JPH03217819A - High polymer/liquid crystal complex - Google Patents

High polymer/liquid crystal complex

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Publication number
JPH03217819A
JPH03217819A JP1466390A JP1466390A JPH03217819A JP H03217819 A JPH03217819 A JP H03217819A JP 1466390 A JP1466390 A JP 1466390A JP 1466390 A JP1466390 A JP 1466390A JP H03217819 A JPH03217819 A JP H03217819A
Authority
JP
Japan
Prior art keywords
liquid crystal
oligomer
monomer
polymer
low
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
Application number
JP1466390A
Other languages
Japanese (ja)
Inventor
Takehisa Asami
剛尚 浅見
Shigeo Shimizu
滋雄 清水
Toshio Konno
昆野 俊男
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Victor Company of Japan Ltd
Original Assignee
Victor Company of Japan Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Victor Company of Japan Ltd filed Critical Victor Company of Japan Ltd
Priority to JP1466390A priority Critical patent/JPH03217819A/en
Publication of JPH03217819A publication Critical patent/JPH03217819A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain the high polymer/liquid crystal complex with which a high change in light transmittance is obtainable by low-voltage driving by irradiating a mixture formed by mixing a liquid crystal of a nematic type of a cyanobiphenyl system, bifunctional polyester oligomer and acrylic acid monomer at specific ratios with UV rays and causing phase sepn. CONSTITUTION:The liquid crystal of the nematic type of the cyanobiphenyl system is used as the liquid crystal. The bifunctional polyester is used as the oligomer and the monomer of the acrylic acid system is used as the monomer. The uniform soln. prepd. by mixing at the ratios of the liquid crystal: (oligomer +monomer)=65 to 75:35 to 25(weight %) and the oligomer/monomer=7/3 to 6.5/4.5 or 4/6 to 2/8 (by weight) is irradiated with the UV rays to cause the phase sepn. The high polymer/liquid crystal complex with which the high change in the light transmittance and the good contrast are obtd. by the low-voltage driving and which is low in viscosity, is easy to handle and is good in productiv ity is obtd. in this way.

Description

【発明の詳細な説明】 [産業上の利用分野1 本発明は、高分子マトリックス中に液晶が分散保持され
た高分子・液晶複合体にかかるものであり、特に、その
電気的,光学的特性の改善に関するものである。
Detailed Description of the Invention [Industrial Field of Application 1] The present invention relates to a polymer/liquid crystal composite in which liquid crystal is dispersed and held in a polymer matrix. It is related to the improvement of

[従来の技術] 高分子・液晶複合体は、ご《微細の液晶が高分子マトリ
ックス中に分散保持されたもので、電界の有無により該
液晶の配向状態が変化するものである。例えば、電界が
ないときには、液晶がランダムな状態にあるため、空間
的な屈折率の差異が生じて光は散乱される。これに対し
、電界が印加されると、液晶が電界方向に配列した状態
となる.その結果、液晶部分と高分子マトリックスの部
分の屈折率が一致し,透明状態となって光が透過するよ
うになる。
[Prior Art] A polymer/liquid crystal composite is one in which very fine liquid crystals are dispersed and held in a polymer matrix, and the alignment state of the liquid crystals changes depending on the presence or absence of an electric field. For example, when there is no electric field, the liquid crystal is in a random state, so a spatial difference in refractive index occurs and light is scattered. On the other hand, when an electric field is applied, the liquid crystals become aligned in the direction of the electric field. As a result, the refractive index of the liquid crystal portion and the polymer matrix portion match, resulting in a transparent state allowing light to pass through.

このような高分子・液晶複合体は、偏光板を必要としな
いために光の透過状態が非常に良好であるとともに、大
面積化が可能であるなどの理由から、感光フィルムや各
種のディスプレイ手段などに対する応用が大いに検討さ
れている。
Such polymer/liquid crystal composites do not require polarizing plates, so light transmission is very good, and they can be made into large areas, so they are suitable for use in photosensitive films and various display devices. Applications are being extensively considered.

