JP2780184B2 - Alignment film and liquid crystal device - Google Patents
Alignment film and liquid crystal deviceInfo
- Publication number
- JP2780184B2 JP2780184B2 JP1045597A JP4559789A JP2780184B2 JP 2780184 B2 JP2780184 B2 JP 2780184B2 JP 1045597 A JP1045597 A JP 1045597A JP 4559789 A JP4559789 A JP 4559789A JP 2780184 B2 JP2780184 B2 JP 2780184B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- alignment film
- polyamic acid
- substrate
- degrees
- 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
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- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Liquid Crystal (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Laminated Bodies (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は液晶表示体用液晶セルの配向膜の作成方法に
関する。The present invention relates to a method for forming an alignment film of a liquid crystal cell for a liquid crystal display.
[従来の技術] 近年、液晶表示体技術の発展は著しく、液晶テレビ等
への応用が可能となった。この液晶表示体は第1図に示
す如く二枚の透明電極12付き基板11と液晶14と配向膜13
よりなっている。[Prior Art] In recent years, the development of liquid crystal display technology has been remarkable, and application to liquid crystal televisions and the like has become possible. As shown in FIG. 1, the liquid crystal display comprises a substrate 11 having two transparent electrodes 12, a liquid crystal 14, and an alignment film 13.
Is made up of
液晶テレビに使われるアクティーブマトリクス駆動の
場合、画素が独立に駆動されるため、配向技術に関して
は従来の技術で問題にはならなかった。しかし、この場
合、歩留まりが悪く高価になる欠点がある。In the case of active matrix driving used in a liquid crystal television, since pixels are driven independently, there was no problem with the conventional technology regarding the alignment technology. However, in this case, there is a disadvantage that the yield is low and the cost is high.
一方、単純マトリクス駆動方式によれば、安価になる
可能性があるためアクティーブ方式の代替が考えられて
いる。On the other hand, according to the simple matrix driving method, there is a possibility that the cost may be reduced, so that an alternative to the active method is considered.
これら代替技術は、SBE方式,NTN方式等とよばれてい
る。These alternative technologies are called SBE system, NTN system and the like.
この技術の重量な点は、従来の液晶表示体の液晶分子
が90度ツイストしているのに対して、180度以上ツイス
トしていることである。The important point of this technology is that the liquid crystal molecules of the conventional liquid crystal display are twisted by 90 degrees or more, but twisted by 180 degrees or more.
このため液晶分子を基板に対して5度以上たたせ、過
度のネジリによる歪を逃がしてやる必要がある。5度以
上立たせる方法の一つとして配向膜による方法がある。For this reason, it is necessary to allow the liquid crystal molecules to be tilted at least 5 degrees with respect to the substrate to release the distortion due to excessive twisting. One of the methods of standing at least 5 degrees is a method using an alignment film.
180度以上液晶分子をツイストさせる従来の配向膜の
作成方法は、単一成分のポリイミド系樹脂を塗布する方
法であった。A conventional method of forming an alignment film in which liquid crystal molecules are twisted by 180 degrees or more has been a method of applying a single-component polyimide resin.
[発明が解決しようとする課題] 液晶表示体のコントラストを最善の状態にするために
は液晶の種類、液晶のネジレ角度に対応して液晶分子と
基板との角度を最適化しなければならない。[Problems to be Solved by the Invention] In order to optimize the contrast of the liquid crystal display, the angle between the liquid crystal molecules and the substrate must be optimized according to the type of liquid crystal and the twist angle of the liquid crystal.
しかし、単一成分を用いるため任意に基板との角度を
変えることはできなかった。However, the angle with the substrate could not be arbitrarily changed because a single component was used.
又多成分によって変えようとしても、単一成分で基板
との角度を大きく変えるような成分が無かったため幅広
く変えることは不可能であった。Further, even if an attempt is made to change by multiple components, it was impossible to change it widely because there was no component that would greatly change the angle with the substrate with a single component.
