JP6089842B2 - Lenticular media with images - Google Patents

Description

The present invention relates to a lenticular media with images.

  Patent Document 1 discloses a light-transmitting base material, a print receiving layer that is fixedly disposed on the back surface of the base material and receives printing ink or toner, and the printing ink or toner received by the print receiving layer. A printed medium comprising: a printed part comprising: an adhesive film fixed to the printed medium so as to cover the printed part; and the adhesive is adhered to an adherend via the adhesive film, In the printed display sheet in which the part is visually recognized from the surface of the base material, the adhesive film has a peelable adhesive layer disposed on the side to be bonded to the adherend, and can be peeled off from the adherend. There is disclosed a printed display sheet characterized in that the printed display sheet can be adhered to the sheet.

  Patent Document 2 discloses an electrophotographic image recording medium having an image receiving layer, a support, and a substrate in this order, wherein the support and the substrate are peelable. It is disclosed.

Patent Document 3 discloses a lenticular lens medium that constitutes a lenticular lens formed by arranging a plurality of semicylindrical or arc-shaped elongated projections, and the volume resistivity value ratio thereof is 1 × 10 ⁷ to 1 × 10 ¹⁴ Ω. Cm and a surface resistivity of 1 × 10 ⁸ to 1 × 10 ¹⁵ Ω / □, the lenticular lens medium is 3 to 100 parts by weight of a hydrophilic polymer (a) made of a graft copolymer, thermoplastic The resin (b) is 0 to 97 parts by weight and comprises a composition comprising 100 parts by weight in total with (a) and 0.1 to 5 parts by weight of an anionic surfactant (c). A lenticular lens medium is disclosed.

JP 2002-169470 A JP 2010-128061 A Japanese Patent No. 4562100

  An object of the present invention is to provide an electrophotographic image recording medium that realizes reuse of an image imparting object (adhesive body) that adheres an image-attached medium having a release substrate peeled from the electrophotographic image recording medium. To do.

The invention according to claim 1
And images an image receiving layer which has been recorded, a support, an adhesive layer comprising a silicone-based adhesive, a release substrate, but are stacked in this order, when the release substrate is peeled, the adhesive An image-attached medium in which the release substrate is peeled from an electrophotographic image recording medium in which a layer remains on the support side, and a lenticular lens in which a plurality of convex portions are arranged are provided on one surface, and the lenticular lens A lenticular medium with an image in which a lenticular medium having the adhesive layer adhered to the back side of the provided surface is laminated.

The invention according to claim 2
2. The lenticular medium with image according to claim 1, wherein a surface resistance value of the image receiving layer is 1.0 × 10 ⁸ Ω / □ or more and 3.2 × 10 ¹³ Ω / □ or less.

The invention according to claim 3
The lenticular medium with an image according to claim 1, wherein the support is white.

The invention according to claim 4
The lenticular medium with an image according to claim 1, wherein the support is transparent.

According to the first aspect of the present invention , the adhesive layer is on the support side when the release substrate is peeled even when the environment changes compared to the case where the adhesive layer is an adhesive layer containing an acrylic adhesive. Thus, a lenticular medium with an image that realizes the reuse of the lenticular medium is obtained.
According to the second aspect of the present invention, compared to the case where the surface resistance value of the image receiving layer is out of the range of 1.0 × 10 ⁸ Ω / □ or more and 3.2 × 10 ¹³ Ω / □ or less, electrophotography When an image is formed by this method, an image-equipped lenticular medium that achieves excellent image formation can be obtained.
According to the invention of claim 3, the lenticular with an image allows the image to be clearly seen when the image formed on the image receiving layer is viewed from the image receiving layer side as compared with the case where a support of a color other than white is applied. A medium is obtained.
According to the invention which concerns on Claim 4, compared with the case where a non-permeable support body is applied, the lenticular medium with an image which implement | achieves the visual recognition from the image provision target object side of the formed image is obtained.

  According to the invention which concerns on Claim 6, the lenticular medium with an image which implement | achieves reuse of a lenticular medium is obtained.

It is sectional drawing which shows an example of the image recording medium for electrophotography which concerns on this embodiment. It is sectional drawing which shows the example which peeled the peeling base material from the image recording medium for electrophotography which concerns on this embodiment. It is a schematic perspective view which shows an example of the lenticular medium which concerns on this embodiment.

  The electrophotographic image recording medium according to this embodiment will be described below.

[Electrophotographic image recording medium]
Hereinafter, a configuration example of an electrophotographic image recording medium will be described in detail with reference to the drawings. However, the configuration of the electrophotographic image recording medium is not limited to the configuration illustrated below.

FIG. 1 is a cross-sectional view showing an example of an electrophotographic image recording medium 100 according to this embodiment. FIG. 2 is a cross-sectional view showing the medium in a state where the peeling substrate 110 is peeled from the electrophotographic image recording medium 100.
An electrophotographic image recording medium 100 shown in FIG. 1 includes a peeling substrate 110, an adhesive layer 120, a support 130, and an image receiving layer 140.
In the electrophotographic image recording medium 100 according to this embodiment, when the peeling substrate 110 is peeled, the adhesive layer 120 remains on the support 130 side (see FIG. 2).

As a method for forming an image on a medium such as an IC card medium or a lenticular medium (hereinafter sometimes collectively referred to as “image-giving object”) and producing an image recording body, for example, a recording medium having an image receiving layer is used. An example is a method in which an image is formed on the image receiving layer, and then the recording medium having the image receiving layer and the image applying object are attached so that the image receiving layer and the surface of the image applying object are in contact with each other. It is done.
However, in the image recording material produced by these methods, an image forming material (for example, toner for developing an electrostatic charge image) adheres on the image application target.
For this reason, when the above-mentioned image imparting object is to be reused, it is necessary to scrape the surface layer in order to remove the image forming material, which is considered to be difficult to reuse.

Therefore, the electrophotographic image recording medium 100 according to the present embodiment has the above-described configuration, and when the image is formed on the image receiving layer 140 and the peeling substrate 110 is peeled off, the image receiving layer 140 to which an image is given. (Hereinafter, the image receiving layer 140 provided with an image may be referred to as an “image receiving layer with image 140”), a support medium 130, and an adhesive medium 120 in which the adhesive layer 120 is laminated in this order, Become.
That is, since the image-added medium 200 has the adhesive layer 120 as the outermost surface layer on the back surface of the surface on which the image is formed, the adhesive layer 120 of the image-added medium 200 is attached to an image application target (not shown). By combining them, an image recording body is obtained.
For this reason, the image recording body is obtained by laminating the image-receiving layer with image 140, the support 130, the adhesive layer 120, and the object to be imaged in this order. The surface of the object does not come into contact with the image formed on the image receiving layer 140.
As a result, even if the object to be imaged is used as a member of the image recording body, without performing the step of scraping the surface layer to remove the image forming material after peeling the image-added medium 200 from the image recording body, It is thought that it can be recovered as an image application object that retains the state before production.

In addition, the adhesive layer 120 of the electrophotographic image recording medium 100 according to the present embodiment is a layer that remains on the support 130 side when the release substrate 110 is peeled and is repeatedly used as the adhesive layer 120. Even when the image-added medium 200 is peeled from the image recording body, it is considered that the adhesive layer 120 remains on the support 130 side, and the adhesive layer 120 does not remain on the image application target side.
As a result, even if the image application object is used as a member of the image recording body, it can be recovered as an image application object that maintains the state before production by peeling the image-added medium 200 from the image recording body. it is conceivable that.

  As described above, the electrophotographic image recording medium 100 according to the present embodiment realizes the reuse of the image imparting target that adheres the image-added medium 200 from which the peeling substrate 110 has been peeled off from the electrophotographic image recording medium 100. .

  Note that “the adhesive layer remains on the support side” specifically indicates that the adhesive layer remains on the support side while maintaining the layer shape.

  In addition to the method of applying the recording medium having the image receiving layer as described above as a method for producing a conventional image recording body, a method of producing an image by directly forming an image on an object to be imaged is exemplified. In the fixing process and transfer process in which an image (for example, a toner image) formed on the image application object is heat-fixed on the image application object, it is necessary to apply heat and pressure. Although deformation and warping tend to occur, when an image recording medium is produced using the electrophotographic image recording medium according to this embodiment, heat and pressure are not applied to the image application object as in the above method. Therefore, it is considered that the occurrence of undulation, deformation, and warpage is suppressed.

  Hereinafter, the configuration and the like of the electrophotographic image recording medium according to the present embodiment will be described in detail. In the following description, reference numerals are omitted.

