JPS5924403B2 - lcd cell - Google Patents
lcd cellInfo
- Publication number
- JPS5924403B2 JPS5924403B2 JP15113178A JP15113178A JPS5924403B2 JP S5924403 B2 JPS5924403 B2 JP S5924403B2 JP 15113178 A JP15113178 A JP 15113178A JP 15113178 A JP15113178 A JP 15113178A JP S5924403 B2 JPS5924403 B2 JP S5924403B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- crystal cell
- epoxy resin
- resin
- adhesive
- 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
Landscapes
- Sealing Material Composition (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
- Liquid Crystal (AREA)
Description
【発明の詳細な説明】 本発明は、液晶セルに関する。[Detailed description of the invention] The present invention relates to a liquid crystal cell.
一般に液晶セルはガラス基板に所定のネサ電極を形成し
た1対の基板を所定の間隔に対向配置し、周囲をシール
し、その間隙に液晶を封入したものである。Generally, a liquid crystal cell is a cell in which a pair of glass substrates with predetermined NESA electrodes formed thereon are arranged facing each other at a predetermined interval, the periphery is sealed, and liquid crystal is sealed in the gap.
ある種のタイプの液晶セルにおいては、さらに、このセ
ルの前面あるいは前面と背面に偏光板を配置し、電極に
電圧を印加すると、液晶分子の配向が変化し、所望の表
示が行なわれるように構成されている。このように用い
られる液晶セルのシール材には、低融点ガラスのような
無機系接着剤、あるいはエポキシ樹脂系、シアノアクリ
レート系、ナイロン系などの有機系接着剤が提案されて
いる。これらシール材の選択は作業性、接着性、耐久性
などのほか液晶の配向性、安定性に及ぼす影響なども関
連して、非常に重要である。無機系のシール材は液晶へ
の影響が少なく、耐久性にすぐれているという長所があ
るが、処理温度が高い(約450℃以上)ため、作業性
が悪い。一方、有機系接着剤では作業は比較的簡単であ
るが、液晶への影響が懸念される。有機系接着剤の中で
エポキシ樹脂系接着剤は、良好な作業性とすぐれた接着
力を有するが、使用する硬化剤によつては液晶の配向性
、寿命に悪影響を及ぼすことが知られ、このことは特開
昭51−120324などでも指摘されている。本発明
者らは各種の硬化剤の特質を検討し、耐湿性にすぐれた
硬化剤とされているフェノールノボラック樹脂が有望と
考えた。しかし、該樹脂硬化エポキシ樹脂でシールした
液晶セルを50℃に長時間放置すると、点灯時の消費電
流が増加する傾向のあることが分つた。この現象は、イ
オン解離し易い不純物が液晶内に入り込み液晶のインピ
ーダンスを低下させ、液晶配向のための見かけの電流が
多くなることであると考え、その原因を究明した。本発
明は、その知見に基づき、液晶の配向性良好で消費電流
変化の少なく、耐湿性にすぐれた液晶セルを提供するも
のである。In some types of liquid crystal cells, polarizing plates are further placed on the front or front and rear sides of the cell, and when a voltage is applied to the electrodes, the orientation of the liquid crystal molecules changes to produce the desired display. It is configured. As sealing materials for liquid crystal cells used in this manner, inorganic adhesives such as low melting point glass, or organic adhesives such as epoxy resin, cyanoacrylate, and nylon adhesives have been proposed. The selection of these sealing materials is very important in terms of workability, adhesiveness, durability, etc., as well as the influence on the alignment and stability of liquid crystals. Inorganic sealing materials have the advantage of having little effect on liquid crystals and being excellent in durability, but the processing temperature is high (approximately 450° C. or higher), resulting in poor workability. On the other hand, organic adhesives are relatively easy to work with, but there are concerns about their effects on liquid crystals. Among organic adhesives, epoxy resin adhesives have good workability and excellent adhesive strength, but it is known that depending on the curing agent used, it has a negative effect on the alignment and lifespan of liquid crystals. This is also pointed out in Japanese Patent Laid-Open No. 51-120324. The present inventors studied the characteristics of various curing agents and found that phenol novolak resin, which is said to be a curing agent with excellent moisture resistance, is promising. However, it has been found that when a liquid crystal cell sealed with the resin-cured epoxy resin is left at 50° C. for a long time, the current consumption during lighting tends to increase. We believe that this phenomenon is due to impurities that are easily ionically dissociated entering the liquid crystal, lowering the impedance of the liquid crystal, and increasing the apparent current for liquid crystal alignment, and investigated the cause. Based on this knowledge, the present invention provides a liquid crystal cell with good liquid crystal orientation, little change in current consumption, and excellent moisture resistance.
