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JPS5924669A - Print lamination method - Google Patents

Print lamination method

Info

Publication number
JPS5924669A
JPS5924669A JP57208760A JP20876082A JPS5924669A JP S5924669 A JPS5924669 A JP S5924669A JP 57208760 A JP57208760 A JP 57208760A JP 20876082 A JP20876082 A JP 20876082A JP S5924669 A JPS5924669 A JP S5924669A
Authority
JP
Japan
Prior art keywords
film
printing paper
resin layer
lamination method
print lamination
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
Application number
JP57208760A
Other languages
Japanese (ja)
Other versions
JPH022411B2 (en
Inventor
健 山本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gunze Ltd
Original Assignee
Gunze Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Gunze Ltd filed Critical Gunze Ltd
Priority to JP57208760A priority Critical patent/JPS5924669A/en
Publication of JPS5924669A publication Critical patent/JPS5924669A/en
Publication of JPH022411B2 publication Critical patent/JPH022411B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Laminated Bodies (AREA)
  • Lining Or Joining Of Plastics Or The Like (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 未発[」1け接着剤、溶剤を用いることなく、印刷紙等
の表rtiiにプラスチックフィルムを簡便な手段でプ
リントラミネーションを行なう方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for print laminating a plastic film onto a surface of printing paper or the like by a simple means without using adhesives or solvents.

周知のように%紙器、出版物、カード、ポスターその他
の印刷物等の紙製品(以下印刷紙等という)には、その
印刷面の保M、#J水、[1油性の何方、更には美麗化
等の目的により、その表面にプラスチックフィルムをラ
ミネートしたものが多く、このような処即を業界では一
般に[プリントラミJもしくニジ「プリントラミネーシ
ョン」と呼称し2ている。
As is well known, paper products such as folding cartons, publications, cards, posters, and other printed matter (hereinafter referred to as printing paper, etc.) are made with In many cases, a plastic film is laminated on the surface for the purpose of printing, etc., and this type of processing is generally referred to as "print lamination" in the industry.

従来このプリントラミネーションは、ラミネータのコー
ティング部において有機溶剤に溶解させだ接清剤をプラ
スチックフィルムに塗布し、乾燥装置において有機溶剤
を飛散させた後、プラスチックフィルムの接着剤塗イ[
1面と印刷紙等とを熱圧湘することによりなされている
。しかるに−に記有機溶剤を使用する方法でH1火災の
危険性等作画の安全性の而並びに臭気の発生、大気の汚
染等環境保全の面で問題があり、捷た省資源の観点から
も好まし、<すく、有機溶剤を使用しないですむラミネ
ーション方法の出現が強く要望されていた。
Conventionally, this print lamination involves applying a cleaning agent dissolved in an organic solvent to the plastic film in the coating section of the laminator, scattering the organic solvent in a drying device, and then applying adhesive to the plastic film.
This is done by applying heat and pressure to one side and printing paper. However, the method using organic solvents has problems in terms of safety in drawing, such as the danger of H1 fires, as well as in terms of environmental protection, such as the generation of odors and air pollution. However, there has been a strong demand for a lamination method that does not require the use of organic solvents.

木発1’!11iJ、前記のような技術的課題に鑑み、
木発明者らは鋭意研究を重ねた結果、接着剤、溶剤を用
いることなく、印刷紙等の表面にプラスチックフイルノ
・を簡便な手段でプリントラミネーシHンを行なう方法
を発す1するに到奥でt・す、その要旨とするところは
、感〆(接着性樹脂層が積層された複合ポリプロピレン
系フィルムの該感熱接着性樹脂層と、印刷紙等の印刷面
とが合わされるように給送12.かつ加熱された金属ロ
ール側に複合ポリプロピレン系フィルムが接し、ゴム!
ゴール側に印刷紙等が接するように金属ロールとゴムロ
ールからなるピング” lj−ル間をim l−、て熱
り一着する。r!i、 [S)る。
Kihatsu 1'! 11iJ, in view of the above technical issues,
As a result of intensive research, the inventors of the wood industry have come up with a method for laminating plastic films onto the surface of printing paper using simple means without using adhesives or solvents. In the back, the gist is that the heat-sensitive adhesive resin layer of the composite polypropylene film on which the adhesive resin layer is laminated is aligned with the printed surface of printing paper, etc. Feeding 12.The composite polypropylene film comes into contact with the heated metal roll side, and the rubber!
Place the printing paper between the metal roll and rubber roll so that it is in contact with the goal side.

