JPH05681B2 - - Google Patents
Info
- Publication number
- JPH05681B2 JPH05681B2 JP33872190A JP33872190A JPH05681B2 JP H05681 B2 JPH05681 B2 JP H05681B2 JP 33872190 A JP33872190 A JP 33872190A JP 33872190 A JP33872190 A JP 33872190A JP H05681 B2 JPH05681 B2 JP H05681B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- polarizing
- adhesive
- polarizing plate
- cellulose acetate
- 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
- 239000000853 adhesive Substances 0.000 claims description 18
- 230000001070 adhesive effect Effects 0.000 claims description 18
- 230000001681 protective effect Effects 0.000 claims description 15
- 229920002301 cellulose acetate Polymers 0.000 claims description 12
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 229920002451 polyvinyl alcohol Polymers 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
- 238000002834 transmittance Methods 0.000 description 6
- 239000012790 adhesive layer Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
- 238000007127 saponification reaction Methods 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- 229920002284 Cellulose triacetate Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 229920001477 hydrophilic polymer Polymers 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 208000028659 discharge Diseases 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- -1 etc.) Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Polarising Elements (AREA)
- Laminated Bodies (AREA)
Description
[産業上の利用分野]
本発明は、偏光板の製造法に関するものであ
る。
[従来の技術]
近年、卓上電子計算機、電子時計、ワープロ、
自動車や機械類の計器類等に液晶表示装置が用い
られ、これに伴い偏光板の需要も増大している。
偏光板は、一般に偏光能を有する偏光膜の両面
に、接着剤層を介して保護膜を形成させたもので
ある。
偏光膜としては例えば、ポリビニルアルコール
系樹脂やエチレン−酢酸ビニル共重合体ケン化物
等のビニルアルコール系一軸延伸フイルムに沃素
を染色させたもの等が代表的に用いられ、保護膜
としては、酢酸セルロース系フイルムが、表面保
護膜として光学的透明性、無配向性などにすぐれ
ているため汎用されている。
ビニルアルコール系フイルムも酢酸セルロース
系フイルムも親水性であるため、親水性の接着剤
を用いて貼合しているが一般的である。このた
め、得られる偏光板は長時間高湿雰囲気下におい
ては吸水率が大きく、吸水するにつれて接着力が
低下し、偏光物性の低下がおこつて、いわゆる耐
湿性や寸法安定性に問題が生じたりする場合があ
る。
この問題を解決するため、例えば、特開昭56−
50301号公報では、保護膜の酢酸セルロース系フ
イルム表面をケン化処理して、接着剤と酢酸セル
ロースとの接着力を強固にし、耐湿性、耐熱性及
び寸法安定性を改善することが提案されている。
又、特開昭61−245107号公報では、偏光膜の表
面をポリビニルアルコール、カルボキシメチルセ
ルロース、ウレタン系、アクリル系、エポキシ系
等の親水性高分子の水溶液又は、接着剤で一度処
理した後、再度接着剤を介して保護膜を接着する
ことによつて、接着強度の改善された偏光板を提
供することが提案されている。
[発明が解決しようとする課題]
しかし、特開昭56−50301号公報に記載の方法
では、保護膜と接着剤層の接着力は改善される
が、偏光膜と接着剤層の接着力に関しては何ら改
善されず、この点も同時に改善することが偏光板
の耐湿性および寸法安定性を改善する上で重要で
ある。
該方法に比較して、特開昭61−245107号公報に
記載の方法では偏光膜と接着剤層、及び接着剤層
と保護膜の接着性の改善を同時にめざしているの
でいくらか実用性の高い製品は得られるものの、
耐湿性及び寸法安定性ではまだ十分満足出来るも
のではなく、更なる改善が望まれるところであ
る。
[課題を解決するための手段]
そこで、本発明者はかかる課題を解決するため
に鋭意研究を行つた結果、ビニルアルコール系偏
光膜の少なくとも一方の面に酢酸セルロース系保
護膜を接着材料を用いて接着してなる偏光板を製
造するに当たり、接着後の偏光板を90〜110℃の
温度で熱処理することにより、耐湿性及び寸法安
定性に優れた偏光板が得られることを見出し、本
発明を完成するに至つた。
本発明のビニルアルコール系偏光膜とは、一軸
延伸したポリビニルアルコール系フイルムやエチ
レン−酢酸ビニル共重合体ケン化物フイルムに沃
素や二色性染料を吸着配向せしめたものが一般的
に用いられる。
ポリビニルアルコール及びエチレン−酢酸ビニ
ル共重合体ケン化物は必ずしもこれに限定される
ものではなく、少量の不飽和カルボン酸(塩、エ
ステル、アミド、ニトリル等を含む)、オレフイ
ン類、ビニルエーテル類、不飽和スルホン酸塩
等、酢酸ビニルあるいは更にエチレンと共重合可
能な成分を含有していても良い。
本発明の偏光膜は公知の任意の方法で製造さ
れ、例えば下記に示す様な手段が採用されるが、
本発明ではこれに限定されるものではない。
沃素又は二色性染料の水溶液、又は更にこの水
溶液に沃化カリウム及び/又は硼酸を加えた水溶
液を常温もしくは加温(30〜60℃)しておき、該
水溶液にポリビニルアルコール系フイルム、又は
