JP6195196B2 - 両面型偏光板及びこれを含む光学装置 - Google Patents
両面型偏光板及びこれを含む光学装置 Download PDFInfo
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- JP6195196B2 JP6195196B2 JP2013548375A JP2013548375A JP6195196B2 JP 6195196 B2 JP6195196 B2 JP 6195196B2 JP 2013548375 A JP2013548375 A JP 2013548375A JP 2013548375 A JP2013548375 A JP 2013548375A JP 6195196 B2 JP6195196 B2 JP 6195196B2
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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
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
- G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
- G02B5/3041—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks
- G02B5/305—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks including organic materials, e.g. polymeric layers
-
- G02B1/105—
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/14—Protective coatings, e.g. hard coatings
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
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Description
特許文献1 特開2010−209126
Si(R1)n(R2)4−n
ポリ(N−シクロヘキシルマレイミド−co−メチルメタクリレート)、スチレン−無水マレイン酸共重合体樹脂及びフェノキシ系樹脂を100:2.5:5の重量比で均一に混合した樹脂組成物を、原料ホッパー(hopper)から押出機までを窒素置換した24Φ押出機に供給し、250℃で溶融して原料ペレット(pellet)を製造した。
上記のような過程により製造されたアクリルフィルムをコロナ処理した後、上記アクリルフィルムの一面に、CK−PUD−F(Chokwang、ウレタン分散液)を純水で希釈して製造された固形分含量10重量%のプライマー組成物にカルボジイミド系架橋剤(日清紡社製、カルボジライトSV−02)10重量部を添加したプライマー組成物を、#7バーでコートした後、TD方向に130℃でテンターを用いて190%延伸し、プライマー層の厚さが400nmであるアクリルフィルム(A)を製造した。
製造例1の(1)により製造されたアクリルフィルムをコロナ処理した後、CK−PUD−F(Chokwang、ウレタン分散液)を純水で希釈して製造された固形分含量10重量%のプライマー組成物にカルボジイミド系架橋剤(日清紡社製、カルボジライトSV−02)20重量部を添加したプライマー組成物を、その上に#7バーでコートした後、TD方向に130℃でテンターを用いて190%延伸し、プライマー層の厚さが400nmであるアクリルフィルム(B)を製造した。
(1)接着剤組成物A
3,4−エポキシシクロへキシルメチル−3,4'−エポキシシクロへキサンカルボン酸25重量%(Dicel社のCelloxide 2021P)、1,4−シクロヘキサンジメタノールジグリシジルエーテル25重量%、3−エチル−3−[(3−エチルオキセタン−3−イル)メトキシメチル]オキセタン(東亞合成株式会社のアロンオキセタンDOX221)35重量%及び3−エチル−3−ヒドロキシメチルオキセタン(東亞合成株式会社のアロンオキセタンOXA)15重量を入れて製造した樹脂組成物100重量部に、カチオン開始剤であるCPI 100P(Sanapro社)5重量部を添加して偏光板用接着剤組成物Aを製造した。
3,4−エポキシシクロへキシルメチル−3,4'−エポキシシクロへキサンカルボン酸25重量%(Dicel社のCelloxide 2021P)、1,4−シクロヘキサンジメタノールジグリシジルエーテル25重量%、3−エチル−3−[(3−エチルオキセタン−3−イル)メトキシメチル]オキセタン(東亞合成株式会社のアロンオキセタンDOX221)50重量を入れて製造した樹脂組成物100重量部に、カチオン開始剤であるCPI 100P(Sanapro社)5重量部、ビニルトリエチルシラン5重量部を添加して偏光板用接着剤組成物Bを製造した。
