JP6832246B2 - 有機el表示装置用粘着剤組成物、有機el表示装置用粘着剤層、有機el表示装置用粘着剤層付き偏光フィルム、および有機el表示装置 - Google Patents
有機el表示装置用粘着剤組成物、有機el表示装置用粘着剤層、有機el表示装置用粘着剤層付き偏光フィルム、および有機el表示装置 Download PDFInfo
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- JP6832246B2 JP6832246B2 JP2017122122A JP2017122122A JP6832246B2 JP 6832246 B2 JP6832246 B2 JP 6832246B2 JP 2017122122 A JP2017122122 A JP 2017122122A JP 2017122122 A JP2017122122 A JP 2017122122A JP 6832246 B2 JP6832246 B2 JP 6832246B2
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- sensitive adhesive
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- LUUMBHMWFNNZPH-UHFFFAOYSA-N tris(3,5-ditert-butyl-4-hydroxyphenyl) phosphite Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(OP(OC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)OC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 LUUMBHMWFNNZPH-UHFFFAOYSA-N 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
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- C09J7/38—Pressure-sensitive adhesives [PSA]
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Description
前記第1粘着剤層、第2粘着剤層、および第3粘着剤層のうち、少なくとも一つの粘着剤層が、前記有機EL表示装置用粘着剤層であることが好ましい。
本発明の有機EL表示装置用粘着剤組成物は、ベースポリマー、ラジカル発生剤、並びに、分子構造中の水酸基が0〜3個である紫外線吸収剤(a)および吸収スペクトルの最大吸収波長が380〜430nmの波長領域に存在する色素化合物(b)から選ばれる少なくとも1種の化合物(A)含むことを特徴とする。
前記(メタ)アクリル系ポリマーは、通常、モノマー単位として、アルキル(メタ)アクリレートを主成分として含有する。なお、(メタ)アクリレートはアクリレートおよび/またはメタクリレートをいい、本発明の(メタ)とは同様の意味である。
本発明の粘着剤組成物に配合されるラジカル発生剤としては、前記(メタ)アクリル系ポリマーの製造の際に用いたラジカル重合開始剤を例示することができる。前記ラジカル重合開始剤のなかでも、粘着剤組成物に配合されるラジカル発生剤は過酸化物が好ましい。
