JPS6215501A - Production of optical filter - Google Patents

Production of optical filter

Info

Publication number
JPS6215501A
JPS6215501A JP15543285A JP15543285A JPS6215501A JP S6215501 A JPS6215501 A JP S6215501A JP 15543285 A JP15543285 A JP 15543285A JP 15543285 A JP15543285 A JP 15543285A JP S6215501 A JPS6215501 A JP S6215501A
Authority
JP
Japan
Prior art keywords
polymer film
liquid crystal
substrate
optical filter
film
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
JP15543285A
Other languages
Japanese (ja)
Inventor
Fumiko Yokoya
横谷 文子
Shoichi Ishihara
將市 石原
Yoshihiro Matsuo
嘉浩 松尾
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP15543285A priority Critical patent/JPS6215501A/en
Publication of JPS6215501A publication Critical patent/JPS6215501A/en
Pending legal-status Critical Current

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  • Liquid Crystal (AREA)
  • Optical Filters (AREA)

Abstract

PURPOSE:To make the removal of a solid polymer film having a cholesteric liquid crystal structure obtd. by photopolymerizing from a substrate composed of a high polymer film easily by using the high polymer film as the translucent substrate. CONSTITUTION:The titled optical filter is produced by interposing the cholesteric liquid crystal composed of a mixed solution of a polypeptide compd. and a photopolymerizable monomer between a pair of the translucent substrates. Namely, the translucent substrates comprises the high polymer film and interposes the cholesteric liquid crystal there-between. After plate-orientation, the solid polymer film is obtd.by performing the optical polymerization, and the removing from the high polymer film substrate, whereby the solid polymer film having the uniform cholesteric liquid crystal structure which is the optical filter is obtd. As the high polymer film has a flexibility, said film can be removed from the prescribed substrate, without applying an unreasonable force to the polymer film, whereby the high polymer film having a good surface condition is obtd.

Description

【発明の詳細な説明】 産業上の利用分野 本発明はディスプレイ、オプトエレクトロニクスなどに
用いる光学フィルタ、例えば光ノツチフィルタ、バンド
パスフィルタ、カラーフィルタ。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to optical filters used in displays, optoelectronics, etc., such as optical notch filters, bandpass filters, and color filters.

元アイソレータなどの製造に適用できる光学フィルタの
製造方法に関する。
The present invention relates to a method for manufacturing an optical filter that can be applied to manufacturing original isolators.

