JPS62127702A - Preparation of color filter having superior characteristics and high precision - Google Patents
Preparation of color filter having superior characteristics and high precisionInfo
- Publication number
- JPS62127702A JPS62127702A JP60268879A JP26887985A JPS62127702A JP S62127702 A JPS62127702 A JP S62127702A JP 60268879 A JP60268879 A JP 60268879A JP 26887985 A JP26887985 A JP 26887985A JP S62127702 A JPS62127702 A JP S62127702A
- Authority
- JP
- Japan
- Prior art keywords
- film layer
- dye
- layer
- activated
- active 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
Links
- 229910052751 metal Inorganic materials 0.000 claims abstract description 32
- 239000002184 metal Substances 0.000 claims abstract description 32
- 238000010438 heat treatment Methods 0.000 claims abstract description 20
- 238000012546 transfer Methods 0.000 claims abstract description 17
- 238000004043 dyeing Methods 0.000 claims abstract description 11
- 239000000758 substrate Substances 0.000 claims abstract description 9
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000011148 porous material Substances 0.000 claims abstract description 4
- 230000000704 physical effect Effects 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000003086 colorant Substances 0.000 claims description 5
- 238000000859 sublimation Methods 0.000 claims 1
- 230000008022 sublimation Effects 0.000 claims 1
- 229920005989 resin Polymers 0.000 abstract description 3
- 239000011347 resin Substances 0.000 abstract description 3
- 230000004927 fusion Effects 0.000 abstract 1
- 239000000975 dye Substances 0.000 description 35
- 239000010408 film Substances 0.000 description 23
- 239000000976 ink Substances 0.000 description 18
- 238000000034 method Methods 0.000 description 14
- 239000011521 glass Substances 0.000 description 7
- 239000001856 Ethyl cellulose Substances 0.000 description 6
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 6
- 235000019325 ethyl cellulose Nutrition 0.000 description 6
- 229920001249 ethyl cellulose Polymers 0.000 description 6
- 238000009834 vaporization Methods 0.000 description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000008016 vaporization Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000009760 electrical discharge machining Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Optical Filters (AREA)
- 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、各種表示装置において用いられる高物性・高
精度カラーフィルターの製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for manufacturing a color filter with high physical properties and high precision used in various display devices.
従来、カラーフィルターの製造方法としては、ゼラチン
をフォトリソグラフィー法により染色する方法が公知で
ある。この方法は、製造工程が煩雑であること、カラー
フィルターの物性が劣ること等の理由から、需要者にお
いて十分に満足し得る方法とは言えなかった。Conventionally, as a method for manufacturing color filters, a method of dyeing gelatin using a photolithography method is known. This method cannot be said to be a method that fully satisfies consumers because the manufacturing process is complicated and the physical properties of the color filter are poor.
そこで、本発明者らは、鋭意研究の結果、先に所謂メタ
ルマスク法を発明した(特願昭59−97210号参照
)。即ち、この方法は、透明基板上に活性アルミナ又は
活性シリカの少なくとも一以上からなる活性膜層を形成
し、該活性膜層上に所定のパターン孔を有するメタルマ
スクを載置する工程、その上に昇華性染料又は/及び熱
溶融藤気化する染料を含むインキ層を有する転写シート
を載置する工程、加熱により前記インキ層中の染料を気
体状態で前記活性膜層に移行させて染着させる工程1次
いで前記転写シート及びメタルマスクを除去する工程か
らなる諸工程を必要な色数に応じて繰り返し行うことに
よって、前記メタルマスクのパターン孔に対応したパタ
ーンを前記活性膜層に順次形成し、最後に前記活性膜層
の微細孔の上部を封孔する為のオーバコート層を設けて
カラーフィルターを製造する方法である。この方法によ
れば、前記したフォトリソグラフィー法の欠点は解決す
ることができたが、次の様な新たな問題点が生じたので
ある。即ち、透明基板と転写シートとの間にメタルマス
クが介在する為、従来の転写捺染の様に密着状態での染
料の熱移行ではなく、染料は必ず蒸気化しメタルマスク
厚に相当する距離を飛翔する必要がある。従って、空気
抵抗等の作用により多大なエネルギー(熱と時間)を必
要とした。その為、メタルマスクの膨張による歪みも相
当量起こり、精度に大きな悪影響を及ぼした。また、使
用する染料は、蒸気化し易くなければならないから、染
料選択範囲が狭められ、染着性や熱安定性等に優れた染
料の使用が不可能となり、カラーフィルターの物性低下
の要因となっていた。そこで、これらの問題を解決する
為に、膜厚の1いメタルマスクの使用を試みた。しかし
、強度不足の為にメタルマスクの破損等が起こり、耐久
