JP5659538B2 - Ink composition and decorative sheet using the same - Google Patents

Description

  The present invention relates to an ink composition and a decorative sheet using the same.

Conventionally, an injection molding simultaneous decorating method is used for decorating a resin molded body having a complicated surface shape such as a three-dimensional curved surface. In the injection molding simultaneous decoration method, the decorative sheet inserted into the mold at the time of injection molding is integrated with the molten injection resin injected and injected into the cavity to decorate the surface of the resin molded body Generally, it is roughly classified into an injection molding simultaneous laminate decoration method and an injection molding simultaneous transfer decoration method depending on the difference in the configuration of the decorative sheet integrated with the resin molded body.
In the injection molding simultaneous transfer decorating method, the transfer layer side of the decorative sheet for injection molding simultaneous transfer decoration is directed into the mold and heated from the transfer layer side by a hot platen, and the decorative sheet is placed in the mold. Molded along the shape, tightly attached to the inner surface of the mold and clamped, then injected the molten injection resin into the cavity to integrate the decorative sheet and the injection resin, then cooled the decorative molded product And after taking out from a metal mold | die, the decorative molded product which transcribe | transferred the transfer layer by peeling a base film can be obtained.

  The decorative molded products thus obtained include notebooks including mobile PCs that can be carried everyday, for example, along with the expansion of the PC market in recent years, in addition to the fields of household appliances and automobile interiors that have been used in the past. Use in the field of personal computers, automobile exteriors, and cellular phones are also attracting attention. In these fields, the decorative sheet is required to have high hardness and scratch resistance, and at the same time, formability that can provide a molded product with a more complicated shape.

  In order to satisfy such a demand, for example, a decorative sheet in which a release layer for protecting a molded product is provided on a base film has been proposed (see, for example, Patent Document 1). However, for a molded product with a more complex shape, such as a three-dimensional curved surface with a high degree of deep drawing, which cannot sufficiently meet the stricter requirements for high hardness and scratch resistance, Following the uneven shape of the mold is not sufficient, and there is a problem of obtaining better moldability.

  For the purpose of obtaining surface properties such as high hardness and scratch resistance, a decorative sheet using a predetermined hard coat agent on the surface of a resin molded product has been proposed (for example, see Patent Document 2). However, due to the properties of the hard coat agent or the agent that forms the protective layer, a certain surface physical property can be obtained because the decorative sheet (transfer sheet) is cured before injection molding. There was a problem that excellent moldability could not be obtained. In addition, for the purpose of improving the transfer to the deep drawing shape while obtaining the above surface properties, a transfer sheet having a protective layer made of an ionizing radiation curable resin is formed in a mold by vacuum and pressure forming, A manufacturing method is disclosed in which a resin molded product is obtained by performing injection molding after irradiating with ionizing radiation and curing the protective layer (see, for example, Patent Document 3). However, even this manufacturing method cannot sufficiently meet demands for more severe surface properties and moldability, and further improvement is necessary. Thus, high hardness, scratch resistance, and moldability are contradictory performances, and it is required to secure these conflicting performances at a high level.

JP 2009-247011 A JP 2008-231220 A Japanese Patent No. 3345668

  Under such circumstances, the present invention provides an ink composition that imparts excellent hardness and scratch resistance to a decorative molded product, and at the same time imparts moldability to obtain a molded product having a more complicated shape. An object is to provide a decorative sheet using the ink composition and a decorative molded product using the decorative sheet.

  As a result of intensive studies to achieve the above problems, the present inventor has found that the problems can be solved by the following invention. That is, the present invention provides the following ink composition, a decorative sheet using the ink composition, a method for manufacturing a decorative molded product using the ink composition, and a decorative molded product obtained by the manufacturing method. is there.

1. It is a manufacturing method of the decorative molded product which has the following process (1)-process (5),
Step (1) Step of arranging a decorative sheet in an injection mold
Step (2) Injection step of injecting molten resin into the cavity, cooling and solidifying, and laminating and integrating the resin molding and the decorative sheet
Step (3) Step of taking out a molded body in which the resin molded body and the decorative sheet are integrated from the mold
Process (4) The process of peeling the base film of a decorating sheet from a molded object
Step (5) a hard coat layer forming step of curing the hard coat layer forming layer provided on the molded body,
The decorative sheet used in the step (1) is a decorative sheet having at least a release layer and a hard coat layer forming layer on one side of the base film in order, and the hard coat layer forming layer is ionizing radiation curable. Polymer having at least one selected from vinyl group, (meth) acryloyl group, allyl group and epoxy group as a functional group and a weight average molecular weight of 20,000 to 150,000 and vinyl ion, (meth) acryloyl group as ionizing radiation curable functional group A monomer having at least one selected from an allyl group and an epoxy group and having a weight average molecular weight of 100 to 10,000, and at least one reactivity selected from a vinyl group, a (meth) acryloyl group, and an allyl group on the surface of the inorganic particles. An ink composition comprising reactive inorganic particles having a functional group, Using an ink composition whose amount is 25% by mass or more based on the total of the polymer and the monomer, and whose content of the reactive inorganic particles in the ink composition is 20 to 60% by mass A method for producing a decorative molded product.
2. The manufacturing method of said 1 whose compounding quantity of the said polymer is 55-100 mass% with respect to the sum total of a polymer and a monomer.
3. 3. The production method according to 1 or 2 above, wherein the inorganic particles are silica particles.
4). The polymer having an ionizing radiation curable functional group is composed of at least one selected from acrylic (meth) acrylate, urethane (meth) acrylate, polyester (meth) acrylate, epoxy (meth) acrylate, and polyether (meth) acrylate. The manufacturing method in any one of said 1-3 which is a polymer.
5. The monomer having an ionizing radiation-curable functional group, which have a functional group 2 or more, the production method according to any one of the above 1 to 4 are urethane (meth) acrylate.
6 . Curing in Engineering as (5) The method according to any one of the above 1 to 5, characterized in that is carried out by irradiating the ionizing radiation in an oxygen concentration of 2% or less atmosphere.
7). The decorating sheet used for the manufacturing method in any one of said 1-6.
8). The decorative molded product obtained by the manufacturing method in any one of said 1-6 .

