JP2000206303A - Polarizing plate protective film and polarizing plate - Google Patents
Polarizing plate protective film and polarizing plateInfo
- Publication number
- JP2000206303A JP2000206303A JP11009393A JP939399A JP2000206303A JP 2000206303 A JP2000206303 A JP 2000206303A JP 11009393 A JP11009393 A JP 11009393A JP 939399 A JP939399 A JP 939399A JP 2000206303 A JP2000206303 A JP 2000206303A
- Authority
- JP
- Japan
- Prior art keywords
- polarizing plate
- protective film
- film
- resin
- photoelastic constant
- 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
Links
- 230000001681 protective effect Effects 0.000 title claims abstract description 39
- 239000011347 resin Substances 0.000 claims abstract description 36
- 229920005989 resin Polymers 0.000 claims abstract description 36
- 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 claims abstract description 15
- 229920002284 Cellulose triacetate Polymers 0.000 claims description 13
- 239000004973 liquid crystal related substance Substances 0.000 claims description 13
- 210000002858 crystal cell Anatomy 0.000 claims description 12
- 230000003287 optical effect Effects 0.000 abstract description 6
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
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- 239000010410 layer Substances 0.000 description 19
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 239000000853 adhesive Substances 0.000 description 10
- 230000001070 adhesive effect Effects 0.000 description 10
- 238000003851 corona treatment Methods 0.000 description 9
- 230000007423 decrease Effects 0.000 description 9
- 239000004417 polycarbonate Substances 0.000 description 9
- 229920000515 polycarbonate Polymers 0.000 description 9
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 8
- 229920002492 poly(sulfone) Polymers 0.000 description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000012790 adhesive layer Substances 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 230000010287 polarization Effects 0.000 description 6
- 229920002451 polyvinyl alcohol Polymers 0.000 description 6
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 208000028659 discharge Diseases 0.000 description 4
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 4
- -1 polyethylene terephthalate Polymers 0.000 description 4
- 239000004926 polymethyl methacrylate Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000004695 Polyether sulfone Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 101150059062 apln gene Proteins 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 238000009820 dry lamination Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 2
- 229920001230 polyarylate Polymers 0.000 description 2
- 229920006393 polyether sulfone Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 102100029777 Eukaryotic translation initiation factor 3 subunit M Human genes 0.000 description 1
- 101001012700 Homo sapiens Eukaryotic translation initiation factor 3 subunit M Proteins 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 239000004419 Panlite Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000009477 glass transition Effects 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
- 238000003475 lamination Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
Landscapes
- Polarising Elements (AREA)
- Liquid Crystal (AREA)
- Surface Treatment Of Optical Elements (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、耐熱性と耐湿熱性
に優れた偏光板保護フィルム、及びそれを用いた偏光板
に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polarizing plate protective film excellent in heat resistance and wet heat resistance, and a polarizing plate using the same.
【0002】[0002]
【従来の技術】近年、液晶ディスプレイ(LCD)は車
両積載機器用や携帯情報機器用として用いられることが
多くなり、高温及び高温多湿環境下におけるLCDの信
頼性が強く要望されている。従来よりLCDに用いられ
る偏光板は、延伸配向したポリビニルアルコール(PV
A)にヨウ素もしくは二色染料を吸着させた偏光子の両
面に、光学等方性を有するフィルムが保護膜として用い
られている。保護膜としては複屈折率が小さいトリアセ
チルセルロース(TAC)が一般的に使用されている。2. Description of the Related Art In recent years, liquid crystal displays (LCDs) are often used for on-board equipment and portable information equipment, and there is a strong demand for the reliability of LCDs under high-temperature and high-temperature and high-humidity environments. Conventionally, polarizing plates used for LCDs are stretched and oriented polyvinyl alcohol (PV).
A film having optical isotropy is used as a protective film on both surfaces of a polarizer having iodine or a dichroic dye adsorbed on A). As a protective film, triacetyl cellulose (TAC) having a small birefringence is generally used.
【0003】しかし、TACは吸水率が高いために高温
多湿環境下において偏光度の低下、変色による透過率の
低下が起こる。又、高温環境下でPVAの配向緩和が起
き、保護膜のTACに応力が発生したとき大きな複屈折
が生じることにより偏光度の低下をもたらし、LCDに
表示むらの発生やコントラスト低下が起こる原因とな
る。However, since TAC has a high water absorption, the degree of polarization decreases and the transmittance decreases due to discoloration in a high-temperature and high-humidity environment. In addition, under the high temperature environment, the orientation of PVA is relaxed, and when a stress is applied to the TAC of the protective film, a large birefringence is caused to cause a decrease in the degree of polarization. Become.
