JP5942369B2 - Method for manufacturing transfer medium - Google Patents

Description

  The present invention relates to a method for manufacturing a transfer medium.

  2. Description of the Related Art Conventionally, transfer media that transfer characters and other image patterns formed by attaching ink onto a substrate onto a transfer medium are known. In this transfer medium, for example, as described in Patent Document 1, a technique is known in which an adhesive liquid is applied onto a pattern using, for example, a screen printing plate in accordance with the pattern shape.

Japanese Patent Laid-Open No. 7-314879

  However, when an image pattern or an adhesive liquid pattern is formed by using a printing plate such as a flexo and a gravure in addition to a screen printing plate, the manufacturing cost increases in the production of a small variety of transfer media. Therefore, in order to keep the manufacturing cost low in the production of small quantities and various types of transfer media, the ink and the adhesive liquid are ejected from the ink jet head and adhered to the base material, whereby the colored layer and the adhesive liquid are formed on the base material. A method of manufacturing a transfer medium by sequentially forming an adhesive layer according to the above is conceivable.

  The following characteristics are required for the ink discharged from the inkjet head for forming the colored layer and the adhesive liquid discharged from the inkjet head for forming the adhesive layer.

  First, when the ink jet head is driven at a high frequency, it is required to have excellent ejection stability of ink and adhesive liquid.

  Second, in the step of forming an adhesive layer pattern by adhering an adhesive liquid onto the colored layer pattern, it is required that a high resolution image be obtained without the colored layer pattern flowing or collapsing. The

  Third, the thermoplastic resin constituting the adhesive layer is efficiently distributed on the colored layer pattern, and when used as a transfer medium, there is no fine character transfer failure or image transfer unevenness, and transfer It is required to have excellent properties.

  Fourth, it is required to have excellent adhesion between the transfer medium (target) or the colored layer after transfer and the adhesive layer.

  Fifth, it is required that the transfer medium is free of tack and has excellent blocking resistance and can be easily stored in a warehouse.

  Therefore, the present invention is excellent in ejection stability when ejecting the ink for forming the colored layer and the adhesive liquid for forming the adhesive layer from the inkjet head, can obtain the pattern of the colored layer with high resolution, and can be transferred. One of the objects is to provide a method for producing a transfer medium having excellent properties, adhesion after transfer, and blocking resistance, a transfer medium obtained by the production method, and a transfer product obtained by transfer of the transfer medium. .

  The present inventors have intensively studied to solve the above problems. As a result, in the method for producing a transfer medium in which a colored layer is formed by ejecting ink and an adhesive layer is formed by ejecting an adhesive liquid, the ink is an aqueous pigment ink, a non-aqueous pigment ink, or an ultraviolet curable pigment ink. And an adhesive liquid is an aqueous liquid containing an emulsion-type polyester resin having a glass transition temperature of 10 ° C. or higher and 70 ° C. or lower, more preferably an emulsion-type polyester resin having a temperature of 10 ° C. or higher and 60 ° C. or lower. The present invention has been completed by finding that the above-mentioned problems can be solved by using an aqueous liquid containing the liquid.

That is, the present invention is as follows.
[1]
A colored layer forming step of forming a colored layer on the substrate by ejecting ink from the inkjet head toward the substrate, and discharging the adhesive liquid from the inkjet head toward the colored layer An adhesive layer forming step of forming an adhesive layer on the layer, wherein the ink is an aqueous pigment ink, a non-aqueous pigment ink, or an ultraviolet curable pigment ink, and the adhesive liquid has a glass transition temperature. A method for producing a transfer medium, which is an aqueous liquid containing an emulsion-type polyester resin having a temperature of 10 ° C. or more and 70 ° C. or less, more preferably an aqueous liquid containing an emulsion-type polyester resin of 10 ° C. or more and 60 ° C. or less.

[2]
The colored layer forming step includes evaporating a liquid component contained in the ink ejected and adhered to the base material so as to satisfy the following (1), (2), or (3): [1] A method for producing a transfer medium according to [1].
(1) When the ink is an aqueous pigment ink, 65 to 95% by mass of the liquid component contained in the ink is evaporated.
(2) When the ink is a non-aqueous pigment ink, 50 to 90% by mass of the liquid component contained in the ink is evaporated.
(3) When the ink is an ultraviolet curable ink, 40 to 70% by mass of the liquid component contained in the ink is evaporated.

[3]
The aqueous pigment ink or the non-aqueous pigment ink contains a water-soluble organic solvent having a boiling point of 70 ° C. or more and 250 ° C. or less at 1 atm, and the water-soluble organic solvent contains lactam, carboxylic acid ester, alkylene glycol ether, and alcohol. The method for producing a transfer medium according to [1] or [2], which is an aqueous liquid containing one or more selected from the group consisting of:

[4]
The adhesive liquid contains a water-soluble organic solvent having a boiling point of 70 ° C. or more and 250 ° C. or less at 1 atm, and the water-soluble organic solvent is selected from the group consisting of lactam, carboxylic acid ester, alkylene glycol ether, and alcohol. The method for producing a transfer medium according to any one of [1] to [3], which is an aqueous liquid containing at least seeds.

[5]
The method for producing a transfer medium according to any one of [1] to [4], wherein the substrate is metal, plastic, or paper.

[6]
A transfer medium obtained by the production method according to any one of [1] to [5].

[7]
A transfer product obtained by transferring the transfer medium according to [6] to a transfer medium.

It is a side view which shows the outline of the whole transfer medium manufacturing apparatus used for the 1st aspect of this embodiment. It is a side view which shows the outline of the image formation part of the transfer medium manufacturing apparatus used for the 1st aspect of this embodiment. It is a schematic diagram which shows the nozzle formation surface of an inkjet head. It is a block diagram of the control structure of a transfer medium manufacturing apparatus. It is a plane schematic diagram of a transfer medium. (A)-(d) is a 6-6 arrow cross section in FIG. 5, Comprising: It is sectional drawing of each manufacturing process of a transfer medium. It is a side view which shows the outline of the whole transfer medium manufacturing apparatus used for the 2nd aspect of this embodiment. It is a side view which shows the outline of the image formation part of the transfer medium manufacturing apparatus used for the 2nd aspect of this embodiment.

  Hereinafter, embodiments for carrying out the present invention will be described in detail. In addition, this invention is not restrict | limited to the following embodiment, A various deformation | transformation can be implemented within the range of the summary.

In the present specification, “ejection stability” refers to the property of ejecting a stable ink or adhesive liquid droplet from the nozzle without clogging of the nozzle.
“Transferability” refers to a property that requires less energy to transfer a colored layer from a transfer medium to a transfer medium (target). The energy depends on one or more of temperature, pressure, and time during transfer, and transferability is good as long as at least one of low temperature, low pressure, and short time is achieved. It can be said.
“Adhesiveness” refers to the property that the adhesion strength of the colored layer transferred to the transfer medium is excellent.

In the present specification, “no tack” (tack free) means that no rub marks are left even when rubbed with a cotton swab. More specifically, when the surface of the transfer medium (the surface with the adhesive layer) is touched with a finger, the time until the surface does not adhere to the finger is evaluated by the viscosity (tack) of the surface. Refers to nature.
“Blocking resistance” means that when the transfer medium is wound around a paper tube using a winder, the adhesive component sticks to the contact surface (the back surface of the transfer medium) and the transfer medium cannot be unwound. In other words, even if it can be unwound, the coloring layer or the adhesive layer does not occur on the back surface of the transfer medium.
“Excellent blocking resistance” means that there is no stickiness on the surface of the transfer medium, so that the transfer medium can be wound using a winder without any problem.

  In this specification, “(meth) acryl” means “acryl” and “methacryl” corresponding thereto, and “(meth) acrylate” means “acrylate” and “methacrylate” corresponding thereto.

  In the present specification, the “solid content” means a substance that is in a solid state under the conditions of 1 atm and 25 ° C.

  In the present specification, “medium boiling point” means that the boiling point at 1 atm is 70 ° C. or more and 250 ° C. or less.

Moreover, in this specification, a "base material" means the support body used in order to transfer the pattern of a colored layer and an adhesive layer.
The “transfer medium” means a medium that includes at least a base material, a colored layer, and an adhesive layer, and is a transfer source medium for transferring to a transfer medium.
The “transfer medium” means a target medium, that is, a target to which at least the colored layer and the adhesive layer are transferred from the transfer medium.

  Further, in this specification, “image” means including characters, and “transfer” means including bonding.

  Further, in this specification, the “heat conduction type” refers to a method of transferring heat from the high temperature part to the low temperature part through the inside of the object. That is, it is a system in which heat is conducted to the substrate side when a high-temperature object comes into contact with the substrate. The “convection type” refers to a method of transferring heat by a fluid such as gas or liquid.

[Method of manufacturing transfer medium]
One embodiment of the present invention relates to a method for manufacturing a transfer medium. The manufacturing method includes a colored layer (colored layer forming step) obtained by discharging ink onto a substrate, and an adhesive layer (adhesive layer forming step) obtained by discharging an adhesive liquid onto the colored layer. , To manufacture a transfer medium for transferring an image to a transfer medium.
Here, the state in which the ink discharged from the inkjet head and the adhesive liquid are attached and deposited for each droplet can be said to be synonymous with the state in which the colored layer and the adhesive layer are formed. That is, even if the clear layer structure cannot be confirmed depending on whether the ink discharged from the inkjet head and the adhesion timing of the adhesive liquid are first or later, it can be determined that a layer is formed.
Here, as the ink, an aqueous pigment ink, a non-aqueous pigment ink, or an ultraviolet curable pigment ink can be used. However, the transfer medium manufacturing apparatus used when manufacturing the transfer medium differs depending on the ink type. Therefore, the transfer medium manufacturing apparatus for each ink type will be described below.

[Transfer medium manufacturing apparatus for water-based pigment ink or non-aqueous pigment ink]
The first aspect of the present embodiment relates to a manufacturing method using a transfer medium manufacturing apparatus suitable for using an aqueous pigment ink or a non-aqueous pigment ink as an ink.

(1. Device configuration)
FIG. 1 is a side view showing an outline of the entire transfer medium manufacturing apparatus 1a used in the first mode of the present embodiment. FIG. 2 is a side view schematically showing the image forming unit 30 of the transfer medium manufacturing apparatus 1a.

  As shown in FIG. 1, the transfer medium manufacturing apparatus 1 a includes a substrate F feeding unit 10, a transport unit 20, an image forming unit 30, a drying device 90, and a discharge unit 70. Among these, the drying apparatus 90 has the 1st drying part 40 which performs the 1st drying process mentioned later, and the 2nd drying part 50 which performs a 2nd drying process.

  The feeding unit 10 is provided so that the roll-shaped base material F can be fed to the transport unit 20. Specifically, the feeding unit 10 has a roll medium holder 11, and the roll medium holder 11 holds a roll-shaped substrate F. And it is comprised so that the base material F can be supplied to the conveyance part 20 of a feed direction downstream by rotating the roll-shaped base material F. As shown in FIG.

  The transport unit 20 is provided so that the substrate F sent from the feeding unit 10 can be transported to the image forming unit 30. More specifically, the transport unit 20 includes a first feed roller 21 and is configured to transport the fed base material F to the image forming unit 30 further downstream in the feed direction.

  The image forming unit 30 sequentially performs image formation (colored layer formation) and adhesive layer formation by sequentially ejecting ink L (see FIG. 2) and adhesive liquid onto the substrate F sent from the transport unit 20. It is provided so that it can. More specifically, the image forming unit 30 includes a platen 34 as a medium support unit and a carriage 31 that houses an inkjet head 32 having a nozzle row 33. Among these, the platen 34 is provided so that the base material F can be supported from the back surface. The carriage 31 faces the platen 34 and moves in the width direction X with respect to the feed direction Y of the substrate F by the power of a carriage motor (not shown) while being guided by a first guide shaft (not shown). It is provided so that you can.

The inkjet head 32 is provided on the carriage 31 so as to be able to move integrally with the carriage 31 in the width direction X. Further, the inkjet head 32 is configured to be able to move relative to the carriage 31 in the feed direction Y. Specifically, the inkjet head 32 is provided so as to be able to move in the feed direction Y by the power of an inkjet head motor (not shown) while being guided by a second guide shaft (not shown). .
That is, the inkjet head 32 is configured to be able to move in the feed direction Y and the width direction X in a range facing the platen 34. Then, the ink L and the adhesive liquid are sequentially ejected from the nozzle row 33 provided on the surface of the inkjet head 32 facing the platen 34, thereby performing image formation and adhesive layer formation on the substrate F. it can.
The nozzle row 33 of the inkjet head 32 will be described in detail later.

  As will be described later, the platen 34 is provided with a first drying unit 40 that evaporates at least a part of the ink L ejected toward the substrate F and the liquid component in the adhesive liquid.

  As shown in FIG. 2, the first drying unit 40 is provided on the platen 34. Specifically, the first drying unit 40 includes a first nichrome wire 42 which is an example of the heat conduction heating means 41. The first nichrome wire 42 is disposed in the entire region of the platen 34 so as to be a certain distance from the upper surface of the platen 34.

  Further, a second feed roller 43 is provided downstream of the platen 34 in the feed direction, as shown in FIG. The second feed roller 43 is configured to feed the image-formed substrate F to the second drying unit 50 on the downstream side in the feed direction. And it is comprised so that the base material F may enter into the 2nd drying part 50 from the inlet_port | entrance 63. FIG.

  The 2nd drying part 50 is comprised so that at least one part of the ink L discharged to the base material F and the residual component in the liquid in adhesive liquid can be further evaporated. A third feed roller 65 is provided in the vicinity of the outlet 64 of the second drying unit 50. The third feed roller 65 is disposed so as to be in contact with the back surface of the base material F, and is configured so as to be able to feed the base material F to the discharge unit 70 on the downstream side in the feed direction.

The discharge part 70 is provided so that the base material F sent from the 2nd drying part 50 can further be sent to a feed direction downstream. Specifically, the discharge unit 70 includes a fourth feed roller 71, a fifth feed roller 72, a sixth feed roller 73, a seventh feed roller 74, and a take-up roller 75.
Among these, the 4th feed roller 71 and the 5th feed roller 72 are arrange | positioned so that the surface of the base material F may be contacted. Moreover, the 6th feed roller 73 and the 7th feed roller 74 are arrange | positioned so that a roller pair may be comprised. And the base material F sent via the 4th feed roller 71, the 5th feed roller 72, the 6th feed roller 73, and the 7th feed roller 74 in order is provided so that it may be wound up by the winding roller 75. It has been.

  In addition, although it does not specifically limit as a specific example of the transfer medium manufacturing apparatus 1a, For example, PX-7550 (Inkjet printer, Seiko Epson Corporation brand name) is mentioned.

  Next, the nozzle row 33 of the inkjet head 32 will be described in detail. FIG. 3 is a schematic diagram illustrating the nozzle formation surface 39 of the inkjet head 32, and FIG. 4 is a block diagram of a control configuration of the transfer medium manufacturing apparatus 1a.

As shown in FIG. 3, a plurality of (six in this embodiment) ink jet heads 32 are provided on the support plate 28 supported on the lower surface side of the carriage 31. Are supported in a staggered arrangement in the width direction X (front-rear direction) orthogonal to the direction indicated by (in order that the rows of inkjet heads 32 adjacent in the feed direction are stepped). .
A plurality of rows (eight rows in this embodiment) of the first to eighth nozzle rows 33a to 33h along the front-rear direction are formed on the left and right sides of the nozzle forming surface 39 which is the lower surface of each inkjet head 32. It is regularly formed with a predetermined interval in the direction. The first to eighth nozzle rows 33 a to 33 h configured as described above are supplied with a plurality of types of liquid from cartridges (not shown) corresponding to the nozzle rows, and correspond to the nozzle rows 33. In accordance with the vibration of the piezoelectric element 56 (see FIG. 4) provided so as to discharge, each nozzle row 33 is discharged.

