JP2543051B2 - Color filter manufacturing method - Google Patents

Color filter manufacturing method

Info

Publication number
JP2543051B2
JP2543051B2 JP27023186A JP27023186A JP2543051B2 JP 2543051 B2 JP2543051 B2 JP 2543051B2 JP 27023186 A JP27023186 A JP 27023186A JP 27023186 A JP27023186 A JP 27023186A JP 2543051 B2 JP2543051 B2 JP 2543051B2
Authority
JP
Japan
Prior art keywords
dye
pigment
color filter
green
resin
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 - Fee Related
Application number
JP27023186A
Other languages
Japanese (ja)
Other versions
JPS63123004A (en
Inventor
眞守 曽我
成広 佐藤
公明 芳野
時彦 清水
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 JP27023186A priority Critical patent/JP2543051B2/en
Publication of JPS63123004A publication Critical patent/JPS63123004A/en
Application granted granted Critical
Publication of JP2543051B2 publication Critical patent/JP2543051B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【発明の詳細な説明】 産業上の利用分野 本発明は顔料系色素を用いたカラーフィルタの製造方
法に関し、特に緑色素層の改良に関する。
TECHNICAL FIELD The present invention relates to a method for producing a color filter using a pigment-based dye, and more particularly to improvement of a green dye layer.

従来の技術 カラーフィルタは液晶カラーディスプレイ、液晶カラ
ーテレビ等に用いられている。カラーフィルタ用の色材
としては、耐光性が良く、分光特性がCRTと同等のもの
がよい。
2. Description of the Related Art Color filters are used in liquid crystal color displays, liquid crystal color televisions and the like. As the color material for the color filter, one having good light resistance and spectral characteristics equivalent to that of CRT is preferable.

一般的に、染料より顔料の方が耐光性が良いので、良
く使われている。緑色素層にはフタロシアニン系色素が
用いられている。しかしながら、フタロシアニン系色素
単独では、透過極大値が500nm付近にあるため、カラー
フィルタ用の緑色素層としては使えない。
In general, pigments are more commonly used because they have better light resistance than dyes. A phthalocyanine dye is used for the green dye layer. However, the phthalocyanine-based dye alone cannot be used as a green dye layer for a color filter because the maximum transmission value is around 500 nm.

このため、フタロシアニン系色素とイソインドリノン
系黄色色素を併用することが提案されている。(特開昭
60−42706号公報) 発明が解決しようとする問題点 しかしながら、フタロシアニン系色素とイソインドリ
ノン系黄色色素の組合せで得られる緑色素層の分光特性
はCRTに比べて劣り、CIE色度図上での色再現性も悪い。
これは、イソインドリノン系黄色色素がフタロシアニン
系色素の青色成分を十分にカットできていないためと考
えられる。
Therefore, it has been proposed to use a phthalocyanine dye and an isoindolinone yellow dye together. (JP Sho
(Problems to be solved by the invention) However, the spectral characteristics of the green pigment layer obtained by the combination of the phthalocyanine pigment and the isoindolinone yellow pigment are inferior to those of the CRT, and the CIE chromaticity diagram is shown. The color reproducibility of is also poor.
It is considered that this is because the isoindolinone yellow dye cannot sufficiently cut the blue component of the phthalocyanine dye.

問題点を解決するための手段 緑色素層の色再現性の優れたカラーフィルタを得るた
めに、透明基板上に、重量比で、ハロゲン化フタロシア
ニン系色素100に対してジスアゾイエロー系色素を5〜5
0の割合で含有する光硬化性樹脂もしくは光硬化性樹脂
と熱硬化性樹脂との混合物を印刷して形成し、500nm以
下の波長および600nm以上の波長の透過率を10%以下の
光学特性を持つ緑色素層を有するカラーフィルタの製造
方法を提供する。
Means for Solving the Problems In order to obtain a color filter having excellent color reproducibility of the green dye layer, the disazo yellow dye is added to the halogenated phthalocyanine dye 100 in a weight ratio of 5 to 5 on the transparent substrate. Five
It is formed by printing a photo-curable resin or a mixture of a photo-curable resin and a thermosetting resin that is contained in a ratio of 0, and has a transmittance of 10% or less with a transmittance of 500 nm or less and 600 nm or more. Provided is a method for manufacturing a color filter having a green dye layer.

