrate.
- the constituent members of the thermal transfer sheet are transferred to the transfer body to such an extent that abnormal noise is generated when the transfer layer is peeled off It means the phenomenon of being integrated with the transfer layer transferred above.
- the transfer target and the thermal transfer sheet are heat-sealed, it becomes a factor that causes a conveyance error in the printer, a transfer failure, and the like. Even if the degree of thermal fusion between the transfer target and the thermal transfer sheet is low, the transfer layer transferred onto the transfer target can be peeled off from the thermal transfer sheet, but the transfer layer is transferred.
- the interface (sometimes referred to as a peeling interface) is roughened, resulting in a decrease in glossiness and the like.
- the energy applied to the thermal transfer sheet is increased, or when using a thermal peeling type printer, etc., in order to support high-speed printing suitability.
- the transferred material and the thermal transfer sheet tend to be thermally fused.
- the thermal transfer sheet according to the embodiment of the present disclosure is a thermal transfer sheet 100 in which a transfer layer 10 is provided on one surface of a substrate 1, as shown in FIGS. Is composed of one or more layers, and among the layers constituting the transfer layer 10, the layer located closest to the substrate 1 is (1) a homopolymer of isobutyl (meth) acrylate, or (2 ) The copolymer is characterized by containing a copolymer having a copolymerization ratio of isobutyl (meth) acrylate of 30% or more in terms of molar ratio.
- the layer located closest to the substrate 1 may be referred to as a “base layer”.
- the transfer layer Although the releasability of the heat transfer sheet tends to decrease, the applied energy was lowered even with a thermal transfer sheet with good releasability of the transfer layer when the applied energy was increased. Sometimes the peelability of the transfer layer is not sufficient. Also, even if the transfer layer has good peelability when the applied energy is lowered, the transfer layer is not sufficiently peelable when the applied energy is increased. There is also. In other words, thermal transfer sheets having a transfer layer that have been proposed to date have not yet fully satisfied the peelability of the transfer layer in a wide applied energy range.
- the thermal transfer sheet according to the embodiment of the present disclosure is a thermal transfer sheet 100 in which a transfer layer is provided on one surface of a substrate as shown in FIGS. Or, the layer that is composed of two or more layers and constitutes the transfer layer 10, the layer located closest to the substrate 1 contains a copolymer of methyl (meth) acrylate and ethyl (meth) acrylate.
- the copolymerization ratio of methyl (meth) acrylate in the copolymer is 60% or more and 90% or less in molar ratio
- the copolymerization ratio of ethyl (meth) acrylate is 10% or more and 40% or less in molar ratio.
- the copolymerization ratio of methyl (meth) acrylate is 80% or more in terms of molar ratio
- the copolymer has a weight average molecular weight (Mw) of 15000 or less
- methyl (meth) Acry If the copolymerization ratio of over bets is less than 80% by molar ratio, weight average molecular weight of the copolymer (Mw) of the polymer is characterized by at 45000 or less.
- the transfer layer 10 transferred onto the transfer target is peeled from the constituent members that are in direct contact with the transfer layer among the constituent members constituting the thermal transfer sheet.
- Peeling force for example, when the transfer layer 10 is directly provided on the substrate 1, it has a close relationship with the peeling force when peeling from the substrate 1, and the peeling By reducing the force, it is presumed that the thermal fusion between the transfer object and the thermal transfer sheet can be suppressed. By the way, it is difficult to accurately measure in a printer the peeling force when peeling the transfer layer 10 transferred onto the transfer body from the constituent members in contact with the transfer layer.
- the peeling force when the transfer layer 10 transferred onto the transfer material is peeled from the constituent member in contact with the transfer layer is correlated with the tensile strength applied to the thermal transfer sheet at the time of peeling. It has been found that the relationship between the tensile strength applied to the thermal transfer sheet at the time of peeling and the thermal fusion between the transfer target and the thermal transfer sheet is also closely related.
- the thermal transfer sheet 100 is a thermal transfer sheet 100 in which the transfer layer 10 is positioned on one surface of the substrate 1, and the thermal transfer sheet 100 and the transfer target are overlapped, As shown in FIG. 7, a thermal transfer sheet supply unit 201, a heating unit 202, a thermal transfer sheet winding unit 203, a thermal transfer sheet positioned between the heating unit 202 and the thermal transfer sheet winding unit 203 and transported along the transport path.
- a printer 200 having a measuring means 204 for measuring the tensile strength of the paper, a peeling means 205 located between the heating means 202 and the measuring means 204, a printing power of 0.15 W / dot, a thermal transfer sheet conveyance speed of 84.6 mm /
- the transfer layer 10 transferred onto the transfer target 300 is thermally transferred while continuously transferring the transfer layer 10 onto the transfer target 300 under the condition of sec. It is characterized in that the tensile strength measured by the measuring means 204 is 0.1 N / cm or less when peeled from the constituent member in contact with the transfer layer 10 of the sheet 100.
- thermal transfer sheet according to the embodiment of the present disclosure will be described with specific examples.
- Thermal transfer sheet of the first embodiment is formed on one surface of the substrate 1 as shown in FIGS.
- the transfer layer 10 is provided.
- the transfer layer 10 is composed of one or more layers, and the thermal transfer sheet 100 according to the first embodiment includes a layer located closest to the substrate 1 among the layers constituting the transfer layer 10 (1). It contains a homopolymer of isobutyl (meth) acrylate, or (2) a copolymer having a copolymerization ratio of isobutyl (meth) acrylate of 30% or more in molar ratio.
- 1 to 3 are schematic cross-sectional views showing an example of the thermal transfer sheet of the first embodiment.
- the constituent member that directly contacts the transfer layer among the constituent members constituting the thermal transfer sheet is a base material.
- the base material and the transfer layer are directly It is not limited to the form which touches automatically, Arbitrary layers can also be provided between a base material and a transfer layer.
- the arbitrary layer is a constituent member in direct contact with the transfer layer.
- (Meth) acrylate as referred to in the thermal transfer sheet of the first embodiment means acrylate or methacrylate.
- a homopolymer of isobutyl (meth) acrylate, and (2) a copolymer having a copolymerization ratio of isobutyl (meth) acrylate of 30% or more in terms of molar ratio are collectively referred to as “specific isobutyl (meth)”.
- acrylate As shown in FIG. 1, when the transfer layer 10 has a single layer configuration, the transfer layer 10 directly becomes a “base layer”.
- the “base layer” contains “specific isobutyl (meth) acrylate”, thereby transferring the transfer layer 10 onto the transfer target. Without being affected by various conditions, it is possible to suppress thermal fusion between the transfer target and the thermal transfer sheet.
- the transfer layer 10 is transferred onto the transfer medium in order to cope with high-speed printing suitability, when the energy applied to the thermal transfer sheet is increased, in other words, the printing power is increased.
- the thermal fusion between the transfer object and the thermal transfer sheet is suppressed. be able to.
- the transfer layer 10 is roughened when the transfer layer 10 is peeled from the substrate 1. Etc. can be suppressed, and the glossiness of the transfer layer 10 transferred onto the transfer medium can also be suppressed from decreasing.
- the “base layer” contains “specific isobutyl (meth) acrylate” on the condition that the “base layer” is a layer located at the transfer interface when the transfer layer 10 is transferred.
- the “base layer” does not contain “specific isobutyl (meth) acrylate”, and the layers constituting the transfer layer 10 other than the “base layer” are “specific isobutyl (meth)”.
- the thermal fusion between the transferred material and the thermal transfer sheet which may occur when the transfer layer is transferred onto the transferred material, cannot be suppressed.
- the “base layer” contains either a homopolymer of isobutyl (meth) acrylate or a copolymer of isobutyl (meth) acrylate and other polymerization components as “specific isobutyl (meth) acrylate”. It may be included, and both may be contained.
- the copolymer of isobutyl (meth) acrylate and another polymerization component is a condition that the copolymerization ratio of isobutyl (meth) acrylate is a copolymer having a molar ratio of 30% or more.
- the copolymerization ratio of isobutyl (meth) acrylate in the copolymer is a molar ratio.
- it is less than 30%, it is because heat fusion between the transfer medium and the thermal transfer sheet, which may occur when the transfer layer is transferred onto the transfer medium, cannot be suppressed.
- the “base layer” contains a copolymer having a copolymerization ratio of isobutyl (meth) acrylate of 50% or more in terms of molar ratio.
- the other polymerization components forming the copolymer such as methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, lauryl (meth) acrylate, isobornyl (meth) acrylate, 2-ethylhexyl.
- (Meth) acrylic acid alkyl esters such as (meth) acrylate and octyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, 2-hydroxy-3-phenoxypropyl (meth)
- examples thereof include (meth) acrylic acid ester having a hydroxyl group in the molecule such as acrylate, and a polymerizable monomer such as styrene.
- methyl (meth) acrylate or ethyl (meth) acrylate is used as a monomer constituting the copolymer, thermal fusion between the transfer target and the thermal transfer sheet can be more effectively suppressed. It can be said that it is a preferable monomer which comprises a copolymer at a point.
- the “base layer” is 30% by mass or more, preferably 50% by mass or more of “specific isobutyl (meth) acrylate” with respect to the total mass of the “base layer”. Contains. There is no limitation in particular about an upper limit, and it is 100 mass%.
- the weight average molecular weight (Mw) of the “specific isobutyl (meth) acrylate” and the glass transition temperature (Tg) are not particularly limited, but the weight average molecular weight (Mw) of the “specific isobutyl (meth) acrylate” is 15000. Or less, more preferably 13000 or less.
- the glass transition temperature (Tg) of “specific isobutyl (meth) acrylate” is preferably 100 ° C. or lower, more preferably 90 ° C. or lower, particularly preferably 80 ° C. or lower, and most preferably 70 ° C. or lower.
- the weight average molecular weight (Mw) mentioned in the present specification means a value measured by gel permeation chromatography using polystyrene as a standard substance, and is measured by a method based on JIS-K-7252-1 (2008). Can do.
- the glass transition temperature (Tg) referred to in the present specification means a temperature obtained based on measurement of a change in calorie (DSC method) by DSC (differential scanning calorimetry) in accordance with JIS-K-7121 (2012). To do.
- the method for forming the “base layer” is not particularly limited, and the “specific isobutyl (meth) acrylate” described above and any additive used as necessary may be dispersed or dissolved in an appropriate solvent.
- the base layer coating solution can be prepared, and this base layer coating solution can be formed by applying and drying the base layer 1 or an arbitrary layer located on the base member 1.
- the range of 0.1 micrometer or more and 50 micrometers or less is preferable, and the range of 0.5 micrometer or more and 10 micrometers or less is more preferable.
- the transfer layer 10 having a single layer structure including only the “base layer” and the transfer layer 10 having a stacked structure including the “base layer” will be described as an example.
- the transfer layer 10 is formed by superimposing the thermal transfer sheet of the first embodiment and the transfer target, and the other surface of the substrate 1 is heated by a heating means such as a thermal head or a heating roll (hereinafter referred to as heating means).
- a layer that is transferred onto a transfer medium by heating and is a laminated structure in which two or more layers are laminated (see FIGS. 1 and 2), or a single layer structure that consists of one layer (FIG. 3). See).
- the transfer layer 10 of the first form includes a transfer layer 10 having a laminated structure in which a “base layer” 10 ⁇ / b> A and a protective layer 3 are laminated in this order on one surface of a substrate 1. positioned.
- the thermal transfer sheet 100 having the transfer layer 10 of the first form transfers the image of the transfer layer 10 of the first form onto the transfer target body, so that an image of the transfer target covered with the transfer layer 10 of the first form, etc. In addition, it is used for imparting durability, weather resistance, etc., and serves as a so-called protective layer transfer sheet.
- the “base layer” in the transfer layer 10 of the first embodiment can be used as it is, and a detailed description thereof is omitted here.
- components of the protective layer 3 include acrylic resins, vinyl chloride-vinyl acetate copolymers, epoxy resins, polyester resins, polycarbonate resins, butyral resins, polyamide resins, and vinyl chloride resins. be able to.
- the protective layer 3 containing a ultraviolet absorber According to the protective layer 3 containing the ultraviolet absorber, the light resistance, weather resistance, etc. of the image of the transfer target covered with the transfer layer 10 of the first form can be transferred by transferring the transfer layer 10 of the first form. Can be improved.
- the ultraviolet absorber include salicylate-based, benzophenone-based, benzotriazole-based, triazine-based, substituted acrylonitrile-based, nickel chelate-based, hindered amine-based and the like, which are conventionally known organic ultraviolet absorbers.
- a polymer in which an addition polymerizable double bond such as a vinyl group, an acryloyl group, or a methacryloyl group, or an alcoholic hydroxyl group, an amino group, a carboxyl group, an epoxy group, or an isocyanate group is introduced into these ultraviolet absorbers.
- the material is an ultraviolet absorbing resin.
- the protective layer 3 is prepared by, for example, preparing a protective layer coating solution in which the above-described components and the like are dispersed or dissolved in an appropriate solvent, and this protective layer coating solution is placed on the “base layer” 10A. It can be formed by coating and drying. Although there is no limitation in particular about the thickness of the protective layer 3, Usually, it is the range of 0.5 micrometer or more and 50 micrometers or less.
- An adhesive layer (not shown) can be positioned on the protective layer 3. According to the transfer layer 10 in the first form in which the adhesive layer is further located on the protective layer 3, the adhesion between the transfer layer 10 and the transfer target can be improved.
- a conventionally known adhesive mainly composed of an acrylic resin, a vinyl resin, a polyester resin, a urethane resin, a polyamide resin, an epoxy resin, a rubber resin, an ionomer resin, etc. Etc.
- the thickness of an contact bonding layer the range of 0.1 micrometer or more and 50 micrometers or less is preferable, and the range of 1 micrometer or more and 10 micrometers or less is more preferable.
- the transfer layer 10 of the second form includes a transfer layer 10 having a laminated structure in which a “base layer” 10 ⁇ / b> A and a receiving layer 2 are laminated in this order on one surface of a substrate 1. positioned.
- the thermal transfer sheet 100 having the transfer layer 10 of the second form forms a thermal transfer image on the receiving layer 2 located farthest from the substrate 1 among the layers constituting the transfer layer 10 of the second form, and the thermal transfer sheet 100
- the transfer layer 10 of the second form including the receiving layer 2 on which an image is formed is used to obtain a printed matter by transferring it onto a transfer target, and serves as a so-called intermediate transfer medium.
- the “base layer” in the transfer layer 10 of the second embodiment can be used as it is, and a detailed description thereof is omitted here.
- the component of the receiving layer 2 examples include polyolefin resins such as polypropylene, halogenated resins such as polyvinyl chloride or polyvinylidene chloride, polyvinyl acetate, vinyl chloride-vinyl acetate copolymers, ethylene-vinyl acetate copolymers.
- polyolefin resins such as polypropylene
- halogenated resins such as polyvinyl chloride or polyvinylidene chloride
- polyvinyl acetate vinyl chloride-vinyl acetate copolymers
- ethylene-vinyl acetate copolymers examples of the component of the receiving layer 2 include polyolefin resins such as polypropylene, halogenated resins such as polyvinyl chloride or polyvinylidene chloride, polyvinyl acetate, vinyl chloride-vinyl acetate copolymers, ethylene-vinyl acetate copolymers.
- Polymers or vinyl resins such as polyacrylates, polyester resins such as polyethylene terephthalate or polybutylene terephthalate, polystyrene resins, polyamide resins, copolymers of olefins such as ethylene or propylene, and other vinyl polymers, ionomers or Examples thereof include cellulose resins such as cellulose diastase and polycarbonate resins.
