JPH0324938A - Preparation of pva type film laminate - Google Patents
Preparation of pva type film laminateInfo
- Publication number
- JPH0324938A JPH0324938A JP1161071A JP16107189A JPH0324938A JP H0324938 A JPH0324938 A JP H0324938A JP 1161071 A JP1161071 A JP 1161071A JP 16107189 A JP16107189 A JP 16107189A JP H0324938 A JPH0324938 A JP H0324938A
- Authority
- JP
- Japan
- Prior art keywords
- polyvinyl alcohol
- water
- resin films
- pref
- 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
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 27
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 27
- 229920005989 resin Polymers 0.000 claims abstract description 20
- 239000011347 resin Substances 0.000 claims abstract description 20
- 238000010030 laminating Methods 0.000 claims abstract description 4
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229920005903 polyol mixture Polymers 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract description 6
- 230000004888 barrier function Effects 0.000 abstract description 6
- 238000010438 heat treatment Methods 0.000 abstract description 6
- 229920005862 polyol Polymers 0.000 abstract description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 3
- 150000003077 polyols Chemical class 0.000 abstract description 3
- 235000011187 glycerol Nutrition 0.000 abstract description 2
- 229920002689 polyvinyl acetate Polymers 0.000 abstract description 2
- 239000011118 polyvinyl acetate Substances 0.000 abstract description 2
- 239000007788 liquid Substances 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 238000009736 wetting Methods 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 229920002978 Vinylon Polymers 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/40—General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
- B29C66/41—Joining substantially flat articles ; Making flat seams in tubular or hollow articles
- B29C66/45—Joining of substantially the whole surface of the articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/01—General aspects dealing with the joint area or with the area to be joined
- B29C66/05—Particular design of joint configurations
- B29C66/10—Particular design of joint configurations particular design of the joint cross-sections
- B29C66/11—Joint cross-sections comprising a single joint-segment, i.e. one of the parts to be joined comprising a single joint-segment in the joint cross-section
- B29C66/112—Single lapped joints
- B29C66/1122—Single lap to lap joints, i.e. overlap joints
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/71—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Laminated Bodies (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、PVA系フィルム積層物の製造法に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to a method for producing a PVA-based film laminate.
更に詳しくは,ポリビニルアルコール系樹脂フィルム同
士を積層し. PVA系フィルム積層物を製造する方法
に関する。More specifically, polyvinyl alcohol resin films are laminated together. The present invention relates to a method of manufacturing a PVA-based film laminate.
ポリビニルアルコール系樹脂フィルムは、水蒸気以外の
気体の透過性がきわめて小さいので、こうしたガスバリ
ャー性を利用してガスケット、ホース、ダイアフラム、
包装用シートなどの各種用途に用いられている。こうし
た用途に用いられる場合、ガスバリャー性を上げるため
にはフィルムの厚さを増す必要があり、一般にはウレタ
ン系、ポリビニルアルコール水溶液などの接着剤を用い
る積層が行われている.
しかしながら、こうした積層方法では,接着剤のコーテ
ィング、乾燥という工程が必要となり、また接着剤コス
トも加わることになる。そこで、ヒートシール法という
ことも考えられるが、ポリビニルアルコール系樹脂は一
般に融点が200℃以上と高く、低い温度では一時的に
積層できても界面剥離を生じ易いという欠点がみられ,
究極的に高いガスバリャー性を確保することができない
。Polyvinyl alcohol resin film has extremely low permeability to gases other than water vapor, so its gas barrier properties can be used to create gaskets, hoses, diaphragms, etc.
It is used for various purposes such as packaging sheets. When used in such applications, it is necessary to increase the thickness of the film in order to improve gas barrier properties, and lamination is generally performed using adhesives such as urethane adhesives or aqueous polyvinyl alcohol solutions. However, such lamination methods require steps such as coating and drying the adhesive, which also adds to the cost of the adhesive. Therefore, a heat sealing method may be considered, but polyvinyl alcohol resins generally have a high melting point of 200°C or higher, and even if they can be temporarily laminated at low temperatures, they have the disadvantage of easily causing interfacial peeling.
