JPH04187427A - Composite panel - Google Patents
Composite panelInfo
- Publication number
- JPH04187427A JPH04187427A JP31674690A JP31674690A JPH04187427A JP H04187427 A JPH04187427 A JP H04187427A JP 31674690 A JP31674690 A JP 31674690A JP 31674690 A JP31674690 A JP 31674690A JP H04187427 A JPH04187427 A JP H04187427A
- Authority
- JP
- Japan
- Prior art keywords
- film
- resin
- primer
- base film
- protective layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 14
- 229920005989 resin Polymers 0.000 claims abstract description 27
- 239000011347 resin Substances 0.000 claims abstract description 27
- 239000000463 material Substances 0.000 claims abstract description 18
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 4
- 239000000057 synthetic resin Substances 0.000 claims abstract description 4
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 3
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 3
- 239000002023 wood Substances 0.000 claims description 6
- 239000010410 layer Substances 0.000 abstract description 14
- 239000011241 protective layer Substances 0.000 abstract description 14
- -1 polypropylene Polymers 0.000 abstract description 10
- 239000004743 Polypropylene Substances 0.000 abstract description 7
- 239000003973 paint Substances 0.000 abstract description 7
- 229920001155 polypropylene Polymers 0.000 abstract description 7
- 239000011120 plywood Substances 0.000 abstract description 6
- 239000006097 ultraviolet radiation absorber Substances 0.000 abstract description 6
- 229920000728 polyester Polymers 0.000 abstract description 5
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 abstract description 4
- 239000012965 benzophenone Substances 0.000 abstract description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- 239000004952 Polyamide Substances 0.000 abstract description 2
- 239000000853 adhesive Substances 0.000 abstract description 2
- 230000001070 adhesive effect Effects 0.000 abstract description 2
- 239000012611 container material Substances 0.000 abstract description 2
- 229920001577 copolymer Polymers 0.000 abstract description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 abstract description 2
- 229920002647 polyamide Polymers 0.000 abstract description 2
- 239000004926 polymethyl methacrylate Substances 0.000 abstract description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000010894 electron beam technology Methods 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 238000007493 shaping process Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 230000007613 environmental effect Effects 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
- 239000010408 film Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000003562 lightweight material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Abstract
Description
[産業上の利用分野]
本発明は、コンテナの材料や、外装および内装用の建材
として使用する複合板に関する。
[従来の技術]
たとえばコンテナを製造する材料としては、鋼板に適宜
の塗装を施したものか代表的である。
鋼板のコンテナは高強度で耐久性が高いが、いうまでも
なく重く、取扱いが容易でない上に比較的高価である。
高強度で軽量な材料としてFRP板が知られているが、
高価なため特殊な用途にしか使用できない。