以1・、木発FJl’lの夾h(Il、aφ様を下記に
訂i71にする。
1. The following is the revision i71 of Kihatsu FJl'l's Il, aφ.

未発rI11におけるボリア°tJピレン糸フィル” 
ト出n−ヘプタノ抽出残分9o%以十、のポリゾロピレ
ノIt’ 独市合体、 Q−オレフィン含有Rtが5モ
ル%以Fのプロピレン−(シーオレフィン共重合体、あ
るいにl−〜タルのプロピレン含有量が95モル%以」
二と在るような配合のプロピレン単独重合体とプロピレ
ン−α−オレフィン共重合体の1% 合%J 。
Boria°tJ pyrene thread fill in undeveloped rI11”
PolyzolopyrenoIt' with a n-heptano extraction residue of 90% or more, a propylene (se-olefin copolymer) with a Q-olefin content of Rt of 5 mol% or more, or Propylene content is 95 mol% or more
1% J of propylene homopolymer and propylene-α-olefin copolymer blended as follows.

及び大発明のフィルムgBB時に発生するフィルム屑を
混合1−だ」二記ポリプロピレン系樹脂等からなるフィ
ルムを指し、 If、さけ特に制限はないが通常15乃
至20μ厚のフィルムが好んで使用される。
and the film of the great invention gBB film scraps generated during BB are mixed 1-2. Refers to a film made of polypropylene resin, etc. If, there is no particular restriction, but usually a film with a thickness of 15 to 20 μm is preferably used. .

なお、ポリプロピレン系フィルムに着色や表面艶消し処
理を施、したものや、滑剤、アンチブロッキング剤、安
定剤、紫外線吸収剤、帯電防止剤等を添加したものも木
発1.1の利用に供されることは云う迄も々い。この際
、ポリプロピレン系フィルム1l−12軸延伸されたも
のが好ましいが、無延伸でも1軸延伸でも差支えない。
Additionally, polypropylene films with coloring or surface matte treatment, as well as those to which lubricants, anti-blocking agents, stabilizers, ultraviolet absorbers, antistatic agents, etc. have been added, can also be used in Kippatsu 1.1. There are so many things that can happen. At this time, it is preferable to use a polypropylene film that has been stretched 1l-12 axes, but it may be unstretched or uniaxially stretched.

また、上記ポリプロピレン系フィルムに積層される複合
ポリプロピレン系フィルムの片面を司どる感熱接着性樹
脂層とけ、ポリエチレンもしく幻、エチレンを少なくと
も70重量%(好ましく(rJ:85%以」二)含む共
重合体、捷たはトータルのエチレン含有量が70重風%
(奸才しくtris 5重M1%)以−tzとなるよう
なif+記重合体の混合物からなる層が望ましい。そし
てエチレンと共重合される単量体については、箱別な制
限はなく、エチレンと共重合可能な単hi体であれば良
い。例えば、プロピレン、ブテン−1、ムギセン−1,
酢酸ビニル。
In addition, the heat-sensitive adhesive resin layer on one side of the composite polypropylene film laminated on the polypropylene film may be made of polyethylene or a material containing at least 70% by weight (preferably (rJ: 85% or more) of ethylene). Polymer, sludge or total ethylene content is 70%
A layer consisting of a mixture of if + polymers such that (skillfully tris 5 weight M1%) or less is desirable. There are no particular restrictions on the monomer to be copolymerized with ethylene, and any monomer that can be copolymerized with ethylene may be used. For example, propylene, butene-1, mugisene-1,
Vinyl acetate.

