JP2000266932A - Polarizing plate protection film and polarizing plate using it - Google Patents
Polarizing plate protection film and polarizing plate using itInfo
- Publication number
- JP2000266932A JP2000266932A JP11066554A JP6655499A JP2000266932A JP 2000266932 A JP2000266932 A JP 2000266932A JP 11066554 A JP11066554 A JP 11066554A JP 6655499 A JP6655499 A JP 6655499A JP 2000266932 A JP2000266932 A JP 2000266932A
- Authority
- JP
- Japan
- Prior art keywords
- polarizing plate
- polarizer
- thermoplastic saturated
- protective film
- norbornene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000011347 resin Substances 0.000 claims abstract description 20
- 229920005989 resin Polymers 0.000 claims abstract description 20
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 18
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 18
- 238000009736 wetting Methods 0.000 claims abstract description 14
- 230000001681 protective effect Effects 0.000 claims description 27
- 125000003518 norbornenyl group Chemical class C12(C=CC(CC1)C2)* 0.000 claims 1
- 150000002848 norbornenes Chemical class 0.000 abstract description 17
- 238000000034 method Methods 0.000 abstract description 11
- 239000000178 monomer Substances 0.000 abstract description 8
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 abstract description 6
- 229920000642 polymer Polymers 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 239000000126 substance Substances 0.000 abstract description 3
- 239000000654 additive Substances 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 238000007142 ring opening reaction Methods 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 8
- 230000007423 decrease Effects 0.000 description 7
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 7
- 229910052753 mercury Inorganic materials 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- XLOVPKCQAPHUKK-UHFFFAOYSA-N 1,2,3,4,4a,5,8,8a-octahydronaphthalene Chemical compound C1C=CCC2CCCCC21 XLOVPKCQAPHUKK-UHFFFAOYSA-N 0.000 description 6
- 230000010287 polarization Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 229920002284 Cellulose triacetate Polymers 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- OJOWICOBYCXEKR-APPZFPTMSA-N (1S,4R)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound CC=C1C[C@@H]2C[C@@H]1C=C2 OJOWICOBYCXEKR-APPZFPTMSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- VIDOPANCAUPXNH-UHFFFAOYSA-N 1,2,3-triethylbenzene Chemical compound CCC1=CC=CC(CC)=C1CC VIDOPANCAUPXNH-UHFFFAOYSA-N 0.000 description 1
- YSSKGAZZZKLMAE-UHFFFAOYSA-N 4,4a,4b,5,8,8a,9,9a-octahydro-1h-fluorene Chemical compound C12CC=CCC2CC2C1CC=CC2 YSSKGAZZZKLMAE-UHFFFAOYSA-N 0.000 description 1
- YRIYXMAKROEVBQ-UHFFFAOYSA-N 5,5-dimethylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C)(C)CC1C=C2 YRIYXMAKROEVBQ-UHFFFAOYSA-N 0.000 description 1
- YSWATWCBYRBYBO-UHFFFAOYSA-N 5-butylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CCCC)CC1C=C2 YSWATWCBYRBYBO-UHFFFAOYSA-N 0.000 description 1
- QHJIJNGGGLNBNJ-UHFFFAOYSA-N 5-ethylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(CC)CC1C=C2 QHJIJNGGGLNBNJ-UHFFFAOYSA-N 0.000 description 1
- PCBPVYHMZBWMAZ-UHFFFAOYSA-N 5-methylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C)CC1C=C2 PCBPVYHMZBWMAZ-UHFFFAOYSA-N 0.000 description 1
- PGNNHYNYFLXKDZ-UHFFFAOYSA-N 5-phenylbicyclo[2.2.1]hept-2-ene Chemical compound C1=CC2CC1CC2C1=CC=CC=C1 PGNNHYNYFLXKDZ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 102100024522 Bladder cancer-associated protein Human genes 0.000 description 1
- 101150110835 Blcap gene Proteins 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- DKNPRRRKHAEUMW-UHFFFAOYSA-N Iodine aqueous Chemical compound [K+].I[I-]I DKNPRRRKHAEUMW-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 101100493740 Oryza sativa subsp. japonica BC10 gene Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 101150059062 apln gene Proteins 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- BMAXQTDMWYDIJX-UHFFFAOYSA-N bicyclo[2.2.1]hept-2-ene-5-carbonitrile Chemical compound C1C2C(C#N)CC1C=C2 BMAXQTDMWYDIJX-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- AEBDJCUTXUYLDC-UHFFFAOYSA-N methyl 5-methylbicyclo[2.2.1]hept-2-ene-5-carboxylate Chemical compound C1C2C(C(=O)OC)(C)CC1C=C2 AEBDJCUTXUYLDC-UHFFFAOYSA-N 0.000 description 1