【0004】偏光板に高温や高温多湿環境に対応させる
ための手段として、ポリカーボネート樹脂やポリメチル
メタクリレート系樹脂よりなるフィルムを用いた保護フ
ィルムが開示されている(特開平7−56017号公
報)。又、平均分子量が3万以上、ガラス転移温度が1
50℃以上であるポリカーボネートフィルムを保護フィ
ルムとして用いることも開示されている(特開平8−6
2419号公報)。As means for adapting a polarizing plate to a high-temperature or high-temperature and high-humidity environment, a protective film using a film made of a polycarbonate resin or a polymethyl methacrylate resin has been disclosed (Japanese Patent Application Laid-Open No. 7-56017). In addition, the average molecular weight is 30,000 or more, and the glass transition temperature is 1
It is also disclosed that a polycarbonate film having a temperature of 50 ° C. or higher is used as a protective film (JP-A-8-6).
2419).
【0005】上記公報に記載のものは、いずれも耐湿性
について改良は認められるが、高温環境下で受ける位相
差変化に伴う表示むらやコントラストの低下に対しては
未だ改良の余地が残されている。[0005] Although all of the publications described in the above publications are improved in terms of moisture resistance, there is still room for improvement with respect to display unevenness and a decrease in contrast due to a change in phase difference under a high temperature environment. I have.
【0006】[0006]
【発明が解決しようとする課題】本発明は上記の問題点
を解消し、偏光板に用いた場合、高温或いは高温多湿の
環境下においても表示むらの発生やコントラストの低下
を生じることのない偏光板保護フィルム、及び光学的特
性に優れた偏光板を提供することを目的とする。SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems and, when used in a polarizing plate, does not cause display unevenness or a decrease in contrast even in a high-temperature or high-temperature and high-humidity environment. It is an object to provide a plate protective film and a polarizing plate having excellent optical characteristics.
【0007】[0007]
【課題を解決するための手段】本発明の偏光板保護フィ
ルムは、トリアセチルセルロースよりも吸湿性が小さく
正の光弾性定数を有する樹脂層と、トリアセチルセルロ
ースよりも吸湿性が小さく負の光弾性定数を有する樹脂
層とが積層され、光弾性定数が10.0×10 -7cm2
/kgf以下であることを特徴とするものである。Means for Solving the Problems The polarizing plate protective film of the present invention is provided.
Lum is less hygroscopic than triacetyl cellulose
A resin layer having a positive photoelastic constant;
Resin with a lower hygroscopicity than base and a negative photoelastic constant
And a photoelastic constant of 10.0 × 10 -7cmTwo
/ Kgf or less.
【0008】又、本発明の偏光板は、請求項1記載の偏
光板保護フィルムが、偏光子の少なくとも液晶セル側の
面に貼り合わされたことを特徴とするものである。Further, the polarizing plate of the present invention is characterized in that the polarizing plate protective film according to claim 1 is bonded to at least the surface of the polarizer on the liquid crystal cell side.
【0009】本発明でいう光弾性定数とは、弾性体が外
力を受けたとき一時的に光学的異方体となって複屈折を
生じ、外力を除いたあと元に戻る光弾性効果を示す物質
において複屈折差の応力依存性を表す定数である。即
ち、複屈折差(Δn)と光弾性定数との関係は次式で表
される。 Δn=C・σ (Cは光弾性定数、σは応力を表す)The photoelastic constant referred to in the present invention refers to a photoelastic effect in which when an elastic body receives an external force, it temporarily becomes an optically anisotropic body, generates birefringence, and returns to its original state after removing the external force. It is a constant representing the stress dependence of the birefringence difference in a substance. That is, the relationship between the birefringence difference (Δn) and the photoelastic constant is represented by the following equation. Δn = C · σ (C is photoelastic constant, σ is stress)
【0010】正の光弾性定数を有する樹脂とは、上記光
弾性定数の符号が正の樹脂であり、負の光弾性定数を有
する樹脂とは上記光弾性定数の符号が負の樹脂である。
上記正、負の光弾性定数を有する樹脂はいずれも透明性
に優れ、TACよりも吸湿性が小さいことが必要であ
る。これらの条件を満たすものであれば単独重合体、共
重合体のいずれでもよい。A resin having a positive photoelastic constant is a resin having a positive photoelastic constant, and a resin having a negative photoelastic constant is a resin having a negative photoelastic constant.
Each of the resins having the positive and negative photoelastic constants is required to be excellent in transparency and to be less hygroscopic than TAC. As long as these conditions are satisfied, either a homopolymer or a copolymer may be used.