ところで,このような高分子・液晶複合体の製造方法と
しては、■乳化状態からの溶媒蒸発,■溶媒蒸発による
相分離.■クエンチによる相分離.■重合による相分離
などが知られている。中でも、構造の安定性.生産性.
構造制御の可能性などから,■の重合による相分離が着
目されている。また、液晶及び高分子マトリックスの種
類としては、液晶・モノマー・才リゴマー系のものが、
上述した構造の安定性などの理由から着目されている(
高分子討論会第38回予稿集P 2 1 5 1 ; 
Polymer Prerints Japan Vo
1.38No.7(19891 ”高分子一液品複合体
(■)〜(II)”参照)。
By the way, methods for manufacturing such polymer/liquid crystal composites include: (1) solvent evaporation from an emulsified state, and (2) phase separation by solvent evaporation. ■Phase separation by quenching. ■Phase separation due to polymerization is known. Above all, structural stability. Productivity.
Phase separation by polymerization (2) is attracting attention because of the possibility of structural control. In addition, the types of liquid crystals and polymer matrices include liquid crystals, monomers, and oligomers.
It is attracting attention for reasons such as the stability of the structure mentioned above (
Proceedings of the 38th Polymer Symposium P 2 1 5 1;
Polymer Prints Japan Vo
1.38 No. 7 (see 19891 "Polymer one-component composites (■) to (II)").

これには、液晶としてBDH社の商品名E−8(シアノ
ビフェニール系)を、モノマーとして2−エチルへキシ
ルアクリレートを、才リゴマーとして2官能ウレタンア
クリレート(分子量2000)を各々使用し、液晶:モ
ノマ一二才リゴマー=6:2.4: 1.6 (重量比
)で混合した均一溶液を,紫外線照射により重合させて
相分離させた高分子・液晶複合体が開示されている。
For this, BDH's product name E-8 (cyano biphenyl type) was used as the liquid crystal, 2-ethylhexyl acrylate was used as the monomer, and bifunctional urethane acrylate (molecular weight 2000) was used as the oligomer. A polymer/liquid crystal composite is disclosed in which a homogeneous solution of 12-year-old oligomers = 6:2.4:1.6 (weight ratio) is polymerized and phase-separated by ultraviolet irradiation.

[発明が解決しようとする課題] かかる従来の高分子・液晶複合膜の駆動電圧と光の透過
率との関係は、・第3図に示すようになる。この図から
明らかなように,駆動電圧は約20Vと高く、またこの
駆動電圧に対する透過率の変化も約70%程度で、十分
に満足し得るコントラストを得ることはできない。更に
、液晶とモノマーと才リゴマーとを混合した均一溶液の
粘度が高いため、取り扱いも容易でなく、生産性がよく
ないという不都合もある。
[Problems to be Solved by the Invention] The relationship between the driving voltage and the light transmittance of such a conventional polymer/liquid crystal composite film is as shown in FIG. As is clear from this figure, the driving voltage is as high as about 20 V, and the change in transmittance with respect to this driving voltage is about 70%, making it impossible to obtain a fully satisfactory contrast. Furthermore, since the viscosity of the homogeneous solution obtained by mixing the liquid crystal, monomer, and oligomer is high, it is not easy to handle, and there are also disadvantages in that productivity is poor.

本発明は、かかる点に鑑みてなされたもので、低い駆動
電圧で高い光透過率の変化と良好なコントラストを得る
ことができるとともに、粘度が低く取り扱いが容易で生
産性のよい高分子・液晶複合体を提供することを、その
目的とするものである。
The present invention has been made in view of these points, and it is possible to obtain a high change in light transmittance and good contrast with a low driving voltage, as well as a polymer/liquid crystal that has a low viscosity, is easy to handle, and has high productivity. The purpose is to provide a complex.

[課題を解決するための手段] 本発明は、シアノビフェニール系のネマチックタイプの
液晶と2官能性ポリエステルオリゴマーとアクリル酸系
モブマーとを、液晶.(オリゴマー+モノマー)=65
〜75 : 35〜25(重量%)であって、かつ才リ
ゴマー/モノマー7/3〜6.5/4.5あるいは4/
6〜2/8(重量比)の比率で混合した均一溶液に、紫
外線を照射して相分離させることを特徴とする。
[Means for Solving the Problems] The present invention combines a cyanobiphenyl-based nematic type liquid crystal, a bifunctional polyester oligomer, and an acrylic acid-based mobmer into a liquid crystal. (oligomer + monomer) = 65
~75: 35 to 25 (wt%), and oligomer/monomer 7/3 to 6.5/4.5 or 4/
It is characterized in that a homogeneous solution mixed at a ratio of 6 to 2/8 (weight ratio) is irradiated with ultraviolet rays to cause phase separation.