性に問題があった。As a result of intensive research, the present inventors have previously invented the so-called metal mask method (see Japanese Patent Application No. 59-97210). That is, this method includes the steps of forming an active film layer made of at least one of activated alumina or activated silica on a transparent substrate, placing a metal mask having a predetermined pattern of holes on the active film layer, and then A step of placing a transfer sheet having an ink layer containing a sublimable dye or/and a dye that vaporizes by heat melting, and by heating, the dye in the ink layer is transferred in a gaseous state to the active film layer and dyed. Step 1 Next, by repeating the steps of removing the transfer sheet and the metal mask according to the number of colors required, patterns corresponding to the pattern holes of the metal mask are sequentially formed in the active film layer, Finally, an overcoat layer is provided to seal the upper part of the fine pores of the active film layer, thereby producing a color filter. According to this method, the drawbacks of the photolithography method described above could be solved, but the following new problems arose. In other words, since a metal mask is interposed between the transparent substrate and the transfer sheet, the dye is not thermally transferred in a close contact state as in conventional transfer printing, but the dye is always vaporized and travels a distance equivalent to the thickness of the metal mask. There is a need to. Therefore, a large amount of energy (heat and time) was required due to effects such as air resistance. As a result, a considerable amount of distortion occurred due to expansion of the metal mask, which had a large negative impact on accuracy. In addition, the dye used must be easily vaporized, which narrows the range of dye selection, making it impossible to use dyes with excellent dyeability and thermal stability, and causing a decline in the physical properties of color filters. was. Therefore, in order to solve these problems, we attempted to use a metal mask with a thin film. However, due to lack of strength, the metal mask was damaged and there were problems with durability.
そこで、本発明者は、前記した従来法の欠点に鑑み鋭意
研究の結果、前記した所謂メタルマスク法を改良するこ
とによって、従来法の諸欠点を解決した本発明を完成す
るに至ったのである。Therefore, as a result of intensive research in view of the drawbacks of the conventional method described above, the present inventor has completed the present invention which solves the various drawbacks of the conventional method by improving the so-called metal mask method described above. .
即ち、本発明は、透明基板上に活性アルミナ又は活性シ
リカの少なくとも一以上からなる活性膜層を形成し、該
活性膜層上に所定のパターン孔を有するメタルマスクを
載置する工程、その上に昇華性染料又は/及び熱溶融蒸
気化する染料を含むインキ層を有する転写シートを載置
する工程、加熱により前記インキ層中の染料を気体状態
で前記活性膜層に移行させて染着させる工程1次いで前
記転写シート及びメタルマスクを除去する工程からなる
諸工程を必要な色数に応じて繰り返し行うことによって
、前記メタルマスクのパターン孔に対応したパターンを
前記活性膜層に順次形成し、最後に前記活性膜層の微細
孔の上部を封孔する為のオーバコート層を設けてカラー
フィルターを製造する方法において;前記加熱を減圧雰
囲気下にて行うことを特徴とする高物性・高精度カラー
フィルターの製造方法である。That is, the present invention includes a step of forming an active film layer made of at least one of activated alumina or activated silica on a transparent substrate, placing a metal mask having a predetermined pattern of holes on the active film layer, and then A step of placing a transfer sheet having an ink layer containing a sublimable dye or/and a dye that is heat-melted and vaporized on the substrate, and by heating, the dye in the ink layer is transferred in a gaseous state to the active film layer and dyed. Step 1 Next, by repeating the steps of removing the transfer sheet and the metal mask according to the number of colors required, patterns corresponding to the pattern holes of the metal mask are sequentially formed in the active film layer, A method for producing a color filter by finally providing an overcoat layer for sealing the upper part of the micropores of the active film layer; characterized in that the heating is performed in a reduced pressure atmosphere with high physical properties and high precision. This is a method for manufacturing a color filter.