コンテナを簡易に製造する材料としては、合板にポリ塩
化ビニルのシートを積層したものが使用されている。
しかしこの材料は、ポリ塩化ビニルシートが耐候性、耐
熱性に乏しく表面硬度も低いため、製品コンテナの耐久
性の面で不満足である。
(発明が解決しようとする課題1
本発明の目的は、安価に製造できて軽く、しかも耐久性
の高い、コンテナ材料をはじめとする種々の用途に適し
た複合板を提供することにある。
[課題を解決するための手段]
本発明の複合板は、図面に示すように、木質基材(1)
上k、熱可塑性合成樹脂のベースフィルム(2)、耐候
性を有するプライマー層(3)、および硬化樹脂の表面
保護層(4)をそなえてなる。
木質基材には、合板、パーチクルボードなど、既知の板
状材料を使用すればよい。
ベースフィルムは、低価格で着色または印刷が容易であ
り、ある程度柔軟性をもつものからえらぶことか好まし
い。 そのような熱可塑性樹脂のフィルムの例をあげれ
ば、ポリエチレン、ポリプロピレン、ポリ塩化ビニル、
ポリ塩化ビニリデン、ポリビニルアルコール、ポリエチ
レンテレフタレート、ポリカーボネート、ナイロン、ポ
リスチレン、エチレン−酢酸ビニル共重合体、■チレン
ービニルアルコール共重合体、アイオノマーのフィルム
でおる。 とくにポリプロピレンのフィルムは、環境の
変化によるクラック発生かはとんどなく、最も好適であ
る。 ベースフィルムの厚さは、0.25〜0.65N
riが適当でおる。
プライマー層は、耐候性にすぐれた材料、たとえばフッ
素樹脂、アクリル樹脂、それらの混合物、あるいはポリ
カーボネートを、塗料の形態にして塗布して形成すると
よい。 アクリル樹脂の塗料には、イソシアネートなど
の架橋剤を添加してもよい。
ベースフィルムおよび(または)プライマー層に耐候性
顔料を含有させて、ざらに耐候性を向上させることは推
奨される態様である。 耐候性顔料としては、キナクリ
ドン、イソインドリノン、フタロシアニンブル−、カー
ボンブラックなどが知られており、それらの中から適宜
選択して使用する。
表面保護層を形成する硬化樹脂は、熱硬化性樹脂や電離
放射線硬化性樹脂を硬化させたものである。
電離放射線硬化性樹脂としては、たとえば、エポキシア
クリレート、ウレタンアクリレート、アクリル酸変性ア
ルキッド、アクリル変性ポリエステルなどをオリゴマー
とし、これに架橋構造の調整や粘度調整などを目的とし
て、ネオペンチルグリコール−ジアクリレート、ペンタ
エリスリトール−トリアクリレート、トリメチロールプ
ロパン−トリアクリレート、トリメチロールプロパン−
トリメタアクリレートなどのモノマーを配合したものが
利用される。 これらは電子線により十分に硬化可能で
あるが、紫外線照射で硬化させる場合には、ベンゾイン
系、アセトフェノン系、ベンジルケタール系、ケトン/
アミン系などの光重合開始剤を添加することが一般的で
ある。 基材シート、中間層、さらには保護層への接着
性を確保するため、それらと同種の、または近縁のプラ
スチックを添加して用いるとよい。
電離放射線は、電子線および紫外線が代表的である。
前者は各種の電子線加速機から放出され、50〜100
0KeV、好ましくは100〜30OKeVの範囲のエ
ネルキーをもつ電子線が用いられ、後者は、高圧水銀灯
、そのほかの紫外線源から発するものを用いる。
熱硬化性樹脂としては、フェノール樹脂、尿素樹脂、ジ
アリルフタレート樹脂、メラミン樹脂、グアナミン樹脂
、不飽和ポリエステル樹脂、ポリウレタン樹脂、エポキ
シ樹脂、アミノアルキッド樹脂、メラミン/尿素共縮合
樹脂、シリコーン樹脂、ポリシロキサン樹脂等があり、
これらに必要に応じて、架橋剤、重合開始剤等の硬化剤
、重合促進剤、溶剤、粘度調整剤、体質顔料等を添加す
る。
表面保護層に耐候性を与えるために、ベンゾトリアゾー
ル、ベンゾフェノン、微粉末酸化第二鉄、微粉末亜鉛華
などの紫外線吸収剤を添加することが好ましい。 ただ
し、表面保護層として紫外線硬化性樹脂を用いる場合に
は、樹脂の硬化を阻害しないように、紫外線吸収剤の吸
収波長帯域が硬化樹脂を劣化させる波長帯域であるが、
樹脂を硬化させる波長帯域とは実質上型ならないように
、紫外線吸収剤を選択する必要がある。 −例を示せば
、ポリエステルアクリレート系の樹脂を紫外線硬化させ
る場合、硬化波長は254〜360nmを中心とする帯
域であり、一方便化樹脂を劣化させる波長は約340n
m以上の帯域であるから、340nm以上の吸収波長を
有する紫外線吸収剤、たとえばベンゾフェノンを使用す
る。
表面保護層は、一般に厚さが10〜15μ瓦程度あれば
、その効果を確保できる。
ベースフィルムなどに絵柄や模様を設けるときは、表面
保護層は無色または着色の透明な樹脂で形成するが、設
けない場合は表面保護層が不透明であってもよい。
保護層の表面を、ツヤ消しにすることもてきる。
ツヤ消しにするには、樹脂へのマット材添加や、賦形フ
ィルムまたはエンボス版を使用した樹脂層への賦形加工
など、既知の手法に従えばよい。
本発明の複合板の製造方法は任意であって、木質基材上
に、ベースフィルム、プライマー層および硬化性樹脂層
を順に積層して、その表面を硬化処理するという工程の
ほか、たとえばベースフィルム上にプライマーを塗布し
、その上に硬化性樹脂を塗布して適宜の硬化処理を施す
ことによって積層フィルムを得、これを木質基材に貼る
ことによっても製造できる。
[作 用]
ベースフィルムの上に設けるプライマー層に耐候性にす
ぐれた材料を使用し、かつ表面保護層として高い表面硬
度を有する硬化樹脂としたことにより、複合板は耐候性
と耐擦傷性が高くなる。
これらの作用は、適度の柔軟さをもつベースフィルムの
存在によって確実なものとなる。[Industrial Field of Application] The present invention relates to a composite board used as a material for containers and as a building material for exterior and interior applications. [Prior Art] For example, a typical material for manufacturing containers is a steel plate coated with an appropriate coating. Containers made of steel plates have high strength and durability, but needless to say, they are heavy, difficult to handle, and relatively expensive. FRP board is known as a high-strength and lightweight material.
