JPS6340283B2 - - Google Patents
Info
- Publication number
- JPS6340283B2 JPS6340283B2 JP2592483A JP2592483A JPS6340283B2 JP S6340283 B2 JPS6340283 B2 JP S6340283B2 JP 2592483 A JP2592483 A JP 2592483A JP 2592483 A JP2592483 A JP 2592483A JP S6340283 B2 JPS6340283 B2 JP S6340283B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- polarizing
- plastic layer
- polarizing plate
- composition
- 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
- 229920003023 plastic Polymers 0.000 claims description 16
- 239000004033 plastic Substances 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 7
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 150000004291 polyenes Chemical class 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- RGYAVZGBAJFMIZ-UHFFFAOYSA-N 2,3-dimethylhex-2-ene Chemical compound CCCC(C)=C(C)C RGYAVZGBAJFMIZ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- -1 2-hydroxypropyl Chemical group 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B5/00—Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
- G11B5/02—Recording, reproducing, or erasing methods; Read, write or erase circuits therefor
- G11B5/027—Analogue recording
- G11B5/035—Equalising
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
- G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
Description
【発明の詳細な説明】
本発明は耐久性、熱安定性及び耐スクラツチ性
に優れる偏光板に関するものである。
偏光板は、一般に偏光フイルムの表面に透明な
プラスチツク層を形成させてなるものが汎用され
ており、その使用分野も従来の電卓や時計などの
小型品から、自動車用メーター、計器といつた大
型品へ拡大されつつある。
かかる使用分野の拡大に伴ない、偏光板に要求
される耐久性及び熱安定性などの特性もより高い
ものが要望されている。
一方、大型化に伴ない偏光板自体の耐スクラツ
チ性が要望されている。これは偏光板の製造工程
中や実装時に、偏光板表面にキズが入ると製品歩
留りが著しく低下すると共に、表示装置の外観や
光学特性を低下させるためである。
本発明の偏光板はかかる要望に従つて開発され
たものであつて、その要旨とするところは、偏光
フイルムの表面に無延伸又は一方向のみに延伸し
てなるプラスチツク層を形成してなる偏光基材の
該プラスチツク層面に、紫外線硬化型アクリルウ
レタン系樹脂にシリカゾルを含む組成物からなる
硬化皮膜層を形成してなることである。
本発明の偏光板によれば、偏光基材のプラスチ
ツク層面に紫外線硬化型アクリルウレタン系樹脂
にシリカゾルを含む組成物からなる硬化皮膜層が
形成されているので、表面硬度が大きく耐スクラ
ツチ性にすぐれ、しかも良好な耐久性及び熱安定
性を有するという特徴を有する。
本発明に使用される紫外線硬化型アクリルウレ
タン系樹脂は、一般にポリエステルポリオールと
にイソシアネートモノマー又はプレポリマーを反
応させ、さらにこれに2−ヒドロキシエチル(メ
タ)アクリレート、2−ヒドロキシプロピル(メ
タ)アクリレートの如き水酸基を有するアクリレ
ート又はメタクリレート系モノマーを反応させる
ことによつて得られ、かかる樹脂を用いることに
より、組成物の紫外線硬化を可能とし、しかもこ
れによつて表面硬度の大きい耐スクラツチ性にす
ぐれる硬化皮膜層が得られることが見い出され
た。
本発明に使用されるシリカゾルは、非晶質で多
孔性のものであり、コロイド状に分散するもので
ある。粒子径としては30mμ以下、好ましくは平
均粒子径5〜25mμであり、その屈折率は約
1.46、見掛け比重は約0.836程度のものである。
紫外線硬化型アクリルウレタン系樹脂とシリカ
ゾルとの割合は、樹脂100重量部に対して、シリ
カゾルが0.1〜35重量部となるように配合するの
が望ましいものである。シリカゾルが0.1重量部
以下では硬化皮膜層の表面硬度が小さく、35重量
部以上では光学特性を低下させるので好ましくな
いものである。
紫外線硬化型アクリルウレタン系樹脂とシリカ
ゾルとの組成物には、皮膜形成性向上や塗工時の
粘度調整を目的として、エチル(メタ)アクリレ
ート、イソプロピル(メタ)アクリレート、ブチ
ル(メタ)アクリレートの如きアルキル(メタ)
アクリレート、スチレン、(メタ)アクリロニト
リル、酢酸ビニルの如きビニルエステルモノマ
ー、(メタ)アクリレート、グリシジルメタクリ
レートの如き官能性モノマーなどのモノマーを添
加することができ、その範囲は1〜40重量%とさ
れるものである。
さらに前記組成物には、染料、顔料、帯電防止
剤などの配合剤を添加でき、また前記樹脂の光重
合剤が配合される。
該開始剤としては、アセトフエノン、ベンゾフ
エノン、ミセラーケトン、ベンジル、ベンゾイン
などの群から選ばれたものが例示でき、また光増
感剤としてアミン、尿素系化合物などを、熱重合
開始剤としてイミダゾール化合物、過酸化物など
を併用することもできる。
このように配合された組成物は、単独或いは該
組成物が塗布硬化される後記プラスチツク層に対
して不活性な有機溶剤に、固形分濃度で20〜95重
量%となるように希釈され、スピンナーコート、
グラビアコータ、リバースコータ、スプレコー
タ、スロツトオリフイスコータなどの一般の塗工
法にて、1〜30g/m2(固形分)となるように塗
布し、乾燥後紫外線硬化されるものである。
かかる組成物からなる硬化皮膜層が形成される
偏光基材は、偏光フイルムの両面又は片面に、塗
設又は貼り合せなどの手段によつて形成した無延
