JPWO2019239817A1 - 粘着剤組成物、及びこれを用いた積層フィルム - Google Patents
粘着剤組成物、及びこれを用いた積層フィルム Download PDFInfo
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- JPWO2019239817A1 JPWO2019239817A1 JP2019548075A JP2019548075A JPWO2019239817A1 JP WO2019239817 A1 JPWO2019239817 A1 JP WO2019239817A1 JP 2019548075 A JP2019548075 A JP 2019548075A JP 2019548075 A JP2019548075 A JP 2019548075A JP WO2019239817 A1 JPWO2019239817 A1 JP WO2019239817A1
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- sensitive adhesive
- pressure
- meth
- acrylate
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- GVIIRWAJDFKJMJ-UHFFFAOYSA-N propan-2-yl 3-oxobutanoate Chemical compound CC(C)OC(=O)CC(C)=O GVIIRWAJDFKJMJ-UHFFFAOYSA-N 0.000 description 1
- CYIRLFJPTCUCJB-UHFFFAOYSA-N propyl 2-methoxypropanoate Chemical compound CCCOC(=O)C(C)OC CYIRLFJPTCUCJB-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 229920006352 transparent thermoplastic Polymers 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229940042596 viscoat Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/08—Macromolecular additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J201/00—Adhesives based on unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/318—Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
- Laminated Bodies (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
測定装置:東ソー株式会社製「HLC−8220 GPC」、
カラム:東ソー株式会社製ガードカラム「HHR−H」(6.0mmI.D.×4cm)+東ソー株式会社製「TSK−GEL GMHHR−N」(7.8mmI.D.×30cm)+東ソー株式会社製「TSK−GEL GMHHR−N」(7.8mmI.D.×30cm)+東ソー株式会社製「TSK−GEL GMHHR−N」(7.8mmI.D.×30cm)+東ソー株式会社製「TSK−GEL GMHHR−N」(7.8mmI.D.×30cm)
検出器:ELSD(オルテックジャパン株式会社製「ELSD2000」)
データ処理:東ソー株式会社製「GPC−8020モデルIIデータ解析バージョン4.30」
測定条件:カラム温度 40℃
展開溶媒 テトラヒドロフラン(THF)
流速 1.0ml/分
試料:固形分換算で1.0質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(5μl)。
標準試料:前記「GPC−8020モデルIIデータ解析バージョン4.30」の測定マニュアルに準拠して、分子量が既知の下記の単分散ポリスチレンを用いた。
東ソー株式会社製「A−500」
東ソー株式会社製「A−1000」
