JPH01297619A - Rubbing material - Google Patents
Rubbing materialInfo
- Publication number
- JPH01297619A JPH01297619A JP12753588A JP12753588A JPH01297619A JP H01297619 A JPH01297619 A JP H01297619A JP 12753588 A JP12753588 A JP 12753588A JP 12753588 A JP12753588 A JP 12753588A JP H01297619 A JPH01297619 A JP H01297619A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- rubbing
- pile
- fibers
- fabric
- 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
- 239000000463 material Substances 0.000 title claims abstract description 18
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 29
- 239000004744 fabric Substances 0.000 abstract description 20
- 230000005611 electricity Effects 0.000 abstract description 10
- 230000003068 static effect Effects 0.000 abstract description 10
- 238000009940 knitting Methods 0.000 abstract 2
- 239000000835 fiber Substances 0.000 description 19
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 239000002216 antistatic agent Substances 0.000 description 9
- 239000004020 conductor Substances 0.000 description 9
- 239000004745 nonwoven fabric Substances 0.000 description 9
- 239000000758 substrate Substances 0.000 description 9
- 229920002994 synthetic fiber Polymers 0.000 description 9
- 239000012209 synthetic fiber Substances 0.000 description 9
- 229920000742 Cotton Polymers 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 6
- 229920002972 Acrylic fiber Polymers 0.000 description 5
- 229920003043 Cellulose fiber Polymers 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 210000002858 crystal cell Anatomy 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- -1 5i02 Polymers 0.000 description 3
- 229920000049 Carbon (fiber) Polymers 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 239000004917 carbon fiber Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 235000006693 Cassia laevigata Nutrition 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920001407 Modal (textile) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000735631 Senna pendula Species 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- DPLVEEXVKBWGHE-UHFFFAOYSA-N potassium sulfide Chemical compound [S-2].[K+].[K+] DPLVEEXVKBWGHE-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229940124513 senna glycoside Drugs 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Liquid Crystal (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はラビング材料に関し、さらに詳しくは静電気除
去効果を有するラビング材料に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a rubbing material, and more particularly to a rubbing material having a static electricity removal effect.
近年、エレクトロニクス産業の急速な進展により、コン
ピューター周辺端末装置市場におけるデイスプレー装置
を中心とした表示装置市場はオフィスオートメーション
、ファクトリオートメーション等の本格的普及期を迎え
、急成長を続けている。In recent years, due to the rapid development of the electronics industry, the display device market, centered on display devices in the computer peripheral terminal device market, has continued to grow rapidly as office automation, factory automation, etc. have entered the period of full-scale popularization.
液晶表示装置はゲームコンピューター、液晶テレビ、フ
ァクシミリ、電話機、時計、カメラなどの表示装置とし
て使用されている。液晶表示装置の製造において、液晶
の配向性を均一にすることが最も重要で゛ある。液晶の
配向を得る方法としてラビング方法がある。Liquid crystal display devices are used as display devices in game computers, liquid crystal televisions, facsimile machines, telephones, watches, cameras, etc. In manufacturing liquid crystal display devices, it is most important to make the alignment of liquid crystals uniform. There is a rubbing method as a method for obtaining alignment of liquid crystal.
ラビング法は液晶セルおよび基板であるガラス板に対し
ては、5i02、ポリイミド、PVAなどの高分子膜を
、また高分子フィルムの表面、例えばポリエステルなど
に対しては、変成PVA。In the rubbing method, a polymer film such as 5i02, polyimide, or PVA is applied to the liquid crystal cell and the glass plate serving as the substrate, and a modified PVA is applied to the surface of the polymer film, such as polyester.
ナイロン−エポキシ−有機チタン系などの膜を配向膜と
して、ガラス板や各配向膜を布などで一方向にこすって
配向を得るものである。A nylon-epoxy-organotitanium film is used as an alignment film, and the glass plate and each alignment film are rubbed in one direction with a cloth or the like to obtain orientation.