  According to the present invention, an ink composition that imparts excellent hardness and scratch resistance to a decorative molded product, and at the same time imparts moldability to obtain a molded product having a more complicated shape, and the ink composition are used. It is possible to provide a decorative sheet and a decorative molded product using the decorative sheet.

It is a schematic diagram which shows the cross section of the decorating sheet of this invention. It is a schematic diagram which shows the cross section of the decorative molded product of this invention.

[Ink composition]
The ink composition of the present invention comprises a polymer and a monomer having at least one selected from vinyl groups, (meth) acryloyl groups, allyl groups and epoxy groups as ionizing radiation-curable functional groups, and reactive functional groups on the surface of inorganic particles. An ink composition comprising reactive inorganic particles having a content of 25% by mass or more based on the total amount of the polymer and the monomer, and the reactive inorganic in the ink composition The ink composition has a particle content of 20 to 60% by mass.

<Polymer having ionizing radiation-curable functional group>
Ionizing radiation curable is one having an energy quantum that can crosslink and polymerize molecules in an electromagnetic wave or charged particle beam, that is, crosslinked by causing a polymerization reaction upon excitation by irradiation with ultraviolet rays or electron beams, It is the ability to cure. The ionizing radiation curable functional group is a functional group capable of expressing the ionizing radiation curable property, and has an ethylenically unsaturated bond such as vinyl group, (meth) acryloyl group and allyl group in the present invention. It is a functional group and an epoxy group.

  The polymer having an ionizing radiation curable functional group is not particularly limited as long as it is a polymer having the above ionizing radiation curable functional group. For example, acrylic (meth) acrylate, urethane (meth) acrylate, polyester (meth) acrylate, epoxy ( Polymers such as (meth) acrylate and polyether (meth) acrylate are preferred. In the present invention, these polymers may be used alone or in combination.

The weight average molecular weight of the polymer used in the present invention is about 5000 to 150,000, preferably 20000 to 100,000. If the weight average molecular weight is within the above range, the thixotropy of the ink composition can be obtained, and good moldability can also be obtained. Here, the weight average molecular weight is a value measured by gel permeation chromatography (GPC), and is a value measured under conditions using polystyrene as a standard sample.
Moreover, from the viewpoint of obtaining excellent high hardness and scratch resistance, the double bond equivalent of the polymer is 50 to 1000, preferably 100 to 1000, and more preferably 100 to 500. Here, the double bond equivalent means the molecular weight per ionizing radiation-curable functional group.

《Monomer having ionizing radiation curable functional group》
The monomer having an ionizing radiation curable functional group used in the present invention is particularly limited as long as it is a monomer having at least one selected from a vinyl group, a (meth) acryloyl group, an allyl group and an epoxy group as an ionizing radiation curable functional group. There is preferably no polyfunctional (meth) acrylate having two or more functional groups in one molecule, more specifically, urethane (meth) acrylate, polyester (meth) acrylate, epoxy (meth) acrylate, And polyfunctional (meth) acrylates such as polyether (meth) acrylate are preferred.

2-16 are preferable, as for the number of functional groups which a monomer has, 2-10 are more preferable, and 2-8 are more preferable. If the number of functional groups is within the above range, excellent high hardness and scratch resistance can be obtained.
The weight average molecular weight of the monomer used in the present invention is preferably about 100 to 10,000, more preferably 1000 to 5,000. When the weight average molecular weight of the monomer is within the above range, excellent high hardness can be obtained. Here, the weight average molecular weight is a value measured in the same manner as described above.

  Moreover, in this invention, polyfunctional (meth) acrylate can also be used as a monomer other than the above. The polyfunctional (meth) acrylate is not particularly limited as long as it is a (meth) acrylate having two or more ethylenically unsaturated bonds in the molecule. Such polyfunctional (meth) acrylates include ethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, 1,4-butanediol di (meth) acrylate, and 1,6-hexanediol di (meth). Acrylate, neopentyl glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, hydroxypivalate neopentyl glycol di (meth) acrylate, dicyclopentanyl di (meth) acrylate, caprolactone modified dicyclopentenyl di (meth) Acrylate, ethylene oxide modified di (meth) acrylate phosphate, allylated cyclohexyl di (meth) acrylate, isocyanurate di (meth) acrylate, trimethylolpropane tri (meth) acrylate , Ethylene oxide modified trimethylolpropane tri (meth) acrylate, dipentaerythritol tri (meth) acrylate, propionic acid modified dipentaerythritol tri (meth) acrylate, pentaerythritol tri (meth) acrylate, propylene oxide modified trimethylolpropane tri (meth) ) Acrylate, tris (acryloxyethyl) isocyanurate, propionic acid modified dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, ethylene oxide modified dipentaerythritol hexa (meth) acrylate, caprolactone modified dipentaerythritol hexa (Meth) acrylate is preferred. These polyfunctional (meth) acrylates may be used singly or in combination of two or more.

<Reactive inorganic particles>
The ink composition of the present invention contains reactive inorganic particles. In the present invention, the reactive inorganic particle has a reactive functional group on the surface of the inorganic particle. Preferred examples of the reactive functional group include an ethylenically unsaturated bond such as a vinyl group, a (meth) acryloyl group, and an allyl group, an epoxy group, a silanol group, and the like, from the viewpoint of improving high hardness and scratch resistance. , Vinyl group, (meth) acryloyl group, and allyl group are more preferable.