以下、本発明の詳細な説明する。本発明において使用す
る透明基板としては、一般に液晶表示装置に用いられる
ものでよく、通常はガラス板を用いるとよい。The present invention will be explained in detail below. The transparent substrate used in the present invention may be one commonly used in liquid crystal display devices, and usually a glass plate is preferably used.
前記した透明基板上には、活性アルミナ又は活性シリカ
の少なくとも1以上からなる活性膜層が形成される。こ
の活性膜層を形成するには、先ず透明基板の表面にコロ
イド性アルミナ、コロイド性シリカ、又は両者の混合物
を塗布し、乾燥した後、350℃〜850℃で10分〜
180分間焼成すればよい。このようにして得た活性膜
層は、透明であり且つ多数の微細孔が形成されており、
これが染着層となる。なお、活性膜層は、その透明性、
表面硬度、染料受容性等を考慮すると0.5μm〜10
μm、好ましくは1.5μm〜5μmの層厚のものが望
ましい。これは、活性膜層の層厚が厚くなると白化して
不透明となり易く、また反対に層厚が薄くなると染料受
容性が減少し染着濃度が得られなくなるためである。An active film layer made of at least one of activated alumina and activated silica is formed on the transparent substrate. To form this active film layer, first coat colloidal alumina, colloidal silica, or a mixture of both on the surface of a transparent substrate, dry it, and then heat it at 350°C to 850°C for 10 minutes.
It is sufficient to bake for 180 minutes. The active membrane layer obtained in this way is transparent and has many micropores formed therein.
This becomes the dyed layer. In addition, the active film layer has its transparency,
Considering surface hardness, dye receptivity, etc., 0.5 μm to 10
A layer thickness of .mu.m, preferably 1.5 .mu.m to 5 .mu.m is desirable. This is because when the thickness of the active film layer increases, it tends to whiten and become opaque, and on the other hand, when the layer thickness decreases, the dye receptivity decreases and dyeing density cannot be obtained.
また、本発明に使用するメタルマスクの材質は、所定の
パターン孔の加工が可能な金属ならば何でも良い。その
膜厚は、0.005〜0.5鶴であり、好ましくは0.
007〜0.05mm程度である。前記した所定のパタ
ーンは、エレクトロホーミング、ケミカルエツチング、
放電加工、レーザー加工等により形成される。目的物が
ドントマトリソクスタイプの液晶表示装置向けのカラー
フィルターである場合には、十分に微細なドア)パター
ン孔精度を有するものでなければならない。Further, the material of the metal mask used in the present invention may be any metal as long as it is possible to form holes in a predetermined pattern. The film thickness is 0.005 to 0.5 mm, preferably 0.005 to 0.5 mm.
It is about 0.007 to 0.05 mm. The above-mentioned predetermined pattern is formed by electrohoming, chemical etching,
It is formed by electrical discharge machining, laser machining, etc. If the object is a color filter for a don't-matrix type liquid crystal display device, it must have a sufficiently fine door pattern hole accuracy.
次に本発明において使用する転写シートは、酎熱性を有
する高分子材料のフィルムや紙等からなるベースシート
と、染料とバインダー等によるインキ層とを最低限必要
な構成層として含むものである。この場合の染料として
は、昇華性染料又は/及び熱溶融蒸気化する染料であり
、具体的には、分散染料、金属を含まない油溶性染料、
カチオン染料等がある。尚、合成樹脂用着色剤層は油溶
性染料と同類であり、使用可能である。Next, the transfer sheet used in the present invention includes a base sheet made of a film or paper made of a polymeric material having heat-induced heat properties, and an ink layer made of a dye, a binder, etc. as the minimum necessary constituent layers. The dye in this case is a sublimable dye or/and a dye that is thermally melted and vaporized, and specifically, disperse dyes, metal-free oil-soluble dyes,
There are cationic dyes, etc. Note that the colorant layer for synthetic resins is similar to oil-soluble dyes and can be used.