【0011】本発明の偏光板保護フィルムは、上記正の
光弾性定数を有する樹脂層と負の光弾性定数を有する樹
脂層との積層体であって、この積層体の光弾性定数が1
0.0×10-7cm2 /kgf以下である。光弾性定数
が上記よりも高いと高温下で位相差変化が激しく、LC
Dとして表示むらやコントラストの低下が顕著に現れ
る。The polarizing plate protective film of the present invention is a laminate of the resin layer having a positive photoelastic constant and the resin layer having a negative photoelastic constant, wherein the laminate has a photoelastic constant of 1
0.0 × 10 −7 cm 2 / kgf or less. If the photoelastic constant is higher than the above, the phase difference changes sharply at high temperature, and LC
As D, display unevenness and a decrease in contrast remarkably appear.
【0012】正の光弾性定数を有する樹脂の例として
は、ポリカーボネート(PC)、ポリサルホン(PS
u)、ポリアリレート、ポリエーテルサルホン、ポリエ
チレンテレフタレート(PET)、ポリスチレン、ノル
ボルネン開環重合水素添加物及びこれらのモノマーユニ
ットが含まれた共重合体等が挙げられる。Examples of the resin having a positive photoelastic constant include polycarbonate (PC) and polysulfone (PS).
u), polyarylate, polyether sulfone, polyethylene terephthalate (PET), polystyrene, norbornene ring-opening polymerization hydrogenated product, and a copolymer containing these monomer units.
【0013】負の光弾性定数を有する樹脂の例として
は、メチルメタクリレート(MMA)、α−メチルスチ
レン等の単独重合体及びこれらのモノマーユニットを含
む共重合体、エチレン−テトラシクロドデセン共重合体
等が挙げられる。Examples of the resin having a negative photoelastic constant include homopolymers such as methyl methacrylate (MMA) and α-methylstyrene, copolymers containing these monomer units, and ethylene-tetracyclododecene copolymer. Coalescence and the like.
【0014】正の光弾性定数を有する樹脂層と負の光弾
性定数を有する樹脂層を積層する方法としては、共押出
成形、押出ラミネートの他、それぞれの樹脂フィルムを
別々に作製し、これをポリウレタン系、ポリエステル
系、ポリアクリル系等の接着剤、又はアクリル系、シリ
コーン系、ゴム系等の粘着剤などを用いる公知の手段で
積層するドライラミネートを採用することができる。As a method of laminating a resin layer having a positive photoelastic constant and a resin layer having a negative photoelastic constant, besides co-extrusion molding and extrusion lamination, respective resin films are separately prepared, Dry lamination using known means, such as a polyurethane-based, polyester-based, or polyacryl-based adhesive, or an acrylic, silicone-, or rubber-based adhesive, can be employed.
【0015】ドライラミネートの場合は接着力を向上さ
せるために、貼り合わせ面にコロナ放電処理などの表面
処理を施しておくことが好ましい。本発明の偏光板保護
フィルムは少なくとも上記2層の樹脂層が必須である
が、必要に応じて他の樹脂層が積層されてもよい。しか
し、透過光の損失を最小限とするために3層以下とする
ことが好ましい。In the case of dry lamination, it is preferable to apply a surface treatment such as a corona discharge treatment to the bonding surface in order to improve the adhesive strength. The polarizing plate protective film of the present invention requires at least the two resin layers described above, but other resin layers may be laminated as necessary. However, in order to minimize the loss of transmitted light, the number of layers is preferably three or less.
【0016】偏光板保護フィルム全体の厚みは10〜1
000μmが好ましく、より好ましくは30〜500μ
mである。10μmよりも薄いと取扱い難く、透湿性が
高くなって耐久性に劣ることになる。又、1000μm
を超えると透明性が悪くなり、LCDの特長である薄型
軽量を達成できなくなる。The total thickness of the polarizing plate protective film is 10 to 1
000 μm is preferable, and more preferably 30 to 500 μm
m. If the thickness is less than 10 μm, it is difficult to handle, the moisture permeability increases, and the durability deteriorates. 1000 μm
When the ratio exceeds, the transparency is deteriorated, and it is impossible to achieve the thin and light weight which is a feature of the LCD.
【0017】正の光弾性定数を有する樹脂層と負の光弾
性定数を有する樹脂層との厚み比は、全体の厚みが上記
範囲内で光弾性定数が10.0×10-7cm2 /kgf
以下となる範囲で適宜選択することができる。The thickness ratio of the resin layer having a positive photoelastic constant to the resin layer having a negative photoelastic constant is such that the total thickness is within the above range and the photoelastic constant is 10.0 × 10 −7 cm 2 / kgf
It can be appropriately selected within the following range.