  That is, as an example, the first to fifth nozzle rows 33a to 33e include cyan, magenta, yellow, and black in order from the first nozzle row 33a that is located on the most upstream side (left side) in the feed direction Y of the base material F. The ink L containing the colorant of each color of white is supplied. Further, metallic ink is supplied as the ink L to the sixth nozzle row 33f located sixth from the left side. Then, when the ink L ejected from the first to sixth nozzle rows 33a to 33f adheres to the base material F, a colored layer 81 (see FIG. 6) as a pattern is formed. The metallic ink is an ink in which a metallic pigment as a colorant is dispersed in a liquid, and is an ink capable of forming the metal coloring layer 81 by being attached to the substrate F.

  Further, an adhesive liquid is supplied to the seventh nozzle row 33g located seventh from the left side. A transparent protective liquid is supplied to the eighth nozzle row 33h located on the most downstream side (right side) in the feed direction Y of the base material F.

Next, control of the transfer medium manufacturing apparatus 1a will be described.
The transfer medium manufacturing apparatus 1a is provided with a control unit 53 (see FIG. 4) composed of a microcomputer or the like that comprehensively controls the drive of the transfer medium manufacturing apparatus 1a. The control unit 53 controls driving of the piezoelectric element 56 and the transport motor 55 based on an input from the operation unit 54 operated by the user.

(2. Manufacturing method)
Next, a manufacturing method for manufacturing the transfer medium 88 using the transfer medium manufacturing apparatus 1a will be described with reference to FIGS. FIG. 5 is a schematic plan view of the transfer medium. 6 is a cross-sectional view taken along the arrow 6-6 in FIG. 5, which is a schematic plan view of the transfer medium, and is a cross-sectional view of each process of manufacturing the transfer medium.

  The transfer medium manufacturing method using the transfer medium manufacturing apparatus 1a for aqueous pigment ink or non-aqueous pigment ink as described above includes at least a colored layer forming step and an adhesive layer forming step.

  As shown in FIG. 6A, a release layer 89 is formed on the surface on the image forming side of the base material F (corresponding to the base material F in FIG. 1) in this embodiment. Yes. The base material F is set on the conveyance path in a state in which the downstream end in the feeding direction Y is wound around the central axis (winding shaft) of the winding roller 75 at the start of manufacturing the transfer medium 88. And

As shown in FIG. 5 and FIG. 6A, when image formation data such as alphabet R is input as image formation data for forming an image pattern by a colored layer 81 described later, first, the control unit 53 A transfer area A to which the ink L is attached is set.
Note that the transfer medium 88 manufactured in the present embodiment transfers the transfer image formed on the transfer medium 88 to the transfer target medium (not shown) by being reversed left and right. Therefore, the control unit 53 sets a transfer area A in which the image corresponding to the image formation data is reversed left and right with respect to the surface of the substrate F on which the image is formed.

  When the operation unit 54 is operated by the user and the production of the transfer medium 88 is started, the control unit 53 vibrates the piezoelectric element 56 and attaches the protective liquid, the ink L, and the adhesive liquid to the substrate F, respectively. Will be allowed to. Hereinafter, each manufacturing process of the transfer medium 88 will be described in detail.

<< Pre-process [FIG. 6B] >>
If desired, as a pre-process for forming the colored layer, the control unit 53 vibrates the piezoelectric element 56 corresponding to the eighth nozzle row 33h in accordance with the movement of the carriage 31, and attaches the protective liquid to at least the transfer region A. As a result, a protective layer 91 is formed on the upper surface of the release layer 89 on the substrate F as shown in FIG.

  At that time, since the first nichrome wire 42 of the heat conduction type heating means 41 in the first drying section 40 generates heat as will be described later, the protective liquid (protective layer 91) attached to the release layer 89 is the base material F. And heated through the release layer 89. As a result, the component excluding the solid content in the protective layer 91, that is, the liquid component evaporates to some extent and the protective layer 91 dries to some extent, but a part of the liquid component remains in the protective layer 91.

<< Colored layer forming step [FIG. 6 (c)] >>
In the colored layer forming step, which is essential in the manufacturing method of the present embodiment, the ink L is ejected from the inkjet head 32 toward the substrate F, and the ink L is attached to a predetermined portion on the substrate F. Thereby, as shown in FIG.6 (c), the pattern of the colored layer 81 is formed in the upper surface of the protective layer 91 on the base material F. As shown in FIG. What is necessary is just to adjust the droplet mass at the time of the ink discharge in this process, for example in the range of 5-15 ng.

In the colored layer forming step, the control unit 53 (see FIG. 4) vibrates the piezoelectric elements 56 corresponding to the first to sixth nozzle rows 33a to 33f in accordance with the movement of the carriage 31. Then, as shown in FIG. 6C, the color layer 81 is formed by ejecting and adhering the ink L to the transfer region A where the protective layer 91 is formed.
For example, when manufacturing the transfer medium 88 for foil transfer, the colored layer 81 is formed using metallic ink. Specifically, first, the metallic ink is attached to the transfer region A, and then the white ink is attached to the transfer region A, whereby the silver colored layer 81 is formed.

This colored layer forming step will be described more specifically with reference to FIG. First, the base material F sent onto the platen 34 of the image forming unit 30 is temporarily stopped. Then, in a state where the inkjet head 32 is located at a position facing the downstream side in the feed direction Y on the platen 34, the carriage 31 moves in the width direction X, and ink L is ejected to perform image formation.
Next, the ink-jet head 32 moves to the upstream side in the feed direction Y with respect to the carriage 31 by the length of the nozzle row 33. Then, the carriage 31 moves in the width direction X, ink L is ejected, and image formation is executed. Further, the inkjet head 32 moves further by the length of the nozzle row 33 toward the upstream side in the feed direction Y with respect to the carriage 31.
Then, the carriage 31 moves in the width direction X, and the ink L is ejected. If the image formation is not completed, the inkjet head 32 moves to a position facing the upstream side in the feed direction Y of the platen 34, and in this state, the carriage 31 moves in the width direction X, and the ink L is ejected again. A series of operations are repeated. On the other hand, if the image formation is completed, the above operation ends. By the end of this operation, the formation of the colored layer 81 (see FIG. 6C) is completed.
In addition, in the colored layer formation process in this embodiment, said aspect is only an example and this embodiment is not limited at all. As a modification mode, when the inkjet head 32 is moved to the upstream side in the feed direction Y in the above mode, a distance shorter than the length of the nozzle row 33 is moved. As a result, the image resolution can be increased.

≪First drying process≫
If desired, a first drying step of evaporating at least part of the liquid component contained in the ink L of the colored layer 81 is further performed. When water-based pigment ink is used as the ink L, the evaporation amount of the liquid component in the ink L ejected and adhered to the substrate F is 65 to 95% by mass with respect to the total mass (100% by mass) of the liquid component. Preferably, 70 to 90% by mass is more preferable. On the other hand, when a non-aqueous pigment ink is used as the ink L, the evaporation amount of the liquid component in the ink L ejected and adhered to the substrate F is 50 to 90 with respect to the total mass (100% by mass) of the liquid component. % By mass is preferable, and 55 to 85% by mass is more preferable. In this way, the liquid component in the ink L ejected and adhered onto the substrate F is evaporated by a certain amount, and then the adhesive liquid is adhered in the next step, so that the pattern of the colored layer 81 on the transfer medium can be made with high resolution. It can be formed and has excellent transferability.

  The first drying step can be executed not only by the heat conduction heating means 41 (platen heater) provided on the platen 34 as described above but also by a hot air heater, an infrared heater, or the like. As an example of the evaporation means in the case of using a platen heater, heating by the platen heater from the back surface of the substrate F, and on the other hand, warm air is brought into contact with the ink L attached to the substrate F. By adopting such an evaporation means, heat is transmitted almost evenly to the ink L on the substrate F, so that the evaporation amount can be easily adjusted, and when the substrate F is paper or the like, curling is performed. Can be prevented. Specifically, the evaporation amount can be adjusted by controlling the heating temperature, heating time, hot air temperature, air volume, and the like of the platen 34 by the heater. It is preferable to set the conditions of the heater by measuring the evaporation amount in advance before the start of manufacture.

  The evaporation amount can be derived by measuring the change in the mass of the ink before and after the liquid component is evaporated under the same conditions as in this step. Therefore, after obtaining the conditions for evaporating the desired amount of the liquid component in advance, the evaporation process in this step may be performed under the same conditions.

  In the first drying step, the control unit 53 (see FIG. 4) is set in advance so that at least a part of the liquid component in the colored layer 81 evaporates and the colored layer 81 is dried to a desired degree. The first nichrome wire 42 of the heat conduction heating means 41 is caused to generate heat. As a result, the ink L (colored layer 81) ejected and adhered to the substrate F is heated via the protective layer 91 depending on the substrate F and the region, and a predetermined amount of the liquid component in the ink L evaporates, thereby coloring Layer 81 is dried. The first drying step may be performed simultaneously with the colored layer forming step or after the colored layer forming step (preferably before the adhesive layer forming step).

  Here, it is preferable that the heat conduction type heating means 41 is not a convection type but a heat conduction type. By adopting the heat conduction type, there is no possibility that hot air is blown directly onto the first to eighth nozzle rows 33a to 33h of the ink jet head 32, so that the state of the nozzle rows 33a to 33h may be affected. There is no. Specifically, when the ink in the nozzles is dried, the viscosity increases, and there is no possibility of defective ejection. Further, the degree of heating by the heat conduction type heating means 41 can be made lower than the degree of heating in the drying furnace 52 described later. The degree may be such that there is no possibility of affecting the state of the first to eighth nozzle rows 33a to 33h of the inkjet head 32.

<< Adhesive layer forming step [FIG. 6 (d)] >>
In the adhesive layer forming step essential in the manufacturing method of the present embodiment, at least a part of the liquid component of the ink L adhering to the substrate F is evaporated, and a predetermined portion on the surface to which the ink L has adhered is applied. Then, the adhesive liquid is discharged from the ink jet head 32 and attached. Thereby, as shown in FIG.6 (d), the pattern of the contact bonding layer 94 is formed on the colored layer 81 (and a part of base material F depending on the case). What is necessary is just to adjust the droplet mass at the time of the adhesive liquid discharge in this process, for example in the range of 5-15 ng.

  In the adhesive layer forming step, the control unit 53 (see FIG. 4) vibrates the piezoelectric elements 56 corresponding to the seventh nozzle row 33g in accordance with the movement of the carriage 31, and as shown in FIG. The adhesive liquid 94 is discharged and adhered to A to form an adhesive layer 94 that is thinner than the colored layer 81.

  This adhesive layer forming step will be described more specifically with reference to FIG. First, the image-formed substrate F, the carriage 31, and the inkjet head 32 operate in the same manner as the colored layer forming step, so that the inkjet head 32 moves toward the colored layer 81 (see FIG. 6D). The adhesive liquid is discharged, and an adhesive layer 94 (see FIG. 6D) is formed on the colored layer. Thereafter, the substrate F is downstream of the feed direction Y by the length of the platen 34 along the feed direction Y, that is, the length along the feed direction Y of the region where the image is formed by the plurality of scans. To the side and pause again. Then, image formation and adhesive layer formation are performed on the substrate F on the platen 34 by a plurality of scans. That is, image formation and adhesive layer formation are performed by so-called intermittent feeding.

  During the layer formation as described above, that is, before pressure bonding, the thickness of the adhesive layer 94 may be smaller than the thickness of the colored layer 81. The reason is that it has excellent transferability. On the other hand, after the crimping, the above relationship becomes more remarkable. The reason is that, since the colored layer 81 is relatively hard, the degree of pressure bonding is smaller, while the adhesive layer 94 is relatively soft, so the degree of pressure bonding is larger.

  The thicknesses of the colored layer 81 and the adhesive layer 94 can be adjusted by the mass of the ink L and the adhesive liquid that adhere to the unit area of the substrate F. Therefore, it is preferable to set the conditions in advance by measuring the thickness of only the colored layer 81 or only the adhesive layer 94 before the start of production.

  Here, the thickness of the layer can be calculated from an enlarged photograph of about 1 to 100,000 times by a cross-sectional observation method called microtome-transmission electron microscopy. A transmission electron microscope (TEM) is a device that irradiates a sample with an electron beam emitted from an electron gun in a vacuum and enlarges the transmission image with a magnetic lens to obtain an enlarged image of a substance. The microtome is a sample preparation method for preparing a slice having a thickness that allows transmission of an electron beam.

Here, in FIG. 6D, the colored layer 81 and the adhesive layer 94 are shown as being separated. However, in practice, the colored layer 81 and the adhesive layer 94 are not necessarily (clearly) separated. This is because the adhesive liquid may be discharged in a state where all the liquid components contained in the colored layer 81 are not evaporated, and in this case, the adhesive liquid can be mixed into the colored layer 81. In addition, when the adhesive layer 94 is provided in a state where the colored layer 81 is not completely dried, it is expected that the fixing strength increases due to a so-called anchor effect.
When the colored layer 81 and the adhesive layer 94 are not (separately) separated from each other, the thickness of each layer is defined by the thickness of the colored layer 81 and the adhesive layer 94 based on the above-described condition setting.

≪Second drying process≫
If desired, a second drying step is further performed. In the second drying step, the liquid component contained in the colored layer 81 and the adhesive layer 94 on the substrate F is forcibly evaporated.

  As a means of evaporation in the second drying step, in addition to heating such as a drying furnace 52 (see FIG. 1) which is an example of the convection heating means 51 in the second drying unit 50, reduced pressure, dry air and hot air are used. It is mentioned to make it contact. When the aqueous pigment ink is used as the ink L, in the second drying step, it is preferable to evaporate more than 95% by mass of the liquid component contained in the ink L and the adhesive liquid adhering to the substrate F. On the other hand, when a non-aqueous pigment ink is used as the ink L, in the second drying step, it is preferable to evaporate over 90% by mass of the liquid component contained in the ink L and the adhesive liquid adhering to the substrate F.

In the second drying step, when the image formation (printing) on the base material F is completed as described above, the control unit 53 (see FIG. 4) drives the transport motor 55 to feed the base material F downstream in the feed direction Y. Then, evaporation and drying are performed in a drying furnace 52 which is an example of the convection heating means 51 in the second drying unit 50. Thereby, the liquid component contained in the colored layer 81 and the adhesive layer 94 evaporates, and the dried protective layer 91, colored layer 81, and adhesive layer 94 are finally fixed on the substrate F. Thereafter, the base material F is wound around the central axis (winding shaft) of the winding roller 75 so that the adhesive layer 94 contacts the back surface of the base material F.
Note that the second drying step may be performed simultaneously with the adhesive layer forming step or after the adhesive layer forming step. Further, the drying furnace 52 is not particularly limited in terms of structure, and a conventionally known one can be used.

  In addition, it is of course possible to evaporate the liquid components contained in the colored layer 81 and the adhesive layer 94 by natural drying after performing the above-described adhesive layer forming step without performing the second drying step.

In addition, when the adhesive liquid 94 is a microcapsule (which includes an adhesive component containing a polyester resin), which will be described later, dispersed in a liquid, the temperature of the drying furnace 52 is set so that the microcapsules in the adhesive layer 94 The temperature is set so that it does not break.
Thereby, the adhesive force between the back surface of the base material F and the adhesive layer 94 is made weaker than the adhesive force between the protective layer 91 and the colored layer 81 and between the colored layer 81 and the adhesive layer 94. Can do. Therefore, when the wound base material F is unwound, the back surface of the base material F and the adhesive layer 94 are peeled off, and the release layer 89 and the protective layer 91 are sequentially formed on the surface of the base material F from the base material F side. Further, the colored layer 81 and the adhesive layer 94 can be formed in a laminated state.

