JPS6323906B2 - - Google Patents
Info
- Publication number
- JPS6323906B2 JPS6323906B2 JP55105318A JP10531880A JPS6323906B2 JP S6323906 B2 JPS6323906 B2 JP S6323906B2 JP 55105318 A JP55105318 A JP 55105318A JP 10531880 A JP10531880 A JP 10531880A JP S6323906 B2 JPS6323906 B2 JP S6323906B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- curable paint
- thickness
- transparent
- ultraviolet curable
- 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.)
- Expired
Links
- 239000003973 paint Substances 0.000 claims description 30
- 238000000576 coating method Methods 0.000 claims description 17
- 239000011248 coating agent Substances 0.000 claims description 16
- 238000004049 embossing Methods 0.000 claims description 9
- 229920001169 thermoplastic Polymers 0.000 claims description 9
- 239000004416 thermosoftening plastic Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 229920003023 plastic Polymers 0.000 claims description 5
- 239000002985 plastic film Substances 0.000 claims description 4
- 229920006352 transparent thermoplastic Polymers 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 238000010924 continuous production Methods 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 18
- 239000004014 plasticizer Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 5
- -1 polypropylene Polymers 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 238000005336 cracking Methods 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 230000002087 whitening effect Effects 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229920005601 base polymer Polymers 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000003825 pressing Methods 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
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Shaping Of Tube Ends By Bending Or Straightening (AREA)
Description
【発明の詳細な説明】
本発明は弱電キヤビネツト用、家具、建材用の
化粧フイルムの製造方法に関し、更に詳しくは耐
スクラツチ性にすぐれかつVカツト工法に適する
化粧フイルムの製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a decorative film for use in light electrical cabinets, furniture, and building materials, and more particularly to a method for producing a decorative film that has excellent scratch resistance and is suitable for V-cut construction.
従来この種のフイルムとしては印刷した着色塩
化ビニルフイルムと透明塩化ビニルフイルムとを
加熱させ、エンボスロールによりエンボスと同時
に熱融着させる通常ダブリングエンボスと称する
方法で行われていた。このダブリングエンボスフ
イルムはVカツト性に優れかつ繊細な木目印刷と
表面の木目道管溝の効果より意匠的にも優れ長く
定着した技術に裏付けられていた。しかしダブリ
ングエンボスフイルムにも表面の耐スクラツチ
性、耐熱性、耐汚染性等の性能面でポリエステル
化粧板、メラミン化粧板、DAP化粧板等の熱硬
化性樹脂を使用した化粧板に比べて劣つていた。 Conventionally, this type of film has been produced by a method commonly called doubling embossing, in which a printed colored vinyl chloride film and a transparent vinyl chloride film are heated and thermally fused using an embossing roll at the same time as embossing. This doubling embossed film had excellent V-cutting properties and was also superior in design due to its delicate woodgrain printing and the effect of woodgrain grooves on the surface, and was backed by long-established technology. However, doubling embossed film is also inferior to decorative laminates using thermosetting resins such as polyester decorative laminates, melamine decorative laminates, and DAP decorative laminates in terms of surface scratch resistance, heat resistance, and stain resistance. was.
特にこれらのうち耐スクラツチ性に関しては、
ダブリングエンボスフイルムを合板あるいはパー
チクルボードに貼合せ、断截、Vカツト、組み立
て等の製造工程中に表面にスリ傷、亀裂、艶変化
等を生じこの解決のために組み立て後に補修や、
表面保護の塗装が行われていた。また近年この様
な問題点を解決するために業界では各種の対策が
行われてきた。それらの中で着色印刷塩化ビニル
シートに紫外線硬化型塗料を塗布した化粧フイル
ムが開発された。フイルムの表面が従来の熱可塑
性フイルムに代り硬化樹脂塗膜を有するために前
記の耐スクラツチ性をかなり解消することができ
た。しかしこの場合も印刷表面上で耐スクラツチ
性を有するには紫外線硬化型塗料の塗膜は最低15
g/m2以上必要であり、Vカツト適性を得るには
この塗膜量を大巾にアツプすることは不可能であ
り、この両者を両立させる為に厳しい塗布量管理
が要求される。次に印刷インキ表面に紫外線硬化
型塗料を直接塗布した場合、インキの色相により
紫外線硬化型塗料の硬化速度が異なるという欠点
である。黒に近い濃色程硬化が遅く透明色や濃度
の低い色の場合は硬化が速い。このため印刷模様
面に直接紫外線硬化型塗料を塗布した場合は色相
により紫外線照射条件を変える必要があり、最大
濃度の硬化条件に合わせなければならない。この
ため印刷模様毎に照射条件を決定することにより
作業は複雑になりまたその管理が不充分の場合に
は濃色部は硬化不足となり、その部分の物性が極
端に劣ること、また硬化速度の差により艶ムラが
生じること等の問題があつた。本発明では上記の
二点の問題を考え、透明熱可塑性フイルム上に紫
外線硬化型塗料を特定量塗布した後、連続して着
色印刷フイルム上にダブリングすることによりこ
の問題を解決した。次にこの内容を説明する。 Especially regarding scratch resistance,
Doubling embossed film is attached to plywood or particle board, and during manufacturing processes such as cutting, V-cutting, and assembly, scratches, cracks, and changes in gloss may occur on the surface.