エチレン−酢酸ビニル共重合体ケン化物フイルム
を含浸染色し3〜5倍に延伸するか、又はあらか
じめ延伸フイルムを上記含浸液に浸漬して染色す
る。得られたフイルムを緊張を保ちながらアルコ
ール又は水で表面を洗浄し、乾燥して偏光膜を得
る。
本発明の酢酸セルロース系保護膜としては二酢
酸セルロース、三酢酸セルロース等のフイルムが
ある。また該保護膜の表面をアルカリでケン化処
理したり、プラズマ処理、グロー放電処理、コロ
ナ放電処理、高周波処理、電子線処理等を行う
と、更に効果的である。
本発明で用いる接着剤は特に制限はなく公知の
ものが任意に用いられ、例えばポリビニルアルコ
ール及びその誘導体、デンプン類、カルボキシメ
チルセルロース等の水溶性高分子あるいはアクリ
ル系樹脂、ウレタン系樹脂、エポキシ系樹脂等の
親水性高分子が挙げられる。
接着剤は実用的には0.5〜40重量%、好ましく
は1〜10重量%の濃度の水溶液で使用される。
上記、接着剤の塗布量としては0.1〜5g/m2、
好ましくは1〜3g/m2が適当である。0.1g/
m2未満の場合は、接着力が不充分であり、一方、
5g/m2をこえる場合は、使用量の割には効果は
増加せず、実用的ではない。
通常、該接着剤は偏光膜あるいは酢酸セルロー
ス保護膜上に均一な膜を形成する様に塗工される
のが有利である。塗工操作は必ずしもロール等を
用いる塗布手段に限定されるものではなく、噴霧
法、浸漬法等の手段も含む。
上記酢酸セルロース系保護膜(又は偏光膜)に
上記接着剤を塗布し、上記偏光膜(又は酢酸セル
ロース系保護膜)の少なくとも一方の面と貼合わ
せ、30〜90℃、好ましくは60〜80℃で0.5〜5分、
好ましくは1〜2分間乾燥を行い、続いて90〜
110℃で0.5〜5分程度熱処理を行うことにより本
発明の偏光板が得られる。90℃以下の温度での熱
処理温度では本発明の効果は得難く、一方110℃
をこえるとフイルムに黄変がおこり障害が発生す
る。
このようにして得られた偏光板は、従来のもの
より、耐湿性及び寸法安定性が優れており、産業
上極めて重要である。
[作用]
本発明の製造方法では、ビニルアルコール系偏
光膜と酢酸セルロース系保護膜を接着した後、90
〜110℃で熱処理することにより、得られる偏光
板の耐熱性、耐湿性及び寸法安定性が著しく改善
される。
[実施例及び対照例]
以下実施例及び対照例を挙げて本発明を更に具
体的に説明する。
本発明における偏光度とは下記の式より求めた
値である。
H‖
;2枚のサンプルを偏光膜の配向方向が同一
方向になるように重ね合わせて透過率を測定し
た(平行透過率)。
H⊥
;2枚のサンプルを偏光膜の配向方向が互い
に直交する方向に重ね合わせて透過率を測定し
た(直交透過率)。
透過率の測定には日本電色工業製Z−1001DP
分光光度計を用いた。
実施例 1
重合度3800、ケン化度99.9モル%、含水率10重
量%、厚さ50μのポリビニルアルコールフイルム
を、沃素5.0g、沃化カリウム250g、硼酸10g、
水1000gからなる40℃の浴に浸漬しながら、約5
分間で4倍まで一軸延伸した。
得られたフイルムを緊張を保ちながらアルコー
ルで表面を洗浄後風乾し、偏光膜を得た。アルカ
リで表面処理した三酢化セルロースフイルムに重
合度1700、ケン化度99.9モル%のポリビニルアル
コールの4重量%水溶液を5μの厚みに塗布し、
偏光膜の両面に貼合わせ、80℃、2分間、熱風乾
燥機中で乾燥後95℃で熱処理を行い偏光板を得
た。
耐湿テストは、得られた偏光板を60℃−90%
RHの恒温恒湿槽に10日間放置後、単体透過率、
偏光度の変化及び寸法変化を測定した。
テストの結果を第1表に示した。
実施例 2
実施例1において熱処理温度を105℃にした以
外は同様に実験を行つた。結果を第1表に示し
た。
実施例 3
実施例1においてポリビニルアルコールフイル
ムの延伸倍率を5倍に変更した以外は同様に実験
を行つた。
実施例 4
実施例1においてポリビニルアルコールフイル
ムの代わりに、エチレン含量40モル%、酢酸ビニ
ル成分のケン化度99.9モル%、揮発分5重量%、
厚さ70μのエチレン−酢酸ビニル共重合体ケン化
物フイルムを用いた以外は実施例1に準じて実験
を行つた。結果を第1表に示した。
対照例 1、2
実施例1において熱処理温度を85℃にした(対
照例1)及び熱処理温度を120℃にした(対照例
2)以外は、実施例1に準じて実験を行つた。
結果を第1表に示した。
[Industrial Field of Application] The present invention relates to a method for manufacturing a polarizing plate. [Conventional technology] In recent years, desktop electronic computers, electronic clocks, word processors,
2. Description of the Related Art Liquid crystal display devices are used in instruments such as automobiles and machinery, and the demand for polarizing plates is increasing accordingly. A polarizing plate is generally made by forming protective films on both sides of a polarizing film having polarizing ability via an adhesive layer. Typical polarizing films used include polyvinyl alcohol resins, saponified ethylene-vinyl acetate copolymers, and other vinyl alcohol uniaxially stretched films dyed with iodine, and protective films include cellulose acetate. These films are widely used as surface protective films because of their excellent optical transparency and non-orientation properties. Since vinyl alcohol films and cellulose acetate films are both hydrophilic, they are generally bonded together using a hydrophilic adhesive. For this reason, the obtained polarizing plate has a high water absorption rate when left in a high humidity atmosphere for a long time, and as water is absorbed, the adhesive strength decreases and the polarizing properties deteriorate, causing problems in so-called moisture resistance and dimensional stability. There may be cases where In order to solve this problem, for example,
