JPWO2010087122A1 - Optical filter film and optical filter for plasma display panel using the same - Google Patents
Optical filter film and optical filter for plasma display panel using the same Download PDFInfo
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- JPWO2010087122A1 JPWO2010087122A1 JP2010548395A JP2010548395A JPWO2010087122A1 JP WO2010087122 A1 JPWO2010087122 A1 JP WO2010087122A1 JP 2010548395 A JP2010548395 A JP 2010548395A JP 2010548395 A JP2010548395 A JP 2010548395A JP WO2010087122 A1 JPWO2010087122 A1 JP WO2010087122A1
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- film
- optical filter
- sensitive adhesive
- meth
- pressure
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Classifications
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Abstract
【課題】架橋型アクリル系樹脂と架橋剤、ネオン光吸収色素を含有した粘着剤により耐光性に優れた光学フィルター用フィルム及びこれを用いたプラズマディスプレイパネル用光学フィルターを開発すること。【解決手段】アルキル基の炭素数が4〜12の(メタ)アクリル酸アルキルエステルを70.1〜99.8重量%、前記(メタ)アクリル酸アルキルエステルと共重合可能な水酸基含有モノマーを0.1〜10重量%および前記(メタ)アクリル酸アルキルエステルと水酸基含有モノマーとに共重合可能な他のモノマーを0.1〜19.9重量%の量で共重合させた架橋型アクリル系樹脂と架橋剤からなる粘着剤を使用することにより、ネオン光吸収色素は粘着剤層において優れた安定性を示し、該粘着剤層を透明基材の片面に設けることにより、優れた耐光性を有する光学フィルター用フィルムおよびこれを用いたプラズマディスプレイパネル用光学フィルターが開発できた。【選択図】なしTo develop an optical filter film having excellent light resistance by an adhesive containing a cross-linkable acrylic resin, a cross-linking agent and a neon light absorbing dye, and an optical filter for a plasma display panel using the same. SOLUTION: 70.1 to 99.8% by weight of a (meth) acrylic acid alkyl ester having 4 to 12 carbon atoms in the alkyl group, and 0% of a hydroxyl group-containing monomer copolymerizable with the (meth) acrylic acid alkyl ester. .1-10% by weight and a cross-linked acrylic resin obtained by copolymerizing 0.1 to 19.9% by weight of another monomer copolymerizable with the (meth) acrylic acid alkyl ester and the hydroxyl group-containing monomer. Neon light-absorbing dye exhibits excellent stability in the pressure-sensitive adhesive layer, and has excellent light resistance by providing the pressure-sensitive adhesive layer on one side of the transparent substrate. An optical filter film and an optical filter for a plasma display panel using the same were developed. [Selection figure] None
Description
本発明は粘着剤層にネオン光吸収色素を含有させた耐久性に優れる光学フィルター用フィルム及びそれを用いたプラズマディスプレイパネル(以下、PDPと記す)用光学フィルターに関する。 The present invention relates to an optical filter film having excellent durability, in which a neon light absorbing dye is contained in an adhesive layer, and an optical filter for a plasma display panel (hereinafter referred to as PDP) using the same.
PDPの原理は2枚の板状ガラスで挟まれたセルに封入した希ガス(ネオン、キセノン等)に電圧をかけ、プラズマ状態になった希ガスが発する紫外線がセル壁面に処理された発光体に当たることで映像に必要な可視光線を発生させるものであるが、可視光線と同時に、近赤外線、人体に有害な電磁波、及びネオンガスに起因し、赤色光の色純度を下げる波長595nm近辺の橙色光線(以下、ネオン光と記す)等の有害な電磁波も一緒に放出されるため、有益な可視光線は透過するが、ネオン光をはじめとした近赤外線や人体に有害な電磁波を遮蔽する必要があり、そのための光学フィルターが必要とされる。(特許文献1参照) The principle of PDP is that a light is applied to the cell wall by applying a voltage to a rare gas (neon, xenon, etc.) enclosed in a cell sandwiched between two sheet-like glasses, and emitting ultraviolet light emitted from the rare gas in a plasma state. The visible light necessary for the image is generated by hitting the light, but at the same time as the visible light, the orange light near the wavelength of 595 nm which reduces the color purity of the red light due to near infrared rays, electromagnetic waves harmful to the human body, and neon gas. Since harmful electromagnetic waves such as neon light (hereinafter referred to as neon light) are also emitted, it transmits useful visible light, but it is necessary to shield near infrared rays including neon light and electromagnetic waves harmful to the human body. Therefore, an optical filter for that purpose is required. (See Patent Document 1)
光学フィルターに用いられる部材としては金属材料による多層スパッタ膜を用いることで、近赤外線と人体に有害な電磁波を同時にカットすることが出来る。(特許文献2、3参照)
しかしながら、ネオン光に関しては別途遮蔽層を設ける必要があり、従来はネオン光を吸収する特定の色素をバインダー樹脂に添加して透明基材に塗布したネオン光吸収フィルムと、近赤外線及び電磁波遮蔽機能を有する基材、防眩および反射防止フィルム等を粘着剤によって貼り合わせた光学フィルターを使用している。上記色素としては、少量の添加で十分な吸収特性があるシアニン色素が主に使用されていた。By using a multilayer sputtered film made of a metal material as a member used for the optical filter, it is possible to simultaneously cut near infrared rays and electromagnetic waves harmful to the human body. (See Patent Documents 2 and 3)
However, it is necessary to provide a separate shielding layer for neon light. Conventionally, a neon light absorbing film in which a specific dye that absorbs neon light is added to a binder resin and applied to a transparent substrate, and a near infrared ray and electromagnetic wave shielding function An optical filter in which a base material having antiglare, an antiglare and antireflection film and the like are bonded together with an adhesive is used. As the dye, a cyanine dye having sufficient absorption characteristics with a small amount of addition was mainly used.