従来の技術 ]レステリツク液晶が選択光散乱、旋光性1円偏光2色
性などの光学的性質を示すことは従来からよく知られて
いた。このコレステリック液晶の光学的性質を九ノツチ
フィルタおよびバンドパスフィルタに応用する技術が発
明されている(特公昭63−2330号公報)。この発
明で用いられているコレステリック液晶フィルムは、コ
レステリック液晶組成物ケー用崩機溶剤(例、ぐifり
「I 11ホル)・、不i l′+tドn−チルなど)
に浴角了さ−Iノー、フィルム状に展開L2だ後、コレ
スデリノク液晶成分が舌プ5性液体に転移する渦電以上
(通常60 ”c+L2)、 l )に加熱し、有機浴
剤成分を:蒸発させ、コl/ステリンク液晶成分を面接
結合さ−)しC1常I′11、+’t、i+i<の77
.1.1Bでコl/ステリック液晶構造ケもつフィル1
1と1−子得たものである。このルスデリソクdk品フ
ィルムのら旋ピップは本質的に温度、 i”t::、 
):+ 、電胃、磁界、化学的蒸気、紫外線などの外部
刺激によ−・1変化する。しだが−)−C1このフィル
i、 f光ツノ’fフィルタなどに実用する/こめにl
−11、その保持温度を一定に保つ恒温槽が必要であり
、斗/こ入気中の水分やアルコールなどの化仝l′的蒸
気かC)フ、イルノ、を保護する/こめの保護膜(ガラ
ス板など)が・1′/・片であり、さらにとのフィル7
・シ1、粘着(’lがあるため、ちり、虫などの異物質
からそ−のノイルly %)保護するだめの保護膜が必
要であるゾCどの欠点’;tイ11−.ていた。
[Prior Art] It has been well known that Lesteric liquid crystals exhibit optical properties such as selective light scattering, optical rotation, and monocircular dichroism. A technique has been invented in which the optical properties of cholesteric liquid crystals are applied to nine-notch filters and bandpass filters (Japanese Patent Publication No. 63-2330). The cholesteric liquid crystal film used in this invention is made of a disintegrating solvent for cholesteric liquid crystal compositions (e.g., ``I 11 hol'', ``I 11 hol'', ``I 11 hol,'' etc.).
After the bath is finished, it is developed into a film L2, and then heated to a temperature above the eddy current (usually 60"C+L2), where the liquid crystal component transforms into a liquid liquid (usually 60"C+L2), and the organic bath agent component is : evaporate and surface-bond C1/Stelink liquid crystal component -) to form C1 normal I'11, +'t, i+i<77
.. 1. Fill 1 with 1B and steric liquid crystal structure
1 and 1- children were obtained. The helical pips of this Rusdelisok dk product film are essentially temperature, i”t::,
): +, -・1 change due to external stimuli such as electrogastric, magnetic field, chemical vapor, and ultraviolet rays. Shidaga -) -C1 This filter is used for optical horn 'f filters, etc./Komeni l
-11. A constant temperature bath is required to keep the temperature constant, and a protective film to protect the water and chemical vapors such as alcohol from the incoming air. (glass plate, etc.) is ・1′/・piece, and furthermore, the fill 7
・1. Adhesive (due to its presence, a protective film is required to protect it from foreign substances such as dust and insects.) What disadvantages? 11-. was.

次に、安定な一ケ「、学フィルタと1−7で実用1に1
制えうるコレスデリソク液晶フィルノ・の製」前方法か
発明さtl、−/こ(11)開明56−139506弓
公報)。との:ルスヴリノクdシ晶ノイルトは、コレス
ブリック液晶成4)と重台性不飽和基♀もつ化合物との
/1゜合溶液から成るす第1・r”Iビ、ツク液晶をカ
ラス等の透ゲC1性茫板にはさみ重合さ−1−r、コl
/スヴリノク液晶構造ケ固定した固体ポリ−〆−フイル
ムであ(パイのフィルムのら旋ピッチは温度、−)Il
′:、¥[);場なとの列部刺激に対1.−.−7T極
め−r安宇である。
Next, a stable one-piece filter and 1-7 are 1 to 1 in practical use.
The method for manufacturing a controllable liquid crystal display was invented (tl.-/ko (11) Kaimei 56-139506 Bow Publication). Rusvlinok d-crystal noilt is a liquid crystal made of a 1/1 degree solution of colesbric liquid crystal compound 4) and a compound having a heavy unsaturated group. Polymerized with translucent C1 plate -1-r, Col.
/ Svrinok liquid crystal structure is a fixed solid poly film (the helical pitch of the film is temperature, -) Il
′:, ¥[); 1 for column stimulation with field. −. -7T mastery-r Yasu.

発明が解決しようと4゛る問題点 このようにコレスデリノク液晶構造を固体ポリマー中に
固定]−2/こポリ−7−フィルム全製造する場合、コ
レステリック液晶頁:挟持−Jるためのカラス等の透C
′l’;性基板が必要であり、ぞし2で、その基板を取
りはがし、フィル7・全取り出寸。従来例のようにガラ
ス基板ケ用いた1JA合、大きなフィルムを1)すると
とはかf61〜く、1/へ、フィルム金ガラス基板から
取りはがす場合、作業哨間か長くかかる。短時間でフィ
ル7、全ガラス基板から取りはがそうとするとフィルム
表面にきすがつき−IZf’;学的特性が悪くなる。
4 Problems to be Solved by the Invention In this way, the cholesteric liquid crystal structure is fixed in a solid polymer. Toru C
'l': A base plate is required, so remove it with 2 steps and fill 7 with all dimensions. In the case of 1JA using a glass substrate as in the conventional example, it takes a long time to remove a large film from the gold glass substrate. If you try to remove the film 7 from the entire glass substrate in a short period of time, the surface of the film will be scratched and the mechanical properties will deteriorate.

