JPH03293635A - Production of color filter - Google Patents
Production of color filterInfo
- Publication number
- JPH03293635A JPH03293635A JP2096914A JP9691490A JPH03293635A JP H03293635 A JPH03293635 A JP H03293635A JP 2096914 A JP2096914 A JP 2096914A JP 9691490 A JP9691490 A JP 9691490A JP H03293635 A JPH03293635 A JP H03293635A
- Authority
- JP
- Japan
- Prior art keywords
- film
- pigment
- color filter
- liquid crystal
- films
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 239000000049 pigment Substances 0.000 claims abstract description 30
- 239000000758 substrate Substances 0.000 claims abstract description 15
- 239000000463 material Substances 0.000 claims abstract description 9
- 239000004094 surface-active agent Substances 0.000 claims abstract description 7
- 238000005868 electrolysis reaction Methods 0.000 claims abstract description 6
- 230000009257 reactivity Effects 0.000 claims abstract description 3
- 239000012860 organic pigment Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 239000007864 aqueous solution Substances 0.000 claims description 7
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 4
- 229910052738 indium Inorganic materials 0.000 claims description 4
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 4
- 150000004703 alkoxides Chemical class 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 19
- 239000004020 conductor Substances 0.000 abstract description 12
- 239000011159 matrix material Substances 0.000 abstract description 8
- 239000000084 colloidal system Substances 0.000 abstract description 3
- 239000000693 micelle Substances 0.000 abstract description 3
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 239000011347 resin Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000002243 precursor Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Chemical compound [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- 239000003513 alkali Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003115 supporting electrolyte Substances 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はカラーデイスプレィ装置に用いるカラーフィル
ターの製造方法に関し、詳しくは液晶デイスプレィ装置
に用いるカラーフィルターの製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method of manufacturing a color filter used in a color display device, and more particularly to a method of manufacturing a color filter used in a liquid crystal display device.
有機顔料をレドックス反応性を有する界面活性剤のミセ
ル水溶液中に分散、コロイド化した後、該ミセル水溶液
中で電解を行ない、有機顔料をアノードとして用いた透
明電極基板上に析出させ、色素膜を形成することによる
カラーフィルターの製造方法を我々は発明した(特願昭
63−175610)。After dispersing the organic pigment in a micellar aqueous solution of a redox-reactive surfactant and turning it into a colloid, electrolysis is performed in the micellar aqueous solution to deposit the organic pigment on a transparent electrode substrate using the anode to form a pigment film. We have invented a method for manufacturing color filters by forming (Japanese Patent Application No. 175610/1983).
しかしなから、上記のカラーフィルターにおいて次の問
題点があった。However, the above color filter had the following problems.
本カラーフィルターの色素膜は有機顔料粒子だけの堆積
層として透明電極上に形成されるが、液晶デイスプレィ
用として用いる場合には、その透明電極が液晶駆動用と
しても用いられるという大きなメリットを持っている。The dye film of this color filter is formed as a deposited layer of organic pigment particles on a transparent electrode, but when used for a liquid crystal display, it has the great advantage that the transparent electrode can also be used to drive the liquid crystal. There is.
すなわち、従来の染色法や顔料分散法のカラーフィルタ
ーの場合には色素膜中に染料もしくは顔料以外にそれら
を固定するためのバインダー樹脂も含まれるため、相対
的に色素膜は厚くなる。従って、それらの色素膜が液晶
駆動用の透明電極上に形成されると、印加電圧のロスを
生じ、液晶駆動性を低下させるという問題がある。特に
単純マトリクスタイプ(STNタイプ)の液晶パネルに
おいて少なくとも1/200 duty以上での駆動が
適用される場合には、十分な駆動特性を得ることは困難
であった。その点に関し、我々の発明のカラーフィルタ
ーは色素膜が有機顔料のみで形成されるため、染色法や
顔料分散法に比べ色素膜を相対的に薄くすることが可能
であるため、1/200duty程度での駆動は十分に
行なえる。ところが、1/400から1/480程度の
高デユーティ−駆動になるとやはり十分な駆動は困難で
あることが判明した。従って、この問題を解決するため
には、色素膜上に液晶駆動用透明電極を設ければよいこ
とが容易と思われるが、実際には製造プロセスが長くな
り、高歩留りも得られず、コストアップもしてしまうと
いう問題があった。That is, in the case of color filters made using the conventional dyeing method or pigment dispersion method, the pigment film contains, in addition to the dye or pigment, a binder resin for fixing them, so the pigment film becomes relatively thick. Therefore, when such a dye film is formed on a transparent electrode for driving a liquid crystal, there is a problem in that a loss of applied voltage occurs and the driving performance of the liquid crystal decreases. In particular, when a simple matrix type (STN type) liquid crystal panel is driven at a duty of at least 1/200 or more, it is difficult to obtain sufficient drive characteristics. Regarding this point, since the color filter of our invention has a pigment film formed only from organic pigments, it is possible to make the pigment film relatively thin compared to the dyeing method or pigment dispersion method, so the duty is about 1/200. It can be driven satisfactorily. However, it has been found that sufficient driving is still difficult when driving at a high duty of about 1/400 to 1/480. Therefore, in order to solve this problem, it seems easy to simply provide a transparent electrode for driving the liquid crystal on the dye film, but in reality, the manufacturing process is long, high yield cannot be obtained, and the cost is high. There was a problem that it was also uploaded.