伸又は一方向のみに延伸してなるプラスチツク層
とから構成される。
従つて、本発明の偏光板には例えば第1〜3図
に図示した形状のものが包合される。
第1図においては、1は偏光フイルム、2はプ
ラスチツク層、3は前記組成物からなる硬化皮膜
層である。
第2図は、層2,2′及び3,3′がフイルム1
の両面に夫々形成されたものである。
第3図は、偏光板をプラスチツク液晶セルの基
板として用いる場合の実例を示すもので、硬化皮
膜からなる層3′の表面にパターン状の透明導電
膜4が形成されたものであり、層3′はキズなど
による膜4の断線を防止する。
前記偏光フイルムとしては、ポリビニルアルコ
ール系フイルム、部分ホルマール化ポリビニルア
ルコール系フイルム、エチレン−酢酸ビニル共重
合体系ケン化フイルムの如き親水性高分子系フイ
ルムに沃素及び/又は二色性染料を吸着配向せし
めた沃素及び/又は二色性染料系偏光フイルム、
ポリビニルアルコール系フイルムを脱水処理する
か、或いはポリ塩化ビニルフイルムを脱塩酸処理
するかしてポリエンを配向せしめたポリエン系偏
光フイルムなどが挙げられ、これらは通常10〜
80μmの厚みを有するものが使用される。
偏光フイルムの片面又は両面に形成される無延
伸又は一方向のみに延伸してなるプラスチツク層
(厚さは約10〜2000μmが好ましい)は、ポリア
クリル系樹脂、ポリウレタン系樹脂の如き塗布硬
化型の樹脂を塗布硬化させるか、ポリエステルフ
イルム、ポリカーボネートフイルム、ポリスルホ
ンフイルム、ポリエーテルフイルム、トリメチル
ペンテンフイルム、ポリエーテルケトンフイル
ム、(メタ)アクリロニトリルフイルムなどの光
学的透明性にすぐれる無方向又は一方向のみに延
伸してなるプラスチツクフイルムをポリエステル
系接着剤、ポリアクリル系接着剤、ポリウレタン
系接着剤、ポリ酢酸ビニル系接着剤の如き光学的
透明性にすぐれる接着剤或いは溶着などの接着手
段を用いて貼り合せるかして構成される。しかし
て、該プラスチツク層に耐薬品性などを望む場合
には、縦軸又は横軸方向にのみ少なくとも5%、
好ましくは50〜800%延伸し、100〜230℃で5〜
60分間熱処理してなるポリエステルフイルムが好
ましいものである。
このような偏光フイルムとプラスチツク層とか
ら構成される偏光基材において、前記組成物が塗
布硬化されるプラスチツク層面には、プラスチツ
ク基材の材質に応じてアルカリ処理、コロナ処理
スパツタ処理などの表面処理やシランカツプリン
グ剤の塗布或いはSi蒸着などによる表面改質処理
を行うことは、プラスチツク層と組成物からなる
硬化皮膜層との接着性向上の点から好ましいこと
である。
このようにして得られた偏光板は、硬化皮膜層
の硬度が高いので良好な耐スクラツチ性を有し、
またアクリルウレタン系樹脂にて皮膜が構成され
ているので耐久性や熱安定性にすぐれるという特
徴を有する。
以下本発明の実施例を示す。
実施例
厚さ50μmの沃素系偏光フイルムの両面に、厚
さ100μmの一軸延伸(延伸率300%)したポリエ
ステルフイルムをポリエステル系接着剤にて接着
して偏光基板を作成した。
この基板の一方のフイルム面に、第1表に示す
組成物をスピンナーコータによりライン速度10
m/分で塗布し、100℃で3分間乾燥後、オゾン
タイプ高圧水銀灯(80W/cm、15cm集光型)2灯
で紫外線照射を行い、平均塗膜厚みが4μmの硬
化皮膜層を有する偏光板を得た。
各偏光板の皮膜層面の表面硬度をJISK5401塗
膜用鉛筆ひつかき試験機で測定した結果、参考例
の皮膜形成前の表面硬度がHであつたのに対し、
本実施例は各れも2〜4Hの硬度を有するもので
あつた。
第1表に組成物(単位重量部)及び測定結果を
示す。第1表中の光透過率及び偏光度は常法によ
り測定した。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polarizing plate having excellent durability, thermal stability and scratch resistance. Polarizing plates are generally made by forming a transparent plastic layer on the surface of a polarizing film, and their use ranges from small items such as conventional calculators and watches to large items such as automobile meters and instruments. It is being expanded to include products. With the expansion of such fields of use, polarizing plates are required to have higher properties such as durability and thermal stability. On the other hand, with the increase in size, there is a demand for the scratch resistance of the polarizing plate itself. This is because if the surface of the polarizing plate is scratched during the manufacturing process or mounting of the polarizing plate, the product yield will be significantly lowered, and the appearance and optical characteristics of the display device will also be degraded. The polarizing plate of the present invention was developed in accordance with such a request, and its gist is that a polarizing plate is produced by forming a plastic layer on the surface of a polarizing film, either unstretched or stretched only in one direction. A cured film layer made of a composition containing silica sol in an ultraviolet curable acrylic urethane resin is formed on the surface of the plastic layer of the base material. According to the