- RMAZRAQKPTXZNL-UHFFFAOYSA-N methyl bicyclo[2.2.1]hept-2-ene-5-carboxylate Chemical compound C1C2C(C(=O)OC)CC1C=C2 RMAZRAQKPTXZNL-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- -1 polyethylene terephthalate Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/40—General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
- B29C66/41—Joining substantially flat articles ; Making flat seams in tubular or hollow articles
- B29C66/45—Joining of substantially the whole surface of the articles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
- B29C59/16—Surface shaping of articles, e.g. embossing; Apparatus therefor by wave energy or particle radiation, e.g. infrared heating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/48—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor using adhesives, i.e. using supplementary joining material; solvent bonding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/01—General aspects dealing with the joint area or with the area to be joined
- B29C66/02—Preparation of the material, in the area to be joined, prior to joining or welding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
- B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
- B29C35/0805—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation
- B29C2035/0827—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation using UV radiation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/71—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0037—Other properties
- B29K2995/0092—Other properties hydrophilic
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2011/00—Optical elements, e.g. lenses, prisms
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Polarising Elements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、偏光板保護フィル
ム及びそれを用いた偏光板に関する。The present invention relates to a polarizing plate protective film and a polarizing plate using the same.
【0002】[0002]
【従来の技術】液晶ディスプレイ等に用いられる偏光板
は、一般に偏光子の両面に保護フィルムが積層されて形
成されている。偏光子としては沃素又は二色性染料が吸
着された延伸ポリビニルアルコールフィルムが使用さ
れ、保護フィルムとしてはトリアセチルセルロースフィ
ルムが使用されている。2. Description of the Related Art A polarizing plate used in a liquid crystal display or the like is generally formed by laminating protective films on both surfaces of a polarizer. A stretched polyvinyl alcohol film on which iodine or a dichroic dye is adsorbed is used as a polarizer, and a triacetyl cellulose film is used as a protective film.
【0003】しかしながら、トリアセチルセルロースフ
ィルムは耐熱性及び耐湿性が充分でなく、高温下若しく
は高湿下で使用すると、偏光子とトリアセチルセルロー
スフィルムが剥離したり、トリアセチルセルロースが加
水分解して透明性が低下し偏光板性能が低下したり、偏
光子の偏光度が低下するという欠点があった。従って、
液晶ディスプレイに用いた場合にも、短期間で画質が低
下するという欠点があった。However, the triacetylcellulose film has insufficient heat resistance and moisture resistance, and when used under high temperature or high humidity, the polarizer and the triacetylcellulose film may peel off or the triacetylcellulose may be hydrolyzed. There are drawbacks that the transparency is reduced and the performance of the polarizing plate is reduced, and the degree of polarization of the polarizer is reduced. Therefore,
Even when used in a liquid crystal display, there is a disadvantage that image quality is reduced in a short period of time.
【0004】この対策として、保護フィルムとして熱可
塑性飽和ノルボルネン系樹脂を使用することが提案され
ている(例えば、特開平8ー5836号公報)。しか
し、熱可塑性飽和ノルボルネン系樹脂は接着性が乏し
く、偏光子との接着が困難なため、特開平5ー2128
28号公報には、偏光子と熱可塑性飽和ノルボルネン系
樹脂シートをアクリル系粘着剤層を介して積層し、1〜
5分間加熱圧着して接着する方法が提案されている。As a countermeasure, it has been proposed to use a thermoplastic saturated norbornene-based resin as a protective film (for example, JP-A-8-5836). However, thermoplastic saturated norbornene resins have poor adhesion and are difficult to adhere to a polarizer.
No. 28, lamination of a polarizer and a thermoplastic saturated norbornene-based resin sheet via an acrylic pressure-sensitive adhesive layer,
A method of bonding by heating and pressing for 5 minutes has been proposed.