- the receiving layer 2 is prepared as a receiving layer coating solution in which the above-described components and the like are dispersed or dissolved in a suitable solvent, and this receiving layer coating solution is applied onto the “base layer” 10A. It can be formed by drying. Although there is no limitation in particular about the thickness of the receiving layer 2, Usually, it is the range of 1 micrometer or more and 10 micrometers or less.
- an arbitrary layer such as an intermediate layer may be provided between the “base layer” 10A and the receiving layer 2.
- An adhesive layer or the like can be provided on the receiving layer 2.
- a transfer layer in which the transfer layer 10 of the first form and the transfer layer 10 of the second form can be combined for example, a thermal transfer sheet in which a transfer layer 10 having a laminated structure in which a “base layer”, a protective layer 3, and a receiving layer 2 are laminated in this order on one surface of the substrate 1 may be used.
- the transfer layer 10 of the third form has a single-layer transfer layer 10 composed of only the “base layer” 10 on one surface of the substrate 1.
- the thermal transfer sheet 100 having the transfer layer 10 according to the third embodiment has various functions in the thermal transfer sheet 100 by adding a functional component to the “base layer” 10A together with the “specific isobutyl (meth) acrylate”. Can be granted.
- the thermal transfer sheet 100 having the transfer layer 10 of the third form as a hot melt ink layer can be obtained.
- wax component examples include microcrystalline wax, carnauba wax, and paraffin wax.
- Fischer-Tropsch wax various low molecular weight polyethylene, wood wax, beeswax, whale wax, ibota wax, wool wax, shellac wax, candelilla wax, petrolactam, polyester wax, partially modified wax, fatty acid ester, fatty acid amide, etc. be able to.
- the colorant can be appropriately selected from known organic or inorganic pigments or dyes.
- a colorant having a sufficient color density and not discolored or discolored by light, heat or the like is preferable.
- it may be a substance that develops color when heated or a substance that develops color when it comes into contact with a component applied to the surface of the transfer target.
- a black colorant can be used.
- the function as a protective layer is provided by incorporating the components of the protective layer 3 described in the transfer layer 10 of the first embodiment together with the “specific isobutyl (meth) acrylate” in the “base layer” 10A. It can also be a “basal layer”.
- the transfer layer 10 including the “base layer” has been described with various forms.
- the thermal transfer sheet 100 according to the first embodiment is closest to the base material 1 among the layers constituting the transfer layer 10.
- thermal fusion between the transferred material and the thermal transfer sheet can occur when the transfer layer 10 is transferred onto the transferred material.
- thermal fusion between the transfer target and the thermal transfer sheet can be suppressed.
- Condition 1 A transfer layer having a single layer or a laminated structure is provided on one surface of a base material.
- Condition 2 Among the layers constituting the transfer layer, the base material 1 is the most. A nearby layer is ⁇ a specific isoform As long as satisfying the containing the chill (meth) acrylate ", but is to be any limitation on other conditions, may be other than in the form illustrated above.
- the thermal transfer sheet 100 of the first embodiment may include an arbitrary layer that does not constitute a transfer layer. As an arbitrary layer, it is provided between the base material 1 and the transfer layer 10, and is provided on a release layer (not shown) for improving the transferability of the transfer layer 10 or on the other surface of the base material 1. And a back layer for improving the heat resistance and the runnability of a heating member such as a thermal head.
- a release layer may be provided between the base material 1 and a “base layer” 10 ⁇ / b> A as a hot-melt ink layer.
- a color material layer (not shown) can be provided on the same surface of one surface of the substrate 1 together with the transfer layers of the above-mentioned various forms in the surface order.
- the base material 1 is an essential configuration in the thermal transfer sheet 100 of the first embodiment, and is provided to hold the transfer layer 10 located on one surface of the base material 1.
- the material of the substrate 1 is not particularly limited, but it is desirable that the material has mechanical characteristics that can withstand heat applied when the transfer layer 10 is transferred onto the transfer target and does not hinder handling.
- Examples of such a substrate 1 include polyesters such as polyethylene terephthalate, polyarylate, polycarbonate, polyurethane, polyimide, polyetherimide, cellulose derivatives, polyethylene, ethylene-vinyl acetate copolymer, polypropylene, polystyrene, acrylic, polychlorinated.
- the thickness of the substrate 1 is not particularly limited, and is generally in the range of 2.5 ⁇ m to 100 ⁇ m.
- the substrate 1 that has been subjected to a surface treatment may be used.
- the surface treatment method include, for example, corona discharge treatment, flame treatment, ozone treatment, ultraviolet treatment, radiation treatment, roughening treatment, chemical treatment, plasma treatment, low temperature plasma treatment, primer treatment, grafting treatment, etc. Can be mentioned.
- Transfer material There is no particular limitation on the transfer target to which the transfer layer 10 of the thermal transfer sheet 100 of the first embodiment is transferred.
- the printer used for transferring the transfer layer 10 of the thermal transfer sheet 100 of the first embodiment onto a transfer target is not particularly limited, and any conventionally known printer including a heating member such as a thermal head can be used.
- the thermal transfer sheet 100 according to the first embodiment suppresses thermal fusion between the transfer target and the thermal transfer sheet even when a printer capable of applying high energy, a thermal peeling type printer, or the like is used. This is particularly suitable when using these printers.
- Thermal transfer sheet of the second embodiment is the thermal transfer sheet 100 of the first embodiment as shown in FIGS.
- the transfer layer 10 is provided on one surface of the substrate 1.
- the transfer layer 10 is composed of one or more layers, and the thermal transfer sheet 100 according to the second embodiment is configured such that, of the layers constituting the transfer layer 10, the layer closest to the substrate 1 is methyl (meta )
- a copolymer of acrylate and ethyl (meth) acrylate, and the copolymerization ratio of methyl (meth) acrylate in the copolymer is 60% or more and 90% or less in terms of molar ratio, and ethyl (meth)
- the copolymerization ratio of acrylate is 10% or more and 40% or less in terms of molar ratio
- the copolymerization ratio of methyl (meth) acrylate is 80% or more in terms of molar ratio
- the weight average molecular weight of the copolymer (Mw) is 15000 or less.
- the copolymerization ratio of methyl (meth) acrylate is less than 80% in terms of molar ratio
- the weight average molecular weight (Mw) of the copolymer is 450. 0 is less than or equal to.
- the description of the copolymerization ratio means a molar ratio.
- the layer located closest to the substrate 1 is any of the following copolymer A and copolymer B: It is characterized by containing either or both.
- Copolymer A A copolymer of methyl (meth) acrylate and ethyl (meth) acrylate, and the copolymer A has a weight average molecular weight (Mw) of 15000 or less, and the copolymer A
- Mw weight average molecular weight
- the copolymerization ratio of methyl (meth) acrylate is 80% or more and 90% or less, and the copolymerization ratio of ethyl (meth) acrylate is 10% or more and 20% or less.
- Copolymer B A copolymer of methyl (meth) acrylate and ethyl (meth) acrylate, and the copolymer B has a weight average molecular weight (Mw) of 45,000 or less.
- Mw weight average molecular weight
- the copolymerization ratio of methyl (meth) acrylate is 60% or more and less than 80%, and the copolymerization ratio of ethyl (meth) acrylate is more than 20% and 40% or less.
- the copolymer A and the copolymer B may be collectively referred to as “specific copolymer”.
- the glass transition temperature (Tg) of the copolymer A and the copolymer B is not particularly limited, but is preferably 40 ° C or higher, more preferably 50 ° C or higher, and 60 ° C or higher. Particularly preferred.
- the copolymer B has a condition that its weight average molecular weight (Mw) is 45,000 or less, but the weight average molecular weight (Mw) is 30000 or less, in particular, the weight average molecular weight (Mw) is 20000 or less. Copolymer B can be preferably used.
- the transfer layer transferred onto the transfer target is transferred to the thermal transfer sheet in a wide applied energy region.
- the peelability when peeling from the base material 1 is good.
- thermal peeling type printer it is possible to improve the peelability when peeling the transfer layer 10 from the substrate 1 in a wide applied energy range. .
- various problems caused by insufficient peelability when the transfer layer 10 is peeled from the substrate 1, for example, thermal fusion between the transfer target and the thermal transfer sheet, or transfer of the transferred transfer layer A decrease in glossiness and the like can be suppressed.
- methyl (meth) acrylate which is one of the polymerization components forming a “specific copolymer”, applies a lower energy to the transfer layer on the transfer target as the copolymerization ratio increases.
- the transfer layer has improved peelability when transferred, while the transfer layer 10 has a property of being lowered when high energy is applied to transfer the transfer layer 10 onto the transfer target. is doing.
- ethyl (meth) acrylate which is another polymerization component that forms a “specific copolymer”, is transferred onto a transfer target by applying higher energy as the copolymerization ratio increases.
- the property that the peelability of the transfer layer when the layer 10 is transferred is improved, while the peelability of the transfer layer is lowered when the transfer layer 10 is transferred onto the transfer object by applying low energy. have.
- a copolymer obtained by copolymerizing methyl (meth) acrylate and ethyl (meth) acrylate as the weight average molecular weight (Mw) increases, high energy is applied to the transferred material. When the transfer layer 10 is transferred, the peelability of the transfer layer tends to decrease.
- the thermal transfer sheet 100 pays attention to the properties of methyl (meth) acrylate and ethyl (meth) acrylate and the weight average molecular weight of a copolymer obtained by copolymerizing these polymerization components, Copolymerization of ethyl (meth) acrylate, which is one of the polymerization components, with a copolymerization ratio of methyl (meth) acrylate, which is one of the polymerization components forming “polymer”, in the range of 60% to 90%.
- the copolymer When the ratio is in the range of 10% to 40% and the copolymerization ratio of methyl (meth) acrylate is 80% or more, the copolymer has a weight average molecular weight (Mw) of 15000 or less. When a copolymer is used and the copolymerization ratio of methyl (meth) acrylate is less than 80%, the copolymer has a weight average molecular weight (Mw) of 45,000 or less.
- the “base layer” contains a copolymer obtained by copolymerizing methyl (meth) acrylate and ethyl (meth) acrylate, methyl (meth) in the copolymer is included.
- the copolymerization ratio of acrylate exceeds 90%, or when the copolymerization ratio of ethyl (meth) acrylate is less than 10%, when the transfer layer 10 is transferred onto the transfer target by applying high energy The peelability of the transfer layer cannot be satisfied.
- the copolymerization ratio of methyl (meth) acrylate in the copolymer is less than 60% or when the copolymerization ratio of ethyl (meth) acrylate exceeds 40%, low energy is applied.
- the peelability of the transfer layer when the transfer layer 10 is transferred onto the transfer body cannot be satisfied. Moreover, even if the copolymerization ratio of methyl (meth) acrylate is 80% or more and 90% or less and the copolymerization ratio of ethyl (meth) acrylate is 10% or more and 20% or less, the weight average molecular weight of this copolymer is (Mw) is not 15000 or less, or the copolymerization ratio of methyl (meth) acrylate is 60% or more and less than 80%, and the copolymerization ratio of ethyl (meth) acrylate is more than 20% and 40% or less. However, when the weight average molecular weight (Mw) of the copolymer is not 45000 or less, high energy is applied to satisfy the peelability of the transfer layer when the transfer layer 10 is transferred onto the transfer target. Can not.
- the upper limit of the weight average molecular weight (Mw) of the copolymer having a copolymerization ratio of methyl (meth) acrylate of 60% or more and less than 80% is set to 45000, whereas the copolymerization ratio of methyl (meth) acrylate is 80.
- the upper limit of the weight average molecular weight (Mw) of the copolymer of not less than 90% and not more than 90% is set to 15000 because the higher the copolymerization ratio of methyl (meth) acrylate, the higher the energy applied. In this case, the weight average molecular weight (Mw) of the copolymer containing methyl (meth) acrylate must be reduced. For example, the peelability of the transfer layer when the transfer layer 10 is transferred onto the transfer medium by applying high energy cannot be satisfied.
- the “specific copolymer” may be a polymer with methyl (meth) acrylate, ethyl (meth) acrylate, and other polymerization components.
- Other polymerization components are not particularly limited.
- copolymerization ratio of the other polymerization components there is no particular limitation on the copolymerization ratio of the other polymerization components, and it may be in a range satisfying the copolymerization ratio of methyl (meth) acrylate and the copolymerization ratio of ethyl (meth) acrylate described above.
- the content of the “specific copolymer” contained in the “base layer” is not particularly limited, and the transfer layer can be applied in a wide applied energy region by the amount containing the “specific copolymer”. However, it is preferably 50% by mass or more, more preferably 70% by mass or more based on the total mass of the “base layer”. There is no limitation in particular about an upper limit, and it is 100 mass%.
- the method for forming the “base layer” is not particularly limited, and a base obtained by dispersing or dissolving methyl (meth) acrylate, ethyl (meth) acrylate, and any additive used as necessary in an appropriate solvent. It can be formed by preparing a layer coating solution, and applying and drying the base layer coating solution on the substrate 1 or an arbitrary layer located on the substrate 1. Although there is no limitation in particular about the thickness of a base layer, the range of 0.1 micrometer or more and 50 micrometers or less is preferable, and the range of 0.5 micrometer or more and 10 micrometers or less is more preferable. By making the thickness of the base layer within this range, the peelability from the substrate can be more effectively controlled.
- the thermal transfer sheet 100 of the first embodiment described above is based on the condition that the base layer 10A contains “specific isobutyl (meth) acrylate”, whereas the thermal transfer sheet 100 of the second embodiment. Is different from the thermal transfer sheet 100 of the first embodiment and the thermal transfer sheet 100 of the second embodiment only in that the base layer 10A contains “a specific copolymer”. In other respects, it is consistent. Therefore, for the configuration other than this difference, the configuration of the thermal transfer sheet 100 of the first embodiment described above can be appropriately selected and used, and detailed description thereof is omitted here. That is, the description of the base layer 10A containing “specific isobutyl (meth) acrylate” may be read as the base layer 10A containing “specific copolymer”.
- the thermal transfer sheet 100 according to the second embodiment has been described above.
- the thermal transfer sheet 100 according to the second embodiment is a “base layer” positioned closest to the base material 1 among the layers constituting the transfer layer 10.
- a “specific copolymer” the peelability of the transfer layer is improved in a wide applied energy region.
- Condition 1 One surface of the substrate
- a transfer layer having a single layer or a laminated structure is provided.
- Condition 2 Of the layers constituting the transfer layer, the layer located closest to the substrate 1 contains a “specific copolymer”. As long as it satisfies the condition, it is not limited in any way other than these conditions, and it may be other than the form exemplified above.
- Thermal transfer sheet of the third embodiment includes a base material 1 and the base material 1 as shown in FIGS. And a transfer layer 10 that is detachable from the transfer layer 10.
- the thermal transfer sheet 100 of the third embodiment is formed by superimposing the thermal transfer sheet 100 and the transfer object, and as shown in FIG. 7, the thermal transfer sheet supply unit 201, the heating unit 202, the thermal transfer sheet winding unit 203, the heating Measuring means 204 for measuring the tensile strength of the thermal transfer sheet which is located between the means 202 and the thermal transfer sheet winding means 203 and which is conveyed along the conveying path, and a peeling means which is located between the heating means 202 and the measuring means 204
- the printer 200 having 205 the transfer layer 10 is continuously transferred onto the transfer target 300 under the conditions of a printing power of 0.15 W / dot and a thermal transfer sheet conveyance speed of 84.6 mm / sec.
- the measuring means 204 The tensile strength measured is 0.1 N / cm or less.
- the constituent member in contact with the transfer layer among the constituent members constituting the thermal transfer sheet is a base material.
- the base material and the transfer layer are in direct contact.
- the present invention is not limited to this form, and an arbitrary layer may be provided between the substrate and the transfer layer. In this case, the arbitrary layer is a constituent member in direct contact with the transfer layer.