本発明は犬き4・フィルム全製造するととができ、製造
し2/こフィルムから高分子フィルノ・基板を容易に取
りはがすことがマ゛き、均一々イ4学特+l k持つフ
ィルムを製造することが可能な製浩法を・提供すること
を11自とする。
The present invention is capable of producing all four films, making it difficult to easily remove the polymer film and substrate from the produced film, and producing a film that uniformly has the following four properties. The 11th objective is to provide a manufacturing method that can make this possible.

問題点を解決するだめの手段 本発明においては、ポリペプチド化合物とi i[1合
件モノマーの混合浴液からなるコt/ステリック液晶を
、2枚の透−W、性高分イノfルノ、基板に挾1.1+
して尤学フィルタを製造する。−Jなわち、透光1−1
基板どして高分子−フィル7、金用い、コレスデリック
液晶を挾持し、プレー1−配向させたのち、)′14Φ
合を行った後、高分Y−ノイルノ、基板を・取りはがし
、尾学フ2イルタである均一な=ルステリック液晶構造
を持つ固体ポリマーフィルムz k (!)る1、作用 このようにし′τイ[Iら#Iだコレステリック液晶構
造金持つ固体ポリマーフィルムは、l’1’j:分子ノ
イルノ、基板と接着せず容易に取りはか−J−ことがで
きる。
Means to Solve the Problems In the present invention, a liquid crystal liquid crystal consisting of a mixed bath solution of a polypeptide compound and a monomer is placed between two sheets of translucent and transparent liquid crystals. , 1.1+ on the board
and manufacture a likelihood filter. -J, that is, transparent light 1-1
After sandwiching the polymer fill 7, gold layer, and cholesderic liquid crystal between the substrates and aligning the substrate, )'14Φ
After performing the polymerization, the substrate is peeled off and a solid polymer film with a homogeneous liquid crystal structure, which is a solid polymer film z k (!), is processed in this way. A solid polymer film with a cholesteric liquid crystal structure can be easily removed without adhesion to a substrate.

高分子ノイルノ・は可撓性である/ζめポリマーフィル
ムに無理な力をかげるととなくはが寸ことができ、表面
状態が良好なものがi!Iられると考えられる。
The polymer film is flexible; if excessive force is applied to the polymer film, it can peel off, and the surface condition is good. It is thought that I will be able to do it.

実施例 本発明の尤学)、イルタの製造方θ−において用いる液
晶原料はポリペプチド化合物で、!枯にポリ酸性アミノ
酸またはポリ酸性アミノ酸エステル誘導体であ才tn良
い。酸性アミノ酸としては、アスパラギン酸、クルタミ
ン酸お、hびオギシグルタミン酸の31Φ類がある。捷
だぞf+らのニスデル誘導体としては、酸性アミノ酸メ
チルエステル、エチルニスデル、ブ1]ビルニr−スj
−ル、フ゛チル玉ステル。
EXAMPLES The liquid crystal raw material used in the method for producing Ilta (the theory of the present invention) is a polypeptide compound, and! Polyacidic amino acids or polyacidic amino acid ester derivatives are particularly useful. Acidic amino acids include the 31Φ classes of aspartic acid, curtamic acid, and glutamic acid. Nisdel derivatives such as acidic amino acid methyl ester, ethyl nisdel, bu1] birnysdel, etc.
-L, plastic ball stell.