(Image receiving layer)
The image receiving layer is not particularly limited as long as it contains a thermoplastic resin. Examples of the thermoplastic resin include styrenes such as styrene, vinyl styrene, and chlorostyrene; and mono-types such as ethylene, propylene, butylene, and isobutylene. Olefins; vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, vinyl butyrate; methyl acrylate, ethyl acrylate, butyl acrylate, dodecyl acrylate, octyl acrylate, phenyl acrylate, methyl methacrylate, Esters of α-unsaturated fatty acid monocarboxylic acids such as ethyl methacrylate, butyl methacrylate, dodecyl methacrylate; vinyl ethers such as vinyl methyl ether, vinyl ethyl ether, vinyl butyl ether; vinyl methyl ketone, vinyl hexyl ketone, vinyl Vinyl ketones such as Le isopropenyl ketone; isoprene, 2-diene monomers of chlorobutadiene and the like; and one or two or more polymerized obtained homopolymer or copolymer of the like.

  Of these, styrenes and esters of α-unsaturated fatty acid monocarboxylic acids are preferably used.

Further, as the thermoplastic resin, a polyester resin is desirable because it is used for an image forming material. By including a resin of the same type in the image receiving layer, image formation on the surface of the image receiving layer is possible. The fixability of the material can be controlled appropriately.
In addition, as said polyester resin, you may use silicone modified polyester resin, urethane modified polyester resin, acrylic modified polyester resin, etc. other than general polyester resin. These polyester resins may be used alone or in combination of two or more.

  The polyester is produced by a reaction between a polyvalent hydroxy compound and a polybasic carboxylic acid or a reactive acid derivative thereof. Examples of the polyvalent hydroxy compound constituting the polyester include diols such as ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, neopentyl glycol, and 1,4-butanediol. Bisphenol A alkylene oxide adducts such as hydrogenated bisphenol A, polyoxyethylenated bisphenol A, and polyoxypropylenated bisphenol A; other dihydric alcohols, divalent phenols such as bisphenol A, and the like.

  Examples of the polybasic carboxylic acid include malonic acid, succinic acid, adipic acid, sebacic acid, alkyl succinic acid, maleic acid, fumaric acid, mesaconic acid, citraconic acid, itaconic acid, glutaconic acid, cyclohexanedicarboxylic acid, phthalic acid Examples include acids (isophthalic acid, terephthalic acid), other divalent carboxylic acids, or reactive acid derivatives such as acid anhydrides, alkyl esters, and acid halides. In addition to these divalent hydroxy compounds and carboxylic acids, in order to make the resulting thermoplastic resin non-linear so that tetrahydroxyfuran insoluble matter is not generated, a trivalent or higher polyvalent hydroxyl compound or a trivalent or higher polyvalent compound is used. Basic carboxylic acid may be added.

  Among these, a linear saturated polyester resin obtained by polycondensation at a predetermined composition ratio using phthalic acid as a divalent carboxylic acid and ethylene glycol and neopentyl glycol as polyvalent hydroxy compounds as a polyvalent hydroxy compound is particularly desirable. It is. The composition ratio is such that terephthalic acid and isophthalic acid have a molar ratio of about 1: 1, and ethylene glycol and neopentyl glycol have a molar ratio of 7: 3 to 1: 9. What mixed and polymerized the monovalent | monohydric hydroxy compound by 1: 1 is desirable.

  Further, the resin constituting the image receiving layer may be configured to contain a curable resin such as a thermosetting resin, a photocurable resin, or an electron beam curable resin in order to increase the film strength.

  Further, the image receiving layer may contain a release agent such as a natural wax or a synthetic wax which is a low adhesion material to the fixing member, or a release resin, a reactive silicone compound or a modified silicone oil.

  Specifically, natural wax such as carnauba wax, beeswax, montan wax, paraffin wax, microcrystalline wax, low molecular weight polyethylene wax, low molecular weight oxidized polyethylene wax, low molecular weight polypropylene wax, low molecular weight oxidized polypropylene wax, high grade Synthetic waxes such as fatty acid waxes, higher fatty acid ester waxes, and sazol waxes can be used, and these are not limited to single use but are used in combination.

  In addition, as the releasable resin, a silicone resin, a fluororesin, or a modified silicone resin that is a modified body of a silicone resin and various resins (for example, a polyester-modified silicone resin, a urethane-modified silicone resin, an acrylic-modified silicone resin, a polyimide-modified resin). Silicone resins, olefin-modified silicone resins, ether-modified silicone resins, alcohol-modified silicone resins, fluorine-modified silicone resins, amino-modified silicone resins, mercapto-modified silicone resins, carboxy-modified silicone resins, etc.), thermosetting silicone resins, light A curable silicone resin may be added.

  Furthermore, a reactive silane compound and a modified silicone oil may be mixed as a release agent in order to achieve lower adhesion.

  These waxes and releasable resins may coexist in the form of particles, etc., but are desirably added to the thermoplastic resin, dispersed and compatible with the resin, and incorporated into the thermoplastic resin. It is desirable to use it.

Further, it is desirable to further use a filler for the image receiving layer.
The filler used is not limited, but when it is composed of organic resin particles, specifically, styrenes such as styrene, vinyl styrene and chlorostyrene; monoolefins such as ethylene, propylene, butylene and isobutylene Vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, vinyl butyrate; methyl acrylate, ethyl acrylate, butyl acrylate, dodecyl acrylate, octyl acrylate, phenyl acrylate, methyl methacrylate, methacryl Esters of α-unsaturated fatty acid monocarboxylic acids such as ethyl acetate, butyl methacrylate, dodecyl methacrylate; vinyl ethers such as vinyl methyl ether, vinyl ethyl ether, vinyl butyl ether; vinyl methyl ketone, vinyl hexyl ketone Vinyl ketones such as vinyl isopropenyl ketone; isoprene, 2-chlorobutadiene and the like by polymerizing one or more diene monomers obtained homopolymer or copolymer are exemplified.

  Among these, styrenes, esters of α-unsaturated fatty acid monocarboxylic acids, etc. are preferable. When these thermoplastic resins are used as fillers, gloss control is achieved by coating with a solvent that does not dissolve these resins. Used as a filler constituting the layer. Desirably, a crosslinking agent or the like is added to these heat-meltable resins to form particles of the thermosetting resin having a crosslinked structure, the thermosetting resin, the photocurable resin, or the electron beam curable resin described above. Is more preferably used.

  When the filler is composed of inorganic particles, specific examples include mica, talc, silica, calcium carbonate, zinc white, halocyto clay, kaolin, hydrochloric magnesium carbonate, quartz powder, titanium dioxide, sulfuric acid. Examples include barium, calcium sulfate, and alumina.

As the shape of the filler, spherical particles are generally used, but may be a plate shape, a needle shape, or an indefinite shape.
The volume average particle diameter of the filler is preferably 0.1 μm or more and 30 μm or less, but considering the image receiving layer thickness, it is preferably 1.2 times or more the image receiving layer thickness.

  The mass ratio (filler: binder) between the filler and the binder (resin component) in the image receiving layer is preferably in the range of 0.01: 100 to 15: 100, and 0.5: 100 to More preferably in the range of 5: 100.

As the filler, inorganic particles other than those described above (for example, SiO ₂ , Al ₂ O ₃ , talc or kaolin) and bead-shaped plastic powder (for example, cross-linked PMMA, polycarbonate, polyethylene terephthalate, polystyrene) may be used in combination.

(Support)
Next, the support will be described.
A plastic film is desirably used as the support.
In response to the fact that polyvinyl chloride, which has been used as a lenticular medium material, is not good for the environment as a dioxin generated by combustion at the time of disposal of combustibles, plastic films are no longer used. The
In the present embodiment, considering the use of a support containing no chlorine, further materials such as polystyrene resin film, ABS resin film, AS (acrylonitrile-styrene) resin film, PET film, polyethylene, polypropylene, etc. A film in which a hot-melt adhesive such as polyester or EVA is added to a polyolefin resin film is also preferably used.

  Specifically, as a plastic film, it is a light transmissive film used as an OHP film, polyacetate film, cellulose triacetate film, nylon film, polyethylene terephthalate film, polyethylene naphthalate film, polycarbonate film, polysulfone film, There are polystyrene film, polyphenylene sulfide film, polyphenylene ether film, cycloolefin film, polypropylene film, cellophane, ABS (acrylonitrile-butadiene-styrene) resin film, among them, polyethylene naphthalate film, polyethylene terephthalate film, polyphenylene sulfide. A film is desirably used.

  Although the manufacturing method of a support body is not specifically limited, Well-known methods, such as a co-extrusion method and a bonding method, are utilized.

  In general, when co-extrusion is performed, a longitudinal stretching process is performed, stretching is performed between two or many rolls having different peripheral speeds, and the film is wound after being adjusted to a target film thickness. In the case of biaxial stretching, the film that has passed through the above process is introduced into the tenter as it is, and stretched 2.5 times or more and 5 times or less in the width direction. A desirable stretching temperature at this time is in a range of 100 ° C. or more and 200 ° C. or less.

