TW201504049A - Melamine decorative board and method of manufacturing melamine decorative board - Google Patents
Melamine decorative board and method of manufacturing melamine decorative board Download PDFInfo
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- TW201504049A TW201504049A TW103126169A TW103126169A TW201504049A TW 201504049 A TW201504049 A TW 201504049A TW 103126169 A TW103126169 A TW 103126169A TW 103126169 A TW103126169 A TW 103126169A TW 201504049 A TW201504049 A TW 201504049A
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- 229920000877 Melamine resin Polymers 0.000 title claims abstract description 169
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 title claims abstract description 127
- 238000004519 manufacturing process Methods 0.000 title claims description 30
- 239000010410 layer Substances 0.000 claims abstract description 219
- 239000002344 surface layer Substances 0.000 claims abstract description 160
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- 239000000463 material Substances 0.000 claims abstract description 48
- 239000011521 glass Substances 0.000 claims abstract description 42
- 239000004640 Melamine resin Substances 0.000 claims abstract description 41
- 239000004744 fabric Substances 0.000 claims abstract description 31
- 229920005989 resin Polymers 0.000 claims description 167
- 239000011347 resin Substances 0.000 claims description 167
- 239000000758 substrate Substances 0.000 claims description 130
- 239000002245 particle Substances 0.000 claims description 104
- 239000011162 core material Substances 0.000 claims description 60
- 238000013461 design Methods 0.000 claims description 56
- 239000002966 varnish Substances 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 23
- 239000012792 core layer Substances 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 9
- 239000011241 protective layer Substances 0.000 claims description 5
- 230000001681 protective effect Effects 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 description 24
- 239000004925 Acrylic resin Substances 0.000 description 21
- 239000007787 solid Substances 0.000 description 21
- 229920000178 Acrylic resin Polymers 0.000 description 20
- 238000005452 bending Methods 0.000 description 20
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 18
- -1 amine ester Chemical class 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 16
- 239000002904 solvent Substances 0.000 description 15
- 238000012360 testing method Methods 0.000 description 15
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 14
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
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- 239000004416 thermosoftening plastic Substances 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 239000000805 composite resin Substances 0.000 description 5
- 239000002612 dispersion medium Substances 0.000 description 5
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- 238000001035 drying Methods 0.000 description 4
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000011258 core-shell material Substances 0.000 description 3
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- 238000002156 mixing Methods 0.000 description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 description 3
- 229920006352 transparent thermoplastic Polymers 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- 208000005156 Dehydration Diseases 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
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- 238000011109 contamination Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
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- 238000005227 gel permeation chromatography Methods 0.000 description 2
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- 238000011056 performance test Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920001342 Bakelite® Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 239000003961 penetration enhancing agent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010421 standard material Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/02—Layered products essentially comprising sheet glass, or glass, slag, or like fibres in the form of fibres or filaments
- B32B17/04—Layered products essentially comprising sheet glass, or glass, slag, or like fibres in the form of fibres or filaments bonded with or embedded in a plastic substance
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/12—Layered products comprising a layer of synthetic resin next to a fibrous or filamentary layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/42—Layered products comprising a layer of synthetic resin comprising condensation resins of aldehydes, e.g. with phenols, ureas or melamines
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B33/00—Layered products characterised by particular properties or particular surface features, e.g. particular surface coatings; Layered products designed for particular purposes not covered by another single class
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/02—Composition of the impregnated, bonded or embedded layer
- B32B2260/021—Fibrous or filamentary layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/04—Impregnation, embedding, or binder material
- B32B2260/046—Synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/10—Inorganic fibres
- B32B2262/101—Glass fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/538—Roughness
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2309/00—Parameters for the laminating or treatment process; Apparatus details
- B32B2309/08—Dimensions, e.g. volume
- B32B2309/10—Dimensions, e.g. volume linear, e.g. length, distance, width
- B32B2309/105—Thickness
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2451/00—Decorative or ornamental articles
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F13/00—Coverings or linings, e.g. for walls or ceilings
- E04F13/07—Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor
- E04F13/08—Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor composed of a plurality of similar covering or lining elements
- E04F13/0866—Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor composed of a plurality of similar covering or lining elements composed of several layers, e.g. sandwich panels or layered panels
Landscapes
- Laminated Bodies (AREA)
- Finished Plywoods (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Finishing Walls (AREA)
Abstract
Description
本發明係關於三聚氰胺裝飾板及三聚氰胺裝飾板之製造方法。 The present invention relates to a method for producing a melamine decorative board and a melamine decorative board.
三聚氰胺裝飾板係表面層中使用有三聚氰胺樹脂之裝飾板,其在對建築物的壁面、電梯或電車的車輛等的內壁面、桌子或書架等家具的表面等施加木紋圖案等設計時被使用。 A decorative sheet of melamine resin is used in the surface layer of the melamine decorative board, and is used when a design such as a wood grain pattern is applied to a wall surface of a building, an inner wall surface of a vehicle such as an elevator or a train, a surface of a table or a bookcase, or the like. .
又,近年來,由使用有三聚氰胺樹脂的表面層與玻璃纖維基材構成之不燃性三聚氰胺裝飾板已成為主流。 Further, in recent years, incombustible melamine decorative sheets composed of a surface layer using a melamine resin and a glass fiber base material have become mainstream.
作為此種不燃性三聚氰胺裝飾板,已知有能夠容易地進行彎曲加工的裝飾板(例如參照專利文獻1)。 As such a non-combustible melamine decorative sheet, a decorative sheet which can be easily bent is known (for example, see Patent Document 1).
專利文獻1所記載之三聚氰胺裝飾板之厚度薄,能夠容易地進行彎曲加工。 The melamine decorative sheet described in Patent Document 1 has a small thickness and can be easily bent.
而且,有時為了凸顯高級感而對三聚氰胺裝飾板的設計面實施鏡面加工。然而,專利文獻1所記載之三聚氰胺裝飾板的表面層之厚度薄,因此,即使實施鏡面加工,表面層亦會受到玻璃纖維基材的表面形狀之影響,難以將設計面設為完美的鏡面。 Moreover, the design surface of the melamine decorative board may be mirror-finished in order to highlight the high-grade feeling. However, since the surface layer of the melamine decorative sheet described in Patent Document 1 has a small thickness, even if mirror surface processing is performed, the surface layer is affected by the surface shape of the glass fiber base material, and it is difficult to make the design surface a perfect mirror surface.
[先前技術文獻] [Previous Technical Literature]
[專利文獻] [Patent Literature]
[專利文獻1]日本特許第5099206號 [Patent Document 1] Japanese Patent No. 5099206
本發明之目的在於提供一種不燃性及彎曲加工性優異,並且具備實施了鏡面加工之設計面,及能夠容易地製造之三聚氰胺裝飾板之製造方法。 An object of the present invention is to provide a method for producing a melamine decorative sheet which is excellent in nonflammability and bending workability, and which has a design surface to be mirror-finished and which can be easily produced.
如上所述之目的由下述(1)~(12)之本發明實現。 The object as described above is achieved by the present invention of the following (1) to (12).
(1)一種三聚氰胺裝飾板,其特徵在於:其係由依序積層有表面層、中間層及芯材層之積層體構成;上述表面層係由包含表面層基材之表面層材料構成,該表面層基材於成為設計面之第1面側承載含有三聚氰胺樹脂之樹脂,且於與上述中間層接觸之第2面側承載熱可塑性樹脂,上述表面層的上述第1面成為鏡面;上述芯材層係由包含玻璃布或包含玻璃布作為基材之預浸布構成之芯材層材料構成;上述中間層係由中間層形成用樹脂構成,上述中間層之平均厚度大於上述芯材層的上述中間層側的面之算術平均粗糙度Ra1。 (1) A melamine decorative board comprising: a layered body having a surface layer, an intermediate layer and a core layer sequentially laminated; wherein the surface layer is composed of a surface layer material comprising a surface layer substrate, the surface The layer substrate carries a resin containing a melamine resin on the first surface side of the design surface, and carries a thermoplastic resin on the second surface side in contact with the intermediate layer, wherein the first surface of the surface layer is a mirror surface; The layer is composed of a core material layer made of a glass cloth or a prepreg containing a glass cloth as a base material; the intermediate layer is made of a resin for forming an intermediate layer, and an average thickness of the intermediate layer is larger than the above-mentioned core layer The arithmetic mean roughness Ra1 of the face on the intermediate layer side.
(2)如上述(1)之三聚氰胺裝飾板,其中,上述表面層的上述第1面之算術平均粗糙度Ra2為300nm以下。 (2) The melamine decorative sheet according to the above (1), wherein the first surface of the surface layer has an arithmetic mean roughness Ra2 of 300 nm or less.
(3)如上述(1)或(2)之三聚氰胺裝飾板,其中,上述中間層之平均厚度為5μm以上。 (3) The melamine decorative board according to the above (1) or (2), wherein the intermediate layer has an average thickness of 5 μm or more.
(4)如上述(1)至(3)中任一項之三聚氰胺裝飾板,其 中,上述算術平均粗糙度Ra1為0.1~10μm。 (4) The melamine decorative board according to any one of the above (1) to (3), In the above, the arithmetic mean roughness Ra1 is 0.1 to 10 μm.
(5)如上述(1)至(4)中任一項之三聚氰胺裝飾板,其中,該三聚氰胺裝飾板之平均厚度為0.4mm以下。 (5) The melamine decorative board according to any one of the above (1) to (4), wherein the melamine decorative board has an average thickness of 0.4 mm or less.
(6)一種三聚氰胺裝飾板之製造方法,其係如上述(1)至(5)中任一項之三聚氰胺裝飾板之製造方法,其特徵在於具有如下步驟:準備具有由上述表面層材料構成之第1層、與由上述中間層形成用樹脂構成之第2層之第1基體與由上述芯材層材料構成之第2基體之步驟;以與上述第1基體的上述第2層側的面相對向之方式,配置上述第2基體之步驟;將具備實施了鏡面加工之上述抵接面之護板以使抵接面與上述第1基體的上述第1層側的面相對向之方式配置,並且將140℃之彈性率為1~50GPa之基材膜以與上述第2基體相對向之方式配置之步驟;一面至少對上述第1基體進行加熱,一面使上述護板與上述基材膜靠近,藉此,對上述第1基體與上述第2基體進行熱壓接,獲得上述三聚氰胺裝飾板之步驟;以及自上述三聚氰胺裝飾板將上述護板與上述基材膜除去之步驟。 (6) A method for producing a melamine decorative sheet, which is characterized in that the method for producing a melamine decorative sheet according to any one of the above (1) to (5) is characterized in that it has a step of preparing a surface layer material. a first layer, a first substrate of the second layer made of the resin for forming the intermediate layer, and a second substrate made of the core material layer; and the surface of the first substrate on the second layer side a step of arranging the second substrate; and a shield having the mirror-processed abutting surface disposed such that the abutting surface faces the surface of the first substrate on the first layer side And a step of disposing a substrate film having an elastic modulus of 140° C. of 1 to 50 GPa so as to face the second substrate; and heating the first substrate to at least the substrate and the substrate film The step of obtaining the melamine decorative sheet by thermocompression bonding the first base body and the second base body, and removing the protective sheet and the base material film from the melamine decorative sheet.
(7)如上述(6)之三聚氰胺裝飾板之製造方法,其中,上述第1層係藉由,將含有上述三聚氰胺樹脂之樹脂清漆供給至上述表面層基材的上述第1面側,並且將含有具有小於上述算術平均粗糙度Ra1之平均粒徑,且由上述熱可塑性樹脂構成之樹脂清漆供給至上述表面層基材的上述第2面側,而形成。 (7) The method for producing a melamine decorative sheet according to the above aspect, wherein the first layer is provided by supplying a resin varnish containing the melamine resin to the first surface side of the surface layer substrate, and A resin varnish having an average particle diameter smaller than the arithmetic mean roughness Ra1 and having the above-mentioned thermoplastic resin is supplied to the second surface side of the surface layer substrate.
(8)如上述(7)之三聚氰胺裝飾板之製造方法,其中,上述第2層係,使用含有:具有大於由上述熱可塑性樹脂構成之粒子的上述平均粒徑,且小於上述算術平均粗糙度Ra1之平均粒徑,且由上述中間層 形成用樹脂構成之粒子之樹脂清漆形成。 (8) The method for producing a melamine decorative sheet according to the above (7), wherein the second layer is used to have an average particle diameter larger than a particle composed of the thermoplastic resin and smaller than the arithmetic mean roughness. Average particle size of Ra1, and the above intermediate layer A resin varnish formed of particles composed of a resin is formed.
(9)如上述(6)至(8)中任一項之三聚氰胺裝飾板之製造方法,其中,上述第2層係,使用含有具有150nm以上之平均粒徑且由上述中間層形成用樹脂構成之粒子之樹脂清漆形成。 (9) The method for producing a melamine decorative sheet according to any one of the above-mentioned (6), wherein the second layer is formed of a resin having an average particle diameter of 150 nm or more and formed of the intermediate layer. The resin varnish of the particles is formed.
(10)如上述(6)至(9)中任一項之三聚氰胺裝飾板之製造方法,其中,上述基材膜之平均厚度為0.1~1.0mm。 (10) The method for producing a melamine decorative sheet according to any one of the above (6), wherein the base film has an average thickness of 0.1 to 1.0 mm.
(11)如上述(6)至(10)中任一項之三聚氰胺裝飾板之製造方法,其中,上述基材膜係由軟化溫度為120~160℃之熱可塑性樹脂構成。 (11) The method for producing a melamine decorative sheet according to any one of the above (6), wherein the base film is made of a thermoplastic resin having a softening temperature of 120 to 160 °C.
(12)如上述(6)至(11)中任一項之三聚氰胺裝飾板之製造方法,其中,上述熱壓接時的加熱溫度為130~150℃,壓力為2~8MPa。 (12) The method for producing a melamine decorative sheet according to any one of the above (6), wherein the heating temperature during the thermocompression bonding is 130 to 150 ° C and the pressure is 2 to 8 MPa.