3,4−エポキシシクロへキシルメチル−3,4'−エポキシシクロへキサンカルボン酸25重量%(Dicel社のCelloxide 2021P)、1,4−シクロヘキサンジメタノールジグリシジルエーテル25重量%、3−エチル−3−[(3−エチルオキセタン−3−イル)メトキシメチル]オキセタン(東亞合成株式会社のアロンオキセタンDOX221)50重量を入れて製造した樹脂組成物100重量部に、カチオン開始剤であるCPI 100P(Sanapro社)5重量部、ビニルアセテート5重量部を添加して偏光板用接着剤組成物Cを製造した。
マイクログラビアコーターを用いて上記製造例1により製造されたアクリルフィルム(A)2枚のプライマー層上に接着剤組成物Aを最終接着剤層の厚さが1μmになるよう夫々塗布した。その後、接着剤組成物が塗布された2枚のアクリルフィルム(A)をPVA素子の両面にラミネートし、UV照射装置(Metal halide lamp)を用いて、PVA素子の片面の方向から500mJ/cm2の紫外線を照射して偏光板を製造した。
接着剤組成物としてBを用いたことを除き、実施例1と同様の方法で偏光板を製造した。
接着剤組成物としてCを用いたことを除き、実施例1と同様の方法で偏光板を製造した。
接着剤層の厚さを3μmにコーティングすることを除き、実施例1と同様の方法で偏光板を製造した。
接着剤層の厚さを3μmにコーティングすることを除き、実施例2と同様の方法で偏光板を製造した。
接着剤層の厚さを3μmにコーティングすることを除き、実施例3と同様の方法で偏光板を製造した。
上記製造例1により製造されたアクリルフィルム(A)のプライマー層上にマイクログラビアコーターを用いて接着剤組成物Aを最終接着剤層の厚さが1μmになるようコーティングした(以下、アクリルフィルム(A−1)とする)。また、上記製造例1により製造されたアクリルフィルム(A)のプライマー層上にマイクログラビアコーターを用いて接着剤組成物Aを最終接着剤層の厚さが3μmになるようコーティングした(以下、アクリルフィルム(A−2)とする)。上記アクリルフィルム(A−1)とアクリルフィルム(A−2)をPVA素子の両面にラミネートし、UV照射装置(Metal halide lamp)を用いて、アクリルフィルム(A−2)が積層された面に500mJ/cm2の紫外線を照射して偏光板を製造した。
上記製造例1により製造されたアクリルフィルム(A)のプライマー層上にマイクログラビアコーターを用いて接着剤組成物Aを最終接着剤層の厚さが3μmになるようコーティングした(以下、アクリルフィルム(A−3)とする)。また、上記製造例1により製造されたアクリルフィルム(A)のプライマー層上にマイクログラビアコーターを用いて接着剤組成物Aを最終接着剤層の厚さが10μmになるようコーティングした(以下、アクリルフィルム(A−4)とする)。上記アクリルフィルム(A−3)とアクリルフィルム(A−4)をPVA素子の両面にラミネートし、UV照射装置(Metal halide lamp)を用いて、アクリルフィルム(A−4)が積層された面に500mJ/cm2の紫外線を照射して偏光板を製造した。
上記製造例1により製造されたアクリルフィルム(B)のプライマー層上にマイクログラビアコーターを用いて接着剤組成物Aを最終接着剤層の厚さが1μmになるようコーティングした(以下、アクリルフィルム(B−1)とする)。また、上記製造例1により製造されたアクリルフィルムのプライマー層上にマイクログラビアコーターを用いて接着剤組成物Aを最終接着剤層の厚さが3μmになるようコーティングした(以下、アクリルフィルム(B−2)とする)。上記アクリルフィルム(B−1)とアクリルフィルム(B−2)をPVA素子の両面にラミネートし、UV照射装置(Metal halide lamp)を用いて、アクリルフィルム(B−2)が積層された面に500mJ/cm2の紫外線を照射して偏光板を製造した。
接着剤層の厚さを5μmにコーティングすることを除き、実施例1と同様の方法で偏光板を製造した。
接着剤層の厚さを5μmにコーティングすることを除き、実施例2と同様の方法で偏光板を製造した。
接着剤層の厚さを5μmにコーティングすることを除き、実施例3と同様の方法で偏光板を製造した。
実施例1〜9及び比較例1〜3により製造された偏光板に対し、第1接着剤層の剥離力を測定した。剥離力は幅20mm、長さ100mmの偏光板を用いて、PVA素子と紫外線非照射面のアクリルフィルムを速度300mm/min、90度で剥離した時の剥離力で測定した。その結果を下表1に示した。剥離力が2N/cmを超える場合をOK、2N/cm以下の場合をNGと表示した。
上記実施例1〜9及び比較例1〜3の偏光板をガラス基板にラミネーション(glass lamination)した後、60℃の恒温槽に浸漬させた。8時間経過後、偏光板の端部の脱色有無で耐水性を判断し、変更のない場合をOK、脱色が生じた場合をNGと表示した。
実施例1〜9及び比較例1〜3により製造された偏光板をガラス基板にラミネーション(glass lamination)し、これを−40℃で30分間放置した後、再び80℃で30分間放置することを100回繰り返して行った。それから、偏光板の外観の変形有無を目視で評価した。偏光板の外観の変形がない場合をOK、クラックが発生した場合をNGと表示した。その結果は下表2に示した。
Claims (5)