Because it is expensive, it can only be used for special purposes. The material used to easily manufacture containers is plywood laminated with polyvinyl chloride sheets.
However, this material is unsatisfactory in terms of the durability of the product container because the polyvinyl chloride sheet has poor weather resistance and heat resistance and has low surface hardness. (Problem to be Solved by the Invention 1) An object of the present invention is to provide a composite board that can be manufactured at low cost, is lightweight, and has high durability, and is suitable for various uses including container materials. Means for Solving the Problem] As shown in the drawings, the composite board of the present invention has a wooden base material (1)
Above, it comprises a thermoplastic synthetic resin base film (2), a weather-resistant primer layer (3), and a cured resin surface protection layer (4). Known plate-like materials such as plywood and particle board may be used as the wooden base material. It is preferable to select a base film that is inexpensive, easy to color or print, and has some degree of flexibility. Examples of such thermoplastic resin films include polyethylene, polypropylene, polyvinyl chloride,
Films of polyvinylidene chloride, polyvinyl alcohol, polyethylene terephthalate, polycarbonate, nylon, polystyrene, ethylene-vinyl acetate copolymer, (2) tyrene-vinyl alcohol copolymer, and ionomer. In particular, a polypropylene film is most suitable because cracks are unlikely to occur due to environmental changes. The thickness of the base film is 0.25-0.65N
ri is appropriate. The primer layer is preferably formed by applying a material with excellent weather resistance, such as a fluororesin, an acrylic resin, a mixture thereof, or polycarbonate, in the form of a paint. A crosslinking agent such as isocyanate may be added to the acrylic resin paint. It is a recommended embodiment to substantially improve weather resistance by incorporating a weather resistant pigment into the base film and/or primer layer. As weather-resistant pigments, quinacridone, isoindolinone, phthalocyanine blue, carbon black, etc. are known, and an appropriate one is selected from these for use. The cured resin forming the surface protective layer is a thermosetting resin or an ionizing radiation-curable resin. Examples of ionizing radiation-curable resins include oligomers such as epoxy acrylate, urethane acrylate, acrylic acid-modified alkyd, and acrylic-modified polyester, and neopentyl glycol diacrylate, etc. for the purpose of adjusting the crosslinking structure and viscosity. Pentaerythritol triacrylate, trimethylolpropane triacrylate, trimethylolpropane
A mixture of monomers such as trimethacrylate is used. These can be sufficiently cured by electron beam, but when curing by ultraviolet irradiation, benzoin type, acetophenone type, benzyl ketal type, ketone/
It is common to add a photopolymerization initiator such as an amine type. In order to ensure adhesion to the base sheet, the intermediate layer, and even the protective layer, plastics of the same type or closely related to these may be added. Typical examples of ionizing radiation are electron beams and ultraviolet rays.
The former is emitted from various electron beam accelerators, and is 50 to 100
An electron beam with an energy key in the range 0 KeV, preferably 100 to 30 OKeV is used, the latter coming from a high-pressure mercury lamp or other ultraviolet source. Thermosetting resins include phenolic resin, urea resin, diallyl phthalate resin, melamine resin, guanamine resin, unsaturated polyester resin, polyurethane resin, epoxy resin, aminoalkyd resin, melamine/urea cocondensation resin, silicone resin, and polysiloxane. There are resins, etc.
If necessary, a crosslinking agent, a curing agent such as a polymerization initiator, a polymerization accelerator, a solvent, a viscosity modifier, an extender, and the like are added. In order to impart weather resistance to the surface protective layer, it is preferable to add an ultraviolet absorber such as benzotriazole, benzophenone, finely powdered ferric oxide, finely powdered zinc white, or the like. However, when using an ultraviolet curable resin as the surface protective layer, the absorption wavelength band of the ultraviolet absorber is the wavelength band that degrades the cured resin, so as not to inhibit the curing of the resin.