上述のように従来技術においては、単純マトリクスタイ
プ(STNタイプ)での高デユーティ−駆動への適用が
困難であるという問題があった。As mentioned above, the conventional technology has a problem in that it is difficult to apply it to high duty drive in a simple matrix type (STN type).
そこで本発明の目的とするところは、色素膜を導電化処
理することにより、液晶駆動時の印加電圧ロスをなくす
ことにより、単純マトリクスタイプ(STN)での高デ
ユーティ−駆動にも十分適用できるカラーフィルターの
製造方法を提供することにある。Therefore, the object of the present invention is to eliminate the applied voltage loss during liquid crystal driving by treating the dye film to conductivity, thereby making the color sufficiently applicable to high-duty driving in a simple matrix type (STN). An object of the present invention is to provide a method for manufacturing a filter.
本発明のカラーフィルターの製造方法は、レドックス反
応性を有する界面活性剤のシセル水溶液中に有機顔料を
分散、コロイド化した後、該シセル水溶液中で電解を行
ない該有機顔料を透明電極基板上に析出させ色素膜を形
成した後、該色素膜中に後処理で導電性物質となる材料
を含浸させ、該後処理で、色素膜中に導電体組織を形成
し色素膜を導電化することを特徴とする。The method for producing a color filter of the present invention involves dispersing an organic pigment in an aqueous solution of a redox-reactive surfactant to form a colloid, and then electrolyzing the organic pigment in the aqueous solution of the latter to transfer the organic pigment onto a transparent electrode substrate. After depositing and forming a pigment film, a material that becomes a conductive substance is impregnated into the pigment film in a post-treatment, and in the post-treatment, a conductive structure is formed in the pigment film to make the pigment film conductive. Features.
以下に具体的に手段を述べる。The means will be specifically described below.
本発明のカラーフィルターは有機顔料微粒子か堆積し成
膜した構造となっている。そのため、その色素膜は顔料
粒子間に多くの空隙が存在することを特徴としている。The color filter of the present invention has a structure in which organic pigment fine particles are deposited to form a film. Therefore, the pigment film is characterized by the presence of many voids between pigment particles.
従って本発明は、インジウムやスズのアルコキサドを一
定濃度の溶液とし加水分解した後、その溶液を色素膜空
隙部に含浸させ、熱処理によりインジウムやスズなどの
酸化物導電体組織を顔料粒子間にマトリクス状に形成し
、色素膜の導電化をはかるものである。Therefore, in the present invention, an alkoxide of indium or tin is made into a solution with a certain concentration, hydrolyzed, the resulting solution is impregnated into the voids of the pigment film, and an oxide conductor structure of indium or tin is formed in a matrix between the pigment particles by heat treatment. It is intended to make the dye film electrically conductive.
色素膜を成膜する隙に用いるレドックス反応性を有する
界面活性剤としては、疎水性末端基にフェロセンを導入
した同口化学製フェロセニルPEGなどがある。この界
面活性剤水溶液中に有機顔料微粒子を超音波処理等を用
い分散、コロイド化した後、電解を行なえば、アノード
として用いた透明電極基板上にミセルの破壊によって析
出する有機顔料のみからなる色素膜が形成できる。Examples of the redox-reactive surfactant used in the gap in which the dye film is formed include Ferrocenyl PEG manufactured by Doguchi Chemical Co., Ltd., which has ferrocene introduced into the hydrophobic end group. After dispersing and colloidizing organic pigment fine particles in this surfactant aqueous solution using ultrasonic treatment or the like, electrolysis is performed, and a dye consisting only of organic pigment is deposited by the destruction of micelles on the transparent electrode substrate used as an anode. A film can be formed.
