JPS6312792B2 - - Google Patents
Info
- Publication number
- JPS6312792B2 JPS6312792B2 JP56032692A JP3269281A JPS6312792B2 JP S6312792 B2 JPS6312792 B2 JP S6312792B2 JP 56032692 A JP56032692 A JP 56032692A JP 3269281 A JP3269281 A JP 3269281A JP S6312792 B2 JPS6312792 B2 JP S6312792B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- ethylene
- heat
- biaxially oriented
- weight
- 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
- 229920006378 biaxially oriented polypropylene Polymers 0.000 claims description 14
- 239000011127 biaxially oriented polypropylene Substances 0.000 claims description 14
- 239000002131 composite material Substances 0.000 claims description 13
- 239000004840 adhesive resin Substances 0.000 claims description 12
- 229920006223 adhesive resin Polymers 0.000 claims description 12
- -1 polyethylene Polymers 0.000 claims description 12
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 10
- 239000005977 Ethylene Substances 0.000 claims description 10
- 238000003475 lamination Methods 0.000 claims description 8
- 238000009736 wetting Methods 0.000 claims description 8
- 238000004381 surface treatment Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 description 9
- 229920001155 polypropylene Polymers 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 239000005038 ethylene vinyl acetate Substances 0.000 description 6
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 6
- 238000003851 corona treatment Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 229920006255 plastic film Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 229920001384 propylene homopolymer Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Laminated Bodies (AREA)
Description
本発明は、印刷紙等とラミネーシヨンを行う際
に、接着剤、溶剤を用いることなく熱圧着のみで
ラミネーシヨンが可能なプリントラミネーシヨン
用フイルムに関する。
周知のように、紙器、出版物、カード、ポスタ
ー、その他の印刷物等紙製品には、その印刷面の
保護、耐水、耐油性の付与、更には美麗化等の目
的により、その表面にプラスチツクフイルムをラ
ミネートしたものが多い。このような処理を当業
界では一般に「プリントラミネーシヨン」と呼称
している。
従来このプリントラミネーシヨンは、ラミネー
ターのコーテイング部において有機溶剤に溶解せ
られた接着剤をプラスチツクフイルムに塗布し、
乾燥部において有機溶剤を飛散せしめた後、プラ
スチツクフイルムの接着剤塗布面と印刷紙とを熱
圧着することによりなされている。
しかるに、上記有機溶剤を使用する方法では、
火災の危険性等作業の安全性の面並びに臭気の発
生、大気の汚染等環境保全の面で問題があり、ま
た省資源の観点からも好ましくなく、有機溶剤を