【0018】請求項2記載の偏光板は、請求項1記載の
偏光板保護フィルムが偏光子の少なくとも片面に積層さ
れたものであるが、偏光子の液晶セル側には必ず該保護
フィルムを使用しなければ高温下での位相差変化を抑え
られない。液晶セルと反対面は複屈折の影響はないの
で、必ずしも本発明の保護フィルムを用いなくてもよ
く、透明で吸水率が低ければ光弾性定数の正負にかかわ
らず樹脂を選択することができる。このような樹脂とし
ては、例えば、ポリカーボネート、ポリサルホン、ポリ
アリレート、ポリエーテルサルホン、ポリエチレンテレ
フタレート、ポリスチレン、ノルボルネン系樹脂、PM
MA、ポリα−メチルスチレン及びこれらのモノマーユ
ニットを含む共重合体等が挙げられる。In the polarizing plate according to the second aspect, the protective film for the polarizing plate according to the first aspect is laminated on at least one side of the polarizer, but the protective film is always used on the liquid crystal cell side of the polarizer. Otherwise, a change in the phase difference at a high temperature cannot be suppressed. Since the surface opposite to the liquid crystal cell is not affected by birefringence, the protective film of the present invention does not necessarily need to be used, and a resin can be selected regardless of the positive or negative photoelastic constant as long as it is transparent and has a low water absorption. Examples of such a resin include polycarbonate, polysulfone, polyarylate, polyethersulfone, polyethylene terephthalate, polystyrene, norbornene-based resin, PM
MA, poly-α-methylstyrene, copolymers containing these monomer units, and the like.
【0019】(作用)本発明の偏光板保護フィルムは、
TACよりも吸湿性が小さい樹脂層が積層されたもので
あるから、高温多湿環境においても偏光子を水分から保
護し、偏光度の低下や変色の発生が抑制される。又、光
弾性定数が10.0×10-7cm2 /kgf以下となさ
れているので、高温環境においてもPVAが収縮するこ
とによる応力が発生しても複屈折が起こり難くなり、偏
光板の表示むらの発生やコントラストの低下が抑制され
る。上記偏光板保護フィルムを用いた偏光板は、高温多
湿環境でも良好な光学的特性を維持できる。(Function) The protective film for polarizing plate of the present invention comprises:
Since the resin layer having lower hygroscopicity than TAC is laminated, the polarizer is protected from moisture even in a high-temperature and high-humidity environment, and a decrease in the degree of polarization and generation of discoloration are suppressed. Further, since the photoelastic constant is set to 10.0 × 10 −7 cm 2 / kgf or less, birefringence hardly occurs even when stress is generated due to shrinkage of PVA even in a high temperature environment, and the The occurrence of display unevenness and a decrease in contrast are suppressed. The polarizing plate using the polarizing plate protective film can maintain good optical characteristics even in a high-temperature and high-humidity environment.
【0020】[0020]
【発明の実施の形態】以下に本発明の実施例を説明す
る。偏光子の作製 鹸化度99%で厚み75μmのPVA未延伸フィルムを
室温の水で洗浄し、縦一軸に5倍延伸した。このフィル
ムの緊張状態を保持したままヨウ素0.5重量%、ヨウ
化カリウム5重量%からなる水溶液に浸漬することによ
り二色性色素を吸着させた。更にホウ酸10重量%、ヨ
ウ化カリウム10重量%からなる50℃の水溶液で5分
間架橋処理を行って偏光子を得た。Embodiments of the present invention will be described below. Preparation of Polarizer An unstretched PVA film having a saponification degree of 99% and a thickness of 75 μm was washed with water at room temperature and stretched 5 times uniaxially. The dichroic dye was adsorbed by immersing the film in an aqueous solution containing 0.5% by weight of iodine and 5% by weight of potassium iodide while maintaining the tension of the film. Further, a cross-linking treatment was carried out for 5 minutes with an aqueous solution of 10% by weight of boric acid and 10% by weight of potassium iodide at 50 ° C. to obtain a polarizer.