本発明の粘着剤組成物には、分子構造中の水酸基が0〜3個である紫外線吸収剤(a)および吸収スペクトルの最大吸収波長が380〜430nmの波長領域に存在する色素化合物(b)から選ばれる少なくとも1種の化合物(A)を配合する。前記紫外線吸収剤(a)に関して、分子構造中の水酸基が0〜3個であることは、前述のように、ラジカルを失活させる原因の水素供与性基を少なくして、ラジカル発生剤の架橋阻害を抑制するうえで有効である。また、水酸基が0〜3個であることは、例えば、水酸基と反応性を有するイソシアネート系架橋剤等を配合する場合には、当該架橋剤による架橋阻害を抑制するうえでも好ましい。また、前記紫外線吸収剤(a)は、水酸基以外のラジカルを失活させる水素供与性基として、フェニル基を分子構造中に有さない化合物を使用することが好ましい。なお、分子構造中に有しないフェニル基は、置換基を有しないフェニル(−C6H5)を示し、置換基を有するフェニル基やフェニレン基等を排除するものではない。また、前記色素化合物(b)についても、前記紫外線吸収剤(a)と同様に、ラジカル発生剤の架橋阻害を防ぐ観点で、分子構造中に水酸基やフェニル基などの水素供与性基が少ない(水酸基は0〜3個)または有しない化合物であることが好ましい。
本発明においては、このような色素化合物(b)と前記紫外線吸収剤(a2)を組み合わせて用いることで、有機EL素子の発光に影響しない領域(波長380nm〜430nm)の光を十分に吸収することができ、かつ、有機EL素子の発光領域(430nmよりも長波長側)は十分に透過することができるものであり、その結果、有機EL素子の外光による劣化を抑制することができる。前記紫外線吸収剤(a)および色素化合物(b)を併用する場合には、前記紫外線吸収剤(a)および色素化合物(b)の合計量が前記化合物(A)としての配合量の範囲内なるように制御するのが好ましい。前記紫外線吸収剤(a)は、ベースポリマー(例えば、(メタ)アクリル系ポリマー)100重量部に対して、0.1〜10重量部であることが好ましく、0.1〜5重量部であることが好ましく、0.5〜3重量部であることがより好ましい。前記色素化合物(b)は、ベースポリマー(例えば、(メタ)アクリル系ポリマー)100重量部に対して、0.1〜10重量部程度であることが好ましく、0.1〜5重量部程度であることがより好ましく、0.5〜3重量部であることがより好ましい。
紫外線吸収剤(a)は、分子構造中の水酸基が0〜3個であれば、特に限定されないが、例えば、トリアジン系紫外線吸収剤、ベンゾトリアゾール系紫外線吸収剤、ベンゾフェノン系紫外線吸収剤、オキシベンゾフェノン系紫外線吸収剤、サリチル酸エステル系紫外線吸収剤、シアノアクリレート系紫外線吸収剤等を挙げることができ、これらを1種単独でまたは2種以上を組み合わせて用いることができる。これらの中でも、トリアジン系紫外線吸収剤、ベンゾトリアゾール系紫外線吸収剤が好ましく、1分子中にヒドロキシル基を2個以下有するトリアジン系紫外線吸収剤、および、1分子中にベンゾトリアゾール骨格を1個有するベンゾトリアゾール系紫外線吸収剤からなる群から選択される少なくとも1種の紫外線吸収剤であることが、アクリル系粘着剤組成物の形成に用いられるモノマーへの溶解性が良好であり、かつ、波長380nm付近での紫外線吸収能力が高いため好ましい。
色素化合物(b)は、吸収スペクトルの最大吸収波長が380〜430nmの波長領域に存在する化合物であればよく、特に限定されるものではないが、前記紫外線吸収剤(a)と同様に、分子構造中に水酸基やフェニル基などの水素供与性基が少ないまたは有しない化合物であることが好ましい。なお、最大吸収波長とは、300〜460nmの波長領域での分光吸収スペクトルにおいて、複数の吸収極大が存在する場合には、その中で最大の吸光度を示す吸収極大波長を意味するものである。
<半値幅の測定方法>