[作用] 本発明では、液晶としてシアノビフェニール系のネマチ
ッククイブのものが用いられる。また、オリゴマーとし
て2官能性ポリエステルが用いられ,千ノマーとしてア
クリル酸系のものが用いられる。そして、これらを混合
した均一溶液に紫外線を照射し、2官能性ポエリエステ
ル才リゴマーの単独重合.アクリル酸系モノマーの単独
重合.あるいは両者の共重合を生起させ、これら単独重
合体と共重合体とが混合した高分子マトリックスを得る
。このとき、同時に、かかる高分子マトリックスと前記
液晶との相分離が生じ、高分子−液品複合体が製造され
る。
[Function] In the present invention, a cyanobiphenyl-based nematic quib is used as the liquid crystal. Furthermore, a bifunctional polyester is used as the oligomer, and an acrylic acid type oligomer is used. The homogeneous solution of these mixtures was then irradiated with ultraviolet rays to homopolymerize the bifunctional polyester oligomer. Homopolymerization of acrylic acid monomers. Alternatively, copolymerization of both may be caused to obtain a polymer matrix in which these homopolymers and copolymers are mixed. At this time, phase separation occurs between the polymer matrix and the liquid crystal, and a polymer-liquid composite is produced.

この高分子一液晶複合体の光透過特性は、後述の実施例
に示すように駆動電圧がIOV程度と極めて低い。また
、この駆動電圧に対する光透過率の変化は約95%以上
と大きく、コントラストも高くなる。
The light transmission characteristics of this polymer-liquid crystal composite are extremely low, with a driving voltage of about IOV, as shown in Examples below. Further, the change in light transmittance with respect to this driving voltage is as large as about 95% or more, and the contrast is also high.

なお、上述した均一溶液中の液晶の混合割合が75重量
%より多いと、駆動電圧が高くなるとともに、この駆動
電圧に対する光透過率の変化も小さくなる。また、液晶
の配向状態変化が良好に生じないため、コントラストも
よくない。粘度も高《なりすぎる。液晶の混合割合が6
5重量%より少ない場合にも同様であり、このため、本
発明では前記液晶の混合割合を75〜65重量%とじて
いる。
Note that when the mixing ratio of liquid crystal in the above-mentioned homogeneous solution is more than 75% by weight, the driving voltage becomes high and the change in light transmittance with respect to this driving voltage becomes small. Further, since the alignment state of the liquid crystal does not change satisfactorily, the contrast is also poor. The viscosity is also too high. The mixing ratio of liquid crystal is 6
The same applies when the amount is less than 5% by weight, and therefore, in the present invention, the mixing ratio of the liquid crystal is limited to 75 to 65% by weight.

また、このときの才リゴマーと千ノマーとの配合比率に
ついては、才リゴマー/モノマーが7/3重量比より大
きいと均一溶液の粘度が高くなりすぎ、逆に2/8重量
比より小さいと高分子マトリックスの作用が良好でない
。また,中間の5/5付近でも、後述の実施例に示すよ
うに、特性は低下する。このため、本発明では、才リゴ
マ一とモノマーとの配合比率を、7/3〜6.5/4.
5あるいは4/6〜2/8(重量比)としている。
Regarding the blending ratio of the oligomer and the monomer at this time, if the weight ratio of the oligomer/monomer is greater than 7/3, the viscosity of the homogeneous solution will be too high, and conversely, if the weight ratio is less than 2/8, the viscosity will be too high. The action of the molecular matrix is not good. Furthermore, the characteristics deteriorate even near the middle 5/5, as shown in the examples described later. For this reason, in the present invention, the blending ratio of Sairigoma and monomer is set to 7/3 to 6.5/4.
5 or 4/6 to 2/8 (weight ratio).

付言するに、前記液晶の粒径としては、低駆動電圧.高
コントラストなどの特性を得るために、2〜3um程度
とすることが好ましい。
In addition, the particle size of the liquid crystal is determined by a low driving voltage. In order to obtain characteristics such as high contrast, the thickness is preferably about 2 to 3 um.

また,前記オリゴマーの分子量としては、上述した単独
重合と共重合を良好に生起させ、かつ良好な高分子マト
リックスを得るため、1000以下.好まし《は650
〜850,特に770程度とすることが好ましい。
In addition, the molecular weight of the oligomer is 1000 or less in order to cause the above-mentioned homopolymerization and copolymerization to occur well and to obtain a good polymer matrix. Preferably << is 650
It is preferably about 850 to 770, particularly about 770.

