JP5623445B2 - 光学フィルムの製造方法 - Google Patents
光学フィルムの製造方法 Download PDFInfo
- Publication number
- JP5623445B2 JP5623445B2 JP2012046186A JP2012046186A JP5623445B2 JP 5623445 B2 JP5623445 B2 JP 5623445B2 JP 2012046186 A JP2012046186 A JP 2012046186A JP 2012046186 A JP2012046186 A JP 2012046186A JP 5623445 B2 JP5623445 B2 JP 5623445B2
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- Prior art keywords
- dope
- flow
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- casting
- 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.)
- Expired - Fee Related
Links
- 239000012788 optical film Substances 0.000 title claims description 21
- 238000004519 manufacturing process Methods 0.000 title claims description 18
- 239000010408 film Substances 0.000 claims description 128
- 238000005266 casting Methods 0.000 claims description 83
- 238000000034 method Methods 0.000 claims description 48
- 229920000642 polymer Polymers 0.000 claims description 36
- 238000007906 compression Methods 0.000 claims description 19
- 238000001035 drying Methods 0.000 claims description 19
- 230000006835 compression Effects 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 13
- 238000013517 stratification Methods 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 239000012528 membrane Substances 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 52
- 229920002678 cellulose Polymers 0.000 description 13
- 239000001913 cellulose Substances 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 238000011144 upstream manufacturing Methods 0.000 description 12
- ODIGIKRIUKFKHP-UHFFFAOYSA-N (n-propan-2-yloxycarbonylanilino) acetate Chemical compound CC(C)OC(=O)N(OC(C)=O)C1=CC=CC=C1 ODIGIKRIUKFKHP-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 125000002252 acyl group Chemical group 0.000 description 9
- 230000003287 optical effect Effects 0.000 description 7
- -1 tridecanoyl group Chemical group 0.000 description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- 238000004804 winding Methods 0.000 description 6
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 5
- 239000002346 layers by function Substances 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000002356 single layer Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 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
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 150000008282 halocarbons Chemical class 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 230000002093 peripheral effect Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000010933 acylation Effects 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000006837 decompression Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 125000000400 lauroyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000005185 naphthylcarbonyl group Chemical group C1(=CC=CC2=CC=CC=C12)C(=O)* 0.000 description 2
- 125000002811 oleoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 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 group 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 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 description 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 125000003074 decanoyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C(*)=O 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 125000000268 heptanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000001419 myristoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- 125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 0.000 description 1
- 125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000009751 slip forming Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
Landscapes
- Physics & Mathematics (AREA)
- Nonlinear Science (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Mathematical Physics (AREA)
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Moulding By Coating Moulds (AREA)
- Polarising Elements (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012046186A JP5623445B2 (ja) | 2012-03-02 | 2012-03-02 | 光学フィルムの製造方法 |
CN201310006166.XA CN103289109B (zh) | 2012-03-02 | 2013-01-08 | 光学膜的制造方法 |
TW102100738A TWI599466B (zh) | 2012-03-02 | 2013-01-09 | 光學膜的製造方法 |
KR1020130010364A KR101965912B1 (ko) | 2012-03-02 | 2013-01-30 | 광학필름의 제조방법 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012046186A JP5623445B2 (ja) | 2012-03-02 | 2012-03-02 | 光学フィルムの製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013180506A JP2013180506A (ja) | 2013-09-12 |
JP5623445B2 true JP5623445B2 (ja) | 2014-11-12 |
Family
ID=49090679
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012046186A Expired - Fee Related JP5623445B2 (ja) | 2012-03-02 | 2012-03-02 | 光学フィルムの製造方法 |
Country Status (4)
Country | Link |
---|---|
JP (1) | JP5623445B2 (zh) |
KR (1) | KR101965912B1 (zh) |
CN (1) | CN103289109B (zh) |
TW (1) | TWI599466B (zh) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6686620B2 (ja) * | 2016-03-29 | 2020-04-22 | コニカミノルタ株式会社 | エンドレスベルトの製造方法 |
JP7326956B2 (ja) * | 2019-07-18 | 2023-08-16 | コニカミノルタ株式会社 | 光学フィルム製造方法 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5094788A (en) * | 1990-12-21 | 1992-03-10 | The Dow Chemical Company | Interfacial surface generator |
JP3978107B2 (ja) * | 2002-09-20 | 2007-09-19 | 富士フイルム株式会社 | 多層フィルムの製膜装置及び製膜方法 |
JP4594131B2 (ja) * | 2005-02-24 | 2010-12-08 | 富士フイルム株式会社 | セルロースアシレートフィルム、位相差板、偏光板、液晶表示装置およびセルロースアシレートフィルムの製造方法 |
JP4620526B2 (ja) * | 2005-05-24 | 2011-01-26 | 帝人デュポンフィルム株式会社 | 多層フィルムの製造方法およびその装置 |
JP5245820B2 (ja) * | 2006-03-22 | 2013-07-24 | コニカミノルタアドバンストレイヤー株式会社 | セルロースエステルフィルム、及びその製造方法 |
JP4989424B2 (ja) * | 2006-11-01 | 2012-08-01 | 富士フイルム株式会社 | 積層フイルムの製造方法及びその製造設備 |
JP5135834B2 (ja) * | 2007-03-16 | 2013-02-06 | 東レ株式会社 | 流体流の分岐合流方法および装置 |
JP5576280B2 (ja) * | 2007-08-24 | 2014-08-20 | イーストマン ケミカル カンパニー | 可塑剤を含み低複屈折である混合セルロースエステル組成物およびそれから液晶ディスプレイ用に形成されるフィルム |
JP5022258B2 (ja) * | 2008-02-04 | 2012-09-12 | 富士フイルム株式会社 | 流延装置、溶液製膜設備及び溶液製膜方法 |
JP5541895B2 (ja) * | 2008-09-30 | 2014-07-09 | 富士フイルム株式会社 | 流延方法、流延装置、溶液製膜方法及び溶液製膜設備 |
KR20110078641A (ko) * | 2009-12-31 | 2011-07-07 | 주식회사 효성 | 셀룰로오스 에스테르 필름 및 그 제조 방법 |
WO2011158819A1 (ja) * | 2010-06-18 | 2011-12-22 | コニカミノルタオプト株式会社 | 樹脂フィルムの製造方法 |
-
2012
- 2012-03-02 JP JP2012046186A patent/JP5623445B2/ja not_active Expired - Fee Related
-
2013
- 2013-01-08 CN CN201310006166.XA patent/CN103289109B/zh active Active
- 2013-01-09 TW TW102100738A patent/TWI599466B/zh not_active IP Right Cessation
- 2013-01-30 KR KR1020130010364A patent/KR101965912B1/ko active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
KR20130100683A (ko) | 2013-09-11 |
CN103289109B (zh) | 2017-04-05 |
TWI599466B (zh) | 2017-09-21 |
TW201336659A (zh) | 2013-09-16 |
KR101965912B1 (ko) | 2019-04-04 |
JP2013180506A (ja) | 2013-09-12 |
CN103289109A (zh) | 2013-09-11 |
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LAPS | Cancellation because of no payment of annual fees |