JP5251383B2 - Molding sheet, resin decorative board and method for producing the same - Google Patents

Description

  The present invention relates to a moldable sheet, a resin decorative board obtained using the moldable sheet, and a method for producing a resin decorative board using the moldable sheet.

As building materials used as furniture, desk top plates, various types of housing equipment such as counters and doors, and interior materials, generally, decorative boards formed with synthetic resin materials, such as melamine resin decorative boards, are widely used.
Conventionally, there are two types of thermosetting resin decorative plates having a concavo-convex shape on the surface, one having a concavo-convex shape formed by an embossing die or a resin concavo-convex sheet, and one having a concavo-convex shape formed by a shaping sheet. However, when an embossing mold having a concavo-convex shape is used, it is necessary to subject the die to surface treatment such as blasting or etching, which limits the concavo-convex shape and the fineness of the pattern. Furthermore, when manufacturing a thermosetting resin decorative board, an expensive template and a spare template are required, which increases the labor and cost of preparing the decorative board, greatly increasing the manufacturing cost and making the product expensive. . Also, in the case of a resin uneven sheet, it is necessary to sandwich an aluminum foil, a polypropylene film, etc. between the mold plate and the thermosetting resin decorative board because it becomes difficult to peel off after the resin is cured. It is very difficult to form a sharp.

By the way, due to the recent trend toward consumer luxury goods, furniture, desks, interior materials, etc. have been required to have a high-class feeling, and the decorative panels used for these have a high-quality appearance. Is desired. For this reason, it is also important to impart a texture, and various methods for imparting a delicate uneven shape to a decorative board have been proposed.
For example, it is a moldable sheet provided with an uneven shape with ionizing radiation curable resin on the surface of the base sheet, and is desired by having a crosslinking density such that the uneven shape is not broken when the formed sheet is peeled off. A shaping sheet has been proposed that faithfully reproduces the pattern shape to be used and can be used repeatedly (see Patent Document 1 and Claims). However, since the step of peeling from the roll intaglio is made when producing the shaping sheet, there is a limit to the expression of the concavo-convex shape when the concave portion is thin.
In addition, this method has a problem that unevenness does not appear cleanly when the concave portion is thin. On the other hand, when there is a concave portion with a certain thickness, an uneven pattern is obtained on the surface of the substrate, but the height of the raised portion is high. For example, in the case of a wood grain pattern, there is a problem that there is no real feeling and the appearance and the touch feeling are not good.

  In addition, a concave / convex layer is formed on the surface of the base sheet using a resin composition comprising an inorganic filler and a binder resin, and a fine concave / convex layer formed on a pattern formed of a liquid repellent resin is formed. A shaped sheet is proposed in which only the resin composition is repelled to form an uneven layer (see Patent Document 2 and Claims). However, because the concavo-convex layer is formed by repelling the resin composition for forming the concavo-convex layer, the lack of stability of the pattern due to the concavo-convex shape, and aging for a certain period to cure the concavo-convex layer, Since it takes a very long time to produce a shaped sheet, there is a problem that it cannot quickly respond to the diversifying needs of consumers.

  On the other hand, when producing a resin decorative board using a shaping sheet, it is preferable to handle the shaping sheet by roll-to-roll from the viewpoint of productivity. However, in the case of requiring a heating step of the shaping sheet in the production of the resin decorative board, if the shaping sheet as described above is handled by roll-to-roll, the heat resistance is insufficient. There is also a problem that the molding sheet shrinks after the process and stable molding cannot be performed, or breakage occurs and continuous stable production cannot be performed.

JP 7-164519 A JP-A-5-92484

  Under such circumstances, the present invention has a delicate and bold concavo-convex shape, is capable of high-quality and precise molding with excellent design and feel, has excellent releasability, and is heat resistant. It aims at providing the manufacturing method of the resin decorative board obtained using the shaping sheet excellent in property, this shaping sheet, and this shaping sheet.

  As a result of intensive research to achieve the above object, the present inventors have an ink layer and a surface shaping layer on a base material, and further provide a concave pattern to form an uneven shape on the surface shaping layer. It has been found that the shaped sheet provided can solve the above-mentioned problems. The present invention has been completed based on such findings.

That is, the present invention
(1) A heat-resistant substrate having a heat shrinkage (150 ° C. × 30 minutes) measured in accordance with JIS C2318 of 2% or less, and a substrate made of a resin having a melting point in the range of 90 to 230 ° C. An ink layer provided at least partially or entirely on the resin base material of the composite base material, and an area on the ink layer that is in contact with the ink layer and the ink layer formed thereon and the ink A surface-forming layer that covers the entire surface including a region where no layer is formed, wherein the surface-forming layer is obtained by crosslinking and curing the curable resin composition, and In the mold layer, the surface of the surface shaping layer located immediately above the ink layer and the upper portion in the vicinity thereof has a convex shape, and further has a concave pattern,
(2) An adhesive layer and a decorative sheet layer are sequentially laminated on the upper surface of the substrate, a resin composition is applied on the decorative sheet layer, and then the shaping sheet is brought into contact with and integrally cured, A resin decorative board having a resin layer formed by peeling a molding sheet, wherein the molding sheet is the resin decorative board described in (1) above, and (3) an adhesive on the upper surface of the substrate Layers, a decorative sheet layer, a resin composition is coated on the decorative sheet layer, and then the molded sheet according to (1) is contacted and cured integrally, and then the molded sheet A method for producing a resin decorative board, wherein a resin layer is formed by peeling
Is to provide.

  According to the present invention, it has a delicate and bold concavo-convex shape, can be applied with a high-quality and high-quality design that is excellent in design and feel, has excellent releasability, and has excellent heat resistance. A mold decorative sheet, a resin decorative board obtained by using the mold decorative sheet, and a method for producing a resin decorative board using the mold decorative sheet can be obtained. Especially when used for delicate patterns such as wood grain patterns, the unevenness of the conduit part can be expressed realistically, and the molded decorative material can obtain the same texture as the material using actual wood .

  The moldable sheet of the present invention comprises a heat-resistant substrate having a heat shrinkage (150 ° C. × 30 minutes) measured in accordance with JIS C2318 of 2% or less, and a resin having a melting point in the range of 90 to 230 ° C. An ink layer provided at least partially or over the entire surface of the resin base material of the composite base material with the base material, and the ink layer is present on and in contact with the ink layer, and the ink layer is formed. And a surface-forming layer that covers the entire surface including the region where the ink layer is not formed, and the surface-forming layer is obtained by crosslinking and curing the curable resin composition. And in the surface shaping layer, the surface of the surface shaping layer located immediately above the ink layer and the upper portion in the vicinity thereof has a convex shape, and further has a concave pattern.

The structure of the shaping sheet of this invention is demonstrated using FIGS. 1-7 is a schematic diagram which shows the cross section of the shaping sheet 1 of this invention. An example shown in FIG. 1 is a uniform and uniform penetration preventing layer 6, an ink layer 3, and a curable resin covering the entire surface of a resin substrate 22 of a composite substrate 2 of a heat resistant substrate 21 and a resin substrate 22. The surface shaping layer 5 obtained by crosslinking and curing the composition is laminated in this order, and the surface shaping layer 5 has a fine uneven surface 13 on the surface thereof. The ink layer 3 exists partially, and an interaction region 4 is formed in the surface shaping layer immediately above and near the ink layer 3. The interaction area 4 is represented by a set of points in the figure.
The upper part of the interaction region 4 on the outermost surface of the surface shaping layer 5 has a raised shape 7 raised with the formation of the ink layer 3. Furthermore, a synthesizing effect by applying the recessed pattern 14 by embossing forms a shaped sheet having a concavo-convex shape as a whole and a fine and bold concavo-convex shape. Further, by changing the thickness of the ink layer 3 as shown in FIG. 3, the raised shape 7 corresponding to the thickness is expressed on the surface of the surface shaping layer 5, thereby providing a richer uneven shape. it can.

The extent of the expansion of the interaction region 4 formed in the surface shaping layer 5 is not particularly limited as long as it is within the range where the effects of the present invention can be achieved. As shown in FIG. It may stay in the middle of the thickness direction of the surface shaping layer 5 from the surface, or may reach the outermost surface of the surface shaping layer 5.
Further, as shown in FIG. 4, the fine ridge shape 12 expressed by adding the fine particles or the calcined kaolin particles 8 to the surface shaping layer 5 is a ridge shape 7 developed over the entire surface of the surface shaping layer 5 and The fine uneven surface 13 is given a partially fine raised shape.
Formed according to the effect of the fine uneven surface 13 by the interaction region 4 in the surface shaping layer 5, the effect of the fine ridge shape 12 by cueing of fine particles on the surface of the surface shaping layer 5, the ink layer 3 and its thickness. By the effect of the raised shape 7 and the concave pattern 14 formed by embossing, it has a delicate and bold uneven shape, and enables high-quality and precise shaping that is excellent in design and feel. A sheet can be obtained.

  In the case where the ink layer 3 is provided over the entire surface, as shown in FIG. 5, since the fine uneven surface and the concave pattern 14 due to the fine uneven surface 13 exist on the outermost surface of the surface shaping layer 5, this is applied. When used as a mold sheet, it is possible to obtain a resin decorative board that is matte on the surface of the decorative board to be molded and that is excellent in touch feeling. Also in this case, the raised shape 7 is obtained according to the ink thickness by changing the thickness of the ink layer 3 as shown in FIG. 7, and the fine particles are formed on the surface shaping layer 5 as shown in FIGS. Alternatively, the fine raised shape 12 can be obtained by adding the calcined kaolin particles 8 as in the case where the ink layer 3 is partially provided. Further, the extent of the interaction region 4 formed in the surface shaping layer 5 is also the same as described above, and is not particularly limited as long as it is within the range where the effect of the present invention is achieved. May remain in the middle of the thickness direction of the surface shaping layer 5 or may reach the outermost surface of the surface shaping layer 5.