  The biaxially stretched film thus obtained is subjected to heat treatment as necessary. The heat treatment is desirably performed in a tenter, and a film having a low heat shrinkage rate can be obtained by performing heat treatment particularly while relaxing in the vertical and horizontal directions. A biaxially stretched film is particularly desirable as the support.

More preferably, one of the supports is subjected to a releasability treatment.
As these releasability treatments, surface treatment of a releasable material is generally performed. The releasable material is not particularly limited, but a silicon-based material is desirable. These silicon-based materials are condensate resins containing at least a silane-based composition, or a mixed composition of these and a colloidal silica dispersion. Further, it is desirable to further contain an organic resin.

  The silane composition is specifically an organic silicon compound, such as a silane compound, a fluorine-containing silane compound, and an isocyanate silane compound, and these undergo a condensation reaction to form a resin composition.

Silane compounds include Si (OCH ₃ ) ₄ , CH ₃ Si (OCH ₃ ) ₃ , HSi (OCH ₃ ) ₃ , (CH ₃ ) ₂ Si (OCH ₃ ) ₂ , CH ₃ SiH (OCH ₃ ) ₂ , C _{6 H 5 Si (OCH 3)} 3, Si (OC 2 H 5) 4, CH 3 Si (OC 2 H 5) 3, (CH 3) 2 Si (OC 2 H 5) 2, H 2 Si (OC 2 H ₅ ) ₂ , C ₆ H ₅ Si (OC ₂ H ₅ ) ₃ , (CH ₃ ) ₂ CHCH ₂ Si (OCH ₃ ) ₃ , CH ₃ (CH ₃ ) ₁₁ Si (OC ₂ H ₅ ) ₃ , CH ₃ Alkoxysilanes such as (CH ₂ ) ₁₅ Si (OC ₂ H ₅ ) ₃ and CH ₃ (CH ₂ ) ₁₇ Si (OC ₂ H ₅ ) ₃ ; Silazanes such as (CH ₃ ) ₃ SiNHSi (CH ₃ ) ₃ ; _((CH 3) SiN _{) 2 CO, tert-C 4} H 9 (CH 3) 2 special silylating agent such as SiCl; silane coupling agent; and _{HSC 3 H 6 Si (OCH 3} ) silane compounds such as _3; and these hydrolysis Products and partial condensates.

  Examples of the silane coupling agent include vinyl silanes such as vinyltris (2-methoxyethoxy) silane, vinyltriethoxysilane, and vinyltrimethoxysilane; acrylic silanes such as 3-methacryloxypropyltrimethoxysilane; 2- (3,4 -Epoxycyclohexyl) Epoxysilanes such as ethyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane; N-2- (aminoethyl) -3-aminopropylmethyldimethoxysilane, 3-aminopropyltriethoxysilane, Examples include aminosilanes such as N-phenyl-3-aminopropyltrimethoxysilane;

As fluorine-containing silane compounds, for example, CF ₃ (CH ₂ ) ₂ Si (OCH ₃ ) ₃ , C ₆ F ₁₃ C ₂ H ₄ Si (OCH ₃ ) ₃ , C ₇ F ₁₅ CONH (CH ₂ ) ₃ Si (OC ₂ H ₅ ) ₃ , C ₈ F ₁₇ C ₂ H ₄ Si (OCH ₃ ) ₃ , C ₈ F ₁₇ C ₂ H ₄ SiCH ₃ (OCH ₃ ) ₂ , C ₈ F ₁₇ C ₂ H ₄ Si (ON _{= C (CH 3) (C} 2 H 5)) 3, C 9 F 19 C 2 H 4 Si (OCH 3) 3, C 9 F 19 C 2 H 4 Si (NCO) 3, (NCO) 3 SiC 2 _{H 4 C 6 F 12 C 2} H 4 Si (NCO) 3, C 9 F 19 C 2 H 4 Si (C 2 H 5) (OCH 3) 2, (CH 3 O) 3 SiC 2 H 4 C 8 F _{16 C 2 H 4 Si (OCH} 3) 3, (C _{3 O) 2 (CH 3)} SiC 9 F 18 C 2 H 4 Si (CH 3) (OCH 3) a fluorine-containing silane compounds such as _2, and silane compounds exemplified such as these hydrolyzate or partial condensate thereof Is done.

As isocyanate silane compounds, (CH ₃ ) ₃ SiNCO, (CH ₃ ) ₂ Si (NCO) ₂ , CH ₃ Si (NCO) ₃ , vinylsilyltriisocyanate, C ₆ H ₅ Si (NCO) ₃ , Si ( _{NCO) 4, C 2 H 5} OSi (NCO) 3, C 8 H 17 Si (NCO) 3, C 18 H 37 Si (NCO) 3, (NCO) 3 SiC 2 H 4 (NCO) 3 , etc. are exemplified The

  Examples of the condensate resin of the silane-based composition include curable silicone resins such as thermosetting (condensation type and addition type) and photo-curable silicone resins. Specific examples are as follows. become.

  Among the thermosetting silicone resins, the condensation type curable silicone resin is composed of a polysiloxane such as polydimethylsiloxane having a silanol group at the terminal as a base polymer and blended with polymethylhydrogensiloxane as a cross-linking agent. A curable silicone resin synthesized by heat condensation in the presence of an organic acid metal salt such as a tin catalyst or amines, or a polydiorganosiloxane having a reactive functional group such as a hydroxyl group or an alkoxy group is reacted. Examples thereof include curable silicone resins synthesized in this manner, and polysiloxane resins synthesized by condensing silanol obtained by hydrolyzing a trifunctional or higher functional chlorosilane or a mixture of these with a 1,2-functional chlorosilane.

  The condensed type is classified into a solution type and an emulsion type in terms of form, and any of them is preferably used.

  Among the thermosetting silicone resins, the addition type curable silicone resin is based on platinum containing polysiloxane such as polydimethylsiloxane containing vinyl groups and polydimethylhydrogensiloxane as a cross-linking agent. Examples thereof include curable silicone resins synthesized by reaction and curing in the presence of a catalyst.

  The addition type is classified into a solvent type, an emulsion type, and a solventless type in terms of form, and any of them is preferably used.

  Examples of the thermosetting silicone resin obtained by the above condensation type and addition type curing include, for example, pure silicone resin, silicone alkyd resin, silicone epoxy resin, silicone polyester resin, silicone acrylic resin, silicone phenol resin, silicone urethane resin, silicone A melamine resin etc. are mentioned suitably.

  Examples of the photocurable silicone resin include a curable silicone resin synthesized using a photocationic catalyst and a curable silicone resin synthesized using a radical curing mechanism. Moreover, the modification | denaturation obtained by carrying out photocuring reaction of the low molecular weight polysiloxane which has a hydroxyl group or an alkoxy group etc. couple | bonded with the silicon atom, and an alkyd resin, a polyester resin, an epoxy resin, an acrylic resin, a phenol resin, a polyurethane, or a melamine resin. Silicone resin is desirably used. These may be used individually by 1 type and may use 2 or more types together.

Note that the electrophotographic image recording medium according to the present embodiment is an electrophotographic image recording medium in which the skin color of a person appears clear when the formed image is viewed from the adhesive layer side because the support is white. It is thought that it becomes.
Further, it is considered that the electrophotographic image recording medium according to the present embodiment realizes visual recognition of the formed image from the adhesive layer side because the support is transparent.
In the present embodiment, “being transparent” means that the light transmittance may be 60% or more (a value measured in a portion where no image forming portion exists).
In addition, the “light transmittance” in the present embodiment means a total light transmittance measured using a spectrophotometer or a color meter also having a photometer function and using 550 nm light.

(Adhesive layer)
The pressure-sensitive adhesive layer is a layer remaining on the support side when the peeling substrate is peeled off.
Examples of the method for leaving the adhesive layer on the support side include various methods. For example, (1) a method of increasing the adhesiveness with the adhesive layer by performing a surface treatment on the surface of the support that contacts the adhesive layer, (2) A method of making the surface of the adhesive layer in contact with the release substrate low-viscosity and making the surface in contact with the support of the adhesive layer the other surface highly adhesive, (3) surface of the release substrate in contact with the adhesive layer And (4) a method of directly applying an adhesive layer to a support, and the like.
The methods (1) to (4) may be carried out singly or in combination.

In the method (1), specific examples of the surface treatment performed on the support include the following treatments.
There are a method in which a strong oxidizing agent such as ozone is sprayed to form a hydroxyl group or a carboxyl group on the surface, thereby improving the adhesion to the adhesive layer resin, and a method of treating with various coupling agents.