その特徴は、2枚の対向配置され周縁をシールされた電
極板の間に液晶を充填してなる液晶セルにおいて、シー
ルに3核体以上のフエノールノボラツク樹脂を硬化剤と
するエポキシ樹脂系接着剤を用いることにある。本発明
において、エポキシ樹脂としては例えばビスフエノール
A型エポキシ樹脂、フエノールノボラツクエポキシ樹脂
、ポリフエノール型エポキシ樹脂、脂環式エポキシ樹脂
などが使用できる。また、硬化剤として使用される3核
体以上のフエノールノボラツク樹脂は一般式(式中Rは
水素、アルキル基、フエニル基、もしくは2−(4−ヒ
ドロキシフエニル)イソプロピル基、nは1以上の数を
表わす)で示される。Its feature is that it is a liquid crystal cell in which liquid crystal is filled between two electrode plates arranged opposite to each other and whose peripheral edges are sealed, and an epoxy resin adhesive with a curing agent of phenol novolak resin having 3 or more nuclear elements is used for the seal. It's about using it. In the present invention, as the epoxy resin, for example, bisphenol A type epoxy resin, phenol novolak epoxy resin, polyphenol type epoxy resin, alicyclic epoxy resin, etc. can be used. In addition, the phenol novolak resin with three or more nuclear bodies used as a curing agent has the general formula (wherein R is hydrogen, an alkyl group, a phenyl group, or a 2-(4-hydroxyphenyl) isopropyl group, and n is 1 or more. ).
次に、本発明を実施例によつて説明する。実施例 1
フエニル10009、30%のホルマリン9209、修
酸4g、および水100gをフラスコに入れ還流温度で
60分反応し、つぎに塩酸2.59を加えて、40分間
縮合させる。Next, the present invention will be explained with reference to examples. Example 1 Phenyl 10009, 30% formalin 9209, 4 g of oxalic acid, and 100 g of water are placed in a flask and reacted at reflux temperature for 60 minutes. Next, 2.59 g of hydrochloric acid is added and condensed for 40 minutes.
そして、冷水を多量添加して反応を停止し、30分間放
置する。次に、サイホンにより水を除き、つぎに120
℃に2時間放置し脱水して、生成した樹脂をとり出す。
このようにして合成したフエノールノボラツク樹脂は造
をとつており、n−0〜20のフエノール樹脂と、未反
応のフエノールが混在していることが、液体クロマトグ
ラフイ一で確認された。Then, a large amount of cold water is added to stop the reaction, and the mixture is left to stand for 30 minutes. Next, water is removed using a siphon, and then 120
Leave it at ℃ for 2 hours to dehydrate and take out the produced resin.
The phenol novolac resin synthesized in this manner was well-structured, and it was confirmed by liquid chromatography that the phenol resin of n-0 to 20 and unreacted phenol were mixed together.
