JP3863151B2 - 光学部材用粘着剤層およびその製造方法ならびに粘着剤付光学部材および画像表示装置 - Google Patents
光学部材用粘着剤層およびその製造方法ならびに粘着剤付光学部材および画像表示装置 Download PDFInfo
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- JP3863151B2 JP3863151B2 JP2004126722A JP2004126722A JP3863151B2 JP 3863151 B2 JP3863151 B2 JP 3863151B2 JP 2004126722 A JP2004126722 A JP 2004126722A JP 2004126722 A JP2004126722 A JP 2004126722A JP 3863151 B2 JP3863151 B2 JP 3863151B2
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- 229910019015 Mg-Ag Inorganic materials 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
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- 239000003513 alkali Substances 0.000 description 1
- 150000001336 alkenes Chemical group 0.000 description 1
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- 229910052782 aluminium Inorganic materials 0.000 description 1
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- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 1
- SEEYREPSKCQBBF-UHFFFAOYSA-N n-methylmaleimide Chemical compound CN1C(=O)C=CC1=O SEEYREPSKCQBBF-UHFFFAOYSA-N 0.000 description 1
- JTHNLKXLWOXOQK-UHFFFAOYSA-N n-propyl vinyl ketone Natural products CCCC(=O)C=C JTHNLKXLWOXOQK-UHFFFAOYSA-N 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
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- 239000012875 nonionic emulsifier Substances 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
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- 238000007254 oxidation reaction Methods 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 238000005502 peroxidation Methods 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
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- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920003009 polyurethane dispersion Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
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- 239000012966 redox initiator Substances 0.000 description 1
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- 238000000926 separation method Methods 0.000 description 1
- 229920006300 shrink film Polymers 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010378 sodium ascorbate Nutrition 0.000 description 1
- 229960005055 sodium ascorbate Drugs 0.000 description 1