東ソー株式会社製「A-2500」
東ソー株式会社製「A−5000」
東ソー株式会社製「F−1」
東ソー株式会社製「F−2」
東ソー株式会社製「F−4」
東ソー株式会社製「F−10」
東ソー株式会社製「F−20」
東ソー株式会社製「F−40」
東ソー株式会社製「F−80」
東ソー株式会社製「F−128」
東ソー株式会社製「F−288」
東ソー株式会社製「F−550」
で表される含フッ素ウレタン(メタ)アクリレートであると、後述する粘着剤(B)、特にはアクリル系粘着剤(b1)又はウレタン系粘着剤(b2)との相溶性が良好であって、粘着層を形成したときの透明性も維持でき、また粘着力の調整も容易となる観点から好ましいものである。
で表される化合物(x2−1)、又は下記一般式(4)
R1O−R’’−OR1 (4)
〔式中、R1は同一又は異なる(メタ)アクリロイル基であり、R’’はオキシアルキレン鎖である。〕
で表される化合物(x2−2)が挙げられる。尚、本発明において(メタ)アクリロイル基はアクリロイル基とメタクリロイル基の一方あるいはその混合物の総称として用いる。
ガラス板に、得られた積層フィルムをそれぞれ2kgfローラー1往復で圧着して貼り付け、貼付してから24時間経過後に、テクスチャーアナライザー TA.XT plus(ステーブルマイクロシステムズ社製)を用い、粘着力を測定した。測定条件は、下記の通りである。
・剥離速度:300mm/min、2400mm/min
・剥離方向:180°
・試料サイズ:25mm×70mm
得られた積層フィルムを25mm×120mmに切断し、真中で湾曲させてガラス板に載せて手を離す。真中から両側50mmまでが濡れるまでの時間を計測する。
粘着力測定時と同様にして、得られた積層フィルムをガラス板に貼り付けた。40℃で1週間保存した後にフィルムを剥がし、糊残りを下記の基準に従って評価した。
○:ガラス板に対して糊残りしない
×:ガラス板の一部に糊残りする
撹拌装置、温度計、冷却管、滴下装置を備えたガラスフラスコに、下記式(1−1−1)で表されるエチレンオキシドとプロピレンオキシドとのブロック共重合体30g、アクリル酸2.8g、溶媒としてトルエン64g、重合禁止剤としてフェノチアジン0.03g及び触媒としてメタンスルホン酸0.6gを仕込み、空気気流下にて攪拌を開始し、120℃へ加熱、還流脱水した。0.63gの脱水を確認後、65℃へ冷却し、トリエチルアミンにて中和した。中和後、85℃へ昇温し、イオン交換水2.3gを加え、分液、下層抜き出しを行った。下層のpHを測定し、pHが7以上となるまで、洗浄操作を繰り返し実施した。冷却後、トルエンにて希釈し、下記式(1−1−1)〜(1−1−3)で表される3種の混合物(1−1)を55質量%含むトルエン溶液を得た。
ガラスフラスコにトルエン300.00gを加え、窒素気流中、撹拌しながら105℃に昇温した。ついで、2−(パーフルオロヘキシル)エチルアクリレート14.25g、混合物(1−1)194.73g、トルエン99.05g、開始剤パーブチルO(日油株式会社製)11.25gを混合させた滴下液、ポリシロキサン結合を有するモノメタクリレート化合物(JNC株式会社製、サイラプレーンFM−0721K)28.65gをトルエン30.00gに溶解させた滴下液をそれぞれ滴下装置にセットし、フラスコ内を105℃に保ちながら両滴下液を4時間かけて滴下した。滴下終了後、105℃で10時間撹拌した。反応終了後、溶媒を留去し、含フッ素化合物(1)を得た。この共重合体をGPCにより分析した結果、重量平均分子量Mw=16,200であった。
含フッ素化合物(1)の合成において、2−(パーフルオロヘキシル)エチルアクリレートを42.90g用い、サイラプレーンFM−0721Kを加えなかった以外は、含フッ素化合物(1)と同様に合成し、含フッ素化合物(2)を得た。この共重合体をGPCにより分析した結果、重量平均分子量Mw=12,700であった。
