JPH0694168B2 - Laminating method - Google Patents
Laminating methodInfo
- Publication number
- JPH0694168B2 JPH0694168B2 JP62145510A JP14551087A JPH0694168B2 JP H0694168 B2 JPH0694168 B2 JP H0694168B2 JP 62145510 A JP62145510 A JP 62145510A JP 14551087 A JP14551087 A JP 14551087A JP H0694168 B2 JPH0694168 B2 JP H0694168B2
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- laminating
- curing
- ethyl acetate
- solid content
- 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 - Lifetime
Links
Landscapes
- Laminated Bodies (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明はフイルム状の軟包装材料のラミネート方法に関
するもので、実用的に硬化のための養生時間を短縮する
ためのラミネート方法に関する。The present invention relates to a method for laminating a film-like soft packaging material, and more particularly to a laminating method for practically shortening curing time for curing.
従来、軟包装材料のラミネート方法としては、ポリウレ
タン/ポリウレタンイソシアネート、ポリエステル/ポ
リイソシアネートのごとき、いわゆるポリオール/ポリ
イソシアネート型の接着剤を使用し、ラミネート後35〜
40℃の養生室に入れて2〜5日養生し、硬化反応を完了
させてから、スリツター,製袋等の後加工工程に移行し
ていた。Conventionally, a so-called polyol / polyisocyanate type adhesive such as polyurethane / polyurethane isocyanate and polyester / polyisocyanate has been used as a laminating method for soft packaging materials, and after laminating
After being placed in a 40 ° C. curing room and cured for 2 to 5 days to complete the curing reaction, it was transferred to post-processing steps such as slitter and bag making.
本発明者等は鋭意研究の結果、これ等のポリオール/ポ
リイソシアネートの反応に湿分の関与が多大なことを見
出し、当初養生中の加湿を検討したが、通常この種の加
工品はウエツブ状で供給され、1000〜4000m巻で取扱わ
れるため、養生中では湿分の浸透に時間を要し、ウエツ
ブの極く外巻き部以外は養生時間の短縮が充分には達成
されないが、ラミネート時にフイルム面または接着剤塗
工面に加湿すれば、全体が均一に養生時間の大幅短縮が
達成されることを知見し、本発明を完成した。As a result of diligent research, the inventors of the present invention found that a large amount of moisture was involved in the reaction of these polyols / polyisocyanates, and initially examined humidification during curing. Since it is supplied at a temperature of 1000 to 4000 m and it takes a long time for moisture to penetrate during curing, the curing time is not sufficiently shortened except for the outermost wound portion of the web, but the film is laminated. The present invention has been completed by finding that if the surface or the adhesive-coated surface is humidified, the curing time can be substantially shortened uniformly.
湿分により硬化反応が促進される理由については必らず
しも明らかでないが、水と過剰のポリイソシアネートの
反応およびその反応生成物であるポリウレタンポリウレ
アの促進効果等が相乗的に寄与しているものと考えられ
る。The reason why the curing reaction is accelerated by moisture is not always clear, but the reaction between water and excess polyisocyanate and the accelerating effect of its reaction product, polyurethane polyurea, contribute synergistically. It is considered to be a thing.
本発明で使用するフイルムには特に制限がなく、通常軟
包装用に用いるフイルムは使用できる。その一例を次に
掲げる。The film used in the present invention is not particularly limited, and a film usually used for soft packaging can be used. An example is given below.
これ等のフイルムに予め塩化ビニリデン等のポリマーコ
ートを施したり、印刷インキで印刷したりすることは、
必ずしも必要ではないが、外観その他の面で有効なこと
が多い。 To apply a polymer coating such as vinylidene chloride to these films in advance, or to print with printing ink,
Although not necessary, it is often effective in terms of appearance and other aspects.
本発明で使用するポリオール/ポリイソシアネート系接
着剤は実質的に水を含まないものであれば特に制限はな
い。ポリオールの水酸基とポリイソシアネートのイソシ
アネート基との反応で硬化する機構の接着剤であれば良
い。代表的なポリオールとしては、フタル酸系ポリエス
テルポリオール,ポリアルキレンエーテルベースポリウ
レタンポリオール,ポリエステルベースポリウレタンポ
リオール等、 を挙げることができ、ポリイソシアネートとしては、ジ
イソシアネートの2量体,3量体,トリメチロールプロパ
ン,グリセリン等の多官能ヒドロキ化合物への付加体い
わゆるイソシアネートアダクト,ポリエーテルウレタン
イソシアネート等、を挙げることができる。The polyol / polyisocyanate adhesive used in the present invention is not particularly limited as long as it does not substantially contain water. Any adhesive may be used as long as it has a mechanism of curing by the reaction between the hydroxyl group of the polyol and the isocyanate group of the polyisocyanate. Typical polyols include phthalic acid-based polyester polyols, polyalkylene ether-based polyurethane polyols, polyester-based polyurethane polyols, and the like. Polyisocyanates include diisocyanate dimers, trimers, and trimethylolpropane. Examples thereof include adducts of glycerin and the like with polyfunctional hydroxy compounds, so-called isocyanate adducts, polyether urethane isocyanates and the like.