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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- 238000010558 suspension polymerization method Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- NMOALOSNPWTWRH-UHFFFAOYSA-N tert-butyl 7,7-dimethyloctaneperoxoate Chemical compound CC(C)(C)CCCCCC(=O)OOC(C)(C)C NMOALOSNPWTWRH-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide 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
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- HTVULPNMIHOVRU-UHFFFAOYSA-N trimethoxy-[2-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CC(C)OCC1CO1 HTVULPNMIHOVRU-UHFFFAOYSA-N 0.000 description 1
- 125000006617 triphenylamine group Chemical group 0.000 description 1
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 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
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Description
粘着ハンドブック(第2版)、粘着テープ工業会編、1995.10.12.第147頁 粘着ハンドブック(第2版)、粘着テープ工業会編、1995.10.12.第121頁および第159頁
モノマー単位として炭素数4以上のアルキル基を有するアクリルエステルを少なくとも50重量%および他のアクリルエステルを含有してなるアクリルポリマー100重量部に対し、過酸化物0.02〜2重量部およびシランカップリング剤0.01〜1重量部を混合して粘着剤組成物を調製する工程、ならびに
前記粘着剤組成物を剥離処理した支持体上に塗布し、乾燥させ、過酸化物架橋処理を行う工程、ここで過酸化物架橋処理後の粘着剤層のゲル分率は35〜90重量%である、
を含むことを特徴とする。
モノマー単位として炭素数4以上のアルキル基を有するアクリルエステルを少なくとも50重量%および他のアクリルエステルを含有してなるアクリルポリマー100重量部に対し、過酸化物0.02〜2重量部、シランカップリング剤0.01〜1重量部および架橋剤0.01〜5重量部を混合して粘着剤組成物を調製する工程、ならびに
前記粘着剤組成物を剥離処理した支持体上に塗布し、乾燥させ、過酸化物架橋処理を行う工程、ここで過酸化物架橋処理後の粘着剤層のゲル分率は35〜90重量%である、
を含むことを特徴とする。
以下に、実施例によって本発明を具体的に説明するが、本発明はこれら実施例によって限定されるものではない。なお、各例中の部および%はいずれも重量基準である。
イソノニルアクリレート70部、ブチルアクリレート25部、アクリル酸5部、および2,2−アゾビスイソブチロニトリル0.1部と酢酸エチル200部を、窒素導入管、冷却管を備えた4つ口フラスコに投入し、充分に窒素置換した後、窒素気流下で撹拌しながら55℃で20時間重合反応を行い、重量平均分子量125万のアクリルポリマーを得た。
実施例1の粘着剤組成物の乾燥および架橋を140℃で3分(計算で得られる過酸化物の分解量は約99%)行い、偏光フィルムに転写し、本発明の粘着剤付光学部材とした。なお、粘着剤のゲル分率は71重量%であった。
実施例1の粘着剤組成物の乾燥および架橋を120℃で9分(計算で得られる過酸化物の分解量は約90%)行い、偏光フィルムに転写し、本発明の粘着剤付光学部材とした。なお、粘着剤のゲル分率は70重量%であった。
実施例1の粘着剤組成物の乾燥および架橋を110℃で3分(計算で得られる過酸化物の分解量は約19%)行い、偏光フィルムに転写し、参考例の粘着剤付光学部材とした。なお、粘着剤のゲル分率は5重量%であった。
実施例1において、ジベンゾイルパーオキシドを0.01部としたこと以外は実施例1と同様にして、比較例の粘着剤付光学部材を得た。なお、粘着剤のゲル分率は0重量%であった。
実施例1において、ジベンゾイルパーオキシドを3部としたこと以外は実施例1と同様にして、比較例の粘着剤付光学部材を得た。なお、粘着剤のゲル分率は95重量%であった。
実施例1において、ジベンゾイルパーオキシドを3部とし、乾燥および架橋を110℃で3分(計算で得られる過酸化物の分解量は約19%)行ったこと以外は実施例1と同様にして、比較例の粘着剤付光学部材を得た。なお、粘着剤のゲル分率は82重量%であった。
実施例1において、3−グリシドキシプロピルトリメトキシシランを0.005部としたこと以外は実施例1と同様にして、比較例の粘着剤付光学部材とした。なお、粘着剤のゲル分率は71重量%であった。