Preferred inorganic particles include metal oxide particles such as silica particles (colloidal silica, fumed silica, precipitated silica, etc.), alumina particles, zirconia particles, titania particles, zinc oxide particles, etc., and high hardness and scratch resistance. From the viewpoint of improving the properties, silica particles and alumina particles are preferable.
Examples of the shape of the inorganic particles include a sphere, an ellipsoid, a polyhedron, a scale shape, and the like, and these shapes are preferably uniform and sized. In the present invention, irregular inorganic particles are not included as inorganic particles. Here, the irregularly shaped inorganic particles mean those composed of a group of inorganic particles in which inorganic particles are connected and aggregated having an average number of connections of 2 to 40.
The average particle diameter of the inorganic particles can be appropriately selected depending on the thickness of the layer formed from the ink composition, but is usually preferably 0.005 to 0.5 μm, and more preferably 0.01 to 0.1 μm. Here, the average particle diameter is a 50% particle diameter (d50: median diameter) when the particles in the solution are measured by a dynamic light scattering method and the particle diameter distribution is expressed as a cumulative distribution. It can be measured using a meter (manufactured by Nikkiso Co., Ltd.).

  Preferred examples of such reactive irregularly shaped inorganic particles include irregularly shaped inorganic particles whose surface is decorated with a silane coupling agent. Examples of the silane coupling agent include known silane coupling agents having an alkoxy group, an amino group, a vinyl group, an epoxy group, a mercapto group, a chloro group, and the like, and more specifically, γ-aminopropyltriethoxysilane. , Γ-methacryloxypropyltrimethoxysilane, γ-methacryloxypropylmethyldimethoxysilane, γ-methacryloxypropyldimethylmethoxysilane, γ-methacryloxypropyltriethoxysilane, γ-methacryloxypropyldimethylethoxysilane, γ-acryloxy Propyltrimethoxysilane, γ-acryloxypropylmethyldimethoxysilane, γ-acryloxypropyldimethylmethoxysilane, γ-acryloxypropyltriethoxysilane, γ-acryloxypropylmethyldiethoxysilane Γ-acryloxypropyldimethylethoxysilane, vinyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, and the like are preferable, and γ-methacryloxypropyltrimethoxysilane is more preferable. Γ-methacryloxypropylmethyldimethoxysilane and γ-methacryloxypropyldimethylmethoxysilane.

  The method of decorating the surface of the inorganic particles with the silane coupling agent is not particularly limited and may be any known method, such as a dry method of spraying the silane coupling agent or silane coupling after dispersing the inorganic particles in a solvent. Examples thereof include a wet method in which an agent is added and reacted.

  Content of the reactive inorganic particle in the ink composition of this invention is 20-60 mass%, Preferably it is 30-60 mass%, More preferably, it is 30-50 mass%. Here, the content of the reactive inorganic particles in the ink composition means the content of the reactive inorganic particles with respect to the total of the polymer, the monomer and the reactive inorganic particles, and the polymer and the monomer are solid contents. When the content of the reactive inorganic particles is within the above range, excellent high hardness and scratch resistance can be obtained.

"solvent"
The ink composition of the present invention may contain a solvent for the purpose of adjusting the viscosity. Solvents include hydrocarbons such as toluene and xylene; alcohols such as methanol, ethanol, isopropyl alcohol, butanol, isobutyl alcohol, methyl glycol, methyl glycol acetate, methyl cellosolve, ethyl cellosolve, butyl cellosolve; acetone, methyl ethyl ketone, methyl isobutyl Ketones such as ketone, cyclohexanone, diacetone alcohol; esters such as methyl formate, methyl acetate, ethyl acetate, ethyl lactate, butyl acetate; nitrogen-containing compounds such as nitromethane, N-methylpyrrolidone, N, N-dimethylformamide; Ethers such as propylene glycol monomethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dioxolane; methylene chloride, chloroform Preferred are halogenated hydrocarbons such as chloromethane, trichloroethane and tetrachloroethane; other substances such as dimethyl sulfoxide and propylene carbonate; or a mixture thereof. More preferred solvents include methyl ethyl ketone and methyl isobutyl ketone.
The amount of the solvent in the ink composition may be appropriately selected according to the viscosity of the composition, but the solid including the polymer, the solid content of the monomer, the reactive inorganic particles, and other photopolymerization initiators described later. The amount is usually 10 to 50% by mass, preferably 20 to 40% by mass.

<< Photopolymerization initiator >>
The ink composition of the present invention can contain a photopolymerization initiator.
Examples of the photopolymerization initiator include acetophenone series, ketone series, benzophenone series, benzoin series, ketal series, anthraquinone series, disulfide series, thioxanthone series, thiuram series, and fluoroamine series. Of these, acetophenone, ketone, and benzophenone are preferred. These photopolymerization initiators can be used alone or in combination of two or more.
The content of the photopolymerization initiator is preferably about 0.5 to 10 parts by mass, more preferably 1 to 8 parts by mass, further preferably 3 with respect to 100 parts by mass of the total amount of the polymer and the monomer. -8 parts by weight, and the polymer and monomer are based on solids.

《Other ingredients》
The ink composition of the present invention may contain various additives depending on the desired physical properties to be obtained. Examples of additives include ultraviolet absorbers, infrared absorbers, light stabilizers, polymerization inhibitors, crosslinking agents, antistatic agents, antioxidants, leveling agents, thixotropic agents, coupling agents, plasticizers, and antifoaming agents. Agents, fillers and the like.

<Polymer blending amount>
The ink composition of the present invention includes the above-described polymer and monomer, and the blending amount of the polymer is required to be 25% by mass or more based on the total of the polymer and the monomer, preferably 55 to 55%. 100% by mass. Here, the blending amount of the polymer is based on the solid content of the polymer and the monomer. When the blending amount of the polymer is within the above range, whitening or the like does not occur when forming a layer with the ink composition, and excellent high hardness, scratch resistance and excellent moldability can be obtained. In addition, when producing a decorative molded product using a decorative sheet prepared using the ink composition of the present invention, the decorative sheet is necessary without performing a curing treatment (precure) using ionizing radiation or the like. Even if it is deep drawn so that the area ratio of the decorative sheet before and after molding becomes 130% or more when it is molded, it does not cause coating cracking or whitening at the maximum stretched part. The hard coat layer that can follow the shape of the mold can be rolled up while suppressing the occurrence of wrinkles and tears (tack-free), and the decorative sheet can be wound up and stored without blocking. It is possible to keep it easy to handle. That is, it becomes possible to improve the tack-free property and the blocking resistance and to improve the ease of winding the decorative sheet.