In the method of (2) above, as a method for making one surface of the adhesive layer low adhesive and making the other surface highly adhesive, for example, the adhesive layer is made of a silicone-based or fluorine-based adhesive and a release substrate. There are a method of forming a layer using an acrylic adhesive on the surface in contact with the surface and a method of adding a non-adhesive additive to the adhesive layer on the surface in contact with the release substrate.
In addition, as such an adhesive layer, specifically, both surfaces manufactured by 3M Co., which are described later, include an adhesive layer to be peeled containing elastic globules and a highly adhesive layer not containing elastic globules. A method using an adhesive film, product number: Y-9415PC is mentioned.

In the above method (3), specifically, as a method of surface treatment to be performed on the release substrate, for example, a method of coating a silicone-based cured resin or a fluorine-based cured resin, a non-adhesive to the aforementioned adhesive layer The method of adding an additive is mentioned.
Moreover, for example, a method of providing a release layer on the surface of the release substrate that is in contact with the adhesive layer can be mentioned.
Specific examples of the release layer include a layer containing the release agent described above.

  Among the above (1) to (4), by (2) making the surface of the adhesive layer in contact with the release substrate low adhesive, and making the surface of the adhesive layer in contact with the support high in the other surface, A method of leaving the adhesive layer on the support side is desirable.

An adhesive layer is a layer containing the adhesive mentioned later, for example, and it is good to have peelability. In order to obtain a peelable adhesive layer, for example, a peelability-imparting component described later may be included.
In addition, it becomes easy to control peeling strength to the range which the adhesion layer contains later and the peelability provision component according to the objective in the range mentioned later.

-Adhesive-
Examples of the pressure-sensitive adhesive include a pressure-sensitive adhesive polymer that exhibits pressure-sensitive adhesive properties at room temperature (for example, 25 ° C.).
The pressure-sensitive adhesive (adhesive polymer) is obtained, for example, by polymerization using a mixed monomer containing a target starting monomer. The polymerization method is a usual method such as solution polymerization, bulk polymerization, emulsion polymerization and the like.
In addition, the compression elastic modulus of the adhesive is preferably 1 × 10 ⁴ dyne / cm ² or more and 1 × 10 ⁸ dyne / cm ² (1 kPa or more and 10 MPa or less).

Specific examples of pressure-sensitive adhesives include acrylic pressure-sensitive adhesives (acrylic polymers), nitrile-butadiene copolymers (NBR, etc.), styrene-butadiene copolymers (SBR, etc.), non-crystalline polyurethane, silicone -Based adhesives (silicone-based polymers) and the like, and silicone-based adhesives, acrylic-based adhesives, and fluorine-based adhesives are desirable, and silicone-based adhesives are more desirable.
The pressure-sensitive adhesive is composed of one kind of these polymers or a mixture of two or more kinds.

The image recording medium for electrophotography according to this embodiment includes a silicone-based pressure-sensitive adhesive in the pressure-sensitive adhesive layer, so that even when the environment fluctuates, the pressure-sensitive adhesive layer is on the support side when the peeling substrate is peeled off. It is considered that the remaining electrophotographic image recording medium is realized.
This is thought to be because the peelability of the pressure-sensitive adhesive layer containing the silicone-based adhesive is maintained. The reason for this is that the pressure-sensitive adhesive layer containing the silicone-based adhesive tends to be less sticky. There is also a reason that this low tackiness tends to be maintained by suppressing a change in tackiness due to environmental changes such as a temperature change.
In addition, it is considered that the electrophotographic image recording medium according to the present embodiment is less likely to cause a zipping phenomenon (discontinuous peeling) when the adhesive layer contains a silicone adhesive.

Specific examples of the silicone pressure-sensitive adhesive include a slightly pressure-sensitive type silicone pressure-sensitive adhesive manufactured by Shin-Etsu Chemical Co., Ltd.
Among these, X-40-3270 having excellent heat resistance and X-40-3306 of ultra-adhesive type are desirable, and ultra-adhesive type is desirable.

−Peelability imparting component−
Examples of the peelability-imparting component include cross-linking agents, elastic globules, and crystalline polymers.
As a specific method, a method of using a relatively large amount of a crosslinking agent, crosslinking the pressure-sensitive adhesive, and increasing the cohesive force of the pressure-sensitive adhesive layer can be mentioned. Moreover, the method of using the elastic small sphere as a peelability provision component and providing the convex part which elastically deforms including an elastic small sphere in the adhesion layer is mentioned. Furthermore, a crystalline polymer is used as a peelability-imparting component, and the tack (adhesive strength) of the pressure-sensitive adhesive layer is controlled to be low, or heat peelability is imparted to the pressure-sensitive adhesive layer.
Hereinafter, a method of suitably combining a pressure-sensitive adhesive and a peelability-imparting component to impart peelability to the pressure-sensitive adhesive will be described in detail later.

First, a method for imparting peelability to the adhesive layer with a crosslinking agent will be described.
As the crosslinking agent, a polyfunctional isocyanate compound, an epoxy compound, a bisamide-based crosslinking agent, or the like is used. These react with a crosslinkable functional group such as a carboxyl group of the pressure-sensitive adhesive or a hydroxyl group contained in accordance with the purpose, thereby cross-linking the pressure-sensitive adhesive and acting to enhance the peelability. The polyfunctional isocyanate compound was synthesized from, for example, a starting material containing one or more diisocyanates selected from isophorone diisocyanate, MDI (diphenylmethane diisocyanate), hydrogenated MDI, and 1,6-hexanediol diisocyanate. Things are used. For example, (A) a compound obtained by urethanation reaction of triol (1,1,1-trimethylolpropane and the like) and the above diisocyanate, or (B) a biuret structure obtained by reacting the above diisocyanates or A compound having an isocyanurate structure is used. In order to adjust the NCO equivalent, a crosslinking agent obtained by reacting the above compound with a diol such as polycaprolactone diol may be used.

  As the epoxy compound, for example, a bisphenol A type epoxy compound, a bisphenol F type epoxy compound, a cresol novolac type epoxy compound, a phenol novolac type epoxy compound, or the like is used. The epoxy equivalent of the epoxy compound is preferably 70 or more and 400 or less, and more preferably 80 or more and 300 or less. As the bisamide-based crosslinking agent, for example, a bisaziridine derivative of a dibasic acid such as isophthaloylbis (2-methylaziridine) is used. Bisamide-based crosslinking agents are particularly desirable in that they can react with a pressure-sensitive adhesive having a carboxyl group at a relatively low temperature to easily obtain a sufficient crosslinking density.

  When using a crosslinking agent as described above and providing the peelability to the adhesive layer without using other peelability-imparting components, the content of the crosslinking agent is 1 part by mass or more and 5 parts by mass with respect to 100 parts by mass of the adhesive. It is 1.2 parts by mass or less, preferably 4 parts by mass or less. When elastic globules and crystalline polymers were not included, the adhesive layer peelability was increased by using a relatively large amount of the crosslinking agent in this way, and the measurement was performed at a peel rate of 300 mm / min and a peel angle of 180 °. It is particularly easy to control the peel strength with respect to the aluminum plate surface to a target range (0.2 N / 25 mm or more and 10 N / 25 mm or less). In addition, when there is too much amount of crosslinking agents, there exists a possibility that adhesive force may fall, and when too small, there exists a possibility that peelability may fall.

A method for imparting peelability to the adhesive layer with elastic spheres will be described.
The peelability of the pressure-sensitive adhesive layer is imparted by forming a pressure-sensitive adhesive layer from an adhesive composition (pressure-sensitive adhesive composition) containing a pressure-sensitive adhesive and elastic spheres.
This is because the elastically deforming convex portions including elastic globules formed on the pressure-sensitive adhesive surface of the pressure-sensitive adhesive layer effectively act to lower the peeling strength at the time of peeling. For example, Japanese Patent Application Laid-Open No. 6-505763 (International Patent Publication WO92 / 13924) discloses a pressure-sensitive adhesive (adhesive) containing a composition containing hollow elastic spheres and an acrylic adhesive. ing. Japanese Patent Application Laid-Open No. 4-306281 contains a solid, sticky elastic sphere and an acrylic adhesive latex, and the elastic sphere has a relatively large amount of latex (for example, 2.5). The pressure-sensitive adhesive contained therein is disclosed.

