JPH1149878A - Production of polarized film - Google Patents

Production of polarized film

Info

Publication number
JPH1149878A
JPH1149878A JP20615397A JP20615397A JPH1149878A JP H1149878 A JPH1149878 A JP H1149878A JP 20615397 A JP20615397 A JP 20615397A JP 20615397 A JP20615397 A JP 20615397A JP H1149878 A JPH1149878 A JP H1149878A
Authority
JP
Japan
Prior art keywords
film
boric acid
polyvinyl alcohol
producing
polarizing 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.)
Granted
Application number
JP20615397A
Other languages
Japanese (ja)
Other versions
JP3505968B2 (en
Inventor
Koji Matsumoto
浩二 松元
Shigetoshi Hayashi
成年 林
Nobuyuki Kurata
信行 蔵田
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP20615397A priority Critical patent/JP3505968B2/en
Publication of JPH1149878A publication Critical patent/JPH1149878A/en
Application granted granted Critical
Publication of JP3505968B2 publication Critical patent/JP3505968B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To enable to obtain a polarized film having a high contrast and useful for outdoor liquid crystal display devices, low power consumption liquid crystal display devices, etc., by orienting a polyvinyl alcohol resin film in a specific ratio in an aqueous boric acid solution. SOLUTION: This method for producing a polarized film comprises monoaxially orienting (A) a polyvinyl alcohol resin film (e.g. the film having a resin polymerization degree of 1,000-10,000) in an orientation ratio of 4-8 times e.g. by a dry method, allowing the film to adsorb (B1 ) iodine or (B2 ) a dichroic dye, immersing the film in (C) an aqueous boric acid solution [e.g. a solution containing 2-18 pts.wt. of boric acid in 100 pts.wt. of water] e.g. in conditions comprising a temperature of >=50 deg.C and an immersion time of 100-1,200 sec and simultaneously again orienting the film in a ratio of 1.1-1.8 times.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、偏光フィルムの製
造方法に関する。
[0001] The present invention relates to a method for producing a polarizing film.

【0002】[0002]

【従来の技術】従来より、偏光フィルムの製造方法とし
ては、例えばポリビニルアルコール系樹脂フィルムにヨ
ウ素または二色性染料を吸着配向させたフィルムをほう
酸水溶液に浸漬する方法が知られている。しかし、かか
る偏光フィルムは、屋外で使用される液晶表示装置や低
消費電力の液晶表示装置に求められるより高いコントラ
ストを満足することが困難であった。
2. Description of the Related Art Conventionally, as a method for producing a polarizing film, for example, a method is known in which a film in which iodine or a dichroic dye is adsorbed and oriented on a polyvinyl alcohol resin film is immersed in an aqueous boric acid solution. However, it has been difficult for such a polarizing film to satisfy a higher contrast required for a liquid crystal display device used outdoors or a low power consumption liquid crystal display device.

【0003】[0003]

【発明が解決しようとする課題】そこで、本発明者ら
は、より高いコントラストの偏光フィルムを製造し得る
方法を開発するべく鋭意検討した結果、ほう酸水溶液中
で特定の倍率に延伸処理することによって、高コントラ
ストの偏光フィルムが得られることを見出し、本発明に
至った。
The inventors of the present invention have made intensive studies to develop a method for producing a polarizing film having a higher contrast, and as a result, by stretching the film in a boric acid aqueous solution to a specific magnification. The present inventors have found that a high-contrast polarizing film can be obtained, and have reached the present invention.

【0004】[0004]

【課題を解決するための手段】すなわち、本発明は、ポ
リビニルアルコール系樹脂フィルムを一軸延伸したのち
ヨウ素または二色性染料を吸着配向させたフィルムを、
ほう酸水溶液に浸漬しながら1.1〜1.8倍に延伸す
ることを特徴とする偏光フィルムの製造方法を提供する
ものである。
That is, the present invention provides a film obtained by uniaxially stretching a polyvinyl alcohol resin film and then adsorbing and orienting iodine or a dichroic dye.
An object of the present invention is to provide a method for producing a polarizing film, wherein the film is stretched 1.1 to 1.8 times while being immersed in an aqueous boric acid solution.

