JPH11961A - Surface protective film or sheet - Google Patents

Surface protective film or sheet

Info

Publication number
JPH11961A
JPH11961A JP15376097A JP15376097A JPH11961A JP H11961 A JPH11961 A JP H11961A JP 15376097 A JP15376097 A JP 15376097A JP 15376097 A JP15376097 A JP 15376097A JP H11961 A JPH11961 A JP H11961A
Authority
JP
Japan
Prior art keywords
film
temperature
pressure
oxygen permeability
thickness
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.)
Pending
Application number
JP15376097A
Other languages
Japanese (ja)
Inventor
Kazuto Okumura
和人 奥村
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.)
Nitto Denko Corp
Original Assignee
Nitto Denko Corp
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 Nitto Denko Corp filed Critical Nitto Denko Corp
Priority to JP15376097A priority Critical patent/JPH11961A/en
Publication of JPH11961A publication Critical patent/JPH11961A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To prevent a float phenomenon from being generated even though a surface protective film or sheet is restored to ordinary temperature by thermopressure fixing with an autoclave or the like by a method wherein a film in which oxygen permeability at specific temperature and specific relative humidity is under specific numerical value is used as a base material, and a pressure-sensitive adhesive layer is provid on its one side. SOLUTION: A film of 25 μm thickness consisting of ethylene-vinyl alcohol copolymer is used as a base material film. One side surface of the film is treated with corona, and a pressure sensitive adhesive is applied to this surface. Though a permeation amount of oxygen receives influences from a thickness of the film, temperature and humidity, the permeation amount is inversely proportional to the thickness of the film, and linearity is realized between a logarithm of the permeation amount and a reciprocal of absolute temperature. Though oxygen transmission at temperature and pressure under the same conditions as those for an autoclave is intrincically important, when a film wherein oxygen permeability at 20 deg.C and 0%RH is under 40 cc/m<2> 24 hrs-atm (a film wherein oxygen permeability at ordinary temperature, ordinary humidity, and ordinary pressure is very low) is used as the base material, occurrence of float is very little.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、表面保護フィルム
またはシートに関し、特に偏光板用の表面保護フィルム
またはシート等のように加熱圧着されるのに適した表面
保護フィルムまたはシートに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a surface protective film or sheet, and more particularly to a surface protective film or sheet suitable for thermocompression bonding, such as a surface protective film or sheet for a polarizing plate.

【0002】[0002]

【従来の技術】従来より偏光板の表面保護フィルムまた
はシートとして、ポリエステルフィルムを使用したもの
が多く使用されてきた。粘着加工された偏光板をガラス
基板によく密着させるために、オートクレーブにより加
熱圧着するが、加熱圧着のあと常温に戻すとフィルムに
気泡状の無数の浮きが発生する。このような気泡がある
と後工程の異物検査ができなくなってしまうという問題
がある。
2. Description of the Related Art Conventionally, a polyester film has often been used as a surface protective film or sheet of a polarizing plate. The adhesive-processed polarizing plate is heated and pressed by an autoclave in order to bring the polarizing plate into close contact with the glass substrate. However, when the temperature is returned to room temperature after the heating and pressing, countless floating bubbles are generated in the film. If such bubbles are present, there is a problem that a foreign substance inspection in a later process cannot be performed.

【0003】ポリエステルフィルムは、ポリエチレンや
ポリプロピレンにくらべ前述の浮き現象は少ないもの
の、皆無ではなく、オートクレーブの温度や圧力が高く
なるほど気泡は発生しやすい。
[0003] Although the above-mentioned floating phenomenon is less in a polyester film than polyethylene and polypropylene, it is not absent, and bubbles tend to be generated as the temperature and pressure of the autoclave become higher.

【0004】[0004]

【発明が解決しようとする課題】本発明は、オートクレ
ーブ等により加熱圧着して常温に戻しても、浮き現象の
発生のない表面保護フィルムまたはシートを提供するこ
とを目的とする。
SUMMARY OF THE INVENTION An object of the present invention is to provide a surface protective film or sheet which does not cause a floating phenomenon even when the temperature is returned to room temperature by heating and pressure bonding in an autoclave or the like.