根據本發明,能夠提供不燃性及彎曲加工性優異,且具備實施了鏡面加工之設計面之三聚氰胺裝飾板。 According to the present invention, it is possible to provide a melamine decorative sheet which is excellent in nonflammability and bending workability and which has a design surface to be mirror-finished.
又,能夠提供能容易地製造此種三聚氰胺裝飾板之三聚氰胺裝飾板之製造方法。 Further, it is possible to provide a method for producing a melamine decorative sheet which can easily produce such a melamine decorative sheet.
10‧‧‧第1基體 10‧‧‧1st matrix
11‧‧‧表面層 11‧‧‧ surface layer
11'‧‧‧第1層 11'‧‧‧1st floor
12、14‧‧‧芯材層 12, 14‧‧‧ core layer
12'‧‧‧第2基體 12'‧‧‧2nd matrix
13‧‧‧中間層 13‧‧‧Intermediate
13'‧‧‧第2層 13'‧‧‧2nd floor
15‧‧‧保護層 15‧‧‧Protective layer
16‧‧‧支持層 16‧‧‧Support layer
20‧‧‧基材膜 20‧‧‧Base film
30‧‧‧護板(鏡面完成護板) 30‧‧‧ Guard plate (mirror finish guard)
100‧‧‧三聚氰胺裝飾板 100‧‧‧melamine decorative board
111‧‧‧第1面 111‧‧‧1st
112‧‧‧第2面 112‧‧‧2nd
圖1係表示本發明之三聚氰胺裝飾板之實施形態之剖面圖。 BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a cross-sectional view showing an embodiment of a melamine decorative sheet of the present invention.
圖2係表示本發明之三聚氰胺裝飾板之製造方法的一例之步驟圖。 Fig. 2 is a flow chart showing an example of a method for producing a melamine decorative sheet of the present invention.
圖3係表示本發明之三聚氰胺裝飾板的構成的其他一例之概念圖。 Fig. 3 is a conceptual view showing another example of the constitution of the melamine decorative sheet of the present invention.
圖4係表示本發明之三聚氰胺裝飾板的構成的其他一例之概念圖。 Fig. 4 is a conceptual view showing another example of the constitution of the melamine decorative sheet of the present invention.
以下,根據隨附圖式所示之較佳實施形態,詳細地對本發明進行說明。 Hereinafter, the present invention will be described in detail based on preferred embodiments shown in the accompanying drawings.
《三聚氰胺裝飾板》 Melamine Decorative Board
首先,對本發明之三聚氰胺裝飾板之較佳實施形態進行說明。 First, a preferred embodiment of the melamine decorative sheet of the present invention will be described.
本發明之三聚氰胺裝飾板貼附於建築物的壁面、電梯或電車的車輛等的內壁面、桌子或書架等家具的表面等,藉此,能夠對上述面賦予美觀性或高級感。又,本發明之三聚氰胺裝飾板具有不燃性。 The melamine decorative board of the present invention is attached to the wall surface of a building, the inner wall surface of a vehicle such as an elevator or a train, the surface of a furniture such as a table or a bookcase, and the like, whereby an aesthetic or high-grade feeling can be imparted to the surface. Further, the melamine decorative board of the present invention is incombustible.
圖1係表示本發明之三聚氰胺裝飾板之實施形態之剖面圖。 BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a cross-sectional view showing an embodiment of a melamine decorative sheet of the present invention.
再者,於以下的說明中,將圖1中的上側稱為「上」,將圖1中的下側稱為「下」。 In the following description, the upper side in FIG. 1 is referred to as "upper", and the lower side in FIG. 1 is referred to as "lower".
如圖1所示,三聚氰胺裝飾板100係由積層有表面層11、中間層13及芯材層12之積層體構成。亦即,三聚氰胺裝飾板100成為如下構成:表面層11與芯材層12透過中間層13而接合。 As shown in FIG. 1, the melamine decorative board 100 is composed of a laminate in which a surface layer 11, an intermediate layer 13, and a core layer 12 are laminated. That is, the melamine decorative sheet 100 has a configuration in which the surface layer 11 and the core layer 12 are joined by the intermediate layer 13.
以下,詳細地對各層進行說明。 Hereinafter, each layer will be described in detail.
<1.表面層> <1. Surface layer>
表面層11具備成為設計面之第1面111(上表面)、及處於第1面111的相反側且與中間層13接觸之第2面112(下表面)。該表面層11係由如下表面層材料構成,該表面層材料包含表面層基材、承載於表面層基材的第1面111側之含有三聚氰胺樹脂之樹脂、及承載於表面層基材的第2面112側之熱可塑性樹脂。又,表面層11的設計面(第1面111)成為鏡面。 The surface layer 11 includes a first surface 111 (upper surface) which is a design surface, and a second surface 112 (lower surface) which is on the opposite side of the first surface 111 and which is in contact with the intermediate layer 13. The surface layer 11 is composed of a surface layer material including a surface layer substrate, a resin containing a melamine resin supported on the first surface 111 side of the surface layer substrate, and a surface supported on the surface layer substrate. Thermoplastic resin on the side of 112 sides. Further, the design surface (first surface 111) of the surface layer 11 is a mirror surface.
再者,於本說明書中,所謂表面層基材承載樹脂,係指如下 狀態:樹脂附著於表面層基材(載體)的表面,或浸漬至表面層基材內部的空隙中。於該狀態下使表面層材料成形之後,承載於表面層基材之樹脂會體現其性能。再者,樹脂亦可不均一地分佈於表面層基材的表面及表面層基材的內部。 Furthermore, in the present specification, the term "surface layer substrate carrying resin" means State: The resin is attached to the surface of the surface layer substrate (carrier) or to the voids inside the surface layer substrate. After the surface layer material is formed in this state, the resin carried on the surface layer substrate exhibits its properties. Further, the resin may be unevenly distributed on the surface of the surface layer substrate and the inside of the surface layer substrate.
表面層基材為片材狀基材,其於第1面111側承載含有三聚氰胺樹脂之樹脂,藉此,於表面層11的第1面111上形成設計面。表面層基材之材質並無特別限定。例如能夠使用紙漿(pulp)、棉絨(linter)、合成纖維、玻璃纖維等各種纖維基材作為表面層基材。又,根據需要,亦能夠使用含有氧化鈦等顏料之含氧化鈦裝飾紙等作為表面層基材。 The surface layer base material is a sheet-like base material, and a resin containing a melamine resin is placed on the first surface 111 side, whereby a design surface is formed on the first surface 111 of the surface layer 11. The material of the surface layer substrate is not particularly limited. For example, various fiber base materials such as pulp, linter, synthetic fiber, and glass fiber can be used as the surface layer base material. Further, if necessary, a titanium oxide-containing decorative paper containing a pigment such as titanium oxide or the like can be used as the surface layer substrate.
表面層基材之基重並無特別限定,但較佳為40~150g/m2。若基重不足上述下限值,則於樹脂浸漬步驟中會發生樹脂斷裂,或獲得之表面層材料(表面層11)容易形成皺褶,因此,有時難以進行浸漬處理(例如塗布處理)。而且,有可能亦難以對分別承載於表面層基材的第1面111側與第2面112側之樹脂的量進行調整。另一方面,若基重超過上述上限值,則有時表面層基材所承載之樹脂的量會產生不均,使三聚氰胺裝飾板100之柔軟性下降,並且該三聚氰胺裝飾板100之生產性下降,導致成本升高。 The basis weight of the surface layer substrate is not particularly limited, but is preferably 40 to 150 g/m 2 . When the basis weight is less than the above lower limit, the resin is broken during the resin impregnation step, or the obtained surface layer material (surface layer 11) is likely to be wrinkled. Therefore, it may be difficult to perform the immersion treatment (for example, coating treatment). Further, there is a possibility that it is difficult to adjust the amount of the resin which is carried on the first surface 111 side and the second surface 112 side of the surface layer substrate, respectively. On the other hand, when the basis weight exceeds the above upper limit value, the amount of the resin carried on the surface layer substrate may be uneven, the flexibility of the melamine decorative sheet 100 may be lowered, and the productivity of the melamine decorative sheet 100 may be produced. Falling, leading to higher costs.
表面層材料係將含有三聚氰胺樹脂之樹脂承載於表面層基材的上表面側(第1面111側)而成。藉此,能夠對表面層11的上表面即表面層11的第1面111(設計面)賦予適當之表面硬度。 The surface layer material is obtained by supporting a resin containing a melamine resin on the upper surface side (the first surface 111 side) of the surface layer substrate. Thereby, an appropriate surface hardness can be given to the first surface 111 (design surface) of the surface layer 11 which is the upper surface of the surface layer 11.
三聚氰胺樹脂並無特別限定,例如能夠使用使三聚氰胺與甲醛於中性或弱鹼條件反應所得之聚合物。 The melamine resin is not particularly limited, and for example, a polymer obtained by reacting melamine with formaldehyde under neutral or weak base conditions can be used.
甲醛相對於三聚氰胺之反應莫耳比(以下,亦僅稱為「反應 莫耳比」)為(甲醛之莫耳量)/(三聚氰胺之莫耳量)之值。該反應莫耳比並無特別限定,但較佳為1.0~4.0,更佳為1.0~2.0,進而較佳為1.1~1.8。能夠較佳地使用以該反應莫耳比而使三聚氰胺與甲醛反應所得之三聚氰胺樹脂。若反應莫耳比不足上述下限值,則有時未反應之三聚氰胺會增加,樹脂保存性下降,並且成本升高。又,若反應莫耳比超過上述上限值,則有時硬化後之樹脂之柔軟性會顯著地下降。再者,既能夠使用僅含有一種三聚氰胺樹脂之樹脂作為承載於表面層基材的上表面側之樹脂,亦能夠使用含有反應莫耳比或重量平均分子量等不同之兩種以上的三聚氰胺樹脂之樹脂作為承載於表面層基材的上表面側之樹脂。 Mohr ratio of formaldehyde to melamine (hereinafter, also referred to as "reaction" Moerby" is the value of (molar amount of formaldehyde) / (molar amount of melamine). The reaction molar ratio is not particularly limited, but is preferably 1.0 to 4.0, more preferably 1.0 to 2.0, still more preferably 1.1 to 1.8. A melamine resin obtained by reacting melamine with formaldehyde at the reaction molar ratio can be preferably used. When the reaction molar ratio is less than the above lower limit, the unreacted melamine may increase, the storage property of the resin may decrease, and the cost may increase. Moreover, when the reaction molar ratio exceeds the above upper limit, the flexibility of the resin after curing may be remarkably lowered. Further, a resin containing only one type of melamine resin can be used as the resin supported on the upper surface side of the surface layer substrate, and a resin containing two or more kinds of melamine resins having a reaction molar ratio or a weight average molecular weight can also be used. As the resin carried on the upper surface side of the surface layer substrate.
又,亦能夠使用住友化學(股)製造的三聚氰胺樹脂等市售品作為上述三聚氰胺樹脂。 Further, a commercially available product such as melamine resin manufactured by Sumitomo Chemical Co., Ltd. can be used as the melamine resin.
三聚氰胺樹脂之重量平均分子量並無特別限定,但較佳為200~500,更佳為250~350。若三聚氰胺樹脂之重量平均分子量小於上述下限值,則有時樹脂中所含之未反應之三聚氰胺會增多,樹脂保存性下降。又,若三聚氰胺樹脂之重量平均分子量大於上述上限值,則有時樹脂對於基材之浸漬性會下降。再者,上述重量平均分子量例如能夠由GPC(凝膠滲透層析法,標準物質:聚苯乙烯轉化)測定。 The weight average molecular weight of the melamine resin is not particularly limited, but is preferably 200 to 500, more preferably 250 to 350. When the weight average molecular weight of the melamine resin is less than the above lower limit, the unreacted melamine contained in the resin may increase, and the storage stability of the resin may decrease. Further, when the weight average molecular weight of the melamine resin is more than the above upper limit, the impregnation property of the resin with respect to the substrate may be lowered. Further, the above weight average molecular weight can be measured, for example, by GPC (gel permeation chromatography, standard material: polystyrene conversion).
承載於表面層基材的上表面(第1面111)側之樹脂中所含之上述三聚氰胺樹脂的量並無特別限定,但較佳為80~100質量%,更佳為95~100質量%。若承載於表面層基材的上表面側之樹脂中所含之三聚氰胺樹脂的量不足上述下限值,則有時表面層11的表面(第1面111)之硬度會下降,或表面之耐污染性會下降。 The amount of the melamine resin contained in the resin on the upper surface (first surface 111) side of the surface layer substrate is not particularly limited, but is preferably 80 to 100% by mass, more preferably 95 to 100% by mass. . When the amount of the melamine resin contained in the resin on the upper surface side of the surface layer substrate is less than the above lower limit, the hardness of the surface (first surface 111) of the surface layer 11 may be lowered or the surface may be resistant. Pollution will decline.
將含有三聚氰胺樹脂之樹脂承載於表面層基材的上表面側(第1面111側)之方法並無特別限定。作為該方法,例如能夠使用如下方法等:使用噴射裝置、淋浴裝置、刮刀吻合式塗布機(Kiss coater)、缺角輪塗布機(Comma coater)等眾所周知之裝置,將上述樹脂溶解於溶劑所得之樹脂清漆塗布於表面層基材之後,以80~130℃左右之溫度進行加熱乾燥。藉此,獲得於上表面側承載有樹脂之表面層基材(以下,有時稱為「樹脂承載基材」)。 The method of supporting the resin containing the melamine resin on the upper surface side (the first surface 111 side) of the surface layer substrate is not particularly limited. As such a method, for example, a method such as a spray device, a shower device, a knife coater, or a Comma coater can be used to dissolve the resin in a solvent. After the resin varnish is applied to the surface layer substrate, it is dried by heating at a temperature of about 80 to 130 °C. Thereby, a surface layer substrate (hereinafter sometimes referred to as a "resin carrier substrate") having a resin supported on the upper surface side is obtained.