実施例1において、3−グリシドキシプロピルトリメトキシシランを2部としたこと以外は実施例1と同様にして、比較例の粘着剤付光学部材とした。なお、粘着剤のゲル分率は71重量%であった。
2−エチルヘキシルアクリレート70部、ブチルアクリレート29部、アクリル酸1.0部、および2,2−アゾビスイソブチロニトリル0.05部と酢酸エチル200部を、窒素導入管、冷却管を備えた4つ口フラスコに投入し、充分に窒素置換した後、窒素気流下で撹拌しながら55℃で20時間重合反応を行い、重量平均分子量146万のアクリルポリマーを得た。
ブチルアクリレート95部、アクリル酸5部、2−ヒドロキシエチルアクリレート0.1部、および2,2−アゾビスイソブチロニトリル0.05部と酢酸エチル200部を、窒素導入管、冷却管を備えた4つ口フラスコに投入し、充分に窒素置換した後、窒素気流下で撹拌しながら55℃で20時間重合反応を行い、重量平均分子量157万のアクリルポリマーを得た。
実施例5のポリマー溶液の固形分100部に対して、ジベンゾイルパーオキシド(1分間半減期130.0℃)0.1部、3−グリシドキシプロピルトリメトキシシラン0.08部、さらに架橋剤としてトリメチロールプロパンのトリレンジイソシアネート付加物からなるポリイソシアネート系架橋剤0.5部を均一に混合した粘着剤組成物を、シリコーン剥離処理した38μmのPETに、粘着剤層の乾燥厚さが25μmになるように塗布し、130℃で3分乾燥および架橋(計算で得られる過酸化物の分解量は約88%)を行い、偏光フィルムに転写し、本発明の粘着剤付光学部材とした。なお、粘着剤のゲル分率は68重量%であった。
実施例6において、ジベンゾイルパーオキシドを使用せずに、ポリイソシアネート系架橋剤を0.8部使用したこと以外は実施例6と同様にして、比較例の粘着剤付光学部材とした。なお、粘着剤のゲル分率は6重量%であった。なお、30℃で1週間エージングした後にゲル分率は68重量%になったが、評価はエージング前のもので行った。
実施例5のポリマー重合時に、2,2−アゾビスイソブチロニトリル0.05部の代わりにジベンゾイルパーオキシド0.2部を用いて重合を行い、重量平均分子量130万のポリマーを得た。また、残存過酸化物の定量を液体クロマトグラフィーで行ったところ、0.06部残存していた。
アクリル酸ブチル70部、アクリル酸2−エチルヘキシル27部、アクリル酸2部、6−ヒドロキシヘキシルアクリレート1部のモノマー混合物を、乳化剤としてポリオキシエチレンジスチレン化フェニルエーテル硫酸アンモニウム3部を用いて、水122部に乳化し、開始剤として2,2−アゾビス(2−アミジノプロパン)二塩酸塩0.05部を用いて、50℃にて3時間重合反応を行い、さらに65℃で2時間反応させて、アンモニア水で粘度を調整し、アクリルポリマーの水分散体を得た。
ポリウレタンディスパージョン(タケラックW−511、三井武田ケミカル株式会社製)を50部(固形分40.0重量%)に、水200部とアクリル酸ブチル77部、6−ヒドロキシヘキシルアクリレート3部の単量体混合物を添加し、ウレタン水分散体に吸収させた。2,2−アゾビス(N−(2−カルボキシエチル)−2−メチル−プロピオンアミジン0.08部を加えて、窒素気流下で55℃に加熱して5時間反応を行ない、乳化剤を使用しないウレタン−アクリルポリマーの水分散体を得た。
乾燥および架橋処理した粘着剤(最初の重量W1)を、酢酸エチル溶液に浸漬して、室温で1週間放置した後、不溶分を取り出し、乾燥させた重量(W2)を測定し、下記式:
ゲル分率(重量%)=(W2/W1)×100
のように求めた。
実施例および比較例で得た幅25mmの光学部材を無アルカリガラス板に2kgのロール1往復で貼付け、50℃、0.5MPaのオートクレーブにて30分処理した後、23℃、50%条件下に3時間放置後、剥離角度90°、剥離速度300mm/分で剥離接着力を測定した。また、オートクレーブ処理の後、70℃に6時間保存し、23℃、50%条件下に3時間放置後、剥離角度90°、剥離速度300mm/分で剥離接着力を測定し、加熱後の接着力とした。
実施例および比較例で得た12インチサイズの光学部材を厚さ0.5mmの無アルカリガラスに貼付け、50℃、0.5MPaのオートクレーブにて30分処理した後、60℃、90%RHの雰囲気に500時間投入して、光学部材の剥がれや浮きがなければ、○とし、あれば×とした。
実施例および比較例の粘着剤付光学部材を、エージング処理を行わずに、プレス機を用いて打ち抜き加工した。その際に、切断刃に粘着剤取られが見られない場合を○とし、粘着剤が取られたり、付着した場合は×とした。
Claims (2)
- モノマー単位として炭素数4以上のアルキル基を有するアクリルエステルを少なくとも50重量%および他のアクリルエステルを含有してなるアクリルポリマー100重量部に対し、過酸化物0.02〜2重量部およびシランカップリング剤0.01〜1重量部を混合して粘着剤組成物を調製する工程、ならびに
前記粘着剤組成物を剥離処理した支持体上に塗布し、乾燥させ、過酸化物架橋処理を行う工程、ここで過酸化物架橋処理後の粘着剤層のゲル分率は35〜90重量%である、
を含む光学部材用粘着剤層の製造方法。 - モノマー単位として炭素数4以上のアルキル基を有するアクリルエステルを少なくとも50重量%および他のアクリルエステルを含有してなるアクリルポリマー100重量部に対し、過酸化物0.02〜2重量部、シランカップリング剤0.01〜1重量部および架橋剤(過酸化物を除く)0.01〜5重量部を混合して粘着剤組成物を調製する工程、ならびに