- conditions for peeling the transferred transfer layer 10 from the substrate 1 onto the transfer target 300 specifically, a thermal transfer sheet supply unit 201, a heating unit 202, a thermal transfer sheet winding unit 203, and a heating unit 202 are used.
- the transfer layer 10 is continuously transferred onto the transfer body 300 under the conditions of a printing power of 0.15 W / dot and a thermal transfer sheet conveyance speed of 84.6 mm / sec.
- the conditions for peeling the transfer layer 10 transferred onto the body 300 from the constituent members in contact with the transfer layer 10 of the thermal transfer sheet are collectively referred to as “specific measurement conditions”.
- the transfer layer 10 is transferred only by satisfying the condition that the tensile strength of the thermal transfer sheet is “0.1 N / cm or less” under “specific measurement conditions”. It is possible to suppress thermal fusion between the transfer target and the thermal transfer sheet that may occur when the transfer layer 10 of the thermal transfer sheet 100 is transferred onto the transfer target 300 without being affected by various conditions. . Specifically, in order to cope with high-speed printing suitability, even when the energy applied to the thermal transfer sheet is increased, in other words, even when the printing power is increased, thermal transfer with the transfer target is performed. Thermal fusion with the sheet can be suppressed.
- the transfer layer 10 of the thermal transfer sheet can be easily peeled from the constituent member in contact with the heat transfer member, and thermal fusion between the transfer target and the thermal transfer sheet can be suppressed.
- the third embodiment can suppress thermal fusion between the transfer target and the thermal transfer sheet, which can occur when the transfer layer 10 of the thermal transfer sheet 100 is transferred onto the transfer target 300.
- the thermal transfer sheet 100 when the transfer layer 10 is peeled from the thermal transfer sheet 100 and the base material 1 of the 100, it is possible to prevent the transfer layer 10 from being roughened and transferred to the transfer target. A decrease in glossiness of the transfer layer 10 can also be suppressed.
- the tensile strength of the thermal transfer sheet under “specific measurement conditions” is 0.08 N / cm or less, and particularly preferably 0.07 N / cm or less.
- the printing power is set to 0.15 W / dot because the tensile strength of the thermal transfer sheet measured by the measuring unit 204 is 0 when the printing power is less than 0.15 W / dot. Even if it is 1 N / cm or less, the tensile strength of the thermal transfer sheet measured by the measuring means 204 when the printing power is 0.15 W / dot must be 0.1 N / cm or less. For example, when the energy applied to the thermal transfer sheet is increased when the transfer layer 10 of the thermal transfer sheet 100 is transferred onto the transfer target 300, the thermal fusion between the transfer target 300 and the thermal transfer sheet 100 is suppressed. By being unable to.
- the printer 200 used when transferring the transfer layer 10 of the thermal transfer sheet 100 onto the transfer target 300 melts or softens the transfer layer 10 if the above-mentioned “specific measurement conditions” can be realized.
- the printer may be a thermal peeling type printer that peels the transferred transfer layer 10 from the substrate 1 of the thermal transfer sheet 100 before the layer is solidified. After the transfer layer 10 is solidified, the transferred transfer layer 10 is transferred. May be a cold peeling type printer that peels from the base material 1 of the thermal transfer sheet 100.
- the transfer layer 10 is transferred onto the transfer target.
- the tensile strength of the thermal transfer sheet measured by the measuring means 204 is preferably 0.1 N / cm or less. According to the thermal transfer sheet 100 of the third embodiment that satisfies this condition, the time from when the application of energy is finished to when the transfer layer 10 is peeled off after the application of energy is shortened using a thermal peeling type printer. Even in such a case, the thermal fusion between the transfer target 300 and the thermal transfer sheet 100 can be suppressed. In other words, the peelability of the transfer layer can be improved.
- the thermal transfer sheet after transferring the transfer layer 10 onto the transfer target 300, transfers the transfer layer 10 transferred onto the transfer target, The thermal transfer sheet 100 is removed from the base material 1 without being peeled off, and is peeled off even when the transfer layer 10 transferred onto the transfer target is peeled 180 degrees from the base material 1 of the thermal transfer sheet 100 outside the printer.
- the tensile strength at the time is 0.1 N / cm or less. According to the thermal transfer sheet 100 of this form, for example, even when a cold peeling type printer is used, thermal fusion between the transfer target 300 and the thermal transfer sheet 100 can be suppressed. In other words, the peelability of the transfer layer can be improved.
- the printer 200 used in the “specific measurement conditions” includes a thermal transfer sheet supply roller as a thermal transfer sheet supply unit 201 that conveys the thermal transfer sheet 100 along a predetermined path, and a thermal transfer sheet winding.
- the transfer layer 10 is transferred onto the transfer object 300 and then transferred from the substrate 1 onto the transfer object 300.
- the platen roller 206 is movable between the heating means 202 and the winding means 203.
- a peeling plate as a peeling means 205 for peeling the transferred layer 10, on the conveyance path of the thermal transfer sheet 100, and a heating means 202 (peeling means 05) and the winding means 203, and the transfer layer 10 transferred onto the transfer target 300 is peeled off from the substrate 1 while continuously transferring the transfer layer 10 onto the transfer target 300.
- a tension meter is provided as a measuring means 204 for measuring the tensile strength applied to the thermal transfer sheet.
- the printer 200 used in the above “specific measurement conditions” is located between the heating unit 202 and the winding unit 203 on the conveyance path of the thermal transfer sheet 100, and the transfer layer 10 is placed on the transfer target 300.
- a printer known in the art is used except that a measuring means 204 is provided for measuring the tensile strength of the thermal transfer sheet when the transfer layer 10 transferred onto the transfer target 300 is peeled off from the substrate 1 while transferring. It can be set appropriately and used.
- any tension meter (ASK-1000 model) manufactured by Okura Industry Co., Ltd. can be used as long as it can measure the tensile strength of the thermal transfer sheet running on the conveyance path.
- the tensile strength referred to in this specification is synonymous with tension, and the value of the tensile strength is transferred from the substrate 1 onto the transfer target 300 after the transfer layer 10 is transferred onto the transfer target 300.
- 3 shows a substantial value of the peeling force when the transfer layer 10 is peeled off.
- the printer 200 in which the measuring unit 204 is positioned between the heating unit 202 and the winding unit 203, the transfer layer 10 is transferred from the substrate 1 to the transfer target 300 by the peeling unit 205.
- the transfer layer 10 transferred onto the transfer target 300 is peeled off. Specifically, while the transfer layer 10 is continuously transferred onto the transfer target 300, the transfer layer 10 transferred onto the transfer target is continuously peeled off from the substrate 1, thereby transferring the transfer layer 10. The substantial peeling force can be measured when the layer 10 is peeled off from the constituent member in contact with the transfer layer 10 of the thermal transfer sheet 100.
- the peeling means 205 may be positioned between the heating means 202 and the peeling means 205 located between the measuring means 204, and the position is not particularly limited. May be arranged at a position where the transfer layer 10 transferred onto the transfer target 300 reaches the peeling means 205 after 0.05 sec. As an example, from the heating means 202 toward the transport direction. It is located 4.5mm away. In addition, based on the distance from the heating unit 202 to the peeling unit 205 and the conveyance speed of the thermal transfer sheet, the time until the transfer layer 10 transferred onto the transfer target 300 is peeled off by the peeling unit 205 is calculated. be able to.
- the thermal transfer sheet 100 of the third embodiment only needs to satisfy the condition that the tensile strength in the above-mentioned “specific measurement conditions” is 0.1 N / cm or less, and any other conditions are not limited. It will never be done. Further, there is no limitation on specific means for adjusting the tensile strength under the above-mentioned “specific measurement conditions” to 0.1 N / cm or less, and the tensile strength under the above-mentioned “specific measurement conditions” is 0.1 N / cm. Any means that can be applied is applicable. Hereinafter, although an example is given and demonstrated about the concrete means for making tensile strength into 0.1 N / cm or less, it is not limited to this means.
- the first means is a means for appropriately selecting components to be contained in the transfer layer 10 and adjusting the tensile strength under the above-mentioned “specific measurement conditions” to be 0.1 N / cm or less. Specifically, it is a means for improving the peelability of the layer located at the transfer interface among the layers constituting the transfer layer.
- the transfer interface By selecting an appropriate resin material to be contained in the release layer 4 located in the above, for example, by considering the molecular weight of the resin material, the glass transition temperature, or the monomer forming the resin material, the above-mentioned “specific measurement” The tensile strength in “condition” can be adjusted to 0.1 N / cm or less.
- the peeling layer 4 located at the transfer interface has a methyl methacrylate (MMA) copolymerization ratio of 50% to 85% in molar ratio and an ethyl methacrylate (EA) copolymerization ratio of 15% or more in molar ratio. 50% or less of a copolymer of methyl methacrylate (MMA) and ethyl methacrylate (EA) is included, or the release layer 4 has a copolymerization ratio of isobutyl methacrylate (iBMA) of more than 20% in molar ratio.
- MMA methyl methacrylate
- iBMA isobutyl methacrylate
- a combination of a resin material contained in the transfer layer 10 and a release agent specifically, a resin material contained in a layer located at the transfer interface among the layers constituting the transfer layer 10
- the tensile strength under the above-mentioned “specific measurement conditions” can be adjusted to 0.1 N / cm or less by appropriately determining the type of release agent and the content thereof.
- the release agent include waxes such as polyethylene wax and silicone wax, silicone resin, silicone modified resin, fluorine resin, fluorine modified resin, polyvinyl alcohol, acrylic resin, heat crosslinkable epoxy-amino resin, and heat crosslinkable alkyd. -Amino resins can be mentioned.
- the transfer layer 10 of the thermal transfer sheet of the third embodiment the transfer layer 10 of the thermal transfer sheet of the first embodiment and the second embodiment is applied, and the tensile strength in “specific measurement conditions” is set to 0. It can also be set as the thermal transfer sheet which satisfy
- a more preferable form of the thermal transfer sheet is a thermal transfer sheet in which the transfer layer 10 is positioned on one surface of the substrate 1, and the transfer layer 10 is composed of one or more layers.
- the “base layer” that is the layer located closest to the substrate 1 is (A): (1) a homopolymer of (1) isobutyl (meth) acrylate, or (2) isobutyl (meta ) A copolymer having an acrylate copolymer ratio of 30% or more in molar ratio, and (B): a copolymer of methyl (meth) acrylate and ethyl (meth) acrylate, or both. .
- the copolymerization ratio of methyl (meth) acrylate in the copolymer of (B) is 60% or more and 90% or less in molar ratio, and the copolymerization ratio of ethyl (meth) acrylate is 10% or more in molar ratio.
- the copolymerization ratio of methyl (meth) acrylate in the copolymer (B) is 80% or more in terms of molar ratio
- the copolymer has a weight average molecular weight (Mw) of 15000 or less.
- the thermal transfer sheet 100 is formed by superimposing the thermal transfer sheet 100 and the transfer target 300, and between the thermal transfer sheet supply unit 201, the heating unit 202, the thermal transfer sheet winding unit 203, and between the heating unit 202 and the thermal transfer sheet winding unit 203.
- the printer 200 having the measuring means 204 for measuring the tensile strength of the thermal transfer sheet conveyed along the conveying path and the peeling means 205 positioned between the heating means 202 and the measuring means 204 is used.
- the transfer layer 10 transferred onto the transfer body 300 is transferred while continuously transferring the transfer layer 10 onto the transfer body 300 under the conditions of 15 W / dot and the transfer speed of the thermal transfer sheet of 84.6 mm / sec.
- the tensile strength measured by the measuring unit 204 is 0.1 N / cm or less.
- the “base layer” is described as “specific isobutyl (meth) acrylate” described in the thermal transfer sheet of the first embodiment and the thermal transfer sheet of the second embodiment.
- One or both of the “specific copolymers” are contained, and the tensile strength of the thermal transfer sheet under the “specific measurement conditions” is 0.1 N / cm or less.
- the thermal transfer sheet in a more preferable form may contain one of “specific isobutyl (meth) acrylate” and “specific copolymer”, or may contain both.
- a more preferable form of the thermal transfer sheet is a configuration in which the configuration of the thermal transfer sheet of the first embodiment and the configuration of the thermal transfer sheet of the third embodiment are appropriately combined, or the thermal transfer sheet of the second embodiment.
- the configuration of the thermal transfer sheet of the third embodiment as appropriate, or the configuration of the thermal transfer sheet of the first embodiment, the configuration of the thermal transfer sheet of the second embodiment, and the third embodiment. It is the structure which combined suitably the structure of the form of the thermal transfer sheet.
- the thermal transfer sheet of a more preferable form contains either “specific isobutyl (meth) acrylate” or “specific copolymer”, “specific isobutyl (meth) acrylate”, “specific copolymer weight”
- the preferable content of “union” is as described in the thermal transfer sheet of the first embodiment and the thermal transfer sheet of the second embodiment.
- the “base layer” contains “specific isobutyl (meth) acrylate” and “specific copolymer”, “specific isobutyl (meta) with respect to the total mass of the“ base layer ”.
- Acrylate ”and“ specific copolymer ” are preferably 30% by mass or more, more preferably 50% by mass or more, and particularly preferably 70% by mass or more.
- the second means is to adjust the thickness of the base material 1 or an arbitrary layer provided on the other surface of the base material 1, for example, the thickness of the back layer to reduce the tensile strength in the above “specific measurement conditions” to 0. It is a means to adjust so that it may become 1 N / cm or less. Specifically, it is a means for increasing the thickness of the base material 1 positioned on the heating member side of the transfer layer 10 or an arbitrary layer. According to the second means, the energy applied from the other surface side of the substrate 1 suppresses the transmission efficiency of the energy transmitted to the transfer layer 10, whereby the tensile strength in the above “specific measurement conditions” is reduced. It can adjust so that it may become 0.1 N / cm or less.
- the tensile strength under the above “specific measurement conditions” is 0.1 N / cm or less. It is a means to adjust to.
- a mold release layer etc. can be mentioned, for example.
- the third means It is preferable to use it as an auxiliary means for adjusting the tensile strength by the first means or the second means, or in combination with the fourth means described later.
- the tensile strength can be adjusted by measures such as increasing the thickness of the release layer.
- a fourth means is a means for adjusting the tensile strength under the above-mentioned “specific measurement conditions” to 0.1 N / cm or less in consideration of the heat resistance of the transfer layer 10 itself.
- means for improving the heat resistance of the transfer layer include a method of containing a cured resin cured by a curing agent. Note that it is difficult to adjust the tensile strength under the above-mentioned “specific measurement conditions” to 0.1 N / cm or less only by the fourth means. From the viewpoint of adjusting the tensile strength, the fourth means It is preferable to combine with the third means as an auxiliary means for adjusting the tensile strength by the first means or the second means.
- the heat resistance of the transfer layer 10 instead of improving the heat resistance of the transfer layer 10 itself, or together with this, the heat resistance of an arbitrary layer provided on the other surface of the substrate 1 may be improved.
- the tensile strength under the “specific measurement conditions” can be adjusted to 0.1 N / cm or less by appropriately combining the first to fourth means.
- the tensile strength under the above “specific measurement conditions” can be adjusted to 0.1 N / cm or less in combination with other methods.
- the thermal transfer sheet 100 according to the third embodiment may be formed by using the above-described means and the like under the above-mentioned “specific measurement conditions”.
- the strength is adjusted to be 0.1 N / cm or less, and other conditions are not limited to the following descriptions.
- the base material 1 is an essential configuration in the thermal transfer sheet 100 of the third embodiment, and is provided to hold the transfer layer 10 provided on one surface of the base material 1.
- the material of the base material 1 is not particularly limited, and for example, the material described in the base material 1 of the thermal transfer sheet 100 of the first embodiment can be appropriately selected and used, and detailed description thereof is omitted here.
- the thickness of the substrate 1 is not particularly limited, and is generally in the range of 2.5 ⁇ m to 100 ⁇ m.