A coating was applied to protect the surface. In recent years, various measures have been taken in the industry to solve these problems. Among these, a decorative film was developed in which a colored printed vinyl chloride sheet was coated with an ultraviolet curable paint. Because the surface of the film has a cured resin coating instead of the conventional thermoplastic film, the scratch resistance mentioned above can be significantly overcome. However, in this case as well, the coating film of UV-curable paint must be at least 15% to have scratch resistance on the printed surface.
g/m 2 or more is required, and it is impossible to increase the coating amount to a large extent in order to obtain V-cut suitability, and strict coating amount control is required to achieve both. Next, when an ultraviolet curable paint is directly applied to the surface of the printing ink, the curing speed of the ultraviolet curable paint differs depending on the hue of the ink, which is a drawback. The darker the color, which is closer to black, the slower the curing process, while the more transparent or low density the color, the faster the curing process. For this reason, when applying an ultraviolet curable paint directly to the printed pattern surface, it is necessary to change the ultraviolet irradiation conditions depending on the hue, and the curing conditions must be adjusted to the maximum density. For this reason, the work becomes complicated by determining the irradiation conditions for each printed pattern, and if the management is insufficient, the dark colored areas will be insufficiently cured, the physical properties of those areas will be extremely poor, and the curing speed will be slow. There were problems such as uneven gloss due to the difference. In the present invention, the above two problems were considered and these problems were solved by applying a specific amount of ultraviolet curable paint onto a transparent thermoplastic film and then doubling it onto a colored printing film. Next, this content will be explained.
一般に紫外線硬化型塗料は、熱可塑性の塩化ビ
ニルに比べ表面硬度や耐スクラツチ性に優れるが
可撓性に乏しく、伸びが少ないためVカツトのよ
うなフイルムが局部的に大きく伸ばされ、折り曲
げられる場合には亀裂や白化が生じ易い。 In general, UV-curable paints have superior surface hardness and scratch resistance compared to thermoplastic vinyl chloride, but they are less flexible and have less elongation, so they can be used when a film such as a V-cut is locally stretched and bent. is prone to cracking and whitening.
一般にVカツトに使用される塩化ビニルフイル
ムの伸び率が室温で50〜200%であるのに対し紫
外線硬化型塗料の伸び率が1〜30%と低いためで
ある。 This is because the elongation rate of vinyl chloride film generally used for V-cuts is 50 to 200% at room temperature, while the elongation rate of ultraviolet curable paints is as low as 1 to 30%.
この問題に対して紫外線硬化型塗料と塩化ビニ
ルフイルムを二層にし、それぞれの厚さを種々変
えて試験をした結果、紫外線硬化型塗料の塗膜厚
さを透明塩化ビニルフイルムの厚さの20%以下に
した場合Vカツトの伸びに充分耐え、亀裂、白化
の生じないことが判つた。試験結果の概要をグラ
フ1に示す。 To solve this problem, we made two layers of UV-curable paint and vinyl chloride film and tested them with various thicknesses. As a result, we found that the coating thickness of UV-curable paint was 20 times the thickness of transparent vinyl chloride film. % or less, it was found that the V-cut could sufficiently withstand the elongation and no cracking or whitening would occur. Graph 1 shows a summary of the test results.