再者,對於加熱乾燥後之樹脂承載基材(例如樹脂浸漬紙)而言,較佳為當將該樹脂承載基材整體之重量設為100質量%時,殘存有2~6質量%之揮發成分(溶劑)。藉此,對於樹脂承載基材之處理變得容易。又,於使用此種樹脂承載基材而製造三聚氰胺裝飾板100之情形下,當進行加熱、加壓處理(加熱成形)時,承載於表面層基材的上表面側(第1面111側)之含有三聚氰胺樹脂之樹脂的樹脂流動性提高。因此,表面層11之設計外觀、表面光澤度良好。另一方面,於揮發成分不足2質量%之情形時,樹脂容易斷裂,因此難以進行處理。又,由於樹脂流動性下降,故而會阻礙表面層11之外觀形成。又,於使用揮發成分超過6%之樹脂而製造三聚氰胺裝飾板100之情形時,三聚氰胺裝飾板100之翹曲(片材捲曲)容易因成形後之乾燥環境而增大。而且,於揮發成分為7.5%以上之情形時,揮發成分會對三聚氰胺裝飾板100的外觀方面之光澤轉印性產生影響。 Further, in the resin-supporting substrate (for example, resin-impregnated paper) after heat drying, it is preferable that when the weight of the entire resin-carrying substrate is 100% by mass, 2 to 6% by mass of volatilization remains. Ingredients (solvent). Thereby, the handling of the resin-carrying substrate becomes easy. In the case where the melamine decorative sheet 100 is produced by using such a resin-supporting substrate, when it is subjected to heating and pressure treatment (heat molding), it is carried on the upper surface side (the first surface 111 side) of the surface layer substrate. The resin of the melamine resin-containing resin has improved fluidity. Therefore, the design appearance and surface gloss of the surface layer 11 are good. On the other hand, when the volatile component is less than 2% by mass, the resin is easily broken, so that it is difficult to carry out the treatment. Further, since the fluidity of the resin is lowered, the appearance of the surface layer 11 is hindered. Further, when the melamine decorative sheet 100 is produced using a resin having a volatile component of more than 6%, the warpage (sheet curl) of the melamine decorative sheet 100 is likely to increase due to the dry environment after molding. Further, when the volatile component is 7.5% or more, the volatile component affects the gloss transfer property of the appearance of the melamine decorative sheet 100.
用以對含有三聚氰胺樹脂之樹脂進行溶解(用以調製樹脂清漆)之溶劑並無特別限定,例如可列舉水、甲醇等。作為此種溶劑,水尤佳。又,亦能夠於不會對樹脂清漆之塗布性等產生不良影響之範圍內,組 合使用不良溶劑。上述樹脂清漆中所含之固體成分(除了溶劑以外之全部成分)的量並無特別限定,但較佳為上述樹脂清漆整體之30~70質量%,更佳為45~60質量%。藉此,能夠使樹脂清漆對於表面層基材之浸漬性提高。 The solvent for dissolving the resin containing the melamine resin (for preparing the resin varnish) is not particularly limited, and examples thereof include water and methanol. As such a solvent, water is particularly preferred. Moreover, it is also possible to form a group within a range that does not adversely affect the coatability of the resin varnish or the like. Use a poor solvent. The amount of the solid component (all components other than the solvent) contained in the resin varnish is not particularly limited, but is preferably 30 to 70% by mass, and more preferably 45 to 60% by mass based on the total of the resin varnish. Thereby, the impregnation property of a resin varnish to a surface layer base material can be improved.
表面層材料係將熱可塑性樹脂承載於與表面層基材的第1面111(設計面)側相反之第2面112側而成。 The surface layer material is formed by supporting the thermoplastic resin on the side of the second surface 112 opposite to the side of the first surface 111 (design surface) of the surface layer substrate.
承載於表面層基材之熱可塑性樹脂亦可為粒子狀、塊狀或將該粒子狀與塊狀加以組合而成之形態,但較佳為以粒子狀之形態包含熱可塑性樹脂。再者,粒子狀的熱可塑性樹脂(熱可塑性樹脂粒子)係,將熱可塑性樹脂分散於溶劑而成為乳液狀態所得之熱可塑性乳液樹脂(樹脂清漆)用作原料,且藉由使其乾燥能夠容易且確實地獲得。 The thermoplastic resin to be carried on the surface layer base material may be in the form of particles, a block, or a combination of the particles and the block, but it is preferable to contain the thermoplastic resin in the form of particles. Further, the particulate thermoplastic resin (thermoplastic resin particles) is a thermoplastic resin (resin varnish) obtained by dispersing a thermoplastic resin in a solvent and being in an emulsion state, and is used as a raw material, and can be easily dried. And indeed obtained.
熱可塑性樹脂粒子具有與金屬或各種素材接著之優異之接著特性。因此,熱可塑性樹脂粒子係以高接著強度承載於表面層基材。尤其即使對表面層基材施加彎曲等之應力而使其變形,亦由於該高接著強度,熱可塑性樹脂亦難以自表面層基材剝離。進而,承載於表面層基材之熱可塑性樹脂粒子彼此發生點接觸,因此會確實地追隨表面層基材之變形。因此,對三聚氰胺裝飾板100賦予柔軟性。其結果,能夠提高三聚氰胺裝飾板100之彎曲加工性。 The thermoplastic resin particles have excellent adhesion properties to metals or various materials. Therefore, the thermoplastic resin particles are carried on the surface layer substrate with high adhesion strength. In particular, even if a stress such as bending is applied to the surface layer substrate to deform it, the thermoplastic resin is also difficult to peel off from the surface layer substrate due to the high adhesion strength. Further, since the thermoplastic resin particles carried on the surface layer substrate are in point contact with each other, the deformation of the surface layer substrate is surely followed. Therefore, the melamine decorative board 100 is imparted with flexibility. As a result, the bending workability of the melamine decorative sheet 100 can be improved.
熱可塑性樹脂並無特別限定,例如可列舉丙烯酸樹脂、胺酯樹脂、醋酸乙烯酯系共聚物、胺酯丙烯酸複合樹脂、苯乙烯丁二烯橡膠(SBR)、腈橡膠(NBR)等各種熱可塑性樹脂。其中,熱可塑性樹脂較佳為含有胺酯丙烯酸複合粒子之熱可塑性樹脂。 The thermoplastic resin is not particularly limited, and examples thereof include various thermoplastics such as an acrylic resin, an amine ester resin, a vinyl acetate copolymer, an amine ester acrylic resin, a styrene butadiene rubber (SBR), and a nitrile rubber (NBR). Resin. Among them, the thermoplastic resin is preferably a thermoplastic resin containing an amine ester acrylic composite particle.
胺酯樹脂之強靭性、彈性、柔軟性尤其優異,丙烯酸樹脂之透明性、耐久性、耐候性、耐藥品性、造膜性尤其優異。因此,於使用胺酯丙烯酸複合樹脂作為熱可塑性樹脂之情形時,能夠使承載於表面層基材之熱可塑性樹脂具有上述胺酯樹脂及丙烯酸樹脂雙方之特性。 The urethane resin is particularly excellent in toughness, elasticity, and flexibility, and is excellent in transparency, durability, weather resistance, chemical resistance, and film-forming property of the acrylic resin. Therefore, when an amine ester acrylic composite resin is used as the thermoplastic resin, the thermoplastic resin supported on the surface layer substrate can have characteristics of both the above-described amine ester resin and acrylic resin.
根據以上內容,承載於表面層基材的第2面112側之熱可塑性樹脂較佳為包含由胺酯丙烯酸複合樹脂構成之粒子即胺酯丙烯酸複合粒子。 According to the above, the thermoplastic resin to be carried on the second surface 112 side of the surface layer base material preferably contains the amine ester acrylic composite particles which are particles composed of the amine ester acrylic composite resin.
再者,於本說明書中,所謂胺酯丙烯酸複合粒子,係指於單一粒子內具有丙烯酸樹脂與胺酯樹脂之異相構造之粒子。又,於本說明書中,所謂「異相構造」,係指於一個粒子內存在包含不同種類之樹脂之複數種相之構造。作為該構造,例如可列舉核殼構造、局部構造、島狀構造等。 In the present specification, the amine ester acrylic composite particles are particles having a heterophase structure of an acrylic resin and an amine ester resin in a single particle. In the present specification, the term "heterophase structure" means a structure in which a plurality of phases including different kinds of resins are present in one particle. Examples of the structure include a core-shell structure, a partial structure, and an island-like structure.
對於此種胺酯丙烯酸複合粒子而言,較佳為各粒子具有以丙烯酸樹脂為核且以胺酯樹脂為殼之核殼構造。當具有上述核殼構造之胺酯丙烯酸複合粒子承載於表面層基材時,表面外廓為胺酯樹脂。因此,能夠使表面層基材的第2面112側具有胺酯樹脂及丙烯酸樹脂雙方之特性,且能夠對外廓賦予胺酯樹脂之特性。 In the urethane-acrylic composite particles, it is preferred that each of the particles has a core-shell structure in which an acrylic resin is used as a core and an amine ester resin is used as a shell. When the amine ester acrylic composite particles having the above-described core-shell structure are supported on a surface layer substrate, the surface profile is an amine ester resin. Therefore, the characteristics of both the amine ester resin and the acrylic resin can be obtained on the second surface 112 side of the surface layer base material, and the characteristics of the amine ester resin can be imparted to the outer surface.
又,上述胺酯丙烯酸複合粒子承載於表面層基材的第2面112側時之粒子排列狀態並無特別限定。此種粒子例如能夠排列為直鏈狀而形成直鏈構造,或取得其他各種排列狀態。粒子構造及粒子排列狀態例如能夠由掃描型電子顯微鏡(SEM)確認。 Further, the state in which the urethane-acrylic acid composite particles are supported on the second surface 112 side of the surface layer substrate is not particularly limited. Such particles can be linearly arranged, for example, to form a linear structure, or to obtain other various alignment states. The particle structure and the particle arrangement state can be confirmed, for example, by a scanning electron microscope (SEM).
再者,作為熱可塑性樹脂,可單獨地包含上述熱可塑性樹脂中的一種熱可塑性樹脂,亦可混合地包含不同之兩種以上之熱可塑性樹脂。 Further, as the thermoplastic resin, one of the above thermoplastic resins may be contained alone, or two or more different thermoplastic resins may be contained in combination.
又,熱可塑性樹脂除了含有上述熱可塑性樹脂的樹脂粒子以 外,根據需要,亦可含有少量之增黏劑、浸透促進劑、消泡劑等。 Further, the thermoplastic resin contains, in addition to the resin particles of the above thermoplastic resin, In addition, a small amount of a tackifier, a penetration enhancer, an antifoaming agent, etc. may be contained as needed.
熱可塑性樹脂粒子之平均粒徑並無特別限定,但較佳為小於後述之芯材層12的中間層13側的面(上表面)之算術平均粗糙度Ra1。而且,熱可塑性樹脂粒子之平均粒徑較佳為30~100nm,更佳為60~90nm。 The average particle diameter of the thermoplastic resin particles is not particularly limited, but is preferably smaller than the arithmetic mean roughness Ra1 of the surface (upper surface) on the intermediate layer 13 side of the core material layer 12 to be described later. Further, the average particle diameter of the thermoplastic resin particles is preferably from 30 to 100 nm, more preferably from 60 to 90 nm.
熱可塑性樹脂粒子之平均粒徑滿足上述條件,藉此,熱可塑性樹脂粒子浸漬至表面層基材的纖維間時之浸漬性提高,從而能夠使熱可塑性樹脂粒子進一步浸漬至表面層基材的內部。因此,能夠對表面層11賦予良好之柔軟性。又,若熱可塑性樹脂粒子之平均粒徑處於上述範圍內,則其充分地小於芯材層12的中間層13側的面之算術平均粗糙度Ra1,因此,表面層11的設計面之設計外觀、表面光澤度進一步提高。 When the average particle diameter of the thermoplastic resin particles satisfies the above conditions, the impregnation property of the thermoplastic resin particles when immersed between the fibers of the surface layer substrate is improved, and the thermoplastic resin particles can be further immersed in the interior of the surface layer substrate. . Therefore, it is possible to impart good flexibility to the surface layer 11. In addition, when the average particle diameter of the thermoplastic resin particles is within the above range, it is sufficiently smaller than the arithmetic mean roughness Ra1 of the surface of the core layer 12 on the intermediate layer 13 side, and therefore, the design appearance of the design surface of the surface layer 11 The surface gloss is further improved.
又,熱可塑性樹脂較佳為非水溶性。藉此,能夠防止熱可塑性樹脂向表面層基材的第1面111側移行而與承載於第1面111側之三聚氰胺樹脂混合。因此,能夠防止損害第1面111側的三聚氰胺樹脂所產生之表面性能。 Further, the thermoplastic resin is preferably water-insoluble. Thereby, it is possible to prevent the thermoplastic resin from moving toward the first surface 111 side of the surface layer substrate and mixing with the melamine resin supported on the first surface 111 side. Therefore, it is possible to prevent damage to the surface properties of the melamine resin on the side of the first surface 111.
將熱可塑性樹脂承載於表面層基材的第2面112側之方法並無特別限定,能夠使用與將含有三聚氰胺樹脂之樹脂承載於表面層基材的第1面111側之上述方法相同之方法。 The method of supporting the thermoplastic resin on the second surface 112 side of the surface layer substrate is not particularly limited, and the same method as the above method in which the resin containing the melamine resin is supported on the first surface 111 side of the surface layer substrate can be used. .
尤其於將熱可塑性乳液樹脂(樹脂清漆)用作原料之情形時,能夠使用如下方法等:使用眾所周知之方法而將熱可塑性乳液樹脂塗布於表面層基材,且進行加熱乾燥。 In particular, when a thermoplastic emulsion resin (resin varnish) is used as a raw material, the following method or the like can be used: the thermoplastic emulsion resin is applied to the surface layer substrate by a well-known method, and dried by heating.
