JPH0768716A - Manufacture of film with fluorine resin film - Google Patents
Manufacture of film with fluorine resin filmInfo
- Publication number
- JPH0768716A JPH0768716A JP21998893A JP21998893A JPH0768716A JP H0768716 A JPH0768716 A JP H0768716A JP 21998893 A JP21998893 A JP 21998893A JP 21998893 A JP21998893 A JP 21998893A JP H0768716 A JPH0768716 A JP H0768716A
- Authority
- JP
- Japan
- Prior art keywords
- film
- dried
- fluororesin
- main
- fluorine resin
- 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
Landscapes
- Laminated Bodies (AREA)
- Moulding By Coating Moulds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、例えばマーキングフィ
ルム等に使用されるフッ素系樹脂膜を有するフィルムの
製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a film having a fluororesin film, which is used as a marking film, for example.
【0002】[0002]
【従来の技術】従来、例えば屋外の看板に貼付された塩
化ビニール製のマーキングフィルムは、ほこり等により
汚れやすく、付着した汚れを洗い落すことも困難であ
り、また時間の経過と共に光沢が低下する欠点があるの
で、該マーキングフィルムの表面にフッ素系樹脂のフィ
ルムをラミネートしたり、フッ素系樹脂を塗布したりす
ることが行なわれている。2. Description of the Related Art Conventionally, for example, a vinyl chloride marking film attached to an outdoor signboard is easily soiled by dust and the like, and it is difficult to wash off the adhered soil, and the gloss decreases with the passage of time. Because of the drawbacks, it has been practiced to laminate a film of a fluororesin on the surface of the marking film or to apply a fluororesin.
【0003】[0003]
【発明が解決しようとする課題】上記のフッ素系樹脂の
フィルムをマーキングフィルムにラミネートすると、そ
の全体の厚さが大きくなり、その結果、腰が強くなって
マーキングフィルムに要求される柔軟性が損なわれ、そ
の加工コストも高くなる不都合がある。また、マーキン
グフィルムにフッ素系樹脂の溶液を塗布すると、該溶液
中の溶剤がマーキングフィルムの樹脂に浸透し、容易に
乾燥しないので残留しやすく、作成したマーキングフィ
ルムを巻き取ったときにその背面にフッ素系樹脂膜がブ
ロッキングして使用困難になり、浸透した溶液を乾燥さ
せために乾燥温度を上げると、該フィルムの熱収縮が大
きくなるため、品質が低下する不都合があった。When the above-mentioned fluororesin film is laminated on a marking film, the total thickness of the film is increased, and as a result, the rigidity is increased and the flexibility required for the marking film is impaired. In addition, the processing cost is high. Also, when a solution of a fluorine-based resin is applied to the marking film, the solvent in the solution penetrates into the resin of the marking film and does not easily dry so that the marking film is likely to remain, and when the created marking film is wound up, the marking film is not applied to the back surface of the marking film. The fluorine-based resin film becomes difficult to use due to blocking, and when the drying temperature is raised to dry the permeated solution, the heat shrinkage of the film becomes large, resulting in the disadvantage that the quality deteriorates.
【0004】本発明は、こうした不都合がなく所望の厚
さに加工でき、安価に高品質のフッ素系樹脂膜を有する
フィルムを製造する方法を提供することを目的とするも
のである。An object of the present invention is to provide a method for producing a film having a high quality fluororesin film which can be processed into a desired thickness without such inconvenience and which is inexpensive.
【0005】[0005]
【課題を解決するための手段】本発明では、工程紙上に
フッ素系樹脂を塗布してこれを乾燥させ、続いて該フッ
素系樹脂膜上に塩化ビニールまたはポリウレタンの主膜
をキャスティングにより形成することにより、上記の目
的を達成するようにした。形成した塩化ビニールまたは
ポリウレタンの主膜の上に更に粘着剤層を形成すると耐
候性、防汚性の良いマーキングフィルムが加工性に問題
なく製造できる。According to the present invention, a fluorocarbon resin is coated on a process paper and dried, and subsequently a vinyl chloride or polyurethane main film is formed on the fluorocarbon resin film by casting. Thus, the above-mentioned object is achieved. If a pressure-sensitive adhesive layer is further formed on the formed vinyl chloride or polyurethane main film, a marking film having good weather resistance and antifouling properties can be produced without problems in processability.
