JPH11109112A - Manufacture of glare preventive treated layer - Google Patents
Manufacture of glare preventive treated layerInfo
- Publication number
- JPH11109112A JPH11109112A JP9287807A JP28780797A JPH11109112A JP H11109112 A JPH11109112 A JP H11109112A JP 9287807 A JP9287807 A JP 9287807A JP 28780797 A JP28780797 A JP 28780797A JP H11109112 A JPH11109112 A JP H11109112A
- Authority
- JP
- Japan
- Prior art keywords
- treatment layer
- stirring
- glare
- filler
- base 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 230000004313 glare Effects 0.000 title abstract description 8
- 230000003449 preventive effect Effects 0.000 title abstract 4
- 229920005989 resin Polymers 0.000 claims abstract description 40
- 239000011347 resin Substances 0.000 claims abstract description 40
- 238000011282 treatment Methods 0.000 claims abstract description 36
- 239000000945 filler Substances 0.000 claims abstract description 22
- 238000003756 stirring Methods 0.000 claims abstract description 19
- -1 polysiloxane Polymers 0.000 claims abstract description 10
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 9
- 238000002156 mixing Methods 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 6
- 230000010355 oscillation Effects 0.000 claims abstract description 6
- 150000002222 fluorine compounds Chemical class 0.000 claims abstract description 5
- 206010052128 Glare Diseases 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 12
- 230000000694 effects Effects 0.000 abstract description 6
- 238000000149 argon plasma sintering Methods 0.000 abstract description 3
- 230000002265 prevention Effects 0.000 abstract description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 14
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 208000003464 asthenopia Diseases 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- FTALTLPZDVFJSS-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl prop-2-enoate Chemical compound CCOCCOCCOC(=O)C=C FTALTLPZDVFJSS-UHFFFAOYSA-N 0.000 description 1
- NLGDWWCZQDIASO-UHFFFAOYSA-N 2-hydroxy-1-(7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-yl)-2-phenylethanone Chemical class OC(C(=O)c1cccc2Oc12)c1ccccc1 NLGDWWCZQDIASO-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 229920006358 Fluon Polymers 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 238000007607 die coating method Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000005401 electroluminescence Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- FEUIEHHLVZUGPB-UHFFFAOYSA-N oxolan-2-yl prop-2-enoate Chemical compound C=CC(=O)OC1CCCO1 FEUIEHHLVZUGPB-UHFFFAOYSA-N 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Landscapes
- Optical Elements Other Than Lenses (AREA)
- Surface Treatment Of Optical Elements (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、防眩処理層の製造
法に関し、更に詳しくは、良好な表示品位と汚れ付着防
止性に優れた防眩処理層の製造法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing an anti-glare treatment layer, and more particularly, to a method for producing an anti-glare treatment layer having good display quality and excellent stain prevention.
【0002】[0002]
【従来の技術】CRTディスプレイ、フラットディスプ
レイ(液晶表示素子、プラズマディスプレイ、ELディ
スプレイ等)においては、画面に外部から光が入射し、
この光が反射して(グレアー、或いはギラツキ等といわ
れている)、表示画像を見づらくするという欠点があ
る。この対策として、各ディスプレイ表面に防眩処理が
行われ、従来、CRTディスプレイの防眩においては、
薬品等による化学エッチングによってブラウン管のガラ
スの画像表示表面を粗面化することがおこなわれてお
り、液晶表示素子等のフラットディスプレイの防眩にお
いては、機械的(サンドブラスト)もしくは化学的にエ
ッチングされたガラス板やプラスチック板を別に載置す
ることや、酸化チタン、酸化ケイ素等の多層蒸着膜を付
加させたガラス板やプラスチック板を別に載置すること
や、防眩処理をしたフィルムをディスプレイに貼り合わ
せることが行われている。2. Description of the Related Art In CRT displays and flat displays (liquid crystal display devices, plasma displays, EL displays, etc.), light is incident on the screen from the outside,
This light is reflected (referred to as glare or glare) and there is a drawback that the displayed image is difficult to see. As a countermeasure against this, an anti-glare treatment is performed on each display surface.
The image display surface of the glass of a cathode ray tube is roughened by chemical etching using chemicals or the like, and in the anti-glare of a flat display such as a liquid crystal display device, it is mechanically (sandblasted) or chemically etched. Separately mounting a glass plate or a plastic plate, separately mounting a glass plate or a plastic plate to which a multi-layer vapor-deposited film of titanium oxide, silicon oxide, etc. has been added, and attaching an anti-glare film to the display Matching is being done.