前記した染料は、加熱によって気体状態で前記活性膜層
に移行して染着される。その加熱の条件としては、前記
染料を含有するインキを用いて、染料が微細孔中に熱移
行するような温度で行う。The above-described dye is transferred in a gaseous state to the active film layer by heating and is dyed therein. The heating conditions are such that an ink containing the dye is used and the temperature is such that the dye is thermally transferred into the micropores.
これは染料の種類によって異なるものであるが、例えば
100°C〜250℃において数秒〜600秒間加熱す
ればよい。Although this differs depending on the type of dye, it may be heated, for example, at 100° C. to 250° C. for several seconds to 600 seconds.
オーバコート層は、アクリル、メラミン、エポキシ、シ
リコン系高分子、ポリイミド等の硬質で透明性の良い樹
脂を前記活性膜層の微細孔上に塗布した後、樹脂が硬化
するような温度で加熱することにより形成する。この他
、珪酸ソーダ、リチウムシリケート等の無機材料の塗布
、加熱によって形成することもできる。このようにして
得られたオーバーコート層は、活性膜層の微細孔中に捕
捉された染料分子の再蒸気化を防ぎ、不必要な物質によ
る汚染を防ぎ、しかも表面の平滑性を向上させることに
役立つものである。For the overcoat layer, a hard and transparent resin such as acrylic, melamine, epoxy, silicone polymer, polyimide, etc. is applied onto the micropores of the active film layer, and then heated at a temperature that hardens the resin. formed by In addition, it can also be formed by coating and heating an inorganic material such as sodium silicate or lithium silicate. The overcoat layer thus obtained prevents re-vaporization of dye molecules trapped in the micropores of the active membrane layer, prevents contamination with unnecessary substances, and improves surface smoothness. It is useful for
本発明において特長とするところは、前記した加熱を減
圧雰囲気下にて行う点にある。その具体的条件は、使用
する染料の種類、メタルマスクの膜厚等によって異なる
。減圧すると染料の蒸気化開始温度は降下するが、そこ
に規則性を見出すことは難しいので、個々の染料により
特定の減圧条件の設定が必要となる。例えば、膜厚0.
05mのメタルマスクと蒸気化開始温度が250°Cの
染料を使用する場合、常圧下では180℃、1分間加熱
しても全く染色されないが、雰囲気を1 torrに減
圧すると、加熱温度・加熱時間が同じでも、十分な染色
濃度を持つ微細染色パターンが得られる。A feature of the present invention is that the above-described heating is performed under a reduced pressure atmosphere. The specific conditions vary depending on the type of dye used, the thickness of the metal mask, etc. When the pressure is reduced, the vaporization start temperature of the dye decreases, but it is difficult to find any regularity therein, so it is necessary to set specific reduced pressure conditions for each dye. For example, the film thickness is 0.
When using a 0.5m metal mask and a dye with a vaporization start temperature of 250°C, no dyeing will occur even if heated at 180°C for 1 minute under normal pressure, but if the atmosphere is reduced to 1 torr, the heating temperature and heating time will change. Even if the values are the same, a fine staining pattern with sufficient staining density can be obtained.