【0006】[0006]
【作用】フッ素系樹脂膜が乾燥しているので、その上に
塩化ビニールまたはポリウレタンの樹脂膜を形成して
も、該塩化ビニールまたはポリウレタンの主膜の乾燥中
或いは乾燥後に該フッ素系樹脂膜に使用されていた有機
溶剤が該主膜に移行することがなく、該主膜の表面のブ
ロッキングや収縮を防げ、該フッ素系樹脂膜は薄いので
フィルム全体を所望の厚みに形成できる。該主膜は塗工
機により簡単に形成でき、フッ素系樹脂膜を備えた品質
のよい安価なフィルムが得られる。[Function] Since the fluororesin film is dried, even if a vinyl chloride or polyurethane resin film is formed on the fluororesin film, the fluororesin film may be formed on the vinyl chloride or polyurethane main film during or after drying. The used organic solvent does not migrate to the main film, prevents blocking and shrinkage of the surface of the main film, and the fluororesin film is thin, so that the entire film can be formed to a desired thickness. The main film can be easily formed by a coating machine, and a high-quality and inexpensive film having a fluororesin film can be obtained.
【0007】[0007]
【実施例】本発明方法の実施例を図面に基づき説明する
と、図1は本発明方法で作成したフィルムの一部断面の
拡大図を示し、同図に於いて符号1は乾燥したフッ素系
樹脂膜、2は該乾燥したフッ素系樹脂膜1の上に形成し
た主膜で、その上に剥離紙4で覆われた粘着剤層3が形
成される。EXAMPLE An example of the method of the present invention will be described with reference to the drawings. FIG. 1 is an enlarged view of a partial cross section of a film produced by the method of the present invention. In the figure, reference numeral 1 is a dry fluororesin. The film 2 is a main film formed on the dried fluororesin film 1, on which the pressure-sensitive adhesive layer 3 covered with a release paper 4 is formed.
【0008】該フッ素系樹脂膜1には、フッ化ビニリデ
ン、テトラフルオロエチレン、ヘキサフルオロプロピレ
ンやこれらのブレンド、或はこれらのフッ素樹脂にアク
リル樹脂をブレンドした系を使用し、塩化ビニール、ポ
リウレタンの主膜2の耐候性を更に向上させるために紫
外線吸収剤を該フッ素系樹脂膜1に添加してもよい。本
発明の方法では、まず上記のフッ素系樹脂の溶液を図2
に示すように、上質紙系やポリエステルフィルムタイプ
の工程紙5にグラビヤダイレクト、マイヤーバー、コン
マコーターで例えば5ミクロンの厚さに直接コーティン
グし、これを乾燥してフッ素系樹脂膜1を形成する。こ
の乾燥したフッ素系樹脂膜1の上に、ポリエステル系等
の可塑剤を混入した塩化ビニールポリマーのゾルやポリ
ウレタン樹脂の溶液を例えば55ミクロンの厚さにオル
ガノゾルキャスト法等のキャスティング製膜により製膜
し、図3に示すように該フッ素系樹脂膜1の上にナイフ
コーターやコンマコーターによって主膜2を形成する。
更に、該粘着剤層3は、別個に用意した剥離紙4の上に
例えばアクリル系粘着剤を30ミクロンの厚さに形成
し、これの粘着面を図4のような上記主膜2に重合させ
る転写を行って形成される。For the fluorine-based resin film 1, vinylidene fluoride, tetrafluoroethylene, hexafluoropropylene, a blend thereof, or a blend of these fluororesins with an acrylic resin is used. An ultraviolet absorber may be added to the fluororesin film 1 in order to further improve the weather resistance of the main film 2. In the method of the present invention, first, the solution of the above-mentioned fluororesin is used as shown in FIG.
