JPH06194520A - Phase-difference film - Google Patents
Phase-difference filmInfo
- Publication number
- JPH06194520A JPH06194520A JP4343671A JP34367192A JPH06194520A JP H06194520 A JPH06194520 A JP H06194520A JP 4343671 A JP4343671 A JP 4343671A JP 34367192 A JP34367192 A JP 34367192A JP H06194520 A JPH06194520 A JP H06194520A
- Authority
- JP
- Japan
- Prior art keywords
- polycarbonate
- film
- retardation
- photoelastic constant
- phase
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、STN−LCDの表示
を白黒化するために用いられる位相差フィルムに関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a retardation film used for black and white display of STN-LCD.
【0002】[0002]
【従来の技術】STN液晶表示素子の複屈折効果による
位相差を補償し、表示を白黒化するためには位相差の補
償板が必要であり、当初は同じタイプの液晶セルで補償
していたが、最近では、軽量、低コストであることか
ら、プラスチックフィルムからなる位相差フィルムが用
いられている。使用されている樹脂としては、ポリカー
ボネート、ポリメチルメタクリレート及びポリビニルア
ルコール及びポリスチレンなどがあり、これらの樹脂か
らなるフィルムを均一に一軸延伸することにより製造さ
れており、原理的には線状高分子の一軸配向により生ず
る複屈折効果を利用したものである。しかしながら、プ
ラスチックの延伸フィルムは、斜めから見た場合、リタ
デーションが大きく変化するため、垂直から見た場合は
白黒表示であっても、斜めから見た場合は著しい着色を
生じたり、表示の反転を生じるため、視野が制限されて
いる。2. Description of the Related Art A phase difference compensating plate is necessary for compensating a phase difference due to a birefringence effect of an STN liquid crystal display element and making a display black and white. Initially, the same type of liquid crystal cell was used for compensation. However, recently, a retardation film made of a plastic film has been used because of its light weight and low cost. As the resin used, there are polycarbonate, polymethylmethacrylate, polyvinyl alcohol, polystyrene, etc., which are produced by uniformly uniaxially stretching a film made of these resins. This utilizes the birefringence effect caused by the uniaxial orientation. However, the stretched plastic film has a large change in retardation when viewed from an oblique direction. Therefore, even if it is displayed in black and white when viewed from a vertical direction, when it is viewed from an oblique direction, remarkable coloring occurs or the display is reversed. As a result, the field of view is limited.
【0003】これを解決するために、いろいろと研究さ
れているが、樹脂の改良及び複合化により解決を試みて
いる例としては、正の複屈折を生ずる樹脂からなる位相
差フィルムと負の複屈折を生ずる樹脂からなる位相差フ
ィルムを組合わせる方法(特開平3-206422号公報)や、
正の複屈折を生ずる樹脂と負の複屈折を生ずる樹脂を共
重合させるか又は混合した樹脂により位相差フィルムを
作製する方法(特開平4-195103,4-194902号公報)が提
案されている。これまでの提案のうち、複屈折の符号の
異なる2枚の位相差フィルムを重ねる方法においては、
2枚の軸を合せる作業が難しいこと、2枚使用するため
透過率が低下し、表示が暗くなること、また2枚のため
材料費が高価になる、等の欠点を有する。また、複屈折
の符号の異なる樹脂を共重合又は混合する方法において
は、光弾性定数が大きく、耐熱性があり、光学的に完全
な相溶性を示す組合せは非常に少ないという欠点があ
る。Various studies have been conducted to solve this problem. As an example of attempting to solve the problem by improving and compounding the resin, a retardation film made of a resin which produces positive birefringence and a negative birefringence film are given. A method of combining retardation films made of a resin that causes refraction (Japanese Patent Laid-Open No. 3-206422),
A method of producing a retardation film by copolymerizing or mixing a resin that produces positive birefringence and a resin that produces negative birefringence (JP-A-4-195103, 4-194902) has been proposed. . Among the proposals so far, in the method of stacking two retardation films having different signs of birefringence,
It has drawbacks that it is difficult to align the axes of two sheets, the transmittance is reduced due to the use of two sheets, the display is dark, and the material cost is high because of the two sheets. Further, the method of copolymerizing or mixing resins having different signs of birefringence has the drawbacks that the photoelastic constant is large, the heat resistance is high, and there are very few combinations showing optical perfect compatibility.