また、強制加湿は加湿装置からの水蒸気またはミスト状
水分をフイルム面にまたは接着剤塗工面に吹き付けて加
湿するだけでよく、吹き付け後貼着すれば養生時間が極
度に短縮される。Further, the forced humidification may be performed by spraying water vapor or mist-like water from the humidifying device onto the film surface or the adhesive coated surface to humidify, and the curing time can be extremely shortened by sticking after spraying.
以下、本発明の実施例について説明する。 Examples of the present invention will be described below.
実施例1 セイカボンドE−263(大日精化工業社製のフタル酸系
ポリエステルポリオールの酢酸エチル溶液で固型分が63
%含まれる)100重量部(主剤)とセイカボンドC−26
(大日精化工業社製のトリメチロールプロパン/TDIアダ
クト体の酢酸エチル溶液で、固型分が40%含まれる)20
重量部(硬化剤)と酢酸エチル100重量部の混合溶液
(固型分が32%)を接着剤として使用し、ラミネート条
件としてグラビヤ塗工式ドライラミネーターを使用し、
乾燥温度設定を第1ゾーンを60℃、第2ゾーンを70℃、
第3ゾーンを80℃、加工速度を120m/分、ニツプロール
温度50℃、基材フイルムとしてPET(ルミラー東レ社
製)、CPP(トレフアンNo.3701東レ社製)を使用し、PE
T(12μ)/CPP(60μ)をラミネートする。Example 1 Seika Bond E-263 (a solid component of 63% was obtained by using an ethyl acetate solution of a phthalic acid type polyester polyol manufactured by Dainichiseika Co.
%) 100 parts by weight (main ingredient) and Seika Bond C-26
(A solution of trimethylolpropane / TDI adduct manufactured by Dainichiseika Kogyo Co., Ltd. in ethyl acetate, containing 40% solid content) 20
A mixed solution of 100 parts by weight of ethyl acetate (part by weight) (hardening agent) is used as an adhesive, and a gravure coating type dry laminator is used as a laminating condition.
The drying temperature setting is 60 ℃ in the first zone, 70 ℃ in the second zone,
The third zone is 80 ℃, the processing speed is 120m / min, the Niprol temperature is 50 ℃, and PET (Lumirror Toray Co., Ltd.) and CPP (Trefuan No.3701 Toray Co.) are used as the base film.
Laminate T (12μ) / CPP (60μ).
上記のラミネート条件で、PET側に接着剤を塗工し、乾
燥後に加湿装置(コロナ超音波加湿機UF−450S 2台使
用)からのミスト状水分を接着剤の塗工面に1/時間
吹き付けて貼り合わせた。Under the above laminating conditions, apply the adhesive to the PET side, and after drying, spray mist-like water from the humidifier (using two corona ultrasonic humidifiers UF-450S) on the adhesive coated surface for 1 hour. Pasted together
実施例2 セイカボンドA−158W(大日精化工業社製のポリアルキ
レンエーテルウレタンポリオールの酢酸エチル溶液で固
型分70%)を100重量部とセイカボンドC−90(大日精
化工業社製のポリアルキレンエーテルウレタンポリイソ
シアネートの酢酸エチル溶液で固型分80%)を100重量
部と酢酸エチル400重量部の混合溶液(固型分25%)を
接着剤として使用し、ラミネート条件としてキスリバー
スロール塗工式ドライラミネーターを使用し、乾燥温度
設定を第1ゾーン60℃、第2ゾーン70℃、第3ゾーン80
℃、加工速度130m/分、ニツプロール温度45℃、基材フ
イルムとしてOPP(FOR二村化学工業社製)、CPP(FHK2
二村化学工業社製)を使用し、OPP(25μ)/CPP(40
μ)をラミネートする。Example 2 100 parts by weight of Seikabond A-158W (70% solid content in a solution of polyalkylene ether urethane polyol manufactured by Dainichiseika Kogyo Co., Ltd. in ethyl acetate) and Seikabond C-90 (polyalkylene manufactured by Dainichiseika Kogyo Co., Ltd.) Kiss reverse roll coating is used as a laminating condition by using a mixed solution of 100 parts by weight of ether urethane polyisocyanate in ethyl acetate (solid content: 80%) and 400 parts by weight of ethyl acetate (solid content: 25%) as an adhesive. Using a dry laminator, set the drying temperature to 60 ℃ in the first zone, 70 ℃ in the second zone and 80 in the third zone.
℃, processing speed 130m / min, Niprol temperature 45 ℃, as base film OPP (FOR Nimura Chemical Co., Ltd.), CPP (FHK2
NIPPON CHEMICAL INDUSTRIES, LTD., OPP (25μ) / CPP (40
μ) is laminated.
上記ラミネート条件でOPP側に接着剤を塗工し乾燥後に
加湿装置からの水蒸気を接着剤の塗工面に吹き付けて貼
り合わせた。An adhesive was applied to the OPP side under the above-mentioned laminating conditions, and after drying, water vapor from a humidifying device was sprayed onto the adhesive-coated surface for bonding.