Publication No. 50301 proposes saponifying the surface of the cellulose acetate film of the protective film to strengthen the adhesive force between the adhesive and cellulose acetate, and improve moisture resistance, heat resistance, and dimensional stability. There is. Furthermore, in JP-A No. 61-245107, the surface of the polarizing film is treated once with an aqueous solution of a hydrophilic polymer such as polyvinyl alcohol, carboxymethyl cellulose, urethane, acrylic, or epoxy, or with an adhesive, and then treated again. It has been proposed to provide a polarizing plate with improved adhesive strength by bonding a protective film with an adhesive. [Problems to be Solved by the Invention] However, although the method described in JP-A-56-50301 improves the adhesive strength between the protective film and the adhesive layer, it does not improve the adhesive strength between the polarizing film and the adhesive layer. There was no improvement in this point, and it is important to improve this point at the same time in order to improve the moisture resistance and dimensional stability of the polarizing plate. Compared to this method, the method described in JP-A-61-245107 aims to improve the adhesion between the polarizing film and the adhesive layer, and between the adhesive layer and the protective film at the same time, so it is somewhat more practical. Although the product is obtained,
Moisture resistance and dimensional stability are still not fully satisfactory, and further improvement is desired. [Means for Solving the Problems] Therefore, as a result of intensive research in order to solve the problems, the inventors of the present invention have developed a method of attaching a cellulose acetate-based protective film to at least one surface of a vinyl alcohol-based polarizing film using an adhesive material. It was discovered that a polarizing plate with excellent moisture resistance and dimensional stability can be obtained by heat treating the bonded polarizing plate at a temperature of 90 to 110°C, and the present invention I was able to complete it. The vinyl alcohol polarizing film of the present invention is generally a uniaxially stretched polyvinyl alcohol film or a saponified ethylene-vinyl acetate copolymer film on which iodine or dichroic dye is adsorbed and oriented. Polyvinyl alcohol and saponified ethylene-vinyl acetate copolymers are not necessarily limited to these, but include small amounts of unsaturated carboxylic acids (including salts, esters, amides, nitriles, etc.), olefins, vinyl ethers, unsaturated It may contain a component copolymerizable with vinyl acetate or further with ethylene, such as a sulfonate. The polarizing film of the present invention can be manufactured by any known method, for example, the following methods may be employed.