- the tensile strength in the above-mentioned “specific measurement conditions” is adjusted to 0.1 N / cm or less by applying the third means and making the thickness of the substrate 1 thicker than the thickness in the general range. You can also.
- various surface treatments such as corona discharge treatment, flame treatment, ozone treatment, ultraviolet treatment, radiation treatment, and surface roughening are performed on the surface of the substrate 1 in order to adjust the adhesion between the substrate 1 and the transfer layer 10.
- Treatment, chemical treatment, plasma treatment, low-temperature plasma treatment, primer treatment, grafting treatment, and the like can also be performed.
- Transfer layer As shown in FIGS. 4 to 6, a transfer layer 10 that can be peeled off from the base material 1 is provided on one surface of the base material 1.
- the transfer layer 10 is an essential component in the thermal transfer sheet 100 of the third embodiment.
- the transfer layer 10 referred to in the thermal transfer sheet 100 of the third embodiment means a layer that is peeled off from the substrate 1 and transferred to a transfer target during thermal transfer. As long as the transfer layer 10 finally satisfies the condition that the tensile strength of the thermal transfer sheet is 0.1 N / cm or less in the above-mentioned “specific measurement conditions”, the layer structure and the components contained in the transfer layer are not limited. It will never be done. As shown in FIGS. 4 and 5, the transfer layer 10 may have a laminated structure in which two or more layers are laminated. As shown in FIG. 6, the transfer layer 10 has a single layer structure. It may be presented. Hereinafter, an example is given and demonstrated about the transfer layer 10 which comprises the thermal transfer sheet 100 of 3rd Embodiment.
- the transfer layer 10 of Embodiment A in the thermal transfer sheet of the third embodiment includes the release layer 4 and the adhesive layer 5 from the substrate 1 side. It has a stacked structure in which layers are stacked in order.
- a protective layer (not shown) can be provided between the release layer 4 and the adhesive layer 5 in place of the embodiment shown in FIG.
- the adhesive layer 5 is not provided on the release layer 4, but a transfer layer 10 having a single-layer structure composed of only the release layer 4 is provided, and the release layer 4 itself is given adhesiveness. You can also.
- the thermal transfer sheet 100 including the transfer layer 10 according to Embodiment A functions as a protective layer transfer sheet that transfers the transfer layer 10 onto the transfer target and protects the surface of the transfer target.
- the adhesive layer 5 and the protective layer conventionally known materials can be appropriately selected and used as the material for the adhesive layer and the protective layer in the fields of the intermediate transfer medium, the protective layer transfer sheet and the like. Further, when the tensile strength under the above-mentioned “specific measurement conditions” is adjusted to 0.1 N / cm or less by means other than the first means, a conventionally known material is appropriately selected and used as the release layer 4. Can do.
- the transfer layer 10 of Embodiment B (hereinafter referred to as the transfer layer of Embodiment B) in the thermal transfer sheet of the third embodiment includes a release layer 4 and a receiving layer 2 from the substrate 1 side.
- a stacked structure is formed by stacking in this order.
- the thermal transfer sheet 100 including the transfer layer 10 of Embodiment B forms a thermal transfer image on the receiving layer of the thermal transfer sheet, transfers the transfer layer including the receiving layer on which the thermal transfer image is formed, onto the transfer target, and prints It functions as an intermediate transfer medium for obtaining products.
- a conventionally known material can be appropriately selected and used as a material for the receiving layer in the field of a thermal transfer image receiving sheet or an intermediate transfer medium.
- the transfer layer 10 of the embodiment A and the embodiment B as described in the first means, the transfer layer 10 is configured and the above-mentioned “specific” is considered in consideration of the components contained in the release layer 4 serving as a transfer interface.
- the tensile strength in the "measurement conditions" may be adjusted to 0.1 N / cm or less, and the tensile strength is 0. 0 by the second means or by appropriately combining the first to fourth means. You may adjust so that it may become 1 N / cm or less.
- the transfer layer 10 of the embodiment A (hereinafter referred to as the transfer layer of the embodiment A) in the thermal transfer sheet of the third embodiment has a single layer configuration composed of a hot-melt ink layer 7 as shown in FIG. ing.
- the thermal transfer sheet 100 including the transfer layer 10 according to Embodiment C has a function of transferring the hot-melt ink layer 7 on the transfer target body and forming a thermal transfer image on the transfer target body.
- the above-mentioned “specific measurement” is performed in consideration of the resin material, components such as a release agent, and the content contained in the hot-melt ink layer 7 constituting the transfer layer 10.
- the tensile strength in “Condition” may be adjusted to 0.1 N / cm or less, and the second to fourth means are appropriately selected so that the tensile strength of the transfer layer 10 is 0.1 N / cm. You may adjust so that it may become the following.
- different transfer layers 10 can be provided on the same surface of the substrate 1 in the surface order.
- a heat transfer ink layer 7 as a transfer layer 10, a release layer 4, and an adhesive layer 5 are laminated in this order, and a transfer layer 10 having a stacked structure is provided in the surface order.
- a thermal transfer sheet 100 may also be used.
- the thermal transfer sheet 100 of the third embodiment may include an arbitrary layer that does not constitute a transfer layer. As an arbitrary layer, it is provided between the base material 1 and the transfer layer 10, and is provided on a release layer (not shown) for improving the transferability of the transfer layer 10 or on the other surface of the base material 1. And a back layer for improving the heat resistance and the layer structure of a heating member such as a thermal head.
- a release layer may be provided between the base material 1 and the hot-melt ink layer 7 as the transfer layer 10.
- Mw means a weight average molecular weight
- Tg means a glass transition temperature
- a copolymerization ratio is a molar ratio
- MMA means methyl methacrylate
- MA means methyl acrylate
- EA means ethyl acrylate
- iBMA means isobutyl methacrylate
- MAA means methacrylic acid
- LA means lauryl acrylate.
- the MMA-EA copolymer is a copolymer of methyl methacrylate and ethyl acrylate
- the iBMA-MA copolymer is a copolymer of isobutyl methacrylate and methyl acrylate
- the MMA-iBMA copolymer is methyl methacrylate.
- iBMA-MAA copolymer means a copolymer of isobutyl methacrylate and methacrylic acid
- MMA-LA copolymer means a copolymer of methyl methacrylate and lauryl acrylate.
- Example 1 Using a polyethylene terephthalate film (Toray Co., Ltd.) having a thickness of 4.5 ⁇ m as a base material, the base layer coating solution 1 having the following composition is formed on one surface of the base material, and the thickness upon drying becomes 1 ⁇ m.
- the base layer was formed by coating and drying as described above.
- the protective layer coating solution 1 having the following composition was applied and dried on the base layer so that the thickness upon drying was 1 ⁇ m, thereby forming a protective layer.
- the back layer coating solution 1 having the following composition is applied and dried so that the thickness upon drying is 1 ⁇ m, and the back layer is formed.
- a transfer layer in which a base layer and a protective layer were laminated on one side was provided, and a thermal transfer sheet of Example 1 was obtained in which a back layer was provided on the other side of the substrate.
- the base layer coating solution 1, the protective layer coating solution 1, and the back layer coating solution 1 were applied by gravure coating.
- Example 2 The base layer coating solution 1 was changed to a base layer coating solution 2 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- Example 3 The base layer coating solution 1 was changed to the base layer coating solution 3 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 3 was obtained in which a transfer layer comprising a layer and a protective layer was provided, and a back layer was provided on the other surface of the substrate.
- Example 4 The base layer coating solution 1 was changed to a base layer coating solution 4 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 4 was obtained in which a transfer layer comprising a layer and a protective layer was provided, and a back layer was provided on the other surface of the substrate.
- ⁇ Base layer coating solution 4> IBMA-MA copolymer (Mw: 13500, Tg: 85 ° C.) 25 parts (iBMA: MA (copolymerization ratio) 50: 50) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Example 5 The base layer coating solution 1 was changed to a base layer coating solution 5 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 5 was obtained in which a transfer layer comprising a layer and a protective layer was provided, and a back layer was provided on the other surface of the substrate.
- ⁇ Base layer coating solution 5> IBMA-MA copolymer (Mw: 13600, Tg: 93 ° C.) 25 parts (iBMA: MA (copolymerization ratio) 30: 70) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Example 6 A polyethylene terephthalate film (Toray Industries, Inc.) having a thickness of 4.5 ⁇ m is used as a base material, and the base layer coating solution 1 is formed on one surface of the base material so that the thickness upon drying becomes 2 ⁇ m.
- the base layer was formed by coating and drying.
- the back layer coating liquid is applied and dried so that the thickness upon drying is 1 ⁇ m, and a back layer is formed.
- a thermal transfer sheet of Example 6 was obtained in which a transfer layer consisting only of a base layer was provided, and a back layer was provided on the other side of the substrate.
- the above-mentioned base layer coating solution 1 and back layer coating solution were applied by gravure coating.
- Example 7 Except for changing the base layer coating solution 1 to the base layer coating solution 2 and forming the base layer, the same procedure as in Example 6 was carried out, and only the base layer was formed on one surface of the substrate. Thus, a thermal transfer sheet of Example 7 was obtained in which a transfer layer comprising: a back layer was provided on the other surface of the substrate.
- Example 8 The base layer coating solution 1 was changed to the base layer coating solution 3 above, except that the base layer was formed, and in the same manner as in Example 6, only the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 8 was obtained in which a transfer layer comprising: a back layer was provided on the other surface of the substrate.
- Example 9 The base layer coating solution 1 was changed to the base layer coating solution 4 and all the steps were performed in the same manner as in Example 6, except that only the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 9 was obtained in which a transfer layer comprising: a back layer was provided on the other surface of the substrate.
- Example 10 The base layer coating solution 1 was changed to the base layer coating solution 5 and the base layer was formed in the same manner as in Example 6 except that only the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 10 was obtained, in which a transfer layer comprising: a back layer was provided on the other surface of the substrate.
- the base layer coating solution 1 was changed to the base layer coating solution A having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- ⁇ Base layer coating solution A> IBMA-MA copolymer (Mw: 13600, Tg: 93 ° C.) 25 parts (iBMA: MA (copolymerization ratio) 20: 80) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Comparative Example 2 The base layer coating solution 1 was changed to the base layer coating solution B having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- ⁇ Base layer coating solution B> IBMA-MA copolymer (Mw: 14000, Tg: 101 ° C.) 25 parts (iBMA: MA (copolymerization ratio) 10: 90) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Example 3 The base layer coating solution 1 was changed to a base layer coating solution C having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- thermal transfer image A solid black image composed of yellow, magenta, and cyan dyes was printed on the receiving layer of the thermal transfer image receiving sheet prepared by the following method under the following thermal transfer image forming conditions to obtain a thermal transfer image (image formed product).
- a thermal transfer image image formed product
- sublimation thermal transfer sheets prepared by the following method were used.
- thermo transfer image receiving sheet A On a porous film layer made of a porous polyethylene film having a thickness of 35 ⁇ m (Toyopearl (registered trademark) SS P4255 Toyobo Co., Ltd.), an intermediate layer coating solution having the following composition was applied by a gravure reverse coating method at the time of drying. The intermediate layer was formed by coating and drying so that the thickness was 1.5 ⁇ m. Next, on the intermediate layer, a receiving layer coating solution having the following composition was applied and dried by a gravure reverse coating method so that the thickness upon drying was 5 ⁇ m, thereby forming a receiving layer.
- an adhesive layer coating solution having the following composition is gravure reverse roll coated so that the thickness upon drying is 5 ⁇ m. Then, coating and drying were performed to form an adhesive layer, and an RC base paper (155 g / m 2 , thickness 151 ⁇ m) (Mitsubishi Paper Co., Ltd.) was bonded to produce a thermal transfer image receiving sheet A.
- Thermal head F3598 (Toshiba Hokuto Electronics Corporation) -Heating element average resistance: 5176 ( ⁇ ) ⁇ Print density in main scanning direction: 300 (dpi) -Sub-scanning direction printing density: 300 (dpi) ⁇ Printing power: 0.12 (W / dot) ⁇ One line cycle: 2 (msec.) ⁇ Pulse duty: 85 (%) -Printing start temperature: 35.5 (° C)
- the tensile strength of the thermal transfer sheet when the thermal transfer sheet of each example and comparative example is peeled off from the image formed product, the winding roll of the thermal transfer sheet in the printer was performed with a tension meter (ASK-1000 model number, Okura Industry Co., Ltd.) provided between the release plate and the release plate.
- Table 1 shows the measurement results of tensile strength (peeling force).
- the tensile strength is measured in a state in which the winding speed by the winding roll is controlled to be constant (conveying speed: 84.6 mm / sec.). The peel force to be measured can be measured.
- the heat transfer sheet has good peelability (releasability) from the image formed product, and the heat transfer between the transfer target and the heat transfer sheet, etc. It can be suppressed.
- the tensile strength measured by a tension meter when the transfer layer transferred onto the thermal transfer image receiving sheet A is peeled off from the substrate is synonymous with the tension, and the value of the tensile strength is the same as that on the thermal transfer image receiving sheet A.
- the figure shows a substantial value of the peeling force when the transfer layer transferred onto the thermal transfer image receiving sheet A is peeled from the substrate after the transfer layer is transferred.
- Example 11 The base layer coating solution 1 was changed to a base layer coating solution 11 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 11 was obtained in which a transfer layer comprising a layer and a protective layer was provided, and a back layer was provided on the other surface of the substrate.
- Example 12 The base layer coating solution 1 was changed to a base layer coating solution 12 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- ⁇ Base layer coating solution 12> MMA-EA copolymer (Mw: 7920, Tg: 75 ° C.) 25 parts (MMA: EA (copolymerization ratio) 83: 17) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Example 13 The base layer coating solution 1 was changed to a base layer coating solution 13 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- ⁇ Base layer coating solution 13> MMA-EA copolymer (Mw: 19800, Tg: 60 ° C.) 25 parts (MMA: EA (copolymerization ratio)) 74:26) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Example 14 The base layer coating solution 1 was changed to a base layer coating solution 14 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- ⁇ Base layer coating solution 14> MMA-EA copolymer (Mw: 41200, Tg: 48 ° C.) 25 parts (MMA: EA (copolymerization ratio) 65: 35) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Example 15 The base layer coating solution 1 was changed to a base layer coating solution 15 having the following composition, and the base layer was formed in the same manner as in Example 1 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 15 was obtained in which a transfer layer comprising a layer and a protective layer was provided, and a back layer was provided on the other surface of the substrate.
- ⁇ Base layer coating solution 15> MMA-EA copolymer (Mw: 19900, Tg: 48 ° C.) 25 parts (MMA: EA (copolymerization ratio) 65: 35) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Example 16 Using a polyethylene terephthalate film (Toray Co., Ltd.) having a thickness of 4.5 ⁇ m as a base material, the base layer coating solution 1 having the above composition on one surface of the base material has a thickness of 2 ⁇ m when dried. Thus, the base layer was formed by coating and drying. Further, on the other surface of the base material, the back layer coating solution 1 having the above composition is applied and dried so that the dry thickness is 0.8 ⁇ m, thereby forming the back layer.
- a thermal transfer sheet of Example 16 was obtained in which a transfer layer consisting only of a base layer was provided on one side of the material, and a back layer was provided on the other side of the substrate. The base layer coating liquid 1 and the back layer coating liquid 1 were applied by gravure coating.
- Example 17 The base layer coating solution 1 was changed to the base layer coating solution 2 having the above composition, and the base layer was formed in the same manner as in Example 16 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 17 was obtained in which a transfer layer consisting of only a layer was provided, and a back layer was provided on the other side of the substrate.