色素化合物(b)の半値幅は、紫外可視分光光度計(U−4100、(株)日立ハイテクサイエンス製)を使用し、以下の条件で色素化合物の溶液の透過吸光スペクトルから測定した。最大吸収波長の吸光度が1.0となるよう濃度を調整して測定した分光スペクトルから、ピーク値の50%になる2点間の波長の間隔(半値全幅)をその色素化合物の半値幅とした。
(測定条件)
溶媒:トルエンまたはクロロホルム
セル:石英セル
光路長:10mm
けい皮酸系化合物としては、SOM−5−0106(商品名、吸収スペクトルの最大吸収波長:416nm、半値幅:50nm、オリエント化学工業(株)製)を、ポルフィリン系化合物としては、FDB−001(商品名、吸収スペクトルの最大吸収波長:420nm、半値幅:14nm、山田化学工業(株)製)を、シアニン系化合物としては、メロシアニン化合物(商品名:FDB−009、吸収スペクトルの最大吸収波長:394nm、半値幅:43nm、山田化学工業(株)製)、ポリメチン化合物(商品名:DAA−247、吸収スペクトルの最大吸収波長:389nm、半値幅:49.5nm、山田化学工業(株)製)等を挙げることができ、中でも、架橋阻害抑制と光学信頼性の観点から、前記シアニン系化合物が好ましく、ポリメチン化合物が特に好ましい。
本発明の粘着剤組成物に配合される酸化防止剤を配合することができる。酸化防止剤は、ラジカル発生剤から発生するラジカルの酸素による阻害を防止して、安定なゲル分率(架橋度)を確保することができ、また、粘着剤層に適用する離型フィルム(セパレータ)の剥離力の上昇を抑制しながら、ゲル分率を上昇させることができる。
さらに、本発明の粘着剤組成物は、架橋剤(前記ラジカル発生剤を除く)を含有することができる。本発明においては、架橋剤として、イソシアネート系架橋剤を併用した場合には、酸素によるラジカル架橋阻害を酸化防止剤により効果的に抑制しつつ、イソシアネート系架橋剤により、粘着剤層の三次元架橋ネットワークを効率良く形成することができる。その結果、偏光フィルム端部での外観異常の発生をさらに効果的に防止することができる。
本発明の有機EL表示装置用粘着剤層は、前記有機EL表示装置用粘着剤組成物から形成されることを特徴とする。
本発明の有機EL表示装置用粘着剤層付き偏光フィルムは、偏光フィルムと、前記有機EL表示装置用粘着剤層とを有することを特徴とする。
偏光子は、特に限定されず、各種のものを使用できる。偏光子としては、例えば、ポリビニルアルコール系フィルム、部分ホルマール化ポリビニルアルコール系フィルム、エチレン・酢酸ビニル共重合体系部分ケン化フィルム等の親水性高分子フィルムに、ヨウ素や二色性染料の二色性物質を吸着させて一軸延伸したもの、ポリビニルアルコールの脱水処理物やポリ塩化ビニルの脱塩酸処理物等ポリエン系配向フィルム等が挙げられる。これらの中でも、ポリビニルアルコール系フィルムとヨウ素等の二色性物質からなる偏光子が好適である。これらの偏光子の厚さは特に制限されないが、一般的に5〜80μm程度である。
透明保護フィルムについては、従来から用いられているものを適宜用いることができる。具体的には、透明性、機械的強度、熱安定性、水分遮断性、等方性等に優れる材料から形成される透明保護フィルムが好ましく、例えば、ポリエチレンテレフタレートやポリエチレンナフタレート等のポリエステル系ポリマー、ジアセチルセルロースやトリアセチルセルロース等のセルロース系ポリマー、ポリメチルメタクリレート等のアクリル系ポリマー、ポリスチレンやアクリロニトリル・スチレン共重合体(AS樹脂)等のスチレン系ポリマー、ポリカーボネート系ポリマー等が挙げられる。