[課題を解決するための手段] 本発明の配向膜は,(1)2種類のポリアミド酸化合
物を含有する配向剤から形成される配向膜であって,一
方のポリアミド酸化合物は下記構造式を有することを特
徴とする。[Means for Solving the Problems] The alignment film of the present invention is (1) an alignment film formed from an alignment agent containing two kinds of polyamic acid compounds, and one polyamic acid compound has the following structural formula. It is characterized by having.
(ただし,nは正の整数,Rは水素またはアルキル基を示
す) また,本発明の液晶装置は,スペーサーを介して一対
の基板間に液晶が封入されてなる液晶装置において,2種
類のポリアミド酸化合物を含有する配向剤から形成され
る配向膜が前記一対の基板に形成されてなり,一方のポ
リアミド酸化合物は下記構造式を有することを特徴とす
る。 (However, n is a positive integer, and R represents hydrogen or an alkyl group.) The liquid crystal device of the present invention is a liquid crystal device in which liquid crystal is sealed between a pair of substrates via a spacer. An alignment film formed from an alignment agent containing an acid compound is formed on the pair of substrates, and one polyamic acid compound has the following structural formula.
(ただし,nは正の整数,Rは水素またはアルキル基を示
す) 基板との角度が低角であるポリイミド配向膜の前駆体
であるポリアミド酸としてはつぎのような化合物が考え
られる。 (However, n represents a positive integer, and R represents hydrogen or an alkyl group.) The following compounds are considered as the polyamic acid which is a precursor of the polyimide alignment film having a low angle with the substrate.
(以上nは正の整数を示す。) このようなポリアミド酸化合物はテトラカルボン酸無
水物とジアミン系化合物を原料として反応させることに
よりでき、上記化合物の原料のほかにも色々考えること
が出来る。 (Herein, n is a positive integer.) Such a polyamic acid compound can be produced by reacting a tetracarboxylic anhydride with a diamine-based compound as a raw material, and can be considered variously in addition to the raw material of the compound.
例えば、テトラカルボン酸無水物としてはヘキサフル
オロブロピリデンジフタル酸無水物,ビフエニルテトラ
カルボン酸無水物,ジアミン系化合物としてはm−フェ
ニレンジアミン,m−キシレンジアミン,1,6−ジアミノヘ
キサン,Bis−M(三井石油化学製),Bis−P(三井石油
化学製)等色々考えられる。For example, as tetracarboxylic anhydride, hexafluoropropylidene diphthalic anhydride, biphenyltetracarboxylic anhydride, and as diamine compound, m-phenylenediamine, m-xylenediamine, 1,6-diaminohexane, Bis -M (manufactured by Mitsui Petrochemical) and Bis-P (manufactured by Mitsui Petrochemical) can be considered.
乾燥,焼成条件,ラビング条件等は従来のポリイミド
系配向膜を作成する条件がそのまま適用出来る。Drying, baking conditions, rubbing conditions, and the like can be directly applied to the conditions for forming a conventional polyimide-based alignment film.
塗布方法としては、スピンコート法,ディピング法,
キャスティング法,ハケ塗り法等いずれも可能であるが
スピンコート法が優れている。Coating methods include spin coating, dipping,
Both the casting method and the brush coating method can be used, but the spin coating method is excellent.
[作用] 本発明の配向膜の作成方法によれば、配向膜はポリイ
ミド樹脂よりなるため、ポリイミドの特徴である耐熱性
に優れるという特性を有する。[Function] According to the method for forming an alignment film of the present invention, since the alignment film is made of a polyimide resin, it has a characteristic of excellent heat resistance, which is a characteristic of polyimide.
基板に対する液晶分子の角度は、2成分のポリアミド
酸の混合割合を変えることにより数度(0〜5度)から
20度まで自由に変えることが出来る。混合することによ
り達成される液晶分子と基板との角度と混合前の2成分
によって達成される角度との間にはほぼ加成性が成り立
つ。The angle of the liquid crystal molecules with respect to the substrate can be varied from several degrees (0 to 5 degrees) by changing the mixing ratio of the two-component polyamic acid.
Can be changed freely up to 20 degrees. Additivity is substantially established between the angle between the liquid crystal molecules and the substrate achieved by mixing and the angle achieved by the two components before mixing.