紫外線硬化型塗料塗膜の厚さ/塩化ビニルフイルム厚
さ×100
この表から判るように塩化ビニルフイルムの厚
さに対して紫外線硬化型塗料の塗膜厚さが20%前
後以下だと伸び率は50%を越えVカツト適性を有
する。次に耐スクラツチ性については従来のよう
に印刷塩化ビニルシートに紫外線硬化型塗料を直
接塗布した場合この塗膜層に万一傷が入つた場合
には直接印刷模様に傷が入り商品価値を著しく落
とす。このため安全を見越して紫外線硬化型塗膜
は必要以上に厚くすることが行われ、その結果V
カツトと両立させることを難しくしていた。上記
の説明の如く耐スクラツチ性を確保するのに最低
量の紫外線硬化型塗料を施しVカツト性を維持し
仮に万一紫外線硬化型塗料の塗膜層に傷が入つて
も透明塩化ビニルフイルムが印刷模様上に被覆さ
れているため印刷模様に傷が入るような致命的欠
点にはならない。以上のように熱可塑性透明フイ
ルム上に紫外線硬化型塗料を熱可塑性フイルムの
厚さの20%の塗膜厚を設けることにより耐スクラ
ツチ性とVカツトの性能を両立させると共に従来
印刷フイルム上に直接紫外線硬化型塗膜を設けた
場合インキの色相、濃度による硬化速度に起因し
た塗膜性能のバラツキや艶ムラを解消しまた紫外
線硬化塗膜に万一傷が入つた場合、直接印刷模様
を傷つける商品上の致命欠点をも解決した。次に
特許請求の範囲2項に記載した内容を説明する。
紫外線硬化型塗料を塗布する場合、離型剤を有す
る透明プラスチツクフイルムを用いることにより
次の3点を改良できる。紫外線硬化型塗料は酸
素阻害性を有し透明フイルムを被覆させて紫外線
照射することにより硬化速度が上ること。硬化
速度が上り照射時間が短かくなり、また直接塗膜
面を照射されないため高圧水銀ランプから発生し
た熱により基体が加熱されて熱伸縮を起しカー
ル、フレアー等を生じる問題を解決できること。
塗膜面が被覆するプラスチツク表面の面に規制
され安定した艶表面を得られること。以上の3点
である。またこの離型性を有する透明フイルムを
紫外線硬化型塗料の硬化後に剥離しないでダブリ
ングエンボスする場合、この透明フイルムは保護
フイルムの役目を果し、キヤビネツト加工時に発
生する傷を皆無にすると共にこのフイルムを使用
するまで汚さずに保管できるという利点を有す
る。 Thickness of UV-curable paint film / Thickness of vinyl chloride film x 100 As can be seen from this table, if the film thickness of UV-curable paint is less than about 20% of the thickness of vinyl chloride film, the elongation rate will be has V-cut suitability of over 50%. Next, regarding scratch resistance, if UV-curable paint is applied directly to a printed vinyl chloride sheet as in the past, if this coating layer is scratched, the printed pattern will be scratched and the product value will be significantly reduced. Drop it. For this reason, UV-curable coatings are made thicker than necessary to ensure safety, and as a result, V
It was making it difficult to balance it with Katsuto. As explained above, in order to ensure scratch resistance, the minimum amount of UV-curable paint is applied to maintain V-cut properties, and even if the UV-curable paint layer is scratched, the transparent vinyl chloride film will remain intact. Since it is coated over the printed pattern, it does not cause fatal defects such as scratches on the printed pattern. As described above, by applying ultraviolet curable paint on a thermoplastic transparent film to a coating thickness of 20% of the thickness of the thermoplastic film, it is possible to achieve both scratch resistance and V-cut performance, and to apply the UV-curable paint directly onto a conventional printed film. When a UV-curable coating film is provided, it eliminates variations in coating performance and uneven luster caused by the curing speed depending on the hue and concentration of the ink, and if the UV-curable coating film is scratched, it will directly damage the printed pattern. The product's fatal flaws were also resolved. Next, the content stated in claim 2 will be explained.
When applying an ultraviolet curable paint, the following three points can be improved by using a transparent plastic film containing a mold release agent. UV curable paints have oxygen inhibiting properties and can be cured faster by covering them with a transparent film and irradiating them with UV rays. The curing speed is increased, the irradiation time is shortened, and since the coating surface is not directly irradiated, the heat generated from the high-pressure mercury lamp heats the substrate, causing thermal expansion and contraction, which can solve the problem of curling, flaring, etc.