作用 ジスアゾイエロ系色素がハロゲン化フタロシアニン系
色素の青色成分を十分にカットし、またハロゲン化フタ
ロシアニン系色素の透過極大値が550nm付近に有るの
で、分光特性がCRTと同等のものが得られると推定され
る。
Action The disazo yellow dye sufficiently cuts the blue component of the halogenated phthalocyanine dye, and the transmission maximum of the halogenated phthalocyanine dye is around 550 nm, so it is presumed that spectral characteristics equivalent to CRT can be obtained. It

実施例 本発明のカラーフィルタの製造方法は、透明基板上
に、重量比でハロゲン化フタロシアニン系色素100に対
してジスアゾイエロ系色素を5〜50の割合で含有する光
硬化性樹脂もしくは光硬化性樹脂と熱硬化性樹脂との混
合物を緑層として印刷することである。
Example A method for producing a color filter of the present invention is a photocurable resin or a photocurable resin containing a disazo yellow dye in a ratio of 5 to 50 with respect to 100 halogenated phthalocyanine dye in a weight ratio on a transparent substrate. And printing a mixture of a thermosetting resin as a green layer.

本発明に用いるハロゲン化フタロシアニン系色素とし
ては、C.I.Pigment Green36(C.I.74265)が代表的なも
のとして挙げられる。
Representative examples of the halogenated phthalocyanine dye used in the present invention include CI Pigment Green 36 (CI74265).

また、本発明で用いるジスアゾイエロ系色素の例とし
ては、Pigment Yellow81(PY81)、PY81、PY87、PY93、
PY94などがあげられる。
Examples of the disazo yellow dye used in the present invention include Pigment Yellow 81 (PY81), PY81, PY87, PY93,
Examples include PY94.

ジスアゾイエロ系色素の料は、重量比でハロゲン化フ
タロシアニン系色素100に対して5〜50の割合が望まし
い。ジスアゾイエロ系色素の量が上記の範囲より多くな
ると、650nm〜700nm透過率が10%以上になる。また、反
対に上記の範囲より少ないとハロゲン化フタロシアニン
系色素の青色成分を十分にカットできなくなり色再現性
が悪くなる。
The amount of the disazo yellow dye is preferably 5 to 50 based on 100 parts by weight of the halogenated phthalocyanine dye. When the amount of the disazo yellow dye exceeds the above range, the transmittance of 650 nm to 700 nm becomes 10% or more. On the other hand, if the amount is less than the above range, the blue component of the halogenated phthalocyanine dye cannot be sufficiently cut, resulting in poor color reproducibility.

本発明に用いられる光硬化性樹脂の例としては、オリ
ゴエステルアクリレート、ウレタンアクリレート、エポ
キシアクリレート等が上げられる。熱硬化性樹脂の例と
してはロジン変性フェノール樹脂、クマロン・インデン
樹脂、石油樹脂、アルキド樹脂、エポキシ樹脂、環化ゴ
ム等が上げられる。
Examples of the photocurable resin used in the present invention include oligoester acrylate, urethane acrylate and epoxy acrylate. Examples of the thermosetting resin include rosin-modified phenol resin, coumarone-indene resin, petroleum resin, alkyd resin, epoxy resin and cyclized rubber.

熱硬化性樹脂の光硬化性樹脂に対する混合割合は0〜
30wt%が良い。熱硬化性樹脂の量がこの範囲を越える
と、光重合反応を阻害するようになる。
The mixing ratio of the thermosetting resin to the photocurable resin is 0 to
30wt% is good. When the amount of the thermosetting resin exceeds this range, the photopolymerization reaction is hindered.

緑色素層を印刷により形成する当たってはオフセット
印刷法、スクリーン印刷法、転写印刷法、活版印刷法等
の印刷法を用いることができる。
In forming the green pigment layer by printing, a printing method such as an offset printing method, a screen printing method, a transfer printing method or a letterpress printing method can be used.

実施例1 ハロゲン化フタロシアニン(Pigment Green36)54g、
ジスアゾイエロ系色素(Pigment Yellow83)6g、光硬化
剤(ダロキュア1173、メルク製)9gをオリゴエステルア
クリレート(アロニックスM−8060、東亜合成化学製)
300gに加え、よくかくはんした後、3本ロールに5回か
けて顔料を分散させた。得られた分散物をオフセット印
刷機でガラス板上に50×50mmのパターンを厚さ1μm印
刷し、次に紫外線(200mJ/cm2)を照射して膜を硬化さ
せた。
Example 1 54 g of halogenated phthalocyanine (Pigment Green36),
6 g of disazo yellow dye (Pigment Yellow83), 9 g of photo-curing agent (Darocur 1173, made by Merck) and oligoester acrylate (Aronix M-8060, made by Toagosei Kagaku)
After adding 300 g and stirring well, the pigment was dispersed 5 times on 3 rolls. The obtained dispersion was printed on a glass plate with a pattern of 50 × 50 mm to a thickness of 1 μm by an offset printing machine, and then irradiated with ultraviolet rays (200 mJ / cm 2) to cure the film.