【0021】アクリル系粘着剤及び粘着剤層の調整 アクリル酸ブチル94.8重量部、アクリル酸5重量
部、2−ヒドロキシエチルメタクリレート0.2重量部
を過酸化ベンゾイル0.3重量部の存在下で酢酸エチル
を溶媒として共重合し、重量平均分子量(Mw)120
万、Mwと数平均分子量(Mn)の比(Mw/Mn)が
3.9であるアクリル系ポリマーの酢酸エチル溶液を得
た。得られたアクリル系ポリマーの酢酸エチル溶液にト
ルエンを加えて希釈しアクリル系ポリマー13重量%の
トルエン溶液とした。この溶液にイソシアネート架橋剤
(日本ポリウレタン社製,商品名「コロネートL」)
2.0重量部を添加し攪拌した溶液を離型フィルムに塗
布し、発泡しないように60℃で5分間、更に100℃
で5分間の2段階で乾燥させて粘着剤層を形成した。上
記粘着剤層面に軽剥離性の離型フィルムを貼り合わせ
た。この方法により平均厚みが10μmと25μmの2
種類の粘着剤層を作製した。Preparation of acrylic pressure-sensitive adhesive and pressure-sensitive adhesive layer 94.8 parts by weight of butyl acrylate, 5 parts by weight of acrylic acid, 0.2 parts by weight of 2-hydroxyethyl methacrylate in the presence of 0.3 parts by weight of benzoyl peroxide With ethyl acetate as a solvent at a weight average molecular weight (Mw) of 120.
An ethyl acetate solution of an acrylic polymer having a ratio (Mw / Mn) of Mw to the number average molecular weight (Mn) of 3.9 was obtained. Toluene was added to the obtained ethyl acetate solution of the acrylic polymer to dilute it to obtain a toluene solution of 13% by weight of the acrylic polymer. An isocyanate crosslinking agent (manufactured by Nippon Polyurethane Co., trade name "Coronate L")
The solution obtained by adding 2.0 parts by weight and stirring was applied to a release film, and then left at 60 ° C. for 5 minutes and further at 100 ° C. so as not to foam.
And dried in two stages for 5 minutes to form an adhesive layer. A light-releasable release film was bonded to the surface of the pressure-sensitive adhesive layer. By this method, the average thickness of 10 μm and 25 μm
Various kinds of pressure-sensitive adhesive layers were produced.
【0022】(実施例1)ポリカーボネート(PC)樹
脂(帝人化成社製,商品名「パンライトL−1225Z
E」)30重量%の塩化メチレン溶液を調製してポリエ
チレンテレフタレート(PET)基材上に流延し、60
℃で5分間、100℃で5分間、更に130℃で5分間
乾燥した後、基材より剥離して厚み10μmと50μm
の2種類のPC樹脂フィルムを作製した。MMA80重
量%、無水マレイン酸15重量%及びアクリル酸ブチル
5重量%を、過酸化ベンゾイル3重量%を開始剤として
80℃で重合を行った。得られたポリマーを30重量%
の塩化メチレン溶液としてPET基材上に流延し、60
℃で5分間、100℃で5分間乾燥し、基材より剥離し
て乾燥後の厚みが75μmのPMMA系フィルムを得
た。(Example 1) Polycarbonate (PC) resin (trade name: Panlite L-1225Z, manufactured by Teijin Chemicals Limited)
E ") A 30% by weight methylene chloride solution is prepared and cast on a polyethylene terephthalate (PET) substrate.
5 minutes at 100 ° C, 5 minutes at 100 ° C, and 5 minutes at 130 ° C.
2 types of PC resin films were produced. Polymerization was carried out at 80 ° C. using 80% by weight of MMA, 15% by weight of maleic anhydride and 5% by weight of butyl acrylate, with 3% by weight of benzoyl peroxide as an initiator. 30% by weight of the obtained polymer
Cast on a PET substrate as a methylene chloride solution of
It dried at 100 degreeC for 5 minutes at 100 degreeC, peeled from the base material, and obtained the 75-micrometer-thick PMMA-type film after drying.
【0023】上記PC樹脂フィルム(厚み10μm)と
PMMA系フィルムのそれぞれの片面に40W/m2 /
minの強さでコロナ放電処理を施した。これらのフィ
ルムのコロナ放電処理面を向き合わせ、平均厚み10μ
mの前記粘着剤層を介して貼り合わせ、PC樹脂フィル
ム/粘着剤層/PMMA系フィルムの構成である積層フ
ィルムを作製した。更に、該積層フィルムの両面にそれ
ぞれ40W/m2 /minでコロナ放電処理を行い、こ
れを液晶セル面側の保護フィルムとした。Each of the PC resin film (thickness: 10 μm) and the PMMA-based film has a surface of 40 W / m 2 /
A corona discharge treatment was performed at a strength of min. Face the corona-discharge treated surfaces of these films, and
Then, a laminated film having a structure of PC resin film / adhesive layer / PMMA-based film was produced by laminating through the above-mentioned adhesive layer. Further, both surfaces of the laminated film were subjected to corona discharge treatment at 40 W / m 2 / min, respectively, to obtain a protective film on the liquid crystal cell surface side.