- Example 18 The base layer coating solution 1 was changed to the base layer coating solution 3 having the above composition, and the base layer was formed in the same manner as in Example 16 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 18 was obtained in which a transfer layer consisting of only a layer was provided, and a back layer was provided on the other side of the substrate.
- Example 19 The base layer coating solution 1 was changed to the base layer coating solution 4 having the above composition, and the base layer was formed in the same manner as in Example 16 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 19 was obtained in which a transfer layer consisting of only a layer was provided, and a back layer was provided on the other side of the substrate.
- Example 20 The base layer coating solution 1 was changed to the base layer coating solution 5 having the above composition, and the base layer was formed in the same manner as in Example 16 except that the base layer was formed on one surface of the substrate.
- a thermal transfer sheet of Example 20 was obtained in which a transfer layer consisting of only a layer was provided, and a back layer was provided on the other side of the substrate.
- Comparative Example 4 The thermal transfer sheet of Comparative Example 4 was obtained in the same manner as in Example 1 except that the base layer coating solution 1 was changed to the base layer coating solution D having the following composition to form a base layer.
- ⁇ Base layer coating solution D> MMA-EA copolymer (Mw: 14000, Tg: 96 ° C.) 25 parts (MMA: EA (copolymerization ratio) 95: 5) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Comparative Example 5 A thermal transfer sheet of Comparative Example 5 was obtained in the same manner as in Example 1 except that the base layer coating solution 1 was changed to the base layer coating solution E having the following composition to form a base layer.
- Comparative Example 6 A thermal transfer sheet of Comparative Example 6 was obtained in the same manner as in Example 1 except that the base layer coating solution 1 was changed to the base layer coating solution F having the following composition to form a base layer.
- Comparative Example 7 A thermal transfer sheet of Comparative Example 4 was obtained in the same manner as in Example 1 except that the base layer coating solution 1 was changed to the base layer coating solution G having the following composition to form a base layer.
- Comparative Example 8 The thermal transfer sheet of Comparative Example 8 was obtained in the same manner as in Example 1 except that the base layer coating solution 1 was changed to the base layer coating solution H having the following composition to form a base layer.
- Comparative Example 9 A thermal transfer sheet of Comparative Example 9 was obtained in the same manner as in Example 1 except that the base layer coating solution I was changed to the base layer coating solution I having the following composition to form a base layer.
- ⁇ Base layer coating solution I> MMA-EA copolymer (Mw: 16000, Tg: 75 ° C.) 25 parts (MMA: EA (copolymerization ratio) 83: 17) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- Comparative Example 10 A thermal transfer sheet of Comparative Example 10 was obtained in the same manner as in Example 1 except that the base layer coating solution 1 was changed to the base layer coating solution J having the following composition to form a base layer.
- Comparative Example 11 A thermal transfer sheet of Comparative Example 11 was obtained in the same manner as in Example 1 except that the base layer coating solution 1 was changed to the base layer coating solution K having the following composition to form a base layer.
- Comparative Example 12 A thermal transfer sheet of Comparative Example 12 was obtained in the same manner as in Example 1 except that the base layer coating solution 1 was changed to the base layer coating solution L having the following composition to form a base layer.
- ⁇ Base layer coating solution L> MMA-EA copolymer (Mw: 20000, Tg: 29 ° C.) 25 parts (MMA: EA (copolymerization ratio) 50: 50) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- the tensile strength of the thermal transfer sheet when the thermal transfer sheet of each example and comparative example is peeled off from the image formed product, the winding roll of the thermal transfer sheet in the printer was performed with a tension meter (ASK-1000 model number, Okura Industry Co., Ltd.) provided between the release plate and the release plate.
- Table 2 shows the measurement results of tensile strength (peeling force).
- the tensile strength is measured in a state in which the winding speed by the winding roll is controlled to be constant (conveying speed: 84.6 mm / sec.). The peel force to be measured can be measured.
- the heat transfer sheet has good peelability (releasability) from the image formed product, and the heat transfer between the transfer target and the heat transfer sheet, etc. It can be suppressed.
- the tensile strength measured by a tension meter when the transfer layer transferred onto the thermal transfer image receiving sheet A is peeled off from the substrate is synonymous with the tension, and the value of the tensile strength is the same as that on the thermal transfer image receiving sheet A.
- the figure shows a substantial value of the peeling force when the transfer layer transferred onto the thermal transfer image receiving sheet A is peeled from the substrate after the transfer layer is transferred.
- thermal transfer sheet 1 A polyethylene terephthalate film (Toray Co., Ltd.) having a thickness of 4.5 ⁇ m is used as the base material, and the transfer layer coating liquid 1 having the following composition is formed on one surface of the base material with a thickness of 1 ⁇ m when dried. As described above, coating and drying were performed to form a transfer layer. In addition, on the other surface of the base material, the back layer coating liquid 2 having the following composition is applied and dried so that the thickness upon drying is 1 ⁇ m, thereby forming the back layer, A thermal transfer sheet 1 was obtained in which a transfer layer was provided on one side and a back layer was provided on the other side of the substrate. The transfer layer coating solution 1 and the back layer coating solution were applied by gravure coating.
- ⁇ Coating liquid 1 for transfer layer> MMA-EA copolymer (Mw: 8000, Tg: 75 ° C.) 25 parts (MMA: EA (copolymerization ratio) 83: 17) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- thermal transfer sheet 2 (Preparation of thermal transfer sheet 2)
- the transfer layer coating solution 1 was changed to a transfer layer coating solution 2 having the following composition, and the transfer layer was formed.
- a thermal transfer sheet 2 having a transfer layer provided thereon and a back layer provided on the other surface of the substrate was obtained.
- ⁇ Coating solution 2 for transfer layer> MMA-EA copolymer (Mw: 41200, Tg: 48 ° C.) 25 parts (MMA: EA (copolymerization ratio) 65: 35) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- thermal transfer sheet 3 (Preparation of thermal transfer sheet 3)
- the transfer layer coating solution 1 was changed to a transfer layer coating solution 3 having the following composition, and the transfer layer was formed.
- a thermal transfer sheet 3 having a transfer layer provided thereon and a back layer provided on the other surface of the substrate was obtained.
- thermal transfer sheet 4 (Preparation of thermal transfer sheet 4)
- the transfer layer coating solution 1 was changed to a transfer layer coating solution 4 having the following composition, and the transfer layer was formed.
- a thermal transfer sheet 4 was obtained in which a transfer layer was provided and a back layer was provided on the other surface of the substrate.
- ⁇ Coating solution 4 for transfer layer> MMA-iBMA copolymer (Mw: 13500, Tg: 85 ° C.) 25 parts (MMA: iBMA (copolymerization ratio) 50: 50) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- thermal transfer sheet 5 (Preparation of thermal transfer sheet 5) The transfer layer coating solution 1 was changed to a transfer layer coating solution 5 having the following composition, and the transfer layer was formed. A thermal transfer sheet 5 was obtained in which a transfer layer was provided and a back layer was provided on the other surface of the substrate.
- thermal transfer sheet 6 (Preparation of thermal transfer sheet 6) Instead of a polyethylene terephthalate film (Toray Industries, Inc.) having a thickness of 4.5 ⁇ m, a polyethylene terephthalate film (Toray Industries, Inc.) having a thickness of 5.7 ⁇ m was used.
- the transfer layer is provided on one surface of the base material in the same manner as the preparation of the thermal transfer sheet 1 except that the transfer layer is formed by changing to the layer coating solution 6, and the other surface of the base material is provided.
- a thermal transfer sheet 6 having a back layer provided thereon was obtained.
- thermo transfer sheet 7 (Preparation of thermal transfer sheet 7)
- the transfer layer coating solution 1 is changed to a transfer layer coating solution 6 having the above composition to form a transfer layer, and the back layer coating solution is applied so that the thickness when dried is 2 ⁇ m.
- the transfer layer was provided on one side of the substrate and the back layer was provided on the other side of the substrate in the same manner as the preparation of the thermal transfer sheet 1 except that the back layer was formed by drying.
- a thermal transfer sheet 7 was obtained.
- thermal transfer sheet A (Preparation of thermal transfer sheet A) The transfer layer coating solution 1 was changed to the transfer layer coating solution 6 having the above composition, and the transfer layer was formed in the same manner as in the preparation of the thermal transfer sheet 1 on one side of the substrate. A thermal transfer sheet A having a transfer layer provided thereon and a back layer provided on the other surface of the substrate was obtained.
- thermal transfer sheet B (Preparation of thermal transfer sheet B) The transfer layer coating solution 1 was changed to a transfer layer coating solution A having the following composition, and the transfer layer was formed. A thermal transfer sheet B having a transfer layer provided thereon and a back layer provided on the other surface of the substrate was obtained.
- ⁇ Coating solution A for transfer layer> MMA-iBMA copolymer (Mw: 13500, Tg: 97 ° C.) 25 parts (MMA: iBMA (copolymerization ratio) 80: 20) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- thermo transfer sheet C (Preparation of thermal transfer sheet C)
- the transfer layer coating liquid 1 was changed to the transfer layer coating liquid B having the following composition, and the transfer layer was formed. Was obtained, and a thermal transfer sheet C was obtained in which a back layer was provided on the other surface of the substrate.
- ⁇ Coating solution B for transfer layer> MMA-LA copolymer (Mw: 17500, Tg: 60 ° C.) 25 parts (MMA: LA (copolymerization ratio) 84: 16) ⁇ Methyl ethyl ketone 67 parts ⁇ Normal propyl acetate 8 parts
- thermo transfer image receiving sheet 1 On one side of the base material (coated paper, thickness 170 ⁇ m, Daio Paper Co., Ltd.), a back surface primer layer coating solution having the following composition was applied so that the thickness when dried was 1.2 ⁇ m. The back primer layer was formed by drying at 110 ° C. for 1 minute. On the back primer layer, a back layer coating solution having the following composition was applied so that the thickness when dried was 1 ⁇ m, and dried at 110 ° C. for 1 minute to form a back layer. Next, a sealing layer coating liquid having the following composition is applied onto the other surface of the base material so that the thickness when dried is 1 ⁇ m, and dried at 110 ° C. for 1 minute to form the sealing layer. Formed.
- a porous layer coating solution having the following composition was applied onto the sealing layer so that the thickness when dried was 30 ⁇ m, and dried at 110 ° C. for 2 minutes to form a porous layer.
- a barrier layer coating solution having the following composition is applied onto the porous layer so that the thickness when dried is 0.5 ⁇ m, and dried at 110 ° C. for 1 minute to form a barrier layer.
- an antistatic layer was formed on this barrier layer.
- a receiving layer is formed by applying the receiving layer coating liquid 1 having the following composition on the antistatic layer so that the thickness upon drying is 3 ⁇ m and drying at 110 ° C. for 1 minute. Then, the back primer layer and the back layer are laminated in this order on one surface of the base material, and the sealing layer, the porous layer, the barrier layer, the antistatic layer, and the receiving layer are formed on the other surface of the base material. Obtained a thermal transfer image-receiving sheet 1 laminated in this order.
- Polyester resin 10 parts (Byron (registered trademark) 200 Toyobo Co., Ltd.) ⁇ Methyl ethyl ketone 10 parts ⁇ Toluene 10 parts
- thermo transfer image receiving sheet 2 A porous polypropylene film (thickness 38 ⁇ m, density 0.7 g / cm 3 ) was prepared as a porous film for forming the porous layer.
- a white base paper uncoated paper, thickness 150 ⁇ m, (Mitsubishi Paper Co., Ltd.), which is a paper base material, was prepared as a base material layer.
- a high density polyethylene resin density 0.956 g
- a primer layer coating solution having the following composition was applied onto the porous polypropylene film with a gravure coater so that the thickness when dried was 2 ⁇ m, and the temperature was 110 ° C. for 1 minute.
- a coating solution 2 for receiving layer having the following composition is applied on it with a gravure coater so that the thickness upon drying is 4 ⁇ m, and dried at 110 ° C. for 1 minute, and then a primer layer and a receiving layer As a result, a thermal transfer image-receiving sheet 2 was obtained.
- the tensile strength of the thermal transfer sheet when the transfer layer transferred to the thermal transfer upper sheet is peeled off from the substrate, the winding roll of the thermal transfer sheet, the heating means (thermal head), was measured with a tension meter (ASK-1000 model number, Okura Industry Co., Ltd.) provided between the two.
- Table 3 shows the measurement results of the tensile strength.
- combinations of a thermal transfer sheet and a thermal transfer image receiving sheet in which both the tensile strength during heat (peeling force during heat) and the cold tensile strength (cold peel force) described later are 0.1 N / cm or less are shown.
- Thermal transfer sheet and thermal transfer in which one or both of the tensile strength during heat (peeling force during heat) and the cold tensile strength (cold peel force) described below are 0.1 N / cm as examples.
- a combination with an image receiving sheet is used as a comparative example.
- thermal transfer sheets and thermal transfer image receiving sheets prepared above are combined in the combinations shown in Table 3 below, and after the transfer layer of the thermal transfer sheet is transferred onto the thermal transfer image receiving sheet using the following test printer 2, the thermal transfer image receiving sheet is placed on the thermal transfer image receiving sheet.
- the transferred transfer layer is taken out from the test printer 2 without being peeled off from the substrate, and is pulled when the transfer layer transferred onto the thermal transfer image receiving sheet is peeled off from the substrate with the following peeling device and peeling conditions. The strength was measured.
- the measurement results are also shown in Table 3.
- the test printer 2 has the same configuration as the test printer 1 except that it does not have a release plate and a tension meter.