従来、ラビング材料として綿布、脱脂綿やポリエステル
、ナイロン等の合成繊維布帛が使用されているが、綿糸
や脱脂綿の場合、ラビング中に綿糸が短繊維であるトめ
、液晶セルの基板に付着する。またポリエステル、ナイ
ロン等の合成繊維布帛の場合、ラビング中に静電気が発
生したり、静電気発生により、基板にごみやリントなど
が付着する。その結果、電極の断線や短絡などを誘発し
、液晶分子の配向むらやシール不良、セグメント電極と
コモン電極間の短絡などの因子となり、液晶表示装置の
異常をきたす。これらの欠点により液晶表示装置の歩留
性が非常に悪くなる。Conventionally, cotton cloth, absorbent cotton, and synthetic fiber cloths such as polyester and nylon have been used as rubbing materials, but in the case of cotton threads and absorbent cotton, the short fibers of the cotton threads adhere to the substrate of the liquid crystal cell during rubbing. Furthermore, in the case of synthetic fiber fabrics such as polyester and nylon, static electricity is generated during rubbing, and dust and lint adhere to the substrate due to static electricity generation. As a result, disconnection or short-circuiting of the electrodes is induced, leading to uneven orientation of liquid crystal molecules, poor sealing, and short-circuiting between the segment electrodes and common electrodes, resulting in abnormalities in the liquid crystal display device. These defects cause the yield of liquid crystal display devices to be extremely poor.
本発明者らは、かかるラビング材料の欠点に漏み、ラビ
ング材料と液晶の配合性について鋭意研究の結果、本発
明を完成するに到った。The present inventors have completed the present invention as a result of extensive research into the compatibility of rubbing materials and liquid crystals, in view of the drawbacks of such rubbing materials.
本発明の目的は、液晶基板のラビングにおいて、液晶の
均一な配向性を得ることができて、これにより液晶表示
装置等において不良品の発生をなくするラビング材料を
提供することにある。An object of the present invention is to provide a rubbing material that can obtain uniform alignment of liquid crystal when rubbing a liquid crystal substrate, thereby eliminating the occurrence of defective products in liquid crystal display devices and the like.
本発明は、構造体の裏面に制電性または導電性を有する
材料を用い、構造体の表面でラビングすることを特徴と
するラビング材料である。The present invention is a rubbing material characterized in that an antistatic or conductive material is used on the back surface of the structure, and the surface of the structure is rubbed.
本発明でいう構造体は織物、編物、不織布およびパイル
構造物等である。織物としては例えば平織物、綾織物、
朱子織物など、編物としては例えバジャーシイ、天竺な
ど、パイル構造物としてはパイル糸を有する構造物で、
例えばベルベント、別珍、コーディロイ等のパイル布帛
、起毛布帛、植毛布帛等があげられるが、これらの形態
は特に限定されない。しかしながら、パイル構造物にお
いてはラビング面はパイル側である。また構造体の素材
は、ポリエステル系合成繊維、ポリアミド系合成繊維、
酢酸セルロース系合成繊維、再生セルロース系繊維(ポ
リノジックも含む)、ポリアクリルニトリル系合成繊維
、ガラス繊維、ポリプロピレン系合成繊維、ポリエチレ
ン系合成繊維等であるが、必ずしもこれらに限定するも
のではない。The structures referred to in the present invention include woven fabrics, knitted fabrics, nonwoven fabrics, pile structures, and the like. Examples of textiles include plain weave, twill weave,
Sateen fabrics, knitted fabrics such as bajashii, jersey, etc., pile structures include structures with pile threads,
Examples include pile fabrics such as velveteen, corduroy, raised fabrics, and flocked fabrics, but the forms thereof are not particularly limited. However, in a pile structure, the rubbing surface is on the pile side. The material of the structure is polyester synthetic fiber, polyamide synthetic fiber,
These include, but are not limited to, cellulose acetate synthetic fibers, regenerated cellulose fibers (including polynosic), polyacrylonitrile synthetic fibers, glass fibers, polypropylene synthetic fibers, and polyethylene synthetic fibers.