Next, each layer which comprises the shaping sheet of this invention is demonstrated in detail.
[Composite substrate 2]
The composite base material 2 used in the present invention is a heat-resistant base material 21 having a heat shrinkage (150 ° C. × 30 minutes) measured in accordance with JIS C2318 of 2% or less, and a melting point of 90 to 230 ° C. It is a composite body with the base material 22 (henceforth a resin base material) which consists of resin inside.

(Heat resistant substrate 21)
In the present specification, the heat-resistant substrate means one having a heat shrinkage (150 ° C. × 30 minutes) measured in accordance with JIS C2318 of 2% or less. As such a heat-resistant base material, in addition to various papers, a base material made of a resin having excellent heat resistance, for example, a polycarbonate resin, a polyimide resin, a polyethylene terephthalate resin, and the like are preferably mentioned. Alternatively, a plurality of them may be used as a heat resistant substrate.
As various papers used as the substrate, thin paper, kraft paper, titanium paper and the like can be used. These paper base materials are used to reinforce the interlaminar strength between the fibers of the paper base material or between the paper base material and the paper base material, and further to these paper base materials, acrylic resin, styrene butadiene rubber, A resin such as a melamine resin or a urethane resin may be added (resin impregnation after paper making or embedded during paper making). For example, inter-paper reinforced paper, resin impregnated paper and the like.
In addition to these, various papers often used in the field of building materials such as linter paper, paperboard, base paper for gypsum board, or a vinyl wallpaper raw material in which a vinyl chloride resin layer is provided on the surface of the paper can be mentioned. Furthermore, coated paper, art paper, sulfuric acid paper, glassine paper, parchment paper, paraffin paper, Japanese paper, or the like used in the office field or normal printing and packaging can also be used. Moreover, although distinguished from these papers, woven fabrics and non-woven fabrics of various fibers having an appearance and properties similar to paper can be used as the base material. Examples of various fibers include inorganic fibers such as glass fibers, asbestos fibers, potassium titanate fibers, alumina fibers, silica fibers, and carbon fibers, or synthetic resin fibers such as polyester fibers, acrylic fibers, and vinylon fibers.

From the viewpoint of dimensional stability, the heat shrinkage rate of the heat-resistant substrate needs to be 0.5% or less, preferably 0.3% or less, and more preferably 0.2% or less. Moreover, if the heat shrinkage rate is within the above range, heat can be sufficiently applied during the formation of the concave pattern, so that a high-quality and dense shaped sheet excellent in design and feel can be obtained.
The thickness of the heat-resistant substrate is not particularly limited, but from the viewpoint of productivity and the like, when the heat-resistant substrate is a paper substrate, the weighing is usually about ²⁰ to 250 g / m ² . preferably in the range of 30 to 150 g / m ^2, more preferably in the range of 30 to 100 g / m ^2, in the case of a substrate heat-resistant substrate is made of resin, 20 to 150 [mu] m is preferred, 30 100 μm is more preferable.

(Resin substrate 22)
The resin base material used in the present invention is a resin having a melting point in the range of 90 to 230 ° C, preferably a resin having a melting point in the range of 120 to 175 ° C, more preferably in the range of 145 to 175 ° C. A base material made of resin. It is preferable that the melting point is in the above range because a good concave pattern can be formed.
Such resins include low density polyethylene resins (including linear low density polyethylene resins), medium density polyethylene resins, high density polyethylene resins, ethylene α-olefin copolymers, polypropylene resins, polymethylpentene resins, polybutene resins, Polyolefin resins such as ethylene-propylene copolymer, propylene-butene copolymer, olefinic thermoplastic elastomer, or a mixture thereof, polyethylene terephthalate resin, polybutylene terephthalate resin, polyethylene naphthalate-isophthalate copolymer resin, polyester Preferred examples include polyester resins such as thermoplastic elastomers. Of these, polyethylene resin, polypropylene resin, and polyethylene terephthalate resin are preferable.

The resin base material can be subjected to physical or chemical surface treatment such as an oxidation method or an unevenness method on one side or both sides, if desired, in order to improve the adhesion with the layers provided above and below the resin base material.
Examples of the oxidation method include corona discharge treatment, chromium oxidation treatment, flame treatment, hot air treatment, ozone / ultraviolet treatment method, and examples of the unevenness method include a sand blast method and a solvent treatment method. These surface treatments are appropriately selected depending on the type of substrate, but generally, a corona discharge treatment method is preferably used from the viewpoints of effects and operability.
In addition, the resin base material may be subjected to a treatment such as forming a primer layer for the purpose of enhancing interlayer adhesion between the base material and each layer.

  Although there is no restriction | limiting in particular about the thickness of a resin base material, The range of 1-100 micrometers is preferable, More preferably, it is 1-50 micrometers, More preferably, it is the range of 10-30 micrometers. If the thickness of the resin substrate is within the above range, it is preferable because good productivity can be secured and a good concave pattern can be applied to the shaped sheet.

[Penetration preventing layer 6]
The permeation prevention layer 6 is a layer provided as desired, and suppresses the penetration of the ink constituting the ink layer 3 and the curable resin constituting the surface shaping layer 5 into the composite substrate 2. It has a function. Therefore, the penetration preventing layer 6 may be located between the composite base material 2 and the ink layer 3. Usually, a uniform and uniform layer obtained by crosslinking and curing a curable resin that forms the surface-forming layer 5 and an adhesive curable resin is formed between the composite substrate 2 and the ink layer 3 as shown in FIG. Provided. This also serves to enhance the adhesion between the composite substrate 2, the ink layer 3, and the surface shaping layer 5.

[Ink layer 3]
The ink layer 3 in the shaping sheet of the present invention is laminated on the permeation preventing layer 6 or the like provided as necessary as shown in FIG. 7 and the layer which produces the fine uneven surface 13.
Although the mechanism by which the fine uneven surface 13 is generated on the surface of the surface shaping layer 5 has not been fully elucidated, the surface shaping layer 5 is formed on the surface of the ink layer 3 based on the results of various experiments, observations and measurements. When the uncured product of the curable resin composition for forming the ink is applied, the resin component of the ink layer 3 and the surface shaping layer are partially selected depending on the combination of the materials and the appropriate selection of the coating conditions. This is presumably due to the development of interactions such as elution, dispersion, and mixing. At this time, each of the resin components in the ink of the ink layer 3 and the uncured product of the curable resin composition is not completely compatible in a short time but is in a suspended state, and is directly above the ink layer 3. And the part which exists in the vicinity and became this suspension state is considered to form the interaction region, and to express the fine uneven surface 13. When this state is fixed by crosslinking and curing the surface shaping layer with this suspended state, the interaction region 4 is partially formed in the surface shaping layer, and the fine uneven surface 13 is formed. It is presumed to be made.

  The ink that forms the ink layer 3 has a property capable of expressing an interaction such as elution, dispersion, and mixing with the curable resin composition that forms the surface shaping layer 5, and the curable resin composition It is appropriately selected in relation to a product (uncured product). Specifically, an ink having a non-crosslinkable resin as the binder resin is preferable, and for example, a thermoplastic (non-crosslinked type) urethane resin is preferable. Here, the content of the urethane resin is 50% by mass or more from the viewpoint of further strengthening the interaction with the curable resin composition forming the surface shaping layer 5 and obtaining a feeling of unevenness of the further pattern. More preferably.

  As the urethane resin, a non-cross-linked type, that is, a three-dimensionally crosslinked thermoplastic resin having a linear molecular structure is selected instead of a network-like three-dimensional molecular structure. It is preferable to do. Examples of such non-crosslinked urethane resins include polyol components such as acrylic polyols, polyester polyols and polyether polyols, and isocyanate components such as tolylene diisocyanate, xylene diisocyanate, diphenylmethane diisocyanate and other aromatic isocyanates, and isophorone diisocyanate. And a urethane resin obtained by reacting an isocyanate such as an aliphatic or alicyclic isocyanate such as hexamethylene diisocyanate and hydrogenated tolylene diisocyanate. Usually, the number of hydroxyl groups in one molecule of polyol and the number of isocyanate groups in one molecule of isocyanate are two on average. The average molecular weight of the urethane resin is about 10,000 to 50,000, and the glass transition temperature (Tg) is preferably about −70 to −40 ° C. for the expression of the interaction region.

  If necessary, a saturated or unsaturated polyester resin, an acrylic resin, or a vinyl chloride-vinyl acetate copolymer is mixed to adjust the degree of expression of the interaction region, that is, the degree of the fine uneven surface 13. can do. Of these, polyester resins are preferable, and unsaturated polyester resins are particularly preferable. The addition amount of the unsaturated polyester resin is preferably in the range of 10 to 50% by mass with respect to the total amount of the binder of the ink. Within this range, a sufficient enhancement effect of expression of the interaction region can be obtained. The unsaturated polyester resin is not particularly limited as long as it is a reaction product of an unsaturated dicarboxylic acid and a glycol. Examples of the unsaturated dicarboxylic acid include maleic acid, fumaric acid, itaconic acid, and the like. Examples include ethylene glycol, diethylene glycol, propylene glycol, and butylene glycol.