【0005】[0005]

【発明の実施の形態】本発明に用いられるポリビニルア
ルコール系樹脂フィルムにおけるポリビニルアルコール
系樹脂とは、例えばポリビニルアルコールや、ビニルア
ルコールを主な共重合成分とする他の単量体との共重合
体であって、その重合度は通常1000〜10000、
好ましくは1500〜10000の範囲である。ポリビ
ニルアルコール系樹脂を通常の方法で製膜することによ
ってポリビニルアルコール系樹脂フィルムが得られる
が、その厚みは通常50〜150μm程度である。かか
るポリビニルアルコール系樹脂フィルムは通常、製膜
後、ケン化されるが、ケン化度は通常85〜100モル
%、好ましくは98〜100モル%程度である。
BEST MODE FOR CARRYING OUT THE INVENTION The polyvinyl alcohol-based resin in the polyvinyl alcohol-based resin film used in the present invention is, for example, a copolymer of polyvinyl alcohol or another monomer having vinyl alcohol as a main copolymerization component. And the degree of polymerization is usually from 1,000 to 10,000,
Preferably it is in the range of 1500-10000. A polyvinyl alcohol-based resin film is obtained by forming the polyvinyl alcohol-based resin by a usual method, and the thickness is usually about 50 to 150 μm. Such a polyvinyl alcohol-based resin film is usually saponified after film formation, and the degree of saponification is usually about 85 to 100 mol%, preferably about 98 to 100 mol%.

【0006】かかるポリビニルアルコール系樹脂フィル
ムの一軸延伸は通常、乾式で行われる。具体的には、熱
ロールを用いて一軸延伸する方法、加熱オーブン内に設
置されたロール間で引張力を加えながら延伸を行うロー
ル間一軸延伸法などが挙げられるが、これらに限定され
るものではない。延伸倍率は通常4〜8倍程度である。
[0006] Uniaxial stretching of such a polyvinyl alcohol-based resin film is usually performed in a dry manner. Specifically, a method of uniaxially stretching using a hot roll, a roll-to-roll uniaxial stretching method of stretching while applying a tensile force between rolls installed in a heating oven, and the like are included, but are not limited thereto. is not. The stretching ratio is usually about 4 to 8 times.

【0007】一軸延伸後、ヨウ素または二色性染料を吸
着配向させる方法は特に限定されないが、例えば緊張状
態を保ったままヨウ素およびヨウ化カリウムの水溶液に
浸漬する方法、二色性染料および芒硝の水溶液に浸漬す
る方法などが挙げられる。ヨウ素およびヨウ化カリウム
の水溶液に浸漬する場合、その組成は通常、水100重
量部あたりヨウ素0.01〜0.5重量部、ヨウ化カリ
ウム0.5〜10重量部であり、水溶液の温度は通常2
0〜50℃の範囲である。二色性染料および芒硝の水溶
液を用いる場合、その組成は通常水100重量部あたり
二色性染料0.001〜1重量部、芒硝1〜10重量部
であり、水溶液の温度は通常30〜80℃程度である。
一軸延伸後のポリビニルアルコール系樹脂フィルムは、
ヨウ素または二色性染料を吸着配向させる前に、水に浸
漬処理されてもよい。
The method of adsorbing and orienting iodine or a dichroic dye after uniaxial stretching is not particularly limited. For example, a method of immersing in an aqueous solution of iodine and potassium iodide while maintaining a tension state, and a method of dichroic dye and sodium sulfate A method of dipping in an aqueous solution may be used. When immersed in an aqueous solution of iodine and potassium iodide, the composition is usually 0.01 to 0.5 parts by weight of iodine and 0.5 to 10 parts by weight of potassium iodide per 100 parts by weight of water. Usually 2
The range is from 0 to 50 ° C. When an aqueous solution of the dichroic dye and sodium sulfate is used, the composition is usually 0.001 to 1 part by weight of dichroic dye and 1 to 10 parts by weight of sodium sulfate per 100 parts by weight of water, and the temperature of the aqueous solution is usually 30 to 80 parts by weight. It is about ° C.
Polyvinyl alcohol-based resin film after uniaxial stretching,
Before iodine or a dichroic dye is adsorbed and oriented, it may be immersed in water.