以下、実施例により本発明の詳細を説明する。 Hereinafter, the present invention will be described in detail with reference to examples.
[実施例] (実施例1) 次の構造式を有す2種のポリアミド酸を表1の割合で
混合した10重量パーセントのN−メチルピロリドン溶液
を作成し、配向剤1−5とした。尚、表の数値は重量の
割合を示す。[Example] (Example 1) A 10 wt% N-methylpyrrolidone solution was prepared by mixing two kinds of polyamic acids having the following structural formulas at the ratio shown in Table 1, and was used as an aligning agent 1-5. In addition, the numerical value of a table shows the ratio of weight.
これらの配向剤をスピンコート法により回転数1500rp
mで透明電極付き基板に塗布した。この基板を90度Cで
2時間乾燥した後、200度Cで2時間焼成した。 These alignment agents are spin-coated at 1500 rpm
m and applied to a substrate with a transparent electrode. The substrate was dried at 90 ° C. for 2 hours, and baked at 200 ° C. for 2 hours.
焼成後、この基板を送り速度0.6メートル/分で、回
転数400rpmで回転している表面にナイロン繊維が植毛さ
れている直径80ミリメートルの回転体の下を移送し、ラ
ビング処理をした。このようにして得た基板をラビング
方向が220度になるようにして、12ミクロンのスペーサ
を介して液晶セルを組立、液晶(ZLI2214メルク社製)
を充填し、磁場配向法により液晶分子と基板との角度を
測定したところ表2の結果が得られた。After firing, the substrate was transferred at a feed rate of 0.6 m / min under a rotating body having a diameter of 80 mm with nylon fibers planted on a surface rotating at a rotation speed of 400 rpm, and subjected to a rubbing treatment. The substrate obtained in this manner is set so that the rubbing direction is 220 degrees, and a liquid crystal cell is assembled through a 12-micron spacer. A liquid crystal (manufactured by Merck, ZLI2214)
Was filled, and the angle between the liquid crystal molecules and the substrate was measured by a magnetic field alignment method. The results shown in Table 2 were obtained.
尚、ポリアミド酸1,ポリアミド酸2のみよりなる10重
量パーセントのN−メチルピロリドン溶液を用いて同様
の処理をし、測定した結果は20.1度と、1.2度であっ
た。 The same treatment was carried out using a 10% by weight solution of N-methylpyrrolidone consisting of only polyamic acid 1 and polyamic acid 2, and the measured results were 20.1 degrees and 1.2 degrees.
(実施例2) 次の構造式を有す2種のポリアミド酸を表3の割合で
混合した10重量パーセントのジメチルホルムアミド溶液
を作成し、配向剤6−10とした。尚、表の数値は重量の
割合を示す。(Example 2) A 10% by weight dimethylformamide solution in which two kinds of polyamic acids having the following structural formulas were mixed at the ratio shown in Table 3 was prepared, and used as an aligning agent 6-10. In addition, the numerical value of a table shows the ratio of weight.
これらの配向剤をスピンコート法により回転数2000rp
mで透明電極付き基板に塗布した。この基板を90度Cで
2時間乾燥した後、200度Cで2時間焼成した。 The rotation speed of these alignment agents was 2,000 rp by spin coating.
m and applied to a substrate with a transparent electrode. The substrate was dried at 90 ° C. for 2 hours, and baked at 200 ° C. for 2 hours.
焼成後、この基板を送り速度0.6メートル/分で、回
転数400rpmで回転している表面にナイロン繊維が植毛さ
れている直径80ミリメートルの回転体の下を移送し、ラ
ビング処理をした。このようにして得た基板をラビング
方向が220度になるようにして、12ミクロンのスペーサ
を介して液晶セルを組立、液晶(ZLI2214 メルク社
製)を充填し、磁場配向法により液晶分子と基板との角
度を測定したところ表4の結果が得られた。After firing, the substrate was transferred at a feed rate of 0.6 m / min under a rotating body having a diameter of 80 mm with nylon fibers planted on a surface rotating at a rotation speed of 400 rpm, and subjected to a rubbing treatment. A liquid crystal cell (ZLI2214 manufactured by Merck) is assembled through a 12-micron spacer so that the rubbing direction of the substrate thus obtained is 220 degrees, and the liquid crystal (ZLI2214 Merck) is filled. Was measured, and the results in Table 4 were obtained.