【0004】[0004]
【発明が解決しようとする課題】本発明は、これらの欠
点を改良するため、光学的に透明性がよく、耐熱性があ
り、光弾性定数も大きく、従って薄い位相差フィルムが
可能であり、またコスト的にも有利な位相差フィルムを
提供するものである。本発明は、単一のレジンを用い、
1枚のフィルムにて、視野の広角化を達成し、視野角の
大きな位相差フィルムを提供するものである。DISCLOSURE OF THE INVENTION In order to improve these drawbacks, the present invention has optical transparency, heat resistance and a large photoelastic constant, so that a thin retardation film is possible. It also provides a retardation film which is advantageous in terms of cost. The present invention uses a single resin,
It is intended to provide a retardation film having a wide viewing angle and a wide viewing angle with a single film.
【0005】[0005]
【課題を解決するための手段】本発明は、ポリカーボネ
ートとなしたときに、ポリカーボネートAの固体の光弾
性定数 > ポリカーボネートBの固体の光弾性定数とな
るようなポリカーボネートAを生成し得るジヒドロキシ
化合物aと、ポリカーボネートBを生成し得るジヒドロ
キシ化合物bとのポリカーボネート共重合体で形成され
た位相差フィルムである。DISCLOSURE OF THE INVENTION The present invention provides a dihydroxy compound a capable of producing a polycarbonate A having a solid photoelastic constant of polycarbonate A> a solid photoelastic constant of polycarbonate B when made into a polycarbonate. And a dihydroxy compound b capable of producing a polycarbonate B, is a retardation film formed of a polycarbonate copolymer.
【0006】[0006]
【作用】本発明においては、上記のような構成を有した
樹脂を用いることにより、延伸後の位相差フィルムの厚
み方向の屈折率の低下を抑えることができ、従って相対
的に厚み方向の屈折率が大きくなり、その結果、リタデ
ーションの角度依存性が小さくなり、視野角を広くする
ことができる。本発明においては、ポリカーボネートA
の光弾性定数 > ポリカーボネートBの光弾性定数であ
り、より効果的には、(ポリカーボネートAの光弾性定
数 −ポリカーボネートBの光弾性定数)≧ 10ブリュー
スター、好ましくは、20ブリュースターであることが望
ましい。In the present invention, by using the resin having the above-mentioned constitution, it is possible to suppress the decrease in the refractive index in the thickness direction of the retardation film after stretching, and thus the relative refractive index in the thickness direction As a result, the angle dependence of retardation is reduced and the viewing angle can be widened. In the present invention, polycarbonate A
Photoelastic constant of Polycarbonate B> more effectively, the photoelastic constant of Polycarbonate A-the photoelastic constant of Polycarbonate B ≧ 10 Brewster, preferably 20 Brewster desirable.
【0007】本発明において用いられるジヒドロキシ化
合物aとしては、種々のものを用いることができるが、
ビスフェノールA及びその誘導体のようなジヒドロキシ
芳香族系化合物が適している。ジヒドロキシ化合物bと
しては、化学的性質及び物性の点から、同様にジヒドロ
キシ芳香族系化合物が好ましいが、特にビスフェノール
Aの中央炭素のメチル基をベンゼン環、シクロヘキサン
環、脂肪族炭化水素基で置換した誘導体や、ビスフェノ
ールAのそれぞれのベンゼン環に中央炭素に対して非対
称に脂肪族基、ベンゼン環、シクロヘキサン環などを導
入したジヒドロキシ芳香族系化合物が好ましい。つま
り、ジヒドロキシ化合物bとしては、生成するポリカー
ボネートの単位分子内での異方性が極力小さくなる構造
を与えるものを用いることが望まれる。As the dihydroxy compound a used in the present invention, various compounds can be used.
