JPH045036A - Composite film on which supporting film is adhered temporarily - Google Patents
Composite film on which supporting film is adhered temporarilyInfo
- Publication number
- JPH045036A JPH045036A JP2105470A JP10547090A JPH045036A JP H045036 A JPH045036 A JP H045036A JP 2105470 A JP2105470 A JP 2105470A JP 10547090 A JP10547090 A JP 10547090A JP H045036 A JPH045036 A JP H045036A
- Authority
- JP
- Japan
- Prior art keywords
- film
- pvc
- treated
- coating
- pvc film
- 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 13
- 229920000915 polyvinyl chloride Polymers 0.000 claims abstract description 46
- 239000004800 polyvinyl chloride Substances 0.000 claims abstract description 46
- 229920005989 resin Polymers 0.000 claims abstract description 8
- 239000011347 resin Substances 0.000 claims abstract description 8
- 239000011248 coating agent Substances 0.000 abstract description 11
- 238000000576 coating method Methods 0.000 abstract description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 6
- 239000002904 solvent Substances 0.000 abstract description 6
- 238000011282 treatment Methods 0.000 abstract description 6
- 238000010438 heat treatment Methods 0.000 abstract description 5
- 229920001225 polyester resin Polymers 0.000 abstract description 5
- 239000004645 polyester resin Substances 0.000 abstract description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 abstract description 4
- 238000007639 printing Methods 0.000 abstract description 4
- 238000003825 pressing Methods 0.000 abstract description 2
- 238000012545 processing Methods 0.000 description 6
- 229920002799 BoPET Polymers 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- 239000011120 plywood Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、ポリ塩化ビニル樹脂の複合フィルム(以下、
PVCフィルムという)に関するものである6さらに詳
しくは本発明は、種々の用途に使用されるPVCフィル
ムが印刷、コーティングまたは加熱処理される際の寸法
安定性を維持するために複合化されたフィルムに関する
ものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a polyvinyl chloride resin composite film (hereinafter referred to as
More particularly, the present invention relates to a composite film for maintaining dimensional stability when PVC films used in various applications are printed, coated or heat treated. It is something.
PVCフィルムは、その有する優れたパーフォーマンス
特性、例えば易加工性、柔軟性、着色性、印刷適性、他
の基材への接着性、難燃性あるいは比較的に低価格であ
る等のために、汎用樹脂の中でも最も多量に使用されて
いる。しかしながらその柔軟性および低い耐熱性の故に
、PVCフィルムが種々加工される工程で、高温度にさ
らされたり、張力がかかったり、溶剤が浸透したりした
場合に寸法安定性が著しく劣り、その結果、加工条件の
幅が狭く、加工方法も限定されるという難点があった。PVC film is popular due to its excellent performance properties, such as ease of processing, flexibility, colorability, printability, adhesion to other substrates, flame retardancy, and relatively low cost. is the most widely used general-purpose resin. However, due to its flexibility and low heat resistance, PVC film exhibits significantly poor dimensional stability when exposed to high temperatures, tension, and solvent penetration during various processing steps. However, the range of processing conditions was narrow and the processing methods were also limited.
この問題を解決するために、従来このPVCフィルムに
、耐熱、耐溶剤性の良い他の材料、例えばポリエステル
樹脂、フッ素系樹脂等のフィルム、紙、不織布等の繊維
系素材、鉄、アルミニウム等の金属箔等を複合した複合
フィルムが使用されている。In order to solve this problem, conventionally, PVC film was replaced with other materials with good heat resistance and solvent resistance, such as polyester resin, fluorine resin films, paper, fibrous materials such as nonwoven fabric, iron, aluminum, etc. A composite film made of metal foil, etc. is used.
しかしながら、従来のこれらの複合フィルムは、PVC
フィルムが本来有する柔軟性、接着性、加工性、例えば
真空成形性等を著しく阻害し、pvCフィルムに意図さ
れた用途に使用できなくなることになる。また、複合化
の結果、価格も上昇しこの面からも用途が制限されるき
らいがある。However, these conventional composite films are made of PVC
This significantly impedes the film's inherent flexibility, adhesiveness, processability, such as vacuum formability, and makes it impossible to use the pvC film for its intended purpose. Moreover, as a result of compounding, the price also increases, which tends to limit the applications.
本発明者らは、この課題を解決するべく鋭意研究を重ね
た結果、PVCフィルムに支持フィルムを剥離自在に接
着させることにより、上記の課題を解決し得ることを見
いだした。The inventors of the present invention have conducted extensive research to solve this problem, and have discovered that the above problem can be solved by attaching a support film to a PVC film in a releasable manner.