使用しないですむラミネーシヨン方法の出現が強
く要望されているところである。
このような技術的課題に鑑み本発明者は鋭意研
究を重ねた結果、印刷紙等とラミネーシヨンを行
う際に、接着剤、溶剤を用いる必要なく熱圧着の
みでラミネーシヨンが可能な新しいプリントラミ
ネーシヨン用フイルムを得るに到つたものであ
る。すなわち、新規プリントラミネーシヨン用フ
イルムの提供に関する本発明の要旨は、
二軸延伸ポリプロピレン系フイルムと、厚さが
1〜5μを有し、かつ表面処理することにより少
なくとも濡れ張力36dyn/cmを保持する感熱接着
性樹脂層との2層からなる印刷紙等に熱圧着可能
な複合二軸延伸ポリプロピレン系フイルムであ
り、前記感熱接着性樹脂層が、ポリエチレンもし
くはエチレンを少なくとも80重量%含む共重合
体、またはトータルのエチレン含有量が80重量%
以上である前記重合体の混合物からなる点にあ
る。
以下、本発明の実施態様を下記に詳述する。
本発明における二軸延伸ポリプロピレン系フイ
ルムとは、沸騰n−ヘプタン抽出残分90%以上の
プロピレン単独重合体、α−オレフイン含有量が
5モル%以下のプロピレン−α−オレフイン共重
合体、あるいはトータルのプロピレン含有量が95
モル%以上となるような配合のプロピレン単独重
合体とプロピレン−α−オレフイン共重合体の混
合物、及び本発明に係るプリントラミネーシヨン
用フイルムの屑を混合した上記ポリプロピレン系
樹脂からなる二軸延伸フイルムを指し、通常15乃
至20μ厚のフイルムが好んで使用される。なお、
二軸延伸ポリプロピレン系フイルムに着色や表面
艶消し処理を施したものも本発明の利用に供され
ることは云う迄もない。
また、上記二軸延伸ポリプロピレン系フイルム
に積層される感熱接着性樹脂層とは、ポリエチレ
ンもしくはエチレンを少なくとも80重量%(好ま
しくは85重量%以上)含む共重合体、またはトー
タルのエチレン含有量が80重量%(好ましくは85
重量%)以上となるような前記重合体の混合物か
らなる層を指し、該感熱接着性樹脂層は表面処理
することにより、濡れ張力が少なくとも36dyn/
cm以上に保持されていることが必要である。エチ
レンと共重合される単量体ついては、特別な制限
はなく、エチレンと共重合可能な単量体であれば
良い。例えば、プロピレン、ブデン−1、酢酸ビ
ニル、アクリル酸エチル、アクリル酸等が例示さ
れる。また、共重合後加水分解や金属イオンによ
る架橋等変性させたものや、無水マレイン酸等を
グラフト重合させたものも、そのトータルのエチ
レン含有量が80重量%以上である場合には、本発
明の利用に供し得る。しかし、トータルエチレン
含有量が80重量%未満の場合では、フイルム製造
工程やスリツト工程で発生するフイルム屑をポリ
プロピレン層にリターンして再利用することがで
きず、省資源の観点から好ましくない。なんとな
らば、これらを敢てリターンした場合では、透明
性、すべり性、寸法安定性等が大巾に悪化し、二
軸延伸ポリプロピレン系フイルムとして実用に耐
えないものが生起されるからである。
二軸延伸ポリプロピレン系フイルムに感熱接着
性樹脂層を積層する方法は、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は、印
刷紙等表面の平滑度、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5μが好ま
しい。このさい1μ未満では接着強度が不足し、
5μを超えると透明性を害するおそれがあり好ま
しくない。
感熱接着性樹脂層は、表面処理により濡れ張力
が少なくとも36dyn/cm、好ましくは38dyn/cm
以上に保持されていることが必要である。すなわ
ち、36dyn/cm未満の濡れ張力では、印刷紙等と
の接着強度が不足し、実用に耐えないからであ
る。その表面処理方法は、フレーム処理、化学薬
品処理等公知の如何なる手段でも良いが、コロナ
放電処理が最も簡便である。なお、ここで濡れ張
力とは、ホルムアミドとエチレングリコールモノ
エチルエーテルとの混合液によるJIS K 6768に
規定された測定方法に基づく値を示している。
かくして得られた複合二軸延伸ポリプロピレン
系フイルム(即ちプリントラミネーシヨン用フイ
ルム)と印刷紙等を熱圧着ラミネートする手段と
しては種々の方法が考えられ、公知の如何なる手
段でも良いが、通常加熱されたピンチロールで行
えば充分である。例えばピンチロールの片方は60
乃至130℃、好ましくは80乃至120℃に加熱された
金属ロール、他方はゴムロールを用い、線圧5
Kg/cm以上、好ましくは20Kg/cm以上で、複合二
軸延伸ポリプロピレン系フイルムの感熱接着性樹
脂層と印刷紙の印刷面とが合わされるようにし、
かつ金属ロールに複合二軸延伸ポリプロピレン系
フイルムが、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り目的が達成され
る。