Furthermore, International Patent Publication No. WO98 / 15298 is an article comprising an adhesive layer fixed to at least one main surface of a substrate, the adhesive layer comprising a matrix containing an adhesive, An adhesive article is disclosed, characterized in that it comprises a composition comprising a plurality of solid elastic globules having adhesiveness. Also, International Patent Publication WO 96/14094 discloses an adhesive article having a relatively light peel strength (adhesive force) using acrylate rubber-based elastic pressure-sensitive adhesive spheres. On the other hand, Japanese Patent Application Laid-Open No. 8-113768 has an adhesive layer including a coating layer of an adhesive composition on the surface of a substrate, and the adhesive composition contains a pressure-sensitive adhesive and elastic spheres, The elastic sphere has an elastic modulus of 1 × 10 ⁴ dyne / cm ² or more and 1 × 10 ⁷ dyne / cm ² (1 kPa or more and 1 MPa or less) and a particle size (volume average diameter) of 10 μm or more and 100 μm or less. An adhesive film (adhesive film) is disclosed.

In the electrophotographic image recording medium according to the present embodiment, the adhesive layer may be formed by containing an adhesive composition disclosed in these publications or a composition obtained by improving such an adhesive composition. .
Preferable examples include the adhesive composition disclosed in the above-mentioned Japanese Patent Application Laid-Open No. 8-113768, or an adhesive composition obtained by improving the composition. The elastic modulus and particle size of the elastic spheres are controlled within the optimal range, air bubble removal is good, air bubbles are not trapped when adhering to the adherend, and the adhesive is not attached to the adherend when peeling. This is because it is desirable not to remain.

The elastic spheres used to form the elastic sphere-containing type adhesive layer are produced by a known synthesis method such as suspension polymerization, emulsion polymerization, seed polymerization or the like.
For example, small spheres containing an acrylic polymer are produced by suspension polymerization as follows. First, deionized water, acrylic monomer, radical polymerization initiator, and other desired additives are placed in a reactor equipped with a mechanical stirrer and mixed well. For example, the polymerization reaction of the monomer component is started by heating to the target temperature while stirring and mixing in a state where the inside of the reactor is purged with an inert gas. The stirring speed is 10 RPM or more and 700 RPM or less, and the reaction temperature is 30 ° C. or more and 120 ° C. or less. Moreover, reaction time is several hours or more and tens of hours or less.

  As the acrylic monomer, alkyl (meth) acrylate (for example, isooctyl acrylate, 2-ethylhexyl acrylate, isononyl acrylate, etc.) and an acrylic unsaturated acid (for example, acrylic acid, methacrylic acid, itaconic acid, maleic acid, etc.) A mixture with is used. The (mass) ratio of alkyl acrylate to acrylic unsaturated acid contained in this mixture is in the range of 99: 1 to 90:10, preferably 95: 5 to 91: 9. Alternatively, a bifunctional crosslinking component such as 1,4-butanediol diacrylate or divinylbenzene may be added to the mixture to crosslink the acrylic polymer.

The elastic modulus of the elastic sphere is represented by a compressive elastic modulus, and is preferably in the range of 1 × 10 ⁴ dyne / cm ^{2 to} 1 × 10 ⁷ dyne / cm ² .
In addition, the compression elastic modulus in this embodiment is measured at 20 degreeC using a viscoelasticity measuring apparatus (Rheometrics company make, model number: RSAII, a product name: Viscoelasticity spectrometer).
Specifically, while giving a compressive strain at a frequency of 1 rad / sec, the temperature was changed in the range of −80 ° C. to 150 ° C., the temperature dependence of the elastic modulus was measured, and the compression elastic modulus was measured with the measured value at 20 ° C. And

  The particle diameter of the elastic sphere is represented by a volume average diameter, and examples thereof include the above-described range (10 μm or more and 100 μm or less). The volume average diameter is a value determined by measuring 1,000 small spheres using an image processing apparatus using an optical microscope and applying the measured value to the following equation (1).

Volume average diameter [μm] = Σ (di4 · ni) / Σ (di3 · ni) (1)
[Wherein, di is the diameter (μm) of the i-th size of the small sphere, and ni is the number of small spheres having the diameter di. ]

The ratio of the elastic globules contained in the adhesive layer is 30 parts by mass or more and 900 parts by mass or less with respect to 100 parts by mass of the adhesive. In the adhesive layer, it is desirable that the elastic spheres form a cluster. The coating weight of the adhesive composition when forming the adhesive layer by applying the adhesive composition is preferably in the range of 4 g / m ^{2 to} 40 g / m ² . The thickness of the adhesive layer is preferably applied so as to be 20% by mass or more and 90% by mass or less of the volume average diameter of the elastic spheres.

In addition, an adhesive composition may contain the crosslinking agent for bridge | crosslinking an adhesive and elastic globules, adhesives, and elastic globules.
The content of the crosslinking agent is preferably 0.05 parts by mass or more and 5 parts by mass or less with respect to 100 parts by mass in total of the pressure-sensitive adhesive and the elastic spheres. On the other hand, you may use a commercially available double-sided adhesive film provided with such an elastic small ball content type adhesion layer. Specific examples of this commercially available product include a double-sided adhesive film manufactured by 3M, product number: Y-9415PC. This double-sided adhesive film includes an adhesive layer to be peeled containing elastic globules and a high adhesive layer not containing elastic spheres.

Next, a method for imparting peelability to the adhesive layer with a crystalline polymer will be described.
The crystalline polymer is used in combination with a pressure-sensitive adhesive, thereby controlling the tackiness of the pressure-sensitive adhesive surface of the pressure-sensitive adhesive layer to a low level or imparting heat peelability to the pressure-sensitive adhesive layer.
As an adhesive composition combining this pressure-sensitive adhesive and a crystalline polymer, for example, US Pat. No. 5,192,612 (corresponding to Japanese Patent No. 3021646), pressure sensitive adhesive basic resin (acrylic polymer etc.) A pressure-sensitive adhesive containing an adhesive), a detackifying resin and detackifying particles is disclosed. As a specific and preferable example of the detackifying resin, linear polycaprolactone having a molecular weight of 3,000 to 342,000 is disclosed. Polycaprolactone is a crystalline polymer that exhibits non-adhesiveness at room temperature (for example, 15 ° C. or higher and 30 ° C. or lower). The pressure-sensitive adhesive is pressed and bonded to the adherend at normal temperature (for example, 15 ° C. or higher and 30 ° C. or lower). On the other hand, the detackifying resin as described above cooperates with the detackifying particles to effectively reduce the tackiness of the adhesive surface at normal temperature (for example, 15 ° C. or higher and 30 ° C. or lower) and improve the peelability. . The detackifying particles are inorganic particles such as silica.

On the other hand, US Pat. No. 5,412,035 (corresponding to JP-A-6-510548) discloses a pressure-sensitive adhesive composition that becomes a pressure-sensitive adhesive at at least one temperature in the range of 20 ° C. to 40 ° C. An adhesive composition (pressure-sensitive adhesive) that is easily peelable by heat and comprises a polymer pressure-sensitive adhesive component (that is, a pressure-sensitive adhesive) and a crystalline polymer is disclosed. The crystalline polymer is non-tacky at room temperature (for example, 15 ° C. or higher and 30 ° C. or lower) and has good compatibility with the polymer pressure-sensitive adhesive component.
The melting temperature of the crystalline polymer itself is Tm ° C., and the melting temperature Ta ° C. of the crystalline polymer is lower than Tm when measured in the composition. In this composition, the peel strength P2 [g / cm] at a certain temperature higher than Ta is smaller than the peel strength P1 [g / cm] at a certain temperature lower than Ta, and the thermal peelability is easy. Have

  The above publication does not disclose the use of polycaprolactone as the crystalline polymer or the use of crystalline polyurethane having a crystalline polyol unit such as polycaprolactone in the main chain molecule. However, a crystalline polymer containing polycaprolactone or crystalline polyurethane having a crystalline polyol unit in the main chain molecule, and an adhesive compatible with the crystalline polymer at a temperature equal to or higher than the melting temperature of the crystalline polymer And an adhesive composition formed by crosslinking the pressure-sensitive adhesive exhibits better ease of thermal peeling than conventional ones.

Preferable examples of the pressure-sensitive adhesive that is compatible with the polycaprolactone and the crystalline polyurethane include, for example, the following acrylic polymers.
That is, (A) (meth) acrylic monomer having a hydroxy group in the molecule, (B) (meth) acrylic monomer having a phenyl group in the molecule, and (C) (meth) acrylic having a carboxyl group in the molecule. It is an acrylic polymer obtained by polymerizing a monomer and (D) a mixed monomer comprising an alkyl acrylate having an alkyl group having 4 to 10 carbon atoms. The above components (A) and (B) are essential for enhancing the compatibility of the pressure-sensitive adhesive with the crystalline polymer. The component (C) is essential for crosslinking the pressure-sensitive adhesive using the above-mentioned crosslinking agent. Moreover, the said (D) component implement | achieves maintenance of the adhesive force (peeling strength) of the adhesive composition with respect to an image provision target object until it heats and heat peelability is expressed.