【0024】一方、PC樹脂フィルム(厚み50μm)
の片面に40W/m2 /minでコロナ放電処理を行
い、これを液晶セル面の背面用の保護フィルムとした。
上記液晶セル面側保護フィルムのPMMA系フィルム層
面とエア面側保護フィルムのコロナ放電処理処理面に、
ポリエステル系接着剤(東洋モートン社製,商品名「T
M−593」)の30重量%酢酸エチル溶液を乾燥後の
厚みが2μmとなるように塗布し、90℃で乾燥した。
前記偏光子の両面に上記接着剤面を貼り合わせて偏光板
とした。On the other hand, a PC resin film (50 μm thick)
Was subjected to a corona discharge treatment at 40 W / m 2 / min to obtain a protective film for the back surface of the liquid crystal cell surface.
On the PMMA-based film layer surface of the liquid crystal cell surface side protective film and the corona discharge treated surface of the air surface side protective film,
Polyester adhesive (trade name “T” manufactured by Toyo Morton Co., Ltd.
M-593 ") was applied so as to have a thickness of 2 μm after drying, and dried at 90 ° C.
The adhesive surface was bonded to both surfaces of the polarizer to form a polarizing plate.
【0025】(実施例2)ポリサルホン(PSu)樹脂
(帝人アモコエンジニアプラスチック社製,商品名「U
DEL,P−3500」)の30重量%アニソール溶液
を調製し、PET基材上に流延し60℃で5分間、12
0℃で5分間、更に170℃で5分間乾燥し、厚み10
μmと50μmの2種類のPSuフィルムを作製した。
エチレン−テトラシクロドデセン共重合体(三井石油化
学社製,商品名「APEL6015」,以下「APE
L」と記す)の30重量%シクロヘキサン溶液を調製
し、PET基材に流延し、60℃で5分間、120℃で
5分間乾燥した後基材より剥離し、厚み70μmのAP
ELフィルムを作製した。(Example 2) Polysulfone (PSu) resin (trade name "U" manufactured by Teijin Amoko Engineer Plastics Co., Ltd.)
DEL, P-3500 ") in a 30% by weight anisole solution, and cast on a PET substrate at 60 ° C. for 5 minutes for 12 minutes.
Dried at 0 ° C for 5 minutes and further at 170 ° C for 5 minutes.
Two types of PSu films of μm and 50 μm were produced.
Ethylene-tetracyclododecene copolymer (trade name “APEL6015”, manufactured by Mitsui Petrochemical Co., Ltd .; hereinafter “APE
L)), cast on a PET substrate, dried at 60 ° C. for 5 minutes and at 120 ° C. for 5 minutes, and then peeled off from the substrate to obtain a 70 μm-thick AP.
An EL film was produced.
【0026】上記PSuフィルム(厚み10μm)とA
PELフィルムの各々の片面に40W/m2 /minで
コロナ放電処理を行い、コロナ放電処理面を向き合わせ
て前記粘着剤層(厚み10μm)を介して貼り合わせ、
PSuフィルム/APELフィルムの積層フィルムと
し、該積層フィルムの両面にそれぞれ40W/m2 /m
inでコロナ放電処理を行い、これを液晶セル側の保護
フィルムとした。The above-mentioned PSu film (thickness 10 μm) and A
A corona discharge treatment is performed on each side of the PEL film at 40 W / m 2 / min, and the corona discharge treatment surfaces are faced to each other, and bonded via the pressure-sensitive adhesive layer (thickness: 10 μm).
A laminated film of a PSu film / APEL film, and 40 W / m 2 / m on both sides of the laminated film
In was subjected to a corona discharge treatment to obtain a protective film on the liquid crystal cell side.
【0027】一方、PC樹脂フィルム(厚み50μm)
の片面に40W/m2 /minでコロナ放電処理を行
い、これを背面用保護フィルムとした。上記液晶セル面
側保護フィルムのAPEL樹脂層面と背面用保護フィル
ムのコロナ放電処理処理面に、ポリエステル系接着剤
(東洋モートン社製,商品名「TM−593」)の30
重量%酢酸エチル溶液を乾燥後の厚みが2μmとなるよ
うに塗布し、90℃で乾燥した。前記偏光子の両面に上
記接着剤面を貼り合わせて偏光板とした。On the other hand, a PC resin film (50 μm thick)
Was subjected to a corona discharge treatment at 40 W / m 2 / min to obtain a back surface protective film. A polyester adhesive (trade name “TM-593”, manufactured by Toyo Morton Co., Ltd.) is applied to the APEL resin layer surface of the liquid crystal cell surface side protective film and the corona discharge treated surface of the back surface protective film.