ガラスフラスコにメチルエチルケトン(MEK)225.00gを加え、窒素気流中、撹拌しながら80℃に昇温した。ついで、2−(パーフルオロヘキシル)エチルアクリレート22.50g、ポリエチレングリコールモノアクリレート(日油株式会社製、ブレンマーAE−400)82.65g、MEK150.00g、開始剤2,2’−アゾビス(イソ酪酸)ジメチル(和光純薬工業株式会社製、MAIB)7.50gを混合させた滴下液、ポリシロキサン結合を有するモノメタクリレート化合物(JNC株式会社製、サイラプレーンFM−0721K)44.85gをMEK75.00gに溶解させた滴下液をそれぞれ滴下装置にセットし、フラスコ内を80℃に保ちながら両滴下液を4時間かけて滴下した。滴下終了後、80℃で2時間撹拌した。その後、MAIB0.75gとMEK7.50gの混合液をフラスコ内を80℃に保ちながら15分かけて滴下した。滴下終了後、80℃で9時間撹拌した。30℃に冷却後、MEKにて希釈し、含フッ素化合物(3)を25質量%含む溶液を得た。この共重合体をGPCにより分析した結果、重量平均分子量Mw=9,100であった。
含フッ素化合物(3)の合成において、2−(パーフルオロヘキシル)エチルアクリレートを67.35g用い、サイラプレーンFM−0721Kを加えなかった以外は、含フッ素化合物(3)と同様に合成し、含フッ素化合物(4)を25質量%含む溶液を得た。この共重合体をGPCにより分析した結果、重量平均分子量Mw=9,600であった。
化合物(2−2)83.0g、ポリシロキサン結合を有するモノメタクリレート化合物(JNC株式会社製、サイラプレーンFM−0721K)11.8g、混合物(1−1)22.5g、メタクリル酸メチル116.0g、メタクリル酸2-ヒドロキシエチル10.0g、MIBK298.3gを混合して混合液Aを調整した。混合液Aの25質量%分とMIBK94.9g、開始剤パーブチルO(日油株式会社製)5.0gをガラスフラスコに仕込み、窒素雰囲気下で30分かけて80℃まで昇温した。昇温後、混合物Aの75質量%分にMIBK30.0gとパーブチルO15.0gを加えて滴下液を調整して、80℃で3時間かけて滴下した。滴下終了後、80℃で3時間撹拌した後、110℃で2.5時間撹拌した。その後、固形分65%まで脱溶剤して、MIBKで希釈して含フッ素化合物(5)を50質量%含む溶液を得た。この共重合体をGPCにより分析した結果、重量平均分子量Mw=18,600であった。
含フッ素化合物(5)合成時の混合液Aにおいて、化合物(2−2)を2−(パーフルオロヘキシル)エチルメタクリレート49.80gに置換え、MIBKを331.52g用いた以外は、含フッ素化合物(5)と同様に合成し、含フッ素化合物(6)を50質量%含む溶液を得た。この共重合体をGPCにより分析した結果、重量平均分子量Mw=16,300であった。
含フッ素化合物(5)合成時の混合液Aにおいて、サイラプレーンFM−0721Kをポリシロキサン結合を有するモノメタクリレート化合物(JNC株式会社製、サイラプレーンFM−0711)11.80gに置換えた以外は、含フッ素化合物(5)と同様に合成し、含フッ素化合物(7)を50質量%含む溶液を得た。この共重合体をGPCにより分析した結果、重量平均分子量Mw=17,200であった。
含フッ素化合物(5)合成時の混合液Aにおいて、化合物(2−2)を102.67g用い、MIBKを290.45g用い、サイラプレーンFM−0721Kを加えなかった以外は、含フッ素化合物(5)と同様に合成し、含フッ素化合物(8)を50質量%含む溶液を得た。この共重合体をGPCにより分析した結果、重量平均分子量Mw=17,200であった。
アクリル系粘着剤(CT−3088:DIC社製)の固形分100部に対して、硬化剤(架橋剤)としてD−100K(DIC社製)を2.9部および得られた含フッ素化合物(1)を固形分0.5部添加し、メチルエチルケトンで固形分が35%となるように希釈し、充分に混合して粘着剤組成物を得た。該粘着剤組成物を粘着層厚が20μmになるように、基材である50μm厚のポリエステルフィルムのコロナー処理面に、自動塗工装置バーコーター(PI−1210:テスター社製)を用いて直接塗工した。その後、85℃で3分間乾燥させて粘着層を形成した後、該粘着層にシリコーンコートされた38μm厚のポリエステルフィルムセパレーターを被覆して、積層フィルムを作製した。更に、上記で得た積層フィルムを、40℃で3日間養生し、評価試験の試料とした。評価結果を表1に示した。
含フッ素化合物(1)を用いなかった以外は、実施例1と同様にして評価試験の試料を作製した。評価結果を表1に示した。
含フッ素化合物(1)を含フッ素化合物(2)に置き換えた以外は、実施例1と同様にして評価試験の試料を作製した。評価結果を表1に示した。