ペンブール1スプル、ヘギシル丁スプル、ンクロへギシ
ルエスデル、ベンジル丁−スデル、クロロベンジルニス
デル着の多くの物質かある。とれらの酸性アミノ酸およ
びその誘導体を重合さ拷て得たポリ酸性アミノ酸寸たは
ポリ酸性アミノ酸ニスデル誘導体ケ液晶原料として用い
る。
There are many substances such as Pembrol 1 sprue, Hegysil sprue, Ncrohegisyl esder, Benzyl sulfate, and Chlorobenzyl nisdel. Polyacidic amino acids or polyacidic amino acid Nisdel derivatives obtained by polymerizing these acidic amino acids and their derivatives are used as raw materials for liquid crystals.

溶gどl−での光重合4<トモツマ−は、(メタ)ア7
.7 クリル酸エステルあるいはその誘導体を含んでいるもの
であり、例えば、メチルアクリレート、工、  チルア
クリレート、メチルメタクリレート、シクロヘキシルア
クリレート、エチレングリコールジメタクリレート、ジ
エチレングリコールジメタクリレート、トリエチレング
リコールジメタクリレート等である。
Photopolymerization in molten glass 4<Tomotsuma is (meth)a7
.. 7 Contains acrylic ester or its derivatives, such as methyl acrylate, methyl acrylate, methyl methacrylate, cyclohexyl acrylate, ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, etc.

高分子フィルム基板としては、(メタ)アクリル酸エス
テルあるいはその誘導体を含まない高分子フィルムが良
く、光透過性を持ち、基板としての強度を持ち、光学フ
ィルタの特性に影響を与えないことが望ましい。例えば
、ポリプロピレン。
As the polymer film substrate, a polymer film that does not contain (meth)acrylic acid ester or its derivatives is preferable, and it is desirable that it has light transmittance, has strength as a substrate, and does not affect the characteristics of the optical filter. . For example, polypropylene.

ポリエチレン、ポリ塩化ビニル、ポリスチレンポリ塩化
ビニリデン、ポリアミド、ポリカーボネートおよび酢酸
ビニル等である。高分子フィルム基板は数μm〜数10
077 mの厚みのものを用いることが望ましく、厚み
の薄い場合には高分子フィルムの外に補助基板等を用い
て製造すればよい。
These include polyethylene, polyvinyl chloride, polystyrene polyvinylidene chloride, polyamide, polycarbonate, and vinyl acetate. Polymer film substrates range from several μm to several tens of micrometers
It is desirable to use a film with a thickness of 0.77 m, and if the film is thin, it may be manufactured using an auxiliary substrate or the like in addition to the polymer film.

高分子フィルムを基板として用いた場合ロール等の巻き
取シによる連続製造が可能であり、大きなフィルムを作
ることが可能である。
When a polymer film is used as a substrate, continuous production by winding up a roll or the like is possible, and it is possible to make a large film.

本発明により製造された光学フィルタの分光光度スペク
トルを測定して求めた光学特性を図に示されるような、
選択的に反射する波長λmaX I半直幅Δλ、λwa
x  における光学密度ムm1LXlλwax以外での
光学密度大。、そして■−ム1na!−人。をそれぞれ
求め評価した。
The optical characteristics obtained by measuring the spectrophotometric spectrum of the optical filter manufactured according to the present invention are as shown in the figure.
Selectively reflected wavelength λmaX I half-normal width Δλ, λwa
The optical density at x is large except for m1LX1λwax. , and■-mu1na! -People. were determined and evaluated.