  Examples of the pressure-sensitive adhesive used in this case include a monomer mixture formed by combining the acrylic monomers described above, and the pressure-sensitive adhesive is prepared by copolymerization by a known method such as solution polymerization. For example, as the (meth) acrylic monomer having a hydroxy group in the molecule (A), 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxy (meth) acrylate Methyl, hydroxy-3-phenoxypropyl acrylate and the like are used. (B) As the (meth) acrylic monomer having a phenyl group in the molecule, phenoxyethyl acrylate, phenoxypropyl acrylate, or the like is used.

  The total proportion (mass ratio) of the units derived from the component (A) and the component (B) in the polymerization units of the whole pressure-sensitive adhesive is 40% by mass or more and 90% by mass or less, preferably 41% by mass or more. It is 85 mass% or less. If there are too few units containing the above two functional groups, the compatibility with the crystalline polymer may be reduced. Conversely, if there are too many components having other functional groups, crosslinkability and adhesiveness will be reduced. May decrease, and the above-described performance may not be effectively improved. For example, a decrease in crosslinkability may impair the adhesive residue preventing effect. Further, the proportion of the unit derived from the component (B) in the polymerization unit of the whole pressure-sensitive adhesive is 0.5 mol% or more, preferably 1 mol% or more, particularly preferably 5 mol% or more and 25 mol% or less. It is.

  The adhesive layer may be a transparent layer, and when the support is transparent, the adhesive layer may be a transparent layer in order to visually recognize the image formed on the image receiving layer from the adhesive layer side. Good.

(Peeling substrate)
Although it does not specifically limit as a peeling base material, For example, a plastic film is typically used. Specifically, for example, polyacetate film, cellulose triacetate film, nylon film, polyester film, polycarbonate film, polysulfone film, polystyrene film, polyphenylene sulfide film, polyphenylene ether film, cycloolefin film, polypropylene film, polyimide film, cellophane ABS (acrylonitrile-butadiene-styrene) resin film is preferably used, and may be opaque such as white.

  Furthermore, a sheet-like material such as paper, metal, plastic, or ceramic is desirable.

  In addition, each site | part of this embodiment may be transparent (light transmissive) as a whole, or may be opaque. When each part is light transmissive, the image formed on the image receiving layer is visually recognized by the light irradiated from the support. In this case, as the support, for example, a light emitting device such as a light box for an internally illuminated signboard is applied. When a medium with an image is attached to the light emitting surface of the light emitting device, the light transmittance of the entire adhesive layer may be 60% or more. For example, when an electrophotographic recording medium is attached to a light source, the adhesive layer is light diffusive. It is desirable to have

(Characteristics of electrophotographic image recording media)
-Layer thickness-
The thickness of the image receiving layer 140 is preferably 5 μm or more and 25 μm or less, and more preferably 7 μm or more and 20 μm or less.
The thickness of the support 130 is preferably 10 μm or more and 200 μm or less, and more preferably 20 μm or more and 150 μm or less.
The thickness of the adhesive layer 120 is preferably 5 μm to 200 μm, and preferably 10 μm to 100 μm.
The thickness of the peeling substrate 110 is preferably 5 μm or more and 200 μm or less, and preferably 50 μm or more and 100 μm or less.

-Surface resistance value of image receiving layer-
The electrophotographic image recording medium according to the present embodiment has a surface resistance value of 1.0 × 10 ⁸ Ω from the viewpoint of realizing excellent image formation when an image is formed by an electrophotographic method. / □ or more and 1.0 × 10 ¹³ Ω / □ or less is preferable.
The surface resistance value is preferably in the range of 1.0 × 10 ⁹ Ω / □ to 1.0 × 10 ¹² Ω / □.

When the surface resistance value is 1.0 × 10 ⁸ Ω / □ or more, it is considered that, for example, the transfer toner from the primary transfer member in the electrophotographic apparatus is prevented from being disturbed. Further, since the surface resistance value is 1.0 × 10 ¹³ Ω / □ or less, for example, it is difficult to transfer toner from the primary transfer member in the electrophotographic apparatus to the surface of the image receiving layer, resulting in transfer failure. This is considered to suppress the occurrence of image defects due to the occurrence of image defects.

When the image receiving layer is provided only on one side of the support, for the same reason, the surface resistance value of the support surface on the side where the image receiving layer is not provided is 1.0 × 10 ⁸ or more. A range of 0 × 10 ¹³ Ω / □ or less is desirable, and a range of 1.0 × 10 ⁹ Ω / □ or more and 1.0 × 10 ¹¹ Ω / □ or less is desirable.

In the electrophotographic image recording medium of the present invention, the surface resistance difference between the front and back surfaces at 23 ° C. and 55% RH is preferably within 4 digits, and more preferably within 3 digits.
It is considered that when the surface resistance difference between the front and back surfaces is within 4 digits, toner transfer failure is less likely to occur and image deterioration is suppressed.

  The surface resistance value is measured according to JIS K6991 using a circular electrode (for example, “HR probe” of Hirester IP manufactured by Mitsubishi Oil Chemical Co., Ltd.) in an environment of 23 ° C. and 55% RH.

When the surface resistance value of the image receiving layer provided on the support surface is controlled within the range of 1.0 × 10 ⁸ Ω / □ or more and 1.0 × 10 ¹³ Ω / □ or less, the image receiving layer is charged. It is desirable to contain a control agent. As the charge control agent, a polymer conductive agent, a surfactant, metal oxide particles, or the like is used.

  In addition, when the image receiving layer is provided only on one side of the support, the surface resistance value of the surface on which the image receiving layer is not provided is controlled by the surface activity when producing a film as a release substrate. Add appropriate agents, polymer conductive agents, conductive particles, etc. into the resin, apply a surfactant on the film surface, deposit a metal thin film, or apply an appropriate amount of surfactant, etc. to the adhesive It is performed by adding.

  Examples of the surfactant used include cationic surfactants such as polyamines, ammonium salts, sulfonium salts, phosphonium salts, and betaine amphoteric salts, anionic surfactants such as alkyl phosphates, and nonionic surfactants such as fatty acid esters. Surfactant is mentioned. Among these surfactants, it is effective to improve transferability to use a cationic surfactant having a large interaction with the recent negatively charged toner for electrophotography.

  Among the cationic surfactants, quaternary ammonium salts are desirable. As the quaternary ammonium salts, compounds represented by the following general formula (I) are desirable.

R ³
│
Formula (I) R ¹ —A—R ² —N ⁺ —R ⁵ · X ⁻
│
R ⁴

In the formula, R ¹ represents an alkyl group, an alkenyl group, or an alkynyl group having 6 to 22 carbon atoms, and R ² represents an alkylene group, an alkenylene group, or an alkynylene group having 1 to 6 carbon atoms. R ³ , R ⁴ , and R ⁵ may be the same or different and each represents an aliphatic group, an aromatic group, or a heterocyclic group. An aliphatic group means a linear, branched or cyclic alkyl group, alkenyl group, or alkynyl group. The aromatic group represents a benzene monocyclic or condensed polycyclic aryl group. These groups may have a substituent such as a hydroxyl group. A represents an amide bond, an ether bond, an ester bond or a phenyl group, but this may not be present. X < ^- > represents a halogen element, sulfate ion, or nitrate ion, and these ions may have a substituent.

-Peel strength of adhesive layer-
The peel strength of the adhesive layer is such that when the peeling substrate is peeled off, the adhesive is peeled off without any adhesive residue, and when the image application target is peeled off from the image recording body, no adhesive residue is left on the image application object. Desirably, it is determined to be peeled off.
The peel strength is measured using Imada's 180 ° peel tester IPT200, with a peel rate of 300 mm / min and a peel angle of 180 degrees, and the peeled substrate surface or the image application object surface as a reference surface.
Then, the composition and thickness of the pressure-sensitive adhesive layer, the surface property (surface roughness) of the pressure-sensitive adhesive surface, etc. are determined so that the peel strength (peel strength AL) with respect to the reference surface is 0.2 N / 25 mm or more and 10 N / 25 mm or less. It is good to do. If the peel strength AL is too small, the peeling substrate or the image application target may be peeled off during use of the electrophotographic image recording medium. Conversely, if the peel strength AL is too large, the peel group When the material or the image application object is peeled off, there is a possibility that the adhesive remains on the peeling substrate or the image application object, or the peeling substrate or the image application object is damaged. From such a viewpoint, the range of the peel strength AL is preferably 0.5 N / 25 mm or more and 5 N / 25 mm or less, and particularly preferably 1 N / 25 mm or more and 3 N / 25 mm or less.