The present invention is not limited to this. An aqueous solution of iodine or dichroic dye, or an aqueous solution prepared by adding potassium iodide and/or boric acid to this aqueous solution, is kept at room temperature or heated (30 to 60°C), and a polyvinyl alcohol film or ethylene is added to the aqueous solution. - A saponified vinyl acetate copolymer film is impregnated and dyed and stretched 3 to 5 times, or the stretched film is immersed in the above-mentioned impregnating liquid in advance and dyed. The surface of the obtained film is washed with alcohol or water while maintaining tension, and dried to obtain a polarizing film. The cellulose acetate-based protective film of the present invention includes films such as cellulose diacetate and cellulose triacetate. Further, it is more effective to subject the surface of the protective film to saponification treatment with an alkali, plasma treatment, glow discharge treatment, corona discharge treatment, high frequency treatment, electron beam treatment, etc. The adhesive used in the present invention is not particularly limited, and any known adhesive may be used, such as polyvinyl alcohol and its derivatives, starches, water-soluble polymers such as carboxymethyl cellulose, acrylic resins, urethane resins, and epoxy resins. Hydrophilic polymers such as Adhesives are practically used in aqueous solutions with a concentration of 0.5 to 40% by weight, preferably 1 to 10% by weight. Above, the amount of adhesive applied is 0.1 to 5 g/m 2 ,
Preferably, 1 to 3 g/m 2 is appropriate. 0.1g/
If it is less than m2 , the adhesive strength is insufficient;
If it exceeds 5 g/m 2 , the effect will not increase in proportion to the amount used, and it is not practical. Usually, it is advantageous to apply the adhesive so as to form a uniform film on the polarizing film or cellulose acetate protective film. The coating operation is not necessarily limited to a coating method using a roll or the like, but also includes methods such as a spraying method and a dipping method. Apply the adhesive to the cellulose acetate-based protective film (or polarizing film), and bond it to at least one side of the polarizing film (or cellulose acetate-based protective film) at 30 to 90°C, preferably 60 to 80°C. for 0.5 to 5 minutes,
Preferably dry for 1 to 2 minutes, followed by 90 to
The polarizing plate of the present invention can be obtained by performing heat treatment at 110°C for about 0.5 to 5 minutes. It is difficult to obtain the effect of the present invention at a heat treatment temperature of 90°C or lower, whereas at a heat treatment temperature of 110°C
If the temperature is exceeded, the film will yellow and cause problems. The polarizing plate thus obtained has better moisture resistance and dimensional stability than conventional ones, and is extremely important industrially. [Function] In the production method of the present invention, after adhering the vinyl alcohol polarizing film and the cellulose acetate protective film,
Heat treatment at ~110°C significantly improves the heat resistance, moisture resistance, and dimensional stability of the resulting polarizing plate. [Examples and Comparative Examples] The present invention will be described in more detail below with reference to Examples and Comparative Examples. The degree of polarization in the present invention is a value determined from the following formula. H|; Transmittance was measured by overlapping two samples so that the orientation directions of the polarizing films were in the same direction (parallel transmittance). H⊥; Transmittance was measured by overlapping two samples in a direction in which the orientation directions of the polarizing films were orthogonal to each other (orthogonal transmittance). Nippon Denshoku Kogyo Z-1001DP was used to measure transmittance.