アクリル酸エチル、アクリル酸等が例示される。Examples include ethyl acrylate and acrylic acid.

甘だ、共重合後方水分解や金属イオンによる架橋qf性
させたものや、無水マレイン酸等をグラフト重合させt
cものも大発明の利/IIK供し得る。しかし、トータ
ルエチレン含有量が70重Jit96未満の場合では、
フィルム製Φ:に稈やスリット工程で発生するフィルム
屑をポリプロピレン層にリターンして4′+1利用する
ことができず、省資源の観、点から好捷しくないことも
あるので注意を要する。なX7とならば、これらを敢て
リターンした場合では、誘明性、すべり性、寸法安定性
等が大「11に悪化し、ポリプロピレン系フィルムと1
−、て実用に酎えないものが生起されることも起り得る
可能性があるからである。
It's too easy to use, after copolymerization, water decomposition or cross-linking with metal ions, or graft polymerization with maleic anhydride, etc.
C items can also provide the benefits of great inventions. However, if the total ethylene content is less than 70 FJit96,
It is necessary to be careful because the culm and film waste generated in the slitting process cannot be returned to the polypropylene layer and used for 4'+1, which may not be preferable from the viewpoint of resource conservation. If X7 were used, and if these were deliberately returned, the attractivity, slipperiness, dimensional stability, etc. deteriorated to 11, and it was compared to polypropylene film.
This is because there is a possibility that something impractical may occur.

従ってトルタルのエチレン含イ〕量は最低70軍M%、
さらにいうと85重lit%以十、が望111.いが勿
論この値は制限されるものでなく、エチレンを主成分と
する重合体であれば十分である。女お感熱接着性樹脂層
中に滑剤、アンチブロッキング剤。
Therefore, the ethylene content of Tortal is at least 70 M%,
More specifically, 85 lit% or more is desirable. However, this value is of course not limited, and any polymer containing ethylene as a main component is sufficient. Lubricant and anti-blocking agent in the heat-sensitive adhesive resin layer.

安定剤、着色剤、紫外線吸収剤、帯電防止剤等を添加し
たものも木発す1の利用に供されることはいう壕でもな
い。
It is also true that products to which stabilizers, colorants, ultraviolet absorbers, antistatic agents, etc. have been added can also be used for wood-based products.

ポリプロピレン系フィルムに感熱接着性樹脂層を積層す
る方法d9.公知の如何なる手段を用いても良い。感熱
接着性樹脂層の厚さり、印刷紙等の表面の平岱度、必要
とする接着強度等により適宜選定すれば良いが、通常1
乃至5 Itが好せしい。
Method of laminating a heat-sensitive adhesive resin layer on a polypropylene film d9. Any known means may be used. It may be selected appropriately depending on the thickness of the heat-sensitive adhesive resin layer, the flatness of the surface of the printing paper, etc., the required adhesive strength, etc., but usually 1.
5 It is preferable.

511以」二の厚さのものの使用を妨げないが、不必要
な層19.となる。
This does not preclude the use of a thickness of 511" or more, but it does not prevent unnecessary layers 19. becomes.

感熱接着性樹脂層は、印刷紙等との熱接着性をイルj与
するため、必要に応じ窒素雰囲気下でコロナ放電処理さ
れると望ましい。該雰囲気中の残存酸素濃度は空俄中の
酸素濃度20.9容積%未満で効果が認められ、残存酸
素濃度が低ければ低いほど効果が大きく、好t l−、
<は5容積%以下である。
The heat-sensitive adhesive resin layer is preferably subjected to a corona discharge treatment in a nitrogen atmosphere, if necessary, in order to provide thermal adhesion to printing paper and the like. The effect is recognized when the residual oxygen concentration in the atmosphere is less than 20.9% by volume, and the lower the residual oxygen concentration, the greater the effect.
< is 5% by volume or less.