【0008】かくしてヨウ素または二色性染料が吸着配
向されたフィルムは、ほう酸水溶液に浸漬しながら延伸
されることが必要である。ほう酸水溶液としては、通常
水100重量部あたり、ほう酸を2〜18重量部、好ま
しくは5〜12重量部程度含有する水溶液が用いられ
る。ヨウ素を吸着配向させた場合には、さらにヨウ化カ
リウムを含有していてもよく、ヨウ化カリウムを使用す
る場合その使用量は水100重量部あたり通常2〜20
重量部である。ほう酸水溶液の温度は通常50℃以上で
フィルム切れを起こさない範囲であり、好ましくは50
〜90℃程度である。かかるほう酸水溶液への浸漬時間
は特に限定されないが、通常100〜1200秒、好ま
しくは150〜600秒、より好ましくは200〜50
0秒程度である。
Thus, the film on which iodine or the dichroic dye is adsorbed and oriented needs to be stretched while being immersed in an aqueous boric acid solution. As the boric acid aqueous solution, an aqueous solution containing about 2 to 18 parts by weight, preferably about 5 to 12 parts by weight of boric acid per 100 parts by weight of water is used. When iodine is adsorbed and oriented, it may further contain potassium iodide. When potassium iodide is used, its amount is usually 2 to 20 parts by weight per 100 parts by weight of water.
Parts by weight. The temperature of the boric acid aqueous solution is usually 50 ° C. or higher and a range that does not cause film breakage, and preferably 50 ° C.
~ 90 ° C. Although the immersion time in the boric acid aqueous solution is not particularly limited, it is generally 100 to 1200 seconds, preferably 150 to 600 seconds, more preferably 200 to 50 seconds.
It is about 0 seconds.

【0009】ヨウ素または二色性染料を吸着配向させた
フィルムをほう酸水溶液に浸漬しながら延伸するには、
例えば該フィルムをほう酸水溶液中で延伸すればよい。
延伸方法としては特に限定されるものではなく、例えば
フィルムに付与する張力を適宜調整することにより延伸
することができる。張力は、ほう酸水溶液の温度や濃度
などに応じて調整される。
In order to stretch a film on which iodine or a dichroic dye is adsorbed and oriented while dipping in a boric acid aqueous solution,
For example, the film may be stretched in an aqueous boric acid solution.
The stretching method is not particularly limited. For example, the stretching can be performed by appropriately adjusting the tension applied to the film. The tension is adjusted according to the temperature and concentration of the boric acid aqueous solution.

【0010】本発明の方法において延伸倍率は重要であ
り、1.1〜1.8倍の範囲であることが必要である。
延伸倍率が1.1倍未満または1.8倍を超えるとコン
トラストの向上が十分ではなく、また1.8倍を超える
とフィルム切れを起こしやすくなるため、好ましくな
い。ほう酸水溶液中で延伸処理された後、通常と同様に
水洗し、乾燥する方法によって、目的の偏光フィルムを
得ることができる。
In the method of the present invention, the draw ratio is important, and it is necessary that the draw ratio is in the range of 1.1 to 1.8.
If the stretching ratio is less than 1.1 times or exceeds 1.8 times, the contrast is not sufficiently improved, and if it exceeds 1.8 times, the film tends to break, which is not preferable. After being stretched in an aqueous boric acid solution, the desired polarizing film can be obtained by a method of washing with water and drying in the same manner as usual.

【0011】かくして得られる偏光フィルムは、通常の
偏光フィルムと同様に、その一方の面または両面に保護
層が貼合されて偏光板として使用することができる。保
護層としては、例えばセルロース系アセテート、アクリ
ル系樹脂、ポリエステル系樹脂、ポリオレフィン系樹
脂、ポリカーボネート系樹脂、ポリエーテルサルホン系
樹脂の板、シートまたはフィルムなどが挙げられる。
The polarizing film thus obtained can be used as a polarizing plate by attaching a protective layer to one or both surfaces thereof in the same manner as a normal polarizing film. Examples of the protective layer include a plate, sheet or film of cellulose acetate, acrylic resin, polyester resin, polyolefin resin, polycarbonate resin, and polyethersulfone resin.

【0012】[0012]

【発明の効果】本発明の方法によれば、高コントラスト
の偏光フィルムを容易に製造することができる。
According to the method of the present invention, a high-contrast polarizing film can be easily produced.

【0013】[0013]