アクリル系粘着剤(CT−3088:DIC社製)の固形分100部に対して、硬化剤(架橋剤)としてD−100K(DIC社製)を2.9部および得られた含フッ素化合物(3)を固形分0.5部添加し、メチルエチルケトンで固形分が35%となるように希釈し、充分に混合して粘着剤組成物を得た。該粘着剤組成物を粘着層厚が20μmになるように、基材である50μm厚のポリエステルフィルムのコロナー処理面に、自動塗工装置バーコーター(PI−1210:テスター社製)を用いて直接塗工した。その後、85℃で3分間乾燥させて粘着層を形成した後、該粘着層にシリコーンコートされた38μm厚のポリエステルフィルムセパレーターを被覆して、積層フィルムを作製した。更に、上記で得た積層フィルムを、40℃で3日間養生し、評価試験の試料とした。評価結果を表2に示した。
含フッ素化合物(3)を用いなかった以外は、実施例2と同様にして評価試験の試料を作製した。評価結果を表2に示した。
含フッ素化合物(3)を含フッ素化合物(4)に置き換えた以外は、実施例2と同様にして評価試験の試料を作製した。評価結果を表2に示した。
ウレタン系粘着剤(APU−505:DIC社製)の固形分100部に対して、硬化剤(架橋剤)としてD−100K(DIC社製)を5.5部および得られた含フッ素化合物(5)を固形分0.5部添加し、酢酸エチルで固形分が50%となるように希釈し、充分に混合して粘着剤組成物を得た。該粘着剤組成物を粘着層厚が60μmになるように、基材である50μm厚のポリエステルフィルムのコロナー処理面に、自動塗工装置バーコーター(PI−1210:テスター社製)を用いて直接塗工した。その後、60℃で3分間、100℃で3分間乾燥させて粘着層を形成した後、該粘着層にシリコーンコートされた38μm厚のポリエステルフィルムセパレーターを被覆して、積層フィルムを作製した。更に、上記で得た積層フィルムを、40℃で3日間養生し、評価試験の試料とした。評価結果を表3に示した。
含フッ素化合物(5)を含フッ素化合物(6)に置き換えた以外は、実施例3と同様にして評価試験の試料を作製した。評価結果を表3に示した。
含フッ素化合物(5)を含フッ素化合物(7)に置き換えた以外は、実施例3と同様にして評価試験の試料を作製した。評価結果を表3に示した。
含フッ素化合物(5)を用いなかった以外は、実施例3と同様にして評価試験の試料を作製した。評価結果を表4に示した。
含フッ素化合物(5)を含フッ素化合物(8)に置き換えた以外は、実施例3と同様にして評価試験の試料を作製した。評価結果を表4に示した。
Claims (10)
- 炭素数1〜6のフッ素化アルキル基(a1)とポリオキシアルキレン鎖(a2)とシリコーン鎖(a3)とを有する含フッ素化合物(A)と、粘着剤(B)とを含有する粘着剤組成物。
- 前記含フッ素化合物(A)のフッ素原子含有率が1〜50質量%の範囲である請求項1記載の粘着剤組成物。
- 前記含フッ素化合物(A)の重量平均分子量が3,000〜300,000の範囲である請求項1又は2記載の粘着剤組成物。
- 前記ポリオキシアルキレン鎖(a2)が、ポリオキシエチレン鎖(a2−1)及び/またはポリオキシプロピレン鎖(a2−2)であり、繰り返し数の平均値が2〜50の範囲である請求項1〜3の何れか1項記載の粘着剤組成物。
- 前記シリコーン鎖(a3)が分子量200〜50,000の範囲である請求項1〜4の何れか1項記載の粘着剤組成物。
- 前記粘着剤(B)がアクリル系粘着剤(b1)又はウレタン系粘着剤(b2)である請求項1〜5の何れか1項記載の粘着剤組成物。
- 前記含フッ素化合物(A)の含有率が、粘着剤組成物の固形分中、0.01〜20質量%である請求項1〜6の何れか1項記載の粘着剤組成物。
- 前記含フッ素化合物(A)が、フッ素化アルキル基含有エチレン性不飽和単量体(x1)と、ポリオキシアルキレン鎖含有エチレン性不飽和単量体(x2)と、シリコーン鎖含有エチレン性不飽和単量体(x3)とを必須の原料とする共重合体である請求項1〜7の何れか1項記載の粘着剤組成物。
- 請求項1〜8の何れか1項記載の粘着剤組成物の粘着層と基材層とを有することを特徴とする積層フィルム。
- 光学部材の表面保護フィルムである請求項9記載の積層フィルム。
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