ネオン光吸収色素を粘着剤層に含有できれば、光学フィルターを構成する任意の層間にネオン光吸収能を付与することができるため、光学フィルター製造の効率が著しく向上することが期待できる。しかしながら、シアニン系色素に代表されるネオン光吸収色素を粘着剤に添加すると、ポリエステル樹脂やアクリル樹脂等の高分子体からなる塗布用バインダー樹脂への添加とは異なり、耐久試験後の色素の劣化が大きくネオン光吸収機能が失われてしまうという粘着剤特有の問題があり、これまで、粘着剤中において不安定なネオン光吸収色素を安定化するには種々の添加剤を用いた検討が行われている。(特許文献4参照) If a neon light-absorbing dye can be contained in the pressure-sensitive adhesive layer, neon light absorption ability can be imparted between any layers constituting the optical filter, so that the efficiency of optical filter production can be expected to be significantly improved. However, when neon light-absorbing dyes typified by cyanine dyes are added to the pressure-sensitive adhesive, the dyes deteriorate after the durability test, unlike additions to binder resins for coatings made of polymers such as polyester resins and acrylic resins. There is a problem peculiar to pressure-sensitive adhesives that the neon light absorption function is largely lost, and so far, various additives have been used to stabilize unstable neon light-absorbing dyes in pressure-sensitive adhesives. It has been broken. (See Patent Document 4)
近年、ネオン光吸収色素としてシアニン色素に替わりテトラアザポルフィリン色素が多く用いられるようになった。(特許文献5参照)
テトラアザポルフィリン色素は添加剤がなくとも粘着剤中において安定で、シアニン色素に比べ耐久性が良い。In recent years, tetraazaporphyrin dyes are often used as neon light absorbing dyes instead of cyanine dyes. (See Patent Document 5)
Tetraazaporphyrin dyes are stable in the pressure-sensitive adhesive without any additives and have better durability than cyanine dyes.
粘着剤としては、汎用性の高い架橋型アクリル系樹脂と架橋剤からなる粘着剤が考えられる。しかしながら、該樹脂のモノマー組成によっては、十分な耐久性、とりわけ十分な耐光性が得られない場合があった。 As the pressure-sensitive adhesive, a pressure-sensitive adhesive composed of a highly versatile crosslinked acrylic resin and a crosslinking agent is considered. However, depending on the monomer composition of the resin, sufficient durability, particularly sufficient light resistance, may not be obtained.
架橋型アクリル系樹脂と架橋剤からなる粘着剤であって、ネオン光吸収色素を含有した該粘着剤からなる粘着剤層が透明基材の一面に設けられている耐光性に優れた光学フィルター用フィルム及びこれを用いたプラズマディスプレイパネル用光学フィルターを開発することが本発明の課題となっている。 A pressure-sensitive adhesive comprising a cross-linkable acrylic resin and a cross-linking agent, wherein the pressure-sensitive adhesive layer comprising the pressure-sensitive adhesive containing a neon light-absorbing dye is provided on one side of a transparent substrate, for an optical filter having excellent light resistance It is an object of the present invention to develop a film and an optical filter for a plasma display panel using the film.
本発明者等は前記課題を解決すべく鋭意研究した結果、特定のモノマー組成からなる架橋型アクリル系樹脂と架橋剤からなる粘着剤を用いることにより、ネオン光吸収色素を含有した該粘着剤からなる粘着剤層が透明基材の一面に設けられている光学フィルム及びこれを用いたプラズマディスプレイパネル用光学フィルターが、耐光試験において優れた安定性を保持できることを見出し本発明を完成させるに至った。 As a result of diligent research to solve the above problems, the present inventors have used a pressure-sensitive adhesive containing a neon light-absorbing dye by using a cross-linkable acrylic resin having a specific monomer composition and a cross-linking agent. It was found that an optical film provided with a pressure-sensitive adhesive layer on one surface of a transparent substrate and an optical filter for a plasma display panel using the same can maintain excellent stability in a light resistance test, and the present invention has been completed. .
すなわち、本発明は
(1)(a)アルキル基の炭素数が4〜12の(メタ)アクリル酸アルキルエステルを70.1〜99.8重量%、(b)前記(a)成分と共重合可能な水酸基含有モノマーを0.1〜10重量%および/又は(c)前記(a)成分と(b)成分とに共重合可能な他のモノマーを0.1〜19.9重量%の量の割合((a)+(b)+(C)が100重量%)で共重合させた架橋型アクリル系樹脂と架橋剤からなる粘着剤であって、該粘着剤からなる粘着剤層を透明基材の片面に設けてなり、該粘着剤層がネオン光吸収色素を含有することを特徴とする光学フィルター用フィルム、
(2)架橋剤がブロック型イソシアネートであることを特徴とする前記(1)に記載の光学フィルター用フィルム、
(3)ネオン光吸収色素がテトラアザポルフィリン色素である前記(1)または(2)に記載の光学フィルター用フィルム、
(4)粘着剤がテルペンフェノール樹脂からなる粘着付与剤を含有することを特徴とする前記(1)乃至(3)のいずれか一項に記載の光学フィルター用フィルム、
(5)粘着剤層を設けた透明基材の粘着剤層を有する面の反対面に、ハードコート層、導電層、防眩層および反射防止層から選ばれた少なくとも一層が積層されていることを特徴とする前記(1)乃至(4)のいずれか一項に記載の光学フィルター用フィルム、
(6)(1)乃至(5)のいずれか一項に記載の光学フィルター用フィルムを近赤外線および/又は電磁波遮蔽機能を有するフィルムもしくは硝子に積層したことを特徴とするプラズマディスプレイパネル用光学フィルター、
に関する。That is, the present invention relates to (1) (a) (meth) acrylic acid alkyl ester having 4 to 12 carbon atoms in the alkyl group, 70.1 to 99.8% by weight, (b) copolymerized with component (a). 0.1 to 10% by weight of a possible hydroxyl group-containing monomer and / or (c) 0.1 to 19.9% by weight of another monomer copolymerizable with the component (a) and the component (b). (A) + (b) + (C) is 100% by weight) and is a pressure-sensitive adhesive comprising a cross-linking acrylic resin and a cross-linking agent, and the pressure-sensitive adhesive layer made of the pressure-sensitive adhesive is transparent. An optical filter film, characterized in that it is provided on one side of a substrate, and the pressure-sensitive adhesive layer contains a neon light-absorbing dye,
(2) The film for optical filters as described in (1) above, wherein the crosslinking agent is a block type isocyanate,
(3) The film for optical filters according to (1) or (2), wherein the neon light absorbing dye is a tetraazaporphyrin dye,
(4) The film for optical filters according to any one of (1) to (3), wherein the pressure-sensitive adhesive contains a tackifier made of a terpene phenol resin,
(5) At least one layer selected from a hard coat layer, a conductive layer, an antiglare layer and an antireflection layer is laminated on the surface opposite to the surface having the adhesive layer of the transparent substrate provided with the adhesive layer. The film for optical filters according to any one of (1) to (4),
(6) An optical filter for a plasma display panel, wherein the optical filter film according to any one of (1) to (5) is laminated on a film or glass having a near infrared ray and / or electromagnetic wave shielding function. ,
About.
本発明で使用する粘着剤は、テトラアザポルフィリン色素に代表されるネオン光吸収色素を含んでいても優れた安定性を示し、該粘着剤層が透明基材の一面に設けられている光学フィルター用フィルムおよびこれを用いたプラズマディスプレイパネル用光学フィルターは優れた耐光性を示す。 The pressure-sensitive adhesive used in the present invention exhibits excellent stability even when it contains a neon light-absorbing dye typified by a tetraazaporphyrin dye, and the pressure-sensitive adhesive layer is provided on one surface of a transparent substrate. Films and optical filters for plasma display panels using the same exhibit excellent light resistance.