すなわち本発明は、PVCフィルムの片面に、耐熱性お
よび寸法安定性に優れた支持フィルムを剥離自在に仮貼
りした複合フィルムを提供することにより、上記の課題
を解決しようとするものである。That is, the present invention aims to solve the above problems by providing a composite film in which a support film with excellent heat resistance and dimensional stability is temporarily attached to one side of a PVC film in a removable manner.
以下に本発明をさらに詳細に説明する。The present invention will be explained in more detail below.
PVCフィルムは、易加工性、柔軟性、着色性、印刷適
性、他の基材への接着性、難燃性等に優れているので、
真空成形、圧空成形したり、他の基材に積層したりされ
るが、それに先立ち、フィルムの上に印刷、コーティン
グしたり、あるいはまた他のフィルムを積層して絵付け
したりされる工程を経ることが多い。そしてこの際に不
可避的に高温、高張力、場合によっては溶剤の浸透など
が起こり、フィルムの延伸または収縮、あるいは変形が
おこり、所期の寸法を維持することは困難である。PVC film has excellent processability, flexibility, colorability, printability, adhesion to other substrates, flame retardancy, etc.
The film may be vacuum formed, pressure formed, or laminated to other substrates, but prior to this, the film may be printed, coated, or laminated with other films and painted. It often goes through At this time, high temperatures, high tensions, and in some cases, penetration of solvents inevitably occur, causing stretching, shrinkage, or deformation of the film, making it difficult to maintain the desired dimensions.
そこで本発明においては、PVCフィルムと支持フィル
ムとを適正な加熱、加圧条件下で熱接着による仮貼りを
行うことにより、加熱や引張りに対する抵抗力を高め、
この複合フィルムに印刷やコーティング、場合によって
は発泡層の被覆等の処理を行っても、寸法変化の少ない
処理フィルムを得ることができるようにした。上記のよ
うなP■Cフィルムの処理を行ったのちに、支持フィル
ムを剥離すれば、寸法変化を受けないあるいは寸法変化
が極めて少ないPvCフィルムが印刷、発泡等の処理を
受けた状態で得ることがてきる。Therefore, in the present invention, the PVC film and the supporting film are temporarily bonded by thermal adhesion under appropriate heating and pressure conditions to increase resistance to heating and tension.
Even if this composite film is subjected to treatments such as printing, coating, and in some cases covering with a foam layer, it is possible to obtain a treated film with little dimensional change. If the supporting film is peeled off after the PvC film is processed as described above, a PvC film that undergoes printing, foaming, or other treatments can be obtained with no or very little dimensional change. It's coming.
このようにして得られた処理フィルムは、PVCフィル
ム単体として、通常の方法で後加工、例えばキャビネッ
ト木工加工、鋼板への被覆等、従来PVCフィルムが使
用されてきた用途に、そのまま利用することができる。The treated film obtained in this way can be used as a single PVC film for post-processing using normal methods, such as cabinet woodworking, coating on steel plates, and other applications for which PVC films have traditionally been used. can.
本発明に使用されるPVCフィルムは、可塑剤を添加し
たものも、添加しないものも使用することができ、その
範囲はO〜100phr程度である。The PVC film used in the present invention can be used with or without a plasticizer added, and the range is about 0 to 100 phr.
またPVCフィルムの厚さは、とくに限定はないが、通
常20〜500μ瀧、好ましくは50〜200μ肩程度
である。The thickness of the PVC film is not particularly limited, but is usually about 20 to 500 microns, preferably about 50 to 200 microns.
支持フィルムとして使用できる樹脂は、それ自身の耐熱
性、耐溶剤性、寸法安定性があり、ポリ塩化ビニルに仮
貼りでき、また簡単に剥離できる樹脂であれば、格別種
類は問わない0例えばポリエステル、ポリアミド、ポリ
カーボネート等の樹脂が使用できるが、最も好ましいの
はポリエステル樹脂、とくに好ましいのはテレフタル酸
またはイソフタル酸とエチレングリコールからなるポリ
エステル樹脂である(以下、PETフィルムという)。The resin that can be used as the support film can be of any type, as long as it has its own heat resistance, solvent resistance, and dimensional stability, can be temporarily attached to polyvinyl chloride, and can be easily peeled off.For example, polyester Although resins such as , polyamide, and polycarbonate can be used, the most preferred is a polyester resin, and particularly preferred is a polyester resin made of terephthalic acid or isophthalic acid and ethylene glycol (hereinafter referred to as PET film).
支持フィルムの厚さは、複合されるPVCフィルムの厚
さにもよるが、通常は10〜150μ履、より好ましく
は12〜75μl、代表的には12〜50μl程度であ
る。The thickness of the support film depends on the thickness of the PVC film to be composited, but is usually about 10 to 150 μl, more preferably 12 to 75 μl, and typically about 12 to 50 μl.