実施例2 ハロゲン化フタロシアニン(Pigment Green36)42g、
ジスアゾイエロ系色素(Pigment Yellow83)18g、光硬
化剤(ダロキュア1173、メルク製)9gをオリゴエステル
アクリレート(アロニックスM−8060、東亜合成化学
製)300gに加え、よく攪拌した後、3本ロールに5回か
けて顔料を分散させた。得られた分散物をオフセット印
刷機でガラス板上に50×50mmのパターンを厚さ1μm印
刷し、次に紫外線(200mJ/cm2)を照射して膜を硬化さ
せた。
Example 2 42 g of halogenated phthalocyanine (Pigment Green36),
18 g of disazo yellow dye (Pigment Yellow83) and 9 g of photo-curing agent (Darocur 1173, manufactured by Merck) were added to 300 g of oligoester acrylate (Aronix M-8060, manufactured by Toagosei Kagaku Co., Ltd.), and the mixture was stirred well and then 5 times in 3 rolls. To disperse the pigment. The obtained dispersion was printed on a glass plate with a pattern of 50 × 50 mm to a thickness of 1 μm by an offset printing machine, and then irradiated with ultraviolet rays (200 mJ / cm 2) to cure the film.

実施例3 ハロゲン化フタロシアニン(Pigment Green36)57g、
ジスアゾイエロ系色素(Pigment Yellow83)3g、光硬化
剤(ダロキュア1173、メルク製)8gをオリゴエステルア
クリレート(アロニックスM−8060、東亜合成化学製)
270gとロジン変性p−第三ブチルフェノール樹脂30gと
の混合物に加え、よく攪拌した後、3本ロールに5回か
けて顔料を分散させた。得られた分散物をオフセット印
刷機でガラス板上に50×50mmのパターンを厚さ1μm印
刷し、次に紫外線(200mJ/cm2)を照射して膜を硬化さ
せ、さらに100℃で30分加熱した。
Example 3 57 g of halogenated phthalocyanine (Pigment Green36),
3 g of disazo yellow dye (Pigment Yellow83), 8 g of photo-curing agent (Darocur 1173, made by Merck) and oligoester acrylate (Aronix M-8060, made by Toagosei)
The mixture was added to a mixture of 270 g and 30 g of rosin-modified p-tert-butylphenol resin, stirred well, and then the pigment was dispersed over three rolls five times. The obtained dispersion is printed on a glass plate with a 50 × 50 mm pattern with a thickness of 1 μm by an offset printing machine, and then irradiated with ultraviolet rays (200 mJ / cm2) to cure the film, and further heated at 100 ° C. for 30 minutes. did.

比較例1 実施例1において、色素をハロゲン化フタロシアニン
60gにし、ジスアゾイエロ系色素を含まない顔料分散物
で試料を作った。
Comparative Example 1 In Example 1, the dye was halogenated phthalocyanine.
A sample was prepared with a pigment dispersion containing 60 g and containing no disazo yellow dye.

比較例2 実施例1において、色素を銅フタロシアニン色素(Pi
gment Blue15)54gとイソインドリノン系黄色色素(C.
I.Pigment yellow110)6gにかえて試料を作った。
Comparative Example 2 In Example 1, the dye was a copper phthalocyanine dye (Pi
gment Blue15) 54g and isoindolinone yellow pigment (C.
I. Pigment yellow110) 6g was used as a sample.

実施例1〜3、比較例1〜2の試料を24×40mmの大き
さに切取り、分光光度計(UV−260、島津製)で400〜70
0nmの範囲の透過スペクトルを測定し、スペクトルからC
IE色度座標を計算した。
Samples of Examples 1 to 3 and Comparative Examples 1 and 2 were cut into a size of 24 × 40 mm, and 400 to 70 with a spectrophotometer (UV-260, made by Shimadzu).
Measure the transmission spectrum in the 0 nm range, and
The IE chromaticity coordinates were calculated.

第1図はそれぞれのCIE色度座標をプロットしたもの
である。図の中で実線はCRTの色再現範囲を示す。光源
は3波長域発光形蛍光ランプ(パルック、松下電器製)
を用いた。
FIG. 1 is a plot of each CIE chromaticity coordinate. In the figure, the solid line indicates the color reproduction range of the CRT. The light source is a three-wavelength emission type fluorescent lamp (Palook, manufactured by Matsushita Electric)
Was used.

第1図からわかるように、比較例の座標はCIE色度図
上で、CRTの緑色からなり離れているが、本発明の実施
例の座標はCRTの緑色近傍にあり、発明のカラーフィル
タが色再現性が良いのがわかる。
As can be seen from FIG. 1, the coordinates of the comparative example are separated from the green of the CRT on the CIE chromaticity diagram, but the coordinates of the embodiment of the present invention are near the green of the CRT, and the color filter of the invention is You can see that the color reproducibility is good.