polarizing plate of the present invention, a cured film layer made of a composition containing silica sol in an ultraviolet curable acrylic urethane resin is formed on the plastic layer surface of the polarizing base material, so the surface hardness is large and the scratch resistance is excellent. Moreover, it has the characteristics of good durability and thermal stability. The UV-curable acrylic urethane resin used in the present invention is generally produced by reacting an isocyanate monomer or prepolymer with a polyester polyol, and then adding 2-hydroxyethyl (meth)acrylate or 2-hydroxypropyl (meth)acrylate to this. It is obtained by reacting an acrylate or methacrylate monomer having a hydroxyl group such as the following, and by using such a resin, it is possible to cure the composition with ultraviolet rays, and this also provides a high surface hardness and excellent scratch resistance. It has been found that a cured film layer can be obtained. The silica sol used in the present invention is amorphous, porous, and colloidally dispersed. The particle size is 30 mμ or less, preferably an average particle size of 5 to 25 mμ, and the refractive index is approximately
1.46, and the apparent specific gravity is about 0.836. It is desirable that the proportion of the ultraviolet curable acrylic urethane resin and silica sol is 0.1 to 35 parts by weight based on 100 parts by weight of the resin. If the amount of silica sol is less than 0.1 parts by weight, the surface hardness of the cured film layer will be low, and if it is more than 35 parts by weight, the optical properties will deteriorate, which is not preferable. The composition of ultraviolet curable acrylic urethane resin and silica sol contains ethyl (meth)acrylate, isopropyl (meth)acrylate, butyl (meth)acrylate, etc. for the purpose of improving film formation and adjusting viscosity during coating. Alkyl (meta)
Monomers such as acrylates, styrene, (meth)acrylonitrile, vinyl ester monomers such as vinyl acetate, functional monomers such as (meth)acrylates, glycidyl methacrylate, etc. can be added in the range of 1 to 40% by weight. It is something. Furthermore, additives such as dyes, pigments, and antistatic agents may be added to the composition, and a photopolymerization agent for the resin may be added. Examples of the initiator include those selected from the group such as acetophenone, benzophenone, micellar ketone, benzyl, and benzoin; photosensitizers include amines and urea compounds, and thermal polymerization initiators include imidazole compounds and urea compounds. Oxides etc. can also be used in combination. The composition thus formulated may be used alone or diluted with an organic solvent inert to the plastic layer to be coated and cured to a solid content of 20 to 95% by weight, and then applied to a spinner. coat,