An extender is preferably contained in the ink composition for forming the ink layer 3. By containing the extender, thixotropy can be imparted to the ink composition, and the shape of the ink composition is maintained when the ink layer 3 is printed using a plate. As a result, the sharpness of the concavo-convex shape at the end portion that transitions from the convex portion to the concave portion can be emphasized, and a sharp design expression is possible.
The extender pigment used in the present invention is not particularly limited, and is suitably selected from, for example, silica, talc, clay, barium sulfate, barium carbonate, calcium sulfate, calcium carbonate, magnesium carbonate and the like. Of these, silica, which is a material having a high degree of freedom in material design such as oil absorption, particle size, pore volume, etc., and excellent in designability, whiteness, and coating stability as an ink, is preferred. Is preferred. As a particle size of a silica, the range of 0.1-5 micrometers is preferable. When it is 0.1 μm or more, the thixotropy of the ink does not become extremely high when it is added to the ink, and the viscosity of the ink does not increase too much, so that printing can be controlled easily. In other words, it becomes easier to control the raised shape. In addition, when trying to express a conduit pattern part in the production of a wood grain pattern, the ink head thickness of the conduit pattern part is usually 5 μm or less, and if the silica particle size is smaller than the application thickness, the particle heads are compared. Since the state of the interaction region expression is natural because the target is not conspicuously pressed, a sense of incongruity of the raised shape hardly occurs, and a natural finish is obtained.
The content of these extender pigments in the ink composition is preferably in the range of 5 to 15% by mass. If it is 5% by mass or more, sufficient thixotropy can be imparted to the ink composition, and if it is 15% by mass or less, the effect of imparting the raised shape 7 and the fine uneven surface 13 is completely reduced. It is preferable.

About the application quantity of the ink which forms the ink layer 3, it is preferable that it is the range of 1-50 g / m < ² >. When the amount is 1 g / m ² or more, the above-described interaction between the ink and the resin composition occurs, and a sufficient interaction area is obtained, so that a sufficient uneven shape is obtained on the surface of the shaping sheet. On the other hand, when it is 50 g / m ² or less, there is no mechanical restriction in printing ink, and it is economically advantageous. From the above viewpoint, the coating amount of the ink further 1 to 30 g / m ^2, preferably in particular from 1 to 10 g / m ^2, and most preferably from 1 to 7 g / m ^2.

Further, by changing the coating amount of the ink composition, the thickness of the ink constituting the ink layer 3 can be made non-uniform, and the degree of the height difference of the raised portion that is expressed thereby is stepwise or continuous. As a result, the pattern of the shaping sheet can be changed to a gradation pattern in which the ridge shape changes stepwise or a continuous pattern in which the undulation of the ridge changes continuously.
This is because, as the coating amount of the ink layer 3 is relatively increased, the interaction between the ink layer 3 and the surface shaping layer 5 is relatively increased, and the degree of the suspended state is further increased. This is considered to be because the undulation of the raised shape becomes larger.

This will be described in detail below with reference to FIGS. 3 and 7, the thicknesses of the inks 3-a, 3-b, and 3-c constituting the ink layer 3 are made different. That is, the film thickness is gradually reduced in the order of 3-a, 3-b, and 3-c. By doing so, the interaction regions 4-a, 4-b, and 4-c can be changed in stages, and the resulting raised shapes are in the order of 7-c, 7-b, 7-a. Raises step by step. This is because the thickness of the ink constituting the ink layer 3 is not uniform and is applied so that the thickness of the ink decreases in the order of 3-a, 3-b, 3-c. It is considered that the undulation of the raised shape becomes more remarkable in the larger portion, and changes so that the undulation of the convex shape becomes smaller in gradation in the order of 3-a, 3-b, and 3-c. By changing the thickness of the ink more finely, the concavo-convex shape can be continuously changed.
With the shaped sheet having such a structure, it becomes possible to give a more diverse and delicate texture. The method of changing the thickness of the ink constituting the ink layer 3 can usually be easily performed by changing the amount of ink applied, and by changing the amount of ink applied continuously, the above steps It is also possible to continuously change the change continuously.

  Next, in the example shown in FIG. 8, the ink layer 3 on the composite base material 2 is continuously changed in thickness in a plane parallel to the base material surface (the central part is thick and heads to the side part). The surface shaping layer 5 in which the curable resin composition is crosslinked and cured is laminated thereon (so as to be thinner). As shown in FIG. 3, the surface shaping layer immediately above and near the ink layer forms an interaction region. In the example of FIG. 8, the interaction regions 4-c, 4-b, 4-a correspond to the thickness of the ink layer increasing in the order of 3-c, 3-b, 3-a. In order, the undulations of the raised shape increase continuously. As a result, in the surface shaping layer 5, the undulation of the raised shape continuously increases in this order.

[Surface shaping layer 5]
(Curable resin composition)
As described above, the surface shaping layer 5 is composed of a material obtained by crosslinking and curing the curable resin composition. Here, the curable resin composition is composed of a curable resin, components added as necessary, various additives, and the like, for example, when the curable resin is an ionizing radiation curable resin described later. Is referred to as an ionizing radiation curable resin composition.
In order to form the surface shaping layer by printing, the curable resin composition needs to have printability. Further, in order to form a pattern by printing, it is necessary to set so that the transferred pattern does not fall when transferred from the gravure plate to the shaping sheet. For these reasons, it is necessary to mainly use a resin having a high viscosity at room temperature. Specifically, it is preferable to use a polymerizable oligomer or a prepolymer as a main resin, and add an extender pigment thereto to improve the thixotropy of the curable resin composition. As the extender, those used in the ink layer 3 described above can be preferably used. Further, solvent dilution is performed, the viscosity is lowered to a printable viscosity, a pattern is formed by printing, solvent drying is performed by heating, and crosslinking and curing is performed by a method such as heating or ionizing radiation irradiation. Further, a polyfunctional polymerizable monomer may be added in order to increase the heat resistance and the crosslinking density.

The curable resin in the curable resin composition is not particularly limited, for example, thermosetting resins such as melamine, urea, epoxy, ketone, diallyl phthalate, unsaturated polyester, and phenol, Or an ionizing radiation-curable resin can be mentioned. Among these, an ionizing radiation curable resin is preferable from the viewpoint of improving the surface strength of the shaping sheet.
Here, the ionizing radiation curable resin is a resin having an energy quantum capable of crosslinking and polymerizing molecules in an electromagnetic wave or a charged particle beam, that is, a resin that is crosslinked and cured by irradiation with ultraviolet rays or electron beams. Say. Specifically, it can be appropriately selected from polymerizable monomers, polymerizable oligomers or prepolymers conventionally used as ionizing radiation curable resins.
Typically, as the polymerizable monomer, a (meth) acrylate monomer having a radically polymerizable unsaturated group in the molecule is suitable. By including the (meth) acrylate monomer, the above-described ink layer is formed. Interaction with the ink composition to be formed occurs, and the difference in the undulation of the raised shape is suitably formed. The content of the (meth) acrylate monomer is 50% by mass or more from the viewpoint of further strengthening the interaction with the ink composition, obtaining a difference in the undulation of the raised shape, and obtaining a fine uneven surface. More preferably.

  As the (meth) acrylate monomer, a polyfunctional (meth) acrylate is preferable. Here, “(meth) acrylate” means “acrylate or methacrylate”. 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. Specifically, ethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, 1,4-butanediol di (meth) acrylate, 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 diphosphate ( (Meth) acrylate, allylated cyclohexyl di (meth) acrylate, isocyanurate di (meth) acrylate, trimethylolpropane tri (meth) acrylate, ethylene oxide modified trimethylo Propane 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, etc. Is mentioned. These polyfunctional (meth) acrylates may be used singly or in combination of two or more.

  In the present invention, a monofunctional (meth) acrylate can be used in combination with the polyfunctional (meth) acrylate as long as the object of the present invention is not impaired, for the purpose of lowering the viscosity. Examples of monofunctional (meth) acrylates include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, cyclohexyl ( Examples include meth) acrylate, 2-ethylhexyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, and isobornyl (meth) acrylate. These monofunctional (meth) acrylates may be used alone or in combination of two or more.

  Next, as the polymerizable oligomer, an oligomer having a radical polymerizable unsaturated group in the molecule, for example, epoxy (meth) acrylate, urethane (meth) acrylate, polyester (meth) acrylate, polyether (meth) acrylate System oligomers and the like. Here, the epoxy (meth) acrylate oligomer can be obtained, for example, by reacting (meth) acrylic acid with an oxirane ring of a relatively low molecular weight bisphenol type epoxy resin or novolak type epoxy resin and esterifying it. . Further, a carboxyl-modified epoxy (meth) acrylate oligomer obtained by partially modifying this epoxy (meth) acrylate oligomer with a dibasic carboxylic acid anhydride can also be used. The urethane (meth) acrylate oligomer can be obtained, for example, by esterifying a polyurethane oligomer obtained by reaction of polyether polyol or polyester polyol and polyisocyanate with (meth) acrylic acid. Examples of polyester (meth) acrylate oligomers include esterification of hydroxyl groups of polyester oligomers having hydroxyl groups at both ends obtained by condensation of polycarboxylic acid and polyhydric alcohol with (meth) acrylic acid, It can be obtained by esterifying the terminal hydroxyl group of an oligomer obtained by adding an alkylene oxide to a carboxylic acid with (meth) acrylic acid. The polyether (meth) acrylate oligomer can be obtained by esterifying the hydroxyl group of the polyether polyol with (meth) acrylic acid.

  Furthermore, other polymerizable oligomers include polybutadiene (meth) acrylate oligomers with high hydrophobicity that have (meth) acrylate groups in the side chain of polybutadiene oligomers, and silicone (meth) acrylate oligomers that have polysiloxane bonds in the main chain. In a molecule such as an aminoplast resin (meth) acrylate oligomer modified with an aminoplast resin having many reactive groups in a small molecule, or a novolak epoxy resin, bisphenol epoxy resin, aliphatic vinyl ether, aromatic vinyl ether, etc. There are oligomers having a cationic polymerizable functional group.