次に、本発明の具体的な実施例を比較例と共に
掲げて説明する。但し、本発明はこれらの実施例
のみに制限されるものでないことはもとよりであ
る。
〈実施例 1〉
結晶性ポリプロピレンの溶融押出フイルム(厚
さ750μ)を130℃においてロール延伸機により縦
方向に5倍に延伸し、次いで該縦一軸延伸フイル
ム上に、酢酸ビニル含有量10重量%、M,I6のエ
チレン−酢酸ビニル共重合体を厚さ30μになるよ
うに溶融押出ラミネートし、しかる後160℃にて
横方向に10倍延伸し、エチレン−酢酸ビニル共重
合体層面を処理強度40W.min/m2でコロナ放電
処理を施こして所期の複合二軸延伸ポリプロピレ
ン系フイルムを得た。
このフイルムの厚さは18μで、このうちエチレ
ン−酢酸ビニル共重合体層の厚さは3μであり、
またエチレン−酢酸ビニル共重合体層面の濡れ張
力と42dyn/cmであつた。
次にこの複合二軸延伸ポリプロピレン系フイル
ムの前記濡れ張力42dyn/cmに保持されたエチレ
ン−酢酸ビニル共重合体層と印刷紙等の印刷面と
を100℃に加熱された金属ロールと線圧50Kg/cm
のシリコンゴム製ピンチロール間で、前期所定の
合わせ状態の下に熱圧着してラミネートした。
かくして得られたラミネート物を剥離すると、
印刷紙が破れ、充分な接着性を具有していること
が確認された。
〈比較例 1〉
コロナ放電処理を実施しないことを除き、上記
実施例1と同様にして複合二軸延伸ポリプロピレ
ン系フイルムを製造した。この複合フイルムのエ
チレン−酢酸ビニル共重合体層面の濡れ張力は
33dyn/cm以下であつた。
しかして、これを実施例1と同様に温度100℃、
線圧50Kg/cmで印刷紙と熱圧着した結果、両者は
全く接着しなかつた。
〈実施例 2〉
感熱接着性樹脂としてアクリル酸エチル含有量
7重量%、M,I4のエチレン−アクリル酸エチル
共重合体を用いた点を除き、実施例1と全く同様
にして複合二軸延伸ポリプロピレン系フイルムを
製造した。
このフイルムのエチレン−アクリル酸エチル共
重合体層面の濡れ張力は41dyn/cmであつた。
次いで、実施例1と同じ装置により、温度110
℃、線圧50Kg/cmで印刷紙と熱圧着した。
かくして得られたラミネート物を剥離すると、
印刷紙が破れ、充分な接着性を具有していること
が確認できた。
〈比較例 2〉
コロナ放電処理を実施しないことを除き、上記
実施例2と同様にして複合二軸延伸ポリプロピレ
ン系フイルムを製造した。この複合フイルムのエ
チレン−アクリル酸エチル共重合体層面の濡れ張
力は33dyn/cm以下であつた。
しかして、これを実施例2と同様に温度110℃、
線圧50Kg/cmで印刷紙と熱圧着した結果、両者は
全く接着しなかつた。
〈実施例 3〉
実施例1で製造した複合二軸延伸ポリプロピレ
ン系フイルムのスリツト工程で発生した端尺を粉
砕したもの10重量部と、実施例1で使用した結晶
ポリプロピレン樹脂100重量部の混合物を溶融押
出し(厚さ750μ)、130℃においてロール延伸機
により縦方向に5倍に延伸し、次いで160℃にて
横方向に10倍延伸して厚さ15μのフイルムを得
た。このフイルムの物性を下表に示す。
〈比較例 3〉
実施例1で使用した結晶性ポリプロピレン樹脂
のみを用いたことを除き、上記実施例3と全く同
様にして厚さ15μのフイルムを得た。このフイル
ムの物性を下表に示す。
The present invention relates to a print lamination film that can be laminated with printing paper or the like by only thermocompression bonding without using adhesives or solvents. As is well known, paper products such as paper cartons, publications, cards, posters, and other printed matter are coated with plastic film for the purpose of protecting the printed surface, imparting water resistance, oil resistance, and beautification. Many are laminated. Such processing is generally referred to as "print lamination" in the art. Conventionally, this print lamination involves applying an adhesive dissolved in an organic solvent to a plastic film in the coating section of a laminator.