本発明に係る高物性・高精度カラーフィルターの製造方
法は、減圧雰囲気下にて加熱を行うので、次の通りの効
果を得ることができる。即ち、空気抵抗等の作用がない
ので、染料分子を十分に分散させることができる。従っ
て、少ないエネルギーで処理できるから、メタルマスク
の膨張による歪みが少なくて寸法再現性が高くなり、又
均−でムラのない染色パターンを有する高精度のカラー
フィルターを得ることができる。また、染料分子の蒸気
化温度が低下するので、染料選択範囲が拡大し、染着性
や熱安定性等に優れた染料の使用が可能となる(例えば
、融解温度が200℃以上で、気化が250°C以上で
ある物性の優れた高温蒸気化性の染料が、180℃以下
で使用できる。)。更に、常圧雰囲気下においては、活
性膜層に吸着されやすい不純物が蒸気化するので、活性
膜層の透明性が向上する。その為、高物性のカラーフィ
ルターを得ることができる。メタルマスク厚の影響が少
ないので、膜厚の厚いメタルマスクの使用が可能となり
、耐久性を持たせることができる。Since the method for manufacturing a color filter with high physical properties and high precision according to the present invention performs heating under a reduced pressure atmosphere, the following effects can be obtained. That is, since there is no effect such as air resistance, the dye molecules can be sufficiently dispersed. Therefore, since processing can be performed with less energy, distortion due to expansion of the metal mask is reduced, dimensional reproducibility is increased, and a highly accurate color filter having a uniform and uniform dyeing pattern can be obtained. In addition, since the vaporization temperature of dye molecules is lowered, the range of dye selection is expanded, and dyes with excellent dyeability and thermal stability can be used (for example, dyes with a melting temperature of 200°C or higher and vaporization High-temperature vaporizable dyes with excellent physical properties that have a temperature of 250°C or higher can be used at 180°C or lower.) Furthermore, in a normal pressure atmosphere, impurities that are easily adsorbed to the active film layer are vaporized, so that the transparency of the active film layer is improved. Therefore, a color filter with high physical properties can be obtained. Since the influence of the metal mask thickness is small, it is possible to use a thick metal mask, and it is possible to provide durability.
以下に、本発明の実施例について説明する。 Examples of the present invention will be described below.
実施例1
アルカリ洗浄した透明ガラス板の片面に、アルミナゾル
−2O0(日産化学社製)をスプレーコートし、70℃
で5分間乾燥した後、550℃で45分間焼成し、この
ようにすることによってガラス板上に約2μmのN厚を
有する活性膜層を得た。Example 1 Alumina sol-2O0 (manufactured by Nissan Chemical Co., Ltd.) was spray coated on one side of a transparent glass plate that had been washed with alkali, and heated at 70°C.
After drying for 5 minutes at 550° C., it was fired for 45 minutes, thereby obtaining an active film layer on the glass plate with an N thickness of about 2 μm.
一方、下記の配合成分からなるものを3本のロールミル
にて練肉混合し、3種類のスクリーンインキを得た。On the other hand, three types of screen inks were obtained by mixing the following ingredients using a three roll mill.
■赤色インキ
エチルセルロースN−7(バーキュレス社製)15部(
重量部)
エチルセルロースN−22(パーキュレス社′yA)5
部
ワタソリンレノドyp (r c r社り 8部ブチ
ルセルソルブ 22部ブチルセルソ
ルブアセテート 20部ツルペッツ150
30部■緑色インキ
エチルセルロースN−7(バーキュレス社製)15部(
重量部)
エチルセルロースN−22(バーキュレス社製)5部
オレヅールファストイエロー5G
(田岡化学社製)6部
ミケトンポリエステルグリーンG
(三井東圧社製)4部
ブチルセルソルブ 20部ブチルセ
ルソルブアセテート 20部ツルベック150
30部■青色インキ
エチルセルロースN−7(バーキュレス社製)15部(
重量部)
エチルセルロースN22(バーキュレス社製)5部
カヤロンポリエステルブルーTS
(日本化薬社製)10部
ブチルセルソルブ 20部ブチルセ
ルソルブアセテート 20部ツルベック150
30部上記スクリーンインキを
用い、それぞれシート上にスクリーン印刷を施し、赤、
緑、青の転写シートを得た。■Red ink ethyl cellulose N-7 (manufactured by Vercules) 15 parts (
Weight parts) Ethyl cellulose N-22 (Percules'yA) 5
Part Watasorin Renodo YP (manufactured by RCR) 8 parts Butyl Cellsolve 22 parts Butyl Cellsolve Acetate 20 parts Tsurupetz 150
30 parts Green ink Ethyl cellulose N-7 (manufactured by Vercules) 15 parts (
(parts by weight) Ethyl cellulose N-22 (manufactured by Vercules) 5 parts Orezur Fast Yellow 5G (manufactured by Taoka Chemical) 6 parts Miketone Polyester Green G (manufactured by Mitsui Toatsu) 4 parts Butyl cellosolve 20 parts Butyl cellosolve Acetate 20 parts Trubec 150
30 parts Blue ink Ethyl cellulose N-7 (manufactured by Vercules) 15 parts (
(parts by weight) Ethyl cellulose N22 (manufactured by Vercules) 5 parts Kayalon Polyester Blue TS (manufactured by Nippon Kayaku Co., Ltd.) 10 parts Butyl Cellusolve 20 parts Butyl Cellusolve Acetate 20 parts Trubec 150
30 copies Screen printed on each sheet using the above screen ink, red,
Green and blue transfer sheets were obtained.