- 偏光子、前記偏光子の一面に形成される第1接着剤層、前記偏光子の他面に形成される第2接着剤層、前記第1接着剤層上に形成される第1透明フィルム、及び前記第2接着剤層上に形成される第2透明フィルムを含む両面型偏光板であって、
前記第1接着剤層及び前記第2接着剤層は活性エネルギー線硬化型接着剤により形成され、
前記第1接着剤層の厚さが0.1〜3μmであり、
活性エネルギー線硬化型接着剤は、(1)分子内に少なくとも2つのエポキシ基を有するエポキシ化合物5〜90重量部;(2)分子内に少なくとも1つのオキセタニル基を有するオキセタン化合物5〜90重量部;及び(3)光カチオン性重合開始剤0.5〜20重量部を含むカチオン性接着剤であり、
前記エポキシ化合物は、エポキシ化脂肪族環基を1つ以上含む第1エポキシ化合物及びグリシジルエーテル基を1つ以上含む第2エポキシ化合物の組み合わせであり、
前記第1エポキシ化合物と前記第2エポキシ化合物は、1:1〜3:1の重量比で混合され、
前記活性エネルギー線硬化型接着剤は、15〜50cPの範囲の粘度を有するか、または、前記活性エネルギー線硬化型接着剤は、硬化後において90℃以上のガラス転移温度を有し、
前記第1接着剤層と前記第1透明フィルムとの間、及び前記第2接着剤層と前記第2透明フィルムとの間のうち少なくとも1つにプライマー層をさらに含み、
前記カチオン性接着剤は、カチオン重合性官能基を含むシランカップリング剤をさらに含み、
前記プライマー層は、1〜50重量部のウレタン高分子、水分散性微粒子0.1〜10重量部、0.1〜30重量部の架橋剤及び残部の水を含むプライマー組成物により形成される、
両面型偏光板。 - 前記第2接着剤層の厚さが0.1〜10μmである、
請求項1に記載の両面型偏光板。 - 前記プライマー層はその厚さが100nm〜1μmである、
請求項1に記載の両面型偏光板。 - 前記第1透明フィルム及び前記第2透明フィルムのうち少なくとも1つはアクリル系フィルムである、
請求項1から3の何れか1項に記載の両面型偏光板。 - 請求項1から4の何れか1項に記載の両面型偏光板を含む、
光学装置。
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US9523792B2 (en) * | 2011-10-14 | 2016-12-20 | Lg Chem, Ltd. | Polarizer having protection films in two sides and optical device comprising the same |
CN103415584B (zh) | 2011-10-14 | 2016-06-08 | Lg化学株式会社 | 用于偏振板的粘合剂和包括该粘合剂的偏振板 |
JP2014534988A (ja) * | 2012-05-30 | 2014-12-25 | エルジー・ケム・リミテッド | 水系組成物、これを含む光学フィルム、これを用いた偏光板及び液晶表示装置 |
KR101462579B1 (ko) * | 2013-02-06 | 2014-11-18 | 동우 화인켐 주식회사 | 편광판 및 이를 포함하는 액정표시장치 |
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KR101697404B1 (ko) * | 2013-09-30 | 2017-01-17 | 주식회사 엘지화학 | 편광판 및 이를 포함하는 화상표시장치 |
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JP6265697B2 (ja) | 2013-11-18 | 2018-01-24 | サムスン エスディアイ カンパニー,リミテッドSamsung Sdi Co.,Ltd. | 偏光板用接着剤組成物 |
JP6349082B2 (ja) * | 2013-12-12 | 2018-06-27 | 住友化学株式会社 | 偏光板及び表示装置 |
KR102262160B1 (ko) * | 2013-12-24 | 2021-06-08 | 동우 화인켐 주식회사 | 편광판 및 이를 포함하는 액정표시장치 |
KR101716958B1 (ko) * | 2014-06-27 | 2017-03-15 | 주식회사 엘지화학 | 접착제 조성물 및 이를 포함하는 편광판 |
JP6376872B2 (ja) * | 2014-07-16 | 2018-08-22 | 日東電工株式会社 | 積層光学フィルムの製造方法 |
JP5871408B1 (ja) * | 2014-09-19 | 2016-03-01 | 日東電工株式会社 | 偏光板および光学積層体 |
KR101813338B1 (ko) * | 2014-12-11 | 2017-12-28 | 주식회사 엘지화학 | 베젤용 감광성 유색 잉크 조성물, 이를 이용하여 형성된 베젤 패턴 및 이를 포함하는 디스플레이 기판 |
KR102527505B1 (ko) * | 2014-12-26 | 2023-04-28 | 스미또모 가가꾸 가부시키가이샤 | 편광판 |
KR101956788B1 (ko) * | 2015-09-24 | 2019-03-11 | 주식회사 엘지화학 | 편광판의 제조방법 및 이를 이용한 편광판 |