本発明で使用する粘着剤は、アルキル基の炭素数が4〜12の(メタ)アクリル酸アルキルエステルを70.1〜99.8重量%、前記(メタ)アクリル酸アルキルエステルと共重合可能な水酸基含有モノマーを0.1〜10重量%および前記(メタ)アクリル酸アルキルエステルと水酸基含有モノマーとに共重合可能な他のモノマーを0.1〜19.9重量%の量で共重合させた架橋型アクリル系樹脂と架橋剤からなる粘着剤である。 The pressure-sensitive adhesive used in the present invention is copolymerizable with 70.1 to 99.8% by weight of a (meth) acrylic acid alkyl ester having 4 to 12 carbon atoms in the alkyl group and the (meth) acrylic acid alkyl ester. 0.1 to 10% by weight of the hydroxyl group-containing monomer and another monomer copolymerizable with the (meth) acrylic acid alkyl ester and the hydroxyl group-containing monomer were copolymerized in an amount of 0.1 to 19.9% by weight. It is a pressure-sensitive adhesive comprising a crosslinkable acrylic resin and a crosslinker.
本発明で使用する(メタ)アクリル酸アルキルエステルとしては、アルキル基の炭素数が4〜12である(メタ)アクリル酸アルキルエステルであれば特に限定されないが、例えば(メタ)アクリル酸ブチル、(メタ)アクリル酸イソブチル、(メタ)アクリル酸s−ブチル、(メタ)アクリル酸t−ブチル、(メタ)アクリル酸ペンチル、(メタ)アクリル酸イソペンチル、(メタ)アクリル酸ネオペンチル、(メタ)アクリル酸ヘキシル、(メタ)アクリル酸ヘプチル、(メタ)アクリル酸2−エチルヘキシル、(メタ)アクリル酸オクチル、(メタ)アクリル酸イソオクチル、(メタ)アクリル酸ノニル、(メタ)アクリル酸イソノニル、(メタ)アクリル酸デシル、(メタ)アクリル酸イソデシル、(メタ)アクリル酸ウンデシル又は(メタ)アクリル酸ドデシルなどが挙げられるが、これらは必要に応じて2種類以上を併用しても良い。これらの中でもアクリル酸ブチルが好適に使用できる。 The (meth) acrylic acid alkyl ester used in the present invention is not particularly limited as long as it is a (meth) acrylic acid alkyl ester having 4 to 12 carbon atoms in the alkyl group. For example, butyl (meth) acrylate, ( Isobutyl acrylate, s-butyl (meth) acrylate, t-butyl (meth) acrylate, pentyl (meth) acrylate, isopentyl (meth) acrylate, neopentyl (meth) acrylate, (meth) acrylic acid Hexyl, heptyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, octyl (meth) acrylate, isooctyl (meth) acrylate, nonyl (meth) acrylate, isononyl (meth) acrylate, (meth) acrylic Decyl acid, isodecyl (meth) acrylate, undecyl (meth) acrylate, (Meth) and dodecyl acrylate and the like, it may be used in combination of two or more as necessary. Among these, butyl acrylate can be preferably used.
前記(メタ)アクリル酸アルキルエステルと共重合可能な水酸基含有モノマーとしては、後記する架橋剤との架橋点などとして機能するものが用いられ、その種類について特に限定はないが、 (メタ)アクリル酸ヒドロキシエチル、(メタ)アクリル酸ヒドロキシプロピルなどが挙げられ、これらは必要に応じて2種類以上を併用しても良い。これらの中でもアクリル酸2−ヒドロキシエチルが好適に使用できる。 As the hydroxyl group-containing monomer copolymerizable with the (meth) acrylic acid alkyl ester, those functioning as a crosslinking point with a crosslinking agent to be described later are used, and the type thereof is not particularly limited, but (meth) acrylic acid Examples thereof include hydroxyethyl and hydroxypropyl (meth) acrylate, and these may be used in combination of two or more as required. Among these, 2-hydroxyethyl acrylate can be preferably used.
(メタ)アクリル酸アルキルエステルと水酸基含有モノマーとに共重合可能な他のモノマーとしては、特に限定されないが、アルキル基の炭素数が1〜3である(メタ)アクリル酸アルキルエステル、(メタ)アクリル酸イソボルニルなどの非芳香族性環含有(メタ)アクリル酸エステル、(メタ)アクリル酸アリールアルキルエステルなどの芳香族性環含有(メタ)アクリル酸エステル、N,N−ジメチル(メタ)アクリルアミドなどの(N−置換)アミド系モノマー、(メタ)アクリル酸グリシジルなどのエポキシ基含有アクリル系モノマーなどが挙げられ、これらは必要に応じて2種類以上を併用しても良い。これらの中でもアクリル酸メチルが好適に使用できる。 Although it does not specifically limit as another monomer copolymerizable with a (meth) acrylic-acid alkylester and a hydroxyl-containing monomer, The (meth) acrylic-acid alkylester whose carbon number of an alkyl group is 1-3, (meth) Non-aromatic ring-containing (meth) acrylic acid ester such as isobornyl acrylate, aromatic ring-containing (meth) acrylic acid ester such as (meth) acrylic acid arylalkyl ester, N, N-dimethyl (meth) acrylamide, etc. (N-substituted) amide monomers, epoxy group-containing acrylic monomers such as glycidyl (meth) acrylate, and the like. These may be used in combination of two or more. Among these, methyl acrylate can be preferably used.
前記モノマーを、通常は、有機溶媒、例えばトルエン、キシレン、ベンゼン、ヘキサン、ヘプタン、酢酸エチル、酢酸ブチル、メチルイソブチルケトン、メチルエチルケトン、アセトン、アルコール類に溶解または分散させ、攪拌しながら、重合開始剤を添加し共重合させることにより架橋型アクリル系樹脂を得ることができる。ここで使用される重合開始剤は、無機系あるいは有機系のいずれの重合開始剤であってもよいが、例えばアゾビスイソブチロニトリル(以下AIBNと略す)、ベンジルパーオキサイドのような有機重合開始剤を使用することが好ましい。重合開始剤の使用量は、通常の使用量であれば良く、例えば、全モノマー成分100重量部に対して0.01〜1重量部程度の範囲から選択することが出来る。 The monomer is usually dissolved or dispersed in an organic solvent such as toluene, xylene, benzene, hexane, heptane, ethyl acetate, butyl acetate, methyl isobutyl ketone, methyl ethyl ketone, acetone, alcohols, and the polymerization initiator is stirred. A cross-linked acrylic resin can be obtained by adding and copolymerizing. The polymerization initiator used here may be either an inorganic or organic polymerization initiator. For example, organic polymerization such as azobisisobutyronitrile (hereinafter abbreviated as AIBN) or benzyl peroxide. It is preferred to use an initiator. The amount of the polymerization initiator used may be a normal amount, and can be selected, for example, from a range of about 0.01 to 1 part by weight with respect to 100 parts by weight of all monomer components.