また、一方、所定のトノI・パターン孔を有する厚さ0
.03鰭のステンレス製メタルマスクを3枚製造した。In addition, on the other hand, a thickness of 0 with a predetermined tonneau I/pattern hole
.. Three stainless steel metal masks with 03 fins were manufactured.
次に、前記方法にて製造したガラス板を180°Cに予
熱し、青色インキ用のメタルマスクをガラス板上の所定
の位置に載置し、その上に青色インキにて印刷された転
写シートをその印刷面がメタルマスクと接するように載
置し、l torr条件下で、JIS硬度50で180
°Cに加熱されたシリコンゴムで1分間加熱加圧した。Next, the glass plate manufactured by the above method was preheated to 180°C, a metal mask for blue ink was placed on a predetermined position on the glass plate, and a transfer sheet printed with blue ink was placed on top of the metal mask. was placed so that its printed surface was in contact with the metal mask, and the hardness was 180 with a JIS hardness of 50 under l torr conditions.
Heat and pressure was applied for 1 minute using silicone rubber heated to °C.
しかる後、転写シート及びメタルマスクを除去すると、
メタルマスクのドツトパターンに対応した青色のドツト
パターンが転写された。After that, when the transfer sheet and metal mask are removed,
A blue dot pattern corresponding to the dot pattern on the metal mask was transferred.
次に、前記工程にて得た青色のドツトパターンが形成さ
れたガラス板上において、該青色のドツトパターン部と
は異なる所定の位置に、緑色インキ用メタルマスクを載
置し、更に、その上に緑色インキにて印刷された転写シ
ートを!32置し、前記方法と同様にして50 tor
r条件下で、180℃、40秒間加熱加圧し、緑色のド
ツトパターンを転写した。Next, on the glass plate on which the blue dot pattern obtained in the above step was formed, a metal mask for green ink was placed at a predetermined position different from the blue dot pattern, and then A transfer sheet printed with green ink! 32 to 50 tor in the same manner as above.
A green dot pattern was transferred by heating and pressing at 180° C. for 40 seconds under r conditions.
次に、赤インキ用のメタルマスクと赤色インキにて印刷
された転写シートとを用い、前記工程と同様にして10
0 torr条件下で、180℃、30秒間加熱加圧す
ることにより赤色のドツトパターンを転写した。Next, using a metal mask for red ink and a transfer sheet printed with red ink, 10
A red dot pattern was transferred by heating and pressing at 180° C. for 30 seconds under 0 torr conditions.
この三原色のドツトパターンが転写されたガラス板上に
、下記の組成からなるオーバーコート剤メラミン樹脂
5部
アクリル樹脂 10部
水 85部
をコーティングして、180°Cで15分間乾熱処理を
行った。On the glass plate onto which the three primary color dot patterns have been transferred, an overcoat agent melamine resin consisting of the following composition is applied.