【0003】[0003]
【発明が解決しようとする課題】特に、近年、ディスプ
レイの大型化、高精細化及び用途の拡大に伴って、表示
品位が良好で、汚れ付着防止性に優れた防眩処理層が望
まれるようになってきた。In particular, in recent years, as the size of the display has been increased, the definition thereof has been increased, and the use thereof has been expanded, an anti-glare treatment layer having good display quality and excellent antifouling property has been desired. It has become
【0004】[0004]
【課題を解決するための手段】そこで、本発明者は、か
かる現況に鑑みて鋭意研究した結果、ベース樹脂および
充填剤を超音波で混合撹拌を行った後、塗工することに
よって製造法された防眩処理層が上記の目的を達成でき
ることを見いだし本発明を完成するに至った。Accordingly, the present inventor has conducted intensive studies in view of the present situation. As a result, the present inventors have found that the production method is achieved by mixing and stirring the base resin and the filler with ultrasonic waves and then applying the resulting mixture. The inventor has found that the anti-glare treatment layer can achieve the above object, and has completed the present invention.
【0005】[0005]
【発明の実施の形態】以下、本発明について具体的に説
明する。本発明の方法により製造される防眩処理層は、
ベース樹脂と充填剤からなり、かかるベース樹脂と充填
剤からなる混合物を塗工・硬化させて防眩処理層とする
もので、本発明においては、かかるベース樹脂と充填剤
の混合物を得るにあたって、その両者を超音波で混合撹
拌を行うことを最大の特徴とするもので、該混合撹拌後
に混合物を塗工して、更に硬化させるものである。本発
明の方法をより具体的に説明する。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described specifically. Anti-glare treatment layer produced by the method of the present invention,
Consisting of a base resin and a filler, a mixture comprising the base resin and the filler is applied and cured to form an anti-glare treatment layer.In the present invention, in obtaining a mixture of the base resin and the filler, The greatest feature is that the two are mixed and stirred by ultrasonic waves, and the mixture is applied after the mixing and stirring, and is further cured. The method of the present invention will be described more specifically.
【0006】本発明に用いるベース樹脂としては特に限
定はされないが、硬化皮膜の透過率が88%以上(更に
は90〜100%)で、光沢度(入射角60°)が60
(%)以上(更には70〜100(%))のものが好ま
しく、かかる透過率が88%未満では、表示素子全体が
暗くなり、また光沢度(入射角60°)が60(%)未
満では、汚れ付着防止性が低下したりシロモヤが発生し
て好ましくない。かかるベース樹脂としては、具体的に
酢酸セルロース系樹脂、アクリルウレタン系樹脂、ポリ
エステルアクリレート系樹脂、エポキシアクリレート系
樹脂、セロファン系樹脂、ポリオレフィン系樹脂、ポリ
カーボネート系樹脂、ポリビニルアルコール系樹脂、ポ
リエーテルエーテルケトン系樹脂、メラミン系樹脂、ポ
リスルフォン系樹脂、フッ素系樹脂等を挙げることがで
き、表面硬度の点と表面に光散乱体を含有・分布させる
等の理由により、上記に記載した樹脂中の熱硬化型,紫
外線硬化型,電子線硬化型の樹脂又はこれらの処理を組
み合わせた型の樹脂が好ましく、更に工業的簡便性の点
では紫外線硬化型樹脂が実用的である。The base resin used in the present invention is not particularly limited, but the cured film has a transmittance of 88% or more (further 90 to 100%) and a glossiness (incident angle of 60 °) of 60%.
(%) Or more (more preferably 70 to 100 (%)). When the transmittance is less than 88%, the entire display element becomes dark, and the gloss (incident angle 60 °) is less than 60 (%). In this case, it is not preferable because the stain prevention property is reduced and slime is generated. Specific examples of such base resins include cellulose acetate resins, acrylic urethane resins, polyester acrylate resins, epoxy acrylate resins, cellophane resins, polyolefin resins, polycarbonate resins, polyvinyl alcohol resins, and polyether ether ketones. -Based resins, melamine-based resins, polysulfone-based resins, fluorine-based resins, and the like. Curable, ultraviolet-curable, electron beam-curable resins, or a combination of these treatments are preferred, and from the viewpoint of industrial simplicity, ultraviolet-curable resins are practical.