【0005】しかしながら、上記接着方法では、フィル
ム全体に均一に一定時間加熱加圧する必要があり、設備
が高価になり、且つ生産効率が悪く、得られた偏光板は
加熱圧着されるので偏光子が退色し偏光機能が低下し、
更に、加熱加圧の際の加熱温度や圧力がばらつくと接着
むらとなって偏光性能が低下するという欠点があった。[0005] However, in the above-mentioned bonding method, it is necessary to heat and press the entire film uniformly for a certain period of time, the equipment becomes expensive and the production efficiency is poor. Fading and polarization function decrease,
Further, there is a disadvantage that if the heating temperature or pressure at the time of heating and pressurization varies, the adhesion becomes uneven and the polarization performance deteriorates.
【0006】[0006]
【発明が解決しようとする課題】本発明の目的は、上記
欠点に鑑み、偏光子と容易に接着することができる偏光
板保護フィルム及びこの偏光板保護フィルムを用いた偏
光板を提供することにある。SUMMARY OF THE INVENTION It is an object of the present invention to provide a polarizing plate protective film which can be easily bonded to a polarizer, and a polarizing plate using the polarizing plate protective film. is there.
【0007】[0007]
【課題を解決するための手段】請求項1記載の偏光板保
護フィルムは、熱可塑性飽和ノルボルネン系樹脂フィル
ムの少なくとも一面が紫外線照射処理されてなり、その
表面のぬれ指数が40ダイン/cm以上であることを特
徴とする。According to a first aspect of the present invention, there is provided a polarizing plate protective film, wherein at least one surface of a thermoplastic saturated norbornene resin film is subjected to an ultraviolet irradiation treatment, and the surface has a wetting index of 40 dynes / cm or more. There is a feature.
【0008】請求項2記載の偏光板は、偏光子の少なく
とも一面に、請求項1記載の偏光板保護フィルムが接着
されていることを特徴とする。[0008] A polarizing plate according to a second aspect is characterized in that the polarizing plate protective film according to the first aspect is adhered to at least one surface of a polarizer.
【0009】[0009]
【発明の実施の形態】以下、本発明の構成について詳述
する。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The configuration of the present invention will be described below in detail.
【0010】上記熱可塑性飽和ノルボルネン系樹脂とし
ては、従来公知の熱可塑性飽和ノルボルネン系樹脂が好
適に使用され、例えば、ノルボルネン系モノマーの開環
重合体の水素添加物、ノルボルネン系モノマーの付加型
重合体、ノルボルネン系モノマーとオレフィン系モノマ
ーの付加型重合体、これら重合体の変性物等が挙げられ
る。As the above-mentioned thermoplastic saturated norbornene-based resin, conventionally known thermoplastic saturated norbornene-based resins are suitably used. For example, hydrogenated products of ring-opened polymers of norbornene-based monomers and addition-type polymerization of norbornene-based monomers And an addition type polymer of a norbornene-based monomer and an olefin-based monomer, and a modified product of these polymers.
【0011】上記ノルボルネン系モノマーとしては、例
えば、5ーメチルー2ーノルボルネン、5ーエチルー2
ーノルボルネン、5ーブチルー2ーノルボルネン、5ー
エチリデンー2ーノルボルネン、5ーメトキシカルボニ
ルー2ーノルボルネン、5,5ージメチルー2ーノルボ
ルネン、5ーシアノー2ーノルボルネン、5ーメチルー
5ーメトキシカルボニルー2ーノルボルネン、5ーフェ
ニルー2ーノルボルネン、5ーフェニルー5ーメチルー
2ーノルボルネン、エチレンーテトラシクロドデセン共
重合体、6ーメチルー1,4:5,8ージメタノー1,
4,4a,5,6,7,8,8aーオクタヒドロナフタ
レン、6ーエチルー1,4:5,8ージメタノー1,
4,4a,5,6,7,8,8aーオクタヒドロナフタ
レン、6ーエチルー1,4:5,8ーエチリデンー1,
4,4a,5,6,7,8,8aーオクタヒドロナフタ
レン、6ークロロー1,4:5,8ージメタノー1,
4,4a,5,6,7,8,8aーオクタヒドロナフタ
レン、6ーシアノー1,4:5,8ージメタノー1,
4,4a,5,6,7,8,8aーオクタヒドロナフタ