再者,胺酯丙烯酸複合樹脂分散於溶劑而成為乳液狀態所得之熱可塑性乳液樹脂尤佳為水性透明型。 Further, the thermoplastic emulsion resin obtained by dispersing the amine ester acrylic composite resin in a solvent to be in an emulsion state is preferably an aqueous transparent type.
再者,水性透明型之熱可塑性乳液樹脂為水溶性,去除水分後之固體成分(塗層膜)為非水溶性,且具有能夠明顯地識別出基底的色彩設計之程度之透明性。因此,於本說明書中,所謂水性透明型之熱可塑性乳液樹脂,係指具有此種特性之樹脂水溶液。使用此種水性透明型之熱可塑性乳液樹脂作為承載於表面層基材的第2面112側之熱可塑性樹脂的原料,藉此,能夠抑制對表面層所具有之設計面的色調產生之影響。 Further, the aqueous transparent thermoplastic emulsion resin is water-soluble, and the solid component (coating film) after moisture removal is water-insoluble, and has transparency to the extent that the color design of the substrate can be clearly recognized. Therefore, in the present specification, the aqueous transparent thermoplastic emulsion resin refers to an aqueous resin solution having such characteristics. By using such a water-based transparent thermoplastic emulsion resin as a raw material of the thermoplastic resin supported on the second surface 112 side of the surface layer substrate, it is possible to suppress the influence of the color tone of the design surface of the surface layer.
再者,對於上述加熱乾燥後之樹脂承載基材(例如樹脂浸漬紙)而言,較佳為當將該樹脂承載基材整體之重量設為100質量%時,殘存有2~6質量%之揮發成分。藉此,對於樹脂承載基材之處理變得容易。又,於使用此種樹脂承載基材而製造三聚氰胺裝飾板100之情形下,當進行加熱、加壓處理(加熱成形)時,承載於表面層基材的上表面側(第1面111側)之含有三聚氰胺樹脂之樹脂的樹脂流動性提高。因此,三聚氰胺裝飾板100之設計外觀、表面光澤度良好。 In addition, it is preferable that the resin-supporting substrate (for example, resin-impregnated paper) after heat-drying has a weight of 100% by mass of the entire resin-supporting substrate, and 2 to 6% by mass remains. Volatile ingredients. Thereby, the handling of the resin-carrying substrate becomes easy. In the case where the melamine decorative sheet 100 is produced by using such a resin-supporting substrate, when it is subjected to heating and pressure treatment (heat molding), it is carried on the upper surface side (the first surface 111 side) of the surface layer substrate. The resin of the melamine resin-containing resin has improved fluidity. Therefore, the melamine decorative panel 100 has a good design appearance and surface gloss.
用以對熱可塑性樹脂進行溶解(用以調製熱可塑性乳液樹脂)之溶劑並無特別限定,例如可列舉水等。又,亦能夠於不會對塗布性等產生不良影響之範圍內,組合使用不良溶劑作為溶劑。上述樹脂中所含之固體成分(除了溶劑以外之全部成分)的量並無特別限定,但較佳為上述樹脂整體之25~60質量%,更佳為30~45質量%。藉此,能夠使樹脂對於表面層基材之浸漬性提高。 The solvent for dissolving the thermoplastic resin (for modulating the thermoplastic emulsion resin) is not particularly limited, and examples thereof include water. Further, it is also possible to use a poor solvent as a solvent in a range that does not adversely affect coating properties and the like. The amount of the solid component (all components other than the solvent) contained in the resin is not particularly limited, but is preferably 25 to 60% by mass, and more preferably 30 to 45% by mass based on the total amount of the resin. Thereby, the impregnation property of a resin with respect to a surface layer base material can be improved.
再者,如上所述,表面層11的設計面(第1面111)成為鏡面,其算術平均粗糙度Ra2較佳為300nm以下,更佳為150nm以下。藉此,表面層11的第1面111變得更平滑,從而能夠進一步提高三聚氰胺裝 飾板100之高級感。 Further, as described above, the design surface (first surface 111) of the surface layer 11 is a mirror surface, and the arithmetic mean roughness Ra2 is preferably 300 nm or less, more preferably 150 nm or less. Thereby, the first surface 111 of the surface layer 11 becomes smoother, so that the melamine loading can be further improved. The high quality of the plaque 100.
<2.芯材層> <2. Core material layer>
芯材層12透過中間層13而接合於表面層11的下表面(第2面112)側。 The core material layer 12 is bonded to the lower surface (second surface 112) side of the surface layer 11 through the intermediate layer 13.
芯材層12係由包含玻璃布或預浸布之芯材層材料構成,該預浸布包含玻璃布作為基材。藉此,能夠對三聚氰胺裝飾板100賦予耐熱性、不燃性、剛性等。 The core material layer 12 is composed of a core material layer material containing a glass cloth or a prepreg, and the prepreg cloth contains a glass cloth as a substrate. Thereby, heat resistance, non-combustibility, rigidity, and the like can be imparted to the melamine decorative sheet 100.
又,於芯材層12的上表面形成有凹凸。芯材層12的凹凸埋入至中間層13,藉此,芯材層12與中間層13藉由錨固效果而牢固地接合(接著)。亦即,能夠提高芯材層12與中間層13之層間接著強度。藉此,能夠確實地防止在對三聚氰胺裝飾板100進行彎曲加工時,芯材層12與中間層13剝離。 Further, irregularities are formed on the upper surface of the core material layer 12. The unevenness of the core material layer 12 is buried in the intermediate layer 13, whereby the core material layer 12 and the intermediate layer 13 are firmly joined by the anchoring effect (and then). That is, the interlayer bonding strength between the core material layer 12 and the intermediate layer 13 can be improved. Thereby, it is possible to reliably prevent the core material layer 12 from being peeled off from the intermediate layer 13 when the melamine decorative sheet 100 is subjected to bending processing.
芯材層12的上表面(中間層13側的面)之算術平均粗糙度Ra1並無特別限定,但較佳為0.1~10μm,更佳為1~7μm。藉此,能夠進一步提高芯材層12與中間層13之層間接著強度。 The arithmetic mean roughness Ra1 of the upper surface (surface on the intermediate layer 13 side) of the core material layer 12 is not particularly limited, but is preferably 0.1 to 10 μm, more preferably 1 to 7 μm. Thereby, the interlayer bonding strength between the core material layer 12 and the intermediate layer 13 can be further improved.
又,作為構成玻璃布之玻璃,例如可列舉E玻璃、C玻璃、A玻璃、S玻璃、D玻璃、NE玻璃、T玻璃、H玻璃等。其中,T玻璃較佳。T玻璃係熱膨脹係數比較小之材料,因此,藉由將該T玻璃用作玻璃布之構成材料,能夠減小玻璃布之熱膨脹係數。 Moreover, examples of the glass constituting the glass cloth include E glass, C glass, A glass, S glass, D glass, NE glass, T glass, and H glass. Among them, T glass is preferred. T glass is a material having a relatively small coefficient of thermal expansion. Therefore, by using the T glass as a constituent material of the glass cloth, the thermal expansion coefficient of the glass cloth can be reduced.
玻璃布之重量並無特別限定,但於需要滿足建築基準法第2條第9號之不燃性適合要件即「不允許在燃燒後龜裂、貫通」之情形時,基重100g/m2以上較佳。又,重量之上限並無特別限制,但若考慮材料成本與加工性,則基重250g/m2以下較佳。 The weight of the glass cloth is not particularly limited, but it is required to satisfy the non-combustibility requirements of Article 2, No. 9 of the Building Standards Law, that is, when it is not allowed to crack or penetrate after burning, the basis weight is 100 g/m 2 or more. Preferably. Further, the upper limit of the weight is not particularly limited, but in consideration of material cost and workability, the basis weight is preferably 250 g/m 2 or less.
預浸布並無特別限定,例如能夠使含有熱可塑性樹脂、熱硬化性樹脂等之樹脂組成物浸漬至上述玻璃布。 The prepreg is not particularly limited, and for example, a resin composition containing a thermoplastic resin or a thermosetting resin can be immersed in the glass cloth.
只要與中間層13之間的層間接著強度足以形成三聚氰胺裝飾板100,則預浸布中所含之樹脂組成物的量並無特別限定。於使用熱可塑性樹脂作為樹脂組成物之情形時,預浸布中所含之熱可塑性樹脂(固體成分)的量較佳為1質量%以上、20質量%以下,更佳為1質量%以上、10質量%以下。藉此,能夠進一步提高中間層13與芯材層12之層間接著強度。 The amount of the resin composition contained in the prepreg is not particularly limited as long as the interlayer adhesion strength with the intermediate layer 13 is sufficient to form the melamine decorative sheet 100. When the thermoplastic resin is used as the resin composition, the amount of the thermoplastic resin (solid content) contained in the prepreg is preferably 1% by mass or more and 20% by mass or less, more preferably 1% by mass or more. 10% by mass or less. Thereby, the interlayer adhesion strength between the intermediate layer 13 and the core material layer 12 can be further improved.
又,於使用熱硬化性樹脂作為樹脂組成物之情形時,預浸布中所含之熱硬化性樹脂(固體成分)的量較佳為1質量%以上、20質量%以下,更佳為2質量%以上、10質量%以下。藉此,能夠進一步提高中間層13與芯材層12之層間接著強度。 In the case where a thermosetting resin is used as the resin composition, the amount of the thermosetting resin (solid content) contained in the prepreg is preferably 1% by mass or more and 20% by mass or less, more preferably 2%. The mass% or more and 10% by mass or less. Thereby, the interlayer adhesion strength between the intermediate layer 13 and the core material layer 12 can be further improved.
熱可塑性樹脂並無特別限定,例如可列舉丙烯酸樹脂、胺酯樹脂、乙烯醋酸乙烯酯樹脂、苯乙烯丁二烯橡膠(SBR)等。其中,較佳為使用丙烯酸樹脂及/或胺酯樹脂作為熱可塑性樹脂。 The thermoplastic resin is not particularly limited, and examples thereof include an acrylic resin, an amine ester resin, an ethylene vinyl acetate resin, and a styrene butadiene rubber (SBR). Among them, an acrylic resin and/or an amine ester resin is preferably used as the thermoplastic resin.
熱硬化性樹脂並無特別限定,例如可列舉酚醛樹脂、環氧樹脂、環氧丙烷樹脂、(甲基)丙烯酸酯樹脂、不飽和聚酯樹脂、酞酸二烯丙酯樹脂、尿素樹脂、馬來醯亞胺樹脂等。其中,根據不燃性、耐熱性、密著性之觀點,較佳為使用酚醛樹脂作為熱硬化性樹脂。該等樹脂能夠單獨或混合地使用。 The thermosetting resin is not particularly limited, and examples thereof include a phenol resin, an epoxy resin, a propylene oxide resin, a (meth) acrylate resin, an unsaturated polyester resin, a diallyl citrate resin, a urea resin, and a horse. Come to imine resin and so on. Among them, a phenol resin is preferably used as the thermosetting resin from the viewpoint of incombustibility, heat resistance, and adhesion. These resins can be used singly or in combination.
預浸布能夠藉由以往眾所周知之方法製造。例如,使樹脂組成物溶解於溶劑所得之樹脂清漆浸漬至上述玻璃布,然後進行乾燥,藉此,能夠獲得該預浸布。 The prepreg can be produced by a method known in the art. For example, the resin varnish obtained by dissolving a resin composition in a solvent is immersed in the glass cloth, and then dried, whereby the prepreg can be obtained.
又,芯材層12亦可在與中間層13接觸之上表面側,進而承載熱可塑性樹脂。作為此種熱可塑性樹脂,能夠使用與承載於表面層基材的第2面112側之熱可塑性樹脂相同之熱可塑性樹脂。又,於該熱可塑性樹脂含有熱可塑性樹脂粒子之情形時,能夠進一步提高芯材層12與中間層13之接著強度,且能夠使三聚氰胺裝飾板100在常溫下具有高彎曲加工性。該熱可塑性樹脂粒子之平均粒徑並無特別限定。又,該熱可塑性樹脂粒子既可為水溶性,亦可為非水溶性。 Further, the core material layer 12 may also be in contact with the intermediate layer 13 on the upper surface side to carry the thermoplastic resin. As such a thermoplastic resin, the same thermoplastic resin as that of the thermoplastic resin on the second surface 112 side of the surface layer substrate can be used. Moreover, when the thermoplastic resin contains thermoplastic resin particles, the adhesion strength between the core material layer 12 and the intermediate layer 13 can be further improved, and the melamine decorative sheet 100 can have high bending workability at normal temperature. The average particle diameter of the thermoplastic resin particles is not particularly limited. Further, the thermoplastic resin particles may be water-soluble or water-insoluble.
再者,承載於芯材層12的與中間層13接觸的面側之熱可塑性樹脂只要對芯材層12賦予柔軟性,且不會對燃燒時之發熱量、氣體有害性產生阻礙,則並無特別限定。 In addition, the thermoplastic resin that is placed on the surface side of the core material layer 12 that is in contact with the intermediate layer 13 is not required to impart flexibility to the core material layer 12, and does not hinder heat generation and gas harmfulness during combustion. There is no special limit.
芯材層12之厚度較佳為100μm以上。藉此,能夠對三聚氰胺裝飾板100賦予充分之耐熱性、不燃性。又,厚度之上限並無特別限定。然而,厚度越大,則三聚氰胺裝飾板100之厚度與重量越大,成本亦越高。因此,較佳為於最終製品(三聚氰胺裝飾板100)的設計上所允許之範圍內,設定芯材層12之厚度,該芯材層12之厚度更佳為350μm以下。 The thickness of the core material layer 12 is preferably 100 μm or more. Thereby, the melamine decorative sheet 100 can be provided with sufficient heat resistance and incombustibility. Further, the upper limit of the thickness is not particularly limited. However, the greater the thickness, the greater the thickness and weight of the melamine decorative panel 100 and the higher the cost. Therefore, it is preferable to set the thickness of the core material layer 12 within the range allowed by the design of the final product (melamine decorative sheet 100), and the thickness of the core material layer 12 is more preferably 350 μm or less.