【0007】ここで使用する紫外線硬化型樹脂は、紫外
線を照射することにより光硬化するものであれば特に限
定されるものでなく、これらの樹脂は通常公知の光増感
剤とともに使用される。かかる樹脂としては、上記の中
でもアクリルウレタン系樹脂、ポリエステルアクリレー
ト系樹脂、エポキシアクリレート系樹脂等を挙げること
ができ、該アクリルウレタン系樹脂としては、一般にポ
リエステルポリオールにイソシアネートモノマーもしく
はプレポリマーを反応させ、得られた生成物に更に2−
ヒドロキシルエチル(メタ)アクリレート、2−ヒドロ
キシルプロピル(メタ)アクリレート等の水酸基を有す
るアクリレート、メタアクリレート系のモノマーを反応
させることにより得られる。該ポリエステルアクリレー
ト系樹脂としては、一般にポリエステルポリオールに、
2−ヒドロキシルエチル(メタ)アクリレート、2−ヒ
ドロキシルプロピル(メタ)アクリレート等の水酸基を
有する、アクリレート、メタアクリレート系のモノマー
を反応させることにより得られる。また該エポキシアク
リレート系樹脂としては、エポキシアクリレートをオリ
ゴマーとし、これに反応性希釈剤、光反応開始剤を添加
し反応させて得られる。反応性希釈剤としては、アクリ
ル酸エトキシエトキシエチル、アクリル酸テトラヒドロ
フリル、酢酸ブチルジューキゾール等が使用され、光反
応開始剤としては、ベンゾインエーテル誘導体、アセト
フェノン誘導体、オキシムケトン誘導体、ベンゾフェノ
ン誘導体、チオキサンケトン誘導体、アントラキノン誘
導体等が使用される。[0007] The ultraviolet-curable resin used here is not particularly limited as long as it can be photocured by irradiating ultraviolet rays, and these resins are usually used together with a known photosensitizer. Examples of such a resin include acrylic urethane-based resins, polyester acrylate-based resins, epoxy acrylate-based resins, and the like.The acrylic urethane-based resins generally include a polyester polyol reacted with an isocyanate monomer or a prepolymer, Further 2-
It is obtained by reacting an acrylate having a hydroxyl group such as hydroxylethyl (meth) acrylate or 2-hydroxylpropyl (meth) acrylate or a methacrylate monomer. As the polyester acrylate resin, generally, a polyester polyol,
It is obtained by reacting an acrylate or methacrylate monomer having a hydroxyl group such as 2-hydroxylethyl (meth) acrylate or 2-hydroxylpropyl (meth) acrylate. The epoxy acrylate-based resin is obtained by using epoxy acrylate as an oligomer, adding a reactive diluent and a photoreaction initiator to the oligomer, and causing the reaction to occur. As the reactive diluent, ethoxyethoxyethyl acrylate, tetrahydrofuryl acrylate, butyl juquizol acetate, etc. are used.As the photoreaction initiator, benzoin ether derivatives, acetophenone derivatives, oxime ketone derivatives, benzophenone derivatives, thioxane Ketone derivatives, anthraquinone derivatives and the like are used.
【0008】また、上記の如きベース樹脂に混合される
充填剤(フィラー)としても特に限定はされないが、透
過率が40%以上(フィラーの材質を10μmの厚み層
状物にした時の値で、更には50%〜100%)が好ま
しく、また屈折率が1.0〜1.7(更には1.3〜
1.6)のものが好ましい。かかる充填剤として、具体
的にはポリシロキサン化合物やフッ素化合物等が挙げら
れ、具体的にはポリシロキサン化合物としては、東芝シ
リコーン社製の『トスパール』、信越シリコーン社製の
『KMPシリーズ』及び『X−52シリーズ』、東レダ
ウコーニング社製の『トレフィル』、富士シリシア化学
社製の『サイシリア』、トクヤマ社製の『トクシール』
等を挙げることができ、好適には東芝シリコーン社製の
『トスパール』が用いられ、また、フッ素化合物として
は、旭アイシーアイフロロポリマーズ社製の『フルオ
ン』及び『ルブリカント』、三井デュポンフロロケミカ
ル社製の『ゾニール』、ダイキン工業社製の『ルブロ
ン』等を挙げることができ、好適には三井デュポンフロ
ロケミカル社製の『ゾニール』、ダイキン工業社製の
『ルブロン』が用いられる。The filler (filler) to be mixed with the base resin as described above is not particularly limited, but has a transmittance of 40% or more (when the material of the filler is a 10 μm thick layered material, Further, the refractive index is preferably 50% to 100%, and the refractive index is 1.0 to 1.7 (furthermore, 1.3 to 1.3).