また、ポリエチレン、ポリプロピレン、シクロ系ないしはノルボルネン構造を有するポリオレフィン、エチレン・プロピレン共重合体等のポリオレフィン系ポリマー、塩化ビニル系ポリマー、ナイロンや芳香族ポリアミド等のアミド系ポリマー、イミド系ポリマー、スルホン系ポリマー、ポリエーテルスルホン系ポリマー、ポリエーテルエーテルケトン系ポリマー、ポリフェニレンスルフィド系ポリマー、ビニルアルコール系ポリマー、塩化ビニリデン系ポリマー、ビニルブチラール系ポリマー、アリレート系ポリマー、ポリオキシメチレン系ポリマー、エポキシ系ポリマー、または、前記ポリマーのブレンド物等も前記透明保護フィルムを形成するポリマーの例として挙げられる。透明保護フィルムは、アクリル系、ウレタン系、アクリルウレタン系、エポキシ系、シリコーン系等の熱硬化型、紫外線硬化型の樹脂の硬化層として形成することもできる。
前記第1粘着剤層、第2粘着剤層、および第3粘着剤層のうち、少なくとも一つの粘着剤層が、前記有機EL表示装置用粘着剤層であればよい。
本発明の有機EL表示装置は、本発明の有機EL表示装置用粘着剤層、および/または本発明の有機EL表示装置用粘着剤層付き偏光フィルムを少なくとも1つ用いたことを特徴とする。
(メタ)アクリル系ポリマーの重量平均分子量(Mw)は、GPC(ゲル・パーミエーション・クロマトグラフィー)により測定した。Mw/Mnについても、同様に測定した。
・分析装置:東ソー社製、HLC−8120GPC
・カラム:東ソー社製、G7000HXL+GMHXL+GMHXL
・カラムサイズ:各7.8mmφ×30cm 計90cm
・カラム温度:40℃
・流量:0.8mL/min
・注入量:100μL
・溶離液:テトラヒドロフラン
・検出器:示差屈折計(RI)
・標準試料:ポリスチレン
冷却管、窒素導入管、温度計および撹拌装置を備えた反応容器にアクリル酸ブチル(BA)99部、およびアクリル酸4−ヒドロキシブチル(HBA)1部を含有するモノマー混合物を仕込んだ。さらに、前記モノマー混合物100部に対して、重合開始剤として2,2’−アゾビスイソブチロニトリル0.1部を酢酸エチル100部と共に仕込み、緩やかに攪拌しながら窒素ガスを導入して窒素置換した後、フラスコ内の液温を55℃付近に保って8時間重合反応を行って、重量平均分子量(Mw)180万、Mw/Mn=4.1のアクリル系ポリマーの溶液(固形分濃度30重量%)を調製した。
冷却管、窒素導入管、温度計および撹拌装置を備えた反応容器にアクリル酸ブチル(BA)94.8部、アクリル酸(AA)5部、およびアクリル酸2−ヒドロキシエチル(HEA)0.2部を含有するモノマー混合物を仕込んだ。さらに、前記モノマー混合物100部に対して、重合開始剤としてベンゾイルパーオキサイド(日本油脂社製の商品名ナイパーBMT)0.3部を酢酸エチル100部と共に仕込み、緩やかに攪拌しながら窒素ガスを導入して窒素置換した後、フラスコ内の液温を55℃付近に保って8時間重合反応を行って、重量平均分子量(Mw)220万、Mw/Mn=4.1のアクリル系ポリマーの溶液(固形分濃度30重量%)を調製した。
冷却管、窒素導入管、温度計および撹拌装置を備えた反応容器に、ブチルアクリレート(BA)73.3部、フェノキシエチルアクリレート(PEA)21部、N−ビニルピロリドン(NVP)5部、アクリル酸(AA)0.3部、4−ヒドロキシブチルアクリレート(HBA)0.4部を含有するモノマー混合物を仕込んだ。さらに、前記モノマー混合物(固形分)100部に対して、重合開始剤として2,2’−アゾビスイソブチロニトリル0.1部を酢酸エチル100部と共に仕込み、緩やかに攪拌しながら窒素ガスを導入して窒素置換した後、フラスコ内の液温を55℃付近に保って8時間重合反応を行って、重量平均分子量(Mw)160万、Mw/Mn=3.8のアクリル系ポリマーの溶液(固形分濃度28重量%)を調製した。
(粘着剤組成物の調製)
上記で製造したアクリル系ポリマー(1)の溶液の固形分100部に対して、
ラジカル発生剤(ベンゾイルパーオキサイド,日本油脂社製の商品名ナイパーBMT)を0.3部、