  In the present invention, the interaction between the ink composition constituting the ink layer 3 and the ionizing radiation curable resin composition constituting the surface shaping layer 5 is important as described above. The ionizing radiation curable resin composition is selected, and the curable resin in the ionizing radiation curable resin composition preferably contains a polyfunctional (meth) acrylate monomer.

  When an ultraviolet curable resin is used as the ionizing radiation curable resin, it is desirable to add about 0.1 to 5 parts by mass of the photopolymerization initiator with respect to 100 parts by mass of the curable resin composition. The initiator for photopolymerization can be appropriately selected from those conventionally used and is not particularly limited. For example, for a polymerizable monomer or polymerizable oligomer having a radically polymerizable unsaturated group in the molecule. Benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin-n-butyl ether, benzoin isobutyl ether, acetophenone, dimethylaminoacetophenone, 2,2-dimethoxy-2-phenylacetophenone, 2,2-diethoxy-2 -Phenylacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-hydroxycyclohexyl phenyl ketone, 2-methyl-1- [4- (methylthio) phenyl] -2-morpholino-propane-1 - 4- (2-hydroxyethoxy) phenyl-2 (hydroxy-2-propyl) ketone, benzophenone, p-phenylbenzophenone, 4,4′-diethylaminobenzophenone, dichlorobenzophenone, 2-methylanthraquinone, 2-ethylanthraquinone, 2 -Tertiary butylanthraquinone, 2-aminoanthraquinone, 2-methylthioxanthone, 2-ethylthioxanthone, 2-chlorothioxanthone, 2,4-dimethylthioxanthone, 2,4-diethylthioxanthone, benzyldimethyl ketal, acetophenone dimethyl ketal It is done.

Examples of the polymerizable oligomer having a cationic polymerizable functional group in the molecule include aromatic sulfonium salts, aromatic diazonium salts, aromatic iodonium salts, metallocene compounds, and benzoin sulfonic acid esters.
Moreover, as a photosensitizer, p-dimethylbenzoic acid ester, tertiary amines, a thiol type sensitizer, etc. can be used, for example.

  In the present invention, it is preferable to use an electron beam curable resin as the ionizing radiation curable resin. This is because the electron beam curable resin can be made solvent-free, is more preferable from the viewpoint of environment and health, and does not require a photopolymerization initiator, and can provide stable curing characteristics.

(Fine particles)
Moreover, it is preferable that fine particles are further blended in the curable resin composition used in the present invention. As the fine particles, those having an average particle diameter that is a value close to the plus side of the maximum thickness of the surface shaping layer 5 located immediately above the ink layer 3 are used. The shaped sheet of the present invention in which fine particles are blended will be described in detail with reference to FIG. FIG. 4 is a schematic view showing a cross section of a shaped sheet in which fine particles are blended in the curable resin composition.

The fine particles 8 (8-a, 8-b) blended in the surface shaping layer have an average particle diameter d _A of the maximum thickness t _M of the surface shaping layer 5 located immediately above the ink layer 3. The value near the plus side, that is, d _A is slightly larger than t _M , and cueing of the fine particles 8-a occurs from the surface of the surface shaping layer 5 located immediately above the ink layer 3. The portion where the cue has occurred forms a fine ridge shape 12, so that a fine unevenness can be formed. At the same time, within the surface shaping layer 5, the interaction between the ink in the ink layer 3 and the curable resin composition constituting the surface shaping layer 5 causes the ink directly on the ink layer 3 and in the vicinity thereof. The interaction area | region 4 which expresses a protruding shape is formed.
On the other hand, the fine particles 8-b located in a portion that is not directly above the ink layer 3 do not cue and contribute to the expression of the convex shape, but the position of the fine particles in the surface shaping layer in this way. There are various effects on the expression of the convex shape.

Therefore, the effect of the fine uneven surface 13 by the interaction region 4 in the surface shaping layer 5 and the fine ridge shape 12 by the cueing of the fine particles on the surface of the surface shaping layer 5, the ink layer 3 and the thickness thereof described above. The rugged shape that appears on the surface of the surface shaping layer due to the effect of the raised shape 7 formed according to the embossing process and the embossed pattern is delicate and bold, and has a high quality design and feel. It will be a delicate and precise one.
The maximum thickness t _M of the surface shaping layer 5 positioned immediately above the ink layer 3 is the thickness of the surface shaping layer 5 when the convex shape associated with the formation of the ink layer 3 is not formed. When the convex shape is formed, the thickness includes the portion.

As the particle size distribution is closer to monodisperse, it is easier to set the amount of use, and the above effect is favorably exhibited with a small amount of use.
In the present invention, the coefficient of variation CV value [(standard deviation of particle size / average particle size) × 100] of the particle size distribution of the fine particles is preferably 30% or less. When the CV value is 30% or less, the fine particles have a practical particle size distribution and can sufficiently exhibit the above effects with an appropriate amount of use. This CV value is more preferably 20% or less, still more preferably 15% or less.

Further, the average particle diameter of the fine particles is d _A , the maximum thickness of the surface shaping layer located immediately above the ink layer is t _M , and the thickness of the surface shaping layer in the region where no ink layer is present is t _G. Formula (I)
1.05 × t _M ≦ d _A ≦ t _G (I)
It is preferable to satisfy the relationship. If the average particle diameter d _{A of the} fine particles is 1.05 × t _M or more, even if the fine particles sink into the ink layer, the surface of the surface shaping layer located immediately above the ink layer In this case, the fine particles are cueed, and the above effect is sufficiently exhibited. Further, when the d _A is equal to or less than t _G , cueing of the fine particles is suppressed in the surface shaping layer in the region where the ink layer does not exist.
The shape of the fine particles is not particularly limited, and fine particles such as spherical, ellipsoidal, and polyhedral shapes can be used, but spherical fine particles are preferable. In the present invention, the particle diameter of the fine particles having a shape other than the spherical shape is a value indicated by the diameter of the circumscribed sphere.

  The content of the fine particles in the curable resin composition is usually selected in the range of 2 to 20% by mass, although it depends on the average particle size of the fine particles and the coefficient of variation CV value of the particle size distribution. When the content is 2% by mass or more, the effect of containing the fine particles is exhibited, and when the content is 20% by mass or less, the unevenness of the uneven shape formed on the surface of the shaped sheet is good. The preferable content of the fine particles is 4 to 16% by mass, and more preferably 4 to 13% by mass.

The fine particles may be either inorganic fine particles or organic fine particles. Examples of the fine particles include inorganic particles such as silica, alumina, aluminosilicate, kaolinite, calcium carbonate, barium sulfate, and glass, and organic fine particles include acrylic resin, polycarbonate resin, and urethane type. Examples thereof include particles such as resin, urea resin, benzoguanamine resin, and benzoguanamine-melamine-formaldehyde condensate.
These fine particles may be used alone or in combination of two or more. From the viewpoint of the effect of the present invention, silica particles are preferred. The fine particles may be used in combination with the calcined kaolin particles having the same effect.

(Baking kaolin particles)
The curable resin composition used in the present invention preferably contains calcined kaolin particles. By including the calcined kaolin particles in the surface shaping layer, the uneven shape on the surface of the shaping sheet becomes fine due to the formation of the fine raised shape 12, and the marring resistance is improved. Here, the term “marling” means that small scratches are generated when the sheet surface is rubbed, and “excellent marring resistance” means that scratches are difficult to be made. By imparting such performance to the shaping sheet, it is possible to strengthen the surface shaping layer, obtain a shaping sheet that can withstand longer use, and reduce the manufacturing cost of the resin decorative board It becomes.

The calcined kaolin particles used to impart a more delicate uneven shape and marling resistance to the surface of the shaped sheet are kaolin particles obtained by calcining general (hydrous) kaolin particles, but as a filler By adding the calcined kaolin particles, the improvement in marling resistance, which could not be realized with silica particles or hydrous kaolin particles before firing, is realized. The particle size of the calcined kaolin particles may be appropriately selected according to the application, required physical properties, etc. For example, those having an average particle size of about 0.5 to 2 μm are used. Moreover, what is necessary is just to select suitably the addition amount of baking kaolin particle | grains according to a use, a required physical property, etc., For example, it is about 5-50 mass parts with respect to 100 mass parts of curable resin compositions.
The calcined kaolin particles are superior in paint stability to the hydrous kaolin particles.

  As the calcined kaolin particles, those whose surfaces are further treated may be used. By using the surface-treated calcined kaolin particles, the effect of improving marring resistance can be further increased. As the surface treatment, there is a surface treatment with a silane coupling agent. Examples of the silane coupling agent include known silane coupling agents having an alkoxy group, amino group, vinyl group, epoxy group, mercapto group, chloro group and the like. For example, γ-aminopropyltriethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-methacryloxypropylmethyldimethoxysilane, γ-methacryloxypropyldimethylmethoxysilane, γ-methacryloxypropyltriethoxysilane, γ-methacryloxy Propyldimethylethoxysilane, γ-acryloxypropyltrimethoxysilane, γ-acryloxypropylmethyldimethoxysilane, γ-acryloxypropyldimethylmethoxysilane, γ-acryloxypropyltriethoxysilane, γ-acryloxypropylmethyldiethoxysilane , Γ-acryloxypropyldimethylethoxysilane, vinyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysila Etc.