レン、6ーピリジルー1,4:5,8ージメタノー1,
4,4a,5,6,7,8,8aーオクタヒドロナフタ
レン、6ーメトキシカルボニルー1,4:5,8ージメ
タノー1,4,4a,5,6,7,8,8aーオクタヒ
ドロナフタレン、1,4ージメタノー1,4,4a,4
b,5,8,8a,9aーオクタヒドロフルオレン、
5,8ーメタノー1,2,3,4,4a,5,8,8a
ーオクタヒドロー2.3ーシクロペンタジエノナフタレ
ン、4,9:5,8ージメタノー3a,4,4a,5,
8,8a,9,9aーオクタヒドロー1Hーベンゾイン
デン、4,11:5,10:6,9ートリメタノー3
a,4,4a,5,5a,6,9,9a,10,10
a,11,11aードデカヒドロー1Hーシクロペンタ
アントラセン等が挙げられる。As the norbornene-based monomer, for example, 5-methyl-2-norbornene, 5-ethyl-2
-Norbornene, 5-butyl-2-norbornene, 5-ethylidene-2-norbornene, 5-methoxycarbonyl-2-norbornene, 5,5-dimethyl-2-norbornene, 5-cyano-2-norbornene, 5-methyl-5-methoxycarbonyl-2-norbornene, 5-phenyl-2-norbornene, 5-phenyl-5-phenyl-5 -Methyl-2-norbornene, ethylene-tetracyclododecene copolymer, 6-methyl-1,4: 5,8-dimethanol 1,
4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-ethyl-1,4: 5,8-dimethanol 1,
4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-ethyl-1,4: 5,8-ethylidene-1,
4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-chloro-1,4: 5,8-dimethanol 1,
4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-cyano 1,4: 5,8-dimethano 1,
4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-pyridyl-1,4: 5,8-dimethanol 1,
4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-methoxycarbonyl-1,4: 5,8-dimethanol 1,4,4a, 5,6,7,8,8a-octahydronaphthalene , 1,4-dimethanoux 1,4,4a, 4
b, 5,8,8a, 9a-octahydrofluorene,
5,8-Methanolau 1,2,3,4,4a, 5,8,8a
-Octahydro-2,3-cyclopentadienonaphthalene, 4,9: 5,8 dimethano 3a, 4,4a, 5
8,8a, 9,9a-octahydro-1H-benzoindene, 4,11: 5,10: 6,9-trimethano 3
a, 4,4a, 5,5a, 6,9,9a, 10,10
a, 11,11a dedecahydro-1H-cyclopentaanthracene;
【0012】上記熱可塑性飽和ノルボルネン系樹脂の数
平均分子量は、小さくなると耐湿性が低下し、大きくな
るとフィルム成形性が低下するので、トルエン溶媒によ
るゲル・パーミュエーション・クロマトグラフで測定し
て、2万5千〜10万が好ましく、より好ましくは3万
〜8万である。When the number average molecular weight of the thermoplastic saturated norbornene resin decreases, the moisture resistance decreases, and when the number average molecular weight increases, the film formability decreases. Therefore, the number average molecular weight is measured by gel permeation chromatography using a toluene solvent. It is preferably 25,000 to 100,000, and more preferably 30,000 to 80,000.
【0013】上記熱可塑性飽和ノルボルネン系樹脂とし
ては、日本ゼオン社より商品名「ZEONOR」、「Z
EONEX」、ジェイエスアール社より商品名「ART
ON」、三井石油化学社より商品名「APEL」として
上市されている。As the above-mentioned thermoplastic saturated norbornene resin, trade names "ZEONOR", "Z
"EONEX", product name "ART" from JSR Corporation
ON ", marketed by Mitsui Petrochemical Company under the trade name" APEL ".
【0014】請求項1記載の偏光板保護フィルムは、上
記熱可塑性飽和ノルボルネン系樹脂よりなるが、その製
造方法は公知の任意の方法が採用されてよく、例えば、
溶液流延法、溶融成形法等が挙げられ、溶液流延法が好
ましい。The polarizing plate protective film according to claim 1 is made of the above-mentioned thermoplastic saturated norbornene-based resin, and its production method may be any known method.
Examples include a solution casting method and a melt molding method, and the solution casting method is preferable.