[Decorative sheet]
The decorative sheet of the present invention has at least a release layer and a hard coat layer forming layer on one side of the base film in order, and the hard coat layer forming layer uses the ink composition of the present invention. It is. Hereinafter, the decorative sheet of the present invention will be described with reference to FIGS. 1 and 2. Drawing 1 is a mimetic diagram showing the section about the desirable one mode of the decorating sheet of the present invention. FIG. 2 is a schematic diagram showing a cross section of a preferred embodiment of the decorative molded product of the present invention.
The decorative sheet 10 of the present invention shown in FIG. 1 has a release layer 12, a hard coat layer forming layer 13, an anchor layer 14, a picture layer 15 and an adhesive layer on one surface of a base film 11 made of a polyester film. 16 are laminated in order. Moreover, the decorative molded product 20 of the present invention shown in FIG. 2 has a hard coat formed by curing the adhesive layer 16, the pattern layer 15, the anchor layer 14, and the hard coat layer forming layer 13 on the surface of the resin molded body 21. The layers 22 are sequentially stacked.

<Base film>
Examples of the base film 11 include polyolefin resins such as polyethylene and polypropylene; vinyl resins such as polyvinyl chloride, polyvinylidene chloride, polyvinyl alcohol, ethylene / vinyl acetate copolymer, and ethylene / vinyl alcohol copolymer; polyethylene terephthalate. Polyester resins such as polybutylene terephthalate; Acrylic resins such as poly (meth) acrylate methyl and poly (meth) ethyl acrylate; Styrene resins such as polystyrene, Acrylonitrile butadiene styrene copolymers, Cellulose triacetate Those made of an elastomeric resin such as cellophane, polycarbonate, and polyurethane are used. Of these, polyester resins, particularly polyethylene terephthalate (hereinafter referred to as “PET”) are preferred from the viewpoint of good moldability and peelability.
The thickness of the base film 11 is preferably in the range of 25 to 150 μm, and more preferably in the range of 50 to 100 μm, from the viewpoints of moldability, shape followability, and easy handling.

<Release layer 12>
The release layer 12 preferably has a transfer layer 17 formed by laminating a hard coat layer forming layer 13, an anchor layer 14, a pattern layer 15, and an adhesive layer 16 in order so that the release layer 12 can be easily peeled off from the base sheet 11 It is a layer to be provided. By having the release layer 12, the transfer layer 17 can be reliably and easily transferred from the decorative sheet of the present invention to the transfer target, and the release layer 18 including the base film 11 and the release layer 12 can be reliably transferred. Can be peeled off.

For the release layer 12, melamine resin release agent, silicone resin release agent, fluororesin release agent, cellulose resin release agent, urea resin release agent, polyolefin resin release agent, paraffin A mold release agent such as a system mold release agent, an acrylic resin mold release agent, or a composite mold release agent thereof is preferably used. Among these, acrylic resin-based release agents and polyolefin resin-based release agents are preferable, and an acrylic-polyethylene-based composite is particularly preferable.
The release layer 12 is formed by applying an ink prepared by dissolving or dispersing the above-described additive added to a release agent in an appropriate solvent onto the base sheet 11 by a known means. -It can dry and can carry out and thickness is preferable about 0.1-5 micrometers.

<< Hard Coat Layer Forming Layer 13 >>
The hard coat layer forming layer 13 is a layer formed using the ink composition of the present invention, and is a layer that forms the hard coat layer 22 in the decorative molded product 20 by curing. The hard coat layer 22 is an outermost layer of the decorative molded product and is a layer for protecting the molded product and the pattern layer from abrasion, light, chemicals, and the like. Therefore, the hard coat layer forming layer 13 is a layer having the performance of being excellent in surface physical properties such as chemical resistance and contamination resistance as well as excellent high hardness and scratch resistance by being cured. Cost. In the present invention, the above-described performance can be imparted to the hard coat layer 22 by using the ink composition of the present invention for forming the hard coat layer forming layer 13.

The hard coat layer forming layer 13 can be formed by coating the ink composition of the present invention by a coating method such as a gravure coating method, a roll coating method or a comma coating method, a gravure printing method, a screen printing method or the like. it can.
The thickness of the hard coat layer forming layer 13 is preferably in the range of 0.5 to 30 μm, more preferably 3 to 15 μm. When the thickness is in the above range, not only excellent high hardness and scratch resistance, but also surface properties such as chemical resistance and stain resistance are obtained, and at the same time, excellent moldability and shape followability are obtained. Can be obtained. It is also economically advantageous.

<< Anchor layer 14 >>
The anchor layer 14 is a layer provided as desired in order to improve the adhesion between the hard coat layer forming layer 13 and the adhesive layer 16.
The anchor layer 14 is a two-component curable urethane resin, a thermosetting urethane resin, a melamine resin, a cellulose ester resin, a chlorine-containing rubber resin, a chlorine-containing vinyl resin, an acrylic resin, an epoxy resin, and a vinyl copolymer. For example, a coating resin such as a gravure coating method, a roll coating method, or a comma coating method, a gravure printing method, a screen printing method, or the like is applied on the hard coat layer forming layer 13 formed as described above using a coalesced resin. Can be formed.
The thickness of the anchor layer 14 is usually about 0.1 to 5 μm, preferably about 1 to 5 μm.

<< Pattern layer 15 >>
The pattern layer 15 is a layer for imparting a desired design to the decorative molded product, and is a layer provided as desired. Although the pattern of the pattern layer 15 is arbitrary, for example, a pattern composed of wood grain, stone pattern, cloth pattern, sand pattern, geometric pattern, character, and the like can be mentioned. In addition, the pattern layer 15 can be provided with a pattern pattern layer expressing the above pattern and a whole surface solid layer alone or in combination, and the whole surface solid layer is usually used as a concealing layer, a colored layer, a colored concealing layer, or the like. .