P、G、Hの3原色からなる一定パターンの色素膜を形
成すればカラーフィルターを形成することができる。A color filter can be formed by forming a dye film in a fixed pattern consisting of the three primary colors P, G, and H.
次にこの色素膜に後処理で導電体組織が形成できる材料
を含浸させればよい。導電体組織が形成できる材料とし
ては、とくに制約はないが、インジウムやスズなとのア
ルコキサイドが好ましい。Next, this dye film may be impregnated with a material capable of forming a conductor structure in a post-treatment. There are no particular restrictions on the material that can form the conductor structure, but alkoxides such as indium and tin are preferred.
この導電体組織の前駆体を色素膜中に含浸させる方法と
しては、その溶液を色素膜に塗布するが、溶液中に色素
膜を形成した基板を浸漬するなどして行なえばよい。た
たし、この場合、その前駆体は基板全面に被覆されるた
め、各透明電極パターン同志を結果的に導通させてしま
うという不都合が生じる。従って、各透明電極間にはあ
らかじめ保護膜をコートし、−旦、基板全体を導電体の
前駆体で被覆し、その前駆体の導電化処理をした後、あ
らかじめ形成した保護膜をストリップすれば、各透明電
極の間には導電体組織は形成されず、電極間のショート
を防止することができる。A method for impregnating the dye film with the precursor of the conductor structure is to apply the solution to the dye film, and may be carried out by immersing the substrate on which the dye film is formed in the solution. However, in this case, since the entire surface of the substrate is coated with the precursor, there arises an inconvenience that the transparent electrode patterns end up being electrically connected to each other. Therefore, if a protective film is coated between each transparent electrode in advance, then the entire substrate is coated with a conductive precursor, and the precursor is treated to become conductive, and then the previously formed protective film is stripped. , no conductor structure is formed between each transparent electrode, and short circuits between the electrodes can be prevented.
この保護膜の形成法としては、−旦、硬化した後、有機
溶剤や弱アルカリ等でストリップできるレジスト材料な
どがよく、色素膜形成前、もしくは後にフォトリソグラ
フィーを用いて透明電極同志のギャップ間に形成するか
、オフセット印刷などを用いて精度よく選択的に電極間
に形成してもよい。A good method for forming this protective film is to use a resist material that can be first hardened and then stripped using an organic solvent or weak alkali. Alternatively, the electrodes may be selectively formed between the electrodes with high precision using offset printing or the like.
(実施例1)
30cm角ガラス基板上にITO膜を形成した後対角約
10インチの長方形領域に、フォトリソグラフィーを用
いて、ITO膜を1920本の幅100μmからなるス
トライプ状透明電極として加工した。各ストライプは2
5μmのギャップをもって配列された。また、ストライ
バパターン端部は駆動ICが実装できるような形状に加
工した。(Example 1) After forming an ITO film on a 30 cm square glass substrate, the ITO film was processed into a striped transparent electrode consisting of 1920 stripes with a width of 100 μm using photolithography on a rectangular area of approximately 10 inches diagonally. . Each stripe has 2
They were arranged with a gap of 5 μm. In addition, the ends of the striver patterns were processed into a shape that allows the drive IC to be mounted.
次にこの基板全体に光硬化性の樹脂をコートしフォトリ
ソグラフィー法により、ITOパターン間にのみ樹脂膜
が残るよう加工した。樹脂膜材としては東京応化工業(
株)製、ポジ型レジスト0FPR−800を用いた。(
第1図(a))次にこの1920本の透明電極上にR,
01Bの色素膜を形成した。色素膜は1色あたり640
本のパターンを使用し、R,G、Bが交互に配列される
ように、選択的導通し電解成膜した。(第1図(b))
電解液の組成は表1に示したものを用いた。電解は各色
素膜とも0,5V (vs、5CE)で定電圧電解によ
り行なった。各色素膜はそれぞれ、R(0,9μm)
、G (0,9μm) 、B (0゜9μm)の膜厚に
形成した。Next, the entire substrate was coated with a photocurable resin and processed by photolithography so that the resin film remained only between the ITO patterns. Tokyo Ohka Kogyo (
A positive resist 0FPR-800 manufactured by Co., Ltd. was used. (
Figure 1(a)) Next, R,
A dye film of 01B was formed. Pigment film is 640 per color
Using a book pattern, selective conduction electrolytic film formation was performed so that R, G, and B were arranged alternately. (FIG. 1(b)) The composition of the electrolytic solution shown in Table 1 was used. Electrolysis was performed for each dye film by constant voltage electrolysis at 0.5 V (vs. 5CE). Each pigment film has R (0.9 μm)
, G (0.9 μm), and B (0°9 μm).