しかし乍ら、勿論このことは制限を受けるものでなく、
例えば空気中で実施してもいつこうに差しつかえない。
However, this is of course not subject to any restrictions;
For example, it can be carried out in the air at any time.

この際、例えば目II Ni! L/だコロナ放電処P
11強度及び処理時のフィルム?品度は所望の接着強J
Srにより適宜選定すれば良いが1通常30−1.50
W、分/nf 、宇溝〜90℃が好適である。寸た蟹素
雰囲気にする方法は公知のいかなるものでも良く1例え
ばコロナ放電処理機構全体をボックスで囲み、中の空気
を窒素ガスで囮換する方法、コロナhQ電バ1くにスリ
ットから窒素ガスを吹伺ける方法等が例示される。
At this time, for example, eye II Ni! L/da corona discharge treatment P
11 Strength and film during processing? The quality is the desired adhesive strength J
It may be selected appropriately depending on Sr, but 1 usually 30-1.50
W, min/nf, Uzo~90°C is suitable. Any method known in the art may be used to create a small carbonaceous atmosphere.For example, the entire corona discharge treatment mechanism may be enclosed in a box and the air inside may be decoyed with nitrogen gas, or nitrogen gas may be introduced into the corona hQ electric bar through a slit. Examples include how to ask questions.

との際、:10ナカ(型処〃11を行わ々〈ても実施で
きるが、一般に印刷紙等との接着強度が劣る場合もある
It can also be carried out by repeating mold treatment 11 for 10 minutes, but in general, the adhesive strength with printing paper etc. may be poor.

かくして得られた複合ポリプロピレン系フィル1− (
fall チーy” IJントラミネーションr+1フ
ィルム)ト。
The composite polypropylene film 1- (
Fall Chee y” IJ Lamination R + 1 Film) To.

印刷紙等とを郊B′:着するのであるが、来光り1では
ピンチロールで行なう。この際ピンチロールの片方e」
60〜130℃、好1しくは80〜120 ”Cに加熱
された金属ロール、他方はゴムロールを用イ、 [11
’I iJ: 20に6以」二で、複合ポリプロピレン
糸フィルムの感熱接着性樹脂層と印刷紙等の印刷面とが
合わさるようにし、かつ金属ロールに前記フィルムが、
他方のゴムロールに印刷紙等がそれぞれ接するようにし
て通すことによって目的が達成される。この際線圧40
0 KV−以上で1.d、熱圧着1桿でしわの発生も考
えられ、好適とはいい難い。
Printing paper, etc., is placed on the roller B', but in the next step 1, it is carried out using pinch rolls. At this time, one side of the pinch roll
A metal roll heated to 60-130°C, preferably 80-120"C, and a rubber roll on the other hand,
'I iJ: 20 to 6 or more' 2, so that the heat-sensitive adhesive resin layer of the composite polypropylene thread film and the printing surface of printing paper etc. are brought together, and the film is placed on a metal roll,
The purpose is achieved by passing the printing paper or the like through the other rubber roll so that they are in contact with each other. At this time, the linear pressure is 40
1.0 KV- or more. d. Wrinkling may occur after one rod is bonded by thermocompression, so it is difficult to say that it is suitable.

な卦前記のようにフィルムを金属ロール側に接するよう
Vこするのは、金属ロールの熱が有効にフィルム側に作
用させるためであシ、寸だ鏡面にしろ、エンボス面にし
ろ、美麗で接着力大なるラミネーションをさせるだめで
ある。
As mentioned above, rubbing the film so that it is in contact with the metal roll side is so that the heat from the metal roll can effectively act on the film side, and whether it is a mirror surface or an embossed surface, it is beautiful. This prevents lamination with high adhesive strength.