<3.中間層> <3. Middle layer>
中間層13係設置於表面層11與芯材層12之間的樹脂層,其上表面與表面層11接觸,其下表面與芯材層12接觸,從而接合上述表面層11與芯材層12。中間層13係具有緩和芯材層12的上表面之表面形狀(凹凸)對於表面層11之影響之功能之層。 The intermediate layer 13 is a resin layer disposed between the surface layer 11 and the core material layer 12, the upper surface of which is in contact with the surface layer 11, and the lower surface thereof is in contact with the core material layer 12, thereby joining the surface layer 11 and the core material layer 12 . The intermediate layer 13 is a layer having a function of relaxing the influence of the surface shape (concavity and convexity) of the upper surface of the core material layer 12 on the surface layer 11.
如此,本發明之特徵在於:於表面層11與芯材層12之間具有中間層13。 Thus, the invention is characterized in that an intermediate layer 13 is provided between the surface layer 11 and the core material layer 12.
由於具有此種特徵,故而能夠減小源於玻璃布之芯材層12的上表面之表面形狀(凹凸)對於表面層11的設計面(第1面111)之影響。藉此,能夠提高表面層11的設計面之平滑性。其結果,能夠提供不燃性及彎曲加工性優異,且具備由鏡面加工產生之高級感之三聚氰胺裝飾板100。 With such a feature, it is possible to reduce the influence of the surface shape (concavity and convexity) of the upper surface of the core material layer 12 derived from the glass cloth on the design surface (first surface 111) of the surface layer 11. Thereby, the smoothness of the design surface of the surface layer 11 can be improved. As a result, it is possible to provide the melamine decorative sheet 100 which is excellent in nonflammability and bending workability and has a high-grade feeling produced by mirror finishing.
又,於該三聚氰胺裝飾板100中,中間層13之平均厚度大於芯材層12的上表面之算術平均粗糙度Ra1。藉此,能夠抑制因芯材層12的上表面的凹凸而使中間層13的上表面產生凹凸,該中間層13的上表面之平滑性提高。其結果,能夠提高表面層11的設計面之設計外觀、表面光澤度。又,中間層13之平均厚度滿足上述條件,藉此,中間層13發揮作為緩衝層之功能,吸收施加至三聚氰胺裝飾板100之應力。因此,能夠確實地防止在對三聚氰胺裝飾板100進行彎曲加工時,芯材層12與中間層13剝離。 Further, in the melamine decorative sheet 100, the average thickness of the intermediate layer 13 is larger than the arithmetic mean roughness Ra1 of the upper surface of the core layer 12. Thereby, it is possible to suppress irregularities on the upper surface of the intermediate layer 13 due to the unevenness of the upper surface of the core layer 12, and the smoothness of the upper surface of the intermediate layer 13 is improved. As a result, the design appearance and surface glossiness of the design surface of the surface layer 11 can be improved. Further, the average thickness of the intermediate layer 13 satisfies the above conditions, whereby the intermediate layer 13 functions as a buffer layer and absorbs the stress applied to the melamine decorative sheet 100. Therefore, it is possible to reliably prevent the core material layer 12 from being peeled off from the intermediate layer 13 when the melamine decorative sheet 100 is subjected to bending processing.
中間層13係由中間層形成用樹脂構成。 The intermediate layer 13 is made of a resin for forming an intermediate layer.
中間層形成用樹脂並無特別限定,但較佳為含有樹脂粒子。再者,將樹脂分散於溶劑而成為乳液狀態所得之乳液樹脂(樹脂清漆)用作原料,使該乳液樹脂(樹脂清漆)乾燥,藉此,能夠容易且確實地獲得上述樹脂粒子。於中間層形成用樹脂含有樹脂粒子之情形時,樹脂粒子埋入至芯材層12的凹凸的凹部。藉此,中間層13的上表面之平滑性進一步提高。藉此,能夠進一步減小源於玻璃布之芯材層12之表面形狀對於表面層11的設計面(第1面111)之影響。 The resin for forming the intermediate layer is not particularly limited, but preferably contains resin particles. In addition, an emulsion resin (resin varnish) obtained by dispersing a resin in a solvent to obtain an emulsion state is used as a raw material, and the emulsion resin (resin varnish) is dried, whereby the resin particles can be easily and surely obtained. When the resin for forming the intermediate layer contains resin particles, the resin particles are buried in the concave portion of the unevenness of the core material layer 12. Thereby, the smoothness of the upper surface of the intermediate layer 13 is further improved. Thereby, the influence of the surface shape of the core material layer 12 derived from the glass cloth on the design surface (the first surface 111) of the surface layer 11 can be further reduced.
樹脂粒子並無特別限定,例如可列舉丙烯酸樹脂、胺酯樹脂、乙酸乙烯酯系共聚物、胺酯丙烯酸複合樹脂、苯乙烯丁二烯橡膠(SBR)、 腈橡膠(NBR)等熱可塑性樹脂的粒子。其中,較佳為使用丙烯酸樹脂的粒子作為樹脂粒子。藉此,能夠更牢固地接合表面層11與芯材層12,並且能夠進一步減小源於玻璃布之芯材層12之表面形狀對於表面層11的設計面(第1面111)之影響。 The resin particles are not particularly limited, and examples thereof include an acrylic resin, an amine ester resin, a vinyl acetate copolymer, an amine ester acrylic composite resin, and a styrene butadiene rubber (SBR). Particles of a thermoplastic resin such as nitrile rubber (NBR). Among them, particles of an acrylic resin are preferably used as the resin particles. Thereby, the surface layer 11 and the core material layer 12 can be joined more firmly, and the influence of the surface shape of the core material layer 12 derived from the glass cloth on the design surface (the first surface 111) of the surface layer 11 can be further reduced.
上述樹脂粒子之平均粒徑並無特別限定。於承載於表面層11的下表面側之熱可塑性樹脂含有熱可塑性樹脂粒子之情形時,大於熱可塑性樹脂粒子之平均粒徑且小於上述算術平均粗糙度Ra1之樹脂粒子較佳。此種尺寸之樹脂粒子埋入至芯材層12的凹凸的凹部,能夠使中間層13的上表面平滑。又,即使於中間層13的表面層11側的面(上表面)形成有微小之凹凸,平均粒徑較該樹脂粒子更小之熱可塑性樹脂的熱可塑性樹脂粒子亦會埋入至該凹凸的凹部。其結果,能夠使表面層11的第1面111(設計面)更平滑,表面層11的設計面之設計外觀、表面光澤度進一步提高。 The average particle diameter of the above resin particles is not particularly limited. When the thermoplastic resin to be carried on the lower surface side of the surface layer 11 contains thermoplastic resin particles, the resin particles larger than the average particle diameter of the thermoplastic resin particles and smaller than the arithmetic mean roughness Ra1 are preferable. The resin particles of such a size are embedded in the concave and convex portions of the core material layer 12, and the upper surface of the intermediate layer 13 can be made smooth. Further, even if the surface (the upper surface) on the surface layer 11 side of the intermediate layer 13 is formed with minute irregularities, the thermoplastic resin particles of the thermoplastic resin having an average particle diameter smaller than the resin particles are buried in the unevenness. Concave. As a result, the first surface 111 (design surface) of the surface layer 11 can be made smoother, and the design appearance and surface glossiness of the design surface of the surface layer 11 can be further improved.
具體而言,樹脂粒子之平均粒徑較佳為150nm以上、0.75×Ra1以下,更佳為200nm以上、0.50×Ra1以下。若中間層形成用樹脂中所含之樹脂粒子之平均粒徑處於上述範圍內,則根據上述作用、效果,能夠使表面層11的第1面111(設計面)更平滑,表面層11的設計面之設計外觀、表面光澤度進一步提高。 Specifically, the average particle diameter of the resin particles is preferably 150 nm or more and 0.75 × Ra 1 or less, more preferably 200 nm or more and 0.50 × Ra 1 or less. When the average particle diameter of the resin particles contained in the resin for forming the intermediate layer is within the above range, the first surface 111 (design surface) of the surface layer 11 can be made smoother according to the above-described actions and effects, and the design of the surface layer 11 can be achieved. The design appearance and surface gloss of the surface are further improved.
而且,能夠更確實地防止上述樹脂粒子浸入至表面層11或芯材層12中,且能夠更確實地發揮如上所述之作為中間層13之功能。相對於此,若樹脂粒子之平均粒徑不足上述下限值,則根據構成表面層11之表面層基材之種類或構成芯材層12之玻璃布之種類,有時在製造三聚氰胺裝飾板100時,樹脂粒子會被表面層11或芯材層12吸收,導致難以形成中間層13。 Further, it is possible to more reliably prevent the resin particles from entering the surface layer 11 or the core material layer 12, and it is possible to more reliably exhibit the function as the intermediate layer 13 as described above. On the other hand, when the average particle diameter of the resin particles is less than the above lower limit, the melamine decorative sheet 100 may be manufactured depending on the type of the surface layer base material constituting the surface layer 11 or the type of the glass cloth constituting the core material layer 12 . At the time, the resin particles are absorbed by the surface layer 11 or the core material layer 12, resulting in difficulty in forming the intermediate layer 13.
再者,亦能夠使用由中間層形成用樹脂構成之膜作為中間層13。 Further, a film made of a resin for forming an intermediate layer can also be used as the intermediate layer 13.
此種膜能夠由丙烯酸樹脂、胺酯樹脂、聚烯烴樹脂、聚酯樹脂等熱可塑性樹脂構成。即使於將此種膜用作中間層13之情形時,亦能夠進一步減小源於玻璃布之芯材層12之表面形狀對於表面層11的設計面(第1面111)之影響。又,於將此種膜用作中間層13之情形時,能夠節省用以形成中間層13之材料(溶劑等)或時間,因此,能夠削減三聚氰胺裝飾板100之製造成本。 Such a film can be composed of a thermoplastic resin such as an acrylic resin, an amine ester resin, a polyolefin resin, or a polyester resin. Even in the case where such a film is used as the intermediate layer 13, the influence of the surface shape of the core material layer 12 derived from the glass cloth on the design surface (the first surface 111) of the surface layer 11 can be further reduced. Moreover, when such a film is used as the intermediate layer 13, the material (solvent or the like) or time for forming the intermediate layer 13 can be saved, and therefore, the manufacturing cost of the melamine decorative sheet 100 can be reduced.
中間層13之平均厚度只要大於芯材層12的上表面之算術平均粗糙度Ra1,則並無特別限定,但較佳為6μm以上,更佳為10~50μm。藉此,能夠更有效果地減小源於玻璃布之芯材層12之表面形狀對於表面層11的設計面(第1面111)之影響。相對於此,若中間層13之平均厚度不足上述下限值,則根據算術平均粗糙度Ra1之值,有時源於玻璃布之芯材層12之表面形狀對於表面層11的設計面(第1面111)之影響會增大。又,若中間層13之平均厚度超過上述上限值,則有時中間層13燃燒時之發熱量會增大,具有上述中間層13之三聚氰胺裝飾板100失去不燃性。 The average thickness of the intermediate layer 13 is not particularly limited as long as it is larger than the arithmetic mean roughness Ra1 of the upper surface of the core layer 12, but is preferably 6 μm or more, and more preferably 10 to 50 μm. Thereby, the influence of the surface shape of the core material layer 12 derived from the glass cloth on the design surface (the first surface 111) of the surface layer 11 can be more effectively reduced. On the other hand, when the average thickness of the intermediate layer 13 is less than the above lower limit value, the surface shape of the core material layer 12 derived from the glass cloth may be derived from the design surface of the surface layer 11 depending on the value of the arithmetic mean roughness Ra1. The influence of one side 111) will increase. Further, when the average thickness of the intermediate layer 13 exceeds the above upper limit value, the amount of heat generated when the intermediate layer 13 is burned may increase, and the melamine decorative sheet 100 having the intermediate layer 13 may lose incombustibility.
對於如上所述之三聚氰胺裝飾板100而言,能夠以使常溫(通常為20~30℃左右)下之最小彎曲半徑達到10mmR以下之方式進行彎曲加工,但彎曲加工之程度(最小彎曲半徑之值)並不限定於此。最小彎曲半徑R係指即使沿著具有半徑R之彎曲部之模具而反復地實施向一個方向進行之常溫彎曲加工,亦不會產生裂痕等問題而能夠獲得100%之良品之最小模具的半徑R。 The melamine decorative sheet 100 as described above can be bent so that the minimum bending radius at normal temperature (usually about 20 to 30 ° C) is 10 mmR or less, but the degree of bending processing (the minimum bending radius value) ) is not limited to this. The minimum bending radius R is a radius R of the smallest mold which can obtain 100% of good products even if the normal temperature bending process in one direction is repeatedly performed along the mold having the curved portion having the radius R, and no problem such as cracks occur. .
又,三聚氰胺裝飾板100之整體厚度較佳為0.4mm以下。藉此,能夠更容易地對三聚氰胺裝飾板100進行彎曲加工。 Further, the overall thickness of the melamine decorative sheet 100 is preferably 0.4 mm or less. Thereby, the melamine decorative board 100 can be bent more easily.
再者,於本實施形態中,作為較佳之例子,說明了承載於表面層基材的第2面112側之熱可塑性樹脂呈粒子狀,但亦可並非呈粒子狀。亦即,例如於使用熱可塑性乳液樹脂(樹脂清漆)而將其承載於表面層基材的第2面112側之情形時,於樹脂清漆乾燥之後,熱可塑性樹脂亦可不保持粒子狀之形態。 In the present embodiment, as a preferred example, the thermoplastic resin placed on the second surface 112 side of the surface layer substrate has a particle shape, but may not be in the form of particles. In other words, for example, when a thermoplastic emulsion resin (resin varnish) is used to carry it on the second surface 112 side of the surface layer substrate, the thermoplastic resin may not remain in a particulate form after the resin varnish is dried.