Dihydroxy aromatic compounds such as bisphenol A and its derivatives are suitable. The dihydroxy compound b is preferably a dihydroxy aromatic compound from the viewpoint of chemical properties and physical properties, but particularly, the methyl group at the central carbon of bisphenol A is substituted with a benzene ring, a cyclohexane ring or an aliphatic hydrocarbon group. A derivative or a dihydroxy aromatic compound in which an aliphatic group, a benzene ring, a cyclohexane ring or the like is introduced into each benzene ring of bisphenol A asymmetrically with respect to the central carbon is preferable. That is, it is desirable to use, as the dihydroxy compound b, a compound that gives a structure in which the anisotropy in the unit molecule of the resulting polycarbonate is as small as possible.
【0008】本発明において、ポリカーボネート共重合
体の組成比は、ジヒドロキシ化合物aとジヒドロキシ化
合物bの共重合体中の重量比が95:5〜5:95、より効果
的には、90:10〜10:90 が好ましい。ジヒドロキシ化
合物bが5より少ないと、角度依存性が改良されない。
またジヒドロキシ化合物bが95より多いと、光弾性定数
が小さくなり過ぎて、延伸しても大きなリタデーション
が得られず、安定した加工ができず、均一なフィルムが
得られにくくなる。In the present invention, the composition ratio of the polycarbonate copolymer is such that the weight ratio of the dihydroxy compound a and the dihydroxy compound b in the copolymer is 95: 5 to 5:95, more effectively 90:10 to. 10:90 is preferable. When the dihydroxy compound b is less than 5, the angle dependence is not improved.
If the dihydroxy compound b is more than 95, the photoelastic constant becomes too small, a large retardation cannot be obtained even when stretched, stable processing cannot be performed, and it becomes difficult to obtain a uniform film.
【0009】コスト的には、特殊なジヒドロキシ化合物
bの比率ができるだけ小さなところで、光学特性が最良
となる配合を見出すことが望まれる。このようにして得
られた共重合体の粘度平均分子量は、20000〜100000が
好ましい。In terms of cost, it is desired to find a composition having the best optical characteristics when the ratio of the special dihydroxy compound b is as small as possible. The viscosity average molecular weight of the copolymer thus obtained is preferably 20000 to 100000.
【0010】[0010]
(実施例1)ビスフェノールAと、4,4'-ヒドロキシテ
トラフェニルメタンとを、重量で 90:10 となるような
ポリカーボネート共重合体を製造した。この場合、ビス
フェノールAのみを用いたポリカーボネートの固体の光
弾性定数は、71ブリュースターであり、4,4'-ヒドロキ
シテトラフェニルメタンのみを用いたポリカーボネート
の固体の光弾性定数は22ブリュースターであった。また
共重合体をの粘度平均分子量は35000であった。次に、
この共重合体を塩化メチレンに溶解し、固形分20%のワ
ニスとし、流延法により厚さ70μmのフィルムを作製し
た。さらにこのフィルムをテンター式延伸機にて、165
℃に加熱し、1.2倍に一軸延伸を行った。Example 1 A polycarbonate copolymer having a weight ratio of bisphenol A and 4,4′-hydroxytetraphenylmethane of 90:10 was produced. In this case, the solid photoelastic constant of the polycarbonate using only bisphenol A is 71 Brewster, and the solid photoelastic constant of the polycarbonate using only 4,4'-hydroxytetraphenylmethane is 22 Brewster. It was The viscosity average molecular weight of the copolymer was 35,000. next,
This copolymer was dissolved in methylene chloride to prepare a varnish having a solid content of 20%, and a film having a thickness of 70 μm was produced by a casting method. Furthermore, this film was 165
It was heated to ℃, and uniaxially stretched 1.2 times.
【0011】得られたフィルムの光学特性を評価したと
ころ、リタデーションは370nmであり、リタデーション
の角度依存性は、入射角45度において、増相方向と減相
方向の平均で9%の変化率であった。この値は、比較例
1の現行品に比し、数段改良されており、液晶セルに装
着し、白黒表示パネルとして使用してみたところ、広い
視野角で表示特性が向上し、使い易く、疲労感の少ない
ものであった。When the optical properties of the obtained film were evaluated, the retardation was 370 nm, and the angle dependence of the retardation was 9% in average in the increasing and decreasing directions at an incident angle of 45 degrees. there were. This value has been improved several times compared to the current product of Comparative Example 1, and when it was attached to a liquid crystal cell and used as a monochrome display panel, the display characteristics were improved in a wide viewing angle, and it was easy to use. There was little feeling of fatigue.