[実施例] 〈第1実施例〉 シアノビフェニール系のネマチックタイプの液晶として
、BDH社製の商品名E−9(室温でネマチック相を示
す)を使用した。2官能性ポリエステルオリゴマーとし
て、KAYARAD社製の商品名HX−620 (分子
量768)を使用した。また、アクリル酸系モノマーと
して、2−エチルへキシルアクリレートを使用した。
[Example] <First Example> As a cyanobiphenyl-based nematic type liquid crystal, BDH Co., Ltd.'s trade name E-9 (which exhibits a nematic phase at room temperature) was used. As the bifunctional polyester oligomer, HX-620 (trade name) manufactured by KAYARAD (molecular weight 768) was used. Furthermore, 2-ethylhexyl acrylate was used as the acrylic acid monomer.

このような液晶とオリゴマーとモノマーとを、 液晶:才リゴマー.モノマー =7: t.8: 1.2 (重量比)の割合で混合す
るとともに、重合開始剤としてKAYARAD社製商品
名Darocur 1 1 7 3を3重量%添加し、
均一溶液を調製した. 次に、この均一溶液を厚さ10μmの透明電極付きガラ
スセルに注入し、波長4 0 0 nm.強さ3mW/
cm”の紫外線を3〜4分照射した.これによって、前
記オリゴマー及びモノマーの単独ないし共重合反応が生
起されるとともに、この重合反応で生成される高分子化
合物の混合体(高分子マトリックス)と前記液晶との相
分離が行なわれる。
These liquid crystals, oligomers, and monomers are called liquid crystals: oligomers. Monomer = 7: t. 8: 1.2 (weight ratio), and 3% by weight of Darocur 1 1 7 3 (trade name, manufactured by KAYARAD) was added as a polymerization initiator.
A homogeneous solution was prepared. Next, this homogeneous solution was injected into a glass cell with a transparent electrode having a thickness of 10 μm, and a wavelength of 400 nm. Strength 3mW/
cm" ultraviolet rays for 3 to 4 minutes. As a result, a single or copolymerization reaction of the oligomer and monomer occurs, and a mixture of polymer compounds (polymer matrix) produced by this polymerization reaction Phase separation from the liquid crystal is performed.

以上のようにして得られた高分子・液晶複合体の光透過
特性は、第1図に示すようになる。なお、このときの光
源としては、上述した第3図の場合と同様に、光波長が
6 3 3 nmのものを使用した。
The light transmission characteristics of the polymer/liquid crystal composite obtained as described above are as shown in FIG. Note that the light source used at this time had a light wavelength of 633 nm, as in the case of FIG. 3 described above.

この図から明らかなように、本実施例にかかる高分子・
液晶複合体によれば、IOV程度の極めて低い電圧で駆
動が行なわれるとともに、この駆動電圧に対する光透過
率の変化は約90%と大きくなっている。また、上述し
たように,重合反応開始前の均一溶液の粘度を低く抑え
ることができる。
As is clear from this figure, the polymer and
According to the liquid crystal composite, driving is performed at an extremely low voltage of about IOV, and the change in light transmittance with respect to this driving voltage is as large as about 90%. Furthermore, as described above, the viscosity of the homogeneous solution before the start of the polymerization reaction can be kept low.