第2図は実施例1及び比較例1の400〜700nmにおける
透過スペクトルである。ハロゲン化フタロシアニン単独
の場合(比較例1)、吸収極大は548nmにあるが、青色
成分を含んでいる。本発明のジスアゾイエロ系色素をハ
ロゲン化フタロシアニンに対して11wt%混ぜることによ
り(実施例1)、吸収極大は552nmとほとんど変化せず
に、500nm以下の青色成分をカットできるのがわかる。
FIG. 2 shows transmission spectra of Example 1 and Comparative Example 1 at 400 to 700 nm. When the halogenated phthalocyanine is used alone (Comparative Example 1), the absorption maximum is at 548 nm, but it contains a blue component. It can be seen that by mixing the disazo yellow dye of the present invention in an amount of 11 wt% with respect to the halogenated phthalocyanine (Example 1), the absorption maximum hardly changed to 552 nm and the blue component of 500 nm or less could be cut.

発明の効果 透明基板上に、重量比でハロゲン化フタロシアニン系
色素100に対してジスアゾイエロ系色素を5〜50の割合
で含有する透明樹脂を印刷して緑色素層を形成すること
により、緑色素層の色再現性の優れたカラーフィルタの
製造方法を提供できる。
Effect of the Invention A green dye layer is formed by printing a transparent resin containing a disazo yellow dye in a ratio of 5 to 50 with respect to 100 parts by weight of a halogenated phthalocyanine dye on a transparent substrate to form a green dye layer. It is possible to provide a method for producing a color filter having excellent color reproducibility.

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

第1図は本発明の実施例及び従来例のカラーフィルタの
CIE色度図、第2図は同カラーフィルタの透過スペクト
ル図である。
FIG. 1 shows color filters of an embodiment of the present invention and a conventional example.
The CIE chromaticity diagram and FIG. 2 are transmission spectrum diagrams of the color filter.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 芳野 公明 門真市大字門真1006番地 松下電器産業 株式会社内 (72)発明者 清水 時彦 門真市大字門真1006番地 松下電器産業 株式会社内 (56)参考文献 特開 昭56−54444(JP,A) 特開 昭60−237403(JP,A) 特開 昭60−237441(JP,A) ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Kimiaki Yoshino 1006 Kadoma, Kadoma-shi, Matsushita Electric Industrial Co., Ltd. (72) Inventor Tokihiko Shimizu 1006 Kadoma, Kadoma-shi, Matsushita Electric Industrial (56) References JP-A-56-54444 (JP, A) JP-A-60-237403 (JP, A) JP-A-60-237441 (JP, A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】透明基板上に、重量比で、ハロゲン化フタ
ロシアニン系色素100に対してジスアゾイエロー系色素
を5〜50の割合で含有する光硬化性樹脂もしくは光硬化
性樹脂と熱硬化性樹脂との混合物を印刷して形成し、50
0nm以下の波長および600nm以上の波長の透過率を10%以
下の光学特性を持つ緑色素層を有するカラーフィルタの
製造方法。
1. A photo-curable resin or a photo-curable resin and a thermosetting resin containing, on a transparent substrate, a disazo yellow dye in a proportion of 5 to 50 with respect to 100 halogenated phthalocyanine dyes on a transparent substrate. Print and form a mixture with 50
A method for producing a color filter having a green dye layer having an optical characteristic of a transmittance of 10% or less at a wavelength of 0 nm or less and a wavelength of 600 nm or more.
JP27023186A 1986-11-13 1986-11-13 Color filter manufacturing method Expired - Fee Related JP2543051B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27023186A JP2543051B2 (en) 1986-11-13 1986-11-13 Color filter manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27023186A JP2543051B2 (en) 1986-11-13 1986-11-13 Color filter manufacturing method

Publications (2)

Publication Number Publication Date
JPS63123004A JPS63123004A (en) 1988-05-26
JP2543051B2 true JP2543051B2 (en) 1996-10-16

Family

ID=17483378

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27023186A Expired - Fee Related JP2543051B2 (en) 1986-11-13 1986-11-13 Color filter manufacturing method

Country Status (1)

Country Link
JP (1) JP2543051B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07306312A (en) * 1994-05-16 1995-11-21 Toyo Ink Mfg Co Ltd Colored composition for color filter and color filter
WO2004010172A1 (en) 2002-07-24 2004-01-29 Dai Nippon Printing Co., Ltd. Green pigment for color filter, green pigment dispersion, photosensitive color comosition, color filter, and liquid crystal panel
KR20210040075A (en) * 2018-08-07 2021-04-12 미쯔비시 케미컬 주식회사 Optical film, film laminate, display unit

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5654444A (en) * 1979-10-11 1981-05-14 Toyo Ink Mfg Co Ltd Colored particle for color image forming

Also Published As

Publication number Publication date
JPS63123004A (en) 1988-05-26

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