前記粘着剤組成物を剥離処理した支持体上に塗布し、乾燥させ、過酸化物架橋処理を行う工程、ここで過酸化物架橋処理後の粘着剤層のゲル分率は35〜90重量%である、
を含む光学部材用粘着剤層の製造方法。
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TW094109556A TWI384043B (zh) | 2004-04-22 | 2005-03-28 | An adhesive composition, a method for producing the same, and a use thereof |
CN 200510067340 CN1690152B (zh) | 2004-04-22 | 2005-04-20 | 粘合剂组合物和其制造方法及其用途 |
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JP2007112901A (ja) * | 2005-10-20 | 2007-05-10 | Nitto Denko Corp | 粘着型光学フィルムおよびその製造方法 |
EP2014738A1 (en) | 2007-07-13 | 2009-01-14 | Cheil Industries Inc. | Adhesive composition and optical member |
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JP4519572B2 (ja) * | 2004-08-26 | 2010-08-04 | 日東電工株式会社 | 光学部材用粘着剤組成物、光学部材用粘着剤層およびその製造方法、粘着剤層付光学部材、ならびに画像表示装置 |
JP4485329B2 (ja) * | 2004-11-18 | 2010-06-23 | 日東電工株式会社 | 光学部材用粘着剤組成物、光学部材用粘着剤層およびその製造方法、粘着剤付光学部材、ならびに画像表示装置 |
JP4880315B2 (ja) * | 2006-02-08 | 2012-02-22 | 日東電工株式会社 | 粘着剤組成物、粘着剤層、および粘着剤付光学部材 |
JP4780766B2 (ja) * | 2006-03-27 | 2011-09-28 | 日東電工株式会社 | 光学用粘着剤、粘着剤付き光学フィルムおよび画像表示装置 |
KR101302779B1 (ko) | 2006-11-24 | 2013-09-02 | 동우 화인켐 주식회사 | 점착제 조성물 및 이를 포함하는 편광판 |
JP5314439B2 (ja) | 2008-01-25 | 2013-10-16 | 日東電工株式会社 | 粘着型光学フィルムの剥離方法、及び粘着型光学フィルム |
CN101307225B (zh) * | 2008-07-11 | 2011-05-18 | 广州有色金属研究院 | 一种防止水性油墨用的超细稀土蓄光发光材料水解的方法 |
JP5687420B2 (ja) * | 2009-09-08 | 2015-03-18 | 日東電工株式会社 | 溶剤系光学部材用粘着剤組成物、粘着剤層、および粘着剤付光学部材 |
CN102464960B (zh) | 2010-10-29 | 2014-10-15 | 第一毛织株式会社 | 粘合剂组合物、光学元件、表面保护膜和粘合剂片 |
JP5636339B2 (ja) * | 2011-06-28 | 2014-12-03 | リンテック株式会社 | 粘着剤および粘着シート |
KR101393895B1 (ko) * | 2011-11-02 | 2014-05-13 | (주)엘지하우시스 | 절단성이 우수한 반도체 웨이퍼 표면보호용 점착필름 |
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JP6423574B2 (ja) | 2012-08-31 | 2018-11-14 | 日東電工株式会社 | 粘着剤層付偏光フィルムおよび画像表示装置 |
DE102016205808A1 (de) * | 2016-04-07 | 2017-10-12 | Tesa Se | Haftklebmasse |
JP6906402B2 (ja) * | 2017-09-07 | 2021-07-21 | 日東電工株式会社 | 半導体ウエハ保護用粘着テープ |
TWI727371B (zh) * | 2019-07-16 | 2021-05-11 | 住華科技股份有限公司 | 偏光板結構及其製造方法 |
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JP2007112901A (ja) * | 2005-10-20 | 2007-05-10 | Nitto Denko Corp | 粘着型光学フィルムおよびその製造方法 |
EP2014738A1 (en) | 2007-07-13 | 2009-01-14 | Cheil Industries Inc. | Adhesive composition and optical member |
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