JP6741440B2 (ja) * | 2016-02-29 | 2020-08-19 | 住友化学株式会社 | 積層光学フィルムの製造方法、及び積層光学フィルムの製造装置 |
JP6964965B2 (ja) * | 2016-04-20 | 2021-11-10 | 日東電工株式会社 | 偏光板およびその製造方法、ならびに該偏光板を用いた画像表示装置 |
TWI568582B (zh) * | 2016-07-05 | 2017-02-01 | 住華科技股份有限公司 | 偏光板 |
CN113917590A (zh) * | 2017-02-28 | 2022-01-11 | 住友化学株式会社 | 光学层叠体 |
KR102244789B1 (ko) * | 2017-12-15 | 2021-04-26 | 주식회사 엘지화학 | 편광판, 편광판-캐리어 필름 적층체, 편광판-캐리어 필름 적층체의 제조방법, 편광판의 제조방법 및 활성 에너지선 경화형 조성물 |
TWI700191B (zh) * | 2017-12-15 | 2020-08-01 | 南韓商Lg化學股份有限公司 | 偏光板-承載膜積層體及其製造方法和使用其製造偏光板的方法及偏光板 |
KR102244791B1 (ko) | 2017-12-15 | 2021-04-26 | 주식회사 엘지화학 | 편광판, 편광판-캐리어 필름 적층체, 편광판-캐리어 필름 적층체의 제조방법, 편광판의 제조방법 및 활성 에너지선 경화형 조성물 |
JP6899339B2 (ja) * | 2018-01-24 | 2021-07-07 | 日東電工株式会社 | 表面保護フィルムおよび保護フィルム付き光学部材 |
CN111527163B (zh) * | 2018-05-21 | 2022-07-15 | 杉金光电(苏州)有限公司 | 偏光板、包括其的图像显示装置和用于偏光板的粘合剂组合物 |
JP6898481B2 (ja) * | 2018-05-31 | 2021-07-07 | 住友化学株式会社 | 偏光板及び表示装置 |
JP2021105731A (ja) * | 2020-01-27 | 2021-07-26 | 住友化学株式会社 | 偏光板及び表示装置 |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4953494B2 (ja) | 1998-12-09 | 2012-06-13 | 株式会社日本触媒 | 透明性耐熱樹脂成形材料、その製造方法とその用途 |
JP4769348B2 (ja) | 1999-11-26 | 2011-09-07 | 株式会社日本触媒 | 透明性耐熱樹脂の製造方法 |
US20020074086A1 (en) * | 2000-09-29 | 2002-06-20 | Koichiro Nakamura | Adhesive composition and optical device using the same |
JP4414080B2 (ja) | 2000-10-18 | 2010-02-10 | 株式会社日本触媒 | 透明熱可塑性樹脂積層体 |
KR100387536B1 (ko) | 2000-10-18 | 2003-06-18 | 주식회사 루밴틱스 | 광학 접착제 수지 조성물 및 광학 접착제 수지의 제조방법 |
ATE410708T1 (de) * | 2003-04-17 | 2008-10-15 | Essilor Int | Fotohärtbare klebstoffe und ihre anwendung auf dem optischen gebiet |
EP1679328A1 (en) * | 2003-09-18 | 2006-07-12 | Kaneka Corporation | Photocuring resin composition containing organic polymer having epoxy group and/or oxethane group-containing silicon group at end, and method for producing same |
US20090115945A1 (en) * | 2006-05-17 | 2009-05-07 | Sumitomo Chemical Company, Limited | Polarizing plate, method for manufacturing the polarizing plate, laminated optical member, and liquid crystal display device |
JP5016266B2 (ja) | 2006-06-30 | 2012-09-05 | 三井化学株式会社 | 光学プラスチックレンズ用プライマー |
KR100773634B1 (ko) | 2006-10-26 | 2007-11-05 | 제일모직주식회사 | 아크릴 바인더 수지조성물를 포함하는 광경화형 점착조성물및 이를 이용한 점착테이프 |