It was coated with 5 parts acrylic resin, 10 parts, and 85 parts water, and was subjected to dry heat treatment at 180°C for 15 minutes.
このようにすることによって、三原色のドツトパターン
が形成されたカラーフィルターを得た。By doing this, a color filter in which a dot pattern of three primary colors was formed was obtained.
比較例
比較の為、加熱を常圧下で行う他−は、前記した実施例
におけると同じ条件で処理した。その結果、各色とも全
く染色されなかった。そこで、加熱条件を厳しくして実
験をしたところ、青色は250’C,120秒、緑色は
250℃、90秒、赤色は250℃、60秒の条件下で
染色が可能であり、三原色のドツトパターンが形成され
たカラーフィルターを得た。Comparative Example For comparison, the treatment was carried out under the same conditions as in the above-mentioned Examples, except that the heating was carried out under normal pressure. As a result, each color was not dyed at all. Therefore, we conducted an experiment with stricter heating conditions, and found that blue dyeing was possible at 250°C for 120 seconds, green dyeing was 250°C for 90 seconds, and red dyeing was possible at 250°C for 60 seconds. A color filter on which a pattern was formed was obtained.
前記した実施例及び比較例で得られたカラーフィルター
の物性及び精度を第1表に示す。Table 1 shows the physical properties and precision of the color filters obtained in the Examples and Comparative Examples described above.
第1表
し
[−1
第1表から明らかなように、実施例で得られたカラーフ
ィルターは、透明性に優れたものである。Table 1: [-1] As is clear from Table 1, the color filters obtained in Examples have excellent transparency.
比較例の場合には、カラーフィルターが高熱条件下で得
られるものである為、転写染色の際にインキ層、転写シ
ートから発生するガス等の不純物が活性膜層に吸着され
、それによって透明性が阻害されたものと考えられる。In the case of the comparative example, since the color filter is obtained under high heat conditions, impurities such as gas generated from the ink layer and transfer sheet during transfer dyeing are adsorbed to the active film layer, which reduces transparency. This is thought to have been inhibited.
更に、実施例の場合の染色されたドツトパターン1ケの
色特性における有効部分は、比較例に対して415倍で
あり、また、有効面積60X60mカラーフィルターの
場合の4角の寸法歪み誤差は7/6倍であった。Furthermore, the effective area in the color characteristics of one dyed dot pattern in the case of the example is 415 times that of the comparative example, and the dimensional distortion error of the four corners in the case of the effective area 60 x 60 m color filter is 7 /6 times.
Claims (1)
くとも一以上からなる活性膜層を形成し、該活性膜層上
に所定のパターン孔を有するメタルマスクを載置する工
程、その上に昇華性染料又は/及び熱溶融蒸気化する染
料を含むインキ層を有する転写シートを載置する工程、
加熱により前記インキ層中の染料を気体状態で前記活性
膜層に移行させて染着させる工程、次いで前記転写シー
ト及びメタルマスクを除去する工程からなる諸工程を必
要な色数に応じて繰り返し行うことによって、前記メタ
ルマスクのパターン孔に対応したパターンを前記活性膜
層に順次形成し、最後に前記活性膜層の微細孔の上部を
封孔する為のオーバコート層を設けてカラーフィルター
を製造する方法において;前記加熱を減圧雰囲気下にて
行うことを特徴とする高物性・高精度カラーフィルター
の製造方法。(1) A step of forming an active film layer made of at least one of activated alumina or activated silica on a transparent substrate, placing a metal mask having a predetermined pattern of holes on the active film layer, and adding a sublimation layer on top of the active film layer. a step of placing a transfer sheet having an ink layer containing a dye or/and a dye that can be thermally melted and vaporized;
The steps of transferring the dye in the ink layer in a gaseous state to the active film layer by heating and dyeing it, and then removing the transfer sheet and metal mask are repeated according to the number of colors required. By this, a pattern corresponding to the pattern holes of the metal mask is sequentially formed on the active film layer, and finally an overcoat layer is provided to seal the upper part of the fine pores of the active film layer, thereby manufacturing a color filter. A method for producing a color filter with high physical properties and high precision, characterized in that the heating is performed under a reduced pressure atmosphere.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60268879A JPS62127702A (en) | 1985-11-28 | 1985-11-28 | Preparation of color filter having superior characteristics and high precision |