After the organic solvent is scattered in a drying section, the adhesive-coated surface of the plastic film and the printing paper are bonded under heat and pressure. However, in the method using the above organic solvent,
There are problems in terms of work safety such as the risk of fire, as well as environmental protection such as the generation of odors and air pollution, and it is also undesirable from the perspective of resource conservation. There is a strong demand for its appearance. In view of these technical issues, the inventor of the present invention has conducted extensive research and has developed a new printed laminate that can be laminated with printing paper, etc. by only thermocompression bonding without the need to use adhesives or solvents. This led to the production of a film for use in photography. That is, the gist of the present invention relates to the provision of a novel film for print lamination, which comprises a biaxially oriented polypropylene film, having a thickness of 1 to 5 μm, and having a wetting tension of at least 36 dyn/cm by surface treatment. A composite biaxially oriented polypropylene film that can be thermocompression bonded to a printing paper or the like, consisting of a two-layer heat-sensitive adhesive resin layer, the heat-sensitive adhesive resin layer being polyethylene or a copolymer containing at least 80% by weight of ethylene; or total ethylene content of 80% by weight
It consists of a mixture of the above-mentioned polymers. Embodiments of the present invention will be described in detail below. The biaxially oriented polypropylene film in the present invention is a propylene homopolymer with a boiling n-heptane extraction residue of 90% or more, a propylene-α-olefin copolymer with an α-olefin content of 5 mol% or less, or a total Propylene content of 95
A biaxially stretched film made of the above-mentioned polypropylene resin, which is mixed with a mixture of a propylene homopolymer and a propylene-α-olefin copolymer in a proportion of mol % or more, and scraps of the film for print lamination according to the present invention. A film with a thickness of 15 to 20 μm is usually used. In addition,
It goes without saying that biaxially oriented polypropylene films subjected to coloring or surface matte treatment can also be used in the present invention. The heat-sensitive adhesive resin layer laminated on the biaxially oriented polypropylene film is polyethylene or a copolymer containing at least 80% by weight (preferably 85% or more) of ethylene, or a total ethylene content of 80% by weight or more. % by weight (preferably 85
% by weight) or more, and the heat-sensitive adhesive resin layer can be surface-treated to have a wet tension of at least 36 dyn/
It is necessary that it is maintained at a height of cm or more. 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. Examples include propylene, butene-1, vinyl acetate, ethyl acrylate, and acrylic acid. In addition, products modified by copolymerization such as hydrolysis or crosslinking with metal ions, or products modified by graft polymerization with maleic anhydride, etc., can also be used in the present invention if their total ethylene content is 80% by weight or more. It can be used for However, if the total ethylene content is less than 80% by weight, film waste generated in the film manufacturing process or slitting process cannot be returned to the polypropylene layer and reused, which is undesirable from the viewpoint of resource conservation. This is because, if these are intentionally returned, the transparency, slipperiness, dimensional stability, etc. will be greatly deteriorated, resulting in a biaxially oriented polypropylene film that cannot be put to practical use. Any known method may be used to laminate the heat-sensitive adhesive resin layer on the biaxially stretched polypropylene film. The thickness of the heat-sensitive adhesive resin layer may be appropriately selected depending on the smoothness of the surface of the printing paper, the required adhesive strength, etc., and is usually preferably 1 to 5 μm. At this time, if it is less than 1μ, the adhesive strength will be insufficient,
If it exceeds 5μ, transparency may be impaired, which is not preferable. The heat-sensitive adhesive resin layer has a wetting tension of at least 36 dyn/cm, preferably 38 dyn/cm due to surface treatment.
It is necessary to maintain the above value. That is, if the wet tension is less than 36 dyn/cm, the adhesive strength with printing paper etc. will be insufficient and it will not be practical. The surface treatment method may be any known means such as flame treatment or chemical treatment, but corona discharge treatment is the simplest. Note that the wetting tension herein refers to a value based on a measurement method specified in JIS K 6768 using a mixed solution of formamide and ethylene glycol monoethyl ether. Various methods can be considered for thermocompression laminating the thus obtained composite biaxially oriented polypropylene film (i.e., film for print lamination) and printing paper, etc., and any known method may be used. A pinch roll is sufficient. For example, one side of the pinch roll is 60
Using a metal roll heated to 130°C to 130°C, preferably 80 to 120°C, and a rubber roll on the other hand, a linear pressure of 5
Kg/cm or more, preferably 20 Kg/cm or more, so that the heat-sensitive adhesive resin layer of the composite biaxially oriented polypropylene film and the printing surface of the printing paper are brought together,
The purpose is achieved by passing a composite biaxially oriented polypropylene film through a metal roll and a printing paper or the like through a rubber roll so that they are in contact with each other. Next, specific examples of the present invention will be described together with comparative examples. However, it goes without saying that the present invention is not limited only to these examples. <Example 1> A melt-extruded crystalline polypropylene film (thickness 750μ) was stretched 5 times in the longitudinal direction using a roll stretching machine at 130°C, and then a vinyl acetate content of 10% by weight was applied onto the longitudinally uniaxially stretched film. , M, I6 ethylene-vinyl acetate copolymer was melt-extruded and laminated to a thickness of 30 μm, and then stretched 10 times in the transverse direction at 160°C, and the ethylene-vinyl acetate copolymer layer surface was processed to give a strength A corona discharge treatment was performed at 40 W.min/m 2 to obtain the desired composite biaxially stretched polypropylene film. The thickness of this film is 18μ, of which the thickness of the ethylene-vinyl acetate copolymer layer is 3μ.