  In addition, the adhesion between the protective layer 91 and the colored layer 81 and between the colored layer 81 and the adhesive layer 94 is stronger than the adhesion between the protective layer 91 and the release layer 89. Therefore, when the colored layer 81 is transferred to the transfer medium, first, an additional process is performed on the adhesive layer 94 to destroy the microcapsules. Then, the adhesive layer 94 exhibiting adhesiveness is adhered to the transfer medium and the substrate F is peeled off, whereby the release layer 89 and the protective layer 91 are peeled off, and the surface of the colored layer 81 is the protective layer 91. Are transferred to a transfer medium in a protected state.

  When the transfer medium manufacturing apparatus 1a is used, the following effects can be obtained.

That is, the ink L adheres to the substrate F and at least a part of the liquid component (preferably 65 to 95% by mass when the ink L is an aqueous pigment ink, and when the ink L is a non-aqueous pigment ink. In the state where 50 to 90% by mass) is evaporated, the adhesive liquid is adhered on the colored layer 81, so that the ink L is adhered to the ink L in a state where the fluidity is lost to some extent.
Therefore, the adhesive liquid can be attached without destroying the pattern of the colored layer 81, and the pattern of the colored layer can be obtained with high resolution. Further, the adhesive liquid may adhere in a state where a part of the liquid component remains in the colored layer 81. In this case, the adhesive force between the colored layer 81 and the adhesive layer 94 is stronger than the adhesive force between the protective layer 91 and the release layer 89, and transfer that allows good transfer to the transfer medium. A medium 88 can be manufactured.
Further, the ink L can be adhered with the liquid component partially remaining on the protective layer 91, and the adhesive liquid can be adhered with the liquid component partially remaining on the colored layer 81. In this case, the adhesive force between the protective layer 91 and the colored layer 81 and between the colored layer 81 and the adhesive layer 94 is stronger than the adhesive force between the protective layer 91 and the release layer 89. Therefore, it is possible to manufacture the transfer medium 88 that can transfer the protective layer 91 well to the transfer medium.

  In addition, by attaching the ink L to the transfer region A to which the protective liquid is attached, the surface of the colored layer 81 is protected by the protective layer 91, and the durability of the colored layer 81 transferred to the transfer medium can be improved. it can. Further, by adhering ink L in a state where a part of the liquid component remains in the protective layer 91, for example, between the colored layer 81 and the protective layer 91 when the liquid component does not substantially remain in the protective layer 91. The adhesion can be strengthened compared to.

  Furthermore, by forming the protective layer 91 between the base material F and the colored layer 81, the colored layer 81 can be formed regardless of the compatibility of the base material F and the ink L. That is, for example, even when an image is formed (printed) with a liquid (ink) colored with a pigment on a water-repellent resin base material F, a transparent coat containing inorganic particles such as silica or a swellable resin By forming the protective layer 91 using an agent, the fixability of the ink L to the substrate F can be improved.

  Further, when the adhesive liquid is obtained by dispersing microcapsules described later in the liquid, the adhesive liquid is maintained in a state where the microcapsules are maintained without being destroyed by vibrating the piezoelectric element 56 and discharging the adhesive liquid. Can be attached to the substrate F. That is, since the adhesive liquid can be discharged in a state where the adhesive force of the adhesive liquid is kept low, clogging of the ink jet nozzle can be suppressed.

  In addition, you may change the said embodiment as follows. First, instead of or in addition to the heat conduction type heating means 41 embedded in the platen 34, a radiant heater that radiates and heats electromagnetic waves on the platen 34, or a blower that blows wind (warm air). An evaporation / drying device such as a device may be provided. Moreover, you may provide separately the head which discharges the ink L, protective liquid, and an adhesive liquid. Furthermore, the protective layer 91 may not be formed without attaching the protective liquid. At this time, the release layer 89 may also have a function as a protective layer.

  Moreover, you may use the film in which the protective layer 91 was formed previously. Furthermore, a mechanism for discharging the release agent to the inkjet head 32 may be further provided, and the release layer 89 may be formed by discharging the release agent to the substrate F. In this case, a release agent may be discharged to the transfer region A, and the release layer 89 may be formed in accordance with the shape of the colored layer 81.

Further, in the manufacturing method of the present embodiment, before the colored layer forming step, the base material F on the surface of the base material F on which the colored layer 81 is to be formed (the base material F includes the release layer 89). In some cases, the protective layer 91 may be formed on the surface of the release layer 89). The protective layer 91 is formed by, for example, attaching a protective liquid to the surface of the base material F (release layer 89) and drying it as necessary.
By forming the protective layer 91, the surface of the colored layer 81 after transfer can be protected by the protective layer 91, and the durability of the colored layer 81 transferred to the transfer medium can be improved. Examples of the protective liquid include acrylic ester resin, methacrylic ester resin, acrylic ester-methacrylic ester copolymer resin, acrylic ester-styrene copolymer resin, acrylic ester-methacrylic ester-styrene copolymer. Examples thereof include a liquid containing a coalesced resin, a polyvinyl alcohol resin, and the like. If the thickness of the protective layer 91 is less than 10 nm, the colored layer 81 cannot be sufficiently protected. On the other hand, if it exceeds 30 nm, it is not preferable from the viewpoint of the production cost of the protective layer 91, or it becomes bulky when a roll-shaped substrate F is used. Therefore, it is preferable that it is 10-30 nm.

[Ultraviolet curing type pigment ink transfer medium manufacturing equipment]
The second aspect of the present embodiment relates to a manufacturing method using a transfer medium manufacturing apparatus, which is suitable when an ultraviolet curable pigment ink is used as the ink L. In addition, since this 2nd aspect can be called the modification of the said 1st aspect, it demonstrates below centering on a different part from a 1st aspect.

  FIG. 7 is a side view showing an outline of the entire transfer medium manufacturing apparatus 1b used in the second mode of the present embodiment. FIG. 8 is a side view schematically showing the image forming unit 130 of the transfer medium manufacturing apparatus 1b.

  As shown in FIG. 7, the transfer medium manufacturing apparatus 1 b includes a substrate F feeding unit 10, a transport unit 20, an image forming unit 130, a fixing unit 190, and a discharge unit 70.

  Among these, in the second mode, the configurations of the image forming unit 130 and the fixing unit 190 are mainly different from the first mode. The fixing unit 190 includes a first fixing unit 140 and a second fixing unit 150.

  Since the first fixing unit 140 has the same function as the first drying unit 40 in the first aspect, description thereof is omitted here. Also, the heat conduction heating means 141 and the first nichrome wire 142 shown in FIG. 8 have the same functions as the heat conduction heating means 41 and the first nichrome wire 42, respectively. Since the image forming unit 130 has the same configuration as the image forming unit in the first aspect, description thereof is omitted here.

  The second fixing unit 150 is configured to be able to irradiate ultraviolet rays or electron beams in order to polymerize and cure the remaining components in the ink L attached to the base material F.

  The second fixing unit 150 includes an ultraviolet irradiation device 152 that is an example of the ultraviolet irradiation unit 151. Inside the ultraviolet irradiation device 152, a first ultraviolet lamp, a second ultraviolet lamp, and a third ultraviolet lamp (all not shown) are provided. When the ultraviolet irradiation device 152 uses a light emitting diode (LED) as an ultraviolet irradiation source, an LED having an emission peak wavelength of 395 nm is a first ultraviolet lamp, an LED having an emission peak wavelength of 380 nm is a second ultraviolet lamp, and the emission peak wavelength is It is preferable to use a 365 nm LED as the third ultraviolet lamp. In addition, the ultraviolet irradiation device 152 is not particularly limited due to its structure, and a conventionally known device can be used.

  You may make it equip the 1st fixing | fixed part 140 with the warm air fan 35 as a convection heating means. By applying warm air on the surface of the base material F on the platen 34, the liquid component in the ink L attached to the base material F can be efficiently evaporated. The hot air fan 35 can be replaced with an infrared lamp, or both, as required.

  In the second mode, the colored layer 81 is formed by drying in the first fixing unit 140 and curing in the second fixing unit 150. Then, the base material F is conveyed to the 1st fixing | fixed part 140, and an adhesive liquid is made to adhere on the colored layer 81 similarly to the said 1st aspect. Furthermore, the adhesive layer 94 is formed by drying the liquid component contained in the adhesive liquid using the platen 34 and the hot air fan 35.

  Further, as a modification of the second aspect, it is possible to provide the first fixing unit with the first heating unit and the ultraviolet irradiation unit and provide the second fixing unit with the second heating unit.

  Specific examples of the ink jet recording apparatus used in the transfer medium manufacturing apparatus 1b include, but are not limited to, PX-5600 (ink jet printer, trade name manufactured by Seiko Epson Corporation).

  Further, a supplementary description will be given of a manufacturing method for manufacturing the transfer medium 88 using the transfer medium manufacturing apparatus 1b. In the first drying step in the manufacturing method, an ultraviolet curable pigment ink is used as the ink L. At this time, the evaporation amount of the liquid component in the ink L ejected and adhered to the substrate F is the total amount of the liquid component. 40-70 mass% is preferable with respect to mass (100 mass%), and 35-65 mass% is more preferable. In this case, as described above, the pattern of the colored layer 81 on the transfer medium can be formed with high resolution, and the transferability can be improved.

  Below, the detail of the base material and various inks which are suitable for implementation of the manufacturing method demonstrated so far as structures other than a manufacturing apparatus is demonstrated.

[Base material]
The substrate F is not particularly limited, and examples thereof include metal, wood, plastic, and paper. Especially, since it is easy to process the base material F into a desired shape, a metal, a plastic, or paper is preferable, and when the viewpoint of cost is considered, a plastic is more preferable.

  As said metal, aluminum is mentioned preferably from a viewpoint of cost. Preferred examples of the plastic include polyolefin resins, polyester resins, polyamide resins, and polycarbonate resins. Preferred examples of the paper include plain paper, high-quality paper, and coated paper.

  Furthermore, a non-ink-absorbing or low-absorbing substrate can also be suitably used as the substrate F. As such a non-ink-absorbing substrate F, for example, a plastic film not subjected to surface treatment for ink jet printing (that is, an ink absorbing layer is not formed), plastic is used on the substrate F such as paper. Examples thereof include those coated and those to which a plastic film is adhered. Examples of the plastic here include polyvinyl chloride, polyethylene terephthalate, polycarbonate, polystyrene, polyurethane, polyethylene, and polypropylene. Examples of the low-ink-absorbing substrate F include printing paper such as art paper, coated paper, and matte paper.

In addition, said non-ink-absorbing and low-absorbing base material refers to a base material whose printed surface has a water absorption amount of 10 mL / m ² or less from the start of contact to 30 msec in the Bristow method. . This Bristow method is the most popular method for measuring the amount of liquid absorbed in a short time, and is also adopted by the Japan Paper Pulp Technology Association (JAPAN TAPPI). For details of the test method, refer to Standard No. of “JAPAN TAPPI Paper Pulp Test Method 2000”. 51 "Paper and paperboard-Liquid absorbency test method-Bristow method".

  The substrate F is preferably in the form of a sheet or film in order to facilitate the use of the transfer medium. The thickness of the base material F is preferably 10 to 50 μm.

  The base material F may be provided with a release layer 89 formed by coating with a release agent on at least one of the side on which the colored layer 81 is to be formed and the opposite side thereof. Since the base material F includes the release layer 89 on the side where the colored layer 81 is to be formed, transfer from the transfer medium to the transfer medium becomes easier. From this point of view, it is preferable that the release layer 89 is provided at least on the side where the colored layer 81 of the substrate F is to be formed. In addition, since the base material F includes the release layer 89 on the side opposite to the side on which the colored layer 81 is to be formed, when the transfer media are stacked, the transfer media are brought into close contact with each other and hardly separated from each other. Can be suppressed. Examples of the release agent include a polyethylene wax release agent, a silicone release agent, and a fluorine release agent. If the thickness of the release layer 89 is less than 10 nm, sufficient transferability cannot be obtained. On the other hand, if it exceeds 30 nm, it is not preferable from the viewpoint of the production cost of the release layer 89, or the roll-shaped base material F is bulky. Therefore, it is preferable that it is 10-30 nm.

[ink]
The ink L is used for forming the colored layer 81. The ink L contains a colorant, and this colorant is a pigment because it can improve the light resistance of the ink. The ink L is an aqueous pigment ink, a non-aqueous pigment ink, or an ultraviolet curable pigment ink.

[Water-based pigment ink]
When an aqueous pigment ink is used as the ink L, the ink ejection stability is particularly excellent. The aqueous pigment ink preferably contains at least the following components.
(1) pigment,
(2) at least one of a pigment dispersant, an emulsion-form thermoplastic resin (hereinafter also referred to as “resin emulsion”), and a water-soluble thermoplastic resin (hereinafter also referred to as “water-soluble resin”);
(3) a medium-boiling water-soluble organic solvent having a boiling point at 1 atm of 250 ° C. or lower (more preferably 70 ° C. or higher and 250 ° C. or lower);
(4) surfactant,
(5) Water.

  The contents of the components (1) to (5) with respect to the total mass (100 mass%) of the ink will be described. The component (1) is preferably 0.2 to 10% by mass. The component (2) is preferably 1.5 to 15% by mass. The component (3) is preferably 5 to 40% by mass. The component (4) is preferably 0.5 to 2% by mass. The component (5) is preferably 50 to 92% by mass. When the content of each component is within the above range, the ejection stability is extremely excellent.

  Although the detail about each said component is mentioned later, each said component may be used individually by 1 type, respectively, and may be used in combination of 2 or more type.

[Non-aqueous pigment ink]
The non-aqueous pigment ink preferably contains at least the following components in order to improve ejection stability.
(6) pigment,
(7) A medium-boiling water-soluble organic solvent having a boiling point at 1 atm of 250 ° C. or lower (more preferably 70 ° C. or higher and 250 ° C. or lower).
Here, it is preferable that the non-aqueous pigment ink of the present invention does not substantially contain water. Here, “substantially does not contain water” includes not only the case where water is not included at all, but also the case where water is contained within a range not inhibiting the dispersion of the pigment. The content of water contained in the non-aqueous pigment ink in the present embodiment is preferably 0.5% by mass or less, for example.

  The contents of the components (6) and (7) with respect to the total mass (100% by mass) of the ink will be described. The component (6) is preferably 0.2 to 10% by mass. The component (7) is preferably 70 to 99.8% by mass. When the content of each component is within the above range, the ejection stability is excellent.

Further, the non-aqueous pigment ink is excellent in adhesion by further including the following component (8).
(8) Thermoplastic resin.

  Although the detail about each said component is mentioned later, each said component may be used individually by 1 type, respectively, and may be used in combination of 2 or more type.

[UV curable pigment ink]
The ultraviolet curable pigment ink preferably contains at least the following components in order to improve discharge stability.
(9) Pigment,
(10) a monomer having a boiling point of 100 ° C. or higher and 250 ° C. or lower,
(11) at least one of a polymerizable oligomer and polymer;
(12) Photopolymerization initiator.

  The contents of the components (9) to (12) with respect to the total mass (100 mass%) of the ink will be described. The component (9) is preferably 0.2 to 10% by mass. The component (10) is preferably 30 to 70% by mass. The component (11) is preferably 10 to 50% by mass. The component (12) is preferably 3 to 10% by mass. When the content of each component is within the above range, the ejection stability is excellent.

Moreover, it is more preferable that the ultraviolet curable pigment ink further includes the following component (13).
(13) At least one of a water-soluble organic solvent having a medium boiling point and a water having a boiling point at 1 atm of 250 ° C. or lower (more preferably 70 ° C. or higher and 250 ° C. or lower).

  Although the detail about each said component is mentioned later, each said component may be used individually by 1 type, respectively, and may be used in combination of 2 or more type.