本発明の構造体の裏面に制電性または導電性を有する材
料を用いることは、109オーム・センナメートル以下
の比抵抗を有する制電性または導電性材料を構造体の表
面に露出しないように用いることをいう。例えば構造体
を二層構造として裏糸として制電性または導電性繊維を
混入したり、二層構造体の裏面に制電性または導電性材
料を混入したフィルム、不織布等を接着したり、二層構
造体の裏面に制電性または導電材料を混入した樹脂でバ
ックコーティングするなどの方法があげられる。本発明
に用いる制電性または導電性材料としては、例えば金属
繊維、炭素繊維、硫化銅アクリル繊維、硫化銅セルロー
ス繊維、硫化銅ポリアミド繊維、金属メツキ繊維、カー
ボン、銀、銅等の金属粉体等であるが、これらに限定す
るものではない。また制電性または導電性材料を他の材
料と混合、混紡、混繊、交撚してもよい。The use of an antistatic or conductive material on the back surface of the structure of the present invention prevents the antistatic or conductive material having a resistivity of 109 ohms or less from being exposed on the surface of the structure. It means to use. For example, the structure may be made into a two-layer structure and antistatic or conductive fibers may be mixed in as the back thread, or a film or nonwoven fabric mixed with an antistatic or conductive material may be adhered to the back side of the two-layer structure. Examples of methods include back-coating the back surface of the layered structure with a resin mixed with an antistatic or conductive material. Examples of antistatic or conductive materials used in the present invention include metal fibers, carbon fibers, copper sulfide acrylic fibers, copper sulfide cellulose fibers, copper sulfide polyamide fibers, metal plating fibers, carbon, metal powders such as silver, copper, etc. etc., but is not limited to these. Further, the antistatic or conductive material may be mixed, blended, mixed, or twisted with other materials.
本発明のラビング材料はラビング面(本発明の構造体の
表面)の素材、形態に係わることな(、反ラビング面(
構造体の裏面)に制電性または導電性材料を用いること
により、ラビング時に発生する静電気を速かに除去し、
これにより液晶基板へのリントの付着を防止すると共に
、静電気による障害をなくし、ひいては液晶の配向性を
均一にするものである。The rubbing material of the present invention has no relation to the material or form of the rubbing surface (the surface of the structure of the present invention) (or the anti-rubbing surface (
By using antistatic or conductive material on the back side of the structure, static electricity generated during rubbing can be quickly removed.
This prevents lint from adhering to the liquid crystal substrate, eliminates problems caused by static electricity, and evens out the alignment of the liquid crystal.
以下、実施例により本発明を詳説する。なお、実施例の
電気的特性は以下の条件で測定したものである。Hereinafter, the present invention will be explained in detail with reference to Examples. Note that the electrical characteristics of the examples were measured under the following conditions.
測定条件: 20℃×20%RH
摩擦帯電圧: JIS−L−1094B法(摩擦布:
綿布)
(液晶基板を摩擦した時の摩擦帯電圧は、ガラス板にポ
リイミド系樹脂を塗布した基板をJIS−L−1094
B法に準じて摩擦した時の摩擦帯電圧を示す。)
半減期: JIS−L−1094A法実施例1
ビスコース法レーヨン糸150d150fを経糸、緯糸
に用いた朱子織物の裏面に第1表記載の各種不織布をホ
ットメルト接着剤にて点接着した。Measurement conditions: 20°C x 20% RH Frictional charging voltage: JIS-L-1094B method (friction cloth:
(Cotton cloth) (Frictional charging voltage when rubbing a liquid crystal board is based on JIS-L-1094 for a glass plate coated with polyimide resin.
It shows the frictional charging voltage when friction is applied according to method B. ) Half-life: JIS-L-1094A Method Example 1 Various nonwoven fabrics listed in Table 1 were dot-bonded with a hot melt adhesive onto the back side of a satin fabric using viscose method rayon yarn 150d150f for the warp and weft.
該朱子織物についての電気的特性を第1表に示す。The electrical properties of the satin fabric are shown in Table 1.
以下余白
第1表
第1表の11h2に示す金属繊維複合不織布はポリオレ
フィン系繊維とステンレス繊維8μm(比抵抗:lo−
3オーム・センナメートル)とを9:1の割合で混合し
て作成した目付40 g/gの不織布(比抵抗:lQ!
iオーム・センチメートル)である。The metal fiber composite nonwoven fabric shown in 11h2 of Table 1 below is made of polyolefin fibers and stainless steel fibers of 8 μm (specific resistance: lo-
Non-woven fabric with a basis weight of 40 g/g (specific resistance: lQ!
i ohm cm).
第1表の隘3に示す硫化銅セルロース繊維複合不織布は
ポリオレフィン系繊維と硫化銅セルロース繊維とを4:
1の割合で混合して作成した日付40 g/%の不織布
である。(比抵抗:10’オーム・センナメートル)。The copper sulfide cellulose fiber composite nonwoven fabric shown in column 3 of Table 1 contains polyolefin fibers and copper sulfide cellulose fibers of 4:
This is a 40 g/% non-woven fabric made by mixing 1 part of each. (Resistivity: 10' ohm senna meter).