【0015】溶液流延法で製膜するには、まず、例え
ば、トルエン、キシレン、エチルベンゼン、クロロベン
ゼン、トリエチルベンゼン、ジエチルベンゼン、イソプ
ロピルベンゼン等の高沸点溶媒又はこれら高沸点溶媒と
シクロヘキサン、ベンゼン、テトラヒドロフラン、ヘキ
サン、オクタン等の低沸点溶媒の混合溶媒に、上記熱可
塑性飽和ノルボルネン系樹脂を好ましくは5〜60重量
%溶解して樹脂溶液を得る。In order to form a film by the solution casting method, first, for example, a high boiling solvent such as toluene, xylene, ethylbenzene, chlorobenzene, triethylbenzene, diethylbenzene, isopropylbenzene, or a solvent having such a high boiling point and cyclohexane, benzene, tetrahydrofuran, The above-mentioned thermoplastic saturated norbornene-based resin is preferably dissolved in a mixed solvent of a low boiling point solvent such as hexane and octane in an amount of 5 to 60% by weight to obtain a resin solution.
【0016】次に、得られた樹脂溶液をバーコーター、
ドクターナイフ、メイアバー、ロール、Tダイ等を用い
て、ポリエチレンテレフタレートなどの耐熱性フィル
ム、スチールベルト、金属箔等上に流延し、加熱乾燥す
る。Next, the obtained resin solution is coated with a bar coater.
It is cast on a heat-resistant film such as polyethylene terephthalate, a steel belt, a metal foil or the like using a doctor knife, a Meyer bar, a roll, a T-die or the like, and dried by heating.
【0017】上記偏光板保護フィルムには、フィルムの
耐熱性、耐紫外線性、平滑性等を向上させるために、フ
ェノール系、リン系などの老化防止剤、フェノール系な
どの熱劣化防止剤、アミン系などの帯電防止剤、脂肪族
アルコールのエステル、多価アルコールの部分エステル
などの滑剤、ベンゾフェノン系、ベンゾトリアゾール系
などの紫外線吸収剤等が添加されても良い。In order to improve the heat resistance, ultraviolet resistance, smoothness and the like of the polarizing plate protective film, a phenol-based or phosphorus-based antioxidant, a phenol-based heat deterioration inhibitor, an amine, etc. An antistatic agent such as a system, a lubricant such as an ester of an aliphatic alcohol and a partial ester of a polyhydric alcohol, and an ultraviolet absorber such as a benzophenone or a benzotriazole may be added.
【0018】上記偏光板保護フィルムの厚さは、薄くな
ると強度が低下し、厚くなると透明性が低下したり、複
屈折率が向上するので、5〜500μmが好ましく、よ
り好ましくは10〜150μmであり、更に好ましくは
15〜100μmである。The thickness of the polarizing plate protective film is preferably from 5 to 500 μm, more preferably from 10 to 150 μm, because the strength decreases as the thickness decreases, and the transparency decreases and the birefringence increases as the thickness increases. And more preferably 15 to 100 μm.
【0019】上記偏光板保護フィルムのぬれ指数は、小
さくなると接着剤で偏光子と接着しにくくなるので、4
0ダイン/cm以上必要であり、好ましくは45ダイン
/cm以上である。尚、ぬれ指数とは、Zismanに
よる臨界表面張力を意味し、JIS K6768に基づ
き標準ぬれ試薬で測定される。When the wetting index of the polarizing plate protective film is small, it becomes difficult to adhere to the polarizer with an adhesive.
It is required to be 0 dynes / cm or more, preferably 45 dynes / cm or more. In addition, the wetting index means a critical surface tension according to Zisman, and is measured with a standard wetting reagent based on JIS K6768.
【0020】偏光板保護フィルムのぬれ指数を40ダイ
ン/cm以上にする方法としては、紫外線照射処理法が
採用される。紫外線照射処理は、300nm以下の短波
長にピークを有するランプで紫外線が照射されるのが好
ましく、ランプとしては、例えば、低圧水銀灯、中圧水
銀灯、高圧水銀灯、超高圧水銀灯、ケミカルランプ、ブ
ラックライトランプ、マイクロウエーブ励起水銀灯、メ
タルハライドランプ等があげられ、低圧水銀灯が好適に
使用される。As a method for setting the wetting index of the polarizing plate protective film to 40 dynes / cm or more, an ultraviolet irradiation treatment method is employed. The ultraviolet irradiation treatment is preferably performed by irradiating ultraviolet rays with a lamp having a peak at a short wavelength of 300 nm or less. Examples of the lamp include a low-pressure mercury lamp, a medium-pressure mercury lamp, a high-pressure mercury lamp, an ultra-high-pressure mercury lamp, a chemical lamp, and a black light. Lamps, microwave-excited mercury lamps, metal halide lamps and the like can be mentioned, and low-pressure mercury lamps are preferably used.