As shown in FIG. 3, a fine paper type or polyester film type process paper 5 is directly coated with a gravure direct, a Meyer bar, or a comma coater to a thickness of, for example, 5 μm, and dried to form a fluororesin film 1. . On the dried fluororesin film 1, a vinyl chloride polymer sol mixed with a plasticizer such as polyester or a solution of polyurethane resin is formed to a thickness of, for example, 55 microns by casting film formation such as organosol casting. Then, as shown in FIG. 3, the main film 2 is formed on the fluororesin film 1 by a knife coater or a comma coater.
Further, the pressure-sensitive adhesive layer 3 is obtained by forming, for example, an acrylic pressure-sensitive adhesive with a thickness of 30 μm on a release paper 4 prepared separately, and the pressure-sensitive adhesive surface of the acrylic pressure-sensitive adhesive is polymerized on the main film 2 as shown in FIG. It is formed by performing the transfer.
【0009】工程紙5にフッ素系樹脂の溶液を塗布して
乾燥したフッ素系樹脂膜1の上に主膜2をキャスティン
グにより形成すると、該フッ素系樹脂膜1の溶剤がすで
に蒸発しており、そのため形成した主膜2の内部へ該フ
ッ素系樹脂の溶剤が浸透することがなく、該主膜2の製
膜を過乾燥で行なう必要がないので収縮もなく、製品と
して巻き取ったときにブロッキングすることのない所定
の厚みの製品特に薄手の製品が得られる。When the main film 2 is formed by casting on the fluororesin film 1 obtained by applying the fluororesin solution to the process paper 5 and drying, the solvent of the fluororesin film 1 has already evaporated, Therefore, the solvent of the fluororesin does not penetrate into the formed main film 2 and the film of the main film 2 does not need to be overdried, so that there is no shrinkage and blocking when wound as a product. It is possible to obtain a product having a predetermined thickness which is not particularly thin, and particularly a thin product.
【0010】本発明をマーキングフィルムの製造に適用
した場合の具体的実施例は次の通りである。 実施例 1 表面に剥離処理を施した100ミクロンのポリエステル
フィルムの工程紙5(リンテック(株)製)に、フッ素
樹脂共重合物とアクリル樹脂をブレンドしたフッ素系樹
脂溶液(ノバコート:大日本色材工業(株)製)をグラ
ビア塗工機で5ミクロンの厚さに塗布し、これを120
℃で1分間乾燥してフッ素系樹脂膜1とし、その上に塩
化ビニールポリマー100部とポリエステル系可塑剤3
5部からなるオルガノゾルをコンマ塗工機で厚さ55ミ
クロンに塗布して190℃で1分間乾燥させることによ
り主膜2を形成し、これをロール状に巻き取った。Specific examples of the case where the present invention is applied to the production of a marking film are as follows. Example 1 A fluorocarbon resin solution prepared by blending a fluorocarbon resin copolymer and an acrylic resin on a process paper 5 (manufactured by Lintec Co., Ltd.) of a 100-micron polyester film whose surface has been subjected to a release treatment (Novacoat: Dainippon Color Material) Kogyo Co., Ltd.) was applied with a gravure coater to a thickness of 5 microns, and this was applied to 120
It is dried at ℃ for 1 minute to make a fluororesin film 1, on which 100 parts of vinyl chloride polymer and 3 parts of polyester plasticizer are added.
The main film 2 was formed by coating 5 parts of organosol with a comma coater to a thickness of 55 μm and drying at 190 ° C. for 1 minute, and this was wound into a roll.
【0011】この工程紙5上にフッ素系樹脂膜1と主膜
2とからなるフィルムは、該フッ素系樹脂膜1が乾燥し
ているので主膜2の製膜を過乾燥で行なう必要がなく、
収縮が発生せずブロッキングも起きず、品質が良好であ
った。このロールを粘着剤層形成のために別工程で解
き、主膜の上に、剥離紙4上に30ミクロンの厚さで塗
布乾燥したアクリル系粘着剤を転写して粘着剤層3を形
成したのち、工程紙5を剥がすと図1に示す断面構造の
フィルムが得られた。これにより得られたマーキングフ
ィルムは、総厚で90ミクロンであり、使用したときの
3次元曲面への追従性も良好であった。The film composed of the fluororesin film 1 and the main film 2 on the process paper 5 does not need to be over-dried because the fluororesin film 1 is dried. ,
No shrinkage occurred and no blocking occurred, and the quality was good. This roll was unwound in a separate step to form a pressure-sensitive adhesive layer, and an acrylic pressure-sensitive adhesive applied and dried on the release paper 4 in a thickness of 30 μm was transferred onto the main film to form a pressure-sensitive adhesive layer 3. After that, the process paper 5 was peeled off to obtain a film having a sectional structure shown in FIG. The marking film thus obtained had a total thickness of 90 μm and had good followability to a three-dimensional curved surface when used.