前記架橋型アクリル系樹脂に使用する架橋剤としては、ポリイソシアネート化合物、メラミン化合物、ジアミン化合物、エポキシ樹脂化合物、尿素樹脂化合物、塩化アルミニウム、塩化第二鉄又は硫酸アルミニウム等の金属塩等が挙げられ、ポリイソシアネート化合物が好ましく、ブロック型のポリイソシアネートが更に好ましい。ブロック型のポリイソシアネートとしては、例えばオキシムブロック型イソシアネートや活性メチレンブロックイソシアネートが挙げられ、スズ化合物などの触媒を必要としない低温硬化型の活性メチレン系ブロックイソシアネートが好適に使用できる。 Examples of the crosslinking agent used for the crosslinked acrylic resin include polyisocyanate compounds, melamine compounds, diamine compounds, epoxy resin compounds, urea resin compounds, metal salts such as aluminum chloride, ferric chloride, and aluminum sulfate. Polyisocyanate compounds are preferred, and block-type polyisocyanates are more preferred. Examples of the block type polyisocyanate include oxime block type isocyanate and active methylene block isocyanate. Low temperature curing type active methylene block isocyanate which does not require a catalyst such as a tin compound can be preferably used.
前記の架橋型アクリル系樹脂と架橋剤を用いた粘着剤は粘着力、凝集力に優れると共に、ポリマー中に不飽和結合がないため光や酸素に対する安定性が高く、また、モノマーの種類や分子量の選択の自由度が高いという理由からも好ましく、エージング作業の前後でのネオン光吸収色素の安定性のために塗布乾燥直後でも十分な架橋密度を持った高分子とするため該重量平均分子量が100万以上であることが好ましい。 Adhesives using the above-mentioned crosslinkable acrylic resins and crosslinkers are excellent in adhesion and cohesion, and are highly stable against light and oxygen because there are no unsaturated bonds in the polymer. Also, the type and molecular weight of the monomer The weight average molecular weight is preferable in order to obtain a polymer having a sufficient crosslinking density immediately after coating and drying for the stability of the neon light absorbing dye before and after the aging operation. It is preferably 1 million or more.
本発明で使用する粘着付与剤としては、テルペン系粘着付与樹脂、フェノール系粘着付与樹脂、ロジン系粘着付与樹脂、エポキシ系粘着付与樹脂、ポリアミド系粘着付与樹脂、ケトン系粘着付与樹脂、エラストマー系粘着付与樹脂などが挙げられ、変性テルペン系樹脂であるテルペンフェノール樹脂が好適に使用できる。 As the tackifier used in the present invention, terpene tackifier resin, phenol tackifier resin, rosin tackifier resin, epoxy tackifier resin, polyamide tackifier resin, ketone tackifier resin, elastomer tackifier Examples thereof include terpene phenol resins, which are modified terpene resins.
本発明で使用するネオン光吸収色素は波長580から600nmに吸収極大を有し、その半値幅が約10nmから60nmであるものが好ましく、例えばシアニン、スクアリリウム、キサンテン、オキソノール、アゾ、テトラアザポルフィリン等の色素から選ばれ、式(1)で表されるテトラアザポルフィリン色素が好適に使用できる。テトラアザポルフィリン色素は、市販もされており、例えば「PD319」(三井化学(株)製)や「TAP2」(山田化学(株)製)が挙げられる(吸収波長ピークは592nm)。 The neon light-absorbing dye used in the present invention preferably has an absorption maximum at a wavelength of 580 to 600 nm and a half width of about 10 to 60 nm. For example, cyanine, squarylium, xanthene, oxonol, azo, tetraazaporphyrin, etc. A tetraazaporphyrin dye represented by the formula (1) can be suitably used. Tetraazaporphyrin dyes are also commercially available, and examples include “PD319” (manufactured by Mitsui Chemicals) and “TAP2” (manufactured by Yamada Chemical Co., Ltd.) (absorption wavelength peak is 592 nm).
色素の配合量は、適宜設定すればよく、吸収の極大値における透過率が5から70%になるように配合することが好適である。
What is necessary is just to set the compounding quantity of a pigment | dye suitably, and it is suitable to mix | blend so that the transmittance | permeability in the maximum value of absorption may be 5 to 70%.
本発明のフィルムを製造するには、例えば上記の架橋型アクリル系樹脂100重量部、架橋剤0.01〜1重量部、ネオン光吸収色素0.01〜1重量部、紫外線吸収剤などのその他の添加剤0.1〜10重量部を溶剤中に分散させて得られる粘着剤を、透明基材上に塗工し、乾燥すればよい。溶剤としては、例えばメタノール、エタノール、イソプロパノール、ジアセトンアルコール、エチルセロソルブ、メチルセロソルブ等のアルコール類、アセトン、メチルエチルケトン、シクロペンタノン、シクロヘキサノン等のケトン類、N,N−ジメチルホルムアミド、N,N−ジメチルアセトアミド等のアミド類、ジメチルスルホキシド等のスルホキシド類、テトラヒドロフラン、ジオキサン、エチレングリコールモノメチルエーテル等のエーテル類、酢酸メチル、酢酸エチル、酢酸ブチル等のエステル類、クロロホルム、塩化メチレン、ジクロロエチレン、トリクロロエチレン等のハロゲン系溶剤、ベンゼン、トルエン、キシレン、モノクロルベンゼン、ジクロルベンゼン等の芳香族類、又はn−へキサン、n−ヘプタン等の脂肪族炭化水素類、テトラフルオロプロピルアルコール、ペンタフルオロプロピルアルコール等のフッ素系溶剤等を用いることができ、各組成物の溶解性がよく、塗工、乾燥等の問題がなく、安全性についても十分配慮して溶剤を選択する必要がある。 In order to produce the film of the present invention, for example, 100 parts by weight of the above-mentioned cross-linked acrylic resin, 0.01 to 1 part by weight of a cross-linking agent, 0.01 to 1 part by weight of a neon light-absorbing dye, and other UV absorbers A pressure-sensitive adhesive obtained by dispersing 0.1 to 10 parts by weight of the above additive in a solvent may be coated on a transparent substrate and dried. Examples of the solvent include alcohols such as methanol, ethanol, isopropanol, diacetone alcohol, ethyl cellosolve and methyl cellosolve, ketones such as acetone, methyl ethyl ketone, cyclopentanone and cyclohexanone, N, N-dimethylformamide, N, N- Amides such as dimethylacetamide, sulfoxides such as dimethylsulfoxide, ethers such as tetrahydrofuran, dioxane, ethylene glycol monomethyl ether, esters such as methyl acetate, ethyl acetate, butyl acetate, chloroform, methylene chloride, dichloroethylene, trichloroethylene, etc. Halogen solvents, aromatics such as benzene, toluene, xylene, monochlorobenzene and dichlorobenzene, or aliphatic charcoal such as n-hexane and n-heptane Fluorine solvents such as hydrogen, tetrafluoropropyl alcohol, pentafluoropropyl alcohol, etc. can be used, the solubility of each composition is good, there is no problem of coating, drying, etc., and sufficient consideration is given to safety It is necessary to select a solvent.