[Adhesive liquid]
The above-mentioned adhesive liquid is used for forming the adhesive layer 94, and preferably contains a polyester resin in order to improve the ease of transfer and the adhesiveness to the transfer medium or the colored layer at the time of transfer. . Examples of the adhesive liquid include an aqueous liquid containing a polyester resin in the form of an emulsion (a liquid containing water as a main component), and the polyester resin that functions as an adhesive can be efficiently distributed on the surface layer. An aqueous liquid containing a polyester resin is preferred.

The aqueous liquid containing the polyester resin (polyester resin emulsion) in the form of an emulsion forms the pattern of the colored layer 81 and the adhesive layer 94 in the transfer medium 88 with high resolution due to its excellent ejection stability, and In order to have excellent transferability, it is preferable that at least the following components (14) to (16) are included as constituent components.
(14) polyester resin emulsion,
(15) a medium-boiling water-soluble organic solvent having a boiling point at 1 atm of 250 ° C. or lower (more preferably 70 ° C. or higher and 250 ° C. or lower);
(16) Water.

  Although the detail about each said component is mentioned later, each said component may be used individually by 1 type, respectively, and may be used in combination of 2 or more type.

  The content of each component described above with respect to the total mass (100% by mass) of the adhesive liquid will be described. The component (14) is preferably 2.5 to 25% by mass. The component (15) is preferably 10 to 40% by mass. The component (16) is preferably 45 to 87.5% by mass. When the content of each component is within the above range, the discharge stability of the adhesive liquid is excellent.

  Here, the adhesive liquid in the present embodiment may be one in which microcapsules enclosing an adhesive component containing a polyester resin are dispersed in a liquid. When such an adhesive liquid is used, adhesiveness can be improved by performing additional treatment such as heat treatment or pressure treatment to break the microcapsules.

[Constituent components of ink and adhesive liquid]
Hereinafter, the components of the ink L and the adhesive liquid will be described in detail.

(Pigment)
As the pigment contained in the ink, either an inorganic pigment or an organic pigment can be used.

  As the inorganic pigment, carbon black (CI pigment black 7) such as furnace black, lamp black, acetylene black and channel black, iron oxide, and titanium oxide can be used.

  Specific examples of the carbon black are not particularly limited. 2300, 900, MCF88, no. 20B, no. 33, no. 40, no. 45, no. 52, MA7, MA8, MA100, No2200B, etc. (all trade names, manufactured by Mitsubishi Chemical Corporation), color black FW1, FW2, FW2V, FW18, FW200, S150, S160, S170, Pretex 35, U , V, 140U, Special Black 6, 5, 4A, 4, 250, etc. (all trade names, manufactured by Degussa AG), Conductex SC, Raven 1255, 5750, 5250, 5000, 3500, 1255, 700 Etc. (all trade names, manufactured by Columbia Carbon Co., Ltd.), Regal 400R, 330R, 660R, Mogul L, Monarch 700, 800, 880, 900, 1000, 1100, 1300, 1400, Elf Tex 12 etc. (all brand names, Cabot (C abot Corporation)).

  These carbon blacks may be used alone or in combination of two or more.

  In addition, pigments contained in achromatic white ink (white ink) include titanium oxide such as chlorine-based titanium oxide (rutile type) CR-50 (trade name, manufactured by ISHIHARA SANGYO KAISHA, LTD.), Sulfuric acid, etc. One or more selected from the group consisting of barium and hollow white resin emulsions are preferred.

  Further, among organic pigments, the organic pigment for chromatic ink is not particularly limited, for example, quinacridone pigment, quinacridone quinone pigment, dioxazine pigment, phthalocyanine pigment, anthrapyrimidine pigment, ansanthrone pigment, Indanthrone pigments, flavanthrone pigments, perylene pigments, diketopyrrolopyrrole pigments, perinone pigments, quinophthalone pigments, anthraquinone pigments, thioindigo pigments, benzimidazolone pigments, isoindolinone pigments, Examples thereof include azomethine pigments and azo pigments.

  Specific examples of the cyan pigment used in the cyan ink are not particularly limited. I. Pigment Blue 1, 2, 3, 15: 3, 15: 4, 15:34, 16, 22, 60 etc., C.I. I. Bat Blue 4, 60 and the like. Of these, C.I. I. Pigment blue 15: 3, 15: 4, and one or more selected from the group consisting of 60.

  Specific examples of the magenta pigment used in the magenta ink are not particularly limited. I. Pigment Red 5, 7, 12, 48 (Ca), 48 (Mn), 57 (Ca), 57: 1, 112, 122, 123, 168, 184, 202, C.I. I. And CI Pigment Violet 19. Of these, C.I. I. Pigment red 122, 202, 209, and C.I. I. One or more selected from the group consisting of CI Pigment Violet 19.

  Specific examples of the yellow pigment used in the yellow ink are not particularly limited. I. Pigment Yellow 1, 2, 3, 12, 13, 14C, 16, 17, 73, 74, 75, 83, 93, 95, 97, 98, 119, 110, 114, 128, 129, 138, 150, 151, 154, 155, 180, and 185. Of these, C.I. I. Pigment Yellow 74, 109, 110, 128, and 138 or more selected from the group consisting of 138.

  Specific examples of the pigment used in the orange pigment dispersion used in the orange ink are not particularly limited. I. Pigment Orange 36 or 43, or a mixture thereof.

  Specific examples of the pigment used in the green pigment dispersion used in the green ink are not particularly limited. I. Pigment Green 7 or 36, or a mixture thereof.

  The metallic pigment used in the metallic ink is not particularly limited as long as it has a function such as metallic luster, but is preferably aluminum or an aluminum alloy, or silver or a silver alloy. Among these, aluminum or an aluminum alloy is preferable in order to reduce the cost and improve the metallic luster. When an aluminum alloy is used, the other metal element or non-metal element that can be added to aluminum is not particularly limited as long as it has a function such as having a metallic luster, but silver, gold, platinum, Examples include nickel, chromium, tin, zinc, indium, titanium, and copper. And at least 1 sort (s) of these single-piece | units or these alloys and these mixtures is used suitably.

  These pigments may be used by dispersing a resin using a conventionally known dispersion resin, or may be used as a self-dispersing pigment by oxidizing or sulfonating the pigment surface with ozone, hypochlorous acid, fuming sulfuric acid, or the like. Also good.

(Dispersant)
The ink preferably contains a dispersant from the viewpoint of improving pigment dispersibility. Although it does not specifically limit as a dispersing agent, For example, the dispersing agent currently used for preparing pigment dispersion liquids, such as a polymer dispersing agent, is mentioned. Specific examples include polyoxyalkylene polyalkylene polyamines, vinyl polymers and copolymers, acrylic polymers and copolymers, polyesters, polyamides, polyimides, polyurethanes, amino polymers, silicon-containing polymers, sulfur-containing polymers, fluorine-containing polymers, and epoxies. The thing which has 1 or more types, such as resin, as a main component is mentioned. As a commercial product of a polymer dispersing agent, Dainichiseika Color & Chemicals Mfg. Co., Ltd. made a recall series (N-509 etc.), Ajinomoto Fine-Techno Co., Inc. ), Adisia series manufactured by Avecia, Dispersic series manufactured by BYKChemie, Disparon series manufactured by Enomoto Kasei. In addition, it is preferable to control the hydrophilicity of the dispersant according to the type of ink (aqueous pigment ink, non-aqueous pigment ink), and the hydrophilicity control is a hydrophilic group (for example, a hydroxyl group, a carboxyl group, and a sulfo group). ) Is preferable.

(Thermoplastic resin)
The ink preferably contains a thermoplastic resin from the viewpoints of ease of transfer and enhancement of adhesion to the transfer medium or adhesive layer during transfer.
Among the thermoplastic resins, those used for the aqueous pigment ink include a resin emulsion and a water-soluble resin as described above.

  The adhesive liquid which concerns on this invention contains a polyester resin among said thermoplastic resins.

  In this embodiment, those listed below are preferable as the aqueous pigment ink, the resin emulsion that can be contained in the adhesive liquid, and the water-soluble resin. Resin may be used individually by 1 type and may be used in combination of 2 or more type.

Even if these resins are water-insoluble, they need to be water-dispersible as described above, and are therefore preferably a polymer having both a hydrophilic portion and a hydrophobic portion, that is, a resin emulsion. When a resin emulsion is used as the thermoplastic resin, the average particle diameter is not particularly limited as long as the emulsion is formed, but is preferably less than 1 μm, more preferably 150 nm or less, and further preferably 5 nm to 100 nm.
In the present specification, the average particle diameter is measured by a particle size analyzer using a dynamic light scattering method unless otherwise specified. Pure water is added to the emulsion to dilute it 100 times, and it is expressed as a 50% by mass number average particle size measured using Nanotrac UPA-EX150 (Nikkiso Co., Ltd.).

  As the thermoplastic resin, those conventionally used in ink jet inks and adhesives can be used.

  Specific examples of the thermoplastic resin used in the aqueous pigment ink are not particularly limited, but poly (meth) acrylic acid ester or a copolymer thereof, polyacrylonitrile or a copolymer thereof, polycyanoacrylate, polyacrylamide, and poly ( (Meth) acrylic polymers such as (meth) acrylic acid, polyethylene, polypropylene, polybutene, polyisobutylene, and polystyrene, and copolymers thereof, and polyolefin-based polymers such as petroleum resins, coumarone-indene resins, and terpene resins. Polymers, polyvinyl acetate or copolymers thereof, polyvinyl acetate or vinyl alcohol polymers such as polyvinyl alcohol, polyvinyl acetal, and polyvinyl ether, polyvinyl chloride or copolymers thereof, polyvinylidene chloride, fluororesin, and vinyl Halogen-containing polymers such as raw rubber, polyvinylcarbazole, polyvinylpyrrolidone or copolymers thereof, nitrogen-containing vinyl polymers such as polyvinylpyridine and polyvinylimidazole, polybutadiene or copolymers thereof, polychloroprene, and polyisoprene ( Diene polymers such as butyl rubber), and other ring-opening polymerization resins, condensation polymerization resins, and natural polymer resins.

  Commercially available products of thermoplastic resins used in aqueous pigment inks include, for example, Hitech E-7525P, Hitech E-2213, Hitech E-9460, Hitech E-9015, Hitech E-4A, Hitech E-5403P, Hitech E-8237. (All trade names, manufactured by TOHO Chemical Industry Co., Ltd.), AQUACER 507, AQUACER 515, AQUACER 840 (all trade names, manufactured by BYK Japan KK), JONCRYL 67 611, 678, 680, and 690 (all are trade names, manufactured by BASF).

  When the thermoplastic resin used in the aqueous pigment ink is obtained in the form of an emulsion, it can be prepared by mixing resin particles with water together with a surfactant if desired. For example, emulsions of (meth) acrylic resins or styrene- (meth) acrylic resins are composed of (meth) acrylic ester resins or styrene- (meth) acrylic ester resins and optionally (meth) acrylic resin. And a surfactant are mixed with water. The mixing ratio of at least one of the resin emulsion and the water-soluble resin and the surfactant is preferably about 50: 1 to 5: 1 in mass ratio. When the amount of the surfactant used is less than the above range, an emulsion is hardly formed. On the other hand, when the amount exceeds the above range, the water resistance of the ink or the adhesive liquid is lowered or the adhesion is deteriorated. There is a tendency.

  The surfactant is not particularly limited, but preferred examples include anionic surfactants such as sodium dodecyl benzan sulfonate, sodium lauryl sulfate, and ammonium salt of polyoxyethylene alkyl ether sulfate, polyoxyethylene alkyl ether, Nonionic surfactants such as polyoxyethylene alkyl ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene alkyl phenyl ether, polyoxyethylene alkyl amine, and polyoxyethylene alkyl amide may be mentioned. These surfactants may be used individually by 1 type, and 2 or more types may be mixed and used for them.

  The emulsion of the thermoplastic resin used in the aqueous pigment ink can also be obtained by emulsion polymerization of at least one monomer of the above-described resin emulsion and water-soluble resin in water in which a polymerization catalyst and an emulsifier are present. be able to. The polymerization initiator, the emulsifier, and the molecular weight modifier used in the emulsion polymerization can be used according to a conventionally known method.

  As the polymerization initiator, those used for normal radical polymerization are used, for example, potassium persulfate, ammonium persulfate, hydrogen peroxide, azobisisobutyronitrile, benzoyl peroxide, dibutyl peroxide, Examples include peracetic acid, cumene hydroperoxide, t-butyl hydroxy peroxide, and paramentane hydroxy peroxide. When the polymerization reaction is performed in water, a water-soluble polymerization initiator is preferable. As an emulsifier, what is generally used as an anionic surfactant, a nonionic surfactant, an amphoteric surfactant other than sodium lauryl sulfate, and a mixture thereof are mentioned, for example. These may be used alone or in combination of two or more.

  Speaking of the ratio between at least one of the resin emulsion and the water-soluble resin and water, it is preferably in the range of 60 to 400 parts by mass, more preferably in the range of 100 to 200 parts by mass with respect to 100 parts by mass of these resins. A range of water is suitable.

  Commercially available resin emulsions can also be used. For example, Microgel E-1002, E-5002 (trade name, manufactured by Nippon Paint Co., Ltd., styrene-acrylic resin emulsion) ), Boncoat 4001 (trade name, acrylic resin emulsion manufactured by DIC), Boncoat 5454 (trade name, styrene-acrylic resin emulsion manufactured by DIC), JONCRYL 67 (Tg 73 ° C.), 611 (Tg 50 ° C.), 680 (Tg 67 ° C), 690 (Tg 102 ° C) (trade name, manufactured by BASF), Polyzol AM-710 (Tg 56 ° C), AM-920 (Tg-20 ° C), AM-2300 (Tg 67 ° C) AP-4735 (Tg 21 ° C.), AT-860 (Tg 60 ° C.) (above, acrylic resin emulsion), poly Zole AP-7020 (Tg 85 ° C.) (styrene / acrylic resin emulsion), Polyzole SH-502 (vinyl acetate resin emulsion, Tg 30 ° C.) (above, trade name manufactured by SHOWA DENKO KK), SAE 1014 (product) Name, styrene-acrylic resin emulsion, manufactured by Nippon Zeon Corporation), Cybinol SK-200 (trade name, acrylic resin emulsion, manufactured by SAIDEN CHEMICAL INDUSTRY CO., LTD.), AE- 120A (trade name, acrylic resin emulsion, Tg-10 ° C., manufactured by JSR), AE373D (trade name, carboxy-modified styrene / acrylic resin emulsion, manufactured by Emulsion Technology Co., Ltd.), Takelac W-6061 (Mitsui) (Trade name, polyurethane resin emulsion manufactured by Mitsui Chemicals, Inc.) Seikadyne 1900W (trade name, manufactured by Dainichi Seika Kogyo Co., Ltd., ethylene / vinyl acetate resin emulsion), vinyl furan 2622 (acrylic resin emulsion, Tg −26 ° C.), 2886 (vinyl acetate / acrylic resin emulsion, Tg 0 ° C.), 5202 ( Acetic acid acrylic resin emulsion, Tg 30 ° C.) (trade name, manufactured by Nissin Chemical Industry CO., Ltd.), Elitel KA-5071S (Tg 67 ° C.), KT-8803 (Tg 61 ° C.) , KT-9204 (Tg 19 ° C.), KT-8701 (Tg 13 ° C.), KT-8904 (Tg 10 ° C.), KT-0507 (Tg-27 ° C.) (above, product name manufactured by Unitika, polyester resin emulsion) , Hi-Tech SN-2002 (Polyester resin emulsion Tg 76 ° C, Toho Chemical Company name).