イソシアネート系架橋剤(三井化学社製の商品名タケネートD110N)0.1部、
紫外線吸収剤(a)として、2,4−ビス−[{4−(4−エチルヘキシルオキシ)−4−ヒドロキシ}−フェニル]−6−(4−メトキシフェニル)−1,3,5-トリアジン(商品名:Tinosorb S,BASF社製)2部、および
シランカップリング剤(信越化学工業(株)製のKBM403)0.1部を配合して、粘着剤組成物を得た。
前記粘着剤組成物を厚さ38μmのセパレータ(表面が剥離処理されたポリエチレンテレフタレート系フィルム:離型フィルム)上に、乾燥後の厚さが20μmとなるように塗布し、155℃で1分間乾燥層させて溶媒を除去し、粘着剤層(A)を得た。
厚さ25μmのシクロオレフィンポリマーフィルム(商品名ゼオノアフィルム,日本ゼオン株式会社製)を用いた。
ヨウ素が含浸された厚さ5μmの延伸ポリビニルアルコールフィルムからなる偏光子を用いた。偏光子(または保護フィルムを貼り合わせた偏光フィルム)の単体透過率Y値は、42.4%、偏光度は99.995であった。
特開2010−284840号公報の製造例1に記載のイミド化MS樹脂100重量部からなる樹脂ペレットを、100.5kPa、100℃で12時間乾燥させ、単軸の押出機にてダイス温度270℃でTダイから押出してフィルム状に成形した(厚さ80μm)。さらに当該フィルムを、その搬送方向に150℃の雰囲気下に延伸し(厚さ40μm)、次いでフィルム搬送方向と直交する方向に150℃の雰囲気下に延伸して、厚さ20μmのアクリル系樹脂フィルムを得た。
厚み56μmのポリカーボネートフィルム(日東電工株式会社製「NRF」、面内位相差Re(550):135nm)を用いた。
温度計、攪拌機、還流冷却管及び窒素ガス導入管を備えたセパラブルフラスコに、ブチルアクリレート95重量部、アクリル酸5重量部、重合開始剤としてアゾビスイソブチロニトリル0.2重量部、及び酢酸エチル233重量部を投入した後、窒素ガスを流し、攪拌しながら約1時間窒素置換を行った。その後、60℃にフラスコを加熱し、7時間反応させて、重量平均分子量(Mw)110万のアクリル系ポリマーを得た。上記アクリル系ポリマー溶液(固形分を100重量部とする)に、イソシアネート系架橋剤として、トリメチロールプロパントリレンジイソシアネート(商品名:コロネートL,日本ポリウレタン工業(株)製)0.8重量部、シランカップリング剤(商品名:KBM−403、信越化学工業(株)製)0.1重量部を加えて粘着剤組成物(溶液)を調製した。
前記粘着剤組成物(溶液)を、厚さ38μmのセパレータ(表面が剥離処理されたポリエチレンテレフタレート系フィルム:離型フィルム)上に、乾燥後の厚さが15μmとなるように塗布し、100℃で3分間乾燥層させて溶媒を除去し、粘着剤層(B)を得た。
実施例1において、粘着剤組成物の調製にあたり、(メタ)アクリル系ポリマーの種類、架橋剤の種類または配合量、紫外線吸収剤の種類または配合量、色素化合物の種類または配合量、酸化防止剤の配合量を表1に示すように変えたこと以外は、実施例1と同様にして、粘着剤層を形成した。また、実施例1と同様にして粘着剤層付き偏光フィルムを作製した。
実施例および比較例で得られた粘着剤層(A)からセパレータを剥離して、粘着剤層(A)を測定用治具に取り付け、分光光度計(製品名:U4100、(株)日立ハイテクノロジーズ製)で測定した。透過率は、波長300nm〜450nmの範囲における透過率を測定した。波長300nm〜400nm、波長400nm〜430nm、波長430nm〜450nmの平均透過率を表1に示す。