A weight% ethyl acetate solution was applied so that the thickness after drying became 2 μm, and dried at 90 ° C. The adhesive surface was bonded to both surfaces of the polarizer to form a polarizing plate.
【0028】(比較例1)TACのアルカリ鹸化フィル
ムをポリビニルアルコール系接着剤(日本合成化学社
製,商品名「ゴーセノールNH17」)の3重量%水溶
液を厚み1μmで塗布し、90℃で乾燥して接着剤層を
形成した。該接着剤層に前記偏光子を貼り合わせて偏光
板とした。(Comparative Example 1) A 3% by weight aqueous solution of a polyvinyl alcohol-based adhesive (trade name “Gohsenol NH17”, manufactured by Nippon Synthetic Chemical Industry Co., Ltd.) was applied to an alkali saponified film of TAC at a thickness of 1 μm and dried at 90 ° C. Thus, an adhesive layer was formed. The polarizer was bonded to the adhesive layer to form a polarizing plate.
【0029】(比較例2)比較例1で用いたものと同じ
TACのアルカリ鹸化フィルムを液晶セル側の保護フィ
ルムとした。実施例1で得たPC樹脂フィルム(厚み5
0μm)の片面に400W/m2 /minでコロナ放電
処理を行い、これを背面用保護フィルムとした。この背
面用保護フィルムのコロナ放電処理処理面及びTACフ
ィルムに比較例と同様の接着剤層を形成し、前記偏光子
を挟んで貼り合わせて偏光板とした。Comparative Example 2 The same TAC alkali saponified film as used in Comparative Example 1 was used as a protective film on the liquid crystal cell side. The PC resin film obtained in Example 1 (thickness 5
(0 μm) was subjected to a corona discharge treatment at 400 W / m 2 / min to obtain a back surface protective film. The same adhesive layer as in the comparative example was formed on the corona discharge treated surface of the back protective film and the TAC film, and bonded to each other with the polarizer interposed therebetween to obtain a polarizing plate.
【0030】〔性能評価〕 (1)液晶セル側の保護フィルム 光弾性定数の測定:保護フィルムを長方形に切り取り、
荷重に対する位相差(入射光550nm)を測定し、そ
の傾きにより求めた。位相差の測定には複屈折測定計
(大塚電子社製,商品名「RETS−2000」)を用
いた。 (2)偏光板:実施例及び比較例で得た液晶セル側の保
護フィルムに、前記アクリル系粘着剤層(厚み25μ
m)を離型フィルムを剥がして貼り合わせ、偏光板粘着
シートとした。該偏光板粘着シートを偏光子吸収軸の角
度が辺に45度の角度をなすように、トムソン打抜機で
12.1インチの長方形に打ち抜いて試験片とした。[Evaluation of Performance] (1) Measurement of Photoelastic Constant of Protective Film on Liquid Crystal Cell Side: The protective film was cut into a rectangle,
The phase difference (incident light at 550 nm) with respect to the load was measured, and the inclination was determined. For the measurement of the phase difference, a birefringence meter (trade name “RETS-2000” manufactured by Otsuka Electronics Co., Ltd.) was used. (2) Polarizing plate: The acrylic pressure-sensitive adhesive layer (thickness: 25 μm) was formed on the protective film on the liquid crystal cell side obtained in Examples and Comparative Examples.
m) was peeled off from the release film and bonded to obtain a polarizing plate adhesive sheet. The polarizing sheet pressure-sensitive adhesive sheet was punched out into a 12.1 inch rectangle by a Thomson punching machine so that the angle of the absorption axis of the polarizer made an angle of 45 degrees with the side to obtain a test piece.
【0031】試験片に残された離型フィルムを剥離し、
粘着面を厚み1.2mmのソーダガラスに卓上ラミネー
ターを用いて貼り付けた。粘着剤層を貼り付けたガラス
板を室温に1時間放置した後、5kgf/cm2 で20
分間オートクレーブ処理し、その後室温で1時間放置し
て耐久試験を行い、試験前後での下記による偏光度、色
差により表示特性を評価した。測定位置は各辺の中央部
で端部から10mmの位置の4点である。The release film left on the test piece was peeled off,
The adhesive surface was attached to soda glass having a thickness of 1.2 mm using a desktop laminator. After the glass plate was stuck the pressure-sensitive adhesive layer was left at room temperature for 1 hour, at 5 kgf / cm 2 20
After an autoclave treatment for one minute, it was left at room temperature for one hour to perform a durability test, and display characteristics were evaluated before and after the test based on the following degree of polarization and color difference. There are four measurement positions at the center of each side, 10 mm from the end.
