JP6223570B2 - 粘着フィルムおよびこれを利用した有機電子装置の製造方法 - Google Patents
粘着フィルムおよびこれを利用した有機電子装置の製造方法 Download PDFInfo
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- JP6223570B2 JP6223570B2 JP2016531542A JP2016531542A JP6223570B2 JP 6223570 B2 JP6223570 B2 JP 6223570B2 JP 2016531542 A JP2016531542 A JP 2016531542A JP 2016531542 A JP2016531542 A JP 2016531542A JP 6223570 B2 JP6223570 B2 JP 6223570B2
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Images
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- 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
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C09J123/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
- C09J123/22—Copolymers of isobutene; Butyl rubber ; Homo- or copolymers of other iso-olefines
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/08—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having four or more carbon atoms
- C08F255/10—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having four or more carbon atoms on to butene polymers
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Description
[一般式1]
△X≦0.3mm
前記化学式1で、R1は水素または炭素数1〜4のアルキル基で、nは2以上の整数であり、Xは炭素数3〜30の直鎖、分枝鎖または環状アルキル基から誘導された残基を表す。前記で、Xが環状アルキル基から誘導された残基である場合、Xは例えば炭素数3〜30、炭素数6〜28、炭素数8〜22、または炭素数12〜20の環状アルキル基から誘導された残基であり得る。また、Xが直鎖型アルキル基から誘導された残基である場合、Xは炭素数3〜30、炭素数6〜25、または炭素数8〜20の直鎖アルキル基から誘導された残基であり得る。また、Xが分枝鎖型アルキル基から誘導された残基である場合、Xは炭素数3〜30、炭素数5〜25、または炭素数6〜20の分枝鎖アルキル基から誘導された残基であり得る。
[一般式2]
ゲル含量(重量%)=B/A×100
11:粘着剤
12:第1フィルム
21:第2フィルム
3:有機電子装置
31:基板
32:有機電子素子
33:粘着剤または封止層
34:カバー基板
封止樹脂としてブチルゴム90g(ANXESS,BUTYL301)、粘着付与剤として水添DCPD系粘着付与樹脂10g(SU-90、Kolon)、活性エネルギー線重合性化合物としてトリシクロデカンジメタノールジアクリレート15g(M262、Miwon)およびラジカル開始剤として2、2-ジメトキシ-1、2-ジフェニルエタン-1-オン1g(Irgacure651、Ciba)を投入して、トルエンで固形分が15重量%程度となるように希釈してコーティング溶液を製造した。
ブチルゴム及び粘着付与樹脂100重量部対比20重量部の水分吸着剤CaO(Aldrich)を添加したことを除いては実施例1と同一にして粘着フィルムを製造した。
トリシクロデカンジメタノールジアクリレート15g(M262、Miwon)および2、2-ジメトキシ-1、2-ジフェニルエタン-1-オン1g(Irgacure651、Ciba)を投入せず、紫外線硬化をしなかったことを除いては実施例1と同一にして粘着フィルムを製造した。
トリシクロデカンジメタノールジアクリレート15g(M262、Miwon)および2、2-ジメトキシ-1、2-ジフェニルエタン-1-オン1g(Irgacure651、Ciba)の代わりにfumed silica 15g(R812、Evonik)を追加したことを除いては実施例1と同一にして粘着フィルムを製造した。
n-ブチルアクリレート99重量部および2-ヒドロキシエチルメタクリレート1重量部、分子量(Mw)が約180万であるアクリル粘着剤に多官能性エポキシ化合物(trimethylolpropanetriglycidylether),光陽イオン開始剤(triarylsulfoniumhexafluoroantimonate)およびガンマ-グリシドキシプロピルトリメトキシシランを配合して、適正濃度に希釈してコーティング液(粘着剤組成物)を製造した。
実施例または、比較例で使われた樹脂を溶媒に溶解して樹脂組成物を製造した。前記樹脂組成物を厚さ38μmの基材フィルム(離型ポリエステルフィルム、RS-21G、SKC(製))に塗布した。引き続き、110℃で10分の間乾燥して、厚さが100μmである粘着フィルム状の層を製造した。その後、基材フィルムを剥離し、フィルム状の層を100゜Fおよび100%の相対湿度に位置させた状態で前記フィルム状の層の厚さ方向に対する透湿度を測定した。前記透湿度はASTMF1249での規定にしたがって測定した。
実施例および比較例で製造したフィルムをバリアフィルム(カバー基板の役割)にラミネーションして、さらに、バリアフィルム上に偏光板をラミネーションする。ラミネーションされたセットをグラスにラミネートして、オートクレーブを利用して50℃、5気圧の条件で加圧加熱圧着した。前記バリアフィルム上に偏光板をさらにラミネーションした後、サンプルを80℃のチャンバーにて約500時間維持しながら、グラス基板と粘着剤層の間の界面で浮きや気泡が発生したか否かを観察した。目視で、グラス基板と粘着剤層の間の界面で浮きや気泡が一つでも発生した場合をX、発生しなかった場合をOで表示した。
前記実施例および比較例に係る粘着剤組成物を含む厚さ50μmの粘着剤層を基材フィルムに付着した後、ガラス板に粘着面を1cm X 1cmで付着し、常温で24時間経過した後、80℃の条件で1kg/fの荷重を1000秒の間加えた時、50秒〜200秒間で前記粘着剤層の押された距離の変化を測定する。
Claims (11)
- 下記の一般式1を満足して、100μm厚さに製造された状態で厚さ方向への透湿度が50g/m2・day以下である粘着剤の架橋物を含み、
前記粘着剤は、ジエンおよび一つの炭素-炭素二重結合を含むオレフィン系化合物の共重合体である封止樹脂、多官能性の活性エネルギー線重合性化合物、ならびに粘着付与剤を含む粘着剤組成物を含み、
前記多官能の活性エネルギー線重合性化合物は、封止樹脂100重量部に対して5重量部〜30重量部で含まれる、粘着フィルム:
[一般式1]
△X≦0.3mm
前記一般式1において、△Xは、架橋後の前記粘着剤を含む厚さ50μmの粘着剤層を一面に形成した基材フィルムを接着面積1cm2のガラス板に付着して、24時間熟成させた後、80℃で1kgの荷重を1000秒の間加えた時、50秒〜200秒間で前記粘着剤層が押された距離の変化を表す。 - 前記一般式1で表示される押された距離が0.01mm〜0.3mmである、請求項1に記載の粘着フィルム。
- 可視光線領域に対して85%以上の光透過度を表す、請求項1に記載の粘着フィルム。
- 3%以下のヘイズを表す、請求項1に記載の粘着フィルム。
- 活性エネルギー線重合性化合物は多官能性アクリレートである、請求項1に記載の粘着フィルム。
- 粘着剤組成物はラジカル開始剤をさらに含む、請求項1に記載の粘着フィルム。
- 粘着剤は水分吸着剤を含む、請求項1に記載の粘着フィルム。
- 前記粘着剤を含む第1層および粘着性樹脂または、接着性樹脂を含む第2層を含む、請求項1に記載の粘着フィルム。
- 基板;基板上に形成された有機電子素子;および前記有機電子素子を封止する請求項1に記載された粘着フィルムを含む、有機電子装置封止製品。
- 上部に有機電子素子が形成された基板に請求項1に記載された粘着フィルムが前記有機電子素子をカバーするように適用する段階;および前記粘着フィルムを硬化する段階を含む、有機電子装置の製造方法。
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