【0012】(実施例2)ビスフェノールAと、2,2'-
ビス(3-シクロヘキシル-4-ヒドロキシフェニル)プロパ
ンとを重量比で 70:30 となるようなポリカーボネート
共重合体を製造した。この場合、2,2'-ビス(3-シクロヘ
キシル-4-ヒドロキシフェニル)プロパンのみを用いたポ
リカーボネートの固体での光弾性定数は、29ブリュース
ターであった。次に、実施例1と同様な方法にて、80μ
m厚のフィルムを作製し、テンター式延伸機にて、160
℃、1.2倍に一軸延伸を行った。このようにして得られ
た位相差フィルムの光学特性を評価したところ、リタデ
ーションは410nmであり、リタデーションの角度依存性
は、入射角45度の傾斜で、増相方向と減相方向を平均し
た値で7%であり、広い視野角を示した。(Example 2) Bisphenol A and 2,2'-
A polycarbonate copolymer having a weight ratio of 70:30 with bis (3-cyclohexyl-4-hydroxyphenyl) propane was produced. In this case, the solid-state photoelastic constant of the polycarbonate using only 2,2′-bis (3-cyclohexyl-4-hydroxyphenyl) propane was 29 Brewster. Next, in the same manner as in Example 1, 80μ
A film with a thickness of m is produced, and the
Uniaxial stretching was carried out at 1.2 ° C and 1.2 times. When the optical properties of the retardation film thus obtained were evaluated, the retardation was 410 nm, and the angle dependence of the retardation was a value obtained by averaging the phase increasing direction and the phase decreasing direction at an inclination of an incident angle of 45 degrees. 7%, showing a wide viewing angle.
【0013】(比較例)粘度平均分子量70000のビスフ
ェノールAのみを用いたポリカーボネートを用いて、実
施例1と同様な方法により、90μmのフィルムを作製し
た。次に、テンター式延伸機にて、170℃、1.2倍の条件
で一軸延伸を行った。得られた位相差フィルムの光学特
性を評価したところ、リタデーションは450nmであり、
リタデーションの角度依存性は、入射角45度で増相方向
及び減相方向の平均で25%であった。この位相差フィル
ムを液晶パネルに装着したところ、視野がかなり狭く、
容易に視野の反転を生じ、表示性が悪く、使用者の視角
が制限され、疲労を感じさせるものであった。(Comparative example) A 90 μm film was prepared in the same manner as in Example 1 using a polycarbonate containing only bisphenol A having a viscosity average molecular weight of 70,000. Next, uniaxial stretching was performed with a tenter type stretching machine at 170 ° C. and 1.2 times. When the optical properties of the obtained retardation film were evaluated, the retardation was 450 nm,
The angle dependence of retardation was 25% on average in the increasing and decreasing directions at an incident angle of 45 degrees. When this phase difference film was attached to the liquid crystal panel, the field of view was quite narrow,
The field of view was easily inverted, the displayability was poor, the viewing angle of the user was limited, and the user felt tired.