The pattern layer 15 is usually a polyvinyl resin, a polyester resin, an acrylic resin, a polyvinyl acetal resin, a cellulosic resin on the hard coat layer forming layer 13 or the anchor layer 14 formed as described above. It is formed by printing with a printing ink containing a resin such as a resin as a binder and a pigment or dye of an appropriate color as a colorant. Examples of the printing method include known printing methods such as gravure printing, offset printing, silk screen printing, transfer printing from a transfer sheet, sublimation transfer printing, and ink jet printing.
The thickness of the pattern layer 15 is preferably 5 to 40 μm and more preferably 5 to 30 μm from the viewpoint of design.

<< Adhesive layer 16 >>
The adhesive layer 16 is a layer formed to transfer the transfer layer 17 to the resin molded body with good adhesiveness. For the adhesive layer 16, a heat-sensitive or pressure-sensitive resin suitable for the material of the resin molded body is appropriately used. For example, when the material of the resin molding is an acrylic resin, it is preferable to use an acrylic resin. If the resin molding is made of polyphenylene oxide / polystyrene resin, polycarbonate resin, or styrene resin, use an acrylic resin, polystyrene resin, polyamide resin, or the like that has an affinity for these resins. Is preferred. Furthermore, when the material of the resin molding is a polypropylene resin, it is preferable to use a chlorinated polyolefin resin, a chlorinated ethylene-vinyl acetate copolymer resin, a cyclized rubber, or a coumarone indene resin.

Examples of the method for forming the adhesive layer 16 include a coating method such as a gravure coating method and a roll coating method, a printing method such as a gravure printing method and a screen printing method. In addition, when the pattern layer 15 has sufficient adhesiveness with respect to a resin molding, the contact bonding layer 16 does not need to be provided.
As for the thickness of the contact bonding layer 16, about 0.1-5 micrometers is preferable normally.

《Use of decorative sheet, etc.》
The decorative sheet of the present invention has excellent moldability such as imparting excellent hardness and scratch resistance to a decorative molded product and obtaining a molded product having a more complicated shape. Moreover, when producing a decoration molded product using the decoration sheet of this invention, a decoration sheet can also be used as it is, and since it is excellent in blocking resistance, it can also be used after winding up in roll shape. Therefore, it is excellent in ease of winding and is excellent in terms of usability. For these reasons, it can be used in a wide range of fields such as household electrical appliances and automobile interior parts, personal computer fields, especially personal computer housings.

[Method of manufacturing decorative molded product]
The method for producing a decorative molded product according to the present invention includes a step (1) a step of arranging the decorative sheet of the present invention in an injection mold; a step (2) injecting a molten resin into the cavity, and cooling and solidifying. Then, an injection step of laminating and integrating the resin molded body and the decorative sheet; step (3) a step of taking out the molded body integrated with the resin molded body and the decorative sheet from the mold; step (4) from the molded body A step of peeling the base film of the decorative sheet; and a step (5) a hard coat layer forming step of curing the hard coat layer forming layer provided on the molded body.

<< Process (1) >>
Step (1) is a step of placing and decorating the decorative sheet of the present invention in a molding die. Specifically, the decorative sheet is placed in a molding die composed of a movable mold and a fixed mold with the transfer layer 17 inside, that is, the base film 11 is on the fixed mold side. Send it in. At this time, a single sheet of decorative sheet may be fed one by one, or a necessary part of a long decorative sheet may be intermittently fed.

  When arranging the decorative sheet in the molding die, it is heated and softened from the transfer layer 17 side using a heating plate, preliminarily molded so that the decorative sheet follows the shape in the die, and the inner surface of the die It is preferable to perform mold clamping so as to be in close contact with each other. The heating temperature at this time is preferably in the range of near the glass transition temperature of the base film 11 and less than the melting temperature (or melting point), and is usually performed at a temperature near the glass transition temperature. In addition, said glass transition temperature vicinity is the range of about glass transition temperature +/- 5 degreeC, and is generally about 70-130 degreeC. Further, for the purpose of bringing the decorative sheet into close contact with the surface of the molding die, vacuuming can be performed when the decorative sheet is heated and softened with a hot platen.

<< Step (2) >>
Step (2) is an injection step in which molten resin is injected into the cavity, cooled and solidified, and the resin molded body and the decorative sheet are laminated and integrated. When the injection resin is a thermoplastic resin, it is made into a fluid state by heating and melting. When the injection resin is a thermosetting resin, the uncured liquid composition is appropriately heated and injected in a fluid state, and then cooled. And solidify. As a result, the decorative sheet is integrally attached to the formed resin molded body, and becomes a decorative molded product. The heating temperature of the injection resin is generally about 180 to 270 ° C. although it depends on the injection resin.

(Injection resin)
The injection resin used for the decorative molded product may be any thermoplastic resin that can be injection-molded or a thermosetting resin (including a two-component curable resin), and various resins can be used. Examples of such thermoplastic resin materials include polystyrene resins, polyolefin resins, ABS resins (including heat-resistant ABS resins), AS resins, AN resins, polyphenylene oxide resins, polycarbonate resins, polyacetal resins, and acrylic resins. Examples thereof include resins, polyethylene terephthalate resins, polybutylene terephthalate resins, polysulfone resins, and polyphenylene sulfide resins. Examples of the thermosetting resin include a two-component reaction curable polyurethane resin and an epoxy resin. These resins may be used alone or in combination of two or more.

<< Step (3) and Step (4) >>
Step (3) is a step of removing from the mold a molded body in which the decorative sheet and the resin molded body are integrated, and step (4) is a step of peeling the base film of the decorative sheet from the molded body. It is. Since the base film 11 has the release layer 12, the release layer 18 including the base film 11 and the release layer 12 is formed at the boundary surface between the release layer 12 and the hard coat layer forming layer 13. The decorative molded product 20 can be easily peeled off. In this manner, a molded product is obtained in which the adhesive layer 16, the pattern layer 15, the anchor layer 14, and the hard coat layer forming layer 13 are sequentially laminated on the surface of the resin molded body 21.