1.6) is preferred. Specific examples of such a filler include a polysiloxane compound and a fluorine compound. Specific examples of the polysiloxane compound include "Tospearl" manufactured by Toshiba Silicone, "KMP Series" manufactured by Shin-Etsu Silicone, and " X-52 Series ", Toray Dow Corning's" Trefill ", Fuji Silysia Chemical's" Sycilia ", Tokuyama's" Toksil "
Preferably, "Tospearl" manufactured by Toshiba Silicone Co., Ltd. is used, and as the fluorine compound, "Fluon" and "Lubricant" manufactured by Asahi ICC Fluoropolymers Co., Ltd., and Mitsui DuPont Fluorochemical Co., Ltd. "Zonil" manufactured by Daikin Industries, Ltd., and "Rublon" manufactured by Daikin Industries, Ltd., and "Rublon" manufactured by Daikin Industries, Ltd. are preferably used.
【0009】また、これら充填剤の配合量は、ベース樹
脂100重量部に対して、0.001〜500重量部
(更には0.1〜100重量部)が好ましく、かかる含
有量が0.001重量部未満では防眩効果が得られず、
逆に500重量部を越えると表示品位の低下が見られて
好ましくない。本発明においては、上述の如く上記のベ
ース樹脂と充填剤を混合するにあたって、超音波撹拌を
行うことを最大の特徴とするもので、かかる撹拌につい
て、詳細に説明する。The amount of the filler is preferably 0.001 to 500 parts by weight (more preferably 0.1 to 100 parts by weight) with respect to 100 parts by weight of the base resin. If the amount is less than the weight part, the anti-glare effect cannot be obtained,
Conversely, when the amount exceeds 500 parts by weight, the display quality is deteriorated, which is not preferable. The most characteristic feature of the present invention is that, when the base resin and the filler are mixed as described above, ultrasonic stirring is performed, and such stirring will be described in detail.
【0010】超音波撹拌を行うにあたっては、特に限定
されないが、10kHz以上(更には10〜500kH
z)の発振周波数を用いることが好ましく、かかる発振
周波数が10kHz未満では十分な撹拌効果が得られず
好ましくない。また、このときの高周波出力は50W以
上(更には50〜1000W)が好ましく、かかる出力
が50W未満では撹拌効果が得られず好ましくない。か
かる撹拌機としては、具体的にシャープ社製の『UT−
104』、イウチ社製の『US−4』等の超音波撹拌機
を挙げることができる。In performing the ultrasonic stirring, there is no particular limitation, but 10 kHz or more (further 10 to 500 kHz)
It is preferable to use the oscillation frequency of z), and if the oscillation frequency is less than 10 kHz, a sufficient stirring effect cannot be obtained, which is not preferable. The high-frequency output at this time is preferably 50 W or more (more preferably 50 to 1000 W). If the output is less than 50 W, the stirring effect cannot be obtained, which is not preferable. As such a stirrer, specifically, "UT-" manufactured by Sharp Corporation
104 "and" US-4 "manufactured by Iuchi Corporation.
【0011】かかる超音波撹拌機を用いた撹拌の一例を
挙げれば、上記の配合物(樹脂、充填剤等)をマヨネー
ズ瓶等の容器の密封して、かかる超音波撹拌機中の溶液
温度を20〜30℃程度に保ちながら、撹拌を行うので
ある。超音波撹拌の後は、塗工されるのであるが、塗工
にあたっては、流延キャスト、ダイキャスト、スプレー
コート、グラビアコート、マイクログラビアコート、ロ
ールコート、バーコート、ダイコート、スピンコート、
ディップコート、静電気ヘリオフォンコーティング等の
公知の方法により製膜或いは塗布させ硬化させることに
より防眩処理層を得ることができる。かかる硬化にあた
っては、ベース樹脂として上記の如き紫外線硬化型樹脂
を用いた場合には、紫外線を照射することにより光硬化
させればよく、用いるベース樹脂の硬化方法を採用すれ
ばよい。As an example of stirring using such an ultrasonic stirrer, the above-mentioned compound (resin, filler, etc.) is sealed in a container such as a mayonnaise bottle and the temperature of the solution in the ultrasonic stirrer is reduced. The stirring is performed while maintaining the temperature at about 20 to 30 ° C. After ultrasonic agitation, it is applied, but in application, casting casting, die casting, spray coating, gravure coating, microgravure coating, roll coating, bar coating, die coating, spin coating,
An anti-glare treatment layer can be obtained by forming or applying a film by a known method such as dip coating or electrostatic heliophone coating and curing. In the case of using such an ultraviolet-curable resin as the base resin for the curing, the resin may be photocured by irradiating ultraviolet rays, and a method of curing the used base resin may be employed.