A spectrophotometer was used. Example 1 A polyvinyl alcohol film with a degree of polymerization of 3800, a degree of saponification of 99.9 mol%, a water content of 10% by weight, and a thickness of 50μ was mixed with 5.0 g of iodine, 250 g of potassium iodide, 10 g of boric acid,
While immersed in a 40℃ bath consisting of 1000g of water,
It was uniaxially stretched up to 4 times in minutes. The surface of the obtained film was washed with alcohol while maintaining tension, and then air-dried to obtain a polarizing film. A 4% aqueous solution of polyvinyl alcohol with a degree of polymerization of 1700 and a degree of saponification of 99.9 mol% was applied to a thickness of 5μ on a cellulose triacetate film whose surface had been surface-treated with alkali.
It was pasted on both sides of the polarizing film, dried at 80°C for 2 minutes in a hot air dryer, and then heat-treated at 95°C to obtain a polarizing plate. Moisture resistance test was performed on the obtained polarizing plate at 60℃ - 90%
After being left in a constant temperature and humidity chamber at RH for 10 days, the single transmittance,
Changes in polarization degree and dimensional changes were measured. The test results are shown in Table 1. Example 2 An experiment was conducted in the same manner as in Example 1 except that the heat treatment temperature was changed to 105°C. The results are shown in Table 1. Example 3 An experiment was conducted in the same manner as in Example 1 except that the stretching ratio of the polyvinyl alcohol film was changed to 5 times. Example 4 In place of the polyvinyl alcohol film in Example 1, ethylene content was 40 mol%, saponification degree of vinyl acetate component was 99.9 mol%, volatile content was 5% by weight,
An experiment was carried out in accordance with Example 1, except that a saponified ethylene-vinyl acetate copolymer film having a thickness of 70 μm was used. The results are shown in Table 1. Control Examples 1 and 2 An experiment was conducted according to Example 1, except that the heat treatment temperature was 85° C. (Control Example 1) and 120° C. (Control Example 2). The results are shown in Table 1.
【表】
[効果]
前記の如く本発明の方法は、ビニルアルコール
系偏光膜と酢酸セルロース系フイルムを接着し、
続いて90〜110℃の温度で熱処理することにより、
得られる偏光板の耐湿性及び寸法安定性が著しく
改善され、工業的に優れた方法を提供するもので
ある。[Table] [Effects] As mentioned above, the method of the present invention involves bonding a vinyl alcohol polarizing film and a cellulose acetate film,
By subsequently heat-treating at a temperature of 90-110℃,
The moisture resistance and dimensional stability of the resulting polarizing plate are significantly improved, providing an industrially excellent method.
Claims (1)
の面に酢酸セルロース系保護膜を接着材料を用い
て接着し、ついで90〜110℃の温度にて熱処理す
ることを特徴とする偏光板の製造方法。1. A method for producing a polarizing plate, which comprises adhering a cellulose acetate-based protective film to at least one surface of a vinyl alcohol-based polarizing film using an adhesive material, and then heat-treating the film at a temperature of 90 to 110°C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP33872190A JPH04204803A (en) | 1990-11-30 | 1990-11-30 | Manufacturing method of polarizing plate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP33872190A JPH04204803A (en) | 1990-11-30 | 1990-11-30 | Manufacturing method of polarizing plate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04204803A JPH04204803A (en) | 1992-07-27 |
| JPH05681B2 true JPH05681B2 (en) | 1993-01-06 |
Family
ID=18320839
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP33872190A Granted JPH04204803A (en) | 1990-11-30 | 1990-11-30 | Manufacturing method of polarizing plate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04204803A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0894834A (en) * | 1994-09-26 | 1996-04-12 | Nippon Synthetic Chem Ind Co Ltd:The | Polarizer |
| US6859241B2 (en) | 2001-10-16 | 2005-02-22 | Nitto Denko Corporation | Method of producing polarizing plate, and liquid crystal display comprising the polarizing plate |
| KR101025466B1 (en) * | 2008-01-17 | 2011-04-04 | 닛토덴코 가부시키가이샤 | Polarizing plate, its manufacturing method, optical film, and image display apparatus |
-
1990
- 1990-11-30 JP JP33872190A patent/JPH04204803A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH04204803A (en) | 1992-07-27 |
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