It is applied by a general coating method such as a gravure coater, reverse coater, spray coater, or slot orifice coater at a concentration of 1 to 30 g/m 2 (solid content), and then cured with ultraviolet light after drying. The polarizing base material on which a cured film layer made of such a composition is formed is a plastic film formed on both or one side of a polarizing film by coating or bonding, and is either non-stretched or stretched only in one direction. It consists of layers. Therefore, the polarizing plate of the present invention may have the shapes shown in FIGS. 1 to 3, for example. In FIG. 1, 1 is a polarizing film, 2 is a plastic layer, and 3 is a cured film layer made of the above composition. Figure 2 shows that layers 2, 2' and 3, 3' are film 1.
are formed on both sides of the . FIG. 3 shows an example of using a polarizing plate as a substrate for a plastic liquid crystal cell, in which a patterned transparent conductive film 4 is formed on the surface of a layer 3' made of a cured film. ' prevents disconnection of the membrane 4 due to scratches or the like. The polarizing film is a hydrophilic polymer film such as a polyvinyl alcohol film, a partially formalized polyvinyl alcohol film, or a saponified ethylene-vinyl acetate copolymer film, on which iodine and/or dichroic dyes are adsorbed and oriented. iodine and/or dichroic dye-based polarizing film,
Examples include polyene polarizing films in which polyenes are oriented by dehydrating a polyvinyl alcohol film or dehydrochlorinating a polyvinyl chloride film, and these films usually have a
A material having a thickness of 80 μm is used. The unstretched or unidirectionally stretched plastic layer (preferably about 10 to 2,000 μm in thickness) formed on one or both sides of the polarizing film is a coating-curable plastic layer such as polyacrylic resin or polyurethane resin. Apply and cure the resin, or use non-directional or unidirectional film with excellent optical transparency such as polyester film, polycarbonate film, polysulfone film, polyether film, trimethylpentene film, polyether ketone film, (meth)acrylonitrile film, etc. The stretched plastic film is pasted using adhesives with excellent optical transparency such as polyester adhesives, polyacrylic adhesives, polyurethane adhesives, polyvinyl acetate adhesives, or adhesive means such as welding. It is composed by combining. If chemical resistance or the like is desired for the plastic layer, at least 5% in the vertical or horizontal direction only.
Preferably 50-800% stretching and 5-800% stretching at 100-230°C.
A polyester film heat-treated for 60 minutes is preferred. In a polarizing base material composed of such a polarizing film and a plastic layer, the surface of the plastic layer on which the composition is applied and cured may be subjected to surface treatment such as alkali treatment, corona treatment, sputtering treatment, etc. depending on the material of the plastic base material. It is preferable to perform a surface modification treatment such as coating with a silane coupling agent or Si vapor deposition from the viewpoint of improving the adhesion between the plastic layer and the cured film layer made of the composition. The polarizing plate obtained in this way has good scratch resistance due to the high hardness of the cured film layer.