第1図は大発明の方法を図で脱明したもので、フィルム
繰出部(1)で繰出された複合ポリプロピレン糸フ、イ
ルム(2)と、給紙部(3)より繰出された印刷紙(4
)は、加熱金属ロール(6)トゴムロー/I/ tel
 (’) 間で熱li、着され1巻取部(7)で巻取ら
れるか、もl、 <け熱圧着された印刷紙は定寸に切断
され断裁物として集積される。
Figure 1 illustrates the method of the great invention, showing the composite polypropylene yarn film (2) fed out by the film feeding section (1) and the printing paper fed out from the paper feeding section (3). (4
) is a heated metal roll (6) Togomuro/I/ tel
The printing paper that has been thermally bonded between (') and then wound up in the first winding section (7) is then cut to a fixed size and accumulated as cut pieces.

第2図は従来のプリントラミネーションの方法を図で説
明l−かもので、フィルム繰出部1(11で繰出された
ポリプロピレン型層フィルムaυは、コーティング部0
2で有機溶剤に溶解せられた接着剤が塗布され、乾燥部
0埠で有機溶剤を飛散させた後、給紙部0荀より繰出さ
れた印刷紙OQと、加熱金属ロールC11とゴムロール
(17)との間で熱1]着され1巻取部(18)で巻取
るか、もしくは断裁物として集積される。
Figure 2 is a diagram explaining the conventional print lamination method;
After applying the adhesive dissolved in an organic solvent in step 2 and scattering the organic solvent in the drying section 0, the printing paper OQ fed out from the paper feed section 0, heating metal roll C11 and rubber roll (17 ) and then wound up in the first winding section (18) or accumulated as cut pieces.

従って、上記従来の方法によれば、コーディング部02
及び乾燥部0[有]は必要不可欠でかつ装置は大がかり
で高価なものになるばかりで〃く、火災の危険性等作業
の安全性並びに臭気の発生、大気の汚染等環境保全のm
−1で問題があり1寸だ省資源の観点からも好寸しくな
いのに対し、大発明では有機溶剤を全く使用しないので
、従来の欠点を解消した優れたプリントラミネーション
方法であることが理解できる。
Therefore, according to the above conventional method, the coding unit 02
A drying section and a drying section are indispensable, and the equipment is large-scale and expensive.It also poses a risk to work safety such as the risk of fire, and to environmental protection such as the generation of odors and air pollution.
-1 has a problem and the size of 1 inch is not good from the perspective of resource saving, but the great invention does not use any organic solvents, so it is understood that it is an excellent print lamination method that eliminates the drawbacks of the conventional method. can.

次に大発明の具体的な実施例を比較例表具に掲げ−(説
り1する。世【7木発1)I Elこれらの実施例に制
限きhるものでないことは勿論である。
Next, specific examples of the great invention are listed as comparative examples.It goes without saying that the present invention is not limited to these examples.

< ’t: ノ)ili 例 1 〉 結晶t′lポリ10ピレノの溶融押出フィルム(厚さ7
5071 )を130°Cにおいてロール延伸機によυ
縦方向に5倍に延伸し1次いで該縦−軸延伸フイルム上
に、酢酸ビニル含有112軍量%、 M112のエチレ
ン−酢酸ビニル共重合体を厚さ3011になるように溶
融神明ラミネートし、しかる後160℃にて横方向に1
0倍延伸し、複合二軸延伸ポリプロピレン系フィルムヲ
flだ。
<'t: ノ)ili Example 1 > Crystalline t′l melt-extruded film of poly-10-pyreno (thickness 7
5071) by a roll drawing machine at 130°C.
The film was stretched 5 times in the longitudinal direction, and then an M112 ethylene-vinyl acetate copolymer containing 112% by weight of vinyl acetate was laminated on the longitudinally-axially stretched film to a thickness of 3011 mm. 1 laterally at 160℃
It is a composite biaxially stretched polypropylene film that has been stretched 0 times.