粘着剤の塗工は、フローコート法、スプレー法、バーコート法、グラビアコート法、ロールコート法、ブレードコート法、エアーナイフコート法、リップコート法、ダイコーター法等の公知の塗工方法で、仕上がりの膜厚が通常5から50μm、好ましくは15〜30μmとなるように塗布され、80〜140℃、好ましくは100〜130℃で乾燥することによって処理層が固定される。通常、この後エージング処理が行われる。エージング処理の条件は使用する樹脂と架橋剤の種類によって条件が異なるが、本粘着剤については25〜50℃の恒温槽中、1日〜1週間程度保管するのが好ましい。 The adhesive is applied by a known coating method such as a flow coating method, a spray method, a bar coating method, a gravure coating method, a roll coating method, a blade coating method, an air knife coating method, a lip coating method, or a die coater method. The film thickness is usually 5 to 50 μm, preferably 15 to 30 μm, and the treatment layer is fixed by drying at 80 to 140 ° C., preferably 100 to 130 ° C. Usually, an aging process is performed thereafter. The conditions for aging treatment vary depending on the type of resin used and the crosslinking agent, but it is preferable to store the pressure-sensitive adhesive in a thermostatic bath at 25 to 50 ° C. for about 1 day to 1 week.
本発明に使用される透明基材は透明性が高く、傷などがなく、光学フィルムとしての使用に耐えられるものであれば特に種類や厚さは限定されないが、10〜500μmの厚さが、作業性が良好で好ましい範囲といえる。具体的にはポリエステル系(以下、PETと記す)、ポリカーボネート系、トリアセテート系、ノルボルネン系、アクリル系、セルロース系、ポリオレフィン系又はウレタン系等の高分子樹脂フィルムが挙げられ、外部からの紫外線を吸収して内部部材の機能の安定化をはかるために紫外線吸収物質が含有されている透明支持フィルムを使用することもできる。また、フィルムの表面には塗工膜との密着性を上げるためにコロナ放電処理、プラズマ処理、グロー放電処理、粗面化処理、薬品処理やアンカーコート剤やプライマー等のコーティングを施しても良い。また、透明基材が、例えば減反射性、防眩・減反射性、帯電防止性、防汚性、近赤外線吸収性、電磁波遮蔽性又は色調調整などの機能を単独あるいは複数有するフィルムであれば更に好ましく、特にこれらにネオン光吸収粘着層を設けた場合は、付与されているこれらの機能とネオン光吸収能を同時に保有できるため、合理的で、優れた形態の前記光学フィルター用フィルム及びこれを用いたプラズマディスプレイパネル用光学フィルターが得られる。 The type and thickness of the transparent substrate used in the present invention is not particularly limited as long as it is highly transparent, has no scratches, and can withstand use as an optical film. It can be said that the workability is good and preferable. Specific examples include polymeric resin films such as polyester (hereinafter referred to as PET), polycarbonate, triacetate, norbornene, acrylic, cellulose, polyolefin, or urethane, and absorbs ultraviolet rays from the outside. In order to stabilize the function of the internal member, a transparent support film containing an ultraviolet absorbing material can also be used. The surface of the film may be coated with corona discharge treatment, plasma treatment, glow discharge treatment, roughening treatment, chemical treatment, anchor coating agent, primer or the like in order to improve adhesion with the coating film. . In addition, if the transparent substrate is a film having one or more functions such as anti-reflection, anti-glare / anti-reflection, antistatic, antifouling, near infrared absorptivity, electromagnetic wave shielding or color tone adjustment More preferably, particularly when a neon light absorbing adhesive layer is provided on them, these functions and the neon light absorbing ability can be held at the same time. An optical filter for a plasma display panel using can be obtained.
次に、前記したような機能性を保持する透明支持フィルムの例について以下に説明するが、これらに限定されるものではない。
減反射フィルムはPETなどの透明支持フィルムの表面に、低屈折率剤をバインダー樹脂及びその他の添加剤と共にコーティングして外部からの光の反射を抑えたフィルム又は透明支持フィルムと低屈折率層との間にハードコート層、高屈折率層を施し、各層による反射光を打ち消すようにコントロールして視認性を良くしたフィルムであり、防眩・減反射フィルムは減反射フィルムの高屈折率層やその他の層に微細粒子を含有させて外部からの光を乱反射させて更に視認性を良くしたフィルムで、アークトップシリーズ(旭硝子(株)製)、カヤコートARSシリーズ(日本化薬(株)製)、カヤコートAGRSシリーズ(日本化薬(株)製)、リアルックシリーズ(日油(株)製)等として未粘着加工の減反射性フィルムが透明支持フィルムとして利用できるが、これらは市場から入手することが可能である。Next, examples of the transparent support film having the above-described functionality will be described below, but the present invention is not limited thereto.
The anti-reflective film is a film or a transparent support film in which reflection of light from the outside is suppressed by coating a surface of a transparent support film such as PET with a low refractive index agent together with a binder resin and other additives, and a low refractive index layer. A film with a hard coat layer and a high refractive index layer in between, and control to cancel reflected light from each layer to improve visibility. A film that contains fine particles in other layers and diffuses light from the outside to improve visibility. ARC Top Series (Asahi Glass Co., Ltd.), Kayacoat ARS Series (Nippon Kayaku Co., Ltd.) , Kayacoat AGRS series (manufactured by Nippon Kayaku Co., Ltd.), Realak series (manufactured by NOF Corporation), etc. Can be used as a beam, these can be obtained from the market.