It is necessary to select an ultraviolet absorber so that it is not substantially different from the wavelength band in which the resin is cured. - For example, when polyester acrylate resin is cured by ultraviolet light, the curing wavelength is centered around 254 to 360 nm, while the wavelength that degrades the facilitative resin is about 340 nm.
Since the wavelength range is 340 nm or more, an ultraviolet absorber having an absorption wavelength of 340 nm or more, such as benzophenone, is used. Generally, the surface protective layer has a thickness of about 10 to 15 μm to ensure its effectiveness. When a picture or pattern is provided on a base film or the like, the surface protective layer is formed of a colorless or colored transparent resin, but if not provided, the surface protective layer may be opaque. The surface of the protective layer can also be made matte. To make it matte, known methods such as adding a matte material to the resin or shaping the resin layer using a shaping film or an embossing plate may be used. The method for manufacturing the composite board of the present invention is arbitrary, and includes a step of sequentially laminating a base film, a primer layer, and a curable resin layer on a wood base material and curing the surface thereof. It can also be produced by applying a primer thereon, then applying a curable resin thereon and subjecting it to an appropriate curing treatment to obtain a laminated film, and pasting this onto a wood base material. [Function] By using a material with excellent weather resistance for the primer layer provided on the base film and using a cured resin with high surface hardness as the surface protective layer, the composite board has excellent weather resistance and scratch resistance. It gets expensive. These effects are ensured by the presence of a base film with appropriate flexibility.
【実施例1】
ベースフィルムとして厚さ0.25mのポリプロピレン
フィルムを使用し、その表面にボロメチルメタクリレー
トと塩ビ酢ビ共重合体の混合樹脂系のプライマー「Dプ
ライマー」 (諸星インキ製)を塗布して乾燥させ、塗
布量15g/mのプライマー層を設けた。
その上に、紫外線吸収剤としてベンゾフェノンを含有す
るポリエステルアクリレート系の紫外線硬化性塗料lN
−1cKX−2J (大日精化工業製)を、乾燥後の
塗1′5量か83/尻となるように塗布した。
この積層フィルムを、4灯のオゾン発生型高圧水銀灯か
らなる紫外線ランプ(出力160W/cm)の下を15
m/minの速度で通過させ、表面の硬化性塗料の塗膜
を硬化させて保護層とした。
厚さ2.7#の合板上にポリアミド系接着剤を塗布し、
上記の積層フィルムをポリプロピレンフィルムを下にし
て積層することにより、本発明の複合板を得た。
[実施例2]
ベースフィルムとして厚さ0.651110のポリプロ
ピレンフィルムを使用し、その上にメタリック顔料を含
有するポリメチルメタクリレートと塩ビ酢ビ共重合体の
混合樹脂系のプライマー「Dプライマー」 (諸星イン
キ製〉を塗布して乾燥させ、塗布量が15!iF/mの
プライマー層を設けた。
その上に、紫外線吸収剤としてヘンシフエノンを含有す
るポリエステルアクリレート系の紫外線硬化性塗料rH
CKX−2J (大日精化工業製)を、乾燥後の塗布
量が129/〆となるように塗布し、このフィルムを実
施例1と同じ紫外線ランプの下を10H/n+inの速
度で通過させて保護層を設けた。
上記の積層フィルムを、実施例1と同様に、木質基材(
合板)に積層して本発明の複合板を得た。[Example 1] A polypropylene film with a thickness of 0.25 m is used as the base film, and a mixed resin primer "D Primer" (manufactured by Moroboshi Ink) of boromethyl methacrylate and vinyl chloride-vinyl acetate copolymer is applied to the surface of the film. After drying, a primer layer was applied at a coating weight of 15 g/m. On top of that, a polyester acrylate-based UV-curable paint lN containing benzophenone as a UV absorber.
-1cKX-2J (manufactured by Dainichiseika Chemical Industry Co., Ltd.) was applied in an amount of 1'5 or 83/l after drying. This laminated film was heated for 15 minutes under an ultraviolet lamp (output 160 W/cm) consisting of four ozone-generating high-pressure mercury lamps.