【0032】偏光度=〔(H1−H2)/(H1+H
2)〕1/2 (但し、H1は平行透過率、H2は直交透過率) 色差:ΔEH L,a,b値より算出 以上の結果を平均値として表1に示した。Degree of polarization = [(H1-H2) / (H1 + H)
2)] 1/2 (where, H1 parallel transmittance, H2 is orthogonal transmittance) Color difference: shown in Table 1 ΔE H L, a, a calculation above results b value as an average value.
【0033】[0033]
【表1】 [Table 1]
【0034】[0034]
【発明の効果】本発明の偏光板保護フィルムは、TAC
よりも吸湿性が低く、光弾性定数が10.0×10-7c
m2 /kgf以下となされているので、偏光板に用いた
場合、高温多湿環境においても偏光度の低下や変色が生
じることが抑制され、良好な光学的特性を維持できる。
又、上記偏光板保護フィルムを用いた偏光板は、高温多
湿環境でも光学的特性が低下することがなく、携帯用機
器や車両積載用のLCDに好適に用いることができる。The polarizing plate protective film of the present invention has a TAC
Has a lower hygroscopicity and a photoelastic constant of 10.0 × 10 −7 c
Since m 2 / kgf or less, when used for a polarizing plate, a decrease in the degree of polarization and discoloration are suppressed even in a high-temperature and high-humidity environment, and good optical characteristics can be maintained.
Further, the polarizing plate using the polarizing plate protective film does not deteriorate its optical characteristics even in a high-temperature and high-humidity environment, and can be suitably used for a portable device or an LCD mounted on a vehicle.
フロントページの続き Fターム(参考) 2H049 BB62 BC14 2H091 FA08X FA08Z FD15 GA16 GA17 LA04 LA06 MA03 MA10 2K009 CC24 CC34 DD01 DD07 EE00 FF02 Continued on the front page F term (reference) 2H049 BB62 BC14 2H091 FA08X FA08Z FD15 GA16 GA17 LA04 LA06 MA03 MA10 2K009 CC24 CC34 DD01 DD07 EE00 FF02
Claims (2)
小さく正の光弾性定数を有する樹脂層と、トリアセチル
セルロースよりも吸湿性が小さく負の光弾性定数を有す
る樹脂層とが積層され、光弾性定数が10.0×10-7
cm2 /kgf以下であることを特徴とする偏光板保護
フィルム。1. A resin layer having a smaller hygroscopic property than triacetyl cellulose and having a positive photoelastic constant and a resin layer having a smaller hygroscopic property than triacetyl cellulose and having a negative photoelastic constant are laminated. Constant is 10.0 × 10 -7
polarizing plate protective film, wherein the at cm 2 / kgf or less.
偏光子の少なくとも液晶セル側の面に貼り合わされたこ
とを特徴とする偏光板。2. The polarizing plate protective film according to claim 1,
A polarizing plate, which is bonded to at least a surface of a polarizer on a liquid crystal cell side.
Priority Applications (1)
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JP11009393A JP2000206303A (en) | 1999-01-18 | 1999-01-18 | Polarizing plate protective film and polarizing plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11009393A JP2000206303A (en) | 1999-01-18 | 1999-01-18 | Polarizing plate protective film and polarizing plate |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000206303A true JP2000206303A (en) | 2000-07-28 |
Family
ID=11719196
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11009393A Pending JP2000206303A (en) | 1999-01-18 | 1999-01-18 | Polarizing plate protective film and polarizing plate |
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Country | Link |
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JP (1) | JP2000206303A (en) |
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TWI402541B (en) * | 2005-06-21 | 2013-07-21 | Zeon Corp | Protective film for polarizing plate (1) |
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WO2014162977A1 (en) * | 2013-04-03 | 2014-10-09 | 住友化学株式会社 | Polarizing plate |
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KR20150139568A (en) * | 2013-04-03 | 2015-12-11 | 스미또모 가가꾸 가부시키가이샤 | Polarizing plate |
JPWO2014162977A1 (en) * | 2013-04-03 | 2017-02-16 | 住友化学株式会社 | Polarizer |
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WO2022224921A1 (en) * | 2021-04-22 | 2022-10-27 | 住友化学株式会社 | Stacked body, and method for manufacturing same |
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