*1
*2
レドックス反応性を有する界面活性剤
フェロセニルPEG (同口化学製)
支持電解質 Li2SO4
色素膜は各色の成膜ごとに120℃で30分焼成し密着
性を向上させた。*1 *2 Surfactant with redox reactivity Ferrocenyl PEG (manufactured by Doguchi Kagaku) Supporting electrolyte Li2SO4 The dye film was baked at 120° C. for 30 minutes after each color film was formed to improve adhesion.
次にこの色素膜を形成した基板を5n(i−OC3H7
)4()リケミカル(株)製)の5 w t%エタノー
ル溶液に浸漬した。このエタノール溶液中には若干の水
分が添加され、あらかじめ5n(i−OC3H))4を
加水分解して用いた。この操作により酸化スズの前駆体
が顔料膜内に含浸される一方、基板全体にも被覆された
。(第1図(C))
この後、この基板を120℃で30分焼成した。Next, the substrate on which this dye film was formed was 5n (i-OC3H7
)4 (manufactured by Lichemical Co., Ltd.) in a 5 wt% ethanol solution. A small amount of water was added to this ethanol solution, and 5n(i-OC3H))4 was previously hydrolyzed and used. This operation impregnated the tin oxide precursor into the pigment film, while also coating the entire substrate. (FIG. 1(C)) Thereafter, this substrate was baked at 120° C. for 30 minutes.
続いて、ITOパターン間に被覆した光硬化性樹脂をア
セトン中に浸漬し、ストリップした。Subsequently, the photocurable resin coated between the ITO patterns was immersed in acetone and stripped.
(第1図(d))
続いて、この基板をさらに200℃で1時間焼成し、色
素膜内に酸化スズをマトリクス状に形成しカラーフィル
ターを完成した。(FIG. 1(d)) Subsequently, this substrate was further baked at 200° C. for 1 hour to form a matrix of tin oxide within the dye film, thereby completing a color filter.
このカラーフィルターを用い所定の液晶パネル化工程を
通すことでSTNタイプのカラーパネルを作成した。1
/400dutyで駆動した結果、色素膜が導電化さ
れたことて、液晶駆動特性が飛躍的に向上し、カラーフ
ィルターかない構造の場合と同等の特性を示した。An STN type color panel was created by using this color filter and passing through a predetermined liquid crystal panel manufacturing process. 1
As a result of driving at a duty of /400, the dye film became conductive, and the liquid crystal driving characteristics were dramatically improved, showing characteristics equivalent to those of a structure without color filters.
(実施例2)
実施例1においては、各色素膜の膜厚を同一膜厚に形成
した結果、色調的には若干不十分なカラフィルタ−とな
った。従って、十分な色調としさらに、液晶セルギャッ
プが各色素間で異ならないように、各色素膜の膜厚か一
定となるように色素膜を電解形成する際に、顔料と透明
樹脂を共析させた。共析膜は膜厚かそれぞれ1.2μm
で同一となるように成膜したが、十分な色調が発現する
よう顔料は必要量析出させ、膜厚を各色素膜で同一にす
るために、透明樹脂の析出量をコントロルした。(Example 2) In Example 1, each dye film was formed to have the same thickness, resulting in a color filter that was slightly unsatisfactory in terms of color tone. Therefore, when electrolytically forming the dye film, the pigment and transparent resin are eutectoid to ensure a sufficient color tone, and to ensure that the liquid crystal cell gap does not differ between each dye, and the thickness of each dye film is constant. Ta. The thickness of each eutectoid film is 1.2 μm.
The pigment was deposited in the necessary amount to develop a sufficient color tone, and the amount of transparent resin deposited was controlled in order to make the film thickness the same for each pigment film.