Ultimately, high gas barrier properties cannot be ensured.
本発明の目的は、積層方法を単純化かつ低コスト化し,
しかも接着性の点からガスバリャー性を高度に確保した
PVA系フィルム積層物の製造法を提供することにある
.
〔課題を解決するための手段〕
本発明のかかる目的を達成せしめるPVA系フイルム積
層物の製造は、ポリビニルアルコール系樹脂フィルム同
士を積層するに際し、少なくとも一方、好ましくは両方
の樹脂フイルムを含水させあるいは水一ポリオール混合
液で湿潤しかつ加熱軟化状態として圧着することにより
行われる。The purpose of the present invention is to simplify the lamination method and reduce the cost.
Moreover, it is an object of the present invention to provide a method for producing a PVA film laminate that ensures a high level of gas barrier properties in terms of adhesiveness. [Means for Solving the Problems] In order to produce a PVA film laminate that achieves the object of the present invention, when polyvinyl alcohol resin films are laminated together, at least one, preferably both resin films are hydrated or This is carried out by moistening with a water-polyol mixture and heating to a softened state and then press-bonding.
ポリビニルアルコール系樹脂フイルムとしては、ポリ酢
酸ビニルの部分けん化物または完全けん化物、エチレン
ー酢酸ビニル共重合体けん化物などのフイルムが用いら
れ、そのフイルム同士を積層するに際しては、例えば次
の如き各種の態様で含水かつ加熱軟化状態での圧着が行
われる。As the polyvinyl alcohol resin film, films such as partially or completely saponified polyvinyl acetate and saponified ethylene-vinyl acetate copolymer are used. In this embodiment, compression bonding is performed in a water-containing and heat-softened state.
(1)キャスティング法
一般にポリビニルアルコール系樹脂濃度約5〜60%、
好ましくは約10〜40%の製膜原液を回転乾燥ドラム
(ロール)またはベルト上にスリットを通して流延しあ
るいはロールコータによって塗布し、このようにしてキ
ャスティングされた製膜直後のポリビニルアルコール系
樹脂のフィルム状物は、多獣の水分を含有しかつ加熱軟
化状態にあるので、フィルム状物をそのまま圧着させる
。(1) Casting method Generally, polyvinyl alcohol resin concentration is about 5 to 60%,
Preferably, about 10 to 40% of the film-forming stock solution is cast onto a rotary drying drum (roll) or belt through a slit or coated with a roll coater, and the polyvinyl alcohol resin immediately after the film is cast in this manner. Since the film-like material contains moisture and is softened by heating, the film-like material is pressed as is.
この際、フィルム状物同士をこのようにして圧着させる
ことが好ましいが、一方の樹脂フィルム上に製膜原液を
フィルム状に流延し、圧着させることもできる。At this time, it is preferable to pressure-bond the film-like materials to each other in this manner, but it is also possible to cast the film-forming stock solution onto one of the resin films in the form of a film and pressure-bond them.
(2)塗布法,吹付法
予め製造されたポリビニルアルコール系樹脂フィルムに
水を噴霧,刷毛塗りなどにより塗布して加熱するか、あ
るいは加熱水蒸気を吹き付けることによって、樹脂フィ
ルムを含水かつ加熱軟化状態となし、圧着させる。(2) Coating method, spraying method Water is applied to a pre-manufactured polyvinyl alcohol resin film by spraying or brushing and heated, or heated steam is sprayed to make the resin film hydrated and softened by heating. None, crimped.
これらの方法を実施するに際し、けん化度の高いポリビ
ニルアルコールでは高い温度でなければ水に溶解し難い
ため,ある程度の加熱を必要とし、また高温下で水の蒸
発が早くなるのを制御するために、柔軟剤としても使用
されているポリオールを水に添加し、そのような水−ポ
リオール混合液で湿潤させることも行われる.