【0012】かくして防眩処理層が得られるわけである
が、かかる層の厚みは0.01〜1000μm(更には
0.1〜100μm)が好ましく、かかる厚みが0.0
1μm未満の時は、表面硬度に付随する硬く脆い力学物
性のため破壊や剥離がしやすく、厚みが1000μmを
越える時は、折れやすく割れやすいという欠点が生じて
好ましくない。Thus, an antiglare treatment layer is obtained. The thickness of such a layer is preferably 0.01 to 1000 μm (more preferably 0.1 to 100 μm), and the thickness is preferably 0.0 to 1000 μm.
When the thickness is less than 1 μm, the material tends to be easily broken or peeled off due to hard and brittle mechanical properties accompanying the surface hardness.
【0013】かくして得られた本発明の防眩処理層は、
液晶表示素子、プラズマ表示素子、CRT、EL(エレ
クトロルミネッサンス)等の各種表示素子(ディスプレ
イ)の表面に設けられて実用に供されるのであるが、該
防眩処理層の表示素子への付与装着の仕方については、
以下の4通りの方法がある。The antiglare treatment layer of the present invention thus obtained comprises:
It is provided on the surface of various display devices (displays) such as a liquid crystal display device, a plasma display device, a CRT, and an EL (electroluminescence), and is provided for practical use. About how to attach,
There are the following four methods.
【0014】(A)該防眩処理層を製膜されたフィルム
の形態にてアクリル系粘着剤により直接各ディスプレイ
の表示素子上に貼り合わせて構成する方法、(B)該防
眩処理層を製膜されたフィルムの形態にて他フィルム
(酢酸セルロース系樹脂やポリエステル系樹脂のフィル
ム)に貼り合わせた後に各ディスプレーの表示素子上に
貼り合わせて構成する方法、(C)該防眩処理層を他フ
ィルム(同上)に塗工した後に各ディスプレイの表示素
子上に貼り合わせて構成する方法、(D)該防眩処理層
を各ディスプレイの表示素子上に直接塗工して構成する
方法で、これらのいずれの方法でもよく、効果は変わら
ないが工業的な簡便さの点より、(C)の方法が実用的
である。(A) a method in which the anti-glare treatment layer is directly laminated on a display element of each display with an acrylic pressure-sensitive adhesive in the form of a formed film, and (B) the anti-glare treatment layer is A method in which the film is bonded to another film (a film of a cellulose acetate resin or a polyester resin) in the form of a formed film and then bonded on a display element of each display; (C) the anti-glare treatment layer Is applied to another film (same as above) and then bonded on the display element of each display, and (D) the antiglare treatment layer is applied directly on the display element of each display. Any of these methods may be used, and the effect is not changed, but the method (C) is practical from the viewpoint of industrial simplicity.
【0015】かくして、本発明の方法で得られた防眩処
理層は、表示品位が良好で、汚れ付着防止性にも優れた
防眩処理層で、ディスプレイ用の防眩処理層、その他窓
や壁等で光の散乱を必要とする用途にも有用である。Thus, the anti-glare treatment layer obtained by the method of the present invention is an anti-glare treatment layer having good display quality and excellent anti-staining properties, such as an anti-glare treatment layer for displays, other windows and It is also useful for applications that require light scattering on walls and the like.
【0016】[0016]
【実施例】次に実施例を挙げて更に詳しく説明する。 実施例1 紫外線硬化型アクリル系樹脂100重量部に平均粒子径
12μmのポリシロキサン系化合物(東芝シリコーン社
製、『トスパール3120』)50重量部と平均長さ7
μm、平均幅7μmの不定形フッ素化合物(ダイキン社
製の『ルブロンL−5』)50重量部を混合して、超音
波撹拌機(イウチ社製、『US−4』、発振周波数38
kHz)を用いて、80Wで、120分間混合撹拌を行
った後、三酢酸セルロースフィルム上に塗工して、10
0℃で2分間加熱して、その後紫外線照射して、厚み1
0μmの防眩処理層を得た。得られた防眩処理層を用い
て、以下の評価を行った。Next, the present invention will be described in more detail with reference to examples. Example 1 50 parts by weight of a polysiloxane compound having an average particle diameter of 12 μm (“Tospearl 3120” manufactured by Toshiba Silicone Co., Ltd.) and an average length of 7 were added to 100 parts by weight of an ultraviolet curable acrylic resin.
μm, 50 parts by weight of an amorphous fluorine compound having an average width of 7 μm (“Rublon L-5” manufactured by Daikin) were mixed, and an ultrasonic stirrer (“US-4” manufactured by Iuchi Co., Ltd., oscillation frequency 38) was mixed.