The wetting tension of the ethylene-vinyl acetate copolymer layer was 42 dyn/cm. Next, the ethylene-vinyl acetate copolymer layer maintained at the wet tension of 42 dyn/cm of this composite biaxially oriented polypropylene film and the printing surface of printing paper etc. are heated to a metal roll heated to 100°C and a linear pressure of 50 kg is applied. /cm
They were then heat-pressed and laminated between silicone rubber pinch rolls under the predetermined alignment conditions. When the laminate thus obtained is peeled off,
The printed paper was torn and it was confirmed that it had sufficient adhesiveness. <Comparative Example 1> A composite biaxially oriented polypropylene film was produced in the same manner as in Example 1 above, except that the corona discharge treatment was not performed. The wetting tension of the ethylene-vinyl acetate copolymer layer surface of this composite film is
It was less than 33 dyn/cm. Then, as in Example 1, the temperature was 100°C.
As a result of thermocompression bonding with printing paper at a linear pressure of 50 kg/cm, the two did not adhere at all. <Example 2> Composite biaxial stretching was carried out in exactly the same manner as in Example 1, except that an ethylene-ethyl acrylate copolymer of M and I4 with an ethyl acrylate content of 7% by weight was used as the heat-sensitive adhesive resin. A polypropylene film was produced. The wetting tension of the ethylene-ethyl acrylate copolymer layer surface of this film was 41 dyn/cm. Then, using the same apparatus as in Example 1, the temperature was set to 110
It was thermocompression bonded to printing paper at ℃ and linear pressure of 50 kg/cm. When the laminate thus obtained is peeled off,
The printed paper was torn and it was confirmed that it had sufficient adhesiveness. <Comparative Example 2> A composite biaxially stretched polypropylene film was produced in the same manner as in Example 2 above, except that the corona discharge treatment was not performed. The wetting tension of the ethylene-ethyl acrylate copolymer layer surface of this composite film was 33 dyn/cm or less. Then, as in Example 2, the temperature was 110°C.
As a result of thermocompression bonding with printing paper at a linear pressure of 50 kg/cm, the two did not adhere at all. <Example 3> A mixture of 10 parts by weight of the end pieces generated in the slitting process of the composite biaxially oriented polypropylene film produced in Example 1 and 100 parts by weight of the crystalline polypropylene resin used in Example 1 was prepared. The film was melt extruded (thickness: 750 μm), stretched 5 times in the machine direction at 130° C. using a roll stretching machine, and then stretched 10 times in the cross direction at 160° C. to obtain a film with a thickness of 15 μm. The physical properties of this film are shown in the table below. <Comparative Example 3> A film with a thickness of 15 μm was obtained in exactly the same manner as in Example 3 above, except that only the crystalline polypropylene resin used in Example 1 was used. The physical properties of this film are shown in the table below.
【表】
以上の実施例及び比較例の結果によると、まず
実施例1,2及び比較例1,2からは感熱接着性
樹脂層を表明処理することにより初めて有効な接
着性が具現されることが確認でき、また実施例3
及び比較例3からは、本発明で使用するフイルム
がその屑のリターンが可能であり、省資源の観点
からもきわめて有利なものであることが確認でき
る。
本発明は以上に述べた通りであつて、本発明に
係るプリントラミネーシヨン用フイルムを用いれ
ば、印刷紙等にラミネートするに際し、これを熱
圧着するのみで足り、これによつて印刷紙等との
充分な接着性が保証されるものである。従つて、
本発明によれば、有機溶剤を使用する従来ラミネ
ート法における問題点が悉く一掃され、しかもそ
のフイルム屑等のリターンも可能であつて省資源
の目的にも合致し得るものとなる。[Table] According to the results of the above Examples and Comparative Examples, first, from Examples 1 and 2 and Comparative Examples 1 and 2, effective adhesiveness is realized only by applying a surface treatment to the heat-sensitive adhesive resin layer. can be confirmed, and Example 3
From Comparative Example 3, it can be confirmed that the film used in the present invention allows for the return of its waste, and is extremely advantageous from the viewpoint of resource saving. The present invention is as described above, and if the film for print lamination according to the present invention is used, when laminating it onto printing paper, etc., it is sufficient to bond it with heat and pressure, thereby making it possible to bond the film to printing paper, etc. This ensures sufficient adhesion. Therefore,
According to the present invention, all of the problems associated with conventional laminating methods that use organic solvents are eliminated, and furthermore, it is possible to return the film waste, etc., and it can also meet the purpose of resource saving.