【0021】紫外線照射処理条件は、保護フィルムの表
面のぬれ指数が40ダイン/cm以上になる条件であれ
ばよく、一般に、0.1〜100mW/cm2が好まし
く、より好ましくは0.5〜50mW/cm2である。The conditions for the ultraviolet irradiation treatment may be such that the surface wetting index of the protective film is 40 dynes / cm or more, and is generally preferably 0.1 to 100 mW / cm 2 , more preferably 0.5 to 100 mW / cm 2. It is 50 mW / cm 2 .
【0022】請求項2記載の偏光板は、偏光子の少なく
とも一面に、請求項1記載の偏光板保護フィルムが、そ
のぬれ指数が40ダイン/cm以上である表面が偏光子
に接するように接着されているが、偏光板の耐熱性、耐
湿性等を向上させるためには、偏光子の両面に偏光板保
護フィルムが接着されているのが好ましい。In the polarizing plate according to the second aspect, the polarizing plate protective film according to the first aspect is bonded to at least one surface of the polarizer such that the surface having a wetting index of 40 dynes / cm or more is in contact with the polarizer. However, in order to improve the heat resistance, moisture resistance and the like of the polarizing plate, it is preferable that a polarizing plate protective film is adhered to both surfaces of the polarizer.
【0023】偏光子と偏光板保護フィルムとの接着は、
偏光板保護フィルムの表面のぬれ指数が40ダイン/c
m以上になれているので、従来公知の(粘)接着剤で容
易に接着される。好ましい(粘)接着剤としては、例え
ば、ポリウレタン系、ポリエステル系、ポリアクリル系
等の接着剤やアクリル系、シリコン系、ゴム系等の粘着
剤が挙げられる。尚、偏光子の偏光機能が低下しない条
件で加熱圧着してもよいことはいうまでもなく、その場
合は、ゆるやかな加熱圧着条件で接着することができ
る。The adhesion between the polarizer and the polarizing plate protective film is as follows:
The surface wetting index of the polarizing plate protective film is 40 dynes / c
m or more, and can be easily bonded with a conventionally known (viscosity) adhesive. Preferred (sticky) adhesives include, for example, polyurethane-based, polyester-based, polyacryl-based adhesives, and acrylic-, silicone-, and rubber-based adhesives. It is needless to say that the thermocompression bonding may be performed under the condition that the polarizing function of the polarizer does not deteriorate. In this case, the bonding can be performed under gentle thermocompression bonding conditions.
【0024】[0024]
【実施例】以下に本発明を実施例により具体的に説明す
るが、本発明は実施例に限定されるものではない。EXAMPLES The present invention will be described below in more detail with reference to examples, but the present invention is not limited to the examples.
【0025】実施例1〜3 熱可塑性飽和ノルボルネン樹脂(日本ゼオン社製、ZE
ONOR1600R)を一軸押出機に供給し、275〜
290℃で押し出して厚さ60μmの熱可塑性飽和ノル
ボルネン樹脂フィルムを得た。Examples 1 to 3 Thermoplastic saturated norbornene resin (ZEON Corporation, ZE
ONOR1600R) to a single screw extruder,
Extruded at 290 ° C. to obtain a 60 μm thick thermoplastic saturated norbornene resin film.
【0026】次いで、低圧水銀灯(センエンジニアリン
グ社製、SUV110GSー36、110W)の管壁か
ら10mm離れて、得られたフィルムを立設し、30秒
間(実施例1)、90秒間(実施例2)及び120秒間
(実施例3)紫外線照射処理を行って保護フィルムを得
た。尚、紫外線照射強度は、254nmにおいて6mW
/cm2であった。Next, the obtained film was erected 10 mm away from the tube wall of a low-pressure mercury lamp (SUV110GS-36, 110W, manufactured by Sen Engineering Co., Ltd.), and set for 30 seconds (Example 1) and 90 seconds (Example 2). ) For 120 seconds (Example 3) to obtain a protective film. The UV irradiation intensity was 6 mW at 254 nm.
/ Cm 2 .
【0027】厚さ75μmの、鹸化度99%ポリビニル
アルコールフィルムを縦一軸に5倍延伸を行い、緊張状
態を保持したまま沃素0.5重量%と沃化カリウム5.