A stable glossy surface can be obtained by controlling the coating surface to the surface of the plastic surface it covers. These are the three points above. In addition, when doubling embossing is performed without peeling off this transparent film that has mold releasability after the UV-curable paint has hardened, this transparent film serves as a protective film and eliminates any scratches that occur during cabinet processing. It has the advantage that it can be stored without getting dirty until it is used.
次に本発明に使用する材料について図面に対比
させて説明する。着色熱可塑性フイルムは通常上
市されている弱電用耐熱塩ビと称されるもので可
塑剤5〜23部(DOP換算)や鋼板塩ビと称され
ている可塑剤30%前後のものに代表される。この
厚みは50μ〜200μ程度である。塩化ビニルフイル
ム以外にABS樹脂やポリプロピレン系樹脂を主
体とした着色シートも使用される。 Next, materials used in the present invention will be explained in comparison with the drawings. Colored thermoplastic films are usually commercially available, called heat-resistant PVC for light electrical use, and are typified by 5 to 23 parts of plasticizer (in terms of DOP), and those called steel sheet PVC, which contain around 30% plasticizer. This thickness is approximately 50μ to 200μ. In addition to vinyl chloride film, colored sheets mainly made of ABS resin or polypropylene resin are also used.
上記の塩化ビニルフイルムはポリ塩化ビニル、
可塑剤、安定剤と着色顔料、充填剤を主体として
構成されている。これらのフイルムにはグラビア
印刷によつて印刷された木目模様や大理石模様等
の絵柄を有するものと無地(印刷柄の無いもの)
に大別される。次に2の透明熱可塑性フイルムは
1に記した着色熱可塑性シートから着色剤を除い
た透明又は半透明のシートで、基本的には樹脂の
内容は1のフイルムと何ら変らない。次に3の紫
外線硬化型塗料について記す。一般に紫外線硬化
型塗料はベースポリマーとしての紫外線硬化型樹
脂と光開始剤とから成る。この紫外線硬化型樹脂
のベースポリマーにはポリエーテルアクリレー
ト、ウレタン系ポリエステルアクリレート、エポ
キシアクリレート等のアクリル系樹脂に代表さ
れ、これらのポリマー、オリゴマーやモノマーを
適宜混合することにより使用される。また光開始
剤は通常増感剤と呼ばれベンゾインメチルエーテ
ル、ベンゾインエチルエーテル、ベンゾインイソ
ブチルエーテル等のベンゾインエーテルやベンゾ
イン、ベンゾフエノン、等や更に必要に応じ第3
級アミンを促進剤として使用する。またマツトの
塗膜が必要の場合はシリカや硫酸バリウム等の無
機質材料を加えることがある。次に紫外線硬化型
塗料を被覆し離型性を有する透明プラスチツクシ
ート4にはポリエステルフイルムやポリプロピレ
ンフイルムが使用され、本発明の目的には厚さ
20μ〜50μのものが作業性と経済性から適切であ
る。 The above vinyl chloride film is polyvinyl chloride,
It is mainly composed of plasticizers, stabilizers, coloring pigments, and fillers. These films include those with patterns such as wood grain patterns and marble patterns printed by gravure printing, and those with plain colors (without printed patterns).
It is broadly divided into Next, the transparent thermoplastic film 2 is a transparent or translucent sheet obtained by removing the colorant from the colored thermoplastic sheet described in 1, and the resin content is basically the same as the film 1. Next, the ultraviolet curable paint No. 3 will be described. Generally, UV-curable paints consist of a UV-curable resin as a base polymer and a photoinitiator. The base polymer of this ultraviolet curable resin is typified by acrylic resins such as polyether acrylate, urethane polyester acrylate, and epoxy acrylate, and these polymers, oligomers, and monomers are used by appropriately mixing them. The photoinitiator is usually called a sensitizer and includes benzoin ethers such as benzoin methyl ether, benzoin ethyl ether, benzoin isobutyl ether, benzoin, benzophenone, etc.
grade amine is used as accelerator. If a pine coating is required, inorganic materials such as silica or barium sulfate may be added. Next, a polyester film or a polypropylene film is used as the transparent plastic sheet 4 coated with an ultraviolet curable paint and having mold releasability.
A thickness of 20μ to 50μ is suitable from the viewpoint of workability and economy.