〈第2実施例〉 更に上記実施例において、液晶= (オリゴマー+モノ
マー)=70・30(重量%)と固定し、才リゴマー/
モノマーの比率を8/2から3/7まで変化させたとき
の光透過特性は、第2図に示したように変化した。同図
において、才リゴマー/モノマーの比率を8/2嚇7/
316/4に変化させると、グラフの傾きはより急峻と
なって行く(同図グラフLl.L2. L3参照).そ
して、オリゴマー/モノマー=6/4で前紀第1実施例
の比率となり、第1図に示した光透過特性を示すように
なる. そして、オリゴマーを減らして、オリゴマー/モノマー
の比率を6/4から5/5とすると、グラフの傾きはし
だいに滑らかになってゆく(同図グラフL3.L4参照
)。更にオリゴマーを減らして、オリゴマ=/千ノマー
の比率を5/5=>4/6=63/7とすると、グラフ
の傾きは再び急峻になってゆく(同図グラフL4. L
5yt.3参照). この実施例に示すように、オリゴマー/モノマの比率を
、好ましくは7/3〜6.5/4.5あるいは4/6〜
2/8の範囲、特に6/4あるいは3/7程度とするこ
とによって,第1実施例とほぼ同様の効果かえられる. [発明の効果] 以上説明したように、本発明によれば、液晶としてシア
ノビフェニール系のネマチックタイプのものを用い、オ
リゴマーとして2官能性ポリエステル主成分とするもの
を用い、千ノマーとしてアクリル酸系のものを用いて、
それらを所定の比率で混合することとしたので、低い駆
動電圧で高い光透過率の変化と良好なコントラストを得
ることができるとともに、粘度が低く取り扱いが容易で
生産性がよいという効果がある.
<Second Example> Furthermore, in the above example, the liquid crystal = (oligomer + monomer) = 70.30 (weight%) was fixed, and oligomer/monomer
When the monomer ratio was changed from 8/2 to 3/7, the light transmission characteristics changed as shown in FIG. 2. In the same figure, the ratio of oligomer/monomer is 8/2 and 7/
When changing to 316/4, the slope of the graph becomes steeper (see graphs L1, L2, and L3 in the same figure). Then, the ratio of oligomer/monomer = 6/4 is that of the first embodiment of the previous century, and the light transmission characteristics shown in FIG. 1 are exhibited. When the oligomer is reduced and the oligomer/monomer ratio is increased from 6/4 to 5/5, the slope of the graph gradually becomes smoother (see graphs L3 and L4 in the same figure). When the number of oligomers is further reduced and the ratio of oligomers = / 1,000 nomers is set to 5/5 = > 4/6 = 63/7, the slope of the graph becomes steeper again (graph L4.L in the same figure).
5yt. (See 3). As shown in this example, the oligomer/monomer ratio is preferably from 7/3 to 6.5/4.5 or from 4/6 to
By setting the range to 2/8, especially about 6/4 or 3/7, almost the same effect as in the first embodiment can be obtained. [Effects of the Invention] As explained above, according to the present invention, a cyanobiphenyl-based nematic type liquid crystal is used, a bifunctional polyester-based oligomer is used as the oligomer, and an acrylic acid-based liquid crystal is used as the oligomer. using the
By mixing them at a predetermined ratio, it is possible to obtain a high change in light transmittance and good contrast with a low driving voltage, as well as low viscosity, easy handling, and high productivity.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明にかかる高分子・液晶複合体の第1実施
例の光透過特性を示すグラフ、第2図は本発明の第2実
施例の光透過特性を示すグラフ、第3図は従来Q高分子
・液晶複合体の光透過特性を示すグラフである。
FIG. 1 is a graph showing the light transmission characteristics of the first example of the polymer/liquid crystal composite according to the present invention, FIG. 2 is a graph showing the light transmission characteristics of the second example of the present invention, and FIG. 2 is a graph showing the light transmission characteristics of a conventional Q polymer/liquid crystal composite.

Claims (1)

【特許請求の範囲】 モノマー・オリゴマー系の高分子マトリックス中に液晶
が分散保持された高分子・液晶複合体において、 シアノビフェニール系のネマチックタイプの液晶と、2
官能ポリエステルオリゴマーと、アクリル酸系モノマー
とを、液晶:(オリゴマー+モノマー)=65〜75:
35〜25(重量%)であって、かつ、オリゴマー/モ
ノマー=7/3〜6.5/4.5あるいは4/6〜2/
8(重量比)で混合した均一溶液に、紫外線を照射して
相分離させたことを特徴とする高分子・液晶複合体。
[Scope of Claim] A polymer/liquid crystal composite in which a liquid crystal is dispersed and held in a monomer/oligomer polymer matrix, comprising: a cyanobiphenyl nematic type liquid crystal;
A functional polyester oligomer and an acrylic acid monomer are combined into a liquid crystal: (oligomer + monomer) = 65 to 75:
35 to 25 (wt%), and oligomer/monomer = 7/3 to 6.5/4.5 or 4/6 to 2/
A polymer/liquid crystal composite characterized by phase-separating a homogeneous solution mixed at a ratio of 8 (weight ratio) by irradiating ultraviolet rays.
JP1466390A 1990-01-23 1990-01-23 High polymer/liquid crystal complex Pending JPH03217819A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1466390A JPH03217819A (en) 1990-01-23 1990-01-23 High polymer/liquid crystal complex

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1466390A JPH03217819A (en) 1990-01-23 1990-01-23 High polymer/liquid crystal complex

Publications (1)

Publication Number Publication Date
JPH03217819A true JPH03217819A (en) 1991-09-25

Family

ID=11867455

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1466390A Pending JPH03217819A (en) 1990-01-23 1990-01-23 High polymer/liquid crystal complex

Country Status (1)

Country Link
JP (1) JPH03217819A (en)

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