なお硫化銅セルロース繊維(比抵抗:100オーム・セ
ンナメートル)は、公知の方法で調整したセルロース濃
度10重量%、アンモニア濃度7重量%、銅濃度3.6
重量%の組成物を有する銅アンモニアセルロース溶液を
直径0.6 vxの孔を2200([1i!を有する紡
口より紡糸し、紡糸水を満した紡糸濾斗中にて充分凝固
を行なわせた。用いた紡糸水の温度と流量は30℃、1
51/分である。引続き1.4重量%の硫酸水溶液中を
0.3秒通過させ繊維表面を再生し、その後、カッター
で38mの長さに切断し、充分水洗し、銅セルロースの
配位化合物を含有した綿(以下、青線と称する)を得た
。The copper sulfide cellulose fiber (resistivity: 100 ohms/cm) was prepared using a known method with a cellulose concentration of 10% by weight, an ammonia concentration of 7% by weight, and a copper concentration of 3.6.
A cuprammonium cellulose solution having a composition of The temperature and flow rate of the spinning water used were 30°C and 1
51/min. Subsequently, the fiber surface was regenerated by passing it through a 1.4% by weight aqueous sulfuric acid solution for 0.3 seconds, and then it was cut into a length of 38 m with a cutter, thoroughly washed with water, and the cotton containing the coordination compound of copper cellulose ( (hereinafter referred to as the blue line) was obtained.
次に硫化カリウム濃度5重量%、温度50℃の水溶液に
20分間浸漬し、その後、水洗乾燥して硫化銅セルロー
ス短繊維(2デニール、繊維長38鰭)を得た。Next, it was immersed in an aqueous solution with a potassium sulfide concentration of 5% by weight and a temperature of 50° C. for 20 minutes, and then washed with water and dried to obtain copper sulfide cellulose short fibers (2 denier, fiber length 38 fins).
第1表の隘4に示す硫化銅アクリル繊維複合不織布はポ
リオレフィン系繊維と硫化銅アクリル繊維とを4:1の
割合で混合して作成した目付40g/mrの不織布であ
る(比抵抗:106オーム・センチメートル)。なお硫
化銅アクリル繊維(比抵抗:100オーム・センナメー
トル)はカシミロン(旭化成工業■製ニアクリル系合成
繊維、2デニール、繊維長38寵)を硫酸銅(0,05
moβ/It’)とチオ硫酸ナトリウム(0,45mo
l/jりを含む水溶液中に浸漬し、85℃で30分間処
理し、水洗、乾燥して、硫化銅アクリル繊維を得た。The copper sulfide acrylic fiber composite nonwoven fabric shown in column 4 of Table 1 is a nonwoven fabric with a basis weight of 40 g/mr made by mixing polyolefin fibers and copper sulfide acrylic fibers at a ratio of 4:1 (specific resistance: 106 ohms). ·Centimeter). Copper sulfide acrylic fiber (resistivity: 100 ohms) is made of copper sulfate (0.05 cm) made of cashmilon (niacrylic synthetic fiber manufactured by Asahi Kasei Corporation, 2 denier, fiber length 38 mm).
moβ/It') and sodium thiosulfate (0,45 mo
The fibers were immersed in an aqueous solution containing l/j, treated at 85° C. for 30 minutes, washed with water, and dried to obtain copper sulfide acrylic fibers.
第1表により明らかな如(、本発明法(磁2、階3、N
14)は優れた制電性を示し、液晶および基板への繊維
の付着は全く認められなかった。しかし、朱子織物の裏
面に制電性または導電性を有する材料を用いないl1h
lは静電気の発生が高く、ラビングによる液晶の配向が
均一でなかった。As is clear from Table 1, the method of the present invention (Magnetic 2, Floor 3, N
No. 14) exhibited excellent antistatic properties, and no fibers were observed to adhere to the liquid crystal or substrate. However, l1h that does not use antistatic or conductive material on the back side of the satin fabric
1 generated a high amount of static electricity, and the alignment of the liquid crystal due to rubbing was not uniform.
実施例2
パイル糸にポリエステル糸50 d/24 fを用い地
糸の経糸および緯糸にポリエステル糸50d/24fよ
り構成されるベルベットを用いて、パイル長は2. O
vr*とした。Example 2 Polyester yarn 50d/24f was used as the pile yarn, velvet made of polyester yarn 50d/24f was used as the warp and weft of the ground yarn, and the pile length was 2. O
It was set as vr*.