<< Step (5) >>
Step (5) is a step of curing the hard coat layer forming layer 13 in the molded product obtained in step (4) to form a hard coat layer. The curing in the step (5) is preferably performed by irradiating with ionizing radiation in an atmosphere having an oxygen concentration of 2% or less. By carrying out curing in this way, while maintaining the shape followability and formability of the decorative sheet, it is possible to achieve the contradictory performance of obtaining excellent high hardness and scratch resistance on a higher standard. It becomes possible.

  The atmosphere having an oxygen concentration of 2% or less can be obtained by, for example, nitrogen, argon, hydrogen, etc., preferably using nitrogen, or performing air suction so that the oxygen concentration is about 2% or less.

The hard coat layer forming layer 13 can be cured by irradiation with ionizing radiation such as electron beams and ultraviolet rays.
When an electron beam is used as the ionizing radiation, the acceleration voltage can be appropriately selected according to the type of polymer or monomer to be used or the thickness of the hard coat layer forming layer 13, but usually an acceleration voltage of about 70 to 300 kV is preferable. The irradiation dose is usually selected in the range of 5 to 300 kGy (0.5 to 30 Mrad), preferably 10 to 50 kGy (1 to 5 Mrad). The electron beam source is not particularly limited. For example, various electron beam accelerators such as a cockroft Walton type, a bandegraft type, a resonant transformer type, an insulated core transformer type, a linear type, a dynamitron type, and a high frequency type. Can be used.
When ultraviolet rays are used as the ionizing radiation, those containing ultraviolet rays having a wavelength of 190 to 380 nm are emitted, and the irradiation dose is about 500 to 1500 mJ. There is no restriction | limiting in particular as an ultraviolet-ray source, For example, a high pressure mercury lamp, a low pressure mercury lamp, a metal halide lamp, a carbon arc lamp, etc. are used.

The decorative molded product thus obtained has excellent high hardness and scratch resistance, and is excellent in surface physical properties such as chemical resistance and stain resistance. In addition, by using the decorative sheet of the present invention that provides moldability that can correspond to a molded product having a more complicated shape, a decorative molded product that is excellent in finish can be obtained.
The decorative molded product of the present invention can be suitably used in a wide range of fields such as household electrical appliances and automobile interior parts, and in the field of personal computers, especially personal computer casings, taking advantage of these excellent characteristics. Can do.

EXAMPLES Next, although an Example demonstrates this invention further in detail, this invention is not limited at all by this example. In addition, the evaluation method in this invention was performed with the following method.
1. Preparation of test sample The ink composition used in each example and comparative example was coated on a PET film (“F99 (product number)”, thickness: 50 μm, manufactured by Toray Industries, Inc.) with a bar coater, and 100 ° C. The sample was dried in an oven for 60 seconds to obtain a test sample. The obtained test sample had an ink coating amount of 6 g / m ² (the thickness of the ink coating layer was 5 μm).
2. Evaluation of Ease of Sheet Rolling Ink blocking tester ("DG-BT (model number)", manufactured by Daiwa Gravure Co., Ltd.) is superimposed on the surface of the ink coating layer of the test sample and the PET film used for preparation of the test sample. The treatment was carried out by the following four methods while applying a load of 1 kg / cm ² .
(I) left in a 40 ° C. oven for 12 hours (ii) left in a 50 ° C. oven for 12 hours (iii) Irradiation dose: after curing at 15 mJ, left in a 40 ° C. oven for 12 hours (iv) irradiation dose : Cured at 15 mJ and then left in an oven at 50 ° C. for 12 hours. Here, the curing process includes a variable output UV lamp system (“DRS-10 / 12QN (model number)”, manufactured by Fusion UV Systems Japan Co., Ltd.). ) Was used. Then, the test sample was taken out and the superimposed PET film was peeled off. The removal (inversion) of the ink coating layer on the peeled PET film was evaluated according to the following criteria.
A: When the treatment of (i) or (ii) was carried out, there was no set-off. B: When the treatment of (i) or (ii) was carried out, there was slight set-up, but there was no problem in practical use. C: There was no set-off when the processing of (iii) or (iv) was performed. D: The processing of (iii) or (iv) was performed. E: Even if any of the processes (i) to (iv) was performed, the set-off was remarkable. Evaluation of High Hardness and Cracking Resistance After the test samples were cured by the curing methods in the Examples and Comparative Examples shown in Tables 1 to 3, a pencil was formed in accordance with JIS K5600-5-4. Pencil hardness was measured using a scratch coating film hardness tester (“D-NP (model number)”, manufactured by Toyo Seiki Seisakusho Co., Ltd.) and a pencil scratch test pencil (manufactured by Mitsubishi Pencil Co., Ltd.).
The test of scratching the ink coating layer with a pencil of each hardness was conducted 5 times, and the pencil hardness of which the scar did not occur 3 times or more was defined as the pencil hardness of the test sample.