- Peeling device HEIDON-14DR Shinto Kagaku Co., Ltd. Peeling speed: 5 (m / min.) Peel angle: 180 (degrees)
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Abstract
Description
本開示の第1の実施の形態に係る熱転写シート(以下、第1実施形態の熱転写シートと言う場合がある)は、図1~図3に示すように、基材1の一方の面上に転写層10が設けられた構成を呈している。転写層10は、1又は2以上の層から構成され、第1実施形態の熱転写シート100は、転写層10を構成する層のうち、基材1から最も近くに位置する層が、(1)イソブチル(メタ)アクリレートの単独重合体、又は(2)イソブチル(メタ)アクリレートの共重合比率がモル比で30%以上の共重合体を含有している。図1~図3は、第1実施形態の熱転写シートの一例を示す概略断面図である。以下、熱転写シートを構成する構成部材のうち転写層と直接的に接する構成部材が基材である場合を中心に説明するが、第1実施形態の熱転写シートは、基材と転写層とが直接的に接している形態に限定されるものではなく、基材と転写層との間に任意の層を設けることもできる。この場合には、当該任意の層が転写層と直接的に接する構成部材となる。
第1形態の転写層10は、図1に示すように、基材1の一方の面上に、「基底層」10A、保護層3がこの順で積層されてなる積層構成の転写層10が位置している。第1形態の転写層10を有する熱転写シート100は、被転写体上に、当該第1形態の転写層10を転写することで、第1形態の転写層10によって覆われる被転写体の画像等に、耐久性や、耐候性等を付与するために用いられ、所謂保護層転写シートとしての役割を果たす。
保護層3の成分としては、例えば、アクリル系樹脂、塩化ビニル-酢酸ビニル共重合体、エポキシ系樹脂、ポリエステル系樹脂、ポリカーボネート系樹脂、ブチラール系樹脂、ポリアミド系樹脂、塩化ビニル系樹脂などを挙げることができる。
また、保護層3上に接着層(図示しない)を位置させることもできる。保護層3上にさらに接着層が位置する第1形態の転写層10によれば、転写層10と被転写体との密着性を向上させることができる。接着層の成分としては、例えば、アクリル系樹脂、ビニル系樹脂、ポリエステル系樹脂、ウレタン系樹脂、ポリアミド系樹脂、エポキシ系樹脂、ゴム系樹脂、アイオノマー樹脂等を主成分とする従来公知の接着剤等を挙げることができる。接着層の厚みについて特に限定はないが、0.1μm以上50μm以下の範囲が好ましく、1μm以上10μm以下の範囲がより好ましい。
第2形態の転写層10は、図2に示すように、基材1の一方の面上に、「基底層」10A、受容層2がこの順で積層されてなる積層構成の転写層10が位置している。第2形態の転写層10を有する熱転写シート100は、第2形態の転写層10を構成する層のうち、基材1から最も遠くに位置する受容層2上に熱転写画像を形成し、当該熱転写画像が形成された受容層2を含む第2形態の転写層10を、被転写体上に転写することで印画物を得るために用いられ、所謂中間転写媒体としての役割を果たす。
受容層2の成分としては、例えば、ポリプロピレン等のポリオレフィン系樹脂、ポリ塩化ビニルもしくはポリ塩化ビニリデン等のハロゲン化樹脂、ポリ酢酸ビニル、塩化ビニル-酢酸ビニル系共重合体、エチレン-酢酸ビニル共重合体もしくはポリアクリル酸エステル等のビニル系樹脂、ポリエチレンテレフタレートもしくはポリブチレンテレフタレート等のポリエステル樹脂、ポリスチレン系樹脂、ポリアミド系樹脂、エチレンもしくはプロピレン等のオレフィンと他のビニルポリマーとの共重合体、アイオノマーもしくはセルロースジアスターゼ等のセルロース系樹脂、ポリカーボネート系樹脂等を挙げることができる。
第3形態の転写層10は、図3に示すように、基材1の一方の面上に、「基底層」10のみからなる単層構成の転写層10が位置している。
第1実施形態の熱転写シート100は、転写層を構成しない任意の層を備えていてもよい。任意の層としては、基材1と転写層10との間に設けられ、転写層10の転写性を向上させるための離型層(図示しない)や、基材1の他方の面上に設けられ、耐熱性や、サーマルヘッド等の加熱部材の走行性を向上させるための背面層等を挙げることができる。例えば、上記第3形態の転写層10を備える熱転写シートにおいて、基材1と、熱溶融インキ層としての「基底層」10Aとの間に離型層を設けることもできる。
基材1は、第1実施形態の熱転写シート100における必須の構成であり、当該基材1の一方の面上に位置する転写層10を保持するために設けられる。基材1の材料については特に限定されないが、転写層10を被転写体上に転写する際に加えられる熱に耐え、取り扱い上支障のない機械的特性を有することが望ましい。このような基材1として、例えば、ポリエチレンテレフタレート等のポリエステル、ポリアリレート、ポリカーボネート、ポリウレタン、ポリイミド、ポリエーテルイミド、セルロース誘導体、ポリエチレン、エチレン-酢酸ビニル共重合体、ポリプロピレン、ポリスチレン、アクリル、ポリ塩化ビニル、ポリ塩化ビニリデン、ポリビニルアルコール、ポリビニルブチラール、ナイロン、ポリエーテルエーテルケトン、ポリサルフォン、ポリエーテルサルフォン、テトラフルオロエチレン-パーフルオロアルキルビニルエーテル共重合体、ポリビニルフルオライド、テトラフルオロエチレン-エチレン共重合体、テトラフルオロエチレン-ヘキサフルオロプロピレン共重合体、ポリクロロトリフルオロエチレン、ポリビニリデンフルオライド等の各種プラスチックフィルムまたはシートを挙げることができる。
第1実施形態の熱転写シート100の転写層10が転写される被転写体について特に限定はなく、普通紙、上質紙、トレーシングペーパー、プラスチックフィルム、塩化ビニル、塩化ビニル-酢酸ビニル共重合体、ポリカーボネートを主体として構成されるプラスチックカード、熱転写受像シート、任意の対象物上に中間転写媒体の転写層が転写されてなる印画物等を挙げることができる。後述する第2実施形態、第3実施形態の熱転写シート100の転写層10が転写される被転写体についても同様である。
第1実施形態の熱転写シート100の転写層10を被転写体上に転写する際に用いられるプリンタについて特に限定はなく、サーマルヘッド等の加熱部材を備える従来公知のあらゆるプリンタを使用可能である。なお、第1実施形態の熱転写シート100は、高いエネルギーを印加可能なプリンタや、熱時剥離タイプのプリンタ等を用いた場合においても、被転写体と熱転写シートとの熱融着を抑制することができ、これらのプリンタを用いる場合に特に好適である。後述する第2実施形態の熱転写シートの転写層10を被転写体上に転写する際に用いられるプリンタについても同様である。
本開示の第2の実施の形態に係る熱転写シート(以下、第2実施形態の熱転写シートと言う場合がある)は、図1~図3に示すように、上記第1実施形態の熱転写シート100と同様に、基材1の一方の面上に転写層10が設けられた構成を呈している。転写層10は、1又は2以上の層から構成され、第2実施形態の熱転写シート100は、転写層10を構成する層のうち、基材1から最も近くに位置する層が、メチル(メタ)アクリレートとエチル(メタ)アクリレートとの共重合体を含有しており、当該共重合体におけるメチル(メタ)アクリレートの共重合比率がモル比で60%以上90%以下であり、エチル(メタ)アクリレートの共重合比率がモル比で10%以上40%以下であり、さらに、メチル(メタ)アクリレートの共重合比率がモル比で80%以上である場合には、当該共重合体の重量平均分子量(Mw)は15000以下であり、一方で、メチル(メタ)アクリレートの共重合比率がモル比で80%未満である場合には、当該共重合体の重量平均分子量(Mw)は45000以下である。以下、共重合比率とある記載は、いずれもモル比を意味する。
(共重合体A):メチル(メタ)アクリレートとエチル(メタ)アクリレートとの共重合体であって、当該共重合体Aの重量平均分子量(Mw)は15000以下であり、当該共重合体Aをなすメチル(メタ)アクリレートの共重合比率が80%以上90%以下であり、エチル(メタ)アクリレートの共重合比率が10%以上20%以下である。
(共重合体B):メチル(メタ)アクリレートとエチル(メタ)アクリレートとの共重合体であって、当該共重合体Bの重量平均分子量(Mw)は45000以下であり、当該共重合体Bをなす、メチル(メタ)アクリレートの共重合比率が60%以上80%未満であり、エチル(メタ)アクリレートの共重合比率は、20%より多く40%以下である。
以下、共重合体A、共重合体Bを総称して、「特定の共重合体」と言う場合がある。
本開示の第3の実施の形態に係る熱転写シート(以下、第3実施形態の熱転写シートと言う場合がある)は、図4~図6に示すように、基材1と、当該基材1から剥離可能に設けられた転写層10とを備えている。
次に、上記「特定の測定条件」にて、被転写体300上に転写層10を転写し、被転写体上に転写された転写層10を、熱転写シート100の基材1から剥離する際に用いられるプリンタについて説明する。
第1の手段は、転写層10に含有せしめる成分を適宜選択して、上記「特定の測定条件」における引張強度を0.1N/cm以下となるように調整する手段である。具体的には、転写層を構成する層のうち、転写界面に位置する層の剥離性を向上させる手段である。
第2の手段は、基材1の厚みや、基材1の他方の面上に設けられる任意の層、例えば、背面層の厚みを調整して上記「特定の測定条件」における引張強度を0.1N/cm以下となるように調整する手段である。具体的には、転写層10よりも加熱部材側に位置する基材1や、任意の層の厚みを厚くする手段である。第2の手段によれば、基材1の他方の面側から印加されるエネルギーが転写層10に伝達されるエネルギーの伝達効率を抑え、これにより、上記「特定の測定条件」における引張強度が0.1N/cm以下となるように調整することができる。また、基材1や、基材1の他方の面上に設けられる任意の層の厚みを調整する方法にかえて、基材1や、基材1の他方の面上に設けられる任意の層の材料として、エネルギーの伝達効率が低い材料を用いることで、基材1の他方の面側に印加されたエネルギーが、転写層10に伝達されるまでのエネルギーの伝達効率を抑えることもできる。
第3の手段は、基材1と転写層10との間に、転写層10の転写性を向上させる任意の層を設け、上記「特定の測定条件」における引張強度を0.1N/cm以下に調整する手段である。任意の層としては、例えば、離型層等を挙げることができる。なお、第3の手段のみによって、上記「特定の測定条件」における引張強度を0.1N/cm以下に調整することは難しく、引張強度の調整の観点からは、第3の手段は、上記第1の手段や、第2の手段により引張強度を調整する補助的な手段として、或いは、後述する第4の手段と組合せて用いること好ましい。また、離型層の材料とともに、離型層の厚みを厚くする等の対策により引張強度の調整を図ることもできる。
第4の手段は、転写層10自体の耐熱性を考慮して、上記「特定の測定条件」における引張強度を0.1N/cm以下に調整する手段である。転写層の耐熱性を向上させる手段としては、例えば、硬化剤によって硬化された硬化樹脂を含有せしめる方法等を挙げることができる。なお、第4の手段のみによって、上記「特定の測定条件」における引張強度を0.1N/cm以下に調整することは難しく、引張強度の調整の観点からは、第4の手段は、上記第1の手段や、第2の手段により引張強度を調整する補助的な手段として、或いは上記第3の手段と組合せることが好ましい。
基材1は、第3実施形態の熱転写シート100における必須の構成であり、当該基材1の一方の面上に設けられる転写層10を保持するために設けられる。基材1の材料について特に限定はなく、例えば、上記第1実施形態の熱転写シート100の基材1で説明したものを適宜選択して用いることができ、ここでの詳細な説明は省略する。
図4~図6に示すように、基材1の一方の面上には、当該基材1から剥離可能な転写層10が設けられている。転写層10は、第3実施形態の熱転写シート100における必須の構成である。
第3実施形態の熱転写シートにおける実施形態Aの転写層10(以下、実施形態Aの転写層と言う)は、図4に示すように、基材1側から剥離層4、接着層5がこの順で積層されてなる積層構成を呈している。また、図4に示す形態にかえて、剥離層4と接着層5との間に保護層(図示しない)を設けることもできる。また、図4に示す形態にかえて、剥離層4上に接着層5を設けずに、剥離層4のみからなる単層構成の転写層10とし、この剥離層4自体に接着性を付与することもできる。実施形態Aの転写層10を備える熱転写シート100は、被転写体上に転写層10を転写して、被転写体の表面を保護する保護層転写シートとしての機能を果たす。接着層5、保護層については、中間転写媒体や、保護層転写シート等の分野において接着層や、保護層の材料として従来公知のものを適宜選択して用いることができる。また、第1の手段以外によって、上記「特定の測定条件」における引張強度を0.1N/cm以下に調整する場合には、剥離層4としては、従来公知の材料を適宜選択して用いることができる。
第3実施形態の熱転写シートにおける実施形態Bの転写層10(以下、実施形態Bの転写層と言う)は、図5に示すように、基材1側から、剥離層4、受容層2がこの順で積層されてなる積層構成を呈している。実施形態Bの転写層10を備える熱転写シート100は、当該熱転写シートの受容層に熱転写画像を形成し、熱転写画像が形成された受容層を含む転写層を被転写体上に転写して、印画物を得るための中間転写媒体としての機能を果たす。受容層2については、熱転写受像シートや、中間転写媒体の分野で受容層の材料として従来公知のものを適宜選択して用いることができる。
第3実施形態の熱転写シートにおける実施形態Aの転写層10(以下、実施形態Aの転写層と言う)は、図6に示すように、熱溶融インキ層7から構成される単層構成を呈している。実施形態Cの転写層10を備える熱転写シート100は、被転写体上に熱溶融インキ層7を層ごと転写して被転写体上に熱転写画像を形成する機能を果たす。
第3実施形態の熱転写シート100は、転写層を構成しない任意の層を備えていてもよい。任意の層としては、基材1と転写層10との間に設けられ、転写層10の転写性を向上させるための離型層(図示しない)や、基材1の他方の面上に設けられ、耐熱性や、サーマルヘッド等の加熱部材の層構成を向上させるための背面層等を挙げることができる。例えば、上記実施形態Cの転写層10を備える熱転写シートにおいて、基材1と転写層10としての熱溶融性インキ層7との間に離型層を設けることもできる。これら任意の層は、上記第1の手段や、第2の手段による引張強度を調整するときの補助的な手段として設けることができる。
基材として厚さ4.5μmのポリエチレンテレフタレートフィルム(東レ(株))を用い、該基材の一方の面上に下記組成の基底層用塗工液1を、乾燥時の厚みが1μmとなるように塗布・乾燥し、基底層を形成した。次いで、基底層上に下記組成の保護層用塗工液1を、乾燥時の厚みが1μmとなるように、塗布・乾燥し、保護層を形成した。また、基材の他方の面上に、下記組成の背面層用塗工液1を、乾燥時の厚みが1μmとなるように、塗布・乾燥し、背面層を形成することで、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例1の熱転写シートを得た。なお、上記の基底層用塗工液1、保護層用塗工液1、背面層用塗工液1は、グラビアコーティングにて塗工した。
・iBMA単独重合体(Mw:12500、Tg:67℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
・塩化ビニル-酢酸ビニル共重合体 20部
(ソルバイン(登録商標)CNL 日信化学工業(株))
・トルエン 40部
・メチルエチルケトン 40部
・ポリビニルブチラール樹脂 10部
(エスレック(登録商標)BX-1 積水化学工業(株))
・ポリイソシアネート硬化剤 2部
(タケネート(登録商標)D218 三井化学(株))
・リン酸エステル 2部
(プライサーフ(登録商標)A208S 第一工業製薬(株))
・メチルエチルケトン 43部
・トルエン 43部
基底層用塗工液1を、下記組成の基底層用塗工液2に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例2の熱転写シートを得た。
・iBMA単独重合体(Mw:8750、Tg:67℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液3に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例3の熱転写シートを得た。
・iBMA単独重合体(Mw:6460、Tg:67℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液4に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例4の熱転写シートを得た。
・iBMA-MA共重合体(Mw:13500、Tg:85℃) 25部
(iBMA:MA(共重合比率)=50:50)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液5に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例5の熱転写シートを得た。
・iBMA-MA共重合体(Mw:13600、Tg:93℃) 25部
(iBMA:MA(共重合比率)=30:70)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基材として厚さ4.5μmのポリエチレンテレフタレートフィルム(東レ(株))を用い、該基材の一方の面上に上記基底層用塗工液1を、乾燥時の厚みが2μmとなるように、塗布・乾燥し、基底層を形成した。また、基材の他方の面上に、背面層用塗工液を、乾燥時の厚みが1μmとなるように、塗布・乾燥し、背面層を形成することで、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例6の熱転写シートを得た。なお、上記の基底層用塗工液1、背面層用塗工液は、グラビアコーティングにて塗工した。
基底層用塗工液1を、上記基底層用塗工液2に変更して、基底層を形成した以外は全て実施例6と同様にして、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例7の熱転写シートを得た。
基底層用塗工液1を、上記基底層用塗工液3に変更して、基底層を形成した以外は全て実施例6と同様にして、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例8の熱転写シートを得た。
基底層用塗工液1を、上記基底層用塗工液4に変更して、基底層を形成した以外は全て実施例6と同様にして、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例9の熱転写シートを得た。
基底層用塗工液1を、上記基底層用塗工液5に変更して、基底層を形成した以外は全て実施例6と同様にして、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例10の熱転写シートを得た。
基底層用塗工液1を、下記組成の基底層用塗工液Aに変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた比較例1の熱転写シートを得た。
・iBMA-MA共重合体(Mw:13600、Tg:93℃) 25部
(iBMA:MA(共重合比率)=20:80)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Bに変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた比較例2の熱転写シートを得た。
・iBMA-MA共重合体(Mw:14000、Tg:101℃)25部
(iBMA:MA(共重合比率)=10:90)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Cに変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた比較例3の熱転写シートを得た。
・MMA単独重合体(Mw:22800、Tg:105℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
下記の方法で作成した熱転写受像シートの受容層上に、以下の熱転写画像形成条件により、イエロー、マゼンタ、シアンの染料からなる黒ベタ画像を印画し、熱転写画像(画像形成物)を得た。イエロー、マゼンタ、シアンの染料としては、下記の方法で作成した昇華型熱転写シートを用いた。
厚さ35μmの多孔質ポリエチレンフィルム(トヨパール(登録商標)SS P4255 東洋紡(株))からなる多孔質フィルム層上に、下記組成の中間層用塗工液を、グラビアリバースコート方式で、乾燥時の厚みが1.5μmとなるように、塗布・乾燥し、中間層を形成した。次いで、中間層上に、下記組成の受容層用塗工液を、グラビアリバースコート方式で、乾燥時の厚みが5μmとなるように、塗布・乾燥し、受容層を形成した。その中間層、受容層の設けられた面と反対面の多孔質ポリエチレンフィルム上に、下記組成の接着層用塗工液を、グラビアリバースロールコート方式で、乾燥時の厚みが5μmとなるように、塗布・乾燥し、接着層を形成し、RC原紙(155g/m2、厚さ151μm)(三菱製紙(株))と貼り合わせ熱転写受像シートAを作製した。
・ポリエステル樹脂 50部
(ポリエスター(登録商標)WR-905 日本合成化学工業(株))
・酸化チタン 20部
(TCA888 (株)トーケムプロダクツ)
・蛍光増白剤 1.2部
(ユビテックス(登録商標)BAC BASFジャパン社)
・水 14.4部
・イソプロピルアルコール 14.4部
・塩化ビニル-酢酸ビニル共重合体 60部
(ソルバイン(登録商標)C 日信化学工業(株))
・エポキシ変性シリコーン 1.2部
(X-22-3000T 信越化学工業(株))
・メチルスチル変性シリコーン 0.6部
(X-24-510 信越化学工業(株))
・メチルエチルケトン 2.5部
・トルエン 2.5部
・ウレタン樹脂 30部
(タケラック(登録商標)A-969V 三井化学(株))
・イソシアネート 10部
(タケネート(登録商標)A-5 三井化学(株))
・酢酸エチル 100部
基材として厚さ4.5μmの易接着処理済みポリエチレンテレフタレートフィルムを用い、この上に、下記組成の耐熱滑性層用塗工液を、乾燥時の厚みが0.8μmとなるように、塗布・乾燥し、耐熱滑性層を形成した。次いで、基材の他方の面に、イエロー染料層用塗工液、マゼンタ染料層用塗工液、シアン染料層用塗工液をそれぞれ、乾燥時の厚みが0.6μmとなるように、面順次に塗布・乾燥して各色の染料層を形成し、昇華型熱転写シートを得た。
・ポリビニルアセタール樹脂 60.8部
(エスレック(登録商標)KS-1 積水化学工業(株))
・ポリイソシアネート 4.2部
(バーノック(登録商標)D750 DIC(株))
・フィラー(ステアリルリン酸亜鉛) 10部
(LBT1830精製 堺化学工業(株))
・フィラー(ステアリン酸亜鉛) 10部
(SZ-PF 堺化学工業(株))
・フィラー(ポリエチレンワックス) 3部
(ポリワックス3000 東洋アドレ(株))
・フィラー(エトキシ化アルコール変性ワックス) 7部
(ユニトックス750 東洋アドレ(株))
・トルエン 200部
・メチルエチルケトン 100部
・Disperse Yellow 201 4.0部
・ポリビニルアセタール樹脂 3.5部
(エスレック(登録商標)KS-5 積水化学工業(株))
・ポリエチレンワックス 0.1部
・メチルエチルケトン 45.0部
・トルエン 45.0部
・Disperse Red 60 1.5部
・Disperse Violet 26 2.0部
・ポリビニルアセタール樹脂 4.5部
(エスレック(登録商標)KS-5 積水化学工業(株))
・ポリエチレンワックス 0.1部
・メチルエチルケトン 45.0部
・トルエン 45.0部
・Solvent Blue 63 2.0部
・Disperse Blue 354 2.0部
・ポリビニルアセタール樹脂 3.5部
(エスレック(登録商標)KS-5 積水化学工業(株))
・ポリエチレンワックス 0.1部
・メチルエチルケトン 45.0部
・トルエン 45.0部
・サーマルヘッド:F3598(東芝ホクト電子(株))
・発熱体平均抵抗値:5176(Ω)
・主走査方向印字密度:300(dpi)
・副走査方向印字密度:300(dpi)
・印画電力:0.12(W/dot)
・1ライン周期:2(msec.)