Among these, as the polyester resin to be contained in the adhesive liquid, a polyester resin having a glass transition temperature (Tg) of 10 ° C. or higher and 70 ° C. or lower is preferable. When the polyester resin has a Tg of 70 ° C. or lower, the transferability and adhesiveness are excellent. On the other hand, when the polyester resin has a Tg of 10 ° C. or higher, the blocking resistance is excellent.
In addition, Tg in this specification is a value obtained by removing a liquid component from a resin emulsion by heating, taking out the resin component, and measuring the resin component with a differential thermothermal gravimetric simultaneous measurement device (TG / DTA). .

  The thermoplastic resin may be mixed as a particle powder with other components in the ink or the adhesive liquid. However, after the resin particles are dispersed in an aqueous medium to form a resin emulsion, the ink or the adhesive liquid is mixed. It is preferable to mix with the component. In order to improve the long-term storage stability and ejection stability of the ink or the adhesive liquid, the particle size of the resin particles in the present embodiment is preferably in the range of 5 to 400 nm, more preferably in the range of 50 to 200 nm. It is.

  In addition, as the water-soluble resin, a synthetic polymer having an ionic hydrophilic group such as an alkali metal salt such as a sulfonic acid group, a carboxylic acid group, or an amino group, an ammonium salt, an inorganic acid salt, or an organic acid salt may be used. it can. More specifically, acrylic resins such as polyethylene glycol, polyvinyl pyrrolidone, polyvinyl alcohol, and polyvinyl acetal, and styrene- (meth) acrylic acid copolymer and (meth) acrylic acid ester- (meth) acrylic acid copolymer. And synthetic polymers such as

  Commercially available water-soluble resins can also be used. For example, JONCRYL 678 and 680 (trade name, acrylic resin manufactured by BASF), Denkapoval H-12 (Denki Kagaku Kogyo KK ) Product name, polyvinyl alcohol).

  At least one of the resin emulsion and the water-soluble resin is preferably contained in the range of 0.5 to 10.0% by mass in terms of solid content with respect to the total mass (100% by mass) of the ink or the adhesive liquid. If the amount of these resins is too small, the ink or adhesive liquid film formed on the surface of the substrate becomes thin, and the adhesion to the surface of the substrate may be insufficient. If there is too much of these resins, the ejection stability of the ink or adhesive liquid is inferior, the dispersion of the resin becomes unstable during storage of the ink or adhesive liquid, or the resin agglomerates and solidifies due to slight evaporation of moisture. In some cases, a uniform film cannot be formed.

  On the other hand, examples of the thermoplastic resin used in the non-aqueous pigment ink include acrylic resin, styrene-acrylic resin, rosin-modified resin, terpene resin, polyester resin, polyamide resin, epoxy resin, vinyl chloride resin, vinyl chloride-acetic acid. Examples include vinyl copolymers, fiber-based resins (for example, cellulose acetate butyrate, hydroxypropyl cellulose), polyvinyl butyral, polyacryl polyol, polyvinyl alcohol, and polyurethane.

  Non-aqueous emulsion type polymer particles can also be used as the thermoplastic resin. This is a dispersion in which particles such as polyurethane resin, acrylic resin, and acrylic polyol resin are stably dispersed in an organic solvent. Examples of the polyurethane resin include Sanprene IB-501 and Sanprene IB-F370 manufactured by Sanyo Chemical Industries. Examples of the acrylic polyol resin include N-2043-60MEX manufactured by Harima Chemicals.

  The resin emulsion is preferably contained in an amount of 0.1 to 10% by mass with respect to the total mass (100% by mass) of the non-aqueous pigment ink in order to improve adhesion. When the content is 0.1% by mass or more, the discharge stability is good. Adhesiveness will become favorable in content being 10 mass% or less.

  The thermoplastic resin in the non-aqueous pigment ink is preferably at least one selected from the group consisting of polyvinyl butyral, cellulose acetate butyrate, and polyacryl polyol, and more preferably cellulose acetate butyrate. . With such a suitable configuration, the fixing property is excellent.

(Water-soluble organic solvent having a boiling point of 250 ° C. or less at 1 atm)
By incorporating a water-soluble organic solvent having a boiling point at 1 atm of 250 ° C. or less (more preferably 70 ° C. or more and 250 ° C. or less) into an ink (aqueous pigment ink or non-aqueous pigment ink) or an adhesive liquid, Thus, the resin can be stabilized, and it is excellent in the ejection stability and volatility of the ink and the adhesive liquid, and can effectively prevent image transfer unevenness.

  The water-soluble organic solvent is preferably an aqueous liquid containing at least one selected from lactam, carboxylic acid ester, alkylene glycol ether, and alcohol because of excellent discharge stability. Among these, an aqueous liquid containing 2-pyrrolidone (γ-butyrolactam), lactic acid ester, alkylene glycol ether, and alcohol is more preferable.

  Although it does not specifically limit as said water-soluble organic solvent, For example, ethanol (boiling point 78 degreeC), N-methyl-2-pyrrolidone (boiling point 204 degreeC), N-ethyl-2-pyrrolidone (boiling point 212 degreeC), 2- Pyrrolidone (bp 245 ° C), dimethyl sulfoxide (bp 189 ° C), methyl lactate (bp 145 ° C), ethyl lactate (bp 155 ° C), isopropyl lactate (bp 168 ° C), butyl lactate (bp 188 ° C), ethylene glycol monomethyl Ether (boiling point 124 ° C), ethylene glycol dimethyl ether (boiling point 85 ° C), ethylene glycol monomethyl ether acetate (boiling point 145 ° C), diethylene glycol monomethyl ether (boiling point 194 ° C), diethylene glycol monopropyl ether (boiling point 212 ° C), diethylene glycol monobutyl Ether (boiling point 230 ° C.), diethylene glycol dimethyl ether (boiling point 162 ° C.), diethylene glycol ethyl methyl ether (boiling point 176 ° C.), diethylene glycol diethyl ether (boiling point 189 ° C.), triethylene glycol monomethyl ether (boiling point 249 ° C.), propylene glycol monomethyl ether ( 120 ° C boiling point), propylene glycol dimethyl ether (bp 97 ° C), dipropylene glycol monomethyl ether (bp 188 ° C), dipropylene glycol dimethyl ether (bp 171 ° C), 1,4-dioxane (bp 101 ° C), ethylene glycol (boiling point) 197 ° C), diethylene glycol (boiling point 244 ° C), propylene glycol (boiling point 188 ° C), dipropylene glycol (boiling point 232 ° C), 1 3-propanediol (boiling point 212 ° C), 1,4-butanediol (boiling point 230 ° C), hexylene glycol (boiling point 198 ° C), 2,3-butanediol (boiling point 77 ° C), n-butanol (boiling point 118 ° C) ), 1,2-hexanediol (boiling point 224 ° C.), and 1,2-pentanediol (boiling point 206 ° C.).

  The water-soluble organic solvent having a boiling point at 1 atm of 250 ° C. or less may be used alone or in combination of two or more.

(Surfactant)
In the present embodiment, the surfactant used in the ink includes one or more surfactants selected from the group consisting of acetylene glycol surfactants and silicone surfactants.

  Examples of the acetylene glycol surfactant include 2,4,7,9-tetramethyl-5-decyne-4,7-diol, 3,6-dimethyl-4-octyne-3,6-diol, 3, 5-dimethyl-1-hexyn-3ol, 2,4-dimethyl-5-hexyn-3-ol. Examples of commercially available acetylene glycol surfactants include Olphine E1010, STG, Y, Surfynol 104E, 104H, 104A, 104BC, 104DPM, 104PA, 104PG-50, 104S, 420, 465, 485, TG, SE, SE-F, 61, 82, DF-110D (all trade names, manufactured by Nissin Chemical Industry CO., Ltd.), acetylenol E00, E00P (all trade names, Kawaken Fine Chemical Co., Ltd. ( Kawaken Fine Chemicals Co., Ltd.) can be used.

  As the silicone surfactant, a polysiloxane compound is preferably used, and a polyether-modified organosiloxane is given as a specific example of the polysiloxane compound. As commercially available silicone surfactants, BYK-306, BYK-307, BYK-333, BYK-341, BYK-345, BYK-346, BYK-347, BYK-348, BYK-UV3500, 3510, 3530, 3570 (all trade names, manufactured by Big Chemie Japan) can be used.

  A particularly preferable surfactant is a combination including both a silicone-based surfactant and an acetylene glycol-based surfactant having an HLB value of 17 or less.

  The surface tension of the ink is preferably in the range of 23.0 mN / m to 40.0 mN / m by combining the above water-soluble organic solvent and the surfactant, and more preferably 25.0 mN / m. It is in the range of ~ 35.0 mN / m. When the surface tension of the ink is within the above range, the ejection stability is excellent.

(Polymerizable compound)
The monomers and oligomers that are polymerizable compounds that can be contained in the ultraviolet curable pigment ink are not particularly limited as long as they are compounds that polymerize and solidify upon irradiation with light such as ultraviolet rays by the action of a photopolymerization initiator described later. However, various monomers and oligomers having a monofunctional group, a bifunctional group, and a polyfunctional group having three or more functional groups can be used.

  Here, the “monomer” in the present specification means a molecule having a number average molecular weight of 100 to 3,000. The “oligomer” in the present specification means a molecule having a number average molecular weight of 500 to 20,000. In the present specification, the number average molecular weight is measured according to a gel permeation chromatography (GPC) method.

  Examples of the monomer include unsaturated carboxylic acids such as (meth) acrylic acid, itaconic acid, crotonic acid, isocrotonic acid, and maleic acid, and salts or esters thereof, urethane, amide and anhydride thereof, acrylonitrile, styrene, various types Unsaturated polyesters, unsaturated polyethers, unsaturated polyamides, and unsaturated urethanes.

  As an oligomer, the oligomer formed from said monomers, such as a linear acrylic oligomer, an epoxy (meth) acrylate, a urethane (meth) acrylate, and polyester (meth) acrylate are mentioned, for example.

Further, the above monomers and oligomers may be allyl compounds. An allyl compound is a compound having a 2-propenyl (—CH ₂ CH═CH ₂ ) structure. The 2-propenyl group is also referred to as an allyl group, and is a common name in the IUPAC nomenclature. The allyl compound has radical polymerizability. Specific examples of allyl compounds include ethylene glycol monoallyl ether, allyl glycol (for example, available from NIPPON NYUKAZAI CO., LTD.), Trimethylolpropane diallyl ether, pentaerythritol triallyl ether, glycerin monoallyl. Ether (above, for example, available from DAISO), polyoxyalkylene compounds having an allyl group, which is a trade name of UNIOX, UNILOP, polyserine, UNISafe (available from NOF CORPORATION) Etc.

  Among these, it is preferable to use allyl glycol. By using allyl glycol as the polymerizable compound, the viscosity of the ultraviolet curable ink can be reduced, and the viscosity can be adjusted to an optimum viscosity (10 mPa · s or less at 25 ° C.) as the ink used in the production method of the present embodiment. Is possible.

  The monomer and oligomer may be an N-vinyl compound. Examples of the N-vinyl compound include N-vinylformamide, N-vinylcarbazole, N-vinylacetamide, N-vinylpyrrolidone, N-vinylcaprolactam, acryloylmorpholine, and derivatives thereof.

(Photopolymerization initiator)
The photopolymerization initiator that can be contained in the ultraviolet curable pigment ink is limited as long as it generates active species such as radicals and cations by the energy of light such as ultraviolet rays and initiates polymerization of the polymerizable compound. However, a radical photopolymerization initiator or a cationic photopolymerization initiator can be used, and among them, it is preferable to use a radical photopolymerization initiator.

  Examples of the radical photopolymerization initiator include aromatic ketones, acylphosphine compounds, aromatic onium salt compounds, organic peroxides, thio compounds, hexaarylbiimidazole compounds, ketoxime ester compounds, borate compounds, Examples thereof include azinium compounds, metallocene compounds, active ester compounds, compounds having a carbon halogen bond, and alkylamine compounds.

  Specific examples of radical photopolymerization initiators include acetophenone, acetophenone benzyl ketal, 1-hydroxycyclohexyl phenyl ketone, 2,2-dimethoxy-2-phenylacetophenone, xanthone, fluorenone, benzaldehyde, fluorene, anthraquinone, triphenyl. Amine, carbazole, 3-methylacetophenone, 4-chlorobenzophenone, 4,4'-dimethoxybenzophenone, 4,4'-diaminobenzophenone, Michler's ketone, benzoin propyl ether, benzoin ethyl ether, benzyldimethyl ketal, 1- (4-isopropyl Phenyl) -2-hydroxy-2-methylpropan-1-one, 2-hydroxy-2-methyl-1-phenylpropan-1-one, thioxanthone, diethyl Thioxanthone, 2-isopropylthioxanthone, 2-chlorothioxanthone, 2-methyl-1- [4- (methylthio) phenyl] -2-morpholino-propan-1-one, bis (2,4,6-trimethylbenzoyl) -phenyl Phosphine oxide, 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, 2,4-diethylthioxanthone, and bis- (2,6-dimethoxybenzoyl) -2,4,4-trimethylpentylphosphine oxide Can be mentioned.

  Examples of commercially available radical photopolymerization initiators include IRGACURE 651 (2,2-dimethoxy-1,2-diphenylethane-1-one), IRGACURE 184 (1-hydroxy-cyclohexyl-phenyl-ketone), DAROCUR. 1173 (2-hydroxy-2-methyl-1-phenyl-propan-1-one), IRGACURE 2959 (1- [4- (2-hydroxyethoxy) -phenyl] -2-hydroxy-2-methyl-1-propane) -1-one), IRGACURE 127 (2-hydroxy-1- {4- [4- (2-hydroxy-2-methyl-propionyl) -benzyl] phenyl} -2-methyl-propan-1-one}), IRGACURE 907 (2-methyl-1- (4-methylthiophenyl) -2-mol Forinopropan-1-one), IRGACURE 369 (2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1), IRGACURE 379 (2- (dimethylamino) -2-[( 4-methylphenyl) methyl] -1- [4- (4-morpholinyl) phenyl] -1-butanone), DAROCUR TPO (2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide), IRGACURE 819 (bis ( 2,4,6-trimethylbenzoyl) -phenylphosphine oxide), IRGACURE 784 (bis (η5-2,4-cyclopentadien-1-yl) -bis (2,6-difluoro-3- (1H-pyrrole)) 1-yl) -phenyl) titanium), IRGACURE OXE 01 (1.2-octanedione, 1- [4- (phenylthio)-, 2- (O-benzoyloxime)]), IRGACURE OXE 02 (ethanone, 1- [9-ethyl-6- (2-methylbenzoyl) ) -9H-carbazol-3-yl]-, 1- (O-acetyloxime)), IRGACURE 754 (oxyphenylacetic acid, 2- [2-oxo-2-phenylacetoxyethoxy] ethyl ester and oxyphenylacetic acid, 2 -(2-hydroxyethoxy) ethyl ester mixture (above, manufactured by Ciba Japan KK), DETX-S (2,4-diethylthioxanthone) (Nippon Kayaku Co., Ltd. ), Lucirin TPO, LR 8893, LR 8970 (above, manufactured by BASF), Ubekrill P36 (manufactured by UCB), etc. It is.

  The said photoinitiator may be used individually by 1 type, and may be used in combination of 2 or more type.

  Although it is possible to omit the addition of a photopolymerization initiator by using a photopolymerizable compound as the polymerizable compound described above, it is easier to start polymerization by using a photopolymerization initiator. It can be adjusted and is preferred.

(Polymerization inhibitor)
The polymerization inhibitor that can be contained in the ultraviolet curable pigment ink is not particularly limited, and for example, IRGASTAB UV10 and UV22 (manufactured by BASF) can be used. By adding a polymerization inhibitor, the storage stability of the ink composition is improved.

(water)
Water is a main solvent when the ink used in the present embodiment is a water-based ink, and is also included in the adhesive liquid. In order to reduce ionic impurities as much as possible, it is preferable to use pure water such as ion exchange water, ultrafiltration water, reverse osmosis water, or distilled water, or ultrapure water. Further, when water sterilized by ultraviolet irradiation or addition of hydrogen peroxide is used, it is preferable because the generation of mold and bacteria can be prevented when the pigment dispersion and the ink using the same are stored for a long period of time. .