又,於本實施形態中,作為較佳之例子,說明了構成中間層13之中間層形成用樹脂呈粒子狀,但亦可並非呈粒子狀。亦即,例如於使用乳液樹脂(樹脂清漆)而形成中間層13之情形時,於樹脂清漆乾燥之後,中間層形成用樹脂亦可不保持粒子狀之形態。 Further, in the present embodiment, as a preferred example, the intermediate layer forming resin constituting the intermediate layer 13 is described as being in the form of particles, but may not be in the form of particles. In other words, for example, when the intermediate layer 13 is formed using an emulsion resin (resin varnish), the resin for forming the intermediate layer may not remain in a particulate form after the resin varnish is dried.
《三聚氰胺裝飾板之製造方法》 "Manufacturing method of melamine decorative board"
其次,說明上述三聚氰胺裝飾板之製造方法。 Next, a method of manufacturing the above melamine decorative sheet will be described.
圖2係表示本發明之三聚氰胺裝飾板之製造方法之一例的步驟圖。 Fig. 2 is a flow chart showing an example of a method for producing a melamine decorative sheet of the present invention.
再者,於以下的說明中,將圖2中的上側稱為「上」,將圖2中的下側稱為「下」。 In the following description, the upper side in FIG. 2 is referred to as "upper", and the lower side in FIG. 2 is referred to as "lower".
首先,形成由上述表面層材料構成之第1層11'。再者,第1層11'係成為上述表面層11之層。 First, the first layer 11' composed of the above surface layer material is formed. Further, the first layer 11' is a layer of the surface layer 11 described above.
於表面層基材的一面(成為設計面之第1面111)側(上表面側)承載含有三聚氰胺樹脂之樹脂,於另一面(第2面112)側(下表面側)承載熱可塑性樹脂,藉此形成第1層11'。更具體而言,將含有如下樹 脂之樹脂清漆供給至表面層基材的第1面111側,該樹脂含有三聚氰胺樹脂,並且將含有由熱可塑性樹脂構成之粒子(熱可塑性樹脂粒子)之樹脂清漆供給至表面層基材的第2面112側,藉此形成上述第1層11'。 The resin containing the melamine resin is carried on one side (the first surface side of the design surface) (the upper surface side) of the surface layer substrate, and the thermoplastic resin is carried on the other surface (the second surface 112 side) (the lower surface side). Thereby, the first layer 11' is formed. More specifically, it will contain the following tree The resin varnish is supplied to the first surface 111 side of the surface layer substrate, and the resin contains a melamine resin, and the resin varnish containing particles (thermoplastic resin particles) composed of a thermoplastic resin is supplied to the surface layer substrate. On the two sides 112 side, the first layer 11' is formed thereby.
再者,在將熱可塑性樹脂承載於表面層基材的第2面112側時所使用之樹脂清漆中,該樹脂清漆中所含之熱可塑性樹脂粒子之平均粒徑較佳為30~100nm,更佳為60~90nm。熱可塑性樹脂粒子之平均粒徑滿足上述條件,藉此,熱可塑性樹脂粒子浸漬至表面層基材的纖維間時之浸漬性提高,從而能夠使熱可塑性樹脂粒子進一步浸漬至表面層基材的內部。因此,能夠對表面層11賦予良好之柔軟性。又,若熱可塑性樹脂粒子之平均粒徑處於上述範圍內,則其充分地小於芯材層12的中間層13側的面之算術平均粗糙度Ra1,因此,表面層11的設計面之設計外觀、表面光澤度進一步提高。 Further, in the resin varnish used when the thermoplastic resin is carried on the second surface 112 side of the surface layer substrate, the average particle diameter of the thermoplastic resin particles contained in the resin varnish is preferably 30 to 100 nm. More preferably 60 to 90 nm. When the average particle diameter of the thermoplastic resin particles satisfies the above conditions, the impregnation property of the thermoplastic resin particles when immersed between the fibers of the surface layer substrate is improved, and the thermoplastic resin particles can be further immersed in the interior of the surface layer substrate. . Therefore, it is possible to impart good flexibility to the surface layer 11. In addition, when the average particle diameter of the thermoplastic resin particles is within the above range, it is sufficiently smaller than the arithmetic mean roughness Ra1 of the surface of the core layer 12 on the intermediate layer 13 side, and therefore, the design appearance of the design surface of the surface layer 11 The surface gloss is further improved.
其次,對第1層11'的下表面(另一個面)賦予中間層形成用樹脂,形成由上述中間層形成用樹脂構成之第2層13'。更具體而言,將含有由中間層形成用樹脂構成之粒子(樹脂粒子)之樹脂清漆供給至第1層11'的下表面,藉此形成第2層13'。第2層13'係成為上述中間層13之層。 Next, the resin for forming an intermediate layer is applied to the lower surface (the other surface) of the first layer 11', and the second layer 13' made of the resin for forming the intermediate layer is formed. More specifically, a resin varnish containing particles (resin particles) composed of a resin for forming an intermediate layer is supplied to the lower surface of the first layer 11' to form a second layer 13'. The second layer 13' is a layer of the above intermediate layer 13.
再者,於形成第2層13'時所使用之樹脂清漆中,該樹脂清漆中所含之樹脂粒子之平均粒徑較佳為150nm以上,更佳為200nm以上。若中間層形成用樹脂中所含之樹脂粒子之平均粒徑處於上述範圍內,則根據上述作用、效果,能夠使表面層11的第1面111(設計面)更平滑,表面層11的設計面之設計外觀、表面光澤度進一步提高。進而,能夠更確實地防止上述樹脂粒子浸入至表面層11或芯材層12中,且能夠更確實地發揮如上所述之作為中間層13之功能。 In the resin varnish used for forming the second layer 13', the average particle diameter of the resin particles contained in the resin varnish is preferably 150 nm or more, and more preferably 200 nm or more. When the average particle diameter of the resin particles contained in the resin for forming the intermediate layer is within the above range, the first surface 111 (design surface) of the surface layer 11 can be made smoother according to the above-described actions and effects, and the design of the surface layer 11 can be achieved. The design appearance and surface gloss of the surface are further improved. Further, it is possible to more reliably prevent the resin particles from entering the surface layer 11 or the core material layer 12, and it is possible to more reliably exhibit the function as the intermediate layer 13 as described above.
根據以上內容,獲得具有由表面層材料構成之第1層11'、與由中間層形成用樹脂構成之第2層13'之第1基體10(參照圖2(a))。 According to the above, the first substrate 10 having the first layer 11' made of the surface layer material and the second layer 13' made of the resin for forming the intermediate layer is obtained (see FIG. 2(a)).
再者,亦可在將熱可塑性樹脂承載於第1層11'的下表面(另一個面)側之同時,形成第2層13'。中間層形成用樹脂的樹脂粒子之粒子徑大於構成表面層11之熱可塑性樹脂的樹脂粒子之粒子徑,該中間層形成用樹脂的樹脂粒子不易浸入至表面層11。換言之,中間層形成用樹脂的樹脂粒子不易承載於表面層基材。因此,能夠將熱可塑性樹脂承載於表面層基材的下表面(第2面112)側,且同時形成中間層。藉此,能夠一次性實施乾燥步驟,從而能夠簡化生產步驟,進而降低成本。 Further, the second layer 13' may be formed while the thermoplastic resin is carried on the lower surface (the other surface) side of the first layer 11'. The particle diameter of the resin particles of the intermediate layer forming resin is larger than the particle diameter of the resin particles constituting the thermoplastic resin of the surface layer 11, and the resin particles of the intermediate layer forming resin are less likely to enter the surface layer 11. In other words, the resin particles of the intermediate layer forming resin are less likely to be carried on the surface layer substrate. Therefore, the thermoplastic resin can be carried on the lower surface (second surface 112) side of the surface layer substrate while forming the intermediate layer. Thereby, the drying step can be carried out at one time, so that the production steps can be simplified and the cost can be reduced.
其次,準備由芯材層材料構成之第2基體12'。第2基體12'係成為上述芯材層12之層。 Next, a second base 12' made of a core material is prepared. The second base 12' is a layer of the core material layer 12.
其次,以與第1基體10的下表面(第2層13'側的面)相對向之方式,配置第2基體12'(參照圖2(b))。 Next, the second base body 12' is disposed so as to face the lower surface (the surface on the second layer 13' side) of the first base 10 (see FIG. 2(b)).
其次,準備140℃下之彈性率為1~50GPa之基材膜20。 Next, a base film 20 having an elastic modulus at 140 ° C of 1 to 50 GPa was prepared.
又,準備兩塊具備實施了鏡面加工之抵接面之護板(鏡面完成護板)30。 Further, two shields (mirror-completed shields) 30 having mirror-processed abutting faces are prepared.
其次,如圖2(c)所示,準備兩組對向配置之第1基體10及第2基體12'之積層體,且以將基材膜20夾在積層體的第2基體12'彼此之間之方式進行配置。亦即,以使各積層體的第2基體12'位於基材膜20側之方式進行配置。 Next, as shown in FIG. 2(c), two sets of the first base body 10 and the second base body 12' which are disposed opposite to each other are prepared, and the base material 20 is sandwiched between the second base bodies 12' of the laminated body. The way between them is configured. In other words, the second substrate 12' of each of the laminates is disposed on the side of the base film 20.
進而,如圖2(c)所示,以使各抵接面與各積層體的第1基體10(第1層11')相對向之方式,配置兩塊鏡面完成護板30。 Further, as shown in FIG. 2(c), the two mirror-finished panels 30 are disposed such that the respective abutting faces face the first base 10 (the first layer 11') of each of the laminated bodies.
然後,一面利用鏡面完成護板30對第1基體10(第1層11')進行加熱,一面使鏡面完成護板30彼此靠近。藉此,因鏡面完成護板30與基材膜20靠近而按壓各積層體,從而對第1基體10與第2基體12'進行熱壓接。藉此,獲得兩塊三聚氰胺裝飾板100。 Then, while the first base 10 (the first layer 11') is heated by the mirror-finished shield 30, the mirror-finished shields 30 are brought closer to each other. Thereby, the first base body 10 and the second base body 12' are thermocompression-bonded by pressing the respective laminated bodies by the mirror-finished shield 30 and the base film 20. Thereby, two melamine decorative panels 100 are obtained.
根據如上所述之製造方法,能夠容易地製造不燃性及彎曲加工性優異,且具備實施了鏡面加工之設計面之三聚氰胺裝飾板100。 According to the manufacturing method as described above, the melamine decorative sheet 100 having excellent non-combustibility and bending workability and having a mirror-finished design surface can be easily produced.
又,將基材膜20設置於第2基體12'側,藉此,當進行熱壓接時,能夠緩和第2基體12'將第1基體10按壓至鏡面完成護板30時之力。藉此,能夠進一步減小構成第2基體12'之玻璃布的表面形狀對於第1基體10的表面(表面層11的設計面)之影響。其結果,能夠將三聚氰胺裝飾板100的設計面設為更平滑之鏡面。 Moreover, when the base film 20 is provided on the side of the second base 12', it is possible to alleviate the force when the second base 12' presses the first base 10 to the mirror-finished panel 30 when the thermocompression bonding is performed. Thereby, the influence of the surface shape of the glass cloth constituting the second base body 12' on the surface of the first base body 10 (the design surface of the surface layer 11) can be further reduced. As a result, the design surface of the melamine decorative panel 100 can be made into a smoother mirror surface.
再者,基材膜20的140℃下之彈性率為1~50GPa,但較佳為15~40GPa。藉此,能夠進一步減小構成第2基體12'之玻璃布的表面形狀對於第1基體10的表面(表面層11的設計面)之影響。 Further, the substrate film 20 has an elastic modulus at 140 ° C of 1 to 50 GPa, preferably 15 to 40 GPa. Thereby, the influence of the surface shape of the glass cloth constituting the second base body 12' on the surface of the first base body 10 (the design surface of the surface layer 11) can be further reduced.
構成基材膜20之材料只要滿足上述特性,則並無特別限定,但較佳為由熱可塑性樹脂構成,且更佳為由軟化溫度為120~160℃之熱可塑性樹脂構成。藉此,當進行熱壓接時,能夠進一步減小構成第2基體12'之玻璃布的表面形狀對於第1基體10的表面(表面層11的設計面)之影響。 The material constituting the base film 20 is not particularly limited as long as it satisfies the above characteristics, but is preferably composed of a thermoplastic resin, and more preferably a thermoplastic resin having a softening temperature of 120 to 160 °C. Thereby, when the thermocompression bonding is performed, the influence of the surface shape of the glass cloth constituting the second base body 12' on the surface of the first base body 10 (the design surface of the surface layer 11) can be further reduced.
又,基材膜20之平均厚度較佳為0.1~1.0mm,更佳為0.1~0.5mm。藉此,能夠進一步減小構成第2基體12'之玻璃布的表面形狀對於第1基體10的表面(表面層11的設計面)之影響。 Further, the average thickness of the base film 20 is preferably from 0.1 to 1.0 mm, more preferably from 0.1 to 0.5 mm. Thereby, the influence of the surface shape of the glass cloth constituting the second base body 12' on the surface of the first base body 10 (the design surface of the surface layer 11) can be further reduced.
再者,根據需要,亦可使用複數片基材膜20。 Further, a plurality of substrate films 20 may be used as needed.
又,對三聚氰胺裝飾板100進行加熱加壓成形(熱壓接)之條件並無特別限定,但較佳為以130~150℃之加熱溫度、2~8MPa之壓力進行加熱加壓成形(熱壓接)。又,熱壓接時間較佳為10~60分鐘。藉此,能夠進一步減小構成第2基體12'之玻璃布的表面形狀對於第1基體10的表面(表面層11的設計面)之影響。 Further, the conditions for the heat and pressure forming (thermocompression bonding) of the melamine decorative sheet 100 are not particularly limited, but it is preferably heated and pressed at a heating temperature of 130 to 150 ° C and a pressure of 2 to 8 MPa (hot pressing). Connect). Moreover, the thermocompression bonding time is preferably from 10 to 60 minutes. Thereby, the influence of the surface shape of the glass cloth constituting the second base body 12' on the surface of the first base body 10 (the design surface of the surface layer 11) can be further reduced.