・パルスDuty:85(%)
・印画開始温度:35.5(℃)
下記熱時剥離タイプのテストプリンタを用いて、上記で得られた熱転写画像(画像形成物)上に、各実施例、及び比較例の熱転写シートの転写層を転写し、各実施例、及び比較例の印画物を得た。
・発熱体平均抵抗値:5241(Ω)
・主走査方向印字密度:300(dpi)
・副走査方向印字密度:300(dpi)
・印画電圧:28(V)
・印画電力:0.15(W/dot)
・1ライン周期:1(msec.)
・パルスDuty:85(%)
・印画開始温度:29.0~36.0(℃)
・発熱ポイントから剥離板までの距離:4.5(mm)
・搬送速度:84.6(mm/sec.)
・印圧:3.5~4.0(kgf)
・評価画像:255諧調ベタ画像
基底層用塗工液1を、下記組成の基底層用塗工液11に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例11の熱転写シートを得た。
・MMA-EA共重合体(Mw:10600、Tg:75℃) 25部
(MMA:EA(共重合比率)=83:17)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液12に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例12の熱転写シートを得た。
・MMA-EA共重合体(Mw:7920、Tg:75℃) 25部
(MMA:EA(共重合比率)=83:17)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液13に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例13の熱転写シートを得た。
・MMA-EA共重合体(Mw:19800、Tg:60℃) 25部
(MMA:EA(共重合比率))=74:26)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液14に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例14の熱転写シートを得た。
・MMA-EA共重合体(Mw:41200、Tg:48℃) 25部
(MMA:EA(共重合比率)=65:35)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液15に変更して、基底層を形成した以外は全て実施例1と同様にして、基材の一方の面上に、基底層、保護層が積層されてなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例15の熱転写シートを得た。
・MMA-EA共重合体(Mw:19900、Tg:48℃) 25部
(MMA:EA(共重合比率)=65:35)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基材として厚さ4.5μmのポリエチレンテレフタレートフィルム(東レ(株))を用い、該基材の一方の面上に上記組成の基底層用塗工液1を、乾燥時の厚みが2μmとなるように、塗布・乾燥し、基底層を形成した。また、基材の他方の面上に、上記組成の背面層用塗工液1を、乾燥時の厚みが0.8μmとなるように、塗布・乾燥し、背面層を形成することで、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例16の熱転写シートを得た。なお、上記の基底層用塗工液1、背面層用塗工液1は、グラビアコーティングにて塗工した。
基底層用塗工液1を、上記組成の基底層用塗工液2に変更して、基底層を形成した以外は全て実施例16と同様にして、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例17の熱転写シートを得た。
基底層用塗工液1を、上記組成の基底層用塗工液3に変更して、基底層を形成した以外は全て実施例16と同様にして、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例18の熱転写シートを得た。
基底層用塗工液1を、上記組成の基底層用塗工液4に変更して、基底層を形成した以外は全て実施例16と同様にして、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例19の熱転写シートを得た。
基底層用塗工液1を、上記組成の基底層用塗工液5に変更して、基底層を形成した以外は全て実施例16と同様にして、基材の一方の面上に、基底層のみからなる転写層が設けられ、基材の他方の面上に背面層が設けられた実施例20の熱転写シートを得た。
基底層用塗工液1を、下記組成の基底層用塗工液Dに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例4の熱転写シートを得た。
・MMA-EA共重合体(Mw:14000、Tg:96℃) 25部
(MMA:EA(共重合比率)=95:5)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Eに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例5の熱転写シートを得た。
・MMA単独重合体(Mw:22800、Tg:105℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Fに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例6の熱転写シートを得た。
・MMA単独重合体(Mw:14000、Tg:105℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Gに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例4の熱転写シートを得た。
・MMA単独重合体(Mw:9400、Tg:105℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Hに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例8の熱転写シートを得た。
・MMA単独重合体(Mw:7040、Tg:105℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Iに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例9の熱転写シートを得た。
・MMA-EA共重合体(Mw:16000、Tg:75℃) 25部
(MMA:EA(共重合比率)=83:17)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Jに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例10の熱転写シートを得た。
・MMA-EA共重合体(Mw:63000、Tg:48℃) 25部
(MMA:EA(共重合比率)=65:35)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Kに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例11の熱転写シートを得た。
・EA単独重合体(Mw:21600、Tg:-22℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基底層用塗工液1を、下記組成の基底層用塗工液Lに変更して、基底層を形成した以外は全て実施例1と同様にして、比較例12の熱転写シートを得た。
・MMA-EA共重合体(Mw:20000、Tg:29℃) 25部
(MMA:EA(共重合比率)=50:50)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
上記テストプリンタ(熱時剥離タイプ)を用いて、上記で得られた熱転写画像(画像形成物)上に、各実施例、及び比較例の熱転写シートの転写層を転写し、各実施例、及び比較例の印画物を得た。なお、印画物の形成は、印画電圧23V(印画電力:0.10W/dot)、印画電圧28V(印画電力:0.15W/dot)のそれぞれについて行った。
基材として厚さ4.5μmのポリエチレンテレフタレートフィルム(東レ(株))を用い、該基材の一方の面上に下記組成の転写層用塗工液1を、乾燥時の厚みが1μmとなるように、塗布・乾燥し、転写層を形成した。また、基材の他方の面上に、下記組成の背面層用塗工液2を、乾燥時の厚みが1μmとなるように、塗布・乾燥し、背面層を形成することで、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シート1を得た。なお、上記の転写層用塗工液1、背面層用塗工液は、グラビアコーティングにて塗工した。
・MMA-EA共重合体(Mw:8000、Tg:75℃) 25部
(MMA:EA(共重合比率)=83:17)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
・ポリビニルブチラール樹脂 10部
(エスレック(登録商標)BX-1 積水化学工業(株))
・ポリイソシアネート硬化剤 2部
(タケネート(登録商標)D218 三井化学(株))
・リン酸エステル 2部
(プライサーフ(登録商標)A208S 第一工業製薬(株))
・メチルエチルケトン 43部
・トルエン 43部
転写層用塗工液1を、下記組成の転写層用塗工液2に変更して、転写層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シート2を得た。
・MMA-EA共重合体(Mw:41200、Tg:48℃) 25部
(MMA:EA(共重合比率)=65:35)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
転写層用塗工液1を、下記組成の転写層用塗工液3に変更して、転写層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シート3を得た。
・iBMA単独重合体(Mw:12500、Tg:67℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
転写層用塗工液1を、下記組成の転写層用塗工液4に変更して、転写層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シート4を得た。
・MMA-iBMA共重合体(Mw:13500、Tg:85℃)25部
(MMA:iBMA(共重合比率)=50:50)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
転写層用塗工液1を、下記組成の転写層用塗工液5に変更して、転写層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シート5を得た。
・iBMA-MAA共重合体(Mw:12500、Tg:81℃)25部
(iBMA:MAA(共重合比率)=85:15)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
厚さ4.5μmのポリエチレンテレフタレートフィルム(東レ(株))にかえて、厚さ5.7μmのポリエチレンテレフタレートフィルム(東レ(株))を用い、転写層用塗工液1を、下記組成の転写層用塗工液6に変更して、転写層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シート6を得た。
・MMA単独重合体(Mw:12500、Tg:81℃) 25部
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
転写層用塗工液1を、上記組成の転写層用塗工液6に変更して、転写層を形成し、背面層用塗工液を、乾燥時の厚みが2μmとなるように塗布・乾燥して背面層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シート7を得た。
転写層用塗工液1を、上記組成の転写層用塗工液6に変更して、転写層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シートAを得た。
転写層用塗工液1を、下記組成の転写層用塗工液Aに変更して、転写層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シートBを得た。
・MMA-iBMA共重合体(Mw:13500、Tg:97℃)25部
(MMA:iBMA(共重合比率)=80:20)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
転写層用塗工液1を、下記組成の転写層用塗工液Bに変更して、転写層を形成した以外は全て熱転写シート1の作成と同様の方法で、基材の一方の面上に転写層が設けられ、基材の他方の面上に背面層が設けられた熱転写シートCを得た。
・MMA-LA共重合体(Mw:17500、Tg:60℃) 25部
(MMA:LA(共重合比率)=84:16)
・メチルエチルケトン 67部
・酢酸ノルマルプロピル 8部
基材(コート紙、厚さ170μm、大王製紙(株))の一方の面上に、下記組成の裏面プライマー層用塗工液を、乾燥時の厚みが1.2μmとなるように、塗布し、110℃で1分間乾燥することにより、裏面プライマー層を形成した。この裏面プライマー層上に、下記組成の裏面層用塗工液を、乾燥時の厚みが1μmとなるように、塗布し、110℃で1分間乾燥することにより、裏面層を形成した。次いで、基材の他方の面上に下記組成の目止め層用塗工液を、乾燥時の厚みが1μmとなるように、塗布し、110℃で1分間乾燥することにより、目止め層を形成した。この目止め層上に下記組成の多孔質層用塗工液を、乾燥時の厚みが30μmとなるように塗布し、110℃で2分間乾燥することにより、多孔質層を形成した。次いで、多孔質層上に、下記組成のバリア層用塗工液を、乾燥時の厚みが0.5μmとなるように、塗布し、110℃で1分間乾燥することにより、バリア層を形成し、このバリア層上に、上記裏面プライマー層と同じ組成の帯電防止層用塗工液を、乾燥時の厚みが1.5μmとなるように、塗布し、110℃で1分間乾燥することにより、帯電防止層を形成した。次いで、電防止層上に、下記組成の受容層用塗工液1を、乾燥時の厚みが3μmとなるように、塗布し、110℃で1分間乾燥することにより、受容層を形成することで、基材の一方の面上に、裏面プライマー層、裏面層がこの順で積層され、基材の他方の面上に、目止め層、多孔質層、バリア層、帯電防止層、受容層がこの順で積層されてなる熱転写受像シート1を得た。
・ポリエステル樹脂(固形分25%) 40部
(バイロナール(登録商標)MD-1480 東洋紡(株))
・充填材 9部
(ラポナイトJS ウイルパー・エリス(株))
・界面活性剤 0.08部
(ダイノール604 信越化学工業(株))
・イソプロピルアルコール 66.7部
・水 133.3部
・ポリビニルブチラール 36部
(BL-7 積水化学工業(株))
・ナイロンフィラー(平均粒径4μm) 7部
(MW330 神東塗料(株))
・トルエン 150部
・イソプロピルアルコール 150部
・ポリエステル樹脂 10部
(バイロン(登録商標)200 東洋紡(株))
・メチルエチルケトン 10部
・トルエン 10部
・中空粒子(固形分36%) 100部
(平均粒径3.5μm 中空率82体積%)
(マイクロスフィア 松本油脂製薬(株))
・アクリルエステル系ラテックス(固形分45%) 133部
(SX1707A 日本ゼオン(株))
・界面活性剤 2部
(ダイノール604 信越化学工業(株))
・イソプロピルアルコール 60部
・水 140部
・アクリル樹脂(固形分37%) 40部
(ボンロン(登録商標)B4100 三井化学(株))
・ポリエステル樹脂(固形分20%) 10部
(WR905 日本合成化学(株))
・アナターゼ型酸化チタン 1部
(TCA-888 堺化学工業(株))
・イソプロピルアルコール 25部
・水 25部
・水酸基含有アクリル樹脂(固形分26%) 100部
(水酸基価29.7mgKOH/g AH90A 藤倉化成(株))
・イソシアネート化合物(固形分75%) 1.74部
(タケネートD110N 三井化学(株))
・両末端カルビノール(ROH)変性シリコーンオイル 0.13部
(KF6003 信越化学工業(株))
・シリカ微粒子(平均粒径2.7μm) 0.128部
(サイリシア310P 富士シリシア化学(株))
・メチルエチルケトン 10部
・トルエン 10部
多孔質層を形成する多孔質フィルムとして、多孔質ポリプロピレンフィルム(厚さ38μm、密度0.7g/cm3)を用意した。また、基材層として、紙基材であるホワイト原紙(非コート紙、厚さ150μm、(三菱製紙(株))を用意した。ホワイト原紙の面上に、高密度ポリエチレン樹脂(密度0.956g/cm3)と低密度ポリエチレン樹脂(密度0.919g/cm3)の混合樹脂(混合比8:2、密度0.949g/cm3)を押し出しラミネート法により押し出して、第2のポリオレフィン樹脂層(厚さ30μm)を形成した。続いて、基材層の第2のポリオレフィン樹脂層と反対側の面上に、上記の低密度ポリエチレン樹脂を押し出しながら、上記の多孔質ポリプロピレンフィルムとホワイト原紙とを貼合して、多孔質層と基材層の間に、該低密度ポリエチレン樹脂からなる第1のポリオレフィン樹脂層(厚さ15μm)を形成して、熱転写受像シート用支持体を得た。次いで、多孔質ポリプロピレンフィルムの上に、下記組成のプライマー層用塗工液を、乾燥時の厚みが2μmとなるように、グラビアコーターで塗布し、110℃で1分乾燥した後、その上に下記組成の受容層用塗工液2を、乾燥時の厚みが4μmとなるように、グラビアコーターで塗布し、110℃で1分乾燥させて、プライマー層及び受容層を形成することで、熱転写受像シート2を得た。
・ポリエステル樹脂 13.1部
(WR-905 日本合成化学(株))
・酸化チタン 26.2部
(TCA-888 トーケムプロダクツ(株))
・蛍光増白剤(ベンゾイミダゾール誘導体) 0.39部
(ユビテックス(登録商標)BAC BASFジャパン社)
・水 40部
・イソプロピルアルコール 20部
・塩化ビニル-酢酸ビニル共重合体 60部
(ソルバイン(登録商標)C 日信化学工業(株))
・エポキシ変性シリコーン 1.2部
(X-22-3000T 信越化学工業(株))
・メチルスチル変性シリコーン 0.6部
(24-510 信越化学工業(株))
・メチルエチルケトン 2.5部
・トルエン 2.5部
上記で作成した各熱転写シート、及び熱転写受像シートを下表3に示す組合せで組合せ、下記熱時剥離タイプのテストプリンタ1を用いて熱転写受像シート上に、熱転写シートの転写層を転写しながら、当該転写された転写層を基材から剥離することで、熱転写受像シート上に転写層が設けられた印画物を得た。この印画物を得るにあたり、熱転写上シートに転写された転写層を基材から剥離するときの熱転写シートの引張強度を、プリンタ内において、熱転写シートの巻取ロールと、加熱手段(サーマルヘッド)との間に設けられたテンションメーター(ASK-1000型番 大倉インダストリー(株))により測定した。表3に引張強度の測定結果を示す。また、表3では、熱時引張強度(熱時剥離力)、及び後述する冷時引張強度(冷時剥離力)がともに0.1N/cm以下となる熱転写シートと熱転写受像シートとの組合せを実施例とし、熱時引張強度(熱時剥離力)、及び後述する冷時引張強度(冷時剥離力)の何れか一方、又は双方の引張強度が0.1N/cmを超える熱転写シートと熱転写受像シートとの組合せを比較例としている。
・発熱体平均抵抗値:5241(Ω)
・主走査方向印字密度:300(dpi)
・副走査方向印字密度:300(dpi)
・印画電圧:28(V)
・印画電力:0.15(W/dot)
・1ライン周期:1(msec.)