  The main solvent mentioned above refers to the solvent having the highest content among all the solvents in the ink.

(Other additives)
The ink and the adhesive liquid in the present embodiment may further contain a preservative / antifungal agent, a pH adjuster, an antioxidant, an organic solvent other than those described above, a metal trapping agent, and the like as necessary.

  Examples of preservatives and fungicides include sodium benzoate, sodium pentachlorophenol, sodium 2-pyridinethiol-1-oxide, sodium sorbate, sodium dehydroacetate, 1,2-dibenzisothiazolin-3-one ( Proxel-CRL, Proxel-BDN, Proxel-GXL, Proxel-XL2, Proxel-TN) manufactured by Arch Chemicals.

  Examples of the pH adjuster include inorganic alkalis such as sodium hydroxide and potassium hydroxide, ammonia, diethanolamine, triethanolamine, triisopropanolamine, morpholine, potassium dihydrogen phosphate, and disodium hydrogen phosphate.

  Examples of the metal trapping agent include disodium ethylenediaminetetraacetate.

  As described above, according to the present embodiment, the color layer forming ink and the adhesive layer forming adhesive liquid are excellent in ejection stability when ejected from the inkjet head, and the color layer pattern can be obtained with high resolution. It is possible to provide a method for producing a transfer medium that is excellent in transferability and excellent in adhesion after transfer.

[Transfer media]
One embodiment of the present invention relates to a transfer medium 88. The transfer medium 88 can be obtained by performing the manufacturing method of the above embodiment. The transfer medium 88 is provided with a colored layer 81 and an adhesive layer 94 laminated on the base material F in this order, and a protective layer 91, between the base material F and the colored layer 81, if necessary. Alternatively, a release layer 89 is provided, or a release layer 89 and a protective layer 91 are laminated in this order from the substrate F side between the substrate F and the colored layer 81.

  In the transfer medium 88, the thickness of the colored layer 81 is preferably 1 to 10 μm, and more preferably 2 to 5 μm. When the thickness of the colored layer 81 is within the above range, the color developability is excellent. Further, the thickness of the adhesive layer 94 is preferably 0.5 to 5 μm, and more preferably 1 to 3.5 μm. When the thickness of the adhesive layer 94 is within such a numerical range, the adhesiveness is excellent.

  Furthermore, when the transfer medium 88 includes the protective layer 91, the thickness of the protective layer 91 is preferably 10 to 30 nm. When the thickness of the protective layer 91 is within the above range, it is excellent from the viewpoint of not being bulky when the roll-shaped substrate F is used, protecting the colored layer 81, or manufacturing cost of the protective layer 91.

[Transcript]
One embodiment of the present invention relates to a transfer product, and is obtained by transferring from the transfer medium 88 of the above embodiment to a transfer medium. Examples of the transfer material include plastics and metals used in automobile interiors, notebook PC exteriors, mobile phone exteriors, cosmetic containers, stationery, and the like. Examples of the transfer medium (material) include plastics such as acrylic resin, polyester resin, polypropylene resin, and ABS resin, and metals such as nickel, iron, SUS, and titanium.

  EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to only these examples.

[Preparation of aqueous pigment ink A]
An aqueous pigment ink A (hereinafter also simply referred to as “ink A”) for forming a colored layer was prepared.

[Ink A-1]
4 parts by mass of diethylene glycol monobutyl ether (hereinafter also referred to as “DEGmBE”), 1 part by mass of BYK-348 (silicone surfactant, trade name manufactured by Big Chemie), and 30 parts by mass of ion-exchanged water were mixed. The mixture was stirred for 20 minutes at room temperature to obtain a premixed solution. Next, 5 parts by mass of JONCRYL 678 (acrylic water-soluble resin, trade name of BASF, molecular weight 8,500, oxidation 215) as a water-soluble resin, and 0.1 parts by mass of potassium hydroxide (as a pH adjuster) KOH) was added to the premix and stirred at 40 ° C. for 1 hour.

  To this liquid after stirring, 10 parts by mass of carbon black MA100 (trade name, manufactured by Mitsubishi Chemical Corporation) was added to obtain a mixed liquid, and 1 of the mixed liquid was obtained in a desktop sand mill (manufactured by Hayashi Shoten). Along with zirconia glass beads (diameter: 1.5 mm) having a mass of 5 times, the mixture was stirred and dispersed at 2,160 rpm for 2 hours. After dispersion, the mixture was filtered through a 0.1 mm SUS mesh filter to prepare a dispersion.

  In the dispersion, 2-pyrrolidone (hereinafter also referred to as “2-Py”), propylene glycol (hereinafter also referred to as “PG”), and Polysol AM-710 (acrylic resin emulsion, manufactured by Showa Denko KK) as a resin emulsion. Name, average particle diameter 150 nm, active ingredient 50.5 mass%), Proxel-XL2 (preservative, trade name manufactured by Arch Chemicals), and ion-exchanged water are added in the amounts (parts by mass) shown in Table 1, Stir at 40 ° C. for 20 minutes. After stirring, the mixture was filtered through a membrane filter having a diameter of 5 μm to prepare a black ink A-1 having the composition shown in Table 1.

[Ink A-2]
3 parts by mass of DEGmBE, 0.5 parts by mass of BYK-348, and 30 parts by mass of ion-exchanged water were mixed and stirred at room temperature for 20 minutes to obtain a premixed solution. Next, 2 parts by weight of JONCRYL680 (acrylic water-soluble resin, trade name of BASF, molecular weight 4,900, oxidation 215) and 0.1% by weight of KOH are added to this premixed solution as a water-soluble resin. And stirred at 40 ° C. for 1 hour.

  To this liquid after stirring, 5 parts by mass of a cyan pigment (CI Pigment Blue 15: 3, manufactured by DIC) was added to obtain a mixed liquid, and then dispersed under the same conditions as in ink A-1. And filtered to prepare a dispersion.

  In the dispersion, 1,2-hexanediol (hereinafter also referred to as “1,2-HD”), 2-Py, PG, and Polysol AM-2300 (styrene / acrylic resin emulsion, manufactured by Showa Denko KK) as a resin emulsion Name, minimum film-forming temperature (MFT) 70 ° C., average particle size 90 nm, active ingredient 40 mass%), Proxel-XL2, and ion-exchanged water are added in the amounts (parts by mass) shown in Table 1, and then the ink The mixture was stirred and filtered under the same conditions as in A-1 to prepare cyan ink A-2 having the composition shown in Table 1.

[Ink A-3]
3 parts by mass of DEGmBE, 0.8 parts by mass of BYK-348, and 30 parts by mass of ion-exchanged water were mixed and stirred at room temperature for 20 minutes to obtain a premixed solution. Next, 1 part by mass of JONCRYL680 and 0.1% by mass of KOH were added to the premixed solution, and the mixture was stirred at 40 ° C. for 1 hour.

  To this stirred liquid, 4 parts by mass of magenta pigment (CI Pigment Red 122, manufactured by BASF) was added to obtain a mixed liquid, and then dispersed and filtered under the same conditions as in ink A-1. Then, a dispersion was prepared.

  In the dispersion, 1,2-HD, 2-Py, PG, AE373D (carboxy-modified styrene / acrylic resin emulsion, trade name, manufactured by Etec, average particle diameter of 150 nm, active ingredient 50% by mass), Proxel-XL2, and ions Exchange water was added in the amount (parts by mass) shown in Table 1, and then stirred and filtered under the same conditions as in ink A-1, so that magenta ink A-3 having the composition shown in Table 1 was obtained. Prepared.

[Ink A-4]
3 parts by mass of DEGmBE, 0.8 parts by mass of BYK-348, and 30 parts by mass of ion-exchanged water were mixed and stirred at room temperature for 20 minutes to obtain a premixed solution. Next, 2 parts by mass of JONCRYL 680 and 0.1% by mass of KOH were added to this premixed solution, and stirred at 40 ° C. for 1 hour.

  To this liquid after stirring, 4 parts by mass of yellow pigment (CI Pigment Yellow 180, manufactured by Dainichi Seika Kogyo Co., Ltd.) was added to obtain a mixed liquid, and then the same conditions as in ink A-1 were used. Dispersion and filtration were performed to prepare a dispersion.

  In the dispersion, 1,2-HD, 2-Py, PG, Polysol AT860 (acrylic resin emulsion, trade name, Showa Denko, trade name, average particle size 120 nm, Tg 60 ° C., active ingredient 50% by mass) as a resin emulsion, Surfynol 465 (acetylene glycol surfactant, product name manufactured by Air Products and Chemicals Inc.), Proxel-XL2, and ion-exchanged water were added in the amounts (parts by mass) shown in Table 1, and then the ink A-1 was added. The mixture was stirred and filtered under the same conditions as in Example 1 to prepare yellow ink A-4 having the composition shown in Table 1.

[Ink A-5]
1 part by weight of BYK-348, 4.7 parts by weight of Denkapoval H-12 (polyvinyl alcohol, trade name, manufactured by Denki Kagaku Kogyo Co., Ltd., pure content: 94% by weight) as water-soluble resin, and 30 parts by weight of ion-exchanged water Were mixed and stirred at 40 ° C. for 1 hour.
9.5 parts by mass of CR-50 (rutile titanium oxide, trade name, manufactured by Ishihara Sangyo Co., Ltd., TiO ₂ active ingredient 95% by mass, average particle size 0.25 μm) as a pigment is added to the liquid after stirring and mixed. A liquid was obtained, and then dispersed and filtered under the same conditions as in ink A-1, to prepare a dispersion.

  To the dispersion, Takelac W-6061 (polyurethane resin emulsion, trade name, manufactured by Mitsui Chemicals, Inc., solid content 30% by mass), 1,2-HD, 2-Py, PG, Proxel-XL2, And ion exchange water was added in the amount (part by mass) shown in Table 1, and the mixture was stirred at 40 ° C. for 20 minutes. After stirring, the mixture was filtered through a 10 μm diameter SUS mesh filter to prepare a white ink A-5 having the composition shown in Table 1.

  Table 1 summarizes the compositions of the ink A-1 to the ink A-5. In Table 1, “resin EM” means a resin emulsion, and the numerical value represents the converted amount (parts by mass) of the resin component. A blank part means no addition. The amount of ion-exchanged water is the amount of ion-exchanged water contained in the obtained ink.

[Preparation of UV-curable pigment ink B]
An ultraviolet curable pigment ink B (hereinafter also simply referred to as “ink B”) for forming a colored layer was prepared.

[Ink B-1]
14 parts by mass of allyl glycol (monomer, manufactured by Nippon Emulsifier Co., Ltd., hereinafter also referred to as “AG”), and 1.2 parts by mass of Discol N-509 (dispersant, polyoxyalkylene polyalkylene polyamine, Dainichi Seika Kogyo) Product name) and mixed at 40 ° C. for 20 minutes.
6 parts by mass of carbon black MA7 (trade name, manufactured by Mitsubishi Chemical Corporation) was added to the liquid after stirring to obtain a mixed liquid, and 1.5 times the mass of this mixed liquid in a tabletop sand mill (manufactured by Hayashi Shoten) And zirconia glass beads (diameter 1.5 mm) were stirred and dispersed at 2,160 rpm for 2 hours. After dispersion, the mixture was filtered through a 0.1 mm SUS mesh filter to prepare a dispersion.
In the dispersion, N-methyl-2-pyrrolidone (hereinafter also referred to as “NMP”), U-15HA (urethane acrylate oligomer, trade name of Shin-Nakamura Chemical Co., Ltd., weight average molecular weight 2,300), Irgacure 127 and 819 (photopolymerization initiator, trade name manufactured by BASF), Irgastab UV-10 (polymerization inhibitor, trade name manufactured by BASF), BYK-UV3500 (surfactant, trade name manufactured by Big Chemie), and AG (residue) Min) was added in the amount (parts by mass) shown in Table 2 and stirred at room temperature for 1 hour. After stirring, the mixture was filtered through a membrane filter having a diameter of 5 μm to prepare black ink B-1 having the composition shown in Table 2. In addition, among 10 mass parts of photoinitiators in Table 2, Irgacure 127 is 7 mass parts, and Irgacure 819 is 3 mass parts.

[Ink B-2]
Carbon black, which is a colorant, was used as a cyan pigment (CI Pigment Blue 15: 4, manufactured by DIC Corporation), and the composition was as described in Table 2 in the same manner as in the preparation of ink B-1. A dispersion was prepared. In addition, 14 mass parts of AG was added at the time of preparation of this dispersion liquid.
Table 2 shows N-vinylformamide (hereinafter also referred to as “NVF”), U-15HA, Irgacure 127 and 819, Irgastab UV-10, BYK-UV3500, and AG (residue) as monomers in the dispersion. It added by the quantity shown (mass part), and stirred at normal temperature for 1 hour. After stirring, the mixture was filtered through a membrane filter having a diameter of 5 μm to prepare cyan ink B-1 having the composition shown in Table 2. In addition, among 69.8 mass parts of monomers in Table 2, AG is 59.8 mass parts and NVF is 10 mass parts. Further, out of 5 parts by mass of the photopolymerization initiator, Irgacure 127 is 3 parts by mass, and Irgacure 819 is 2 parts by mass.

[Ink B-3]
Dispersion liquid was prepared in the same manner as ink B-1 except that carbon black as a colorant was used as a magenta pigment (CI Pigment Violet 19, manufactured by BASF) and the composition was as shown in Table 2. Was made. In addition, 14 mass parts of AG was added at the time of preparation of this dispersion liquid.
To the dispersion, 2-Py, U-15HA, Irgacure 127 and 819, Irgastab UV-10, BYK-UV3500, AG (residue), and ion-exchanged water were added in the amounts (parts by mass) shown in Table 2. The mixture was stirred at room temperature for 1 hour. After stirring, the mixture was filtered through a membrane filter having a diameter of 5 μm to prepare magenta ink B-3 having the composition shown in Table 2. In addition, Irgacure127 is 2 mass parts among 3 mass parts of photoinitiators in Table 2, and Irgacure819 is 1 mass part.

[Ink B-4]
Carbon black as a colorant was used as a yellow pigment (CI Pigment Yellow 150, manufactured by Wynn Chemical Co.), and dispersed in the same manner as in the preparation of ink B-1, except that the composition was as shown in Table 2. A liquid was prepared. In addition, 14 mass parts of AG was added at the time of preparation of this dispersion liquid.
To the dispersion, 2-Py, U-15HA, Irgacure 127 and 819, Irgastab UV-10, BYK-UV3500, and AG (residue) are added in the amounts (parts by mass) shown in Table 2, and 1 at room temperature. Stir for hours. After stirring, the mixture was filtered through a membrane filter having a diameter of 5 μm to prepare yellow ink B-4 having the composition shown in Table 2. In addition, Irgacure 127 is 3 mass parts among 5 mass parts of photoinitiators in Table 2, and Irgacure 819 is 2 mass parts.

[Ink B-5]
Carbon black, which is a colorant, was used as a cyan pigment (CI Pigment Blue 15: 4, manufactured by DIC Corporation), and the composition was as described in Table 2 in the same manner as in the preparation of ink B-1. A dispersion was prepared. In addition, 14 mass parts of AG was added at the time of preparation of this dispersion liquid.
To the dispersion, NVF, U-15HA, Irgacure 127 and 819, Irgastab UV-10, BYK-UV3500, and AG (residue) were added in the amounts (parts by mass) shown in Table 2, and stirred at room temperature for 1 hour. did. After stirring, the mixture was filtered through a membrane filter having a diameter of 5 μm to prepare light cyan ink B-5 having the composition shown in Table 2. In addition, AG is 34.4 mass parts among 44.4 mass parts of monomers in Table 2, and NVF is 10 mass parts. Moreover, among 5 mass parts of photoinitiators in Table 2, Irgacure 127 is 3 mass parts, and Irgacure 819 is 2 mass parts.