実施例1 液晶材料としてポリーレーグルタミン酸−nブチルエス
テルを60重量%、光重合性モノマーとしてトリエチレ
ングリコールジメタクリレートを50重量%秤量し、3
6〜4Q’cの温度に保持しながら両者を充分に攪拌し
た。この様にして得た均一な液晶溶液を100A1+1
厚のスペーサを介して2枚の厚み16μmのポリ塩化ビ
ニリデンの高分子フィルム基板に挾持し、30°Cの一
定温度に3時間保持した。その後、引き続き30’Cの
一定温度に保持しながら紫外線を3時間照射して厚み1
00μlのポリマーフィルム人を得た。その際、基板と
して用いた高分子フィルムはポリマーフィルム9べ一/ ムから容易に取りはがすととができた。
Example 1 Weighed 60% by weight of polyurethane glutamic acid-n-butyl ester as a liquid crystal material and 50% by weight of triethylene glycol dimethacrylate as a photopolymerizable monomer.
Both were sufficiently stirred while maintaining the temperature at 6 to 4 Q'c. The uniform liquid crystal solution obtained in this way was 100A1+1
It was sandwiched between two 16 μm thick polyvinylidene chloride polymer film substrates via a thick spacer, and kept at a constant temperature of 30° C. for 3 hours. After that, while maintaining the temperature at a constant temperature of 30'C, UV rays were irradiated for 3 hours to create a thickness of 1.
00 μl of polymer film was obtained. At that time, the polymer film used as a substrate could be easily removed from the polymer film 9 base.

次に、比較のために同様に均一混合した液晶溶液を10
0μl厚のスペーサを介して、2枚のガラス基板に挾持
し、30℃の一定温度に3時間保持した。その後、引き
継き30’Oの一定温度に保持しながら紫外線を3時間
照射して厚み100μmのポリマーフィルムBi得た。
Next, for comparison, 10% of the liquid crystal solution was mixed uniformly in the same manner.
It was sandwiched between two glass substrates via a 0 μl thick spacer and kept at a constant temperature of 30° C. for 3 hours. Thereafter, while maintaining the temperature at a constant temperature of 30'O, ultraviolet rays were irradiated for 3 hours to obtain a polymer film Bi having a thickness of 100 μm.

ガラス基板をポリマーフィルムBから取りはがすだめに
6時間の作業時間を要した。
It took 6 hours of working time to remove the glass substrate from polymer film B.

これらのポリマーフィルム人、Bの分光光度スペクトル
、λmaXIΔλ、Δムおよびム。を測定し、その値を
第1表に示した。結果は1α角のポリマーフィルム内で
5点測定したものである。この結果からみてわかるよう
に、ポリマーフィルムBに比べてポリマーフィルム人は
ム。がそろっておりフィルム表面にきすがなく光学特性
の均一な光学フィルタである。
The spectrophotometric spectra of these polymer films, B, λmaXIΔλ, Δam and Mu. was measured and the values are shown in Table 1. The results were measured at five points within the 1α angle polymer film. As you can see from this result, compared to polymer film B, the polymer film is more effective. It is an optical filter with uniform optical properties and no scratches on the film surface.

(以 下金 白) 10、\−/゛ 11  、 実施例2 液晶(−4料とL2てボリーレーグルタミン酸−nブチ
ルエステルを60中−Rt)0、−尾市合1′f−f:
ノマー−一してトリエチレングリコールジメタクリl/
 −1−%)60重Wf”f)秤fjt +/、36〜
4o ”C(7) rr(’+ e K (’A持tな
がら両渚呑・充分に晴拌した。との様に+、 −r イ
:tt、:均一・な液晶溶液を200 /I m lワ
Cハスベー恨有媚17で2枚のJ?み50 /7 Il
lのボリゾ「1ピL/、/のj’;i1分−r7 イ#
 、1一基板V(A40S L、26 ”Cty)−A
if7tiA度に3 ++、g間保持1〜だ。その後、
引き続き26 ”(:の一定温度に保持l、7ながら紫
外線(t−3時間照射してJj7み20011mのポリ
マーフィルムCを得た。−その際、〕L(Iスと1−2
で用いた高分子ノイルノ・はボリマーフィルノ・Cから
容易に取りCIかすととができた。
(Hereinafter referred to as Kinshiro) 10,\-/゛11, Example 2 Liquid crystal (-Rt in -4 material and L2 Boryley glutamic acid n-butyl ester in 60) 0, -Oichigo 1'f-f:
Nomer-triethylene glycol dimethacrylate/
-1-%) 60 weight Wf”f) Scale fjt +/, 36~
4o ``C(7) rr('+ e K ('While holding A, both sides were swallowed and thoroughly stirred. +, -r I: tt,: A homogeneous liquid crystal solution was prepared at 200/I. m lwa C hasbe grudge 17 and 2 J?mi 50 /7 Il
l's bolizo "1 pi L/, /'s j'; i1 minute - r7 i #
, 1-board V (A40S L, 26”Cty)-A
If7tiA degree is 3 ++, and g is maintained at 1~. after that,
Subsequently, the film was kept at a constant temperature of 26" (l, 7) and irradiated with ultraviolet light (t) for 3 hours to obtain a polymer film C with a length of 20011 m.
The polymer Noylno. used in the above was easily removed from the polymer Filno.C to yield CI dregs.