Example 1
(1) Production of polymer Into a 2-liter four-necked flask equipped with a cooler, a dropping funnel and a thermometer, 40 g of toluene and 40 g of methyl ethyl ketone (MEK) were charged together with an azo-based initiator, and 2-hydroxyethyl methacrylate (HEMA) 38 g, 30 g of methyl methacrylate (MMA), 7 g of methacrylic acid (MAA), 7 g of isobornyl methacrylate (IBM), 30 g of toluene and 20 g of MEK were dropped at about 100 to 110 ° C. over about 2 hours through a dropping funnel. After reacting for 8 hours under temperature, the mixture was cooled to room temperature. To this was added 46 g of 2-isocyanatoethyl methacrylate (“Karenz MOI (trade name)”, Showa Denko KK), 20 g of propylene glycol monomethyl ether acetate and 20 g of MEK, and an addition reaction using dibutyltin laurate as a catalyst. I let you. The reaction was completed after confirming the disappearance of the absorption peak at 2200 cm ⁻¹ by IR analysis of the reaction product.
(2) Manufacture of decorative sheet Coating on base film (“F99 (product number)”, thickness: 50 μm, manufactured by Toray Industries, Inc.) using acrylic resin as binder resin and silicone resin as release agent The release liquid was formed by gravure printing the coating liquid at a coating amount of 4 g / m ² , and a hard coat layer forming layer was formed by gravure printing the ink composition shown below at a coating amount of 8 g / m ² . . Next, the anchor layer is formed by gravure printing with a coating based on cellulose ester resin at a coating amount of 4 g / m ² , and then the gravure pattern is printed with an acrylic printing ink at a coating amount of 8 g / m ^2. The decorative layer of Example 1 was obtained by printing to form a pattern layer and further applying an acrylic coating solution with a thickness of 4 μm to form an adhesive layer.
(Ink composition)
4.65 parts by mass of polymer prepared in (1) above (2 parts by mass of solid content): acrylic acrylate (molecular weight 40000, double bond equivalent: 430 g / mol)
Monomer 4 parts by mass (solid content 4 parts by mass): Urethane acrylate ("purple UV 1700B (product number)", Nippon Synthetic Chemical Co., Ltd., molecular weight: 2000, functional group number: 6 or more)
4 parts by mass of reactive inorganic particles (“MIBK-SD-L (product number)”, manufactured by Nissan Chemical Industries, Ltd., reactive colloidal silica particles, average particle diameter d50: 44 nm)
0.4 parts by mass of photopolymerization initiator: 1-hydroxycyclohexyl phenyl ketone (ketone type, “IRGACURE 184 (product number)”, manufactured by Ciba Japan Co., Ltd.)
Solvent 21.6 parts by mass: Mixed solvent of toluene and methyl ethyl ketone (blending ratio 50:50)
(3) Manufacture of decorative molded product The decorative sheet obtained in (2) above is heated at a hot platen temperature of 70 ° C to soften the decorative sheet, and air suction is performed to mold the shape inside the mold. Was molded so as to be in close contact with the inner surface of the mold. The mold used was of a shape with a high degree of deep drawing, having a 80 mm square size, a 10 mm rise and a 3R tray shape.
On the other hand, ABS resin (“Crustic MTH-2 (product number)”, manufactured by Nippon A & L Co., Ltd.) was used as the injection resin, and this was melted at 230 ° C. and then injected into the cavity. After cooling and taking out from the mold, the base film was peeled off to obtain a molded product having an adhesive layer, a printing layer, an anchor layer and a hard coat layer forming layer on the surface of the resin molded product in this order. Furthermore, in an atmosphere with an oxygen concentration of 1% using a nitrogen stream, a variable output UV lamp system (“DRS-10 / 12QN (model number)”, manufactured by Fusion UV Systems Japan Co., Ltd.) was used, and the irradiation dose was 1000 mJ. Then, the molded article was irradiated with ultraviolet rays to cure the hard coat layer forming layer, and the resin molded article of Example 1 was obtained as a hard coat layer.
About the obtained resin molding, the external appearance (moldability) was evaluated on the following reference | standard.
○: No coating cracks or whitening were observed in the hard coat layer (and its formation layer), and the shape of the mold was satisfactorily observed. Δ: Fine coating cracks and minor changes in the hard coat layer (and its formation layer) Although whitening was confirmed, there was no problem in practical use. ×: Remarkable paint cracking and whitening were confirmed in the hard coat layer (and its formation layer).

Examples 2 to 5 and Comparative Example 1
In Example 1, a decorative sheet and a decorative molded product were obtained in the same manner as in Example 1 except that the ink composition and the curing conditions are shown in Table 1. Said external appearance evaluation was performed about the obtained decorative molded product. The results are shown in Table 1.

Example 6
In Example 1, a decorative sheet and a decorative molded product were obtained in the same manner as in Example 1 except that ultraviolet irradiation was performed in the atmosphere. Said external appearance evaluation was performed about the obtained decorative molded product. The results are shown in Table 1.

＊１，ポリマー固形分とモノマー固形分との合計に対するポリマー固形分の配合量（質量％）である。
＊２，ポリマー固形分、モノマー固形分及び反応性無機粒子の合計に対する反応性無機粒子の含有量（質量％）である。
＊３，ポリマー、モノマー、反応性無機粒子、光重合開始剤及び溶剤の合計に対するポリマー固形分、モノマー固形分、反応性無機粒子及び光重合開始剤の合計の含有量（質量％）である。
＊４，電離放射線（紫外線及び電子線）の照射条件は以下の通りである。
紫外線照射条件
出力可変型ＵＶランプシステム：
（「ＤＲＳ−１０／１２ＱＮ（型番）」，フュージョンＵＶシステムズ・ジャパン株式会社製）
照射線量：１０００ｍＪ
電子線照射条件
電子線照射装置：「ＬＢ１０２３（型番）」，株式会社アイ・エレクトロンビーム製
加速電圧：１６５ｋＶ，照射線量：３０ＫＧｙ
＊５，酸素濃度は、ポケッタブル酸素モニターＯＣ−９５（理研計器株式会社製）を用いて測定した値である。

* 1, It is the blending amount (mass%) of the polymer solid content with respect to the total of the polymer solid content and the monomer solid content.
* 2. Reactive inorganic particle content (% by mass) relative to the total of polymer solids, monomer solids and reactive inorganic particles.
* 3 Total content (% by mass) of polymer solids, monomer solids, reactive inorganic particles and photopolymerization initiator relative to the total of polymer, monomer, reactive inorganic particles, photopolymerization initiator and solvent.
* 4. Irradiation conditions for ionizing radiation (ultraviolet rays and electron beams) are as follows.
UV irradiation conditions Variable output UV lamp system:
("DRS-10 / 12QN (model number)", manufactured by Fusion UV Systems Japan)
Irradiation dose: 1000mJ
Electron beam irradiation conditions Electron beam irradiation device: “LB1023 (model number)”, manufactured by I Electron Beam Co., Ltd. Acceleration voltage: 165 kV, irradiation dose: 30 KGy
* 5 The oxygen concentration is a value measured using a pocketable oxygen monitor OC-95 (manufactured by Riken Keiki Co., Ltd.).