JP2008134385A (ja) | 2006-11-28 | 2008-06-12 | Kyoritsu Kagaku Sangyo Kk | 液晶表示用偏光板 |
JP5448024B2 (ja) * | 2007-03-15 | 2014-03-19 | 住友化学株式会社 | 光硬化性接着剤、該光硬化性接着剤を用いた偏光板およびその製造方法、光学部材および液晶表示装置 |
US7782537B2 (en) | 2007-10-15 | 2010-08-24 | Seiko Epson Corporation | Optical article and process for producing optical article |
JP2009107171A (ja) | 2007-10-29 | 2009-05-21 | Fujifilm Corp | 光学用積層シート及びその製造方法 |
KR20100117591A (ko) | 2008-01-08 | 2010-11-03 | 스미또모 가가꾸 가부시키가이샤 | 편광판 |
KR101105424B1 (ko) | 2008-04-30 | 2012-01-17 | 주식회사 엘지화학 | 수지 조성물 및 이를 이용하여 형성된 광학 필름 |
JP5354733B2 (ja) | 2008-07-29 | 2013-11-27 | 日東電工株式会社 | 偏光子保護フィルムおよび偏光子保護フィルムを用いた偏光板および画像表示装置 |
JP5120715B2 (ja) | 2008-09-10 | 2013-01-16 | 住友化学株式会社 | 偏光板およびその製造方法、ならびに光学部材、液晶表示装置 |
TWI443169B (zh) | 2008-10-24 | 2014-07-01 | Cheil Ind Inc | 黏著劑組成物以及光學零件 |
JP5098060B2 (ja) | 2008-10-27 | 2012-12-12 | フジコピアン株式会社 | 光硬化型接着剤組成物及びそれを用いた偏光板 |
KR20100068178A (ko) | 2008-12-12 | 2010-06-22 | 동우 화인켐 주식회사 | 편광판 및 이것이 구비된 액정표시장치 |
JP5446902B2 (ja) | 2009-03-05 | 2014-03-19 | Dic株式会社 | カチオン重合性接着剤及びそれを用いて得られた偏光板 |
JP5296575B2 (ja) | 2009-03-06 | 2013-09-25 | 住友化学株式会社 | 光硬化性接着剤組成物、偏光板とその製造法、光学部材及び液晶表示装置 |
JP2011039362A (ja) * | 2009-08-14 | 2011-02-24 | Sumitomo Chemical Co Ltd | 偏光板および液晶表示装置 |
JP4561936B1 (ja) | 2009-09-04 | 2010-10-13 | 東洋インキ製造株式会社 | 偏光板及び偏光板形成用光硬化性接着剤 |
JP5661293B2 (ja) * | 2010-02-08 | 2015-01-28 | 太陽ホールディングス株式会社 | 光硬化性樹脂組成物、ドライフィルム、硬化物及びプリント配線板 |
JP5495906B2 (ja) * | 2010-04-06 | 2014-05-21 | 東亞合成株式会社 | 光硬化性接着剤組成物、偏光板とその製造法、光学部材及び液晶表示装置 |
JP2011236389A (ja) * | 2010-05-13 | 2011-11-24 | Toyo Ink Sc Holdings Co Ltd | 偏光板形成用光硬化性接着剤及び偏光板 |
KR101072371B1 (ko) | 2010-09-20 | 2011-10-11 | 주식회사 엘지화학 | 편광판용 접착제 및 이를 포함하는 편광판 |
TWI537356B (zh) * | 2010-12-17 | 2016-06-11 | Toagosei Co Ltd | Photo-curable adhesive composition, polarizing plate and manufacturing method thereof, optical member and liquid crystal display device (1) |
JP2014513325A (ja) | 2011-04-13 | 2014-05-29 | エルジー・ケム・リミテッド | 光学フィルム |
JP5229433B2 (ja) * | 2011-04-19 | 2013-07-03 | Dic株式会社 | カチオン重合性接着剤及びそれを用いて得られた偏光板 |
JP5674729B2 (ja) | 2011-08-31 | 2015-02-25 | 富士フイルム株式会社 | 帯電防止性ハードコート層形成用組成物、光学フィルム、光学フィルムの製造方法、偏光板、及び画像表示装置 |
WO2013055154A2 (ko) | 2011-10-14 | 2013-04-18 | 주식회사 엘지화학 | 양면형 편광판 및 이를 포함하는 광학 장치 |
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