ゲル分率は、前記粘着剤層(A)を0.2gとり、あらかじめ重量を測定したフッ素樹脂(TEMISH NTF−1122日東電工(株)製)(Wa)に包み、粘着剤が漏れないように縛った後、重量(Wb)を測定し、サンプル瓶にいれた。酢酸エチルを40cc加えて7日間放置した。その後、フッ素樹脂を取り出し、アルミカップ上で130℃、2時間乾燥させ、サンプルを含むフッ素樹脂の重量(Wc)を測定し、次式(I)によりゲル分率を求めた。
式(I):ゲル分率=(Wc−Wa)/(Wb−Wa)×100(重量%)
ゲル分率の測定は、粘着剤層(A)を形成した直後(4時間以内)と、粘着剤層(A)を形成した後、室温(23℃)で1週間放置した後について行った。
得られた粘着剤層付き偏光フィルムを一辺の長さが270mmの正方形に打ち抜いたものについて、粘着剤層(A)の糊打痕、端部の糊欠け、端部の糊汚れを以下の基準で評価した。
○・・・問題なし。
△・・・糊かけ、糊汚れ、糊打痕による一部外観不良がある。
×・・・糊かけ、糊汚れ、糊打痕による外観不良が著しい。
得られた粘着剤層付き偏光フィルム(縦290mm×横220mm)からセパレータを剥離し、粘着剤層(A)側を、厚さ0.7mmの無アルカリガラス板の両面にクロスニコル状態になるように貼着した。次いで、50℃、5atmで15分間オートクレーブ処理を施し、完全に密着させてサンプルを調製した。当該サンプルを85の条件下でそれぞれ500時間処理した後、発泡・剥れ・浮きの状態を以下の基準で目視観察した。
〇・・・発泡・剥れ・浮きなどがない。
△・・・実用上問題は無いレベルだが、目視でわずかにレベルが悪い。
×・・・実用上問題がある。
得られた粘着剤層付き偏光フィルムから、長さ100mm、幅50mmのシート片を切り出したものをサンプルとした。得られたサンプルについて、引張試験機(装置名:オートグラフ AG−IS、(株)島津製作所製)を用い、JIS Z0237に準拠して、23℃、50%R.H.の雰囲気下、引張速度300mm/分、剥離角度180°の条件でサンプルからセパレータを引きはがし、180°引き剥がし剥離力(N/50mm)を測定した。
ラジカル発生剤は、ベンゾイルパーオキサイド(日本油脂社製の商品名ナイパーBMT);
D110Nは、イソシアネート系架橋剤(三井化学社製の商品名タケネートD110N);
C/Lは、イソシアネート系架橋剤(東ソー社製の商品名コロネートL);
紫外線吸収剤のa1は、2,4−ビス−[{4−(4−エチルヘキシルオキシ)−4−ヒドロキシ}−フェニル]−6−(4−メトキシフェニル)−1,3,5-トリアジン(商品名:Tinosorb S,BASF社製);
紫外線吸収剤のa2は、2,2’,4,4’テトラヒドロキシベンゾフェノン(商品名:SeeSorb106,シプロ化成社製);
色素化合物のb1は、メロシアニン系化合物(商品名:FDB−009,吸収スペクトルの最大吸収波長:394nm,半値幅:43nm,山田化学工業(株)製);
色素化合物のb2は、ポリメチン化合物(商品名:DAA−247、吸収スペクトルの最大吸収波長:389nm、半値幅:49.5nm、山田化学工業(株)製);
色素化合物のb3は、アルキルフェニルインドールシアノアクリナート誘導体(インドール化合物)(商品名:BONASORB UA3912,吸収スペクトルの最大吸収波長:386nm,半値幅:53nm,オリエント化学工業(株)製);
酸化防止剤は、フェノール系酸化防止剤(BASFジャパン社製の商品名IRGANOX 1010);を示す。
2 粘着剤層
3 透明保護フィルム
4 偏光子
5 位相差フィルム
6 偏光フィルム
7 カバーガラスまたはカバープラスチック
8 有機ELパネル
9 接着剤層
10 センサー層
Claims (17)