Claims (1)
が1〜5μを有し、かつ表面処理することにより
少なくとも濡れ張力36dyn/cmを保持する感熱接
着性樹脂層との2層からなる印刷紙等に熱圧着可
能な複合二軸延伸ポリプロピレン系フイルムであ
り、前記感熱接着性樹脂層が、ポリエチレンもし
くはエチレンを少なくとも80重量%含む共重合
体、またはトータルのエチレン含有量が80重量%
以上である前記重合体の混合物からなることを特
徴とするプリントラミネーシヨン用フイルム。1 A printing paper, etc. consisting of two layers, a biaxially oriented polypropylene film and a heat-sensitive adhesive resin layer having a thickness of 1 to 5 μm and having a wetting tension of at least 36 dyn/cm by surface treatment, is heated. It is a composite biaxially oriented polypropylene film that can be pressure-bonded, and the heat-sensitive adhesive resin layer is made of polyethylene or a copolymer containing at least 80% by weight of ethylene, or the total ethylene content is 80% by weight.
A film for print lamination comprising a mixture of the above polymers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3269281A JPS57146653A (en) | 1981-03-05 | 1981-03-05 | Film for printed lamination |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3269281A JPS57146653A (en) | 1981-03-05 | 1981-03-05 | Film for printed lamination |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59143808A Division JPS60132738A (en) | 1984-07-10 | 1984-07-10 | Print lamination method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57146653A JPS57146653A (en) | 1982-09-10 |
JPS6312792B2 true JPS6312792B2 (en) | 1988-03-22 |
Family
ID=12365906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3269281A Granted JPS57146653A (en) | 1981-03-05 | 1981-03-05 | Film for printed lamination |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57146653A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60109834A (en) * | 1983-11-18 | 1985-06-15 | グンゼ株式会社 | Film for laminating print |
JPS60198223A (en) * | 1984-03-22 | 1985-10-07 | Showa Denko Kk | Preparation of multi-layered film |
JPS6150436U (en) * | 1984-09-05 | 1986-04-04 | ||
JP2007204931A (en) * | 2006-01-31 | 2007-08-16 | Shuji Endo | Joist keeper, joist system, and double floor |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4969784A (en) * | 1972-10-26 | 1974-07-05 | ||
JPS49101420A (en) * | 1972-10-17 | 1974-09-25 | ||
JPS5268279A (en) * | 1975-12-04 | 1977-06-06 | Toyobo Co Ltd | Composite films of polypropylene withexcellent processability |
JPS5292694A (en) * | 1976-01-30 | 1977-08-04 | Shigekazu Takeda | Film for wrapping skin |
JPS52126487A (en) * | 1976-04-16 | 1977-10-24 | Toyobo Co Ltd | Laminated films of polypropylene |
JPS53114886A (en) * | 1977-03-17 | 1978-10-06 | Asahi Chem Ind Co Ltd | Skin packaging film |
JPS54106583A (en) * | 1978-02-09 | 1979-08-21 | Nippon Petrochemicals Co Ltd | Method of making laminate |
JPS5516666U (en) * | 1978-07-17 | 1980-02-01 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5755078Y2 (en) * | 1978-12-26 | 1982-11-29 |
-
1981
- 1981-03-05 JP JP3269281A patent/JPS57146653A/en active Granted
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS49101420A (en) * | 1972-10-17 | 1974-09-25 | ||
JPS4969784A (en) * | 1972-10-26 | 1974-07-05 | ||
JPS5268279A (en) * | 1975-12-04 | 1977-06-06 | Toyobo Co Ltd | Composite films of polypropylene withexcellent processability |
JPS5292694A (en) * | 1976-01-30 | 1977-08-04 | Shigekazu Takeda | Film for wrapping skin |
JPS52126487A (en) * | 1976-04-16 | 1977-10-24 | Toyobo Co Ltd | Laminated films of polypropylene |
JPS53114886A (en) * | 1977-03-17 | 1978-10-06 | Asahi Chem Ind Co Ltd | Skin packaging film |
JPS54106583A (en) * | 1978-02-09 | 1979-08-21 | Nippon Petrochemicals Co Ltd | Method of making laminate |
JPS5516666U (en) * | 1978-07-17 | 1980-02-01 |
Also Published As
Publication number | Publication date |
---|---|
JPS57146653A (en) | 1982-09-10 |
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