次に、比較の/こめに同様に1り一混合した液晶kt教
を20077 m厚のスペーサを介して、2枚のガラス
基鈑に挾持し、26”Cの−・定7晶度に3時間保持し
た。その後、引き継き26°’(Eの一’ >I’ 7
!、、1.度に保持し寿がら紫夕1線を31〕j[il
j p(j、射L5.て)すみ200/Jmのポリマー
フィルムDを得/こ。ガシス基板4でポリマーフィルム
Dから取りに1、がJ−ために6 tLlllt!、1
の作業時間を要した。
Next, for comparison, liquid crystal kt crystals, which were mixed one by one, were sandwiched between two glass substrates via a 20,077 m thick spacer, and heated to a crystallinity of 26"C - constant 7. After that, it was taken over and 26°'(E'>I' 7
! ,,1. 31〕j[il
A polymer film D of 200/Jm was obtained. 1 to take from polymer film D on gasis substrate 4, but 6 tLllllt for J-! ,1
It took a lot of work time.

これらのポリマーノイルAC、Dの分M、 w−用スペ
クトル その値全第2表に示した。結果は1 (’m角のポリ−
7−フィルム内で6点測定したものである。C.の結果
からノドでわかるように、ポリマーノイルシJ、Dに比
べてポリマーフィルムCは人。かぞろー、て1,・リノ
,イルム表面にきーtがなく、−尾学%(’.1の均一
な尾学フィルタである。
The spectra and values of these polymer noils AC and D for M and W are all shown in Table 2. The result is 1 ('m square poly-
7 - Measurements were taken at 6 points within the film. C. As can be clearly seen from the results, polymer film C was more sensitive than polymer films J and D. There are no keys on the surface of Kazoro, Te1, Reno, and Illum, and it is a uniform tail filter with -tail filter % ('.1).

(以 下金 白) 1 3 ・−7 1 4 、、 発明の効果 本発明によれは光学ノfルタの製造「稈に」、・いて透
光性x板としてKl・1分子フィルム部用いるととによ
り、光重合してイ)すたコレス゛j゛リック液晶構造を
持つ固体ポリマーフィル” k lX□:j分子フィル
ム基板から容易に取りC1−がlととができる。]1,
)分子フィルム基板を用いるととで、固体ポリマーフィ
ルムと透光性基板との取りはがしに要する作業時間を短
縮でき、取りはがした固体ボリマーノーイルムの表面状
態が良好とhる/(め、菫学ノイルタとしての特性に影
響を及はさず均一・4.+I” I’l k持つ光学フ
ィルタケ作ることができる。−4 f(連続的に光学フ
ィルタを製造するととができ、きわめて千1−効な発明
である。
(hereinafter referred to as Kinshiro) 1 3 ・-7 1 4 , Effects of the Invention According to the present invention, when manufacturing an optical filter, and using the Kl 1 molecule film part as a translucent x plate, By photopolymerizing, a) a solid polymer film having a coreless liquid crystal structure can be easily removed from the molecular film substrate to form C1- and L.]1.
) By using a molecular film substrate, the working time required to remove the solid polymer film and the transparent substrate can be shortened, and the surface condition of the removed solid polymer film is good. , it is possible to make an optical filter with uniform 4.+I"I'k without affecting the characteristics of the violet filter. 1- It is an effective invention.