次に実施例により本発明の製造工程を述べる。 Next, the manufacturing process of the present invention will be described with reference to Examples.
〔実施例 1〕
可塑剤含有量15部厚さ60μの透明塩化ビニルフ
イルム上にグラビアロールによりマツト剤3%を
含むポリエーテルアクリレートを主体とした紫外
線硬化型塗料を10g/m2(厚さ10μ)塗布し
80W/cmの照射量を有する高圧水銀ランプ3本の
下を20m/分の速度で通し塗膜を硬化させた。次
いで該フイルムとグラビア印刷により木目模様を
印刷した可塑剤含有量15部の着色塩化ビニルフイ
ルムとを重ねて加熱ドラムに巻きつけてエンボス
ロールで押圧することによつて熱融着させ木目道
管溝のエンボスを施した。このように作られたフ
イルムは、表面硬度が鉛筆硬度2Hでホフマンス
クラツチテスターを用いた500gの荷重の引つか
きに耐え、厚さ12mmのパーチクルボードとこのフ
イルムを貼合せたものはVカツトで亀裂、白化を
生じることなく、弱電用キヤビネツト材に供し
た。[Example 1] On a transparent vinyl chloride film with a plasticizer content of 15 parts and a thickness of 60μ, an ultraviolet curable paint mainly composed of polyether acrylate containing 3% of a matting agent was applied using a gravure roll at 10g/m 2 (thickness of 10μ). ) applied
The coating was cured by passing it under three high-pressure mercury lamps with an irradiance of 80 W/cm at a speed of 20 m/min. Next, this film and a colored vinyl chloride film with a plasticizer content of 15 parts printed with a wood grain pattern by gravure printing are overlapped, wrapped around a heated drum, and heated and fused by pressing with an embossing roll to form wood grain grooves. Embossed. The film made in this way has a surface hardness of 2H pencil hardness and can withstand a 500g load using a Hoffman scratch tester, and when this film is laminated to a 12mm thick particle board, it has a V-cut. It was used as a low-power cabinet material without cracking or whitening.
〔実施例 2〕
可塑剤含有量30部厚さ60μの鋼板用透明塩化ビ
ニルフイルム上に10μの厚さにウレタン系ポリエ
ステルアクリレートを主体とした紫外線硬化型塗
料を塗布した後厚さ20μのポリプロピレンフイル
ムを重ね、高圧水銀灯で照射し硬化させた。ポリ
プロピレンフイルムを剥離せず木目印刷模様を有
する可塑剤含有量30部の鋼板塩化ビニルフイルム
とダブリングエンボスを行つた。このものは保護
フイルム付の鋼板用塩化ビニルフイルムとなり、
これを厚さ0.4m/mの亜鉛鉄板に貼合せたもの
はデユポン衝撃試験及び1丁の折り曲げ試験に合
格し加工用塩ビ鋼板に使用できた。[Example 2] Plasticizer content: 30 parts A transparent vinyl chloride film for steel plates with a thickness of 60μ is coated with an ultraviolet curing paint mainly composed of urethane polyester acrylate to a thickness of 10μ, and then a polypropylene film with a thickness of 20μ is formed. They were layered and cured by irradiation with a high-pressure mercury lamp. Doubling embossing was performed on a steel plate with a vinyl chloride film containing 30 parts of plasticizer and having a woodgrain print pattern without peeling the polypropylene film. This is a vinyl chloride film for steel plates with a protective film.
When this was laminated to a galvanized iron plate with a thickness of 0.4 m/m, it passed the Dupont impact test and the single bending test, and could be used as a processing PVC steel plate.
図面は本発明の実施例を示すものであり、第1
図は本発明によつて得られる化粧フイルムの断面
図を、第2図は本発明方法の製造工程図を各々示
す。
1…着色熱可塑性フイルム、2…透明熱可塑性
フイルム、3…紫外線硬化型塗料塗膜、4…離型
フイルム、5…模様、6…紫外線硬化型塗料塗工
部、7…高圧水銀灯、8…冷却ロール、9…赤外
線ランプ、10…エンボスロール。
The drawings show embodiments of the present invention.
The figure shows a sectional view of a decorative film obtained by the present invention, and FIG. 2 shows a manufacturing process diagram of the method of the present invention. 1...Colored thermoplastic film, 2...Transparent thermoplastic film, 3...UV curable paint film, 4...Release film, 5...Pattern, 6...UV curable paint coating section, 7...High pressure mercury lamp, 8... Cooling roll, 9...Infrared lamp, 10... Embossing roll.