- ベースポリマー、加熱によりラジカル活性種を発生するラジカル発生剤、並びに、分子構造中の水酸基が0〜3個である紫外線吸収剤(a)および吸収スペクトルの最大吸収波長が380〜430nmの波長領域に存在する色素化合物(b)から選ばれる少なくとも1種の化合物(A)含むことを特徴とする有機EL表示装置用粘着剤組成物。
- 前記化合物(A)が、前記紫外線吸収剤(a)および前記色素化合物(b)の両方を含むことを特徴とする請求項1に記載の有機EL表示装置用粘着剤組成物。
- 前記紫外線吸収剤(a)の吸収スペクトルの最大吸収波長が、300〜400nmの波長領域に存在することを特徴とする請求項1または2記載の有機EL表示装置用粘着剤組成物。
- 前記ラジカル発生剤が、過酸化物であることを特徴とする請求項1〜3のいずれかに記載の有機EL表示装置用粘着剤組成物。
- 前記ベースポリマーが、(メタ)アクリル系ポリマーであることを特徴とする請求項1〜4のいずれかに記載の有機EL表示装置用粘着剤組成物。
- 前記ラジカル発生剤を、前記ベースポリマー100重量部に対して0.01〜2重量部含有することを特徴とする請求項1〜5のいずれかに記載の有機EL表示装置用粘着剤組成物。
- 前記化合物(A)を、前記ベースポリマー100重量部に対して0.1〜25重量部含有することを特徴とする請求項1〜6のいずれかに記載の有機EL表示装置用粘着剤組成物。
- さらに酸化防止剤を含むことを特徴とする請求項1〜7のいずれかに記載の有機EL表示装置用粘着剤組成物。
- さらに、架橋剤を含有することを特徴とする請求項1〜8のいずれかに有機EL表示装置用粘着剤組成物。
- 請求項1〜9のいずれかに記載の有機EL表示装置用粘着剤組成物から形成されることを特徴とする有機EL表示装置用粘着剤層。
- 波長300〜400nmの平均透過率が12%以下であり、波長400nm〜430nmの平均透過率が30%以下であり、波長430〜450nmの平均透過率が70%以上であることを特徴とする請求項10に記載の有機EL表示装置用粘着剤層。
- 波長300〜400nmの平均透過率が12%以下であり、波長400nm〜430nmの平均透過率が30%を超え95%以下であり、波長430〜450nmの平均透過率が80%以上であることを特徴とする請求項10に記載の有機EL表示装置用粘着剤層。
- 偏光フィルムと、請求項10〜12のいずれかに記載の有機EL表示装置用粘着剤層とを有することを特徴とする有機EL表示装置用粘着剤層付き偏光フィルム。
- 前記偏光フィルムが、偏光子の一方の面に透明保護フィルムが設けられ、他方の面に位相差フィルムを有するものであって、前記有機EL表示装置用粘着剤層が、前記位相差フィルムの偏光子と接する面と反対側の面、および/または、前記透明保護フィルムの偏光子と接する面と反対側の面に設けられることを特徴とする請求項13に記載の有機EL表示装置用粘着剤層付き偏光フィルム。
- 第1粘着剤層、透明保護フィルム、偏光子、第2粘着剤層、位相差フィルム、第3粘着剤層をこの順に有する有機EL表示装置用粘着剤層付き偏光フィルムであって、
前記第1粘着剤層、第2粘着剤層、および第3粘着剤層のうち、少なくとも一つの粘着剤層が、前記有機EL表示装置用粘着剤層であることを特徴とする請求項13に記載の有機EL表示装置用粘着剤層付き偏光フィルム。 - 前記位相差フィルムが1/4波長板であって、前記偏光フィルムが円偏光フィルムであることを特徴とする請求項14または15に記載の有機EL表示装置用粘着剤層付き偏光フィルム。
- 請求項10〜12のいずれかに記載の有機EL表示装置用粘着剤層、または請求項13〜16のいずれかに記載の有機EL表示装置用粘着剤層付き偏光フィルムを少なくとも1つ用いたことを特徴とする有機EL表示装置。
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