電磁波を遮蔽する方法には銅などの金属の極細線を網目のような幾何学模様を透明基材に保持させたメッシュタイプと、光透過性を有する範囲で金属の極薄膜を透明基材または硝子に保持させた薄膜タイプがある。薄膜タイプは一般的に近赤外線を反射し透過させないので、別に近赤外線吸収層を必要としない。本発明に使用される、その他の機能性を有する透明基材としては、紫外線吸収性、帯電防止性、防汚性、色調調整等の、機能を単独あるいは複数で保持させたフィルムがあるが、これらはそれらの性能を有する化合物を含有するバインダー樹脂組成物から成形する方法などによりそれ自体公知の方法に準じて調製することが出来る。 The method of shielding electromagnetic waves is a mesh type in which a fine pattern of metal such as copper is held on a transparent base material with a fine metal wire such as copper, and an ultra-thin metal film within a transparent base There is a thin film type held in glass. The thin film type generally reflects and does not transmit near-infrared light, and therefore does not require a separate near-infrared absorbing layer. As the transparent substrate having other functionality used in the present invention, there is a film that has a single function or a plurality of functions such as ultraviolet absorptivity, antistatic property, antifouling property, and color tone adjustment. These can be prepared according to a method known per se by a method of molding from a binder resin composition containing a compound having these properties.
次に、本発明の光学フィルターは、透明基材上に本粘着層が設けられている本発明のネオン光吸収フィルムを最低限の構成要素として、該ネオン光吸収フィルムとその他の機能を有する透明基材または硝子(例えば、近赤外線および/又は電磁波遮蔽機能を有するフィルムもしくは硝子)とを積層して得られる。本発明の光学フィルターはあらかじめ硝子板やプラスチック板に貼合してプラズマディスプレイの前面に取り付けてもよいし、直接貼合して使用してもよい。 Next, the optical filter of the present invention has the neon light-absorbing film of the present invention in which the present adhesive layer is provided on a transparent substrate as a minimum component, and the neon light-absorbing film and other functions are transparent. It is obtained by laminating a substrate or glass (for example, a film or glass having a near infrared ray and / or electromagnetic wave shielding function). The optical filter of the present invention may be bonded in advance to a glass plate or a plastic plate and attached to the front surface of the plasma display, or may be used by directly bonding.
以下実施例により本発明を更に具体的に説明するが、本発明はかかる実施例に限定されるものではない。尚、実施例において部は重量部を、%は重量%をそれぞれ意味する。 Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to the examples. In Examples, “part” means “part by weight” and “%” means “% by weight”.
使用した粘着剤の重量平均分子量は、GPC(ゲルパーミエーションクロマトグラフィー)法の下記条件にて測定した。
分析装置:昭和電工製、GPC SYSTEM−21 Shodex
カラム:昭和電工製、KF−803L+KF−803L+KF−803L
カラム温度:40℃
流速:1ml/min
溶離液:テトラヒドロフラン
検出器:示差屈折計
標準試料:ポリスチレンThe weight average molecular weight of the used adhesive was measured on the following conditions of GPC (gel permeation chromatography) method.
Analyzer: Showa Denko, GPC SYSTEM-21 Shodex
Column: Showa Denko KF-803L + KF-803L + KF-803L
Column temperature: 40 ° C
Flow rate: 1 ml / min
Eluent: Tetrahydrofuran Detector: Differential refractometer Standard sample: Polystyrene
実施例1
<アクリル系樹脂の作製>
重合容器に、アクリル酸ブチル90部、アクリル酸メチル9.5部、アクリル酸2−ヒドロキシエチル0.5部、酢酸エチル150部を仕込み、室温で1時間窒素置換を行った。その後、攪拌下で75℃に昇温し、重合開始剤としてAIBN0.02部を添加し、75℃にて6時間重合を行って、アクリル酸エステル系重合物を作製した。このアクリル酸エステル系重合物の重量平均分子量は100万であった。
<ネオン光吸収フィルムの作製>
前記作製のアクリル酸エステル系重合物(アクリル系樹脂)を使用し下表に示す各材料を均一になるように混合溶解した塗工液を、MRF−38(商品名、剥離PETフィルム、三菱化学ポリエステルフィルム製)上にコンマコーターで0.8m/分の塗工速度、乾燥温度110℃により、粘着層の厚さが18μmになるように塗工して粘着剤層を形成した。次に、KAYACOAT ARS−E105−100UV(商品名、減反射フィルム、日本化薬製)の減反射面の反対面に当該粘着剤層が形成されるように2枚のフィルムを貼り合わせることにより減反射性を有するネオン光吸収フィルムを得た。
<PDP用光学フィルターの作製>
粘着剤層を有する金属多層スパッタ膜を有するフィルム上に、前記ネオン光吸収フィルムを貼合し、PDP用光学フィルターを得た。このフィルターはPDPモジュールの前面に直接貼っても、ガラス板のような透明板に貼ってモジュールの前に取り付けてもよく、PDPフィルターとして必要な性能を十分に発揮するものであった。Example 1
<Production of acrylic resin>
A polymerization vessel was charged with 90 parts of butyl acrylate, 9.5 parts of methyl acrylate, 0.5 part of 2-hydroxyethyl acrylate, and 150 parts of ethyl acetate, and purged with nitrogen at room temperature for 1 hour. Then, it heated up at 75 degreeC under stirring, 0.02 part of AIBN was added as a polymerization initiator, and it superposed | polymerized at 75 degreeC for 6 hours, and produced the acrylic ester polymer. The weight average molecular weight of this acrylate ester polymer was 1 million.
<Preparation of neon light absorption film>
A coating solution prepared by mixing and dissolving the materials shown in the following table using the prepared acrylic acid ester polymer (acrylic resin) so as to be uniform was used as MRF-38 (trade name, release PET film, Mitsubishi Chemical Corporation). A pressure-sensitive adhesive layer was formed on a polyester film by a comma coater at a coating speed of 0.8 m / min and a drying temperature of 110 ° C. so that the thickness of the pressure-sensitive adhesive layer was 18 μm. Next, the two films are bonded together so that the adhesive layer is formed on the opposite side of the anti-reflection surface of KAYACOAT ARS-E105-100UV (trade name, anti-reflection film, manufactured by Nippon Kayaku Co., Ltd.). A reflective neon light absorbing film was obtained.
<Production of optical filter for PDP>
The neon light-absorbing film was bonded onto a film having a metal multilayer sputtered film having an adhesive layer to obtain an optical filter for PDP. This filter may be directly attached to the front surface of the PDP module, or may be attached to a transparent plate such as a glass plate and attached to the front of the module, and sufficiently exhibits the performance required as a PDP filter.