(Reactive silicone)
The curable resin composition used in the present invention preferably further contains reactive silicone. This is because the surface-forming layer 5 contains reactive silicone to improve the releasability and improve the resistance to repeated continuous use. In addition, when an additive such as a pearl pigment or a filler is included in the object to be molded, it prevents the additive or filler contained in the object to be removed during the process of manufacturing the decorative board. effective.

Here, the reactive silicone means a modified silicone oil in which an organic group is introduced into the side chain or terminal and has reactivity depending on the nature of the introduced organic group. The reactive silicone is specifically modified silicone oil side chain type, modified silicone oil both end type, modified silicone oil one end type, modified silicone oil side chain both end type, etc. Examples thereof include epoxy modification, mercapto modification, carboxyl modification, carbinol modification, phenol modification, methacryl modification, and different functional group modification.
The reactive silicone reacts and bonds with the curable resin when the surface shaping layer is cured to be integrated. Therefore, when the decorative board of the present invention is molded by hot pressing, it does not bleed out (does not bleed out) on the surface of the decorative board, so that the adhesion between the shaped sheet of the present invention and the decorative board is significantly improved. Thus, it becomes possible to mold a delicate design having a fine uneven shape into a decorative material.

  The amount of the reactive silicone used is in the range of about 0.1 to 50 parts by mass, preferably in the range of about 0.5 to 10 parts by mass per 100 parts by mass of the curable resin. When the amount of the reactive silicone used is 0.1 parts by mass or more, the decorative plate and the surface of the shaping sheet are sufficiently peeled off, the uneven shape of the surface of the shaping sheet is maintained, and it can withstand long-term use. sell. On the other hand, if the amount of the reactive silicone used is 50 parts by mass or less, no repellency occurs when the curable resin composition is applied to the base material, so the surface of the coating film is not roughened and the coating stability is improved. To do.

(Various additives)
Moreover, various additives are mix | blended with the curable resin composition used by this invention according to the desired physical property of the obtained cured resin layer. Examples of additives include a weather resistance improver, an abrasion resistance improver, a polymerization inhibitor, a crosslinking agent, an infrared absorber, an antistatic agent, an adhesion improver, an antioxidant, a leveling agent, a thixotropic agent, and a cup. A ring agent, a plasticizer, an antifoaming agent, a filler, a solvent, etc. are mentioned.

  Here, as the weather resistance improving agent, an ultraviolet absorber or a light stabilizer can be used. It is added for long-term use of the shaped sheet. The ultraviolet absorber may be either inorganic or organic, and as the inorganic ultraviolet absorber, titanium dioxide, cerium oxide, zinc oxide or the like having an average particle diameter of about 5 to 120 nm can be preferably used. Examples of the organic ultraviolet absorber include benzotriazole-based compounds, specifically 2- (2-hydroxy-5-methylphenyl) benzotriazole, 2- (2-hydroxy-3,5-di-tert-). Amylphenyl) benzotriazole, 3- [3- (benzotriazol-2-yl) -5-tert-butyl-4-hydroxyphenyl] propionic acid ester of polyethylene glycol, and the like. On the other hand, examples of the light stabilizer include hindered amines, specifically 2- (3,5-di-tert-butyl-4-hydroxybenzyl) -2′-n-butylmalonate bis (1,2,2). , 6,6-pentamethyl-4-piperidyl), bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, tetrakis (2,2,6,6-tetramethyl-4-piperidyl)- 1,2,3,4-butanetetracarboxylate and the like. Further, as the ultraviolet absorber or light stabilizer, a reactive ultraviolet absorber or light stabilizer having a polymerizable group such as a (meth) acryloyl group in the molecule can be used.

  Examples of the wear resistance improver include, for inorganic substances, spherical particles such as α-alumina, silica, kaolinite, iron oxide, diamond, and silicon carbide. Examples of the particle shape include a sphere, an ellipsoid, a polyhedron, a scale shape, and the like. Organic materials include synthetic resin beads such as cross-linked acrylic resin and polycarbonate resin. The particle size is usually about 30 to 200% of the film thickness. Among these, spherical α-alumina is particularly preferable because it has high hardness and a large effect on improving wear resistance, and it is relatively easy to obtain spherical particles.

Examples of the polymerization inhibitor include hydroquinone, p-benzoquinone, hydroquinone monomethyl ether, pyrogallol, and t-butylcatechol. Examples of the crosslinking agent include a polyisocyanate compound, an epoxy compound, a metal chelate compound, an aziridine compound, and an oxazoline compound. Used.
As the filler, for example, barium sulfate, talc, clay, calcium carbonate, aluminum hydroxide and the like are used.
As the infrared absorber, for example, a dithiol metal complex, a phthalocyanine compound, a diimmonium compound, or the like is used.

(Formation of surface shaping layer 5)
In the present invention, curable resins such as polymerizable monomers and polymerizable oligomers that are the curable components, components added as necessary, and various additives are uniformly mixed at a predetermined ratio, respectively. A curable resin composition is prepared. The viscosity of this curable resin composition should just be a viscosity which can form an uncured resin layer on the surface of a base material by the below-mentioned coating system, and there is no restriction | limiting in particular.
In the present invention, gravure coating, bar coating, roll coating, and reverse roll are applied to the surface of the substrate so that the thickness after curing of the curable resin composition thus prepared is 1 to 20 μm. It coats by well-known systems, such as a coat and a comma coat, preferably a gravure coat, and forms an uncured resin layer. When the thickness after curing is 1 μm or more, a cured resin layer (surface shaping layer) having a desired function is obtained. The thickness of the surface shaping layer after curing is preferably about 2 to 20 μm.

In the present invention, the uncured resin layer formed in this manner is irradiated with ionizing radiation such as heat, electron beam, and ultraviolet rays to cure the uncured resin layer to obtain a surface shaping layer. Here, when an electron beam is used as the ionizing radiation, the acceleration voltage can be appropriately selected according to the resin used and the thickness of the layer, but the uncured resin layer is usually cured at an acceleration voltage of about 70 to 300 kV. preferable.
In addition, in electron beam irradiation, the transmission capability increases as the acceleration voltage increases, so when using a base material that deteriorates due to the electron beam as the base material, the penetration depth of the electron beam and the thickness of the uncured resin layer By selecting an accelerating voltage so as to be substantially equal, it is possible to suppress the irradiation of the extra electron beam to the base material, and to minimize the deterioration of the base material due to the excess electron beam. it can.

The irradiation dose is preferably such that the crosslinking density of the curable resin in the surface shaping layer is saturated, and 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). .
Further, 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. 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.

  In this way, various additives are added to the formed surface shaping layer so as to have various functions, for example, high hardness and scratch resistance, so-called hard coat function, anti-fogging coat function, antifouling function. A coating function, an antiglare coating function, an antireflection coating function, an ultraviolet shielding coating function, an infrared shielding coating function, and the like can also be imparted.

[Concave pattern 14]
The concave pattern 14 is provided on the shaping sheet by embossing or the like, and gives a high-class feeling excellent in design and touch feeling by the shaping sheet by giving a deep concave shape to the surface of the surface shaping layer 5. Is.
This concave pattern 14 is heated by an embossing plate from the upper surface of the surface shaping layer 5, that is, the outermost layer side, when the shaping sheet of the invention in the manufacturing process is at a temperature at which it can be embossed by any means. It can be formed by pressing. As shown in FIGS. 1 to 9, the unevenness formed by heating and pressing with an embossed plate preferably has the deepest portion reaching the upper surface of the composite substrate 2, and reaching the heat resistant substrate 21. It may be. Moreover, there is no restriction | limiting in particular in the place which forms the concave pattern 14. FIG.

The above embossable temperature is normally selected within a range of about 80 to 250 ° C., gives a good concave shape, and gives a high-class feeling excellent in design and touch feeling by the shaping sheet. Is preferably 100 to 250 ° C, more preferably 150 to 250 ° C, and still more preferably 180 to 240 ° C.
Although the depth of the unevenness | corrugation by the concave pattern 14 is based also on the thickness of a shaping sheet, it is 20-200 micrometers normally, 20-80 micrometers is preferable and 30-60 micrometers is more preferable. A well-known sheet or rotary embossing machine is used to form the concave pattern 14, and the shape of the concave pattern 14 includes a wood grain conduit groove, stone surface unevenness, cloth surface texture, satin, sand, hairline. , There are many strips. Further, by synchronizing with the pattern applied with the ink layer 3 described above, the effect of the present invention becomes more remarkable, but a sufficient effect can be obtained without synchronization.

[Resin decorative board]
(Resin decorative board-1)
The resin decorative board of the present invention is not particularly limited as long as it is produced using the shaping sheet of the present invention. However, as a preferred embodiment, the resin decorative board is bonded to the upper surface of the substrate shown in FIG. The agent layer and the decorative sheet layer are laminated in order, the resin composition is applied onto the decorative sheet layer, and then the molded sheet of the present invention is contacted and cured integrally, and then the molded sheet is peeled off. And a resin decorative board-1 obtained by forming a resin layer.

<< Substrate 10 >>
The substrate 10 of the resin decorative board is not particularly limited, and a plastic film, a plastic sheet metal plate, a wooden board such as wood, a ceramic material, and the like can be appropriately selected depending on the application. When these substrates, particularly plastic sheets, are used as substrates, physical or chemical surface treatment such as oxidation or unevenness is applied to one or both sides as desired in order to improve adhesion to the decorative material. Can be applied. The oxidation method and the uneven method are the same as those described above for the base material of the shaping sheet of the present invention.