Claims (1)
が該フイルムの厚さの20%以下になるように、艶
調整をした紫外線硬化型塗料を塗布する第一工
程、被塗物を冷却しつつ紫外線により硬化させる
第二工程、被塗物を硬化させた後、着色又は/及
び印刷を施した熱可塑性フイルム上に該フイルム
を熱融着させると同時にエンボスロールを用いて
エンボスを施す第三工程よりなる連続工程によつ
て製造することを特徴とするウエブ状の化粧フイ
ルムの製造方法。 2 紫外線硬化型塗料を塗布した被塗物に該紫外
線硬化型塗料と離型剤を有する透明プラスチツク
フイルムを被覆し、被塗物を冷却しつつ紫外線を
硬化させた後に、該透明プラスチツクフイルムを
剥離するか、あるいは剥離せずに付着した状態で
着色又は/及び印刷を施した熱可塑性フイルムと
熱融着させエンボスすることを特徴とする特許請
求の範囲第1項記載の化粧フイルムの製造方法。[Claims] 1. A first step of applying a gloss-adjusted ultraviolet curable paint to a transparent thermoplastic film so that the coating thickness is 20% or less of the thickness of the film; The second step is to cure the object with ultraviolet rays while cooling it. After the object to be coated is cured, the film is heat-sealed onto the colored and/or printed thermoplastic film, and at the same time, embossing is performed using an embossing roll. 1. A method for producing a web-like decorative film, characterized in that it is produced by a continuous process consisting of a third step of applying. 2. A transparent plastic film containing the ultraviolet curable paint and a release agent is coated on an object coated with an ultraviolet curable paint, and after curing the ultraviolet rays while cooling the object, the transparent plastic film is peeled off. 2. The method for producing a decorative film according to claim 1, wherein the decorative film is embossed by being heat-sealed to a thermoplastic film that has been colored and/or printed while being adhered without being peeled off.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10531880A JPS5729455A (en) | 1980-07-30 | 1980-07-30 | Manufacture of decorative film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10531880A JPS5729455A (en) | 1980-07-30 | 1980-07-30 | Manufacture of decorative film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5729455A JPS5729455A (en) | 1982-02-17 |
JPS6323906B2 true JPS6323906B2 (en) | 1988-05-18 |
Family
ID=14404353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10531880A Granted JPS5729455A (en) | 1980-07-30 | 1980-07-30 | Manufacture of decorative film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5729455A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0376502A (en) * | 1989-08-16 | 1991-04-02 | Kobashi Kogyo Co Ltd | Side drive type deep tillage rotor |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3418282A1 (en) * | 1984-05-17 | 1985-11-21 | Hoechst Ag, 6230 Frankfurt | DECORATIVE PLATE WITH IMPROVED SURFACE PROPERTIES |
JP2523574B2 (en) * | 1987-02-05 | 1996-08-14 | 松下電器産業株式会社 | Method for manufacturing coating film |
JPS6432181U (en) * | 1987-08-20 | 1989-02-28 | ||
JP2639951B2 (en) * | 1988-01-11 | 1997-08-13 | 大日本印刷株式会社 | Manufacturing method of decorative sheet |
JP5507807B2 (en) * | 2007-11-30 | 2014-05-28 | 日東電工株式会社 | Conductive water repellent member having conductive particle unevenly distributed polymer layer |
JP5507806B2 (en) * | 2007-11-30 | 2014-05-28 | 日東電工株式会社 | Conductive member having conductive material unevenly distributed polymer layer |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54139223A (en) * | 1978-04-21 | 1979-10-29 | Kohkoku Chem Ind | Floor material that have excellent tobaccoofire resistance and its preparation |
-
1980
- 1980-07-30 JP JP10531880A patent/JPS5729455A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54139223A (en) * | 1978-04-21 | 1979-10-29 | Kohkoku Chem Ind | Floor material that have excellent tobaccoofire resistance and its preparation |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0376502A (en) * | 1989-08-16 | 1991-04-02 | Kobashi Kogyo Co Ltd | Side drive type deep tillage rotor |
Also Published As
Publication number | Publication date |
---|---|
JPS5729455A (en) | 1982-02-17 |
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