・パルスDuty:85(%)
・印画開始温度:29.0~36.0(℃)
・発熱ポイントから剥離板までの距離:4.5(mm)
・搬送速度:84.6(mm/sec.)
・印圧:3.5~4.0(kgf)
・評価画像:255諧調ベタ画像
上記で作成した各熱転写シート、及び熱転写受像シートを下表3に示す組合せで組合せ、下記テストプリンタ2を用いて熱転写受像シート上に、熱転写シートの転写層を転写した後、熱転写受像シート上に転写された転写層を基材から剥離することなく、テストプリンタ2から取り出し、以下の剥離装置、及び剥離条件にて、熱転写受像シート上に転写された転写層を基材から剥離するときの引張強度を測定した。測定結果を表3に併せて示す。なお、テストプリンタ2は、剥離板、及びテンションメーターを有していない点を除いて、テストプリンタ1と同様の構成をとる。
剥離速度:5(m/min.)
剥離角度:180(度)
・発熱体平均抵抗値:5241(Ω)
・主走査方向印字密度:300(dpi)
・副走査方向印字密度:300(dpi)
・印画電圧:28(V)
・印画電力:0.15(W/dot)
・1ライン周期:1(msec.)
・パルスDuty:85(%)
・印画開始温度:29.0~36.0(℃)
・搬送速度:84.6(mm/sec.)
・印圧:3.5~4.0(kgf)
・評価画像:255諧調ベタ画像
表3に示す各実施例、及び比較例の熱転写シートと、熱転写受像シートとの組合せにおいて、以下の評価基準に基づいて、上記熱時剥離タイプのテストプリンタ1を用いて熱転写受像シート上に転写層を転写したときの熱融着の評価を行った。評価結果を表3に併せて示す。
A:熱融着の発生がなく、基材から転写層を良好に剥離することができる。
NG:転写層の一部又は全部で熱融着が発生し、基材から転写層の一部又は全部を剥離することができない。
2…受容層
3…保護層
4…剥離層
5…接着層
7…熱溶融インキ層
10A…基底層
10…転写層
100…熱転写シート
200…プリンタ
201…熱転写シート供給手段
202…加熱手段
203…熱転写シート巻取り手段
204…測定手段
205…剥離手段
300…被転写体
Claims (4)
- 基材の一方の面上に転写層が位置する熱転写シートであって、
前記熱転写シートは、
前記熱転写シートと被転写体とを重ね合わせ、熱転写シート供給手段、加熱手段、熱転写シート巻取り手段、前記加熱手段と前記熱転写シート巻取り手段との間に位置し搬送経路に沿って搬送される熱転写シートの引張強度を測定する測定手段、前記加熱手段と前記測定手段との間に位置する剥離手段を有するプリンタを用い、印画電力0.15W/dot、熱転写シートの搬送速度84.6mm/sec.の条件にて、前記被転写体上に前記転写層を転写しながら、前記被転写体上に転写された前記転写層を前記熱転写シートの当該転写層と接する構成部材から剥離したときに、前記測定手段により測定される引張強度が0.1N/cm以下であることを特徴とする熱転写シート。 - 基材の一方の面上に転写層が位置する熱転写シートであって、
前記転写層は、1又は2以上の層から構成され、
前記転写層を構成する層のうち、前記基材から最も近くに位置する層は、
(A):(1)イソブチル(メタ)アクリレートの単独重合体、又は(2)イソブチル(メタ)アクリレートの共重合比率がモル比で30%以上の共重合体、及び、
(B):メチル(メタ)アクリレートとエチル(メタ)アクリレートとの共重合体の何れか一方又は双方を含有しており、
前記(B)の共重合体における前記メチル(メタ)アクリレートの共重合比率は、モル比で60%以上90%以下であり、前記エチル(メタ)アクリレートの共重合比率は、モル比で10%以上40%以下であり、
前記(B)の共重合体における前記メチル(メタ)アクリレートの共重合比率がモル比で80%以上である場合には、当該共重合体の重量平均分子量(Mw)は15000以下であり、一方で、
前記(B)の共重合体における前記メチル(メタ)アクリレートの共重合比率がモル比で80%未満である場合には、当該共重合体の重量平均分子量(Mw)は45000以下であり、
前記熱転写シートは、
前記熱転写シートと被転写体とを重ね合わせ、熱転写シート供給手段、加熱手段、熱転写シート巻取り手段、前記加熱手段と前記熱転写シート巻取り手段との間に位置し搬送経路に沿って搬送される熱転写シートの引張強度を測定する測定手段、前記加熱手段と前記測定手段との間に位置する剥離手段を有するプリンタを用い、印画電力0.15W/dot、熱転写シートの搬送速度84.6mm/sec.の条件にて、前記被転写体上に前記転写層を転写しながら、前記被転写体上に転写された前記転写層を前記熱転写シートの当該転写層と接する構成部材から剥離したときに、前記測定手段により測定される引張強度が0.1N/cm以下であることを特徴とする熱転写シート。 - 基材の一方の面上に転写層が設けられた熱転写シートであって、
前記転写層は、1又は2以上の層から構成され、
前記転写層を構成する層のうち、前記基材から最も近くに位置する層が、(1)イソブチル(メタ)アクリレートの単独重合体、又は(2)イソブチル(メタ)アクリレートの共重合比率がモル比で30%以上の共重合体を含有していることを特徴とする熱転写シート。 - 基材の一方の面上に転写層が設けられた熱転写シートであって、
前記転写層は、1又は2以上の層から構成され、
前記転写層を構成する層のうち、前記基材から最も近くに位置する層は、メチル(メタ)アクリレートとエチル(メタ)アクリレートとの共重合体を含有し、
前記共重合体における前記メチル(メタ)アクリレートの共重合比率は、モル比で60%以上90%以下であり、前記エチル(メタ)アクリレートの共重合比率は、モル比で10%以上40%以下であり、
前記共重合体における前記メチル(メタ)アクリレートの共重合比率がモル比で80%以上である場合には、当該共重合体の重量平均分子量(Mw)は15000以下であり、一方で、
前記共重合体における前記メチル(メタ)アクリレートの共重合比率がモル比で80%未満である場合には、当該共重合体の重量平均分子量(Mw)は45000以下であることを特徴とする熱転写シート。
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Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS511781A (ja) * | 1974-06-28 | 1976-01-08 | Toyo Boseki | |
JPS5280912A (en) * | 1975-12-26 | 1977-07-07 | Okuno Chem Ind Co | Transfer sheet |
JPS59135184A (ja) * | 1983-01-24 | 1984-08-03 | Shoichi Yamada | マ−ク転写法 |
JPH02139294A (ja) * | 1988-11-21 | 1990-05-29 | Ricoh Co Ltd | 熱転写記録媒体 |
JPH06262859A (ja) * | 1993-03-16 | 1994-09-20 | Toppan Printing Co Ltd | 熱転写記録媒体 |
JPH07101155A (ja) * | 1993-09-30 | 1995-04-18 | Toppan Printing Co Ltd | 熱転写記録媒体 |
US5674805A (en) * | 1996-11-27 | 1997-10-07 | Eastman Kodak Company | Binder for thermal transfer pigment donor element |
JPH09290576A (ja) | 1996-04-26 | 1997-11-11 | Toray Ind Inc | 溶融型感熱転写材 |
JPH11263079A (ja) | 1998-03-17 | 1999-09-28 | Dainippon Printing Co Ltd | 中間転写記録媒体 |
JP2001246845A (ja) | 2000-03-03 | 2001-09-11 | Dainippon Printing Co Ltd | 保護層転写シート |
JP2009073190A (ja) * | 2007-08-30 | 2009-04-09 | Fujifilm Corp | 感熱転写方式による画像形成方法 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0999648A (ja) * | 1995-10-04 | 1997-04-15 | Toppan Printing Co Ltd | 感熱転写記録媒体 |
JPH1067174A (ja) * | 1996-06-19 | 1998-03-10 | Ricoh Co Ltd | 熱転写記録方法並びに熱転写記録媒体及びその製造方法 |
JPH1165098A (ja) * | 1997-08-19 | 1999-03-05 | Mitsubishi Chem Corp | 感光性平版印刷版の製版方法 |
JP3883264B2 (ja) * | 1997-09-08 | 2007-02-21 | 大日本印刷株式会社 | シール用熱転写受像シート及びその製造方法 |
JPH11227348A (ja) * | 1998-02-19 | 1999-08-24 | Ricoh Co Ltd | 熱転写記録方法及び熱転写記録媒体 |
DE69917844T2 (de) | 1998-03-06 | 2005-06-23 | Dai Nippon Printing Co., Ltd. | Zwischenträger eines übertragungsaufzeichnungsmaterials, verfahren zur herstellung eines druckes, sowie entsprechendes druckerzeugnis |
JP2001030642A (ja) * | 1999-05-19 | 2001-02-06 | Konica Corp | 熱転写受像材料及び熱転写記録方法 |
JP2004202731A (ja) * | 2002-12-24 | 2004-07-22 | Sumitomo Chem Co Ltd | 大型導光板の製造方法 |
JP5458737B2 (ja) * | 2009-08-18 | 2014-04-02 | ソニー株式会社 | 樹脂組成物、被熱転写シート及び被熱転写シートの製造方法 |
JP5856867B2 (ja) | 2012-02-16 | 2016-02-10 | リンテック株式会社 | 粘着シート、粘着シートの使用方法及び粘着シートの製造方法 |
WO2014041779A1 (ja) * | 2012-09-11 | 2014-03-20 | 凸版印刷株式会社 | 感熱転写記録媒体 |
-
2016
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- 2016-12-22 EP EP16878983.2A patent/EP3388244B1/en active Active
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- 2016-12-22 US US16/064,147 patent/US10569588B2/en active Active
- 2016-12-22 CN CN201680073853.5A patent/CN108472969B/zh active Active
- 2016-12-22 WO PCT/JP2016/088509 patent/WO2017111097A1/ja active Application Filing
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS511781A (ja) * | 1974-06-28 | 1976-01-08 | Toyo Boseki | |
JPS5280912A (en) * | 1975-12-26 | 1977-07-07 | Okuno Chem Ind Co | Transfer sheet |
JPS59135184A (ja) * | 1983-01-24 | 1984-08-03 | Shoichi Yamada | マ−ク転写法 |
JPH02139294A (ja) * | 1988-11-21 | 1990-05-29 | Ricoh Co Ltd | 熱転写記録媒体 |
JPH06262859A (ja) * | 1993-03-16 | 1994-09-20 | Toppan Printing Co Ltd | 熱転写記録媒体 |
JPH07101155A (ja) * | 1993-09-30 | 1995-04-18 | Toppan Printing Co Ltd | 熱転写記録媒体 |
JPH09290576A (ja) | 1996-04-26 | 1997-11-11 | Toray Ind Inc | 溶融型感熱転写材 |
US5674805A (en) * | 1996-11-27 | 1997-10-07 | Eastman Kodak Company | Binder for thermal transfer pigment donor element |
JPH11263079A (ja) | 1998-03-17 | 1999-09-28 | Dainippon Printing Co Ltd | 中間転写記録媒体 |
JP2001246845A (ja) | 2000-03-03 | 2001-09-11 | Dainippon Printing Co Ltd | 保護層転写シート |
JP2009073190A (ja) * | 2007-08-30 | 2009-04-09 | Fujifilm Corp | 感熱転写方式による画像形成方法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP3388244A4 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2021133546A (ja) * | 2020-02-25 | 2021-09-13 | 大日本印刷株式会社 | 熱転写シート、及び該熱転写シートと、中間転写媒体との組合せ |
JP7421750B2 (ja) | 2020-02-25 | 2024-01-25 | 大日本印刷株式会社 | 熱転写シート、及び該熱転写シートと、中間転写媒体との組合せ |
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