【0005】[0005]

【課題を解決するための手段】本発明者は鋭意研究の結
果、20℃、0%RH(相対湿度)での酸素透過率が4
0(cc/m2 ・24hrs・atm)未満、好ましく
は30(cc/m2 ・24hrs・atm)以下、さら
に好ましくは20(cc/m2 ・24hrs・atm)
以下であるフィルムを基材とすることによって、浮きを
防止した表面保護シートが得られることを見い出し本発
明を完成するに至った。
Means for Solving the Problems As a result of intensive studies, the present inventors have found that the oxygen permeability at 20 ° C. and 0% RH (relative humidity) is 4%.
0 (cc / m 2 · 24 hrs · atm), preferably 30 (cc / m 2 · 24 hrs · atm) or less, more preferably 20 (cc / m 2 · 24 hrs · atm)
By using the following film as a base material, it has been found that a surface protective sheet in which floating is prevented can be obtained, and the present invention has been completed.

【0006】酸素透過量は、フィルムの厚さや温度・湿
度に影響を受けるが、透過量はフィルムの厚みに反比例
し、透過量の対数と絶対温度の逆数との間に直線性が成
り立つことが分かっている。
Although the amount of oxygen permeation is affected by the thickness of the film and the temperature and humidity, the amount of permeation is inversely proportional to the thickness of the film, and linearity is established between the logarithm of the amount of permeation and the reciprocal of the absolute temperature. I know it.

【0007】実際の使用上、オートクレーブと同一条件
の温度・圧力での酸素透過率が本来重要であるが、20
℃、0%RHでの酸素透過率が40(cc/m2 ・24
hrs・atm)未満であるフィルム(即ち、そもそも
常温・常湿度・常圧下において酸素透過率の非常に低い
フィルム)を基材とすれば、実用上のオートクレーブ条
件では前記浮きの発生が極めて少ないことを見い出し
た。
In actual use, the oxygen permeability at the same temperature and pressure as the autoclave is originally important.
Oxygen permeability at 40 ° C. and 0% RH is 40 (cc / m 2 · 24
When the base material is a film having an oxygen permeability at room temperature, normal humidity, and normal pressure, the occurrence of the float is extremely small under practical autoclave conditions. I found

【0008】本発明における基本となるべき酸素透過率
の低いプラスチックフィルムとしては、厚み10〜30
μm程度での20℃、0%RHでの酸素透過率が40
(cc/m2 ・24hrs・atm)未満であるプラス
チックフィルムが好ましく、例えばエチレンビニルアル
コール共重合体、ポリビニルアルコール、塩化ビニリデ
ン、塩化ビニリデン−アクリル酸メチル共重合体、アク
リロニトリル共重合体、ポリアミドなどが用いられる。
これらを単独で基材フィルムとしても良いし、これらの
複合多層フィルムやその他の樹脂(例えば一般的なポリ
エチレン・ポリプロピレン・ポリエステル等)との多層
フィルムでも、上記の酸素透過率の条件を満たすもので
あればなんら問題はない。また、プラスチックフィルム
の厚みについても上記の酸素透過率の条件を満たすもの
であれば特に限定されないが、好適には10〜200μ
m、特に15〜40μmである。
[0008] The plastic film having a low oxygen permeability, which is the basis of the present invention, has a thickness of 10 to 30.
Oxygen permeability at 20 ° C. and 0% RH at about μm is 40
(Cc / m 2 · 24 hrs · atm), a plastic film of less than 10 g is preferred, for example, ethylene vinyl alcohol copolymer, polyvinyl alcohol, vinylidene chloride, vinylidene chloride-methyl acrylate copolymer, acrylonitrile copolymer, polyamide and the like. Used.
These may be used alone as a base film, or a multilayer film of these composite multilayer films or other resins (for example, general polyethylene, polypropylene, polyester, etc.) that satisfies the above oxygen permeability conditions. If there is no problem. Also, the thickness of the plastic film is not particularly limited as long as it satisfies the above oxygen permeability conditions, but is preferably 10 to 200 μm.
m, especially 15 to 40 μm.

【0009】酸素透過率の測定は、乾燥状態の酸素を利
用し、気体透過度測定用セルマノメータを使用してJI
S Z 1707に準じて行なう。
The oxygen permeability is measured by using oxygen in a dry state and using a gas permeation measuring selmanometer according to JI.
Performed according to SZ1707.

【0010】かかる酸素透過率の基材は、例えばプラス
チックフィルムの材料の選択、厚みの調整、異種フィル
ムとの複合等によって得ることができる。
The substrate having such an oxygen permeability can be obtained, for example, by selecting the material of the plastic film, adjusting the thickness, and combining with a different kind of film.