このフィルムの厚さは1871で、このうちエチレン−
酢酸ビニル共重合体層の厚さは3 /Zであった。
The thickness of this film is 1871 mm, of which ethylene-
The thickness of the vinyl acetate copolymer layer was 3/Z.

〈実施例2〉 実Mi 例1で得だフィルムのエチレン−酢酸ビニル共
lj合体層面を、窒素と酸素の混合比を種々変えた雰囲
気下で、フィルム温度60℃、処理強度60W1分/n
fでコロナ放電処理を施した。
<Example 2> Actual Mi The ethylene-vinyl acetate combined layer surface of the film obtained in Example 1 was treated at a film temperature of 60°C and a treatment strength of 60W 1 min/n in an atmosphere with various nitrogen and oxygen mixing ratios.
Corona discharge treatment was performed at f.

次いでこの複合二軸延伸ポリプロピレン系フィルムと印
刷をMli したアート紙とを種々の温度に加熱された
金属ロールと線圧50ψのゴム製ピンチロール間で、前
記所定の合わせ状態の下に20m/う〕の速度で熱LT
E着してラミネートした。
Next, this composite biaxially oriented polypropylene film and Mli-printed art paper were rolled for 20 m/fur in the predetermined alignment condition between metal rolls heated to various temperatures and rubber pinch rolls with a linear pressure of 50 ψ. Heat LT at the speed of ]
I arrived at E and laminated it.

かくして得られたラミネート製品のカール状態、接着強
度を第3図に示す。同図において縦軸は金属ロールの温
度((力を、横軸に窒素/酸素の容積比を示17たもの
で、Aゾーンは製品がカールし、Bゾーンt−J良好な
製品が<Xられ、Cゾーンは接着強度不足を示す。なお
第3図に、4.:実hni例における好せl−い温度範
囲を示したものであってこれに限定されるものでない。
The curl state and adhesive strength of the thus obtained laminate product are shown in FIG. In the figure, the vertical axis shows the temperature ((force) of the metal roll, and the horizontal axis shows the volume ratio of nitrogen/oxygen. In the A zone, the product curls, and in the B zone t-J, the good product is <X The C zone shows insufficient adhesion strength. Fig. 3 shows the preferable temperature range in the actual example 4., but is not limited thereto.

製品によってはカールしても問題のないものもあるし1
寸た接着強度が若干不足しても使用可能なものもあり、
腸に接着強度は印刷紙等の桐質によって変動するのが′
超で、要するに木発す1け加熱された金属ロールを用い
る限り実施例
Depending on the product, there may be no problem even if it curls.1
There are some products that can be used even if the adhesive strength is slightly insufficient.
The strength of adhesion to the intestines varies depending on the material of the printing paper, etc.
In other words, as long as a metal roll heated by wood is used, it is an example.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は未発IJ’l方法の説明図、第2図は従来方法
の脱FV1図、第3図は木兄FlliK係る一実施例を
示すフィルムを使用してラミネートした場合のカール状
態、接着強度の試験結果を示したグラフである。 m・・・フィルム静出部、(2)・・・複合ポリプロピ
レン糸フィルム、(3)・・・給紙部、(4)・・・印
刷紙、(5)・・・加熱金属ロール、 (61・・・ゴ
ムロール、 +71・・・巻取部。
Fig. 1 is an explanatory diagram of the undeveloped IJ'l method, Fig. 2 is an explanatory diagram of the conventional method of removing FV1, and Fig. 3 is a curl state when laminated using a film showing an example of Kinoe FlliK. It is a graph showing the test results of adhesive strength. m...Film ejection part, (2)...Composite polypropylene thread film, (3)...Paper feeding part, (4)...Printing paper, (5)...Heating metal roll, ( 61... Rubber roll, +71... Winding section.