Comparative Example 2
In Example 1, a decorative sheet and a decorative molded product were obtained in the same manner as in Example 1 except that the ink composition was changed to the ink composition shown below. Said external appearance evaluation was performed about the obtained decorative molded product. The results are shown in Table 3.
(Ink composition)
2.3 parts by mass of the polymer produced in (1) of Example 1 (1 part by mass of solid content)
Acrylic acrylate monomer 5 parts by mass (solid content 5 parts by mass): Urethane acrylate ("purple light UV1700B (product number)", Nippon Synthetic Chemical Industry Co., Ltd., molecular weight: 2000, functional group number: 6 or more)
4 parts by mass of inorganic particles: unreactive colloidal silica particles (“MEK-ST-L (product number)”, manufactured by Nissan Chemical Industries, Ltd., average particle diameter d50: 40 nm)
0.4 parts by mass of photopolymerization initiator: 1-hydroxycyclohexyl phenyl ketone (ketone type, “IRGACURE 184 (product number)”, manufactured by Ciba Japan Co., Ltd.)
22.3 parts by mass of solvent: mixed solvent of toluene and methyl ethyl ketone (blending ratio 50:50)

Comparative Examples 3-6
In Comparative Example 2, a decorative sheet and a decorative molded product were obtained in the same manner as in Comparative Example 2 except that the ink composition and the curing conditions are shown in Table 1. Said external appearance evaluation was performed about the obtained decorative molded product. The results are shown in Table 2.

  From the results of the examples, the ink composition of the present invention imparts excellent hardness and scratch resistance to the decorative molded product, and at the same time, obtains moldability to obtain a molded product with a more complicated shape. I understood. On the other hand, Comparative Examples 2 to 5 in which no reactive inorganic particles were used were not sufficient in terms of pencil hardness (high hardness and scratch resistance). In Comparative Example 6, the ink composition was gravure-printed and hard coat layer was used. When the formation layer was formed, whitening occurred and it was not able to withstand use. Also, from the viewpoint of ease of sheet winding, if a curing process is performed with ionizing radiation after heat drying, excellent sheet winding ease can be obtained in all the examples, and only the heat drying process can be reversed. It was confirmed that the ink compositions of Examples 3 to 6 which are difficult to use are excellent and excellent in terms of usability.

  According to the present invention, an ink composition that imparts excellent hardness and scratch resistance to a decorative molded product, and at the same time imparts moldability to obtain a molded product having a more complicated shape, and the ink composition are used. It is possible to provide a decorative sheet and a decorative molded product using the decorative sheet. Therefore, the present invention is effective in a wide range of fields such as household electric appliances, automobile interior parts, automobile exteriors, and mobile phone fields, and personal computer fields, especially personal computer housings.

DESCRIPTION OF SYMBOLS 10 Decorating sheet 11 Base film 12 Release layer 13 Hard coat layer forming layer 14 Anchor layer 15 Picture layer 16 Adhesive layer 17 Transfer layer 18 Peeling layer 20 Decorated molded body 21 Resin molded body 22 Hard coat layer

Claims (8)

It is a manufacturing method of the decorative molded product which has the following process (1)-process (5) ,
Step (1) Step of placing the decorative sheet in the injection mold (2) Injection of the molten resin into the cavity, cooling and solidifying, and laminating and integrating the resin molded body and the decorative sheet Step (3) Step of removing a molded body in which the resin molded body and the decorative sheet are integrated from the mold (4) Step of peeling the base film of the decorative sheet from the molded body (5) The molded body A hard coat layer forming step of curing the hard coat layer forming layer provided thereon ,
The decorative sheet used in the step (1) is a decorative sheet having at least a release layer and a hard coat layer forming layer on one side of the base film in order, and the hard coat layer forming layer is ionizing radiation curable. Polymer having at least one selected from vinyl group, (meth) acryloyl group, allyl group and epoxy group as a functional group and a weight average molecular weight of 20,000 to 150,000 and vinyl ion, (meth) acryloyl group as ionizing radiation curable functional group A monomer having at least one selected from an allyl group and an epoxy group and having a weight average molecular weight of 100 to 10,000, and at least one reactivity selected from a vinyl group, a (meth) acryloyl group, and an allyl group on the surface of the inorganic particles. An ink composition comprising reactive inorganic particles having a functional group, Using an ink composition whose amount is 25% by mass or more based on the total of the polymer and the monomer, and whose content of the reactive inorganic particles in the ink composition is 20 to 60% by mass A method for producing a decorative molded product. The production method according to claim 1, wherein the blending amount of the polymer is 55 to 100% by mass with respect to the total of the polymer and the monomer. The production method according to claim 1 or 2, wherein the inorganic particles are silica particles. The polymer having an ionizing radiation curable functional group is composed of at least one selected from acrylic (meth) acrylate, urethane (meth) acrylate, polyester (meth) acrylate, epoxy (meth) acrylate, and polyether (meth) acrylate. It is a polymer, The manufacturing method in any one of Claims 1-3. The monomer having an ionizing radiation-curable functional group, to perforated two or more functional groups, The process according to any one of claims 1 to 4 is a urethane (meth) acrylate. Curing in step (5) The production method according to any one of claims 1 to 5, characterized in that is carried out by irradiating the ionizing radiation in an oxygen concentration of 2% or less atmosphere. The decorating sheet used for the manufacturing method in any one of Claims 1-6. The decorative molded product obtained by the manufacturing method in any one of Claims 1-6 .

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