再者,對三聚氰胺裝飾板100進行熱壓接時,除了利用鏡面完成護板30對第1基體10進行加熱、加壓之方法以外,亦能夠使用如下所述之方法。例如能夠對各積層體噴射熱風或進行雷射照射,並且藉由鏡面完成護板30按壓各積層體,藉此獲得三聚氰胺裝飾板100。 Further, when the melamine decorative sheet 100 is thermocompression bonded, the method described below can be used in addition to the method of heating and pressurizing the first base 10 by the mirror finish guard 30. For example, it is possible to eject hot air or laser irradiation to each of the laminated bodies, and press the respective laminated bodies by the mirror finish guard 30, thereby obtaining the melamine decorative board 100.
再者,根據需要,亦可將離型膜夾在基材膜20與第2基體12'之間。作為離型膜,能夠使用眾所周知之離型膜。 Further, if necessary, the release film may be sandwiched between the base film 20 and the second substrate 12'. As the release film, a well-known release film can be used.
以上,說明了本發明之三聚氰胺裝飾板之較佳實施形態,但本發明並不限定於此。 Although the preferred embodiment of the melamine decorative board of the present invention has been described above, the present invention is not limited thereto.
例如,本發明之三聚氰胺裝飾板並不限定於圖1所示之三聚氰胺裝飾板100之形態。例如於欲提高三聚氰胺裝飾板之機械強度等之情形時,如圖3所示,亦可進而將由其他芯材層材料構成之其他芯材層積層於芯材層的下側。亦即,亦可積層2個芯材層而形成表面層11、中間層13、芯材層12、芯材層14之四層構成。又,亦可具有表面層、中間層及芯材層以外之其他層,例如如圖4所示,亦可於設計面側(圖4中的上側)的最外層具有保護層15,或於芯材層側(圖4中的下側)的最外層具有支持層16。 For example, the melamine decorative sheet of the present invention is not limited to the form of the melamine decorative sheet 100 shown in FIG. For example, when it is desired to increase the mechanical strength of the melamine decorative sheet or the like, as shown in FIG. 3, another core material composed of another core material layer material may be laminated on the lower side of the core material layer. In other words, two core material layers may be laminated to form a four-layer structure of the surface layer 11, the intermediate layer 13, the core material layer 12, and the core material layer 14. Further, it may have other layers than the surface layer, the intermediate layer, and the core material layer. For example, as shown in FIG. 4, the outermost layer on the design surface side (upper side in FIG. 4) may have a protective layer 15, or a core. The outermost layer of the material layer side (the lower side in FIG. 4) has a support layer 16.
保護層15並無特別限定,例如單獨使三聚氰胺樹脂浸漬至基重為10~50g/m2之紙基材,或使如下樹脂組成物浸漬至基重為10~50g/m2之紙基材,且進行乾燥,藉此,能夠獲得該保護層15,上述樹脂組成物係使三聚氰胺樹脂中含有選自氫氧化鋁、氫氧化鎂或二氧化矽之無機填充材所得之樹脂組成物。 The protective layer 15 is not particularly limited, and for example, the melamine resin is separately impregnated to a paper substrate having a basis weight of 10 to 50 g/m 2 , or the following resin composition is impregnated to a paper substrate having a basis weight of 10 to 50 g/m 2 . The protective layer 15 is obtained by drying, and the resin composition is a resin composition obtained by containing an inorganic filler selected from the group consisting of aluminum hydroxide, magnesium hydroxide or cerium oxide in the melamine resin.
支持層16並無特別限定,例如能夠使用預浸布或金屬箔等作為與上述表面層基材相同之基材,該預浸布係使能夠承載於表面層的上側(第1面側)或下側(第2面側)之樹脂浸漬至玻璃布等而成。 The support layer 16 is not particularly limited, and for example, a prepreg or a metal foil can be used as the same substrate as the surface layer substrate, and the prepreg can be supported on the upper side (first surface side) of the surface layer or The resin on the lower side (the second surface side) is immersed in a glass cloth or the like.
再者,於上述實施形態中,作為製造方法,說明了同時製造2個三聚氰胺裝飾板之方法,但並不限定於此,亦可為逐個地製造三聚氰胺裝飾板之方法。 Further, in the above embodiment, a method of simultaneously producing two melamine decorative sheets is described as a manufacturing method. However, the present invention is not limited thereto, and a method of producing a melamine decorative sheet one by one may be employed.
以下,根據實施例及比較例而詳細地對本發明進行說明,但本發明並不限定於此。 Hereinafter, the present invention will be described in detail based on examples and comparative examples, but the present invention is not limited thereto.
1.三聚氰胺裝飾板之製造 1. Manufacture of melamine decorative board
(實施例1) (Example 1)
準備基重為80g/m2之含氧化鈦裝飾紙(大日本印刷(股)製造)作為表面層基材。 A titanium oxide-containing decorative paper (manufactured by Dainippon Printing Co., Ltd.) having a basis weight of 80 g/m 2 was prepared as a surface layer substrate.
其次,將固體成分為40g/m2之胺酯丙烯酸複合樹脂乳液(中央理化工業(股)製造,商品名為「SU-100」,平均粒徑:84nm,分散媒:水)塗布至上述含氧化鈦裝飾紙的一個面側(第2面側)。 Next, an amine ester acrylic resin composite emulsion (manufactured by Central Chemical Industry Co., Ltd., trade name "SU-100", average particle diameter: 84 nm, dispersion medium: water) having a solid content of 40 g/m 2 was applied to the above-mentioned content. One surface side (second surface side) of the titanium oxide decorative paper.
接著,將固體成分為50g/m2之三聚氰胺樹脂(反應莫耳比為1.4,樹脂 固體成分為50質量%)塗布至上述含氧化鈦裝飾紙的另一個面側(第1面側(設計面側))。 Next, a melamine resin having a solid content of 50 g/m 2 (reaction molar ratio of 1.4 and a resin solid content of 50% by mass) was applied to the other surface side of the titanium oxide-containing decorative paper (first surface side (design surface) side)).
然後,利用120℃之熱風乾燥機,對上述胺酯丙烯酸複合樹脂乳液及三聚氰胺樹脂進行90秒之乾燥。如此獲得於含氧化鈦裝飾紙的第2面側承載胺酯丙烯酸複合粒子,並且於含氧化鈦裝飾紙的第1面側(設計面側)承載三聚氰胺樹脂,樹脂比率為53%、揮發成分率為3%之第1層。 Then, the above-mentioned amine ester acrylic composite resin emulsion and melamine resin were dried for 90 seconds by a hot air dryer at 120 °C. The urethane-acrylic composite particles were supported on the second surface side of the titanium oxide-containing decorative paper, and the melamine resin was carried on the first surface side (design surface side) of the titanium oxide decorative paper, and the resin ratio was 53%, and the volatile component ratio was 53%. It is the first layer of 3%.
再者,藉由如下方法合成上述三聚氰胺樹脂,該方法係指於反應容器中,以特定調配比率調配(裝入)原料三聚氰胺與甲醛液,添加觸媒後,升溫至沸點為止而進行回流反應。然後,在確認三聚氰胺已溶解完畢後,於到達反應終點時,利用脫水處理調整樹脂固體成分且進行冷卻。 Further, the melamine resin is synthesized by a method in which a raw material melamine and a formaldehyde liquid are prepared (charged) in a specific mixing ratio in a reaction container, and after adding a catalyst, the temperature is raised to a boiling point to carry out a reflux reaction. Then, after confirming that the melamine has been dissolved, when the reaction end point is reached, the resin solid content is adjusted by dehydration treatment and cooled.
其次,將固體成分為20g/m2之丙烯酸樹脂乳液(日本ZEON(股)製造,商品名為「Nipol LX-851E」,平均粒徑:200nm,分散媒:水)塗布至上述第1層的第2面側。 Next, an acrylic resin emulsion (manufactured by ZEON Co., Ltd., trade name "Nipol LX-851E", average particle diameter: 200 nm, dispersion medium: water) having a solid content of 20 g/m 2 was applied to the above first layer. The second side.
然後,利用120℃之熱風乾燥機進行90秒之乾燥,形成第2層(中間層)。藉此,獲得具有第1層與第2層且樹脂比率為58%、揮發成分率為4%之第1基體。 Then, it was dried by a hot air dryer at 120 ° C for 90 seconds to form a second layer (intermediate layer). Thereby, the first substrate having the first layer and the second layer and having a resin ratio of 58% and a volatile component ratio of 4% was obtained.
使基重為104g/m2之玻璃布(臺灣南亞公司製造,商品名為「Nanya-2116」)作為第2基體(芯材層)而重疊於所獲得之第1基體的第2面側,製成第1基體與第2基體之積層體。進而,反復進行上述步驟,製成重疊有第1基體與第2基體之其他積層體,準備2組積層體。 A glass cloth having a basis weight of 104 g/m 2 (manufactured by Taiwan Nanya Corporation, trade name "Nanya-2116") was placed as a second substrate (core material layer) on the second surface side of the obtained first substrate. A laminate of the first substrate and the second substrate is formed. Further, the above steps were repeated to form another laminate in which the first substrate and the second substrate were superposed, and two sets of laminates were prepared.
其次,準備兩塊基材膜(住友培(Sumitomo Bakelite)(股)製造,商品名為「CEL E911B」,厚度:0.12mm,軟化溫度:140℃)及兩塊 離型膜(東麗(Toray)(股)製造,商品名為「TORAYFAN SRP」)。 Next, prepare two base film (manufactured by Sumitomo Bakelite), trade name "CEL E911B", thickness: 0.12mm, softening temperature: 140 °C) and two pieces. Release film (manufactured by Toray Co., Ltd., trade name "TORAYFAN SRP").
以包夾兩塊基材膜之方式設置兩塊離型膜之後,以包夾離型膜及基材膜之方式,將該離型膜及基材膜配置於上述積層體的第2基體彼此之間。其次,以使各抵接面與各積層體的第1基體相對向之方式,配置具備實施了鏡面加工之抵接面之2個鏡面完成護板(作為不銹鋼板的由光澤度計測定出之測定值為300以上之鏡面完成不銹鋼板),包夾積層體與基材膜。 After the two release films are provided so as to sandwich the two base film, the release film and the base film are placed on the second substrate of the laminate in a manner of sandwiching the release film and the base film. between. Next, two mirror-finished shields having a mirror-finished abutting surface are disposed so that the respective abutting faces are opposed to the first base of each of the laminated bodies (measured by a gloss meter as a stainless steel plate) A mirror-finished stainless steel plate having a measured value of 300 or more is formed, and the laminated body and the substrate film are sandwiched.
於該狀態下,使鏡面完成護板彼此靠近(使鏡面完成護板與基材膜靠近),在140℃、8MPa之條件下進行40分鐘之熱加壓成形(熱壓接),獲得厚度為0.3mm之三聚氰胺裝飾板。 In this state, the mirror-finished panels are brought close to each other (the mirror surface is completed close to the substrate film), and subjected to hot press forming (thermocompression bonding) at 140 ° C and 8 MPa for 40 minutes to obtain a thickness of 0.3mm melamine decorative board.
(實施例2) (Example 2)
於第2層之形成過程中,將固體成分為10g/m2之丙烯酸樹脂乳液塗布至第1層的第2面側。 In the formation of the second layer, an acrylic resin emulsion having a solid content of 10 g/m 2 was applied to the second surface side of the first layer.
又,使用以如下方式形成之預浸布作為第2基材(芯材層)。首先,將固體成分為2g/m2之胺酯丙烯酸複合樹脂乳液(中央理化工業(股)製造,商品名為「SU-100」,平均粒徑:84nm,分散媒:水)塗布至基重為104g/m2之玻璃布(臺灣南亞公司製造,商品名為「Nanya-2116」)。然後,利用120℃之熱風乾燥機進行150秒之乾燥,製成樹脂比率為2%、揮發成分率為3%之預浸布(第2基材)。 Further, a prepreg formed in the following manner was used as the second base material (core material layer). First, an amine ester acrylic resin composite emulsion (manufactured by Central Chemical Industry Co., Ltd., trade name "SU-100", average particle diameter: 84 nm, dispersion medium: water) having a solid content of 2 g/m 2 was applied to the basis weight. It is a glass cloth of 104 g/m 2 (manufactured by Taiwan Nanya Corporation, trade name "Nanya-2116"). Then, it was dried by a hot air dryer at 120 ° C for 150 seconds to prepare a prepreg (second substrate) having a resin ratio of 2% and a volatile component ratio of 3%.
除了上述以外,與上述實施例1同樣地獲得厚度為0.3mm之三聚氰胺裝飾板。 A melamine decorative board having a thickness of 0.3 mm was obtained in the same manner as in the above Example 1 except the above.
(實施例3) (Example 3)
於第2層之形成過程中,將固體成分為5g/m2之丙烯酸樹脂乳液塗布至 第1層的第2面側。 In the formation of the second layer, an acrylic resin emulsion having a solid content of 5 g/m 2 was applied to the second surface side of the first layer.
除了上述以外,與上述實施例1同樣地獲得厚度為0.3mm之三聚氰胺裝飾板。 A melamine decorative board having a thickness of 0.3 mm was obtained in the same manner as in the above Example 1 except the above.
(實施例4) (Example 4)
以如下方式形成具有第1層與第2層之第1基體。 The first substrate having the first layer and the second layer is formed as follows.