After mixing and stirring at 80 W for 120 minutes using a
Heat at 0 ° C. for 2 minutes, and then irradiate with ultraviolet light to obtain a thickness of 1
An antiglare layer having a thickness of 0 μm was obtained. The following evaluation was performed using the obtained anti-glare treatment layer.
【0017】かかる防眩処理層を有する三酢酸セルロー
スフィルムを、偏光板(日本合成化学工業社製、『PH
N18442S』)のマスキングフィルム側面(つまり
は非粘着面)に、マスキングフィルムを剥がした後に、
アクリル系粘着剤にて貼り合わせて偏光板を得た。一
方、TFT液晶表示素子(富士通社製、『UL−210
07』、21.3インチモデル、1280×1024ド
ット)の外側の偏光板を剥がし、得られた上記防眩処理
層を有する偏光板を貼り合わせ液晶表示素子を得た。A cellulose triacetate film having such an anti-glare treatment layer is coated on a polarizing plate (manufactured by Nippon Synthetic Chemical Industry Co., Ltd., “PH
N18442S "), after peeling off the masking film on the side of the masking film (that is, the non-adhesive surface),
A polarizing plate was obtained by bonding with an acrylic pressure-sensitive adhesive. On the other hand, a TFT liquid crystal display device (manufactured by Fujitsu Limited, "UL-210
07 ”, 21.3 inch model, 1280 × 1024 dots), and the resulting polarizing plate having the anti-glare layer was bonded to obtain a liquid crystal display device.
【0018】得られた液晶表示素子を使い、暗室に液晶
表示素子と100W蛍光灯1本を4m離して配置し、以
下の〜の評価を10人の評価人(パネラー)にて目
視評価を行った。尚、評価基準は10人のパネラーの
内、8人以上が良好と評価したものを○とし、そうでな
いものを×とした。 写りこみ:液晶表示素子の画面表面の、蛍光灯の写り
こみの状況を観察し、見やすさを評価した。 ギラツキ:液晶表示素子の画面表面の防眩処理層フィ
ラーによる乱視的局所散乱光の明欠陥の状況(つまりは
微小領域や各画素間での輝度ムラの状況)を観察し、見
やすさを評価した。 シロモヤ:液晶表示素子の画面表面の防眩処理層フィ
ラーによる乱視的局所散乱光の暗欠陥の状況(つまりは
微小領域や各画 素間での白化ムラの状況)を観察し、
見やすさを評価した。 目の疲れ:液晶表示素子を用い、ワープロ作業を連続
12時間にわたって行った後に、評価人の目の疲れを評
価した。 汚れ除去性:液晶表示素子の画面表面の防眩処理層を
指の指紋で汚した後、3日間放置した後、汚れをイソプ
ロピルアルコール20%、水80%のクリーナー液を浸
した脱脂綿により1回拭き除去し、表示素子の表面の汚
れの状況を観察した。 汚れ除去後の視認性:液晶表示素子の画面表面の防眩
処理層を指の指紋で汚した後、3日間放置した後、汚れ
をイソプロピルアルコール20%アセトン20%水60
%のクリーナー液を浸した脱脂綿により1回拭き除去し
た後、上記の写りこみ、ギラツキ、シロモヤを総合評価
した。 汚れ除去後の目の疲れ:液晶表示素子の画面表面の防
眩処理層を指の指紋で汚した後、3日間放置した後、汚
れをイソプロピルアルコール20%アセトン20%水6
0%のクリーナー液を浸した脱脂綿により1回拭き除去
した後、ワープロ作業を連続12時間にわたって行った
後に、評価人の目の疲れを評価した。Using the obtained liquid crystal display device, the liquid crystal display device and one 100 W fluorescent lamp were placed in a dark room at a distance of 4 m, and the following evaluations were visually evaluated by 10 evaluators (panels). Was. In addition, the evaluation criteria were evaluated as good when 8 or more panelists out of 10 panelists evaluated it as good, and as poor when not. Reflection: The state of reflection of the fluorescent light on the screen surface of the liquid crystal display element was observed, and the visibility was evaluated. Glare: The state of the bright defect of astigmatic local scattered light due to the filler of the anti-glare treatment layer on the screen surface of the liquid crystal display element (that is, the state of luminance unevenness between minute pixels and between pixels) was observed, and the visibility was evaluated. . Shiromoya: Observing the state of dark defects of astigmatic local scattered light due to the anti-glare treatment layer filler on the screen surface of the liquid crystal display element (that is, the state of whitening unevenness in minute areas and between pixels)
The visibility was evaluated. Eye fatigue: Using a liquid crystal display device, after performing a word processing operation for 12 hours continuously, the eyestrain of the evaluator was evaluated. Stain removal property: The anti-glare treatment layer on the screen surface of the liquid crystal display element is stained with a finger fingerprint, and then left for 3 days. The stain is washed once with absorbent cotton soaked with a cleaner solution of 20% isopropyl alcohol and 80% water. After wiping off, the state of contamination on the surface of the display element was observed. Visibility after removing dirt: After the anti-glare treatment layer on the screen surface of the liquid crystal display element is stained with fingerprints of a finger, and left for 3 days, the dirt is removed from isopropyl alcohol 20% acetone 20% water 60.