0重量%を含有する水溶液に浸漬し、二色性色素を吸着
させた。次いで、ほう酸10重量%と沃化カリウム1
0.0重量%を含有する50℃の水溶液で5分間架橋処
理を行い偏光子を得た。A polyvinyl alcohol film having a thickness of 75 μm and having a saponification degree of 99% is stretched 5 times uniaxially in a longitudinal direction, and 0.5% by weight of iodine and potassium iodide 5.
It was immersed in an aqueous solution containing 0% by weight to adsorb the dichroic dye. Then, boric acid 10% by weight and potassium iodide 1
Crosslinking treatment was performed for 5 minutes with an aqueous solution at 50 ° C. containing 0.0% by weight to obtain a polarizer.
【0028】ポリエステルポリオール溶液(東洋モート
ン社製、TMー593)100重量部とイソシアネート
系硬化剤溶液(東洋モートン社製、CATー56)18
重量部を混合し、酢酸エチルを追加して、固形分30重
量%の接着剤を得た。得られた接着剤を偏光子の両面に
塗布し、80℃で1分間乾燥して、厚さ3μmの接着剤
層が積層された偏光子を得た。100 parts by weight of a polyester polyol solution (manufactured by Toyo Morton, TM-593) and 18 parts of an isocyanate-based curing agent solution (manufactured by Toyo Morton, CAT-56) 18
By weight, ethyl acetate was added to obtain an adhesive having a solid content of 30% by weight. The obtained adhesive was applied on both surfaces of the polarizer and dried at 80 ° C. for 1 minute to obtain a polarizer having a 3 μm-thick adhesive layer laminated thereon.
【0029】偏光子の両面に保護フィルムを紫外線照射
処理面が接するように積層し、80℃に加熱された5K
gのロールを一往復することにより接着した後、40℃
で2日間養生して偏光板を得た。A protective film is laminated on both surfaces of the polarizer so that the surfaces irradiated with ultraviolet rays come into contact with each other, and is heated to 80 ° C.
g by one reciprocation of the roll, and then 40 ° C.
For 2 days to obtain a polarizing plate.
【0030】比較例1 紫外線処理を行わない以外は、実施例1で行ったと同様
にして偏光板を得た。Comparative Example 1 A polarizing plate was obtained in the same manner as in Example 1 except that no ultraviolet treatment was performed.
【0031】比較例2 偏光板保護フィルムと偏光子を90℃で2分間加熱した
後、積層し、5Kgのロールで一往復して圧着した以外
は実施例1で行ったと同様にして偏光板を得た。COMPARATIVE EXAMPLE 2 A polarizing plate was heated in the same manner as in Example 1 except that the polarizing plate protective film and the polarizer were heated at 90 ° C. for 2 minutes, laminated, and reciprocated with a 5 kg roll once. Obtained.
【0032】得られた偏光板保護フィルム及び偏光板の
物性を以下のようにして測定し、結果を表1に示した。 (1)ぬれ指数 JIS K 6768に準拠し、標準
ぬれ試薬を用いて測定した。The physical properties of the obtained polarizing plate protective film and polarizing plate were measured as follows, and the results are shown in Table 1. (1) Wetting index Measured using a standard wetting reagent according to JIS K 6768.
【0033】(2)偏光度 JIS K 7105に準
拠し、全光線透過率を測定し、下記式により偏光度を求
めた。 偏光度(%)={(Y0−Y90)/(Y0+Y90)}1/2
×100 式中、Y0は2枚の偏光板の平行軸を平行に揃えた際の
全光線透過率であり、Y9 0は2枚の偏光板の平行軸を直
交させた際の全光線透過率である。(2) Degree of polarization According to JIS K 7105
The total light transmittance was measured, and the degree of polarization was determined by the following equation.
I did. Degree of polarization (%) = {(Y0-Y90) / (Y0+ Y90)}1/2
× 100 where Y0Is when the parallel axes of the two polarizing plates are aligned in parallel.
Total light transmittance, Y9 0Is the parallel axis of the two polarizing plates
This is the total light transmittance when crossed.