Claims (1)

【特許請求の範囲】 1 感熱接着性樹脂層が積層された複合ポリプロピレン
系フィルムの訪感熱接着性樹脂層と、印刷紙等の印刷面
とが合わされるように給送させ、かつ加熱された金属ロ
ール側に複合ポリプロピレン系フィルムが接し、ゴムロ
ール側に印刷紙等が接するように金属ロールとゴムロー
ルからなるピンチロール間を通して熱圧着することを4
;r徴とするプリントラミネーション方法。 2.1色熱接着性樹脂層がエチレンを主成分とする重合
体である1′漬許請求の範囲第1項記載のプリントラミ
ネーション方法。 3 熱圧着する際の線圧が20 !1y/c+++以上
、であるね許請求の範囲第1項記載のプリントラミネー
ション方法。
[Scope of Claims] 1. A heat sensitive adhesive resin layer of a composite polypropylene film laminated with a heat sensitive adhesive resin layer and a printed surface of printing paper etc. are fed and heated. The composite polypropylene film is in contact with the roll side, and the printing paper, etc. is in contact with the rubber roll side.
;Print lamination method with r sign. 2. The print lamination method according to claim 1, wherein the one-color thermoadhesive resin layer is a polymer containing ethylene as a main component. 3 Linear pressure during thermocompression bonding is 20! 1y/c+++ or more. The print lamination method according to claim 1.
JP57208760A 1982-11-26 1982-11-26 Print lamination method Granted JPS5924669A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57208760A JPS5924669A (en) 1982-11-26 1982-11-26 Print lamination method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57208760A JPS5924669A (en) 1982-11-26 1982-11-26 Print lamination method

Publications (2)

Publication Number Publication Date
JPS5924669A true JPS5924669A (en) 1984-02-08
JPH022411B2 JPH022411B2 (en) 1990-01-18

Family

ID=16561626

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57208760A Granted JPS5924669A (en) 1982-11-26 1982-11-26 Print lamination method

Country Status (1)

Country Link
JP (1) JPS5924669A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60166450A (en) * 1984-02-10 1985-08-29 日本石油化学株式会社 Manufacture of reinforced laminate
JPS60184826A (en) * 1984-03-03 1985-09-20 Gunze Ltd Print lamination
JPS60236727A (en) * 1984-05-10 1985-11-25 Gunze Ltd Print lamination

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52126487A (en) * 1976-04-16 1977-10-24 Toyobo Co Ltd Laminated films of polypropylene
JPS54106583A (en) * 1978-02-09 1979-08-21 Nippon Petrochemicals Co Ltd Method of making laminate
JPS55137136A (en) * 1979-04-13 1980-10-25 Tokuyama Soda Co Ltd Production of polypropylene composition film
JPS5642652A (en) * 1979-09-17 1981-04-20 Gunze Kk Film for print laminate which can thermally be attached on printing paper* etc*
JPS56109726A (en) * 1980-02-04 1981-08-31 Gunze Ltd Manufacture of laminate film

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52126487A (en) * 1976-04-16 1977-10-24 Toyobo Co Ltd Laminated films of polypropylene
JPS54106583A (en) * 1978-02-09 1979-08-21 Nippon Petrochemicals Co Ltd Method of making laminate
JPS55137136A (en) * 1979-04-13 1980-10-25 Tokuyama Soda Co Ltd Production of polypropylene composition film
JPS5642652A (en) * 1979-09-17 1981-04-20 Gunze Kk Film for print laminate which can thermally be attached on printing paper* etc*
JPS56109726A (en) * 1980-02-04 1981-08-31 Gunze Ltd Manufacture of laminate film

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60166450A (en) * 1984-02-10 1985-08-29 日本石油化学株式会社 Manufacture of reinforced laminate
JPH0466695B2 (en) * 1984-02-10 1992-10-26 Nippon Petrochemicals Co Ltd
JPS60184826A (en) * 1984-03-03 1985-09-20 Gunze Ltd Print lamination
JPS60236727A (en) * 1984-05-10 1985-11-25 Gunze Ltd Print lamination

Also Published As

Publication number Publication date
JPH022411B2 (en) 1990-01-18

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