After wiping and removing once with absorbent cotton soaked with a% cleaner solution, the above-mentioned reflection, glare and shiromoya were comprehensively evaluated. Eye fatigue after removing stains: After the anti-glare treatment layer on the screen surface of the liquid crystal display element is stained with finger prints and allowed to stand for 3 days, the stains are washed with isopropyl alcohol 20% acetone 20% water 6
After wiping off once with absorbent cotton soaked with 0% cleaner solution, a word processing operation was performed continuously for 12 hours, and then the eyestrain of the evaluator was evaluated.
【0019】実施例2 実施例1において、超音波撹拌の条件を高周波電力を8
0Wから200Wとした以外は同様に行って、防眩処理
層を得て、同様に評価を行った。Example 2 In Example 1, the condition of the ultrasonic stirring was changed to a high frequency power of 8
An anti-glare treatment layer was obtained in the same manner except that the power was changed from 0 W to 200 W, and the evaluation was similarly performed.
【0020】実施例3 実施例1において、超音波撹拌の条件を発振周波数を3
8kHzから40kHzとした以外は同様に行って、防
眩処理層を得て、同様に評価を行った。Example 3 In Example 1, the condition of the ultrasonic stirring was changed to an oscillation frequency of 3
An anti-glare treatment layer was obtained in the same manner except that the frequency was changed from 8 kHz to 40 kHz, and the same evaluation was performed.
【0021】実施例4 実施例1において、充填剤を三井デュポンフロロケミカ
ル社製の『ゾニールTLP−10F−1』(平均粒子径
3μm)とした以外は同様に行って、防眩処理層を得
て、同様に評価を行った。Example 4 An antiglare treatment layer was obtained in the same manner as in Example 1 except that the filler was changed to “Zonyl TLP-10F-1” (average particle diameter: 3 μm) manufactured by Du Pont-Mitsui Fluorochemicals. And evaluated similarly.
【0022】実施例5 実施例1において、充填剤の配合量をそれぞれ25重量
部ずつとした以外は同様に行って、眩処理層を得て、同
様に評価を行った。Example 5 A glaze-treated layer was obtained in the same manner as in Example 1, except that the blending amount of the filler was changed to 25 parts by weight.
【0023】比較例1 実施例1において、超音波撹拌機に変えて、スクリュー
型撹拌機を用いてベース樹脂と充填剤の混合撹拌を行っ
た以外は同様に行って、防眩処理層を得て、同様に評価
を行った。実施例と比較例の評価結果を表1に示す。Comparative Example 1 An antiglare treatment layer was obtained in the same manner as in Example 1, except that mixing and stirring of the base resin and the filler were performed using a screw-type stirrer instead of the ultrasonic stirrer. And evaluated similarly. Table 1 shows the evaluation results of the examples and the comparative examples.
【0024】[0024]
【表1】 評 価 項 目 実施例1 ○ ○ ○ ○ ○ ○ ○ 〃 2 ○ ○ ○ ○ ○ ○ ○ 〃 3 ○ ○ ○ ○ ○ ○ ○ 〃 4 ○ ○ ○ ○ ○ ○ ○ 〃 5 ○ ○ ○ ○ ○ ○ ○ 比較例1 × × × × × × × [Table 1]Evaluation item Example 1 ○ ○ ○ ○ ○ ○ ○ 〃 2 ○ ○ ○ ○ ○ ○ ○ 〃 3 ○ ○ ○ ○ ○ ○ ○ ○ 4 4 ○ ○ ○ ○ ○ ○ ○〃 5 ○ ○ ○ ○ ○ ○ ○ Comparative Example 1 × × × × × × ×
【0025】[0025]
【発明の効果】本発明においては、防眩処理層の製造法
にあたり、ベース樹脂と充填剤を超音波により混合撹拌
を行っているため、(1280×1024ドットという
画素が非常に多い表示面内の)表示品位が良好で、汚れ
付着防止性にも優れた防眩処理層を得ることができ、ワ
ープロ、パソコン、テレビジョン、カーナビゲーション
等のディスプレー用の防眩処理層やその他窓や壁等で光
の散乱を必要とする用途にも有用である。According to the present invention, since the base resin and the filler are mixed and agitated by ultrasonic waves in the method of manufacturing the anti-glare treatment layer, (1280 × 1024 dots) in the display surface having a very large number of pixels. A) An anti-glare treatment layer having good display quality and excellent anti-staining properties can be obtained, and an anti-glare treatment layer for displays such as word processors, personal computers, televisions, car navigation systems, and other windows and walls. It is also useful for applications requiring light scattering.