EP86906953A EP0246334B1 (en) | 1985-11-28 | 1986-11-28 | High-precision color filter having excellent properties and method of producing the same |
PCT/JP1986/000608 WO1987003381A1 (en) | 1985-11-28 | 1986-11-28 | High-precision color filter having excellent properties and method of producing the same |
DE8686906953T DE3687977T2 (en) | 1985-11-28 | 1986-11-28 | COLOR FILTER HIGHEST ACCURACY WITH EXCELLENT PROPERTIES AND THEIR PRODUCTION. |
US07/086,128 US4776671A (en) | 1985-11-28 | 1986-11-28 | High property, high precision color filter and method for manufacturing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60268879A JPS62127702A (en) | 1985-11-28 | 1985-11-28 | Preparation of color filter having superior characteristics and high precision |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62127702A true JPS62127702A (en) | 1987-06-10 |
Family
ID=17464525
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60268879A Pending JPS62127702A (en) | 1985-11-28 | 1985-11-28 | Preparation of color filter having superior characteristics and high precision |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62127702A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03120516A (en) * | 1989-10-04 | 1991-05-22 | Stanley Electric Co Ltd | Manufacture of color filter |
JP2007175788A (en) * | 2005-12-27 | 2007-07-12 | Tungaloy Corp | Throwaway tip |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5521031A (en) * | 1978-07-31 | 1980-02-14 | Dainippon Printing Co Ltd | Production of color separating filter |
JPS55166607A (en) * | 1979-06-15 | 1980-12-25 | Canon Inc | Color filter |
JPS5651321A (en) * | 1979-09-15 | 1981-05-08 | Yorkshire Imperial Plastics | Manufacturing device for thermoplastic pipe |
JPS59114508A (en) * | 1982-12-22 | 1984-07-02 | Seiko Instr & Electronics Ltd | Manufacture of multicolored surface coloring body |
JPS6180124A (en) * | 1984-09-27 | 1986-04-23 | Dainippon Printing Co Ltd | Formation of colored image |
JPS61252501A (en) * | 1985-05-02 | 1986-11-10 | Ricoh Co Ltd | Manufacture of multicolor color filter |
JPS61268761A (en) * | 1985-05-24 | 1986-11-28 | Mitsui Toatsu Chem Inc | Naphthoquinone-based green dyestuff and its preparation |
-
1985
- 1985-11-28 JP JP60268879A patent/JPS62127702A/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5521031A (en) * | 1978-07-31 | 1980-02-14 | Dainippon Printing Co Ltd | Production of color separating filter |
JPS55166607A (en) * | 1979-06-15 | 1980-12-25 | Canon Inc | Color filter |
JPS5651321A (en) * | 1979-09-15 | 1981-05-08 | Yorkshire Imperial Plastics | Manufacturing device for thermoplastic pipe |
JPS59114508A (en) * | 1982-12-22 | 1984-07-02 | Seiko Instr & Electronics Ltd | Manufacture of multicolored surface coloring body |
JPS6180124A (en) * | 1984-09-27 | 1986-04-23 | Dainippon Printing Co Ltd | Formation of colored image |
JPS61252501A (en) * | 1985-05-02 | 1986-11-10 | Ricoh Co Ltd | Manufacture of multicolor color filter |
JPS61268761A (en) * | 1985-05-24 | 1986-11-28 | Mitsui Toatsu Chem Inc | Naphthoquinone-based green dyestuff and its preparation |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03120516A (en) * | 1989-10-04 | 1991-05-22 | Stanley Electric Co Ltd | Manufacture of color filter |
JP2007175788A (en) * | 2005-12-27 | 2007-07-12 | Tungaloy Corp | Throwaway tip |
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