【実施例】以下、実施例により本発明をより詳細に説明
するが、本発明はこれら実施例により限定されるもので
はない。なお、偏光フィルムのコントラスト(Cr)は
以下の方法により求めた。 (1)平行位透過率(Tp)および直交位透過率(Tc
の測定 得られた偏光フィルム2枚をその吸収軸が互いに平行に
なるように重ね合せた場合の透過率を平行位透過率(T
p)、吸収軸が互いに直交するように重ね合せた場合の
透過率を直交位透過率(Tc)とした。透過率は、分光
光度計(島津UV−2200)を用いて波長領域400
〜700nmで10nm毎に測定した分光透過率〔τ
(λ)、ここでλは波長を示す。〕から、計算式(1) 〔式中、P(λ)は標準光(C光源)の分光分布、y
(λ)は2度視野等色関数をそれぞれ示す。〕により算
出した。 (2)コントラスト(Cr)の計算 平行位透過率(Tp)および直交位透過率(Tc)から、
計算式(2) Cr=Tp/Tc (2) により算出した。
EXAMPLES The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples. The contrast ( Cr ) of the polarizing film was determined by the following method. (1) Parallel transmittance (T p ) and orthogonal transmittance (T c )
The transmittance when two polarizing films obtained are superimposed so that their absorption axes are parallel to each other is referred to as the parallel transmittance (T
p ), and the transmittance in the case where the absorption axes are overlapped so as to be orthogonal to each other is defined as orthogonal transmittance (T c ). The transmittance was measured in a wavelength range of 400 using a spectrophotometer (Shimadzu UV-2200).
The spectral transmittance [.tau.
(Λ), where λ indicates the wavelength. ], The calculation formula (1) [Where P (λ) is the spectral distribution of standard light (C light source), y
(Λ) indicates a two-degree visual field color matching function. ]. (2) Contrast calculated parallel position transmittance (C r) (T p) and the perpendicular position transmittance (T c),
It was calculated by equation (2) C r = T p / T c (2).

【0014】実施例1 ポリビニルアルコールのフィルム(厚み75μm、重合
度2400、ケン化度99.9%以上)を乾式で一軸延
伸し(延伸倍率5倍)、緊張状態を保ったままヨウ素お
よびヨウ化カリウムの水溶液〔ヨウ素:ヨウ化カリウ
ム:水=0.05:5:100(重量比)〕に28℃で
60秒間浸漬した。次いで、ほう酸水溶液(ほう酸7.
5重量部、ヨウ化カリウム6重量部、水100重量部)
に76℃で300秒間浸漬しながら延伸倍率1.3倍に
延伸した。その後、15℃の純水で10秒間水洗し、5
0℃で乾燥して、偏光フィルム(Cr=1800)を得
た。
Example 1 A polyvinyl alcohol film (thickness: 75 μm, degree of polymerization: 2400, degree of saponification: 99.9% or more) was uniaxially stretched in a dry system (stretching ratio: 5 times), and iodine and iodine were kept in a tensioned state. It was immersed in an aqueous solution of potassium [iodine: potassium iodide: water = 0.05: 5: 100 (weight ratio)] at 28 ° C. for 60 seconds. Next, a boric acid aqueous solution (boric acid 7.
(5 parts by weight, potassium iodide 6 parts by weight, water 100 parts by weight)
The film was stretched to 1.3 times the draw ratio while being immersed at 76 ° C. for 300 seconds. Then, wash with pure water at 15 ° C for 10 seconds,
After drying at 0 ° C., a polarizing film (C r = 1800) was obtained.

【0015】実施例2 ほう酸水溶液中での延伸倍率を1.7倍とした以外は、
実施例1と同様に操作して、偏光フィルム(Cr=20
00)を得た。
EXAMPLE 2 Except that the stretching ratio in an aqueous boric acid solution was 1.7 times,
By operating in the same manner as in Example 1, a polarizing film (C r = 20)
00).

【0016】比較例1 ほう酸水溶液中での延伸倍率を1.05倍とした以外
は、実施例1と同様に操作して、偏光フィルム(Cr
1000)を得た。
Comparative Example 1 The same procedure as in Example 1 was carried out except that the stretching ratio in an aqueous solution of boric acid was changed to 1.05, to obtain a polarizing film (C r =
1000).

【0017】比較例2 ほう酸水溶液中での延伸倍率を2.0倍にしようと試み
たが、フィルム切れを起して、延伸できなかった。
COMPARATIVE EXAMPLE 2 An attempt was made to increase the draw ratio in an aqueous boric acid solution to 2.0 times, but the film was cut and could not be drawn.