將固體成分為50g/m2之混合液塗布至基重為80g/m2之含氧化鈦裝飾紙(大日本印刷(股)製造)的一個面側(第2面側),該混合液以100:30之固體成分重量比,混合有胺酯丙烯酸複合樹脂乳液(中央理化工業(股)製造,商品名為「SU-100」,平均粒徑:84nm,分散媒:水)、與丙烯酸樹脂乳液(日本ZEON(股)製造,商品名「Nipol LX-851E」,平均粒徑:200nm,分散媒:水)。 A mixed liquid having a solid content of 50 g/m 2 was applied to one surface side (second surface side) of a titanium oxide decorative paper (manufactured by Dainippon Printing Co., Ltd.) having a basis weight of 80 g/m 2 , and the mixture was 100:30 solid content by weight, mixed with an amine ester acrylic resin emulsion (manufactured by Central Chemical Industry Co., Ltd., trade name "SU-100", average particle size: 84 nm, dispersing medium: water), and acrylic resin Emulsion (manufactured by Japan ZEON Co., Ltd., trade name "Nipol LX-851E", average particle diameter: 200 nm, dispersion medium: water).
接著,將固體成分為50g/m2之三聚氰胺樹脂(反應莫耳比為1.4,樹脂固體成分為50質量%)塗布至上述含氧化鈦裝飾紙的另一個面側(第1面側(設計面側))。 Next, a melamine resin having a solid content of 50 g/m 2 (reaction molar ratio of 1.4 and a resin solid content of 50% by mass) was applied to the other surface side of the titanium oxide-containing decorative paper (first surface side (design surface) side)).
然後,利用120℃之熱風乾燥機,對上述混合液及三聚氰胺樹脂進行90秒之乾燥。如此,在形成第1層之同時,於第1層的第2面側形成包含丙烯酸樹脂粒子之中間層,從而獲得第1基體,該第1層於含氧化鈦裝飾紙的第2面側承載胺酯丙烯酸複合粒子,並且於含氧化鈦裝飾紙的第1面側(設計面側)承載三聚氰胺樹脂。再者,該第1基體的樹脂比率為58%,揮發成分率為4%。 Then, the mixture and the melamine resin were dried for 90 seconds by a hot air dryer at 120 °C. In this manner, an intermediate layer containing acrylic resin particles is formed on the second surface side of the first layer while forming the first layer, and the first substrate is obtained, and the first layer is carried on the second surface side of the titanium oxide-containing decorative paper. The urethane-acrylic composite particles are loaded with a melamine resin on the first surface side (design side) of the titanium oxide-containing decorative paper. Further, the first substrate had a resin ratio of 58% and a volatile component ratio of 4%.
除了上述以外,與上述實施例1同樣地獲得厚度為0.3mm之三聚氰胺裝飾板。 A melamine decorative board having a thickness of 0.3 mm was obtained in the same manner as in the above Example 1 except the above.
(實施例5) (Example 5)
首先,準備丙烯酸膜((株)KANEKA製造,商品名為「SANDUREN SD001NAT」)。 First, an acrylic film (manufactured by KANEKA, trade name "SANDUREN SD001NAT") was prepared.
其次,於第1基體之形成過程中未形成中間層,除此以外,與上述實施例1同樣地獲得第1基體。又,與上述實施例1同樣地獲得第2基體。 Next, the first substrate was obtained in the same manner as in Example 1 except that the intermediate layer was not formed during the formation of the first substrate. Further, a second substrate was obtained in the same manner as in the above Example 1.
將上述丙烯酸膜、所獲得之第2基體依序重疊於所獲得之第1基體的第2面側,形成在第1基體與第2基體之間插入有丙烯酸膜之積層體。除了使用此種積層體以外,與上述實施例1同樣地獲得厚度為0.35mm之三聚氰胺裝飾板。 The acrylic film and the obtained second substrate are sequentially superposed on the second surface side of the obtained first substrate, and a laminate in which an acrylic film is interposed between the first substrate and the second substrate is formed. A melamine decorative board having a thickness of 0.35 mm was obtained in the same manner as in Example 1 except that the laminate was used.
(比較例) (Comparative example)
準備基重為80g/m2之含氧化鈦裝飾紙(大日本印刷(股)製造)作為表面層基材。 A titanium oxide-containing decorative paper (manufactured by Dainippon Printing Co., Ltd.) having a basis weight of 80 g/m 2 was prepared as a surface layer substrate.
其次,將固體成分為40g/m2之胺酯丙烯酸複合粒子乳液(中央理化工業(股)製造,商品名為「SU-100」,平均粒徑:84nm,分散媒:水)塗布至上述含氧化鈦裝飾紙的一個面側(第2面側)。 Next, an amine ester acrylic acid composite particle emulsion having a solid content of 40 g/m 2 (manufactured by Central Chemical Industry Co., Ltd., trade name "SU-100", average particle diameter: 84 nm, dispersion medium: water) was applied to the above-mentioned content. One surface side (second surface side) of the titanium oxide decorative paper.
接著,將固體成分為50g/m2之三聚氰胺樹脂(反應莫耳比為1.4,樹脂固體成分為50質量%)塗布至上述含氧化鈦裝飾紙的另一個面側(第1面側(設計面側))。 Next, a melamine resin having a solid content of 50 g/m 2 (reaction molar ratio of 1.4 and a resin solid content of 50% by mass) was applied to the other surface side of the titanium oxide-containing decorative paper (first surface side (design surface) side)).
然後,利用120℃之熱風乾燥機,對上述胺酯丙烯酸複合粒子乳液及三聚氰胺樹脂進行90秒之乾燥,獲得樹脂比率為53%、揮發成分率為3%的表面層材料(第1層)。 Then, the amine ester acrylic acid composite particle emulsion and the melamine resin were dried by a hot air dryer at 120 ° C for 90 seconds to obtain a surface layer material (first layer) having a resin ratio of 53% and a volatile component ratio of 3%.
再者,藉由如下方法合成上述三聚氰胺樹脂,該方法係指於 反應容器中,以特定調配比率調配(裝入)原料三聚氰胺與甲醛液,添加觸媒後,升溫至沸點為止而進行回流反應。然後,在確認三聚氰胺已溶解完畢後,於到達反應終點時,利用脫水處理調整樹脂固體成分且進行冷卻。 Furthermore, the above melamine resin is synthesized by the following method, which means In the reaction vessel, the raw material melamine and the formaldehyde liquid are prepared (charged) at a specific mixing ratio, and after adding a catalyst, the temperature is raised to the boiling point to carry out a reflux reaction. Then, after confirming that the melamine has been dissolved, when the reaction end point is reached, the resin solid content is adjusted by dehydration treatment and cooled.
使基重為104g/m2之玻璃布(臺灣南亞公司製造,商品名為「Nanya-2116」)作為芯材層而重疊於所獲得之第1層的第2面側,獲得積層體。在140℃、8MPa之條件下,對該積層體進行40分鐘之加熱加壓成形,獲得厚度為0.3mm之三聚氰胺裝飾板。 A glass cloth having a basis weight of 104 g/m 2 (manufactured by Taiwan Nanya Corporation, trade name "Nanya-2116") was placed as a core material layer and superposed on the second surface side of the obtained first layer to obtain a laminated body. The laminate was subjected to heat and pressure molding at 140 ° C and 8 MPa for 40 minutes to obtain a melamine decorative sheet having a thickness of 0.3 mm.
將各實施例及比較例之三聚氰胺裝飾板各層的構成材料等表示於表1。 The constituent materials and the like of each layer of the melamine decorative sheets of the respective examples and comparative examples are shown in Table 1.
2.測試方法 2. Test method
對上述各實施例及比較例中所獲得之三聚氰胺裝飾板進行以下評測。 The following evaluations were performed on the melamine decorative sheets obtained in the above respective examples and comparative examples.
(1)不燃性測試 (1) Non-combustibility test
根據日本建築綜合試驗所的業務標準「防耐火性能測試、評測業務方法書」4.10不燃性能測試、評測方法中的「(2)ii)4.10.2的發熱性測試、評測方法及4.10.3的氣體有害性測試評測方法」實施。 According to the business standard of the Japan Buildings Comprehensive Testing Institute, "Fracture resistance test, evaluation business method book" 4.10 Non-combustible performance test, evaluation method "(2) ii) 4.10.2 heat test, evaluation method and 4.10.3 Implementation of gas hazard test evaluation method".
上述業務標準「防耐火性能測試、評測業務方法書」的上述項目中,記載有與基於建築基準法第2條第9號(不燃材料)之規定之認定相關的性能評測方法。 In the above-mentioned items of the above-mentioned business standard "anti-fire resistance performance test and evaluation business method book", a performance evaluation method relating to the certification based on the provisions of Article 2, No. 9 (non-combustible materials) of the Building Standard Law is described.
(2)耐煮沸性測試 (2) Boiling resistance test
藉由遵從JIS K6902之耐煮沸性測試之方法進行處理,確認在沸水中浸漬2小時後的測試片有無發生膨脹、層間剝離。 The test was carried out in accordance with the method of boiling resistance test according to JIS K6902, and it was confirmed whether or not the test piece after immersion in boiling water for 2 hours was swelled or peeled off between layers.
(3)耐污染性測試 (3) Pollution resistance test
藉由遵從JIS K6902之耐污染性測試之方法進行處理,確認試料表面有無殘留污染材料。 The surface of the sample was confirmed to have any residual contamination material by following the method of the contamination resistance test of JIS K6902.
(4)彎曲成形性測試 (4) Bending formability test
遵從JIS K6902之彎曲成形性測試(A法),於室溫下,以10mmR進行外彎曲及內彎曲成形,確認裝飾片材表面有無裂痕。 According to the bending formability test (A method) of JIS K6902, external bending and inner bending molding were performed at 10 mmR at room temperature, and it was confirmed whether or not the surface of the decorative sheet was cracked.
(5)表面硬度(鉛筆硬度)測試 (5) Surface hardness (pencil hardness) test
藉由遵從JIS K5600之鉛筆硬度測試進行評測。 Evaluation was performed by following the pencil hardness test of JIS K5600.
(6)算術平均粗糙度 (6) Arithmetic mean roughness
使用光干涉型表面形狀粗糙度測定裝置(Veeco公司製造,商品名為 「Wyko NT1100」),對各實施例及比較例之三聚氰胺裝飾板的設計面之算術平均粗糙度Ra2進行測定。 Optical interference type surface shape roughness measuring device (manufactured by Veeco, trade name) "Wyko NT1100"), the arithmetic mean roughness Ra2 of the design surface of the melamine decorative sheet of each of the examples and the comparative examples was measured.
將上述結果一併表示於表1。再者,於表1中,各實施例及比較例中的芯材層的「中間層側的面之算術平均粗糙度Ra1」係指芯材層(第2基體)的第1面側的面(中間層側的面)之算術平均粗糙度Ra1使用上述(6)中所使用之裝置而測定該算術平均粗糙度Ra1。 The above results are shown together in Table 1. In addition, in the core material layer of each of the examples and the comparative examples, the arithmetic mean roughness Ra1 of the surface on the intermediate layer side refers to the surface on the first surface side of the core material layer (second substrate). The arithmetic mean roughness Ra1 of the (surface on the intermediate layer side) is measured by the apparatus used in the above (6).
根據表1可知:本發明之三聚氰胺裝飾板表現出了良好之彎曲加工性及不燃性,並且具有良好之鏡面。相對於此,於比較例中,未能夠形成良好之鏡面。 According to Table 1, the melamine decorative board of the present invention exhibits good bending workability and incombustibility, and has a good mirror surface. On the other hand, in the comparative example, a good mirror surface could not be formed.
[產業上之可利用性] [Industrial availability]
根據本發明,能夠提供不燃性及彎曲加工性優異,且具備實施了鏡面加工之設計面之三聚氰胺裝飾板。又,能夠提供能容易地製造此種三聚氰胺裝飾板之三聚氰胺裝飾板之製造方法。因此,本發明具有產業上之可利用性。 According to the present invention, it is possible to provide a melamine decorative sheet which is excellent in nonflammability and bending workability and which has a design surface to be mirror-finished. Further, it is possible to provide a method for producing a melamine decorative sheet which can easily produce such a melamine decorative sheet. Therefore, the present invention has industrial applicability.
11‧‧‧表面層 11‧‧‧ surface layer
12‧‧‧芯材層 12‧‧‧ core layer
13‧‧‧中間層 13‧‧‧Intermediate
100‧‧‧三聚氰胺裝飾板 100‧‧‧melamine decorative board
111‧‧‧第1面 111‧‧‧1st
112‧‧‧第2面 112‧‧‧2nd
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| JP7091774B2 (en) * | 2018-03-29 | 2022-06-28 | 住友ベークライト株式会社 | Decorative board and manufacturing method of Decorative board |
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| JPS61290610A (en) * | 1985-06-17 | 1986-12-20 | 日立化成工業株式会社 | Manufacture of prepreg sheet |
| JP4344055B2 (en) * | 1999-12-24 | 2009-10-14 | 株式会社エーアンドエーマテリアル | Mirror surface decorative plate manufacturing method |
| JP2004338270A (en) * | 2003-05-16 | 2004-12-02 | Mitsubishi Rayon Co Ltd | Method for producing fiber-reinforced resin composite material and fiber-reinforced resin composite material |
| JP4349161B2 (en) * | 2004-03-08 | 2009-10-21 | 住友ベークライト株式会社 | Finished surface repair method and decorative board |
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| JP5222684B2 (en) * | 2008-10-02 | 2013-06-26 | シーアイ化成株式会社 | Non-flammable decorative veneer |
| JP5201173B2 (en) * | 2009-09-14 | 2013-06-05 | 住友ベークライト株式会社 | Surface layer material and melamine decorative board |
| JP5099206B2 (en) * | 2010-11-30 | 2012-12-19 | 住友ベークライト株式会社 | Melamine decorative board |
| JP5685930B2 (en) * | 2010-12-27 | 2015-03-18 | 住友ベークライト株式会社 | Release film |
| JP5842673B2 (en) * | 2012-02-29 | 2016-01-13 | 住友ベークライト株式会社 | Manufacturing method of decorative panel |
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| WO2015016255A1 (en) | 2015-02-05 |
| JP2015044407A (en) | 2015-03-12 |
| JP6484946B2 (en) | 2019-03-20 |
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