実施例3 セイカボンドE−320(大日精化工業社製フタル酸系ポ
リエステルポリオールの酢酸エチル溶液で固型分60%)
100重量部とセイカボンドC−75N(大日精化工業社製ト
リメチロールプロパン/HMDIアダクト体の酢酸エチルで
固型分75%)10部と酢酸エチル110部の混合溶液(固型
分30.7%)を接着剤として使用し、ラミネート条件とし
てグラビア塗工式ドライラミネーターを使用し、乾燥温
度を第1ゾーン65℃、第2ゾーン75℃、第3ゾーン85
℃、加工速度100m/分、ニツプロール温度55℃、基材フ
イルムとしてPET(12μ)/Al箔(9μ)/CPP(60μ)を
ラミネートする。Example 3 Seika Bond E-320 (60% solid content in ethyl acetate solution of phthalic acid polyester polyol manufactured by Dainichiseika Co., Ltd.)
100 parts by weight of Seika Bond C-75N (75% solid content of trimethylolpropane / HMDI adduct manufactured by Dainichiseika Kogyo Co., Ltd. in ethyl acetate 75%) and 110 parts of ethyl acetate mixed solution (solid content 30.7%) It is used as an adhesive, and a gravure coating type dry laminator is used as a laminating condition.
Laminate PET (12μ) / Al foil (9μ) / CPP (60μ) as the base material film at ℃, processing speed 100m / min, Niprol temperature 55 ° C.
上記のラミネート条件で、PET側及びアルミ箔側に接着
剤を塗工し、乾燥後に加湿装置からの水蒸気を接着剤の
塗工面に吹きつけて貼り合わせた。Under the above-mentioned laminating conditions, the PET side and the aluminum foil side were coated with an adhesive, and after drying, water vapor from a humidifying device was sprayed onto the coated surface of the adhesive for bonding.
比較例1 実施例1の使用接着剤およびラミネート条件が同一で加
湿をしないラミネート。Comparative Example 1 A laminate in which the adhesive used and the laminating conditions of Example 1 were the same and were not humidified.
比較例2 実施例2の使用接着剤およびラミネート条件が同一で加
湿をしないラミネート。Comparative Example 2 A laminate in which the adhesive used and the laminating conditions of Example 2 were the same and were not humidified.
比較例3 実施例3の使用接着剤およびラミネート条件が同一で加
湿をしないラミネート。Comparative Example 3 A laminate in which the adhesive used and the laminating conditions in Example 3 were the same and were not humidified.
上記の実施例および比較例の硬化速度を測定した結果を
次の表に示す。(但し、硬化速度の判定方法については
赤外域のNCO基吸収(2250cm-1)の消費率で判定する事
で、消費率100%を硬化完了したものとする。) 〔発明の効果〕 以上の例からも明らかなように、比較例(1)では硬化
100%になるのが5日間要したものが、加湿を行つた実
施例(1)では1.5日間で100%になつた。The following table shows the results obtained by measuring the curing rates of the above-mentioned examples and comparative examples. (However, regarding the method for determining the curing rate, the rate of consumption of NCO group absorption (2250 cm -1 ) in the infrared region is used to determine that the curing rate is 100%.) [Effects of the Invention] As is clear from the above example, curing in Comparative Example (1)
It took 5 days to reach 100%, but in Example (1) where humidification was performed, it reached 100% in 1.5 days.
また、比較例(2)では5日間要したものが1日で硬化
100%となつた。比較例(3)では7日間要したものが
2日間で100%になつた。In Comparative Example (2), what took 5 days was cured in 1 day.
It was 100%. In Comparative Example (3), what took 7 days became 100% in 2 days.
このように本発明は強制加湿をすることにより養生時間
を短縮することができる効果を奏するものである。As described above, the present invention has the effect of shortening the curing time by performing forced humidification.
Claims (1)
るに当たり、実質的に水を含まないポリオールポリイソ
シアネート接着剤を使用し、ラミネートする際にフィル
ム面または接着剤塗工面に強制加湿を行うことを特徴と
するラミネート方法1. When laminating web-shaped films, a polyol polyisocyanate adhesive containing substantially no water is used, and the film surface or the adhesive coated surface is forcibly humidified when laminating. Laminating method
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62145510A JPH0694168B2 (en) | 1987-06-11 | 1987-06-11 | Laminating method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62145510A JPH0694168B2 (en) | 1987-06-11 | 1987-06-11 | Laminating method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63309427A JPS63309427A (en) | 1988-12-16 |
| JPH0694168B2 true JPH0694168B2 (en) | 1994-11-24 |
Family
ID=15386915
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62145510A Expired - Lifetime JPH0694168B2 (en) | 1987-06-11 | 1987-06-11 | Laminating method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0694168B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6137825B2 (en) * | 2012-12-18 | 2017-05-31 | 昭和電工パッケージング株式会社 | Dry lamination method and method for producing molding packaging material |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5811911A (en) * | 1981-07-15 | 1983-01-22 | 吉村光学株式会社 | Optical filter |
-
1987
- 1987-06-11 JP JP62145510A patent/JPH0694168B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63309427A (en) | 1988-12-16 |
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