[Ink B-6]
Dispersion liquid was prepared in the same manner as ink B-1 except that carbon black as a colorant was used as a magenta pigment (CI Pigment Violet 19, manufactured by BASF) and the composition was as shown in Table 2. Was made. In addition, 14 mass parts of AG was added at the time of preparation of this dispersion liquid.
To the dispersion, 2-Py, U-15HA, Irgacure 127 and 819, Irgastab UV-10, BYK-UV3500, AG (residue), and ion-exchanged water were added in the amounts (parts by mass) shown in Table 2. The mixture was stirred at room temperature for 1 hour. After stirring, the mixture was filtered through a membrane filter having a diameter of 5 μm, and light magenta ink B-6 having the composition shown in Table 2 was prepared. In addition, Irgacure127 is 2 mass parts among 3 mass parts of photoinitiators in Table 2, and Irgacure819 is 1 mass part.

  The compositions from the ink B-1 to the ink B-6 are summarized in Table 2. In Table 2, the amount of monomer is the amount of monomer contained in the obtained ink. A blank part means no addition.

[Preparation of non-aqueous pigment ink C]
A non-aqueous pigment ink C (hereinafter also simply referred to as “ink C”) for forming a colored layer was prepared.

[Ink C-1]
Cellulose acetate butyrate (butylation rate: 35 to 39% by mass, manufactured by KANTO CHEMICAL CO., INC) 5.0% by mass and diethylene glycol diethyl ether (manufactured by Nippon Emulsifier Co., Ltd.) on a PET film having a thickness of 100 μm ) A resin layer coating solution consisting of 95.0% by mass was applied by spin coating and dried to form a resin layer having a thickness of 10 μm on the PET film. The spin coating method was performed at 500 rpm for 10 seconds and then at 2,000 rpm for 30 seconds. The drying conditions were 100 ° C. for 30 minutes. The thickness of the obtained resin layer was 10 μm.

  Next, an aluminum vapor deposition layer having an average film thickness of 20 nm is formed on the above resin layer using a vacuum vapor deposition apparatus (VE-1010 type vacuum vapor deposition apparatus manufactured by VACUUM DEVICE INC.). Obtained.

  Next, the above laminate was simultaneously peeled, refined and dispersed in diethylene glycol diethyl ether using a VS-150 ultrasonic disperser (manufactured by AS ONE Corporation), and subjected to ultrasonic dispersion treatment time. An aluminum pigment dispersion having an (integrated value) of 12 hours was produced.

  The obtained aluminum pigment dispersion was filtered through a SUS mesh filter having an opening of 5 μm to remove coarse particles. The filtrate was then placed in a round bottom flask and diethylene glycol diethyl ether was distilled off using a rotary evaporator. Thus, the aluminum pigment dispersion was concentrated, and then the concentration of the metallic pigment dispersion was adjusted to obtain an aluminum pigment dispersion having a pigment concentration of 5% by mass.

Using a particle diameter / particle size distribution measuring apparatus (FPIA-3000S manufactured by Sysmex Corporation), a cumulative 50 mass% average particle diameter R50 of equivalent circle diameters obtained from a cumulative curve in which the total area of the aluminum pigment population is 100 mass% is The calculated value was 1.0 μm.
Here, “circle equivalent diameter” means the diameter of a circle having an area equal to the projected area of the substantially flat surface (XY plane) of the tabular grains of aluminum pigment. The “substantially flat surface” means a surface on which the projected area of the tabular grains is maximized. Since the aluminum pigment is produced by crushing the deposited film, it has a substantially flat surface (XY plane) and a substantially uniform thickness (20 nm in this embodiment). went.

  Ink C-1 was prepared with the composition shown in Table 3 using the above aluminum pigment dispersion. In Table 3, “CAB” represents cellulose acetate butyrate, “γ-BL” represents γ-butyrolactone, and “DEGdEE” represents diethylene glycol diethyl ether. In addition, the unit of Table 3 is mass%.

[Preparation of adhesive liquid]
An adhesive liquid for forming an adhesive layer was prepared.

[Adhesive fluid B-1]
1,2-HD, 2-Py, PG, Eritel KA-5071S (Tg 67 ° C.), BYK-348, and ion-exchanged water are mixed as a polyester resin emulsion, stirred at 40 ° C. for 20 minutes, and then a membrane having a diameter of 5 μm. It filtered with the filter and prepared the adhesive liquid B-1 which shows a composition in Table 4.

[Adhesive fluid B-2]
1,2-HD, PG, Eritel KT-8803 (Tg 61 ° C), BYK-348, and ion-exchanged water are mixed as a polyester resin emulsion, stirred at 40 ° C for 20 minutes, and then filtered through a membrane filter with a diameter of 5 µm. Then, an adhesive liquid B-2 having a composition shown in Table 4 was prepared.

[Adhesive fluid B-3]
Diethylene glycol monobutyl ether, 1,2-HD, 2-Py, PG, Eritel KT-9204 (Tg 19 ° C.), BYK-348, Surfynol 465, and ion-exchanged water are mixed as a polyester resin emulsion. After stirring for 5 minutes, it was filtered through a membrane filter having a diameter of 5 μm to prepare an adhesive liquid B-3 having the composition shown in Table 4.

[Adhesive fluid B-4]
1,2-HD, 2-Py, PG, Eritel KT-8701 (Tg 13 ° C.), BYK-348, and ion-exchanged water are mixed as a polyester resin emulsion and stirred at 40 ° C. for 20 minutes, and then a membrane having a diameter of 5 μm. It filtered with the filter and prepared the adhesive liquid B-4 which shows a composition in Table 4.

[Adhesive fluid B-5]
1,2-HD, 2-Py, PG, Eritel KT-8904 (Tg 10 ° C.), BYK-348, and ion-exchanged water are mixed as a polyester resin emulsion, and the mixture is stirred at 40 ° C. for 20 minutes. It filtered with the filter and prepared the adhesive liquid B-5 which shows a composition in Table 4.

[Adhesive fluid B-6]
1,2-HD, 2-Py, PG, polyester resin emulsion KT-0507 (Tg-27 ° C.), BYK-348, and ion-exchanged water are mixed, and the mixture is stirred at 40 ° C. for 20 minutes. It filtered with the filter and prepared the adhesive liquid B-6 which shows a composition in Table 4.

[Adhesive fluid B-7]
1,2-HD, 2-Py, PG, Hitec SN-2002 (Tg 76 ° C.), BYK-348, and ion-exchanged water are mixed as a polyester resin emulsion, and the mixture is stirred at 40 ° C. for 20 minutes. It filtered with the filter and prepared the adhesive liquid B-7 which shows a composition in Table 4.

  Table 4 summarizes the compositions from the adhesive liquid B-1 to the adhesive liquid B-7. In Table 4, “resin EM” means a resin emulsion, and the numerical value represents the converted amount (part by mass) of the resin component. A blank part means no addition.

[Inkjet head discharge preparation]
The ejection experiment using the ink jet head using each ink and each adhesive liquid described above was performed using PX-G5300 (ink jet printer, manufactured by Seiko Epson Corporation), but this experiment limits the present invention. It is not a thing.
Ink was put into the ink cartridges of the respective color inks, and the adhesive liquid was put into the ink cartridges of the gloss optimizer for preparation. Each ink cartridge was mounted on the printer, and the ink jet head was filled. Thereafter, it was confirmed that the ink was discharged from the inkjet head, and printing preparation was performed.

[Evaluation of ejection stability]
The ejection stability of ink and adhesive liquid by an inkjet head was evaluated. In an environment of a temperature of 25 ° C. and a relative humidity of 40 mass% RH, the ink and the adhesive liquid were continuously discharged from the inkjet head. The discharge conditions were a response frequency of 25 kHz, a resolution of 5,760 dpi × 1,440 dpi, an ink droplet weight of 2 ng, and a 100 mass% duty, and so-called solid printing was performed. Here, “duty” is a value calculated by the following equation.
duty (mass%) = actual printing dot number / (vertical resolution × horizontal resolution) × 100
(In the formula, “number of actual printing dots” is the number of actual printing dots per unit area, and “vertical resolution” and “horizontal resolution” are resolutions per unit area, respectively.)
The evaluation criteria are as follows.
A: The missing dot or flying curve did not occur even after 15 minutes, or occurred within 15 minutes but recovered by the cleaning operation.
C: A missing dot or a flying curve occurred within 15 minutes and did not recover even after a cleaning operation.

  The evaluation results were “A” in all inks (A-1 to A-5, B-1 to B-6, C-1) and all adhesive liquids (B-1 to B-7). . Therefore, it was confirmed that both the prepared ink and the adhesive liquid were excellent in ejection stability.

[Preparation of base material for transfer medium]
[Preparation of transfer medium base I]
On a biaxially stretched PET film having a roll width of 600 mm and a thickness of 12 μm, a low density polymerized polyethylene wax (trade name: High Wax 110P, manufactured by Mitsui Chemicals) was applied to a thickness of 20 nm to form a release layer. . Furthermore, a thermosetting melamine resin layer produced from a melamine resin (trade name: Amirac 1000, manufactured by Kansai Paint Co., Ltd.) is applied to a thickness of 10 nm, and then cured by heating at 130 ° C. for 5 minutes to form a protective layer. Base substrate I was prepared.

[Preparation of transfer medium base II]
An acrylic resin (nonvolatile content: 45% by mass, trade name: ACRYDIC A-166, manufactured by DIC Corporation) containing silicone oil is applied to a roll-like biaxially stretched PET film having a width of 600 mm and a thickness of 16 μm to a thickness of 50 nm. Then, it was heated and dried at 150 ° C. for 10 minutes to form a release layer and a protective layer, and a base substrate II of a roll-shaped transfer medium was produced.

[Preparation of base substrate III for bonding media]
A roll-shaped biaxially stretched PET film having a width of 600 mm and a thickness of 38 μm is subjected to a discharge treatment for 3 seconds at a distance of 10 mm using an air plasma APW-602 (Corona treatment machine, product name manufactured by Kasuga Denki Co., Ltd.) The base material III of the transfer medium was produced.

[Production of transfer medium]
[Preparation of transfer medium I-1]
The base material I of the roll-shaped transfer medium is applied to the transfer medium manufacturing apparatus shown in FIG. 1 (however, as shown in FIG. 2, the hot air fan 35 is provided and the second drying unit 50 is not provided). Installed. Then, using a software program for printing, by changing the piezo element drive voltage waveform of the head, the droplet weight is appropriately adjusted in the range of 2 to 10 ng, and the resolution is set to 5,760 dpi × 1,440 dpi. did.

First, a colored layer was formed. Ink from the head of the transfer medium manufacturing apparatus is heated at 50 ° C. from the back surface of the base substrate I by the heater of the platen 34 which is the first drying unit, and further, 40 ° C. hot air is passed through the surface of the base substrate I. The ink was discharged and adhered, and dried under the condition that 65% by mass of the liquid component contained in the ink was evaporated. Thus, a colored layer was formed on the surface of the base substrate I. Thus, an image pattern was formed on the base substrate I of the transfer medium.
In the image pattern composed of the above colored layers, the white ink A-5 is formed on the surface of the image formed by each of the black, cyan, magenta, and yellow inks A-1, 2, 3, and 4. It was made to adhere so that it might cover.

  Next, an adhesive layer was formed. The adhesive liquid B-1 was discharged from the head and adhered onto the colored layer. At that time, the adhesive liquid B-1 was adhered on the ink adhesion portion with a discharge amount of 2 ng at a resolution of 2,880 dpi × 1,440 dpi. Thereafter, it is sent to the second drying unit 50, where the adhesive layer is formed by promoting the evaporation and drying of the ink and the adhesive liquid B-1, while passing warm air of 80 ° C. over the surface of the base substrate I. A transfer medium I-1 was produced. In addition, about the obtained transfer medium I-1, the evaporation amount of the liquid component contained in the ink and the adhesive liquid B-1 was measured from the mass of the base substrate I and the adhesion amounts of the ink and the adhesive liquid B-1. However, it was 97 mass%.

[Preparation of transfer medium I-2]
Except that the adhesive liquid B-2 is used instead of the adhesive liquid B-1 and the liquid component contained in the ink is dried under the condition of evaporating 95% by mass, it is the same as the production of the transfer medium I-1. Thus, a transfer medium I-2 was produced.

[Preparation of transfer medium I-3]
Except that the adhesive liquid B-3 is used instead of the adhesive liquid B-1, and the liquid component contained in the ink is dried under the condition of evaporating 80% by mass, the same as the case of the transfer medium I-1. Thus, a transfer medium I-3 was produced.

[Preparation of transfer medium I-4]
Except that the adhesive liquid B-4 is used instead of the adhesive liquid B-1 and the liquid component contained in the ink is dried under the condition of evaporating 80% by mass, it is the same as the production of the transfer medium I-1. Thus, a transfer medium I-4 was produced.

[Preparation of transfer medium I-5]
Except that the adhesive liquid B-5 is used instead of the adhesive liquid B-1, and the liquid component contained in the ink is dried under the condition of evaporating 80% by mass, the same as the case of the transfer medium I-1. Thus, a transfer medium I-5 was produced.

[Preparation of transfer medium I-6]
Except that the adhesive liquid B-6 is used instead of the adhesive liquid B-1 and the liquid component contained in the ink is dried under the condition of evaporating 80% by mass, it is the same as the case of producing the transfer medium I-1. Thus, a transfer medium I-6 was produced.

[Preparation of transfer medium I-7]
Except for using the adhesive liquid B-7 instead of the adhesive liquid B-1 and further drying it under the condition of evaporating 80% by mass of the liquid components contained in the ink, it is the same as the case of producing the transfer medium I-1. Thus, a transfer medium I-7 was produced.

[Preparation of transfer medium I-8]
A transfer medium I-8 was produced in the same manner as in the production of the transfer medium I-2 except that the liquid component contained in the ink was dried under a condition of evaporating 97% by mass or more.

[Preparation of transfer medium II-1]
The base material II of the roll-shaped transfer medium was mounted on the transfer medium manufacturing apparatus 1b shown in FIG. Then, by changing the piezo element driving voltage waveform of the head using a software program for printing, the droplet mass is appropriately adjusted in the range of 2 to 10 ng, and the resolution is set to 5,760 dpi × 1,440 dpi. did.

First, a colored layer was formed. The heater (heat conduction heating means 141) of the platen 34 as the first fixing unit 140 is heated at 50 ° C. from the back surface of the base substrate II, and further hot air of 40 ° C. is passed through the surface of the base substrate II. Then, ink was ejected from the head of the transfer medium manufacturing apparatus and adhered to the surface of the base substrate II. At the same time, it was dried under the condition that 40% by mass of the liquid component excluding the solid content contained therein was evaporated. Thereafter, the ink was sent to the second fixing unit 150, and the ink adhered to the base substrate II was cured by irradiating with ultraviolet rays, thereby forming a colored layer on the surface of the base substrate II. The ultraviolet irradiation was performed for 10 seconds using a D lamp manufactured by Fusion System as the first to third ultraviolet lamps, with an irradiation intensity of 100 mW / cm ² .

  In this way, an image pattern was formed on the base substrate II of the transfer medium.

  Next, an adhesive layer was formed. First, the base substrate II was returned from the second fixing unit 150 to the first fixing unit 140, and the adhesive liquid B-1 was discharged from the head and adhered. At that time, the adhesive liquid B-1 was adhered on the ink adhesion portion with a discharge amount of 2 ng at a resolution of 2,880 dpi × 1,440 dpi. Thereafter, the platen 34 is kept stationary, and warm air of 80 ° C. is passed over the base substrate II by the warm air fan 35 to form an adhesive layer by promoting evaporation / drying of the adhesive liquid B-1. Transfer medium II-1 was produced.