ポリオールとしては、エチレングリコール、ジエチレン
グリコール、プロピレングリコール,グリセリンなどが
用いられる。これらの使用割合が多い程高温下での制御
が容易となるが,コスト面ばかりではなく,柔軟性、ガ
スバリャー性などの面との兼合いで、一般には水に対し
て約5〜400重量2、好ましくは約20〜150重量
%の割合で用いられる。When carrying out these methods, polyvinyl alcohol with a high degree of saponification is difficult to dissolve in water unless the temperature is high, so a certain amount of heating is required, and in order to control the rapid evaporation of water at high temperatures. Polyols, which are also used as softeners, are added to water and wetted with such water-polyol mixtures. As the polyol, ethylene glycol, diethylene glycol, propylene glycol, glycerin, etc. are used. The higher the proportion of these used, the easier it is to control at high temperatures, but considering not only cost but also flexibility, gas barrier properties, etc. , preferably in a proportion of about 20 to 150% by weight.
圧着は、約50〜180℃、好ましくは約70〜120
℃の温度で、熱プレス、加熱ロール,ヒートシーラなど
を用いて、全面的または部分的に行われる。Crimping is performed at about 50-180°C, preferably about 70-120°C.
It is carried out in whole or in part at a temperature of °C using a heat press, a heat roll, a heat sealer, etc.
一対のロール状ヒートシーラを用いれば,袋状物や深絞
り戒形品についての部分的な積層も可能である.また、
熱プレスを用いて全面的に積層する場合には、減圧下で
圧着させると、しわやエア入り部分が生じ難い。By using a pair of roll-shaped heat sealers, it is also possible to partially laminate bags and deep-drawn articles. Also,
When laminating the entire surface using a hot press, crimp and air-filled areas are less likely to occur if the layers are bonded under reduced pressure.
本発明方法によれば,ポリビニルアルコール系樹脂フィ
ルムを含水かつ加熱軟化状態で圧着するだけで樹脂フィ
ルムを積層させることができ,工程的、コスト的にすぐ
れているばかりではなく、接着性、柔軟性の点でもすぐ
れているPVA系フィルム積層物が得られる。According to the method of the present invention, resin films can be laminated simply by pressing polyvinyl alcohol resin films in a water-containing and heat-softened state, which is not only superior in terms of process and cost, but also in terms of adhesiveness and flexibility. A PVA-based film laminate which is also excellent in the following points can be obtained.
次に、実施例について本発明を説明する。 Next, the present invention will be explained with reference to examples.
実施例
A:2枚のポリビニルアルコールフィルム(クラレ製品
ビニロンフィルム#6500、けん化度99.5%以上
、厚さ65μm,伸び390%)に、それぞれ水を8n
+ Q /m”の塗布量で吹き付け,100℃の加熱ロ
ールで圧着し、その後50℃で30分間二一ジングした
B:上記Aにおいて、Aの代わりに水一エチレングリコ
ール等重量混合液が同じ塗布量で用いられた。Example A: Two polyvinyl alcohol films (Kuraray product Vinylon Film #6500, degree of saponification 99.5% or more, thickness 65 μm, elongation 390%) were each coated with 8 n of water.
+Q/m'' coating amount, pressed with a heating roll at 100℃, and then heated at 50℃ for 30 minutes B: In the above A, the same weight mixture of water and ethylene glycol was used instead of A. It was used in a coating amount.
C:ウレタン系接着剤(ロートファーイースト社製品タ
イセル7012)を3倍量の酢酸エチルで希釈した接着
剤を2枚のポリビニルアルコールフィルムに吹き付け、
乾燥させた後100℃の加熱ロールで圧着し、50℃で
10時間二一ジングした
D:前記Aにおいて、ポリビニルアルコール(重合度1
500.けん化度80%)の5重量%水溶液が同じ塗布
量で用いられた。C: Spray an adhesive prepared by diluting urethane adhesive (Tycel 7012, a product of Roto Far East Co., Ltd.) with 3 times the amount of ethyl acetate onto two polyvinyl alcohol films.