【0012】実施例 2 表面に剥離処理を施した100ミクロンのポリエステル
フィルムの工程紙5(リンテック(株)製)に、フッ素
樹脂共重合物とアクリル樹脂をブレンドしたフッ素系樹
脂溶液(ノバコート:大日本色材工業(株)製)をグラ
ビア塗工機で5ミクロンの厚さに塗布し、これを120
℃で1分間乾燥してフッ素系樹脂膜1とし、その上に溶
剤系ウレタン樹脂(レザミン:大日精化(株)製)をコ
ンマ塗工機で厚さ45ミクロンとなるように塗布し、1
00℃で1分間乾燥させて主膜2を形成し、これをロー
ル状に巻き取った。これにより得られたフッ素系樹脂膜
を有するポリウレタンフィルムは、収縮やブロッキング
がなく、また、粘着加工を施してマーキングフィルムと
したときの3次元曲面への追従性も良好であった。Example 2 A fluorocarbon resin solution (Novacoat: Large) in which a fluorocarbon resin copolymer and an acrylic resin were blended with a process paper 5 (manufactured by Lintec Co., Ltd.) of a 100-micron polyester film whose surface was subjected to a release treatment. Nihon Kyoku Kogyo Co., Ltd. was applied to a thickness of 5 microns with a gravure coater, and this was applied to 120
It is dried at ℃ for 1 minute to make a fluorinated resin film 1, and a solvent-based urethane resin (Resamine: Dainichiseika Co., Ltd.) is coated on it with a comma coater to a thickness of 45 microns.
The film was dried at 00 ° C. for 1 minute to form the main film 2, which was wound into a roll. The polyurethane film having the fluororesin film thus obtained had no shrinkage or blocking, and had good followability to the three-dimensional curved surface when the adhesive film was applied to the marking film.
【0013】比較例 1 上記実施例1で製造した本発明のフィルムとの比較のた
め、塩化ビニール100部とポリエステル系可塑剤35
部からなる混合物を50ミクロン厚にカレンダー製膜機
により製膜して主膜を得、これの片面にフッ素系樹脂膜
の形成のために上記のフッ素系樹脂(ノバコート)を5
ミクロンの厚さで塗布し乾燥してフィルムとしたとこ
ろ、塩化ビニールの主膜に浸透した該フッ素系樹脂の溶
剤が完全に乾燥せず、巻き取ったフィルムはフッ素系樹
脂膜が塩化ビニールの主膜の表面にブロッキングし、溶
剤の完全な乾燥のために温度を上げると、主膜が収縮し
て粘着加工が不可能になり、実用に適さなかった。Comparative Example 1 For comparison with the film of the present invention produced in Example 1 above, 100 parts of vinyl chloride and 35 of a polyester plasticizer were used.
Part of the mixture was formed into a main film by a calender film forming machine to a thickness of 50 μm, and the above-mentioned fluororesin (Novacoat) was used to form a fluororesin film on one side of the main film.
When applied to a film with a thickness of micron and dried to form a film, the solvent of the fluororesin that permeated the main film of vinyl chloride did not completely dry, and the film wound up had the fluororesin film mainly composed of vinyl chloride. When the surface of the film was blocked and the temperature was raised to completely dry the solvent, the main film contracted and the adhesive processing became impossible, which was not suitable for practical use.