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

図は、本発明により製造された光学フィルタの光学特性
評価の要素を示−ずグラノである。
The figure does not show elements for evaluating the optical characteristics of the optical filter manufactured according to the present invention.

Claims (4)

【特許請求の範囲】[Claims] (1)ポリペプチド化合物と光重合性モノマーの混合溶
液からなるコレステリック液晶を2枚の透光性高分子フ
ィルム基板に挾持し、プレーナ配向をさせたのち、光重
合させ、2枚の高分子フィルム基板を取りはがし、コレ
ステリック液晶構造を持つ固体ポリマーフィルムを得る
光学フィルタの製造方法。
(1) A cholesteric liquid crystal made of a mixed solution of a polypeptide compound and a photopolymerizable monomer is sandwiched between two transparent polymer film substrates, planarly oriented, and then photopolymerized to form two polymer films. A method for manufacturing optical filters in which a substrate is removed to obtain a solid polymer film with a cholesteric liquid crystal structure.
(2)高分子フィルム基板が、ポリプロピレン、ポリエ
チレン、ポリ塩化ビニル、ポリスチレン、ポリ塩化ビニ
リデン、ポリアミド、ポリカーボネートおよび酢酸ビニ
ルのうちの少なくとも1種であることを特徴とする特許
請求の範囲第1項記載の光学フィルタの製造方法。
(2) Claim 1, wherein the polymer film substrate is at least one of polypropylene, polyethylene, polyvinyl chloride, polystyrene, polyvinylidene chloride, polyamide, polycarbonate, and vinyl acetate. A method for manufacturing an optical filter.
(3)ポリペプチド化合物がポリ酸性アミノ酸またはポ
リ酸性アミノ酸エステルの誘導体であることを特徴とす
る特許請求の範囲第1項記載の光学フィルタの製造方法
(3) The method for producing an optical filter according to claim 1, wherein the polypeptide compound is a derivative of a polyacidic amino acid or a polyacidic amino acid ester.
(4)光重合性モノマーが少なくとも1種類の(メタ)
アクリル酸エステルあるいはその誘導体を含んでいるこ
とを特徴とする特許請求の範囲第1項記載の光学フィル
タの製造方法。
(4) At least one type of photopolymerizable monomer (meth)
2. The method for producing an optical filter according to claim 1, wherein the optical filter contains an acrylic ester or a derivative thereof.
JP15543285A 1985-07-15 1985-07-15 Production of optical filter Pending JPS6215501A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15543285A JPS6215501A (en) 1985-07-15 1985-07-15 Production of optical filter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15543285A JPS6215501A (en) 1985-07-15 1985-07-15 Production of optical filter

Publications (1)

Publication Number Publication Date
JPS6215501A true JPS6215501A (en) 1987-01-23

Family

ID=15605890

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15543285A Pending JPS6215501A (en) 1985-07-15 1985-07-15 Production of optical filter

Country Status (1)

Country Link
JP (1) JPS6215501A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996012209A1 (en) * 1994-10-13 1996-04-25 The Secretary Of State For Defence Liquid crystal polymer devices
GB2308371A (en) * 1994-10-13 1997-06-25 Secr Defence Liquid crystal polymer devices
WO2002010807A1 (en) * 2000-07-27 2002-02-07 Shiseido Co., Ltd. Optical sheets containing cholesteric liquid crystal layer and data recording media, data recording method and data discriminating method by using the same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996012209A1 (en) * 1994-10-13 1996-04-25 The Secretary Of State For Defence Liquid crystal polymer devices
GB2308371A (en) * 1994-10-13 1997-06-25 Secr Defence Liquid crystal polymer devices
GB2308371B (en) * 1994-10-13 1999-03-24 Secr Defence Liquid crystal polymer devices
WO2002010807A1 (en) * 2000-07-27 2002-02-07 Shiseido Co., Ltd. Optical sheets containing cholesteric liquid crystal layer and data recording media, data recording method and data discriminating method by using the same

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