The plastic film and the plastic sheet are the same as those described above in the base material of the shaping sheet of the present invention.
As a metal plate, what consists of aluminum, iron, stainless steel, or copper can be used, for example, and what gave these metals by plating etc. can also be used.
Examples of wood-based boards include veneer of various materials such as cedar, firewood, firewood, pine, lawan, teak and melapie, and wood materials such as wood veneer, wood plywood, particle board, and medium density fiber board (MDF). . These can be used alone or in a laminated manner. The wooden board includes not only a wooden board but also a plastic board containing paper powder and reinforced paper having strength.
Examples of the ceramic material include ceramic building materials such as a gypsum plate, a calcium silicate plate, and a wood piece cement plate, ceramics, glass, firewood, fired tiles, plates made mainly of volcanic ash, and the like.
In addition to these, composites of various materials such as a fiber reinforced plastic (FRP) plate, a paper honeycomb on which both sides of an iron plate are attached, and a polyethylene resin sandwiched between two aluminum plates can be used as the substrate.

<< Adhesive layer 9 >>
The adhesive layer 9 is a layer provided to adhere the substrate 10 and the decorative sheet layer 17.
The adhesive used for the adhesive layer 9 is applied using an application device such as a spray, a spreader, or a bar coater. As this adhesive, urea-based, vinyl acetate resin-based, urea resin-based, melamine resin-based, phenolic resin-based, isocyanate-based adhesives, etc. can be used, either alone or as a mixed adhesive that is arbitrarily mixed. . As needed, talc, calcium carbonate, clay, titanium white and other inorganic powders, wheat flour, wood flour, plastic powder, coloring agents, insect repellents, fungicides and the like can be added and mixed in the adhesive. . In general, the adhesive is applied to the substrate surface with a solid content of 35 to 80% by mass and an application amount of 50 to 300 g / m ² .

  Adhesion of the decorative sheet layer 17 on the substrate 10 is usually performed by forming the adhesive layer 9 on the back surface of the decorative sheet layer 17 and adhering the substrate 10 or applying an adhesive on the substrate 10. For example, the sheet layer 17 is attached. For the sticking, a sticking apparatus such as a cold press, hot press, roll press, laminator, wrapping, edge sticking machine, vacuum press or the like can be used.

<Decoupling sheet layer 17>
The decorative sheet layer 17 gives decorativeness to the resin decorative board of the present invention, and a solid print layer 17-b and a pattern layer 17-c provided in order on the sheet layer 17-a are provided in order. It is what was done.
The sheet layer 17-a is not particularly limited as long as it is normally used as a base material for a decorative sheet, and various papers, plastic films, plastic sheets, and the like can be appropriately selected depending on the application. Each of these materials may be used alone, but may be a laminate of any combination such as a composite of paper or a composite of paper and a plastic film.
When using these substrates, particularly plastic films or plastic sheets, as a substrate, an oxidation method or a concavo-convex method may be applied to one or both sides as desired in order to improve the adhesion to the layer provided thereon. Physical or chemical surface treatment can be applied. The oxidation method and the uneven method are the same as those described above for the base material of the shaping sheet of the present invention. Further, the substrate may be subjected to a treatment such as forming a primer layer, or a coating for adjusting the color or a pattern from a design viewpoint may be formed in advance.

Various papers, plastic films, and plastic sheets used as the sheet layer 17-a are the same as those described above in the base material of the shaping sheet of the present invention.
The thickness of the sheet layer 17-a is not particularly limited, but when a sheet made of plastic is used, the thickness is usually in the range of about 20 to 150 μm, preferably 30 to 100 μm. When using the material, the basis weight is usually about ²⁰ to 250 g / m ² , preferably 30 to 150 g / m ² , more preferably 30 to 100 g / m ² .

  The solid print layer 17-b provided on the sheet layer 17-a is also referred to as a concealing layer provided as desired in order to enhance the design of the resin decorative board of the present invention. The solid printing layer 17-b is formed when the surface color on the sheet layer 17-a is adjusted so that the sheet layer 17-a itself is colored or uneven in color. It gives the intended color to the surface of the. Usually, it is formed with an opaque color, but it may be formed with a colored transparent color to make use of the pattern of the base. When taking advantage of the fact that the sheet layer 17-a is white, or when the sheet layer 17-a itself is appropriately colored, it is not necessary to form the solid print layer 17-b.

As the ink used for the formation of the solid printing layer 17-b, an ink in which a binder, a colorant such as a pigment or a dye, an extender pigment, a solvent, a stabilizer, a plasticizer, a catalyst, or a curing agent is appropriately mixed is used. . The binder is not particularly limited, and examples thereof include polyurethane resins, vinyl chloride / vinyl acetate copolymer resins, vinyl chloride / vinyl acetate / acrylic copolymer resins, chlorinated polypropylene resins, acrylic resins, and polyesters. Arbitrary resins, polyamide resins, butyral resins, polystyrene resins, nitrocellulose resins, cellulose acetate resins and the like may be used alone or in combination of two or more.
Colorants include carbon black (black), iron black, titanium white, antimony white, yellow lead, titanium yellow, petal, cadmium red, ultramarine, cobalt blue and other inorganic pigments, quinacridone red, isoindolinone yellow, phthalocyanine Organic pigments or dyes such as blue, metallic pigments composed of scaly foil pieces such as aluminum and brass, pearlescent pigments composed of scaly foil pieces such as titanium dioxide-coated mica and basic lead carbonate, and the like are used.

The pattern layer 17-c gives decorativeness to the sheet layer 17-a, and various patterns are formed on the sheet layer 17-a or the solid printing layer 17-b using ink and a printing machine. Formed by printing. As patterns, there are stone patterns imitating the surface of rocks such as wood grain patterns, marble patterns (for example, travertine marble patterns), fabric patterns imitating cloth and cloth patterns, tiled patterns, brickwork patterns, etc. There are also patterns such as marquetry and patchwork that combine these. These patterns are formed by multicolor printing with the usual yellow, red, blue and black process colors, as well as by multicolor printing with special colors prepared by preparing the individual color plates that make up the pattern. Is done.
As the pattern ink used for the pattern layer 17-c, the same ink as that used for the solid print layer 17-b can be used.

<Resin layer 18>
The resin layer 18 is a layer formed by applying the resin composition on the decorative sheet layer 17 and then bringing the shaping sheet into contact with and curing it, and then peeling the shaping sheet. the thickness of the resin layer 18 is preferably from 100 to 500 g / m ^2, more preferably 100~350g / m ^2, more preferably 150 to 250 g / m ^2.
The resin composition is a composition comprising a resin and a polymerization initiator, a polymerization accelerator, a polymerization inhibitor, and other additives that are added as necessary.

  The resin in the resin composition used in the present invention is not particularly limited as long as it is cured at room temperature or by heating, for example, silicone resin, unsaturated polyester resin, saturated polyester resin, melamine resin, diallyl Phthalate resin (DAP), polycarbonate resin, phenol resin, polyamide, ketone resin, epoxy resin, urethane resin, urea resin, acrylic resin, vinyl resin, alkyd resin, aminoalkyd resin, hydrocarbon resin (aromatic and aliphatic) ), Rubber resins, fluororesins, and the like. Of these, unsaturated polyester resins are preferred.

A polymerization initiator, a polymerization accelerator, and a polymerization inhibitor are added to adjust the curing rate of the resin composition.
As the polymerization initiator, for example, a peroxide such as methyl ethyl ketone peroxide, benzoyl peroxide, and hydroperoxide, and a radical initiator such as azobisisobutyronitrile are appropriately selected and used. 0.5-3 mass% is preferable and, as for the addition amount in the resin composition of a polymerization initiator, 0.5-2.0 mass% is more preferable.

As the polymerization accelerator, for example, a cobalt compound such as cobalt naphthenate, a metal compound such as a vanadium compound or a manganese compound, an amine compound such as dimethylnitrile, or the like is preferably 0.1 to 2.0 mass with respect to the resin composition. %, More preferably 0.3 to 1.0% by mass. As the polymerization inhibitor, for example, hydroquinone, trihydroquinone, benzoquinone, trihydrobenzene and the like can be used. As other additives, for example, in order to adjust the coating viscosity and to crosslink the resin, a compound having a vinyl group such as a styrene monomer can be preferably mentioned, and the addition amount in the resin composition is 10 to 40 mass. % Is preferable, and 15 to 30% by mass is more preferable.
These curing rate modifiers and other additives can be used alone or in combination.

(Resin decorative board-2)
As a preferable aspect of the resin decorative board of the present invention, the molded sheet of the present invention shown in FIG. 12 is inserted and molded between a molded product molded by pressing between the heated pressure plates and molded. Later, a resin decorative sheet-2 obtained by sticking a resin decorative sheet obtained by peeling off the shaping sheet to a substrate via an adhesive layer may also be mentioned.

  The resin decorative sheet 15 has a hard surface, is excellent in heat resistance and stain resistance, and can be selected from a variety of colors in terms of design, so a melamine resin decorative sheet, a diallyl phthalate (DAP) resin decorative sheet , Polycarbonate resin decorative sheets, polyester decorative sheets, and melamine resin decorative sheets and diallyl phthalate (DAP) resin decorative sheets are particularly suitable. In addition, the adhesive used for the substrate 10 and the adhesive layer 9 to be adhered are as described above.

(Method for producing resin decorative board-1)
The resin decorative board of the present invention preferably has an adhesive layer 9 and a decorative sheet layer 17 sequentially laminated on the upper surface of the substrate 10 shown in FIG. 10, and a resin composition is applied on the decorative sheet layer. Next, the molding sheet of the present invention is brought into contact with and cured integrally, and then the molding sheet is peeled off to form the resin layer 18. The exfoliation of the shaping sheet 1 is performed as shown in FIG. 11 to obtain the resin decorative board 11 having a certain shape.