そこで、前記のフエノール樹脂を150℃、1mmHg
の減圧下に放置し、放置時間と未反応フエノール量およ
びnが0,1,2のフエノール樹脂の量との関係を調べ
た。その結果は第1表の通りであつた。これら滝1〜6
の各樹脂249と、分子量約900のビスフエノールA
型エポキシ樹脂1009、ブチルセロソルブ609を1
00℃で混合撹拌し、完全に溶解する。次に、上記溶液
を1009とり、これに、充填材として、微粉末シリカ
15g、液晶セルの間隙制御材として、10μmのガラ
ス繊維29を入れ、捕潰機で混合して接着剤を調合した
。Therefore, the above phenolic resin was heated at 150°C and 1mmHg.
The relationship between the standing time, the amount of unreacted phenol, and the amount of phenolic resin with n of 0, 1, and 2 was investigated. The results were as shown in Table 1. These waterfalls 1-6
each resin 249 and bisphenol A with a molecular weight of about 900.
Type epoxy resin 1009, butyl cellosolve 609 1
Mix and stir at 00°C to completely dissolve. Next, the above solution 1009 was taken, 15 g of finely powdered silica was added as a filler, and 10 μm glass fiber 29 was added as a gap control material for the liquid crystal cell, and mixed with a crusher to prepare an adhesive.
このようにして調合した接着剤の番号をそれぞれ./1
61A〜屋6Aと命名する。そして、これらの接着剤を
用いて、液晶セルを下記の方法で作成した。所定の位置
にネサ電極、および配向制御膜の付いたガラス板の周囲
にスクリーン印刷により、接着剤を印刷する。The number of each adhesive prepared in this way. /1
Name it 61A~ya6A. Then, a liquid crystal cell was created using these adhesives in the following manner. Adhesive is printed by screen printing around the glass plate with the Nesa electrode and the alignment control film at predetermined positions.
12『C1時間放置して、接着剤の溶剤を乾燥させた後
、もう1枚のネサ電極、配向制御膜の付いたガラス板を
位置合せを行なつた後貼り合せ、加圧しながら210℃
で2時間硬化する。12 "C" After leaving for 1 hour to dry the adhesive solvent, another glass plate with the Nesa electrode and alignment control film was aligned and bonded, and heated at 210°C while applying pressure.
Cure for 2 hours.
このようにして作成した液晶セルの前面と背面に偏光板
を貼り付け電圧を印加して、点灯時の液晶セルの消費電
流を測定した。Polarizing plates were pasted on the front and back sides of the liquid crystal cell thus created, voltage was applied, and the current consumption of the liquid crystal cell during lighting was measured.
さらに、液晶セルを50℃の恒温槽内に1000時間放
置した後の液晶セルの消費電流を測定した。その結果は
第2表に示す如くであつた。表から、未反応フエノール
やメチレンジフエノールのような低分子量成分の存在が
大きく影響していることが分る。Furthermore, the current consumption of the liquid crystal cell was measured after the liquid crystal cell was left in a constant temperature bath at 50° C. for 1000 hours. The results were as shown in Table 2. From the table, it can be seen that the presence of low molecular weight components such as unreacted phenol and methylene diphenol has a large influence.
液晶セルの特性としては、上記50℃,1000時間の
寿命試験後の消費電流は2.0μA以下であることを要
し、従つて、接着剤として用いるノボラツク型フエノー
ル樹脂は3核体以上でなければならない。同様にして、
フエノール樹脂の原料を、クレゾールエチルフエノール
、p−ターシヤリブチルフエノール、p−フエニルフエ
ノール、ビスフエノールAを用いた系で行なつた。As for the characteristics of a liquid crystal cell, the current consumption after the above-mentioned 50°C, 1000 hour life test must be 2.0 μA or less. Therefore, the novolac type phenolic resin used as an adhesive must have three or more nuclear elements. Must be. Similarly,
A system using cresol ethylphenol, p-tertiarybutylphenol, p-phenylphenol, and bisphenol A was used as the raw materials for the phenolic resin.