[Preparation of transfer medium II-2]
Except that the adhesive liquid B-2 is used instead of the adhesive liquid B-1, and the liquid component contained in the ink is dried under the condition of evaporating 70% by mass, it is the same as the production of the transfer medium II-1. Thus, transfer medium II-2 was produced.

[Preparation of transfer medium II-3]
Except for using the adhesive liquid B-3 instead of the adhesive liquid B-1 and further drying it under the condition of evaporating 55% by mass of the liquid components contained in the ink, the same as in the case of producing the transfer medium II-1. Thus, transfer medium II-3 was produced.

[Preparation of transfer medium II-4]
Except for using the adhesive liquid B-4 instead of the adhesive liquid B-1 and further drying it under the condition of evaporating 55% by mass of the liquid components contained in the ink, it is the same as in the production of the transfer medium II-1. Thus, transfer medium II-4 was produced.

[Preparation of transfer medium II-5]
Except for using the adhesive liquid B-5 instead of the adhesive liquid B-1 and further drying it under the condition of evaporating 55% by mass of the liquid components contained in the ink, the same as the case of producing the transfer medium II-1. Thus, transfer medium II-5 was produced.

[Preparation of transfer medium II-6]
Except for using the adhesive liquid B-6 instead of the adhesive liquid B-1 and further drying it under the condition of evaporating 55% by mass of the liquid components contained in the ink, it is the same as the production of the transfer medium II-1. Thus, transfer medium II-6 was produced.

[Preparation of transfer medium II-7]
Except that the adhesive liquid B-7 is used instead of the adhesive liquid B-1, and the liquid component contained in the ink is dried under the condition of evaporating 55% by mass, the same as the case of the transfer medium II-1. Thus, transfer medium II-7 was produced.

[Preparation of transfer medium II-8]
A transfer medium II-8 was produced in the same manner as in the production of the transfer medium II-2 except that the liquid component contained in the ink was dried under the condition of evaporating 80% by mass or more.

[Preparation of transfer medium III-1]
The transfer medium base substrate I was used as a transfer medium.

  The base material I of the roll-shaped transfer medium is applied to the transfer medium manufacturing apparatus shown in FIG. 1 (however, as shown in FIG. 2, the hot air fan 35 is provided and the second drying unit 50 is not provided). Installed. Then, using a software program for printing, by changing the piezo element drive voltage waveform of the head, the droplet weight is appropriately adjusted in the range of 2 to 10 ng, and the resolution is set to 5,760 dpi × 1,440 dpi. did.

  First, a colored layer was formed. Ink from the head of the transfer medium manufacturing apparatus is heated at 70 ° C. from the back surface of the base substrate I by the heater of the platen 34 which is the first drying unit, and further hot air of 80 ° C. is passed through the surface of the base substrate I. And the liquid component contained in the ink C-1 was dried under the condition of evaporating 50% by mass. Thus, a colored layer was formed on the surface of the base substrate I. Thus, an image pattern was formed on the base substrate I of the transfer medium.

  Next, an adhesive layer was formed. The adhesive liquid B-1 was discharged from the head and adhered onto the colored layer. At that time, the adhesive liquid B-1 was adhered on the ink adhesion portion with a discharge amount of 2 ng at a resolution of 2,880 dpi × 1,440 dpi. Thereafter, the platen 34 is stopped and sent to the second drying unit 50, where hot air of 80 ° C. is passed through the surface of the base substrate I, and the evaporation and drying of the ink and the adhesive liquid B-1 are promoted. An adhesive layer was formed to prepare transfer medium III-1. In addition, about the obtained transfer medium III-1, the evaporation amount of the liquid component contained in the ink and the adhesive liquid B-1 was measured from the mass of the base substrate I and the adhesion amount of the ink and the adhesive liquid B-1. However, it was 92 mass%.

[Preparation of transfer medium III-2]
Except that the adhesive liquid B-2 is used instead of the adhesive liquid B-1 and the liquid component contained in the ink is dried under the condition of evaporating 90% by mass, it is the same as the case of producing the transfer medium I-1. Thus, transfer medium III-2 was produced.

[Preparation of transfer medium III-3]
Except that the adhesive liquid B-3 is used instead of the adhesive liquid B-1, and the liquid component contained in the ink is dried under the condition of evaporating 70% by mass, the same as in the production of the transfer medium I-1. Thus, transfer medium III-3 was produced.

[Preparation of transfer medium III-4]
Except that the adhesive liquid B-4 is used instead of the adhesive liquid B-1, and the liquid component contained in the ink is dried under the condition of evaporating 70% by mass, the same as the case of the transfer medium I-1. Thus, transfer medium III-4 was produced.

[Preparation of transfer medium III-5]
Except that the adhesive liquid B-5 is used instead of the adhesive liquid B-1, and the liquid component contained in the ink is dried under the condition of evaporating 70% by mass, it is the same as in the case of producing the transfer medium I-1. Thus, transfer medium III-5 was produced.

[Preparation of transfer medium III-6]
Except that the adhesive liquid B-6 is used instead of the adhesive liquid B-1, and the liquid component contained in the ink is dried under the condition of evaporating 70% by mass, the same as the case of manufacturing the transfer medium I-1. Thus, transfer medium III-6 was produced.

[Preparation of transfer medium III-7]
Except for using the adhesive liquid B-7 instead of the adhesive liquid B-1 and further drying under the condition of evaporating 70% by mass of the liquid components contained in the ink, the same as in the case of producing the transfer medium I-1. Thus, transfer medium III-7 was produced.

[Preparation of transfer medium III-8]
A transfer medium III-8 was produced in the same manner as in the production of the transfer medium III-2 except that the liquid component contained in the ink was dried under the condition of evaporating 95% by mass or more.

[Production of Pasting Medium IV-1]
The base material III of the roll-shaped bonding medium was mounted on the transfer medium manufacturing apparatus shown in FIG. Then, by changing the piezo element driving voltage waveform of the head using a software program for printing, the droplet mass is appropriately adjusted in the range of 2 to 10 ng, and the resolution is set to 5,760 dpi × 1,440 dpi. did.

First, a colored layer was formed. Heating is performed at 50 ° C. from the back surface of the base substrate III by the heater (heat conduction heating means 141) of the platen 34 that is the first fixing unit 140, and hot air of 40 ° C. is passed through the surface of the base substrate III. Then, ink was ejected from the head of the transfer medium manufacturing apparatus and adhered to the surface of the base substrate III. At the same time, it was dried under the condition that 55% by mass of the liquid component excluding the solid content contained therein was evaporated. Thereafter, the ink was sent to the second fixing unit 150, and the ink adhered to the base substrate III was cured by irradiating ultraviolet rays there, thereby forming a colored layer on the surface of the base substrate III. The ultraviolet irradiation was performed for 10 seconds using a D lamp manufactured by Fusion System as the first to third ultraviolet lamps, with an irradiation intensity of 100 mW / cm ² .

  In this way, an image pattern was formed on the base substrate III of the bonding medium.

  Next, an adhesive layer was formed. First, the base substrate III was returned from the second fixing unit 150 to the first fixing unit 140, and the adhesive liquid B-3 was discharged and adhered from the head. At that time, the adhesive liquid B-3 was adhered on the ink adhesion portion with a discharge amount of 2 ng at a resolution of 2,880 dpi × 1,440 dpi. Thereafter, the platen 34 is kept stationary, and warm air of 80 ° C. is passed through the base substrate III by the warm air fan 35 to form an adhesive layer by promoting evaporation / drying of the adhesive liquid B-3. Bonding medium IV-1 was produced.

[Evaluation item]
[Print resolution evaluation]
The printing resolution was evaluated. The evaluation criteria are as follows. The evaluation results are shown in Tables 5 to 8 below.
A: A 5-point image (characters; MS Mincho, full-width hiragana) was also clearly readable.
C: A 5-point image (characters; MS Mincho, full-width hiragana) was unreadable.

[Transferability evaluation 1]
A transfer medium slitted to a width of 100 mm is mounted at a predetermined position of a hot stamping machine R415F-TP (trade name, roll-on type, manufactured by AMAGASAKI MACHINERY Co., Ltd), and the thermocompression roller temperature is 150 ° C. The pressure was 30 kg / cm ² and the speed was 20 cm / sec.
The evaluation criteria are as follows. The evaluation results are shown in Tables 5 to 8 below.
AA: A 4-point image (characters; MS Mincho, full-width hiragana) could be completely transferred.
A: The transfer of the 4-point image (characters; MS Mincho, full-width hiragana) was incomplete, but the 6-point image (characters; MS Mincho, full-width hiragana) could be completely transferred.
C: The transfer of a 6-point image (characters; MS Mincho, full-width hiragana) was incomplete.

[Transferability evaluation 2]
A transfer medium slitted to a width of 100 mm is mounted at a predetermined position of a hot stamping machine R415F-TP (trade name, roll-on type, manufactured by AMAGASAKI MACHINERY Co., Ltd.), and the thermocompression roller temperature is 180 ° C. The pressure was 30 kg / cm ² and the speed was 20 cm / sec.
The evaluation criteria are as follows. The evaluation results are shown in Tables 5 to 8 below.
AA: A 4-point image (characters; MS Mincho, full-width hiragana) could be completely transferred.
A: The transfer of the 4-point image (characters; MS Mincho, full-width hiragana) was incomplete, but the 5-point image characters; MS Mincho, full-width hiragana) could be completely transferred.
B: The transfer of the 5-point image (characters; MS Mincho, full-width hiragana) was incomplete, but the 6-point image (characters; MS Mincho, full-width hiragana) could be completely transferred.
C: Although the transfer of the 6-point image (characters; MS Mincho, full-width hiragana) was incomplete, the 8-point image (characters; MS Mincho, full-width hiragana) was completely transferred.
F: The transfer of an 8-point image (characters; MS Mincho, full-width hiragana) was incomplete.

[Adhesion evaluation]
In accordance with JIS D0202-1988, a cross-cut tape peeling test was performed on the colored layer on the acrylic resin plate transferred in the above transferability evaluation. Cellophane tape (registered trademark) (CT24 [trade name], manufactured by Nichiban Co., Ltd.) was pressed on the colored layer with the belly of the finger and adhered, and then the cellophane tape was peeled off. . It was determined by expressing the number of squares from which the colored layer was peeled out of 100 squares. That is, the case where the colored layer did not peel at all was defined as “0/100”, and the case where the colored layer completely separated was defined as “100/100”. The evaluation criteria are as follows. The evaluation results are shown in Tables 5 to 8 below.
A: It was less than 30/100.
C: 30/100 or more.

[Evaluation of blocking resistance]
Each transfer medium (I, II) on which a colored layer and an adhesive layer were formed to a length of 20 m was wound around a φ3 inch paper tube by a winder. Next, each transfer medium after winding was allowed to stand at 40 ° C. for one week, and the unwinding performance of each transfer medium was evaluated.
Evaluation is made such that an adhesive component such as a polyester resin adheres to the contact surface (PET back surface), and the transfer medium cannot be unwound, or even if unrolled, a colored layer or an adhesive layer remains on the PET back surface. This was performed depending on whether or not a phenomenon (blocking) occurred. The evaluation criteria are as follows. The evaluation results are shown in Tables 5 to 8 below.
A: Not generated.
C: It occurred.

なお、Ｎｏ．IV−１の転写性の評価結果がない理由は、転写フィルムと異なり基材が転写物に残る貼合フィルムとして使ったためである。

In addition, No. The reason why there is no evaluation result of the transferability of IV-1 is that, unlike the transfer film, the base material is used as a bonding film that remains on the transfer.

  From the results of Table 5 to Table 7, the adhesive liquid is an aqueous liquid containing a polyester resin in the form of an emulsion having a glass transition temperature of 10 ° C. or higher and 70 ° C. or lower, more preferably an emulsion having a temperature of 10 ° C. or higher and 60 ° C. or lower. By forming the aqueous liquid containing the polyester resin in the form, the ink for forming the colored layer and the adhesive liquid for forming the adhesive layer are excellent in ejection stability when ejected from the inkjet head, and the pattern of the colored layer is high resolution. It was found that the transfer medium was excellent in transferability, adhesion after transfer, and blocking resistance.

  DESCRIPTION OF SYMBOLS 1a, 1b ... Transfer medium manufacturing apparatus, 10 ... Feeding part, 11 ... Roll medium holder, 20 ... Conveying part, 21 ... First feeding roller, 28 ... Support plate, 30 ... Image forming part, 31 ... Carriage, 32 ... Inkjet head, 33 ... nozzle row, 33a ... first nozzle row, 33b ... second nozzle row, 33c ... third nozzle row, 33d ... fourth nozzle row, 33e ... fifth nozzle row, 33f ... sixth nozzle row, 33g ... seventh nozzle row, 33h ... eighth nozzle row, 34 ... platen, 35 ... warm air fan, 39 ... nozzle forming surface, 40 ... first drying section, 41 ... heat conduction heating means, 42 ... first nichrome Wires 43 ... second feed roller 50 ... second drying unit 51 ... convection heating means 52 ... drying furnace 53 ... control unit 54 ... operation unit 55 ... conveyance motor 56 ... piezoelectric element 63 ... Entrance, 64 ... Exit, 6 ... 3rd feed roller, 70 ... discharge part, 71 ... 4th feed roller, 72 ... 5th feed roller, 73 ... 6th feed roller, 74 ... 7th feed roller, 75 ... take-up roller, 81 ... colored layer, DESCRIPTION OF SYMBOLS 88 ... Transfer medium, 89 ... Release layer, 90 ... Drying apparatus, 91 ... Protective layer, 94 ... Adhesive layer, 130 ... Image forming part, 140 ... First fixing part, 150 ... Second fixing part, 151 ... Ultraviolet irradiation Means 152... UV irradiation device, 190... Fixing portion, A... Transfer region, F .. base material, L .. ink, X.

Claims (4)

A colored layer forming step of forming a colored layer on the substrate by discharging ink from an inkjet head toward the substrate,
An adhesive layer forming step of forming an adhesive layer on the colored layer by discharging an adhesive liquid from an inkjet head toward the colored layer;
Including, and
The ink is an aqueous pigment ink, a non-aqueous pigment ink, or an ultraviolet curable pigment ink,
The adhesive liquid is an aqueous liquid containing a polyester resin in an emulsion form having a glass transition temperature of 10 ° C. or higher and 70 ° C. or lower,
The coloring layer forming step includes evaporating a liquid component contained in the ink ejected and adhered to the base material so as to satisfy the following (1), (2), or (3) A method for manufacturing a medium.
(1) When the ink is an aqueous pigment ink, 65 to 95% by mass of the liquid component contained in the ink is evaporated.
(2) When the ink is a non-aqueous pigment ink, 50 to 90% by mass of the liquid component contained in the ink is evaporated.
(3) When the ink is an ultraviolet curable ink, 40 to 70% by mass of the liquid component contained in the ink is evaporated. The water-based pigment ink or the non-aqueous pigment ink contains a water-soluble organic solvent having a boiling point at 1 atm of 70 ° C. or higher and 250 ° C. or lower,
The method for producing a transfer medium according to claim 1, wherein the water-soluble organic solvent is an aqueous liquid containing at least one selected from the group consisting of lactams, carboxylic acid esters, alkylene glycol ethers, and alcohols. The adhesive liquid contains a water-soluble organic solvent having a boiling point of 70 ° C. or more and 250 ° C. or less at 1 atm,
The method for producing a transfer medium according to claim 1 or 2, wherein the water-soluble organic solvent is an aqueous liquid containing at least one selected from the group consisting of lactams, carboxylic acid esters, alkylene glycol ethers, and alcohols.   The manufacturing method of the transfer medium of any one of Claims 1-3 whose said base material is a metal, a plastics, or paper.

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