(Method for producing resin decorative board-2)
Further, the resin decorative board of the present invention is preferably molded by inserting a shaping sheet between a molded product and a pressure plate, which are molded by pressing between heated pressure plates, as shown in FIG. After the pressure molding, the resin decorative sheet 15 having a certain shape obtained by peeling the moldable sheet from the molded body is adhered to the substrate 10 via the adhesive layer 9. Is. The exfoliation of the shaping sheet 1 is performed as shown in FIG. 11 to obtain the resin decorative board 11 having a certain shape.

  At this time, an embossed surface of the pressure plate can be suitably used. By using such a pressure plate, it is possible to give the resin decorative plate of the present invention a high-quality feeling with a further increased touch feeling. The depth of the unevenness of the embossing by this pressure plate is usually 20 to 80 μm, preferably 30 to 60 μm, and the shape is wood grain conduit groove, plate surface unevenness, cloth surface texture, satin texture, sand texture, hairline, line There are strips. Further, by synchronizing with the pattern applied with the ink layer 3 described above, the effect of the present invention becomes more remarkable, but a sufficient effect can be obtained without synchronization.

  The resin decorative sheet 15 is not particularly limited as long as it is a publicly known and generally used method. Among them, preferred melamine resin decorative sheets and diallyl phthalate (DAP) resin decorative sheets are generally described below. It can be obtained by the production method mentioned.

The melamine resin decorative sheet is formed by laminating a melamine resin-impregnated sheet on about 4 phenol resin-impregnated core papers, and further overlaying a melamine resin-impregnated sheet thereon, and sandwiching the sheet between two mirror metal plates. For example, the mold sheet is inserted, heat-pressed at 0.98 MPa and 160 ° C. for 20 minutes, allowed to cool to room temperature, and then peeled off from the mold sheet.
The diallyl phthalate (DAP) resin decorative sheet is obtained by sequentially stacking diallyl phthalate resin-impregnated paper on a plate-like base material, and, similar to the manufacturing method of the melamine resin decorative sheet, It is obtained by using and pressing at 140 to 150 ° C., 0.98 MPa for about 10 minutes, allowing to cool to room temperature, and then peeling the shaped sheet. In any case, the decorative board has a delicate and bold uneven shape.

  The resin decorative sheet 15 obtained in this way can be used as a resin decorative sheet by sticking to various substrates. Specifically, the resin decorative board 11 is obtained by sticking the decorative board 11 to the substrate 10 via the adhesive layer 9 as shown in FIG. The adhesive and the bonding method used for the substrate 10 and the adhesive layer 9 to be adhered are as described above.

[Resin decorative board]
The resin decorative board produced by the method of the present invention has the effect of the raised shape formed according to the ink layer and its thickness in the shaped sheet of the present invention, the effect of the fine uneven surface, the effect of cueing of the fine particles (fine It is delicate and bold due to the effect of the raised shape), the concave pattern applied by embossing, and the effect of embossing on the heated pressure plate used to make the resin decorative board. It will be precise. From the viewpoint of exhibiting such an effect, the surface roughness of the resin decorative board at the portion subjected to embossing is preferably 20 to 200 μm, more preferably 20 to 80 μm, and more preferably 30 to 60 μm. Moreover, 0.1-10 micrometers is preferable and, as for the surface roughness of the resin decorative board in the part applicable to a protruding shape and a fine uneven surface, 1-8 micrometers is more preferable.

  The resin decorative board of the present invention can be arbitrarily cut and subjected to optional decoration such as grooving and chamfering on the surface and the mouth using a cutting machine such as a router or a cutter. And various uses, for example, interior or exterior materials of buildings such as walls, ceilings, floors, window frames, doors, handrails, skirting boards, surrounding edges, surface decorative panels for fittings such as malls, kitchens, furniture or light electrical appliances, It can be used for surface decorative boards of cabinets such as OA equipment, interiors and exteriors of vehicles.

EXAMPLES Next, although an Example demonstrates this invention further in detail, this invention is not limited at all by this example.
(Evaluation method)
The shaping sheet and decorative board obtained in each example were evaluated by the following methods.
(1) Measurement of surface roughness The decorative plate is 400 mm long x 400 mm wide, and the surface roughness (arithmetic average surface roughness) is measured using a three-dimensional non-contact surface shape measurement system (Micromap manufactured by Ryoka System Co., Ltd.). ) Was measured.
(2) Peelability The peel strength of the shaped sheet was measured using a tensile / compression tester (Orientec Co., Ltd. RTC-1250A). The sample to be evaluated was 25 mm wide × 50 mm long, and the test was performed at a peeling speed of 300 mm / min, a peeling direction of 180 ° (vertical direction), a load cell load of 10 N, and a measurement environment temperature of 23 ° C. (room temperature).
(3) Suitability for continuous molding The molding was carried out 10 times with the same shaped sheet, the peel strength for each molding was measured, and the peel stability when the shaped sheet was repeatedly used was measured.
(4) Evaluation of embossed design The embossed design of the shaped sheet obtained in the examples and comparative examples was visually evaluated.
(5) Embossing rate About the decorative board obtained by the Example and the comparative example, the embossing rate was measured using the said surface roughness meter, and the following reference | standard evaluated.
○: Embossing rate 60% or more and 100% or less △: Embossing rate 40% or more and less than 60% ×: Embossing rate 0% or more and less than 40% (6) Emboss fastness obtained in Examples and Comparative Examples The decorative board was immersed in an oil bath at 120 ° C. for 1 minute. The embossing after dipping and the gloss were visually checked and evaluated according to the following criteria.
◎: No wrinkle return and no change in gloss ○: Some wrinkle return and some change in gloss, but no problem for practical use △: There is a return to wrinkle and change in gloss, but no problem for practical use ×: (7) Embossability (heat resistance)
In Examples and Comparative Examples, the state of the shaped sheet when the shaped sheet was heated to 200 ° C. and embossed was evaluated according to the following criteria.
A: The shaped sheet did not stretch at all and could be sufficiently embossed.
○: Although the shaped sheet was slightly stretched, there was no practical problem and sufficient embossing could be performed.
X: The shaped sheet was broken and could not be used.

Example 1: Production of a shaping sheet High-density polyethylene film surface of high-density polyethylene laminated paper ("Eryorium transfer paper 50 g" manufactured by Eiwa Co., Ltd., base paper weighing: 50 g / m ² , high-density polyethylene film thickness: 15 μm) After the corona treatment, a primer ink (acrylic ink “EBF tuning primer” manufactured by Showa Ink Industries, Ltd.) was gravure-printed on the entire treated surface to form a penetration preventing layer (primer layer).
Next, ink (urethane-based conduit ink “conduit MINI (B)” manufactured by The Inktec Co., Ltd.) was printed on the conduit portion of the wood grain pattern by a pattern plate to form an ink layer. Further, an electron beam curable resin obtained by adding 5% by mass of calcined kaolin particles and 2% by mass of reactive silicone methacrylate to an electron beam curable resin ("REB-GE" manufactured by Dainichi Seika Kogyo Co., Ltd.) on these ink layers. The composition was applied at a coating amount of 4 g / m ² by a gravure offset coater method. After coating, an electron beam with an acceleration voltage of 175 kV and an irradiation dose of 30 kGy (3 Mrad) was irradiated to cure the electron beam curable resin composition to form a surface shaping layer. The molding sheet thus obtained was heated to 230 ° C. with a preheater, and immediately, from the surface molding layer side, embossing using an embossing roll (58.8 N / m ² pressure) was performed, A concave pattern in synchronization with the ink layer formed above was applied. The shaped sheet was a film with a high-class feeling and a delicate wood grain expression.

Example 2: Production of resin decorative board A melamine resin impregnated sheet was laminated on about 4 phenol resin impregnated core papers, and an overlay paper impregnated with melamine resin on an overlay paper of about 35 g / m ² was laminated thereon. A molded sheet manufactured in Example 1 between two mirror surface metal plates (including a metal plate that is in contact with the surface side of the resin decorative plate is embossed) and has a concavo-convex shape on the surface. Was inserted and heated and pressed at 0.98 MPa and 160 ° C. for 20 minutes. After cooling to room temperature, the molded sheet is peeled off, so that the surface roughness of the part formed by the uneven surface by the fine uneven surface and the raised shape of the formed sheet is 2 to 4 μm, and embossing is performed. A melamine resin decorative sheet having a delicate and bold concavo-convex shape having a surface roughness of 10 to 12 μm and excellent in design and feel was obtained. Moreover, the obtained melamine resin decorative sheet had a texture similar to that of a material using actual wood, in which the unevenness of the conduit portion was realistically expressed.
Moreover, the shaping sheet obtained by Example 1 was rich in durability, and even if molding was repeated 10 times, the surface shape and the releasability after shaping (ease of peeling) were not changed at all.