Claims (7)

【特許請求の範囲】[Claims] 【請求項1】ポリビニルアルコール系樹脂フィルムを一
軸延伸したのちヨウ素または二色性染料を吸着配向させ
たフィルムを、ほう酸水溶液に浸漬しながら1.1〜
1.8倍に延伸することを特徴とする偏光フィルムの製
造方法。
1. A film obtained by uniaxially stretching a polyvinyl alcohol-based resin film and then adsorbing and orienting iodine or a dichroic dye in a boric acid aqueous solution.
A method for producing a polarizing film, comprising stretching the film 1.8 times.
【請求項2】ポリビニルアルコール系樹脂フィルムの一
軸延伸が乾式で行われる請求項1に記載の偏光フィルム
の製造方法。
2. The method for producing a polarizing film according to claim 1, wherein the uniaxial stretching of the polyvinyl alcohol-based resin film is performed in a dry manner.
【請求項3】ポリビニルアルコール系樹脂フィルムの一
軸延伸における延伸倍率が4〜8倍である請求項1に記
載の偏光フィルムの製造方法。
3. The method for producing a polarizing film according to claim 1, wherein the stretching ratio in uniaxial stretching of the polyvinyl alcohol-based resin film is 4 to 8 times.
【請求項4】ほう酸水溶液が、水100重量部あたりほ
う酸を2〜18重量部含有する請求項1に記載の偏光フ
ィルムの製造方法。
4. The method for producing a polarizing film according to claim 1, wherein the boric acid aqueous solution contains 2 to 18 parts by weight of boric acid per 100 parts by weight of water.
【請求項5】ほう酸水溶液の温度が50℃以上である請
求項1に記載の偏光フィルムの製造方法。
5. The method for producing a polarizing film according to claim 1, wherein the temperature of the boric acid aqueous solution is 50 ° C. or higher.
【請求項6】ほう酸水溶液への浸漬時間が100〜12
00秒である請求項1に記載の偏光フィルムの製造方
法。
6. An immersion time in an aqueous solution of boric acid of 100 to 12 hours.
The method for producing a polarizing film according to claim 1, wherein the time is 00 seconds.
【請求項7】ポリビニルアルコール系樹脂の重合度が1
000〜10000である請求項1に記載の偏光フィル
ムの製造方法。
7. The polymerization degree of the polyvinyl alcohol resin is 1
The method for producing a polarizing film according to claim 1, wherein the number is from 000 to 10,000.
JP20615397A 1997-07-31 1997-07-31 Manufacturing method of polarizing film Expired - Fee Related JP3505968B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20615397A JP3505968B2 (en) 1997-07-31 1997-07-31 Manufacturing method of polarizing film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20615397A JP3505968B2 (en) 1997-07-31 1997-07-31 Manufacturing method of polarizing film

Publications (2)

Publication Number Publication Date
JPH1149878A true JPH1149878A (en) 1999-02-23
JP3505968B2 JP3505968B2 (en) 2004-03-15

Family

ID=16518683

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Country Status (1)

Country Link
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JP2001296428A (en) * 2000-04-17 2001-10-26 Nitto Denko Corp Method for manufacturing polarizing plate and liquid crystal display device
US6833090B2 (en) 2000-12-19 2004-12-21 Nitto Denko Corporation Process for making a polarizing film
CN100381841C (en) * 2001-05-10 2008-04-16 住友化学株式会社 Polarizing plate and method for producing the same
JP2002350638A (en) * 2001-05-28 2002-12-04 Nishi Kogyo Kk Method and apparatus for manufacturing polarizing film
JP4593827B2 (en) * 2001-05-28 2010-12-08 西工業株式会社 Polarizing film manufacturing method and manufacturing apparatus
US6760156B2 (en) 2001-09-20 2004-07-06 Nitto Denko Corporation Process of producing a polarizer, polarizer, polarizing plate, and visual display
KR100880976B1 (en) * 2001-09-20 2009-02-03 닛토덴코 가부시키가이샤 Process of producing a polarizer, polarizer, polarizing plate, and visual display
JP2003240944A (en) * 2002-02-14 2003-08-27 Nitto Denko Corp Method for manufacturing polarizer, polarizer, polarizing plate, and image display device
US8012383B2 (en) 2002-12-12 2011-09-06 Sumitomo Chemical Company, Limited Method for producing polarizing film
KR100781271B1 (en) * 2006-02-14 2007-11-30 엘지전자 주식회사 Apparatus and method for focusing image
US9194989B2 (en) 2008-11-27 2015-11-24 Nitto Denko Corporation Iodine polarizing film, method of producing the same, and polarizing plate comprising the same
JP2014052647A (en) * 2010-09-03 2014-03-20 Nitto Denko Corp Method for manufacturing thin polarizing film
US9081146B2 (en) 2011-03-23 2015-07-14 Nitto Denko Corporation Polarizing membrane and polarizing film
JP2017076116A (en) * 2015-10-14 2017-04-20 日東電工株式会社 Polarizer and method for producing the same

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