It passed through at a speed of m/min to cure the curable paint film on the surface to form a protective layer. Apply polyamide adhesive on 2.7# thick plywood,
A composite plate of the present invention was obtained by laminating the above laminated films with the polypropylene film facing down. [Example 2] A polypropylene film with a thickness of 0.651110 was used as the base film, and a mixed resin primer "D Primer" of polymethyl methacrylate and vinyl chloride-vinyl acetate copolymer containing a metallic pigment was used on the base film (Moroboshi). A primer layer with a coating amount of 15!iF/m was applied and dried. On top of that, a polyester acrylate-based ultraviolet curable paint rH containing hensifhenone as an ultraviolet absorber was applied.
CKX-2J (manufactured by Dainichiseika Kagyo Kogyo) was applied so that the coating amount after drying was 129/㎜, and this film was passed under the same ultraviolet lamp as in Example 1 at a speed of 10 H/n+in. Provided with a protective layer. The above laminated film was coated on a wood base (
The composite board of the present invention was obtained by laminating the composite board on plywood.
本発明の複合板は、材料が木質のものと合成樹脂である
から軽い。 特別な材料や装置を使用せずに製造でき、
安価である。 しがも高い耐久性をもつ。
この′複合板は、コンテナの材料として好適であるほか
、内装または外装用の建材としても使用でき、広い用途
がある。The composite board of the present invention is light because it is made of wood and synthetic resin. Can be manufactured without using special materials or equipment,
It's cheap. It also has high durability. In addition to being suitable as a material for containers, this 'composite board can also be used as an interior or exterior building material, and has a wide range of uses.
図面は、本発明の詳細な説明するための、模式的な断面
図である。
1・・・木質基材 2・・−ベースフィルム3・
・・プライマー@ 4・・・表面保護層特許出願人
大日本印刷株式会社
代理人 弁理士 須 賀 総 夫The drawings are schematic cross-sectional views for explaining the present invention in detail. 1...Wood base material 2...-Base film 3.
・・Primer @ 4・・Surface protective layer patent applicant
Dai Nippon Printing Co., Ltd. Representative Patent Attorney Souo Suga
Claims (1)
耐候性を有するプライマー層および硬化樹脂の表面保護
層をそなえてなる複合板。Thermoplastic synthetic resin base film on wood base material,
A composite board comprising a weather-resistant primer layer and a hardened resin surface protection layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2316746A JP3055171B2 (en) | 1990-11-21 | 1990-11-21 | Composite board |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2316746A JP3055171B2 (en) | 1990-11-21 | 1990-11-21 | Composite board |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04187427A true JPH04187427A (en) | 1992-07-06 |
JP3055171B2 JP3055171B2 (en) | 2000-06-26 |
Family
ID=18080450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2316746A Expired - Lifetime JP3055171B2 (en) | 1990-11-21 | 1990-11-21 | Composite board |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3055171B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001193267A (en) * | 2000-01-12 | 2001-07-17 | Dainippon Printing Co Ltd | Decorative material for floor material |
KR20030039570A (en) * | 2001-11-13 | 2003-05-22 | 심대근 | panel for plastic door |
US6794055B2 (en) | 2003-02-03 | 2004-09-21 | Ppg Industries Ohio, Inc. | Alkyd-based free radical cured wood stains |
US7001667B2 (en) | 2002-07-17 | 2006-02-21 | Ppg Industries Ohio, Inc. | Alkyd-based free radical wood coating compositions |
-
1990
- 1990-11-21 JP JP2316746A patent/JP3055171B2/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001193267A (en) * | 2000-01-12 | 2001-07-17 | Dainippon Printing Co Ltd | Decorative material for floor material |
KR20030039570A (en) * | 2001-11-13 | 2003-05-22 | 심대근 | panel for plastic door |
US7001667B2 (en) | 2002-07-17 | 2006-02-21 | Ppg Industries Ohio, Inc. | Alkyd-based free radical wood coating compositions |
US7387843B2 (en) | 2002-07-17 | 2008-06-17 | Ppg Industries Ohio, Inc. | Alkyd-based free radical wood coating compositions |
US6794055B2 (en) | 2003-02-03 | 2004-09-21 | Ppg Industries Ohio, Inc. | Alkyd-based free radical cured wood stains |
Also Published As
Publication number | Publication date |
---|---|
JP3055171B2 (en) | 2000-06-26 |
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