【0011】20℃、0%RHでの酸素透過率が40
(cc/m2 ・24hrs・atm)以上であると、オ
ートクレーブによる加熱圧着のあと、常温に戻すと気泡
状の浮きが発生する。これは、酸素透過率が高い基材フ
ィルムを使用すると、オートクレーブ中に多量の空気が
基材フィルムを通過して浸入し、偏光板表面と粘着剤と
の界面に圧縮される。常温に戻すと、この圧縮された空
気が膨張し、気泡状の浮きが発生するものと考えられ
る。
Oxygen permeability at 20 ° C. and 0% RH is 40
If it is more than (cc / m 2 · 24 hrs · atm), after heating and pressure bonding by an autoclave, when the temperature is returned to normal temperature, bubble-like floating occurs. When a base film having a high oxygen permeability is used, a large amount of air enters the autoclave through the base film and is compressed at the interface between the polarizing plate surface and the adhesive. It is considered that when the temperature is returned to normal temperature, the compressed air expands, and a bubble-like floating occurs.

【0012】本発明に用いられる粘着剤は、アクリル系
・合成ゴム系・ゴム系のいずれの粘着剤組成物でも構わ
ないが、組成により粘着力をコントロールしやすいアク
リル系の粘着剤が望ましい。粘着剤はプラスチックフィ
ルムの基材の片側に、乾燥後の厚みが1〜50μm、好
ましくは5〜30μmとなるように塗布される。
The pressure-sensitive adhesive used in the present invention may be any of a pressure-sensitive adhesive composition of an acrylic type, a synthetic rubber type, and a rubber type, but an acrylic pressure-sensitive adhesive whose adhesive strength is easily controlled by the composition is desirable. The pressure-sensitive adhesive is applied to one side of the base material of the plastic film so that the thickness after drying is 1 to 50 μm, preferably 5 to 30 μm.

【0013】[0013]

【実施例】以下、実施例及び比較例を示して、本発明を
より具体的に説明する。なお、本発明はこれら実施例に
限定されるものではない。
The present invention will now be described more specifically with reference to examples and comparative examples. Note that the present invention is not limited to these examples.

【0014】〔粘着剤の作成〕常用の方法を用い、酢酸
エチル中で2−エチルヘキシルアクリレート(96モ
ル)、ヒドロキシエチルアクリレート(4モル)からな
る平均分子量70万(ポリスチレン換算)のアクリル酸
エステル共重合体(25%溶液)を得た。この溶液10
0部(固形分)に対し、架橋剤(ポリイソシアネート、
日本ポリウレタン工業(株)製、商品名コロネートL)
3部を添加して、粘着剤組成物を得た。
[Preparation of Pressure-Sensitive Adhesive] An acrylic ester of 2-ethylhexyl acrylate (96 mol) and hydroxyethyl acrylate (4 mol) having an average molecular weight of 700,000 (polystyrene equivalent) in ethyl acetate was prepared using a conventional method. A polymer (25% solution) was obtained. This solution 10
With respect to 0 parts (solid content), a crosslinking agent (polyisocyanate,
Nippon Polyurethane Industry Co., Ltd., trade name Coronate L)
Three parts were added to obtain a pressure-sensitive adhesive composition.

【0015】以下の各実施例・比較例の基材フィルム
に、乾燥後の厚みが20μmになるように粘着剤組成物
を塗布し、表面保護シートを得た。なお、各実施例・比
較例の基材フィルムの20℃、0%RHでの酸素透過率
を表1に示す。
The pressure-sensitive adhesive composition was applied to the substrate films of the following Examples and Comparative Examples so that the thickness after drying was 20 μm to obtain a surface protection sheet. Table 1 shows the oxygen permeability at 20 ° C. and 0% RH of the base films of the respective examples and comparative examples.

【0016】実施例1 基材フィルムとして、エチレンビニルアルコール共重合
体からなる厚さ25μmのフィルム(エバールEF−
F、(株)クラレ製)を用いた。フィルムの片面をコロ
ナ処理し、この面に粘着剤を塗布した。
Example 1 As a substrate film, a 25 μm-thick film made of an ethylene vinyl alcohol copolymer (EVAL EF-
F, manufactured by Kuraray Co., Ltd.). One surface of the film was subjected to corona treatment, and an adhesive was applied to this surface.

【0017】実施例2 基材フィルムとして、ポリビニルアルコールからなる厚
さ25μmのフィルム(ボブロン、日本合成化学工業
(株)製)を用いた。フィルムの片面をコロナ処理し、
この面に粘着剤を塗布した。
Example 2 A 25 μm-thick film made of polyvinyl alcohol (Boblon, manufactured by Nippon Synthetic Chemical Industry Co., Ltd.) was used as a base film. Corona treatment on one side of the film,
An adhesive was applied to this surface.