実施例2て用いた導電化材料としては実施例1と同材料
を用いた。他の作成法もすべて実施例1と同様にし、液
晶パネルも同様に作成した。As the conductive material used in Example 2, the same material as in Example 1 was used. All other manufacturing methods were the same as in Example 1, and the liquid crystal panel was also created in the same manner.
その結果、液晶駆動性が飛躍的に向上し、かっ色調的に
も十分な液晶パネルを作成することがてきた。As a result, we have been able to dramatically improve liquid crystal drive performance and create liquid crystal panels with satisfactory dark gray tones.
以上のように本発明により、液晶駆動特性を飛躍的に向
上させるカラーフィルターの製造が可能となった。なお
、本発明は、特に高デニーティ駆動の単純マトリクスタ
イプの液晶パネル用カラーフィルターへの適用にあたり
顕著な効果を示すことがわかったが、同様にMIMアク
ティブマトリクスタイプ液晶パネル用カラーフィルター
の作成に適用しても同様の効果が得られると考える。As described above, the present invention has made it possible to manufacture a color filter that dramatically improves liquid crystal driving characteristics. It has been found that the present invention is particularly effective when applied to color filters for high-denity drive simple matrix type liquid crystal panels, but it can also be similarly applied to the creation of color filters for MIM active matrix type liquid crystal panels. I think the same effect can be obtained.
第1図は本発明のカラーフィルターの製造方法の一例を
示す図。
ガラス基板
光硬化性樹脂
透明電極
色素膜
導電化材料前駆体
6 目
・色素膜+導電化材料
以
上FIG. 1 is a diagram showing an example of the method for manufacturing a color filter of the present invention. Glass substrate photocurable resin transparent electrode pigment film conductive material precursor 6 eye/pigment film + conductive material or more
Claims (2)
溶液中に有機顔料を分散、コロイド化した後、該ミセル
水溶液中で電解を行ない該有機顔料を透明電極基板上に
析出させ色素膜を形成するカラーフィルターの製造方法
において、該色素膜を形成後、該色素膜中に後処理で導
電性物質となる材料を含浸させ、該後処理で該色素膜中
に導電体組織を形成することを特徴とするカラーフィル
ターの製造方法。(1) After dispersing and colloidizing an organic pigment in a micellar aqueous solution of a surfactant having redox reactivity, electrolysis is performed in the micellar aqueous solution to deposit the organic pigment on a transparent electrode substrate to form a pigment film. The method for producing a color filter is characterized in that after forming the pigment film, a material that becomes a conductive substance is impregnated into the pigment film in a post-treatment, and a conductive structure is formed in the pigment film in the post-treatment. A method for manufacturing a color filter.
、スズなどの金属アルコキシドを用いることを特徴とす
る請求項1記載のカラーフィルターの製造方法。(2) The method for manufacturing a color filter according to claim 1, characterized in that a metal alkoxide such as indium or tin is used as the material that becomes a conductive substance in post-treatment.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9691490A JP2676972B2 (en) | 1990-04-12 | 1990-04-12 | Color filter manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9691490A JP2676972B2 (en) | 1990-04-12 | 1990-04-12 | Color filter manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03293635A true JPH03293635A (en) | 1991-12-25 |
JP2676972B2 JP2676972B2 (en) | 1997-11-17 |
Family
ID=14177632
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9691490A Expired - Fee Related JP2676972B2 (en) | 1990-04-12 | 1990-04-12 | Color filter manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2676972B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0481804A (en) * | 1990-07-25 | 1992-03-16 | Idemitsu Kosan Co Ltd | Production of color filter and production and driving method of color liquid crystal panel |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0224603A (en) * | 1988-07-13 | 1990-01-26 | Seiko Epson Corp | Color filter |
JPH0235402A (en) * | 1988-05-20 | 1990-02-06 | Commiss Energ Atom | Electroconductive composite color filer and manufacture thereof |
-
1990
- 1990-04-12 JP JP9691490A patent/JP2676972B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0235402A (en) * | 1988-05-20 | 1990-02-06 | Commiss Energ Atom | Electroconductive composite color filer and manufacture thereof |
JPH0224603A (en) * | 1988-07-13 | 1990-01-26 | Seiko Epson Corp | Color filter |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0481804A (en) * | 1990-07-25 | 1992-03-16 | Idemitsu Kosan Co Ltd | Production of color filter and production and driving method of color liquid crystal panel |
Also Published As
Publication number | Publication date |
---|---|
JP2676972B2 (en) | 1997-11-17 |
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