After drying, it was pressed with a heated roll at 100°C, and then heated at 50°C for 10 hours.D: In the above A, polyvinyl alcohol (polymerization degree 1
500. A 5% by weight aqueous solution with a degree of saponification of 80%) was used at the same coating weight.
以上で得られた各PVA系フィルム積層物について、接
着強度(フィルム破断強度)および伸び(柔軟性の目安
となる)の測定を行い、次の表に示されるような結果を
得た。For each of the PVA film laminates obtained above, the adhesive strength (film breaking strength) and elongation (a measure of flexibility) were measured, and the results shown in the following table were obtained.
表
接着強度(kg/cm) 独3ε七〇一2.3
311102.0
420
2.0 70
2.1 180Surface adhesive strength (kg/cm) German 3ε7012.3
311102.0
420 2.0 70 2.1 180
Claims (1)
るに際し、少なくとも一方の樹脂フィルムを含水かつ加
熱軟化状態として圧着することを特徴とするPVA系フ
ィルム積層物の製造法。 2、ポリビニルアルコール系樹脂フィルム同士を積層す
るに際し、少なくとも一方の樹脂フィルムを水−ポリオ
ール混合液で湿潤しかつ加熱軟化状態として圧着するこ
とを特徴とするPVA系フィルム積層物の製造法。[Claims] 1. A method for producing a PVA-based film laminate, characterized in that when polyvinyl alcohol-based resin films are laminated together, at least one of the resin films is compressed in a hydrated and heat-softened state. 2. A method for producing a PVA-based film laminate, which comprises, when laminating polyvinyl alcohol-based resin films, moistens at least one of the resin films with a water-polyol mixture, heats it to a softened state, and then press-bonds it.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1161071A JP2850372B2 (en) | 1989-06-23 | 1989-06-23 | Method for producing PVA-based film laminate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1161071A JP2850372B2 (en) | 1989-06-23 | 1989-06-23 | Method for producing PVA-based film laminate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0324938A true JPH0324938A (en) | 1991-02-01 |
JP2850372B2 JP2850372B2 (en) | 1999-01-27 |
Family
ID=15728071
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1161071A Expired - Lifetime JP2850372B2 (en) | 1989-06-23 | 1989-06-23 | Method for producing PVA-based film laminate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2850372B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH069797A (en) * | 1992-06-23 | 1994-01-18 | Kuinraito Denshi Seiko Kk | Solvent welding of synthetic resin sheets and solvent welding apparatus |
JP2007171897A (en) * | 2005-11-22 | 2007-07-05 | Nitto Denko Corp | Manufacturing method of polarizing film, polarizing film, optical film, liquid crystal display device and image display device |
JP2017097011A (en) * | 2015-11-18 | 2017-06-01 | 三星エスディアイ株式会社Samsung SDI Co., Ltd. | Method for manufacturing polyene based polarizing film, polyene based polarizing film, laminated polarizing film and display device |
-
1989
- 1989-06-23 JP JP1161071A patent/JP2850372B2/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH069797A (en) * | 1992-06-23 | 1994-01-18 | Kuinraito Denshi Seiko Kk | Solvent welding of synthetic resin sheets and solvent welding apparatus |
JP2007171897A (en) * | 2005-11-22 | 2007-07-05 | Nitto Denko Corp | Manufacturing method of polarizing film, polarizing film, optical film, liquid crystal display device and image display device |
JP4734172B2 (en) * | 2005-11-22 | 2011-07-27 | 日東電工株式会社 | Polarizing film manufacturing method and stretching apparatus |
JP2017097011A (en) * | 2015-11-18 | 2017-06-01 | 三星エスディアイ株式会社Samsung SDI Co., Ltd. | Method for manufacturing polyene based polarizing film, polyene based polarizing film, laminated polarizing film and display device |
Also Published As
Publication number | Publication date |
---|---|
JP2850372B2 (en) | 1999-01-27 |
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