【0034】(3)耐熱試験及び耐湿試験 試験後、目
視により、偏光子と保護フィルムの剥がれ状態及び発泡
状態を観察し以下の通り評価した。 ○ 剥がれも発泡もなし △ 剥がれてはいないが気泡が発生した × 剥がれが発生した 尚、耐熱試験は偏光板を80℃の乾燥機に700時間保
持した。又、耐湿試験は偏光板を60℃、90%RHの
乾燥機に700時間保持した。(3) Heat resistance test and moisture resistance test After the test, the peeled state and the foamed state of the polarizer and the protective film were visually observed and evaluated as follows. ○ Neither peeling nor foaming △ No peeling but bubbles were generated × Peeling occurred In the heat resistance test, the polarizing plate was kept in a dryer at 80 ° C. for 700 hours. In the moisture resistance test, the polarizing plate was kept in a dryer at 60 ° C. and 90% RH for 700 hours.
【0035】[0035]
【表1】 [Table 1]
【0036】[0036]
【発明の効果】請求項1記載の偏光板保護フィルムは、
熱可塑性飽和ノルボルネン系樹脂よりなり、少なくとも
一面が紫外線照射処理されてなり、その表面のぬれ指数
が40ダイン/cm以上であるから、耐熱性及び耐湿性
が優れていると共に偏光子との接着性が優れている。The polarizing plate protective film according to claim 1 is
It is made of a thermoplastic saturated norbornene resin, at least one surface of which has been subjected to an ultraviolet irradiation treatment, and has a surface wetting index of 40 dynes / cm or more, so that it has excellent heat resistance and moisture resistance, and has an adhesive property with a polarizer. Is better.
【0037】請求項2記載の偏光板は偏光子の少なくと
も一面に請求項1記載の偏光板保護フィルムが接着され
ているものなので、長時間加熱加圧することなく任意の
(粘)接着剤で容易かつ連続的に生産性よく接着するこ
とができる。従って、偏光板の偏光子が褪色して偏光機
能が低下したり、接着の際に偏光機能が低下することが
なく、液晶ディスプレイ等において好適に使用できる。Since the polarizing plate according to the second aspect has the polarizer protective film according to the first aspect adhered to at least one surface of the polarizer, it can be easily applied with an arbitrary (sticky) adhesive without heating and pressing for a long time. In addition, it is possible to continuously adhere with high productivity. Therefore, the polarizer of the polarizing plate does not fade and the polarizing function is not deteriorated, and the polarizing function is not deteriorated at the time of bonding, and can be suitably used in a liquid crystal display or the like.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) // C08L 65:00 Fターム(参考) 2H049 BA02 BA25 BA26 BB13 BB22 BB43 BB51 BC09 BC10 4F071 AA69 AA69B AF58 AG15 AH19 BA02 BB02 BC01 BC12 CB01 CB02 CB03 CC01 CD01 CD03 4F073 AA01 BA34 BB01 CA45 4J004 AA07 AB01 BA02 FA04 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) // C08L 65:00 F term (Reference) 2H049 BA02 BA25 BA26 BB13 BB22 BB43 BB51 BC09 BC10 4F071 AA69 AA69B AF58 AG15 AH19 BA02 BB02 BC01 BC12 CB01 CB02 CB03 CC01 CD01 CD03 4F073 AA01 BA34 BB01 CA45 4J004 AA07 AB01 BA02 FA04
Claims (2)
ムの少なくとも一面が紫外線照射処理されてなり、その
表面のぬれ指数が40ダイン/cm以上であることを特
徴とする偏光板保護フィルム。1. A polarizing plate protective film, wherein at least one surface of a thermoplastic saturated norbornene resin film is subjected to an ultraviolet irradiation treatment, and the surface has a wetting index of 40 dynes / cm or more.
載の偏光板保護フィルムが接着されていることを特徴と
する偏光板。2. A polarizing plate, wherein the polarizing plate protective film according to claim 1 is adhered to at least one surface of a polarizer.
Priority Applications (1)
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JP11066554A JP2000266932A (en) | 1999-03-12 | 1999-03-12 | Polarizing plate protection film and polarizing plate using it |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11066554A JP2000266932A (en) | 1999-03-12 | 1999-03-12 | Polarizing plate protection film and polarizing plate using it |
Publications (1)
Publication Number | Publication Date |
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JP2000266932A true JP2000266932A (en) | 2000-09-29 |
Family
ID=13319262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11066554A Pending JP2000266932A (en) | 1999-03-12 | 1999-03-12 | Polarizing plate protection film and polarizing plate using it |
Country Status (1)
Country | Link |
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JP (1) | JP2000266932A (en) |
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WO2001048518A1 (en) * | 1999-12-28 | 2001-07-05 | Gunze Co., Ltd | Polarizing plate and liquid-crystal display containing the same |
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