Claims (5)
撹拌を行った後、塗工することを特徴とする防眩処理層
の製造法。1. A method for producing an anti-glare treatment layer, comprising mixing and stirring a base resin and a filler by ultrasonic waves, and then applying the mixture.
ことを特徴とする請求項1記載の防眩処理層の製造法。2. The method of claim 1, wherein the high frequency power of the ultrasonic wave is 50 W or more.
あることを特徴とする請求項1または2記載の防眩処理
層の製造法。3. The method for producing an anti-glare treatment layer according to claim 1, wherein the oscillation frequency of the ultrasonic wave is 10 kHz or more.
を0.001〜500重量部混合することを特徴とする
請求項1〜3いずれか記載の防眩処理層の製造法。4. The method for producing an antiglare layer according to claim 1, wherein 0.001 to 500 parts by weight of a filler is mixed with respect to 100 parts by weight of the base resin.
またはフッ素化合物であることを特徴とする請求項1〜
4いずれか記載の防眩処理層の製造法。5. The method according to claim 1, wherein the filler is a polysiloxane compound and / or
Or a fluorine compound.
4. The method for producing an anti-glare treatment layer according to any one of 4.
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JP28780797A JP3929569B2 (en) | 1997-10-02 | 1997-10-02 | Manufacturing method of antiglare treatment layer |
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ID=17722018
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Citations (7)
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---|---|---|---|---|
JPS61254637A (en) * | 1985-05-02 | 1986-11-12 | Toyobo Co Ltd | Slippery transparent film and production thereof |
JPH01172801A (en) * | 1987-12-28 | 1989-07-07 | Asahi Chem Ind Co Ltd | Light diffusion plate having light transmittability |
JPH0616851A (en) * | 1991-11-25 | 1994-01-25 | Dainippon Printing Co Ltd | Mar-resistant antiglaring film, polarizing plate and production thereof |
JPH0798452A (en) * | 1993-09-28 | 1995-04-11 | Toppan Printing Co Ltd | Reflection type liquid crystal display device |
JPH07104272A (en) * | 1993-09-29 | 1995-04-21 | Toppan Printing Co Ltd | Reflection type liquid crystal display device |
JPH07290652A (en) * | 1994-04-20 | 1995-11-07 | Dainippon Printing Co Ltd | Reflection preventing film having excellent optical characteristics and production thereof |
JPH09220518A (en) * | 1995-12-15 | 1997-08-26 | Sekisui Chem Co Ltd | Article bearing water-repelling coating film and manufacture thereof |
-
1997
- 1997-10-02 JP JP28780797A patent/JP3929569B2/en not_active Expired - Fee Related
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61254637A (en) * | 1985-05-02 | 1986-11-12 | Toyobo Co Ltd | Slippery transparent film and production thereof |
JPH01172801A (en) * | 1987-12-28 | 1989-07-07 | Asahi Chem Ind Co Ltd | Light diffusion plate having light transmittability |
JPH0616851A (en) * | 1991-11-25 | 1994-01-25 | Dainippon Printing Co Ltd | Mar-resistant antiglaring film, polarizing plate and production thereof |
JPH0798452A (en) * | 1993-09-28 | 1995-04-11 | Toppan Printing Co Ltd | Reflection type liquid crystal display device |
JPH07104272A (en) * | 1993-09-29 | 1995-04-21 | Toppan Printing Co Ltd | Reflection type liquid crystal display device |
JPH07290652A (en) * | 1994-04-20 | 1995-11-07 | Dainippon Printing Co Ltd | Reflection preventing film having excellent optical characteristics and production thereof |
JPH09220518A (en) * | 1995-12-15 | 1997-08-26 | Sekisui Chem Co Ltd | Article bearing water-repelling coating film and manufacture thereof |
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