Example 3
As the base material, a reinforced paper with a weight of 30 g / m ² of rice is used, and on one side, acrylic resin and nitrified cotton are used as a binder, and titanium white, petal, and yellow lead are used as colorants. A solid printing layer having a work amount of 5 g / m ² was applied by gravure printing. On top of this, a woodgrain pattern layer was formed by gravure printing using an ink containing a nitrified cotton as a binder and a colorant mainly composed of a dial, and a decorative sheet layer was obtained. Subsequently, after roll-coating the urea-vinyl acetate adhesive on the MFD of the substrate, the obtained decorative sheet layer was bonded.
Thereafter, a polyester resin composition obtained by mixing unsaturated polyester and peroxide was applied to the entire upper surface of the decorative sheet layer at a coating amount of 200 g / m ² , and obtained in Example 1 thereon. The shaped sheet was covered and contacted while aligning with the registration mark, and rolled and defoamed five times at 0.98 MPa / 930 m / m using a rubber roll so that the position does not shift. The polyester resin was cured at room temperature by heating at 40 ° C. for 2 hours. After curing, after curing for 1 hour and allowing to cool to room temperature, the unevenness of the conduit part is realistically expressed in the same manner as in Example 2, and the material using actual wood A polyester decorative board having the same texture was obtained. The results of evaluation are shown in Table 1.
Moreover, the shaping sheet obtained by Example 1 was rich in durability, and even if molding was repeated 10 times, the surface shape and the releasability after shaping (ease of peeling) were not changed at all.

Comparative Example 1
Prepare a polypropylene resin-based colored film (“PB023 (thickness: 60 μm)” manufactured by Mitsubishi Plastics, Inc.) as a base sheet, and after corona treatment is performed on the surface on which the ink layer is provided, A primer ink (acrylic ink “EBF tuning primer” manufactured by Showa Ink Industries, Ltd.) was gravure-printed to form a penetration preventing layer (primer layer).
Next, ink (urethane-based conduit ink “conduit MINI (B)” manufactured by The Inktec Co., Ltd.) was printed on the conduit portion of the wood grain pattern by a pattern plate to form an ink layer. Further, an electron beam curable resin obtained by adding 5% by mass of calcined kaolin particles and 2% by mass of reactive silicone methacrylate to an electron beam curable resin (“REB-CON” manufactured by Dainichi Seika Kogyo Co., Ltd.) on these ink layers. The composition was applied at a coating amount of 4 g / m ² by a gravure offset coater method. After coating, an electron beam with an acceleration voltage of 175 kV and an irradiation dose of 30 kGy (3 Mrad) was irradiated to cure the electron beam curable resin composition to form a surface shaping layer. When the shaped sheet thus obtained was heated to 230 ° C. with a preheater in order to perform embossing, the shaped sheet was broken. Then, it heated to 150 degreeC by which a shaping sheet does not fracture | rupture with a preheater, and immediately performed the embossing (58.8N / m < ² > pressurization) using an embossing roll from the surface shaping layer side, and formed above. A concave pattern in sync with the ink layer was applied. Since the shaped sheet could not be heated sufficiently, the recessed pattern due to embossing was insufficient, resulting in a film having a sweet wood grain expression.
Using the shaped sheet thus obtained, the same operation as in Example 2 was performed to produce a melamine resin decorative board.
The decorative board according to Comparative Example 1 could not express a delicate uneven shape. The results of evaluation are shown in Table 1. The durability and peelability were the same as in Example 2.

Comparative Example 2
Gravure printing of primer ink (acrylic ink “EBF tuning primer” from Showa Ink Industries, Ltd.) on the easy adhesion surface of PET film (“PTM38 (38 μm)” manufactured by Unitika Co., Ltd.) that has already been subjected to easy adhesion treatment Thus, a penetration preventing layer (primer layer) was formed.
Next, ink (urethane-based conduit ink “conduit MINI (B)” manufactured by The Inktec Co., Ltd.) was printed on the conduit portion of the wood grain pattern by a pattern plate to form an ink layer. Further, an electron beam curable resin obtained by adding 5% by mass of calcined kaolin particles and 2% by mass of reactive silicone methacrylate to an electron beam curable resin (“REB-CON” manufactured by Dainichi Seika Kogyo Co., Ltd.) on these ink layers. The composition was applied at a coating amount of 4 g / m ² by a gravure offset coater method. After coating, an electron beam with an acceleration voltage of 175 kV and an irradiation dose of 30 kGy (3 Mrad) was irradiated to cure the electron beam curable resin composition to form a surface shaping layer. In order to emboss, the shaped sheet thus obtained was heated to 230 ° C. with a preheater, the shaped sheet was stretched, and the surface shaped layer was cracked. It could not be used as a sheet. Then, it heated to 200 degreeC which a shaping sheet does not extend with a preheater, and immediately performed the embossing (58.8N / m < ² > pressurization) using an embossing roll from the surface shaping layer side, and formed above. A concave pattern in sync with the ink layer was applied. Since the shaped sheet could not be heated sufficiently, the recessed pattern due to embossing was insufficient, resulting in a film having a sweet wood grain expression.
Using the shaped sheet thus obtained, the same operation as in Example 2 was performed to produce a melamine resin decorative board.
The decorative board according to Comparative Example 2 could not express a delicate uneven shape. The results of evaluation are shown in Table 1. The durability and peelability were the same as in Example 2.

  According to the present invention, it has a delicate and bold concavo-convex shape, can be applied with a high-quality and high-quality design that is excellent in design and feel, has excellent releasability, and has excellent heat resistance. A mold decorative sheet, a resin decorative board obtained by using the mold decorative sheet, and a method for producing a resin decorative board using the mold decorative sheet can be obtained. Especially when used for delicate patterns such as wood grain patterns, the unevenness of the conduit part can be expressed realistically, and the molded decorative material can obtain the same texture as the material using actual wood .

It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the resin decorative board of this invention. It is a schematic diagram which shows the peeling process of the shaping sheet of this invention. It is a schematic diagram which shows the cross section of the resin decorative board of this invention.

Explanation of symbols

1. Molding sheet 2. Composite substrate 21. Heat resistant substrate 22. Resin substrate 3. Ink layer 3-a. Ink 3-b. Ink 3-c. Ink 4. Interaction region 4-a. Interaction region 4-b. Interaction region 4-c. 4. Interaction region 5. Surface shaping layer 6. Penetration prevention layer Raised shape 7-a. Raised shape 7-b. Raised shape 7-c. 7. Raised shape Fine particles or calcined kaolin particles 8-a. Fine particles or calcined kaolin particles 8-b. 8. Fine particles or calcined kaolin particles Adhesive layer 10. Substrate 11. Resin decorative board 12. Fine ridge shape 13. Fine uneven surface 14. Recessed pattern 15. Resin decorative sheet 17. Cosmetic sheet layer 17-a. Sheet layer 17-b. Solid printing layer 17-c. Pattern layer 18. Resin layer

Claims (15)

  A composite group of a heat-resistant substrate having a heat shrinkage (150 ° C. × 30 minutes) measured in accordance with JIS C2318 of 2% or less and a substrate made of a resin having a melting point in the range of 90 to 230 ° C. An ink layer provided at least partially or entirely on the resin substrate of the material, and an area on which the ink layer is formed and the ink layer are formed while being on and in contact with the ink layer A molding sheet having a surface molding layer covering the entire surface including a region that is not formed, wherein the surface molding layer is obtained by crosslinking and curing the curable resin composition, and in the surface molding layer The molding sheet in which the surface of the surface molding layer located immediately above the ink layer and the upper portion in the vicinity thereof has a convex shape and further has a concave pattern.   The heat-resistant base material is a paper base material, a base material made of polycarbonate and a base material made of polyethylene terephthalate, or a combination of one or two or more, and the resin base material is made of a polyolefin resin. The shaping sheet according to claim 1. Heat-resistant substrate is a paper substrate having a basis weight of 20 to 250 g / m ^2, and shaping sheet according to claim 2 the thickness of the resin substrate is 1 to 100 [mu] m.   The surface shaping layer contains fine particles, and the average particle diameter of the fine particles is a value close to the plus side of the maximum thickness of the surface shaping layer located immediately above the ink layer. The shaping sheet according to any one of the above.   The moldable sheet according to any one of claims 1 to 4, wherein the curable resin composition is an ionizing radiation curable resin composition.   6. The shaped sheet according to claim 5, wherein the ionizing radiation curable resin composition is an electron beam curable resin composition.   The ink constituting the ink layer contains a non-crosslinked urethane resin as a binder, and the ionizing radiation curable resin composition contains a (meth) acrylate monomer. The shaping sheet as described in 1.   The shaping sheet according to claim 7, wherein the ink constituting the ink layer contains a non-crosslinked urethane resin and an unsaturated polyester resin as binders.   An adhesive layer and a decorative sheet layer are sequentially laminated on the upper surface of the substrate, a resin composition is applied onto the decorative sheet layer, and then the molded sheet is brought into contact with and integrally cured, and then the molded sheet The resin decorative board which peeled and formed the resin layer, Comprising: This molded sheet is a resin decorative board as described in any one of Claims 1-8.   The resin decorative board according to claim 9, wherein the resin in the resin composition is an unsaturated polyester resin.   The molding sheet according to any one of claims 1 to 8 is inserted and molded between a molded product molded by pressing between a heated pressure plate and a pressure plate, and then the molding sheet is peeled off. The resin decorative board formed by sticking the resin decorative sheet to a board | substrate through an adhesive bond layer.   The resin decorative board according to claim 11, wherein the resin decorative sheet is a melamine resin decorative board.   The resin decorative board according to claim 11, wherein the resin decorative sheet is a diallyl phthalate (DAP) resin decorative board.   An adhesive layer and a decorative sheet layer are sequentially laminated on the upper surface of the substrate, a resin composition is applied on the decorative sheet layer, and then the shaping sheet according to any one of claims 1 to 8 is contacted and integrated. A method for producing a resin decorative board, comprising: after curing, and then peeling off the shaping sheet to form a resin layer.   After the shaping sheet according to any one of claims 1 to 8 is inserted and molded between a molded product and a pressure plate that are molded by pressing between heated pressure plates, the shaping sheet is peeled off. A method for producing a resin decorative board, comprising sticking the obtained resin decorative sheet to a substrate through an adhesive layer.

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