材 料 使用量
アクリル系樹脂 14.0部
架橋剤(商品名K6000;旭化成ケミカルズ(株)製) 0.07部
添加剤(商品名K140;ヤスハラケミカル(株)製) 0.25部
紫外線吸収剤(商品名チヌビン109;チバガイギー(株)製) 0.2部
ネオン光吸収色素(商品名PD319;三井化学(株)製) 0.005部
メチルエチルケトン 14.5部Materials Amount used Acrylic resin 14.0 parts Crosslinking agent (trade name K6000; manufactured by Asahi Kasei Chemicals Corporation) 0.07 part additive (trade name K140; manufactured by Yasuhara Chemicals Co., Ltd.) 0.25 parts UV absorber ( Brand name Tinuvin 109; Ciba Geigy Co., Ltd.) 0.2 parts Neon light absorbing dye (trade name PD319; Mitsui Chemicals Co., Ltd.) 0.005 parts Methyl ethyl ketone 14.5 parts
実施例2
<アクリル系樹脂の作製>
重合容器に、アクリル酸2-エチルヘキシル70部、アクリル酸メチル29.5部、アクリル酸2−ヒドロキシエチル0.5部、酢酸エチル150部を仕込み、室温で1時間窒素置換を行った。その後、攪拌下で75℃に昇温し、重合開始剤としてAIBN0.02部を添加し、75℃にて6時間重合を行って、アクリル酸エステル系重合物を作製した。このアクリル酸エステル系重合物の重量平均分子量は105万であった。
<ネオン光吸収フィルムの作製>
実施例1のアクリル系樹脂を変更する以外は実施例1と同様の方法で減反射性を有するネオン光吸収フィルムを得た。
<PDP用光学フィルターの作製>
粘着剤層を有する金属多層スパッタ膜フィルム上に、前記ネオン光吸収フィルムを貼合し、PDP用光学フィルターを得た。このフィルターはPDPモジュールの前面に直接貼っても、ガラス板のような透明板に貼ってモジュールの前に取り付けてもよく、PDPフィルターとして必要な性能を十分に発揮するものであった。Example 2
<Production of acrylic resin>
A polymerization vessel was charged with 70 parts of 2-ethylhexyl acrylate, 29.5 parts of methyl acrylate, 0.5 parts of 2-hydroxyethyl acrylate, and 150 parts of ethyl acetate, and was purged with nitrogen at room temperature for 1 hour. Then, it heated up at 75 degreeC under stirring, 0.02 part of AIBN was added as a polymerization initiator, and it superposed | polymerized at 75 degreeC for 6 hours, and produced the acrylic ester polymer. The weight average molecular weight of this acrylic ester polymer was 1,050,000.
<Preparation of neon light absorption film>
A neon light-absorbing film having reduced reflectivity was obtained in the same manner as in Example 1 except that the acrylic resin in Example 1 was changed.
<Production of optical filter for PDP>
The neon light-absorbing film was bonded onto a metal multilayer sputtered film having an adhesive layer to obtain an optical filter for PDP. This filter may be directly attached to the front surface of the PDP module, or may be attached to a transparent plate such as a glass plate and attached to the front of the module, and sufficiently exhibits the performance required as a PDP filter.
実施例3
<アクリル系樹脂の作製>
重合容器に、アクリル酸ブチル90部、アクリル酸メチル2部、アクリル酸2−ヒドロキシエチル0.5部、アクリル酸グリシジルメチル7.5部、酢酸エチル150部を仕込み、室温で1時間窒素置換を行った。その後、攪拌下で75℃に昇温し、重合開始剤としてAIBN0.02部を添加し、75℃にて6時間重合を行って、アクリル酸エステル系重合物を作製した。このアクリル酸エステル系重合物の重量平均分子量は104万であった。
<ネオン光吸収フィルムの作製>
実施例1のアクリル系樹脂を変更する以外は実施例1と同様の方法で減反射性を有するネオン光吸収フィルムを得た。
<PDP用光学フィルターの作製>
粘着剤層を有する金属多層スパッタ膜フィルム上に、前記ネオン光吸収フィルムを貼合し、PDP用光学フィルターを得た。このフィルターはPDPモジュールの前面に直接貼っても、ガラス板のような透明板に貼ってモジュールの前に取り付けてもよく、PDPフィルターとして必要な性能を十分に発揮するものであった。Example 3
<Production of acrylic resin>
A polymerization vessel is charged with 90 parts of butyl acrylate, 2 parts of methyl acrylate, 0.5 part of 2-hydroxyethyl acrylate, 7.5 parts of glycidyl methyl acrylate, and 150 parts of ethyl acetate, and nitrogen replacement is performed at room temperature for 1 hour. went. Then, it heated up at 75 degreeC under stirring, 0.02 part of AIBN was added as a polymerization initiator, and it superposed | polymerized at 75 degreeC for 6 hours, and produced the acrylic ester polymer. The weight average molecular weight of this acrylic ester polymer was 1,040,000.
<Preparation of neon light absorption film>
A neon light-absorbing film having reduced reflectivity was obtained in the same manner as in Example 1 except that the acrylic resin in Example 1 was changed.
<Production of optical filter for PDP>
The neon light-absorbing film was bonded onto a metal multilayer sputtered film having an adhesive layer to obtain an optical filter for PDP. This filter may be directly attached to the front surface of the PDP module, or may be attached to a transparent plate such as a glass plate and attached to the front of the module, and sufficiently exhibits the performance required as a PDP filter.
比較例1
<アクリル系樹脂の作製>
重合容器に、アクリル酸ブチル80部、アクリル酸メチル18部、アクリル酸2部、酢酸エチル150部を仕込み、室温で1時間窒素置換を行った。その後、攪拌下で75℃に昇温し、重合開始剤としてAIBN0.02部を添加し、75℃にて6時間重合を行って、アクリル酸エステル系重合物を作製した。このアクリル酸エステル系重合物の重量平均分子量は100万であった。
<ネオン光吸収フィルムの作製>
実施例1のアクリル系樹脂を変更する以外は実施例1と同様の方法で減反射性を有するネオン光吸収フィルムを得た。Comparative Example 1
<Production of acrylic resin>
A polymerization vessel was charged with 80 parts of butyl acrylate, 18 parts of methyl acrylate, 2 parts of acrylic acid, and 150 parts of ethyl acetate, and was purged with nitrogen at room temperature for 1 hour. Then, it heated up at 75 degreeC under stirring, 0.02 part of AIBN was added as a polymerization initiator, and it superposed | polymerized at 75 degreeC for 6 hours, and produced the acrylic ester polymer. The weight average molecular weight of this acrylate ester polymer was 1 million.
<Preparation of neon light absorption film>
A neon light-absorbing film having reduced reflectivity was obtained in the same manner as in Example 1 except that the acrylic resin in Example 1 was changed.