【0014】比較例 2 更に上記実施例1で製造した本発明のフィルムとの比較
のために、塩化ビニール100部とポリエステル系可塑
剤35部からなる混合物を50ミクロン厚にカレンダー
製膜機により製膜して主膜を得、これの表面に市販のフ
ッ素系樹脂のフィルムを積層してフッ素系樹脂膜を有す
るフィルムを作成した。その1つの主膜には厚さ50ミ
クロンのAT-50Y(呉羽化学工業(株)製)のフッ素系樹
脂フィルムを積層し、もう1つの主膜には厚さ25ミク
ロンのテドラー(デュポン社製)のフッ素系樹脂フィル
ムを積層し、更にもう1つの主膜には厚さ50ミクロン
のアフレックス(旭硝子(株)製)のフッ素系樹脂フィ
ルムを積層し、これらの積層のために厚さ30ミクロン
のアクリル系粘着剤を使用した。これらのフィルムの総
厚は本発明の上記実施例や上記のフッ素系樹脂を塗布し
た比較例に較べ50〜80ミクロンも厚くなっており、
フィルムの腰が強くなりすぎ、実施例1の場合と同様の
粘着加工を施しても3次元曲面に充分に追従しなかっ
た。Comparative Example 2 Further, for comparison with the film of the present invention produced in Example 1 above, a mixture of 100 parts of vinyl chloride and 35 parts of a polyester-based plasticizer was made to a thickness of 50 μm by a calender film forming machine. A main film was obtained by laminating the film, and a commercially available film of a fluororesin was laminated on the surface of the main film to prepare a film having a fluororesin film. A 50-micron-thick AT-50Y (Kureha Chemical Industry Co., Ltd.) fluororesin film is laminated on one main film, and a 25-micron thick Tedlar (Dupont Co., Ltd.) is formed on the other main film. ) Fluorine resin film is laminated, and another main film is laminated with Fluorine resin film of Aflex (manufactured by Asahi Glass Co., Ltd.) having a thickness of 50 μm. A micron acrylic adhesive was used. The total thickness of these films is 50 to 80 microns thicker than the above-mentioned examples of the present invention and the comparative examples coated with the above-mentioned fluororesin,
The film became too stiff and did not sufficiently follow the three-dimensional curved surface even when the same adhesive processing as in Example 1 was applied.
【0015】本発明の上記実施例で得られたフィルムを
マーキングフィルムとして屋外に6カ月間暴露して使用
し、その後、乾いた布で拭いたところ、表面の汚れは完
全に拭き取れた。これに対し、フッ素系樹脂膜のない主
膜のみからなるフィルムをマーキングフィルムとして使
用し、同期間暴露したのち汚れを水洗したが、汚れを完
全に除去することは出来なかった。The films obtained in the above-mentioned examples of the present invention were used as a marking film after being exposed outdoors for 6 months, and then wiped with a dry cloth, whereby the surface stains were completely wiped off. On the other hand, a film consisting of only the main film without the fluorine-based resin film was used as a marking film, and the stains were washed with water after being exposed for the same period, but the stains could not be completely removed.
【0016】更に、本発明の上記実施例で得られたフィ
ルムのマーキングフィルムをサンシャインウエザーメー
ター(スガ試験機(株)製、条件120サイクル内18
分降雨、ブラックパネル温度63°±3℃)で3000
時間暴露し、暴露後の外観を目視で判断した。同期間暴
露したフッ素系樹脂膜のないマーキングフィルムと比較
して光沢の低下、変色、退色、チョーキングが優れてい
た。Further, the marking film of the film obtained in the above-mentioned embodiment of the present invention was used as a sunshine weather meter (manufactured by Suga Test Instruments Co., Ltd., under the condition 120 cycles 18
Minute rainfall, black panel temperature 63 ° ± 3 ° C) 3000
It was exposed for a period of time, and the appearance after the exposure was visually judged. Compared to the marking film without the fluororesin film exposed for the same period, the deterioration of gloss, discoloration, fading and chalking were excellent.