In addition, the peel strength measured at a peel speed of 300 mm / min and a peel angle of 180 ° with respect to the actual peel substrate or the substrate surface of the object to be imaged is preferably 0.2 N / 25 mm or more and 10 N / 25 mm or less. , 0.5N / 25mm or more and 5N / 25mm or less is desirable, and particularly preferably 1N / 25mm or more and 3N / 25mm or less, the composition and thickness of the adhesive layer, the surface property (surface roughness) of the adhesive surface, etc. It is good to decide.
By setting the peel strength within the above range, it is considered that an electrophotographic image recording medium capable of reusing an image-giving object that adheres the medium from which the substrate has been peeled off from the electrophotographic image recording medium can be obtained.

(Method for producing electrophotographic image recording medium)
The electrophotographic image recording medium is prepared by, for example, applying a composition containing an adhesive serving as an adhesive layer on one surface of a support and attaching the release substrate to the adhesive layer of the support. It can be formed by coating an uncoated surface with a coating layer to be an image receiving layer.
The electrophotographic image recording medium is, for example, coated with a composition containing an adhesive that becomes an adhesive layer on one side of a support, and an application layer that becomes an image receiving layer on an uncoated surface of the support. After coating, the release substrate may be attached to the adhesive layer on the support.

  The image receiving layer coating liquid is a coating liquid in which components such as wax, resin, and particles are mixed using an organic solvent or water and dispersed by an apparatus such as an ultrasonic wave, a wave blower, an attritor or a sand mill. Is made. The image receiving layer is formed by coating or impregnating the surface of the support with the coating liquid as it is.

  Examples of the coating or impregnation method include blade coating, wire bar coating, spray coating, dip coating, bead coating, air knife coating, curtain coating, and roll coating. Adopted.

  The drying for forming the coating layer on the surface of the support may be air drying, but is easily dried by heat drying. As the drying method, a commonly used method such as a method of putting in an oven, a method of passing through an oven, or a method of contacting with a heating roller is adopted.

  In actual use, the coefficient of static friction on the surface of the image receiving layer is preferably 2 or less, and more preferably 1 or less. The coefficient of dynamic friction on the surface of the image receiving layer is preferably in the range of 0.2 to 1 and more preferably in the range of 0.3 to 0.65.

  For example, in this embodiment, a toner image is formed as an image on the surface of an electrophotographic image recording medium. When a toner image is formed, the formed toner image is fixed so that the temperature of the surface of the electrophotographic image recording medium (the surface on which the image receiving layer is formed) is equal to or lower than the melting temperature of the toner. It is desirable to do this. In consideration of the melting temperature of the toner, it is desirable that the surface temperature of the electrophotographic image recording medium be 130 ° C. or lower, more preferably 110 ° C. or lower.

Even in the case of fixing under the above conditions, in the case of the electrophotographic image recording medium according to the present embodiment, the release substrate may enter a temperature region in which thermal deformation occurs. In this case, the stiffness of the image receiving layer is particularly weak, and it becomes easy to wind around the heating roll of the fixing device. In this case, the image can be transported in an overlapping manner with paper or the like to compensate for the stiffness of the image receiving layer in the fixing device, or the inside of the fixing device can be modified / adjusted so that the guide hits the edge portion of the electrophotographic image recording medium. desirable.
In this embodiment, the toner image formed by the electrophotographic image forming apparatus is described as the image formed on the surface of the electrophotographic image recording medium. However, the present invention is not limited to this. For example, an image may be formed using ink or the like.

[Image Recorder and Method for Producing Image Recorder]
Next, an image recording body using the electrophotographic image recording medium described above will be described.
The image recording material of the present embodiment is obtained by laminating an object to be imaged and an image-attached medium in which an image is recorded on an image receiving layer and the base material is peeled off from the electrophotographic image recording medium on which the image is formed. Is obtained.
Here, although there is no restriction | limiting in particular about an image provision object, For example, the thing of materials, such as resin and a ceramic, is mentioned. The shape of the object to be imaged is preferably a film.
Specific examples of the object to be imaged include lenticular media, IC card media, window glass, building walls, and automobile bodies such as automobiles.
Hereinafter, a lenticular medium with an image using a lenticular medium as an image application target will be described.

A lenticular medium with an image will be described with reference to the drawings.
FIG. 3 is a schematic perspective view showing the lenticular medium 400 with an image according to the present embodiment.
The lenticular medium 400 with an image according to the present embodiment includes the lenticular medium 300 in which a lenticular lens having a plurality of convex portions arranged on one surface and the image 150 recorded on the image receiving layer 140 described above. The image-recording medium 100 is a laminate of the image-bearing medium 200 from which the release substrate 110 has been peeled off.
The lenticular medium with image 400 according to the present embodiment realizes the reuse of the lenticular lens by adopting the above configuration.
Specifically, in the image-added medium 200, an image receiving layer 140 on which an image 150 is formed, a support 130, and an adhesive layer 120 are laminated in this order, and the adhesive layer 120 includes a lenticular medium. The back surface of the surface provided with 300 lenticular lenses is adhered.
In the lenticular medium with image 400 according to the present embodiment, the image 150 of the image receiving layer 140 is exposed.

Next, a method for producing an image-equipped lenticular medium according to the present embodiment will be described.
In the following description, reference numerals are omitted.

  The image-forming lenticular medium according to the present embodiment is an image forming process for forming an image composed of an image forming material by an electrophotographic method on the surface on which the image receiving layer of the electrophotographic image recording medium is provided, A positioning step of stacking the electrophotographic image recording medium so that the back surface of the surface on which the lenticular lens is provided and the adhesive layer on the back surface of the surface on which the fixed image is formed face each other. It is made after.

  In electrophotographic image formation, first, the surface of an electrophotographic photosensitive member (image holding member) is charged and charged, and then the obtained image information is exposed to the surface. A latent image is formed. Next, toner as an image forming material is supplied from the developing device to the electrostatic latent image on the surface of the photoreceptor, so that the electrostatic latent image is visualized and developed with the toner (a toner image is formed). Furthermore, the formed toner image is transferred to the surface on which the image receiving layer is formed, and finally the toner image is fixed on the surface of the image receiving layer by heat, pressure, etc., and the image is formed for electrophotography. The medium is ejected from the electrophotographic apparatus.

  The electrophotographic image recording medium on which the image is formed is the lens surface of the lenticular medium with the surface of the pressure-sensitive adhesive layer (the surface opposite to the surface on which the image receiving layer is provided) remaining on the support side after peeling the release substrate. Therefore, when forming an electrostatic latent image on the surface of the photoconductor, the image is exposed to the surface of the photoconductor. It is desirable that forward image information is provided as the image information.

The lenticular medium used in this embodiment is plastic, ceramic or the like, and these are preferably film-like.
The lenticular medium used in the present invention is preferably transparent so that an image formed when it is used as an image recording body is easily visible, and a lenticular medium having a transparent shape is typically used.

  As the resin for the lenticular medium, those similar to those used for the support of the electrophotographic image recording medium may be used. Polyacetate film, cellulose triacetate film, nylon film, polyester film, polycarbonate film, A polystyrene film, a polyphenylene sulfide film, a polypropylene film, a polyimide film, a cellophane, an ABS (acrylonitrile-butadiene-styrene) resin film, or the like is desirably used.

  Among the above, polyester film, particularly PETG in which about half of the ethylene glycol component of PET (polyethylene terephthalate) is replaced with 1,4-cyclohexanemethanol component, and the PET is mixed with polycarbonate to be alloyed. Further, non-biaxially stretched PET, and amorphous polyester called A-PET is more preferably used.

  In the present invention, as a further material, a polystyrene resin film, an ABS resin film, an AS (acrylonitrile-styrene) resin film, a PET film, a polyolefin resin film such as polyethylene or polypropylene, and a hot melt such as polyester or EVA. A film to which a system adhesive is added is desirably used.

  As the lenticular medium used in the present invention, it is desirable to use a film composed of a plastic having a thickness in the range of 200 μm to 5000 μm, and it is more desirable to use a PETG film having a thickness in the range of 300 μm to 3000 μm.

  The lenticular medium 400 with an image according to the present embodiment manufactured as described above is applied to various uses, and examples thereof include 3D photographs, 3D advertising media, 3D posters, and animation. Since reuse is realized, it is particularly suitable for use in a large advertising medium (for example, A0 size), an application in which an image application object such as a width 1189 mm × length 6000 mm, a width 1189 mm × length 30000 mm is expensive. Conceivable.

Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited thereto. In the following examples and comparative examples, “part” means “part by mass”, and “%” means “% by mass”. In addition, Example 2 is to be read as Reference Example 1.

[Example 1]
<Preparation of resistance adjustment layer solution A-1>
Cross-linked acrylic spherical particles (manufactured by Soken Chemical Co., Ltd .: MX-150) as fillers in 100 parts by mass of an acrylic polymer solution (cation produced by Soken Chemical Co., Ltd .: Elecondo QO-101, solid concentration 50%) which is a cationic antistatic agent The average particle size: 1.5 μm) 0.5 parts by mass and 200 parts by mass of ethanol were mixed and stirred to prepare a resistance adjustment layer solution A-1 for controlling the surface resistivity.