【0018】実施例3 基材フィルムとして、ポリエステルフィルムに塩化ビニ
リデン樹脂をコートした多層フィルム(厚さ:PET
(ポリテレフタル酸エチレン)=12μm、塩化ビニリ
デン樹脂層=2μm)(セネシKET#6000、ダイ
セル化学工業(株)製)を用いた。ポリエステル側に粘
着剤を塗布した。
Example 3 As a base film, a multilayer film in which a vinylidene chloride resin was coated on a polyester film (thickness: PET)
(Polyethylene terephthalate) = 12 μm, vinylidene chloride resin layer = 2 μm) (Seneshi KET # 6000, manufactured by Daicel Chemical Industries, Ltd.) was used. An adhesive was applied to the polyester side.

【0019】実施例4 基材フィルムとして、OPP(延伸ポリプロピレンフィ
ルム)20μm/エバールEF−F15μm/CPP
(Tダイ法(キャスト)によるポリプロピレンフィル
ム)50μmの3層フィルム(ウレタン系接着剤を用い
たラミネート品)を用いた。OPP側をコロナ処理し、
この面に粘着剤を塗布した。
Example 4 As a base film, OPP (stretched polypropylene film) 20 μm / EVAL EF-F 15 μm / CPP
(Polypropylene film by T-die method (cast)) A 50 μm three-layer film (laminated product using a urethane-based adhesive) was used. Corona treatment on OPP side,
An adhesive was applied to this surface.

【0020】実施例5 基材フィルムとして、厚さ20μmのポリアミド(ナイ
ロン−6)フィルムを用いた。このフィルムの片側に粘
着剤を塗布した。
Example 5 A 20 μm thick polyamide (nylon-6) film was used as a base film. An adhesive was applied to one side of the film.

【0021】比較例1 基材フィルムとして、二軸延伸ポリエステルフィルム
(厚さ25μm)を用いた。このフィルムの片側に粘着
剤を塗布した。
Comparative Example 1 A biaxially stretched polyester film (25 μm in thickness) was used as a base film. An adhesive was applied to one side of the film.

【0022】比較例2 基材フィルムとして、二軸延伸ポリプロピレンフィルム
(厚さ40μm)を用いた。このフィルムの片側に粘着
剤を塗布した。
Comparative Example 2 A biaxially stretched polypropylene film (thickness: 40 μm) was used as a base film. An adhesive was applied to one side of the film.

【0023】〔試験方法〕実施例および比較例で得られ
た表面保護シートを偏光板にラミネータにて貼り付けた
後、偏光板をガラス板にラミネータにて貼り付けた。粘
着加工した偏光板として、日東電工(株)製NPF−F
1225DUAG25を用いた。また、粘着加工した偏
光板を貼り付ける基板として、厚さ0.7mmの無アル
カリガラス板を用いた。
[Test Method] After the surface protective sheets obtained in Examples and Comparative Examples were attached to a polarizing plate with a laminator, the polarizing plate was attached to a glass plate with a laminator. NPF-F manufactured by Nitto Denko Corporation as an adhesive-processed polarizing plate
1225 DUAG25 was used. A 0.7 mm-thick non-alkali glass plate was used as a substrate to which the adhesive-processed polarizing plate was attached.

【0024】オートクレーブにて、70℃、5atmで
30分間加熱圧着し、その後常温・常湿度に戻して、表
面保護シートの浮き現象を観察した。その結果を表1に
まとめた。
In an autoclave, it was heated and pressed at 70 ° C. and 5 atm for 30 minutes, and then returned to normal temperature and normal humidity, and the floating phenomenon of the surface protective sheet was observed. Table 1 summarizes the results.

【0025】[0025]

【表1】 [Table 1]

【0026】[0026]