【0017】以上の実施例と比較例に於いて、積層加工
時の収縮、フィルム全体の残留溶剤、3次元曲面への追
従性、及びデラミネーションを検討した結果を総約する
と、次表の通りである。デラミネーションとは積層樹脂
間(フッ素樹脂膜・主膜)の自然剥離性のことで、冷熱
衝撃試験(100℃と−30℃を5サイクル行なった)
で確認した。In the above Examples and Comparative Examples, the results of examining shrinkage during lamination processing, residual solvent of the entire film, conformability to a three-dimensional curved surface, and delamination are summarized as follows. Is. Delamination is the natural peelability between laminated resins (fluorine resin film / main film), and thermal shock test (100 ° C and -30 ° C for 5 cycles).
Confirmed in.
【0018】 [0018]
【0019】[0019]
【発明の効果】以上のように本発明によるときは、乾燥
したフッ素系樹脂膜の上に塩化ビニールまたはポリウレ
タンの主膜を形成するので、所定の厚みに形成でき、収
縮がなく品質のよいフッ素系樹脂膜を有するフィルムが
安価に得られる等の効果がある。As described above, according to the present invention, since the main film of vinyl chloride or polyurethane is formed on the dried fluororesin film, it can be formed to a predetermined thickness, and it does not shrink and has good quality. There is an effect that a film having a resin film can be obtained at low cost.
【図1】 本発明の実施例の要部の拡大断面図FIG. 1 is an enlarged cross-sectional view of a main part of an embodiment of the present invention.
【図2】 本発明のフィルムの製造工程の一部拡大断面
図FIG. 2 is a partially enlarged cross-sectional view of the film manufacturing process of the present invention.
【図3】 本発明のフィルムの製造工程の一部拡大断面
図FIG. 3 is a partially enlarged cross-sectional view of the film manufacturing process of the present invention.
【図4】 本発明のフィルムの製造工程の一部拡大断面
図FIG. 4 is a partially enlarged cross-sectional view of the film manufacturing process of the present invention.
1 フッ素系樹脂膜 2 主膜 3 粘着剤層 4 剥離紙 5 工程紙 1 Fluorine-based resin film 2 Main film 3 Adhesive layer 4 Release paper 5 Process paper
Claims (2)
を乾燥させ、続いて該フッ素系樹脂膜上に塩化ビニール
またはポリウレタンの主膜をキャスティングにより形成
したことを特徴とするフッ素系樹脂膜を有するフィルム
の製造方法。1. A fluororesin film characterized in that a fluororesin is coated on a process paper, dried, and subsequently, a main film of vinyl chloride or polyurethane is formed on the fluororesin film by casting. A method for producing a film having:
主膜の形成後にその上に粘着剤層を形成したことを特徴
とする請求項1に記載のフッ素系樹脂膜を有するフィル
ムの製造方法。2. The method for producing a film having a fluororesin film according to claim 1, wherein an adhesive layer is formed on the main film of vinyl chloride or polyurethane after the main film is formed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21998893A JP2884461B2 (en) | 1993-09-03 | 1993-09-03 | Method for producing film having fluorine-based resin film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21998893A JP2884461B2 (en) | 1993-09-03 | 1993-09-03 | Method for producing film having fluorine-based resin film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0768716A true JPH0768716A (en) | 1995-03-14 |
JP2884461B2 JP2884461B2 (en) | 1999-04-19 |
Family
ID=16744170
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21998893A Expired - Lifetime JP2884461B2 (en) | 1993-09-03 | 1993-09-03 | Method for producing film having fluorine-based resin film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2884461B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5459065A (en) * | 1985-02-19 | 1995-10-17 | Utah State University Foundation | Process for the degradation of coal tar and its constituents by Phanerochaete chrysosporium |
JP2011148115A (en) * | 2010-01-19 | 2011-08-04 | Lintec Corp | Laminated film, and method for manufacturing the same |
-
1993
- 1993-09-03 JP JP21998893A patent/JP2884461B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5459065A (en) * | 1985-02-19 | 1995-10-17 | Utah State University Foundation | Process for the degradation of coal tar and its constituents by Phanerochaete chrysosporium |
JP2011148115A (en) * | 2010-01-19 | 2011-08-04 | Lintec Corp | Laminated film, and method for manufacturing the same |
Also Published As
Publication number | Publication date |
---|---|
JP2884461B2 (en) | 1999-04-19 |
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