該ベルベットの裏側にボンコートR−3380−A(ア
クリル系樹脂:大日本インキ■製)5重量%、スミテッ
クスレジンM−3(メラミン系樹脂:住友化学■製)0
.3重量%、スミテックスアクセレーターACX (有
機アミン系触媒:住友化学@製)0.05重量%と炭素
繊維(2デニール、繊維長3n)(比抵抗:10−1オ
ーム・センチメートル)を10重量%含有する樹脂液を
バンクコーティングした。On the back side of the velvet, 5% by weight of Boncoat R-3380-A (acrylic resin: manufactured by Dainippon Ink ■), 0% Sumitex Resin M-3 (melamine resin: manufactured by Sumitomo Chemical ■)
.. 3% by weight, 0.05% by weight of Sumitex Accelerator ACX (organic amine catalyst: manufactured by Sumitomo Chemical @) and 10% of carbon fiber (2 denier, fiber length 3n) (specific resistance: 10-1 ohm cm). Bank coating was performed using a resin solution containing % by weight.
なお比較として、実施例2と同様のベルベットの裏側に
実施例2のバックコーティング樹脂液の炭素繊維を含有
しないものをバックコーティングした。For comparison, the back side of the same velvet as in Example 2 was back coated with the back coating resin liquid of Example 2 which did not contain carbon fiber.
該ベルベ・/トについての電気的特性を第2表に示す。The electrical properties of the velvet/metal are shown in Table 2.
第2表 (注)摩擦はパイル側より実施した。Table 2 (Note) Friction was performed from the pile side.
第2表により明らかな如く、本発明法は優れた制電性を
示し、ラビングによる液晶の配向は極めて均一であり、
液晶および基板への繊維の付着は全くなかった。これに
対し、比較例は静電気も高く、ラビングによる液晶の配
向は均一でなかった。As is clear from Table 2, the method of the present invention exhibits excellent antistatic properties, and the alignment of liquid crystals by rubbing is extremely uniform.
There was no adhesion of fibers to the liquid crystal or substrate. On the other hand, the comparative example had high static electricity, and the alignment of the liquid crystal due to rubbing was not uniform.
本発明のラビング材料によれば、液晶セルおよびその基
板等のラビングにおいて、液晶の均一な配向性を得るこ
とができるので、ラビング時に発生する液晶セルおよび
その基板への繊維の付着もなく、また静電気の発生も極
めて少なく、安定した液晶の配向が得られる。According to the rubbing material of the present invention, uniform orientation of the liquid crystal can be obtained when rubbing the liquid crystal cell and its substrate, so that there is no adhesion of fibers to the liquid crystal cell and its substrate during rubbing. The generation of static electricity is extremely low, and stable liquid crystal alignment can be obtained.
代理人 弁理士 川 北 武 長Agent: Patent Attorney Kawakita Takecho
Claims (1)
て、該構造体の裏面に制電性または導電性を有する材料
を用いたことを特徴とするラビング材料。(1) A rubbing material for rubbing the surface of a structure, characterized in that a material having antistatic properties or conductivity is used on the back surface of the structure.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12753588A JPH01297619A (en) | 1988-05-25 | 1988-05-25 | Rubbing material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12753588A JPH01297619A (en) | 1988-05-25 | 1988-05-25 | Rubbing material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01297619A true JPH01297619A (en) | 1989-11-30 |
Family
ID=14962418
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12753588A Pending JPH01297619A (en) | 1988-05-25 | 1988-05-25 | Rubbing material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01297619A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008149847A1 (en) * | 2007-06-06 | 2008-12-11 | Toray Industries, Inc. | Rubbing cloth |
JP2009079315A (en) * | 2007-09-26 | 2009-04-16 | Toray Ind Inc | Rubbing cloth for orientation treatment |
-
1988
- 1988-05-25 JP JP12753588A patent/JPH01297619A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008149847A1 (en) * | 2007-06-06 | 2008-12-11 | Toray Industries, Inc. | Rubbing cloth |
JP2009015317A (en) * | 2007-06-06 | 2009-01-22 | Toray Ind Inc | Rubbing cloth |
JP2009079315A (en) * | 2007-09-26 | 2009-04-16 | Toray Ind Inc | Rubbing cloth for orientation treatment |
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