その結果でも、2核体以下ではいずれも消費電流に悪影
響を及ぼすことがわかつた。これらの真相は明らかでは
ないが、エポキシ樹脂との反応性に関連しており、単量
体や2核体はエポキシ樹脂と反応して網状構造中に組込
まれる確率が少なく、接着剤中に残存するためであろう
と考えられる。As a result, it was found that in any case below a binuclear body, the current consumption was adversely affected. Although the truth behind this is not clear, it is related to the reactivity with the epoxy resin, and monomers and binuclear bodies have a low probability of reacting with the epoxy resin and being incorporated into the network structure, and are more likely to remain in the adhesive. It is thought that this is to do so.
実施例 2
実施例1で合成したフエノール樹脂および、比較のため
他の硬化剤を含むエポキシ樹脂系接着剤を、第3表に示
す組成に従い各素材を捕潰機で混合することにより調製
した。Example 2 An epoxy resin adhesive containing the phenolic resin synthesized in Example 1 and another curing agent for comparison was prepared by mixing each material in a crusher according to the composition shown in Table 3.
それらの接着剤を用い実施例1と同様にして液晶セルを
作成した。この際の接着剤の硬化条件は第3表に付記し
た如くである。接着剤の耐湿性を検討するために、作成
した各液晶セルを6『C,95%RH雰囲気中に放置し
該セルのシール部がはくりし始めるまでの時間を測つた
。A liquid crystal cell was prepared using these adhesives in the same manner as in Example 1. The curing conditions for the adhesive at this time are as shown in Table 3. In order to examine the moisture resistance of the adhesive, each of the prepared liquid crystal cells was left in a 6'C, 95% RH atmosphere, and the time until the seal portion of the cell began to peel off was measured.
その結果、フエノールノボラツク樹脂を硬化剤とする接
着剤A67と滝8(第3表)を用いたセルでは、500
時間経過後もはくりが認められなかつた。これに対し滝
9,10,11および12を用いたセルはそれぞれ38
0時間、420時間、480時間、および360時間で
はくりした。このように、フエノールノボラツク樹脂を
硬化剤とするエポキシ樹脂系接着剤はシール材として耐
湿性にすぐれている。As a result, in a cell using adhesive A67, which uses phenol novolac resin as a hardening agent, and Taki 8 (Table 3), 500
No peeling was observed even after the passage of time. On the other hand, cells using waterfalls 9, 10, 11 and 12 each have 38
It was cut off at 0 hours, 420 hours, 480 hours, and 360 hours. As described above, epoxy resin adhesives using phenol novolac resin as a curing agent have excellent moisture resistance as sealing materials.
Claims (1)
に液晶を充填してなる液晶セルにおいて3核体以上のフ
ェノールノボラック樹脂を硬化剤とし、これをエポキシ
樹脂に混合した接着剤でシールしたことを特徴とする液
晶セル。1. In a liquid crystal cell formed by filling liquid crystal between two electrode plates arranged opposite to each other and sealed at the periphery, a phenol novolac resin having 3 or more nuclear bodies is used as a curing agent, and this is sealed with an adhesive mixed with epoxy resin. A liquid crystal cell featuring
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15113178A JPS5924403B2 (en) | 1978-12-08 | 1978-12-08 | lcd cell |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15113178A JPS5924403B2 (en) | 1978-12-08 | 1978-12-08 | lcd cell |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5577722A JPS5577722A (en) | 1980-06-11 |
| JPS5924403B2 true JPS5924403B2 (en) | 1984-06-09 |
Family
ID=15512035
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15113178A Expired JPS5924403B2 (en) | 1978-12-08 | 1978-12-08 | lcd cell |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5924403B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3863253B2 (en) * | 1997-06-27 | 2006-12-27 | 株式会社日立製作所 | Liquid crystal display element and manufacturing method thereof |
-
1978
- 1978-12-08 JP JP15113178A patent/JPS5924403B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5577722A (en) | 1980-06-11 |
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