Furthermore, since the film is made of acrylic urethane resin, it has excellent durability and thermal stability. Examples of the present invention will be shown below. Example A polarizing substrate was prepared by adhering a 100 μm thick uniaxially stretched (stretching ratio: 300%) polyester film to both sides of a 50 μm thick iodine polarizing film using a polyester adhesive. The composition shown in Table 1 was applied onto one film surface of this substrate using a spinner coater at a line speed of 10.
After drying at 100℃ for 3 minutes, UV irradiation was performed using two ozone-type high-pressure mercury lamps (80W/cm, 15cm condensing type) to create a cured film layer with an average coating thickness of 4μm. Got the board. The surface hardness of the film layer surface of each polarizing plate was measured using a JISK5401 paint film pencil scratch tester, and the surface hardness of the reference example before film formation was H.
Each of the examples had a hardness of 2 to 4H. Table 1 shows the composition (parts by weight) and measurement results. The light transmittance and degree of polarization in Table 1 were measured by conventional methods. 【table】
第1〜3図は本発明の偏光板の実例を示す部分
拡大側面図である。
3……硬化皮膜層。
1 to 3 are partially enlarged side views showing examples of the polarizing plate of the present invention. 3...Cured film layer.
Claims (1)
に延伸してなるプラスチツク層を形成してなる偏
光基材の該プラスチツク層面に、紫外線硬化型ア
クリルウレタン系樹脂にシリガゾルを含む組成物
からなる硬化皮膜層を形成してなることを特徴と
する偏光板。1 A cured film made of a composition containing siligasol in an ultraviolet curable acrylic urethane resin is applied to the surface of the plastic layer of a polarizing base material formed by forming a plastic layer unstretched or stretched only in one direction on the surface of a polarizing film. A polarizing plate characterized by forming layers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2592483A JPS59151110A (en) | 1983-02-17 | 1983-02-17 | Polarizing plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2592483A JPS59151110A (en) | 1983-02-17 | 1983-02-17 | Polarizing plate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59151110A JPS59151110A (en) | 1984-08-29 |
JPS6340283B2 true JPS6340283B2 (en) | 1988-08-10 |
Family
ID=12179319
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2592483A Granted JPS59151110A (en) | 1983-02-17 | 1983-02-17 | Polarizing plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59151110A (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6289907A (en) * | 1985-06-19 | 1987-04-24 | Sumitomo Bakelite Co Ltd | Transparent conductive film united with polarizing film |
JP2530537B2 (en) * | 1991-12-13 | 1996-09-04 | 日本製紙株式会社 | Hard coat film |
EP2233607A1 (en) | 2000-12-12 | 2010-09-29 | Konica Corporation | Dielectric coated electrode, and plasma discharge apparatus using the electrode |
CN100568067C (en) | 2005-08-30 | 2009-12-09 | 柯尼卡美能达精密光学株式会社 | Liquid crystal indicator |
EP2278047A1 (en) | 2005-08-31 | 2011-01-26 | Konica Minolta Holdings, Inc. | Plasma discharge treatment apparatus, and method of manufacturing gas barrier film |
JP5633566B2 (en) * | 2010-08-25 | 2014-12-03 | コニカミノルタ株式会社 | Hard coat film, polarizing plate and liquid crystal display device |
JP2012173677A (en) * | 2011-02-24 | 2012-09-10 | Konica Minolta Advanced Layers Inc | Phase difference film and method for manufacturing the same, elongated polarizing plate, and liquid crystal display device |
JPWO2014010562A1 (en) | 2012-07-13 | 2016-06-23 | コニカミノルタ株式会社 | Infrared shielding film |
EP2881769A4 (en) | 2012-08-06 | 2016-03-09 | Konica Minolta Inc | Light-reflective film, and light reflector produced using same |
-
1983
- 1983-02-17 JP JP2592483A patent/JPS59151110A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59151110A (en) | 1984-08-29 |
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