PVCフィルムと支持フィルムとの仮貼りは、PVCフ
ィルムの処理中に剥離しない程度に密着し、処理後には
簡単に剥離できるような複合方法であればどのような仮
貼り方法であってもよいが、最も好ましい方法は熱板貼
りによる方法である。The temporary attachment of the PVC film and the support film may be done by any combination method that allows the PVC film to adhere to the extent that it does not peel off during processing and is easily peeled off after processing. The most preferred method is a method using a hot plate.
すなわちPVCフィルムと支持フィルムとを重ねて加熱
下に圧着することにより、両者を容易に仮貼りすること
ができる。具体的には例えば、加熱された鏡面ドラムと
圧接ローラの間を連続的に通過させることにより仮貼を
行うことができる。圧着温度は、支持フィルムとしてP
ETフィルムを使用する場合は140°C程度が好まし
い。That is, by overlapping the PVC film and the support film and pressing them under heat, they can be easily temporarily attached. Specifically, for example, temporary pasting can be performed by continuously passing between a heated mirror drum and a pressure roller. The pressure bonding temperature is P as the support film.
When using ET film, the temperature is preferably about 140°C.
以下に、実施例により本発明をさらに詳細に説明する。Below, the present invention will be explained in more detail with reference to Examples.
夾1
(熱板貼り)
PVCフィルム(理研ビニル工業(株)製、厚み100
μ!、幅:100cz、可塑剤添加量:20phr)と
PETフィルム(ユニチカ(株)製、厚み25μz、)
を、2枚重ねにして、140℃に加熱された金属ロール
とゴムロールの間にツブ間隔0 、1 zz)を通し、
熱板貼り複合フィルムを形成した(第1図参照)。この
仮貼りフィルムの剥離強度は5g/インチ(2,54c
i+)であった。1 (hot plate pasted) PVC film (manufactured by Riken Vinyl Industries Co., Ltd., thickness 100
μ! , width: 100 cz, plasticizer addition: 20 phr) and PET film (manufactured by Unitika Co., Ltd., thickness 25 μz)
are stacked and passed between a metal roll and a rubber roll heated to 140°C with a spacing of 0 and 1 zz).
A hot plated composite film was formed (see Figure 1). The peel strength of this temporary film is 5 g/inch (2,54 c
i+).
(コーティング、加熱試験)
上記のようにして得られた複合フィルムに、溶剤系塗料
(固形分20%、トルエン+MEK=3:2)を、ウェ
ットで150μ層の厚さにコーティングし、表1に示す
ような温度にそれぞれ設定された乾燥炉を、5分間通過
させた後のフィルムの幅方向の収縮を測定した(第2図
参照)。(Coating, heating test) The composite film obtained as described above was wet coated with a solvent-based paint (solid content 20%, toluene + MEK = 3:2) to a thickness of 150 μm, as shown in Table 1. The shrinkage of the film in the width direction was measured after passing through a drying oven set at the temperatures shown for 5 minutes (see Figure 2).
比較のためにPVCフィルム単体に同様の処理をした結
果も測定した。これらの結果を表1に示す。For comparison, the results of the same treatment on a PVC film alone were also measured. These results are shown in Table 1.
表−1
表1から判るように、本発明における複合フィルムは、
PVCフィルム単体に比べ、幅収縮を著しく減少させる
ことができた。Table-1 As can be seen from Table 1, the composite film of the present invention is
Width shrinkage could be significantly reduced compared to PVC film alone.
(支持フィルムの剥離)
前述のようにしてコーティングおよび乾燥が終了した複
合フィルムを、二軸の巻取り装置のついた巻返し機を用
いて連続的に巻返したところ、PVCフィルムとPET
フィルムとは容易に剥離し、この際PVCフィルムには
なんらの損傷や延伸も起きなかった(第3図参照)。(Peeling of support film) When the composite film coated and dried as described above was continuously rewound using a rewinding machine equipped with a biaxial winding device, the PVC film and PET
The film was easily peeled off without any damage or stretching to the PVC film (see Figure 3).
(合板への応用)
上記のようにして得た処理PVCフィルムを、建材用合
板(スターウッド)に、汎用のPVCラミネート合板用
の接着剤(中央理化(株)製エチレン・酢酸ビニル共重
合体エマルジョンタイプ)を使用して貼合わせしたとこ
ろ、従来のPVC合板用のPVCフィルムと同様の接着
強度を示した。(Application to plywood) The treated PVC film obtained as described above was applied to plywood for building materials (Starwood) using a general-purpose PVC laminated plywood adhesive (ethylene-vinyl acetate copolymer manufactured by Chuo Rika Co., Ltd.). When laminated using a PVC film (emulsion type), it showed the same adhesive strength as conventional PVC film for PVC plywood.