尚、ポリアミド酸1,ポリアミド酸3のみよりなる10重
量パーセントのジメチルホルムアミド溶液を用いて同様
の処理をし、測定した結果は20.0度と、0.2度であっ
た。 The same treatment was performed using a 10% by weight dimethylformamide solution consisting of only polyamic acid 1 and polyamic acid 3, and the measured results were 20.0 degrees and 0.2 degrees.
以上実施例を述べたが、本発明は上記実施例に限定さ
れるものではなく、広く、他の原料,溶媒,塗布条件,
乾燥,焼成条件においても適用出来るものである。Although the embodiments have been described above, the present invention is not limited to the above-described embodiments, but is broadly applicable to other raw materials, solvents, coating conditions,
It can be applied under drying and firing conditions.
[発明の効果] 以上述べたように本発明によれば、液晶の種類、ネジ
レの角度等に合わせ配向剤を用意する必要がなく、2種
類のポリアミド酸を用意することにより全てに対応出来
るという効果を有する。[Effects of the Invention] As described above, according to the present invention, it is not necessary to prepare an alignment agent according to the type of liquid crystal, the angle of twist, and the like, and it is possible to cope with all by preparing two types of polyamic acids. Has an effect.
第1図は、液晶表示体の概念図である。 11……基板 12……電極 13……配向膜 14……液晶 FIG. 1 is a conceptual diagram of a liquid crystal display. 11 ... Substrate 12 ... Electrode 13 ... Alignment film 14 ... Liquid crystal
Claims (2)
向剤から形成される配向膜であって,一方のポリアミド
酸化合物は下記構造式を有することを特徴とする配向
膜。 (ただし,nは正の整数,Rは水素またはアルキル基を示
す)An alignment film formed from an alignment agent containing two kinds of polyamic acid compounds, wherein one of the polyamic acid compounds has the following structural formula. (However, n is a positive integer, R is hydrogen or an alkyl group)
封入されてなる液晶装置において,2種類のポリアミド酸
化合物を含有する配向剤から形成される配向膜が前記一
対の基板に形成されてなり,一方のポリアミド酸化合物
は下記構造式を有することを特徴とする液晶装置。 (ただし、nは正の整数,Rは水素またはアルキル基を示
す)2. In a liquid crystal device in which liquid crystal is sealed between a pair of substrates via a spacer, an alignment film formed from an alignment agent containing two kinds of polyamic acid compounds is formed on the pair of substrates. Wherein one polyamic acid compound has the following structural formula. (However, n is a positive integer, R represents hydrogen or an alkyl group)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1045597A JP2780184B2 (en) | 1989-02-27 | 1989-02-27 | Alignment film and liquid crystal device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1045597A JP2780184B2 (en) | 1989-02-27 | 1989-02-27 | Alignment film and liquid crystal device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02223917A JPH02223917A (en) | 1990-09-06 |
JP2780184B2 true JP2780184B2 (en) | 1998-07-30 |
Family
ID=12723759
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1045597A Expired - Lifetime JP2780184B2 (en) | 1989-02-27 | 1989-02-27 | Alignment film and liquid crystal device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2780184B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5783656A (en) * | 1996-02-06 | 1998-07-21 | Japan Synthetic Rubber Co., Ltd. | Polyamic acid, polyimide and liquid crystal aligning agent |
JP4029452B2 (en) * | 1997-12-29 | 2008-01-09 | チッソ株式会社 | Polyamic acid composition, liquid crystal alignment film, and liquid crystal display element |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0752264B2 (en) * | 1987-06-17 | 1995-06-05 | 株式会社日立製作所 | Liquid crystal display element |
-
1989
- 1989-02-27 JP JP1045597A patent/JP2780184B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH02223917A (en) | 1990-09-06 |
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