【0014】[0014]
【発明の効果】本発明の位相差フィルムを用いることに
より、大きな視角の変化に対しても、着色による白黒表
示の色調の変化を最小限にとどめ、STN液晶表示素子
の視野特性を改良し、表示特性の改善を図ることができ
る。The use of the retardation film of the present invention minimizes the change in color tone of black and white display due to coloring even with a large change in viewing angle, and improves the visual field characteristics of the STN liquid crystal display device. The display characteristics can be improved.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 坂元 秀治 千葉県袖ケ浦市上泉1280番地 出光興産株 式会社中央研究所内 (72)発明者 宮本 秀幸 千葉県袖ケ浦市上泉1280番地 出光興産株 式会社中央研究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Shuji Sakamoto 1280 Kamizumi, Sodegaura, Chiba Prefecture Central Research Institute of Idemitsu Kosan Co., Ltd. (72) Hideyuki Miyamoto 1280, Uezumi, Sodegaura, Chiba Idemitsu Kosan Co., Ltd. Central Research Center
Claims (1)
カーボネートAの固体の光弾性定数 > ポリカーボネー
トBの固体の光弾性定数となるようなポリカーボネート
Aを生成し得るジヒドロキシ化合物aと、ポリカーボネ
ートBを生成し得るジヒドロキシ化合物bとのポリカー
ボネート共重合体で形成された位相差フィルム。1. A dihydroxy compound a capable of producing a polycarbonate A and a polycarbonate B capable of producing a polycarbonate having a photoelastic constant of a solid of polycarbonate A> a solid photoelastic constant of polycarbonate B when formed into a polycarbonate. A retardation film formed of a polycarbonate copolymer with a dihydroxy compound b.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34367192A JP3312937B2 (en) | 1992-12-24 | 1992-12-24 | Retardation film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34367192A JP3312937B2 (en) | 1992-12-24 | 1992-12-24 | Retardation film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06194520A true JPH06194520A (en) | 1994-07-15 |
JP3312937B2 JP3312937B2 (en) | 2002-08-12 |
Family
ID=18363344
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP34367192A Expired - Fee Related JP3312937B2 (en) | 1992-12-24 | 1992-12-24 | Retardation film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3312937B2 (en) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0259702A (en) * | 1988-08-25 | 1990-02-28 | Sumitomo Chem Co Ltd | Phase difference plate |
JPH03155502A (en) * | 1989-11-14 | 1991-07-03 | Nippon Carbide Ind Co Inc | Phase difference film-like material |
JPH0484107A (en) * | 1990-07-27 | 1992-03-17 | Toyo Chem Co Ltd | Production of phase difference film |
JPH05288933A (en) * | 1992-04-10 | 1993-11-05 | Toray Ind Inc | Phase difference film and phase difference film integrated polarizing film formed by using this film |
JPH0625398A (en) * | 1992-07-07 | 1994-02-01 | Teijin Chem Ltd | Polycarbonate resin with high refractive index and low birefringence |
JPH0675113A (en) * | 1992-08-26 | 1994-03-18 | Idemitsu Kosan Co Ltd | Phase difference compensation film |
JPH0682624A (en) * | 1992-09-04 | 1994-03-25 | Idemitsu Kosan Co Ltd | Phase-difference compensating film |
JPH06148426A (en) * | 1992-11-05 | 1994-05-27 | Idemitsu Petrochem Co Ltd | Phase difference compensation film and its production |
-
1992
- 1992-12-24 JP JP34367192A patent/JP3312937B2/en not_active Expired - Fee Related
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0259702A (en) * | 1988-08-25 | 1990-02-28 | Sumitomo Chem Co Ltd | Phase difference plate |
JPH03155502A (en) * | 1989-11-14 | 1991-07-03 | Nippon Carbide Ind Co Inc | Phase difference film-like material |
JPH0484107A (en) * | 1990-07-27 | 1992-03-17 | Toyo Chem Co Ltd | Production of phase difference film |
JPH05288933A (en) * | 1992-04-10 | 1993-11-05 | Toray Ind Inc | Phase difference film and phase difference film integrated polarizing film formed by using this film |
JPH0625398A (en) * | 1992-07-07 | 1994-02-01 | Teijin Chem Ltd | Polycarbonate resin with high refractive index and low birefringence |
JPH0675113A (en) * | 1992-08-26 | 1994-03-18 | Idemitsu Kosan Co Ltd | Phase difference compensation film |
JPH0682624A (en) * | 1992-09-04 | 1994-03-25 | Idemitsu Kosan Co Ltd | Phase-difference compensating film |
JPH06148426A (en) * | 1992-11-05 | 1994-05-27 | Idemitsu Petrochem Co Ltd | Phase difference compensation film and its production |
Also Published As
Publication number | Publication date |
---|---|
JP3312937B2 (en) | 2002-08-12 |
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