丸L1ユ
実施例1で使用した塗料に、発泡剤としてアゾビスイソ
ブチロニトリルを1重量%になるように加え、ウェット
で100μlの厚みになるようにコーティングを行った
。これを140℃の乾燥炉を通したところ、250μl
厚みの発泡層を有するPVC複合フィルムを得た。冷却
後の幅100c1当たりの収縮は1811であった。Azobisisobutyronitrile was added as a foaming agent to the paint used in Example 1 at a concentration of 1% by weight, and wet coating was performed to a thickness of 100 μl. When this was passed through a drying oven at 140℃, 250 μl
A PVC composite film with a thick foam layer was obtained. The shrinkage per 100 c1 of width after cooling was 1811.
一方、PVCフィルム単体では乾燥炉内で切れを生じて
、満足な製品は得られなかった。On the other hand, when the PVC film was used alone, it broke in the drying oven, and a satisfactory product could not be obtained.
本発明においては、上記のようにPVCフィルムに支持
フィルムをあらかじめ仮貼りをするので、PVCにコー
ティングその他の処理を施す間も、PVCフィルムには
収縮や変形が起こらず、処理後は支持フィルムを剥離す
ることにより、本来のPVC単体として使用できる。こ
のため、PVCフィルムの収縮を懸念することなく、自
由に印刷、コーティング、発泡等の処理を行うことがで
き、用途の幅が拡大できる。In the present invention, since the support film is temporarily attached to the PVC film as described above, the PVC film does not shrink or deform while coating or other treatments are applied to the PVC, and the support film is not attached after the treatment. By peeling it off, it can be used as the original PVC alone. Therefore, processing such as printing, coating, and foaming can be freely performed without worrying about shrinkage of the PVC film, and the range of uses can be expanded.
第1図はPVCフィルムにPETフィルムを熱板貼した
図である。
第2図はPVCフィルム上にコーティングを施した図で
ある。
第3図はPETフィルムを剥離した図である。
1:PVcフィルム
2:PETフィルム
3・コーテング
特許出願人 理研ビニル工業株式会社FIG. 1 is a diagram showing a PET film pasted onto a PVC film on a hot plate. FIG. 2 shows a coating applied to a PVC film. FIG. 3 is a diagram showing the PET film peeled off. 1: PVc film 2: PET film 3 Coating patent applicant Riken Vinyl Industries Co., Ltd.
Claims (1)
寸法安定性のある支持フィルムを剥離自在に仮貼りした
複合フィルム。A composite film in which a heat-resistant and dimensionally stable support film is temporarily attached to one side of a polyvinyl chloride resin film in a removable manner.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2105470A JP2971509B2 (en) | 1990-04-23 | 1990-04-23 | Composite film with support film temporarily attached |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2105470A JP2971509B2 (en) | 1990-04-23 | 1990-04-23 | Composite film with support film temporarily attached |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH045036A true JPH045036A (en) | 1992-01-09 |
JP2971509B2 JP2971509B2 (en) | 1999-11-08 |
Family
ID=14408479
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2105470A Expired - Fee Related JP2971509B2 (en) | 1990-04-23 | 1990-04-23 | Composite film with support film temporarily attached |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2971509B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6375786B1 (en) * | 1996-03-04 | 2002-04-23 | Awi Licensing Company | Surface covering having a precoated, E-beam cured wearlayer coated film and process of making the same |
KR100437302B1 (en) * | 2001-10-23 | 2004-06-25 | 주식회사지엠피 | A layer film for laminating |
US6908663B1 (en) | 2000-11-15 | 2005-06-21 | Awi Licensing Company | Pigmented radiation cured wear layer |
CN102896928A (en) * | 2011-07-29 | 2013-01-30 | 上海大巨龙蓬盖新材料有限公司 | Mesh fabric and transparent film double-sided jet drawing material and manufacturing method thereof |
-
1990
- 1990-04-23 JP JP2105470A patent/JP2971509B2/en not_active Expired - Fee Related
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6375786B1 (en) * | 1996-03-04 | 2002-04-23 | Awi Licensing Company | Surface covering having a precoated, E-beam cured wearlayer coated film and process of making the same |
US6616792B2 (en) | 1996-03-04 | 2003-09-09 | Awi Licensing Company | Surface covering having a precoated, E-beam cured wearlayer coated film and process of making the same |
US6908663B1 (en) | 2000-11-15 | 2005-06-21 | Awi Licensing Company | Pigmented radiation cured wear layer |
US6908585B2 (en) | 2000-11-15 | 2005-06-21 | Awi Licensing Company | Pigmented radiation cured wear layer |
KR100437302B1 (en) * | 2001-10-23 | 2004-06-25 | 주식회사지엠피 | A layer film for laminating |
CN102896928A (en) * | 2011-07-29 | 2013-01-30 | 上海大巨龙蓬盖新材料有限公司 | Mesh fabric and transparent film double-sided jet drawing material and manufacturing method thereof |
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