<Preparation of image-receiving layer coating solution B-1>
20 parts by mass of a polyester resin (by Toyobo Co., Ltd .: Byron 200) as a thermoplastic resin, 1 part by mass of a surfactant (manufactured by NOF Corporation: Elegan 264WAX), and a cross-linked acrylic spherical particle (by Soken Chemical Co., Ltd .: MX-) as a filler (1500, average particle size: 15 μm) 3 parts by mass and 50 parts by mass of methyl ethyl ketone were added and stirred to prepare image-receiving layer coating solution B-1.

<Preparation of adhesive layer coating liquid C-1>
Silicone pressure-sensitive adhesive (manufactured by Shin-Etsu Chemical Co., Ltd .: X-40-3306, solid content concentration 30% by mass) 33.3 parts by mass, 0.02 parts by mass of the curing agent (CAT-PL-50T), 20 masses of toluene Then, the mixture was diluted and stirred to prepare an adhesive layer coating solution C-1.

<Preparation of electrophotographic image recording medium 1>
On one side of biaxially stretched polyethylene terephthalate (Lumirror T60 manufactured by Toray Industries, Inc., thickness 25 μm) as a peeling substrate, the resistance adjusting layer solution A-1 is applied using a wire bar and dried at 120 ° C. for 1 minute. A resistance adjustment layer having a thickness of 0.2 μm was formed.

  On the other hand, the adhesive layer coating liquid C-1 was applied to one side of biaxially stretched polyethylene terephthalate (Toray Co., Ltd. Lumirror T60, thickness 75 μm) as a support using a wire bar at 130 ° C. It was dried for 1 minute to form a 5 μm thick adhesive layer.

  On the surface on which this adhesive layer was formed, the uncoated surface of the release substrate prepared above was bonded at a bonding speed of 0.2 m / min and a cylinder pressure of 588 KPa at room temperature (22 ° C.).

The image receiving layer coating solution B-1 was applied to the untreated support surface of the laminated body using a wire bar and dried at 120 ° C. for 1 minute to form an image receiving layer having a thickness of 10 μm. .
Thereafter, it was cut into A4 size (210 mm × 297 mm) to produce an electrophotographic image recording medium 1 having a total thickness of 115 μm.

<Evaluation of electrophotographic image recording medium 1>
(Surface resistance and peel strength)
The surface resistivity of the image receiving layer of the electrophotographic image recording medium 1 was 2.9 × 10 ⁸ Ω on the resistance adjusting layer surface and 3.1 × 10 ¹⁰ Ω on the image receiving layer surface.
Further, the peel strength of the adhesive layer when the peelable substrate of the electrophotographic image recording medium 1 was peeled was measured by the above-described method. As a result, the peel strength was 0.02 N / 25 mm in a low temperature environment (22 ° C.). Under the environment (60 ° C.), it was 0.03 N / 25 mm.

(Evaluation after peeling the peeling substrate)
-Image formation-
First, an image forming apparatus (“Color Copier DocuColor1255CP Remodeling Machine” manufactured by Fuji Xerox Co., Ltd.) is applied to the image receiving layer surface of the electrophotographic image recording medium 1 (image is not formed) to form an image for electrophotography. A color image consisting of 12 viewpoints was formed on the image receiving layer of film 1.

Next, the electrophotographic image recording medium 1 on which the image has been formed is allowed to stand for 24 hours in a low temperature environment (22 ° C.) and a high temperature environment (60 ° C.), and then a release substrate is removed from each electrophotographic image recording medium. It peeled and the image-added medium 1 was produced.
After peeling the release substrate, the adhesive layer and the release substrate were visually confirmed. As a result, the electrophotographic image recording medium 1 left in a low temperature environment and the electrophotographic image recording medium 1 left in a high temperature environment were: In either case, the adhesive layer remained on the support side, and no adhesive layer remained on the release substrate side.
Moreover, in any case, peeling of the peeling base material was easy.

<Production of lenticular medium 1 with image>
First, a 30 lpi (30 lenticular lenses per inch) lenticular medium (trade name lenticular lens, manufactured by Nippon Koban Co., Ltd., thickness 1320 μm) composed of PET-G (glycol-modified polyester) was prepared.
Next, the back surface of the surface on which the lenticular lens of the lenticular medium was provided and the adhesive layer surface of the image-coated medium 1 produced above were aligned and bonded together.
This laminated body was cooled to normal temperature (22 degreeC), and the lenticular medium 1 with an image was produced.
Note that no image defects were observed.

<Evaluation of lenticular medium 1 with image>
(Evaluation of lenticular medium with image after image medium is peeled)
Next, after leaving the lenticular medium 1 with an image in a low temperature environment (22 ° C.) and a high temperature environment (60 ° C.) for 24 hours, the imaged medium was peeled from each image lenticular medium.
When the adhesive layer after peeling was visually confirmed, the lenticular medium 1 with an image left in a low temperature environment and the lenticular medium 1 with an image left in a high temperature environment both had an adhesive layer remaining on the support side, and the lenticular medium The adhesive layer did not remain on the medium. Further, no adhesion of the image forming material was observed on the lenticular medium.
Furthermore, in both cases, the image-bearing medium was easily peeled off.

[Example 2]
Except that the adhesive layer coating solution was changed to the following adhesive layer-coated substrate, an electrophotographic image recording medium 2 was prepared in the same manner as in Example 1, and after the image was formed, the release substrate was peeled off. Evaluation similar to Example 1 was performed.

<Base material with adhesive layer>
A base material with an acrylic pressure-sensitive adhesive (manufactured by Panac Co., Ltd .: trade name Panaprotect ET, base material with an adhesive layer having a PET base material thickness of 50 μm and an adhesive layer of 5 μm) was prepared.

<Evaluation of electrophotographic image recording medium 2>
The peel strength when the peelable substrate of the pressure-sensitive adhesive layer of the electrophotographic image recording medium 2 was peeled was measured by the method described above, and it was 0.08 N / 25 mm in a low temperature environment (22 ° C.). At (60 ° C.), it was 0.10 N / 25 mm.
Regarding the evaluation after peeling the release substrate, the electrophotographic image recording medium 2 left in a low temperature environment has an adhesive layer remaining on the support side and no adhesive layer remaining on the release substrate side. It was.
On the other hand, in the electrophotographic image recording medium 2 which was left in a high temperature environment, the pressure-sensitive adhesive layer remained on the support side and some pressure-sensitive adhesive layer remained on the release substrate side, but the amount was not a problem. .
In either case, the release substrate could be peeled off, but zipping occurred particularly in a high temperature environment.

<Evaluation of lenticular medium 2 with image>
Next, using the electrophotographic image recording medium 2, an image-equipped lenticular medium 2 was produced in the same manner as in Example 1, the lenticular medium was peeled off, and the same evaluation as in Example 1 was performed.
When the adhesive layer after peeling was visually confirmed, the lenticular medium 2 with an image left in a low-temperature environment had an adhesive layer remaining on the support side, and no adhesive layer remained on the lenticular medium side. There was no adhesion of material.
On the other hand, in the lenticular medium 2 with an image left in a high temperature environment, the adhesive layer remained on the support side and some adhesive layer remained on the lenticular medium side, but the amount was not a problem. Further, no adhesion of the image forming material was observed on the lenticular medium.
Furthermore, in both cases, the image-bearing medium was easily peeled off.

  From these results, it became clear that the lenticular media used for the lenticular media with images 1 and 2 can be reused regardless of environmental changes.

DESCRIPTION OF SYMBOLS 100 Electrophotographic image recording medium 110 Peeling base material 120 Adhesive layer 130 Support body 140 Image receiving layer 150 Image 200 Recording medium 300 with image Lenticular medium (object to be imaged)
400 Lenticular medium with image (image recording medium)

Claims (4)

And images an image receiving layer which has been recorded, a support, an adhesive layer comprising a silicone-based adhesive, a release substrate, but are stacked in this order, when the release substrate is peeled, the adhesive A medium with an image in which the release substrate is peeled from an electrophotographic image recording medium having a layer remaining on the support side;
A lenticular lens in which a plurality of convex portions are arranged is provided on one surface, and the adhesive layer is adhered to the back side of the surface on which the lenticular lens is provided; and
Lenticular media with images laminated. 2. The lenticular medium with an image according to claim 1, wherein a surface resistance value of the image receiving layer is 1.0 × 10 ⁸ Ω / □ or more and 3.2 × 10 ¹³ Ω / □ or less.   The lenticular medium with an image according to claim 1, wherein the support is white.   The lenticular medium with an image according to claim 1, wherein the support is transparent.

Images