【発明の効果】本発明の表面保護フィルムまたはシート
は、オートクレーブ等により加熱圧着して常温に戻して
も、浮き現象の発生を防ぐことができる。従って、偏光
板用の表面保護フィルムまたはシートとして用いた場
合、気泡の発生を抑え、後工程の異物検査が容易とな
る。
The surface protective film or sheet of the present invention can prevent the occurrence of a floating phenomenon even when the surface protective film or sheet is heated and pressed by an autoclave or the like to return to room temperature. Therefore, when used as a surface protective film or sheet for a polarizing plate, generation of bubbles is suppressed, and foreign matter inspection in a later step is facilitated.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 20℃、0%RHでの酸素透過率が40
(cc/m2 ・24hrs・atm)未満であるプラス
チックフィルムを基材として、その片側に粘着剤層を設
けた表面保護フィルムまたはシート。
1. Oxygen permeability at 20 ° C. and 0% RH is 40
(Cc / m 2 · 24 hrs · atm) A surface protection film or sheet comprising a plastic film as a base material and an adhesive layer provided on one side thereof.
【請求項2】 偏光板用の表面保護フィルムまたはシー
トである請求項1記載の表面保護フィルムまたはシー
ト。
2. The surface protective film or sheet according to claim 1, which is a surface protective film or sheet for a polarizing plate.
JP15376097A 1997-06-11 1997-06-11 Surface protective film or sheet Pending JPH11961A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15376097A JPH11961A (en) 1997-06-11 1997-06-11 Surface protective film or sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15376097A JPH11961A (en) 1997-06-11 1997-06-11 Surface protective film or sheet

Publications (1)

Publication Number Publication Date
JPH11961A true JPH11961A (en) 1999-01-06

Family

ID=15569541

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15376097A Pending JPH11961A (en) 1997-06-11 1997-06-11 Surface protective film or sheet

Country Status (1)

Country Link
JP (1) JPH11961A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011132567A1 (en) 2010-04-20 2011-10-27 日東電工株式会社 Water-dispersing acrylic adhesive composition and adhesive sheet
JP2012021167A (en) * 2011-10-19 2012-02-02 Nitto Denko Corp Surface-protective film of polarizing plate, polarizing plate protected by the surface-protective film and method for protecting surface of polarizing plate using the surface-protective film
EP2511357A1 (en) 2011-04-13 2012-10-17 Nitto Denko Corporation Removable water-dispersible acrylic pressure-sensitive adhesive composition and pressure-sensitive adhesive sheet
WO2013058208A1 (en) 2011-10-19 2013-04-25 日東電工株式会社 Removable water-dispersible acrylic-based adhesive composition and adhesive sheet
EP2690149A1 (en) 2012-07-27 2014-01-29 Nitto Denko Corporation Re-Peelable Water Dispersion Type Acryl-Based Pressure-Sensitive Adhesive Composition, Pressure-Sensitive Adhesive Sheet, and Optical Member
US9096781B2 (en) 2012-05-11 2015-08-04 Nitto Denko Corporation Re-peelable water dispersion type acryl-based pressure-sensitive adhesive composition, and pressure-sensitive adhesive sheet
JP2017013306A (en) * 2015-06-30 2017-01-19 クラレプラスチックス株式会社 Multilayer laminate film and manufacturing method therefor

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011132567A1 (en) 2010-04-20 2011-10-27 日東電工株式会社 Water-dispersing acrylic adhesive composition and adhesive sheet
WO2011132565A1 (en) 2010-04-20 2011-10-27 日東電工株式会社 Water-dispersible acrylic adhesive agent composition and adhesive sheet
WO2011132566A1 (en) 2010-04-20 2011-10-27 日東電工株式会社 Removable water-dispersing acrylic adhesive composition and adhesive sheet
EP2511357A1 (en) 2011-04-13 2012-10-17 Nitto Denko Corporation Removable water-dispersible acrylic pressure-sensitive adhesive composition and pressure-sensitive adhesive sheet
JP2012021167A (en) * 2011-10-19 2012-02-02 Nitto Denko Corp Surface-protective film of polarizing plate, polarizing plate protected by the surface-protective film and method for protecting surface of polarizing plate using the surface-protective film
WO2013058208A1 (en) 2011-10-19 2013-04-25 日東電工株式会社 Removable water-dispersible acrylic-based adhesive composition and adhesive sheet
US9096781B2 (en) 2012-05-11 2015-08-04 Nitto Denko Corporation Re-peelable water dispersion type acryl-based pressure-sensitive adhesive composition, and pressure-sensitive adhesive sheet
EP2690149A1 (en) 2012-07-27 2014-01-29 Nitto Denko Corporation Re-Peelable Water Dispersion Type Acryl-Based Pressure-Sensitive Adhesive Composition, Pressure-Sensitive Adhesive Sheet, and Optical Member
KR20140014004A (en) 2012-07-27 2014-02-05 닛토덴코 가부시키가이샤 Aqueous dispersion type acrylic pressure-sensitive adhesive composition, pressure-sensitive adhesive sheet, and optical member for repeeling
JP2017013306A (en) * 2015-06-30 2017-01-19 クラレプラスチックス株式会社 Multilayer laminate film and manufacturing method therefor

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