比較例2
<アクリル系樹脂の作製>
重合容器に、アクリル酸ブチル96部、アクリル酸4部、酢酸エチル150部を仕込み、室温で1時間窒素置換を行った。その後、攪拌下で75℃に昇温し、重合開始剤としてAIBN0.02部を添加し、75℃にて6時間重合を行って、アクリル酸エステル系重合物を作製した。このアクリル酸エステル系重合物の重量平均分子量は109万であった。
<ネオン光吸収フィルムの作製>
実施例1のアクリル系樹脂を変更する以外は実施例1と同様の方法で減反射性を有するネオン光吸収フィルムを得た。Comparative Example 2
<Production of acrylic resin>
A polymerization vessel was charged with 96 parts of butyl acrylate, 4 parts of acrylic acid, and 150 parts of ethyl acetate, and was purged with nitrogen at room temperature for 1 hour. Then, it heated up at 75 degreeC under stirring, 0.02 part of AIBN was added as a polymerization initiator, and it superposed | polymerized at 75 degreeC for 6 hours, and produced the acrylic ester polymer. The weight average molecular weight of this acrylate ester polymer was 1.09 million.
<Preparation of neon light absorption film>
A neon light-absorbing film having reduced reflectivity was obtained in the same manner as in Example 1 except that the acrylic resin in Example 1 was changed.
比較例3
<アクリル系樹脂の作製>
重合容器に、アクリル酸ブチル80部、アクリル酸メチル13部、アクリル酸2部、アクリル酸N,N−ジメチルアミド5部、酢酸エチル150部を仕込み、室温で1時間窒素置換を行った。その後、攪拌下で75℃に昇温し、重合開始剤としてAIBN0.02部を添加し、75℃にて6時間重合を行って、アクリル酸エステル系重合物を作製した。このアクリル酸エステル系重合物の重量平均分子量は107万であった。
<ネオン光吸収フィルムの作製>
実施例1のアクリル系樹脂を変更する以外は実施例1と同様の方法で減反射性を有するネオン光吸収フィルムを得た。Comparative Example 3
<Production of acrylic resin>
A polymerization vessel was charged with 80 parts of butyl acrylate, 13 parts of methyl acrylate, 2 parts of acrylic acid, 5 parts of acrylic acid N, N-dimethylamide, and 150 parts of ethyl acetate, and was purged with nitrogen at room temperature for 1 hour. Then, it heated up at 75 degreeC under stirring, 0.02 part of AIBN was added as a polymerization initiator, and it superposed | polymerized at 75 degreeC for 6 hours, and produced the acrylic ester polymer. The weight average molecular weight of this acrylate ester polymer was 1.70 million.
<Preparation of neon light absorption film>
A neon light-absorbing film having reduced reflectivity was obtained in the same manner as in Example 1 except that the acrylic resin in Example 1 was changed.
<試験方法>
各実施例フィルム及び各比較例フィルムの試験片の視感透過率(Y/%)および色度座標(x、y)を測定し、カーボンアークフェードメーターにより100時間かけて18kJ/cm2のエネルギーを照射し、その後、再び視感透過率(Y/%)および色度座標(x、y)を測定した。
測定はUV−3150(商品名、分光光度計、島津製作所製)を使用し、視感透過率(Y/%)および色度座標(x、y)はJIS Z 8701のXYZ表色系による色の表示方法に準拠して算出した。
カーボンアークフェードメーターは紫外線フェードメーターU48H(スガ試験機製)を使用した。<Test method>
The luminous transmittance (Y /%) and chromaticity coordinates (x, y) of the test piece of each example film and each comparative example film were measured, and an energy of 18 kJ / cm 2 over 100 hours using a carbon arc fade meter. Then, luminous transmittance (Y /%) and chromaticity coordinates (x, y) were measured again.
The measurement uses UV-3150 (trade name, spectrophotometer, manufactured by Shimadzu Corporation), and luminous transmittance (Y /%) and chromaticity coordinates (x, y) are colors according to the XYZ color system of JIS Z 8701. It was calculated in accordance with the display method.
As the carbon arc fade meter, an ultraviolet fade meter U48H (manufactured by Suga Test Instruments) was used.
耐光性試験前後での結果を表1に示した。 The results before and after the light resistance test are shown in Table 1.
<結果の考察>
実施例1から3は耐光性試験前後での色目の変化が少なく、592nmにおけるネオン光吸収能の変化においても良好な結果が得られた。比較例1から3は耐光性試験前後での色目の変化が大きく、ネオン光吸収能の変化も大きかった。<Consideration of results>
In Examples 1 to 3, there was little change in color before and after the light resistance test, and good results were obtained even in the change in neon light absorption ability at 592 nm. In Comparative Examples 1 to 3, the color change before and after the light resistance test was large, and the change in neon light absorption ability was also large.
Claims (6)
An optical filter for a plasma display panel, wherein the optical filter film according to any one of claims 1 to 5 is laminated on a film or glass having a near-infrared ray and / or electromagnetic wave shielding function.
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JP2009019000 | 2009-01-30 | ||
JP2009019000 | 2009-01-30 | ||
PCT/JP2010/000223 WO2010087122A1 (en) | 2009-01-30 | 2010-01-18 | Film for optical filter and optical filter comprising same for plasma display panel |
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JPWO2010087122A1 true JPWO2010087122A1 (en) | 2012-08-02 |
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KR (1) | KR20110108327A (en) |
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JP5699529B2 (en) * | 2010-10-22 | 2015-04-15 | 日油株式会社 | Film for 3D display |
CN102721991B (en) * | 2012-07-03 | 2015-11-11 | 四川世创达电子科技有限公司 | Straight pad pasting |
JP7008467B2 (en) * | 2017-10-24 | 2022-01-25 | リンテック株式会社 | Adhesive sheet and display |
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JPH04212498A (en) * | 1990-03-24 | 1992-08-04 | Canon Inc | Conductive adhesive member, preparation of the same, and conductive component/electronic equipment using the same |
JP2006196737A (en) * | 2005-01-14 | 2006-07-27 | Dainippon Printing Co Ltd | Light transparent electromagnetic wave shield sheet |
JP2007266239A (en) * | 2006-03-28 | 2007-10-11 | Dainippon Printing Co Ltd | Method of manufacturing sheet-like composite filter for plasma display and sheet-like composite filter for plasma display |
JP5035236B2 (en) * | 2006-08-18 | 2012-09-26 | 大日本印刷株式会社 | Front filter for plasma display and plasma display |
JP2008182145A (en) * | 2007-01-26 | 2008-08-07 | Dainippon Printing Co Ltd | Sheet shape composite filter for plasma display, and its manufacturing method |
JP2008209575A (en) * | 2007-02-26 | 2008-09-11 | Fujimori Kogyo Co Ltd | Optical filter for display |
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2010
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- 2010-01-18 JP JP2010548395A patent/JPWO2010087122A1/en not_active Withdrawn
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CN102272639A (en) | 2011-12-07 |
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