CN113493575A - 光学膜及柔性显示装置 - Google Patents

光学膜及柔性显示装置 Download PDF

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Publication number: CN113493575A
Authority: CN; China
Prior art keywords: optical film; film; formula; group; resin
Prior art date: 2020-03-18
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

Application number

CN202110278578.3A

Other languages

English (en)

Chinese (zh)

Inventor

大松一喜

福井仁之

唐泽真义

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Sumitomo Chemical Co Ltd

Original Assignee

Sumitomo Chemical Co Ltd

Priority date (The priority date 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 date listed.)

2020-03-18

Filing date

2021-03-15

Publication date

2021-10-12

2021-03-15 Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd

2021-10-12 Publication of CN113493575A publication Critical patent/CN113493575A/zh

Status Pending legal-status Critical Current

Links

239000012788 optical film Substances 0.000 title claims abstract description 429
230000009975 flexible effect Effects 0.000 title claims abstract description 47
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238000004519 manufacturing process Methods 0.000 claims abstract description 60
230000003287 optical effect Effects 0.000 claims abstract description 59
239000009719 polyimide resin Substances 0.000 claims abstract description 34
238000002834 transmittance Methods 0.000 claims abstract description 24
239000011347 resin Substances 0.000 claims description 185
229920005989 resin Polymers 0.000 claims description 184
238000005452 bending Methods 0.000 claims description 59
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238000012360 testing method Methods 0.000 claims description 22
239000000945 filler Substances 0.000 claims description 19
238000002310 reflectometry Methods 0.000 claims description 5
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239000004952 Polyamide Substances 0.000 abstract description 6
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125000004432 carbon atom Chemical group C* 0.000 description 141
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238000010438 heat treatment Methods 0.000 description 111
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125000000962 organic group Chemical group 0.000 description 52
125000005843 halogen group Chemical group 0.000 description 49
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NVKGJHAQGWCWDI-UHFFFAOYSA-N 4-[4-amino-2-(trifluoromethyl)phenyl]-3-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC(N)=CC=C1C1=CC=C(N)C=C1C(F)(F)F NVKGJHAQGWCWDI-UHFFFAOYSA-N 0.000 description 31
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ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
MXPYJVUYLVNEBB-UHFFFAOYSA-N 2-[2-(2-carboxybenzoyl)oxycarbonylbenzoyl]oxycarbonylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)OC(=O)C1=CC=CC=C1C(=O)OC(=O)C1=CC=CC=C1C(O)=O MXPYJVUYLVNEBB-UHFFFAOYSA-N 0.000 description 11
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238000005160 1H NMR spectroscopy Methods 0.000 description 9
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125000004122 cyclic group Chemical group 0.000 description 9
239000000975 dye Substances 0.000 description 9
229910052751 metal Inorganic materials 0.000 description 9
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ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 8
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
239000000654 additive Substances 0.000 description 8
150000004984 aromatic diamines Chemical class 0.000 description 8
229910052801 chlorine Inorganic materials 0.000 description 8
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 8
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235000019422 polyvinyl alcohol Nutrition 0.000 description 8
238000003672 processing method Methods 0.000 description 8
125000006158 tetracarboxylic acid group Chemical group 0.000 description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 7
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WKDNYTOXBCRNPV-UHFFFAOYSA-N bpda Chemical compound C1=C2C(=O)OC(=O)C2=CC(C=2C=C3C(=O)OC(C3=CC=2)=O)=C1 WKDNYTOXBCRNPV-UHFFFAOYSA-N 0.000 description 7
125000003700 epoxy group Chemical group 0.000 description 7
125000003709 fluoroalkyl group Chemical group 0.000 description 7
239000010954 inorganic particle Substances 0.000 description 7
125000002950 monocyclic group Chemical group 0.000 description 7
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229920000728 polyester Polymers 0.000 description 7
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239000005020 polyethylene terephthalate Substances 0.000 description 7
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238000002360 preparation method Methods 0.000 description 7
239000007870 radical polymerization initiator Substances 0.000 description 7
238000010526 radical polymerization reaction Methods 0.000 description 7
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 6
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 6
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 6
JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 6
239000004372 Polyvinyl alcohol Substances 0.000 description 6
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WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
239000003086 colorant Substances 0.000 description 6
125000000524 functional group Chemical group 0.000 description 6
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
239000007788 liquid Substances 0.000 description 6
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239000002244 precipitate Substances 0.000 description 6
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150000000000 tetracarboxylic acids Chemical class 0.000 description 6
VQBBXLZPRXHYBO-UHFFFAOYSA-N 2-methoxyterephthalic acid Chemical compound COC1=CC(C(O)=O)=CC=C1C(O)=O VQBBXLZPRXHYBO-UHFFFAOYSA-N 0.000 description 5
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LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 5
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NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 4
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CN202110278578.3A 2020-03-18 2021-03-15 光学膜及柔性显示装置 Pending CN113493575A (zh)

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Citations (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20110311796A1 (en) *	2007-08-20	2011-12-22	Kolon Industries, Inc.	Polyimide film
KR20140005103A (ko) *	2012-07-03	2014-01-14	주식회사 엘지화학	폴리아믹산 고분자 복합체 및 이의 제조방법
WO2019208610A1 (ja) *	2018-04-27	2019-10-31	住友化学株式会社	光学フィルム、光学積層体及びフレキシブル画像表示装置
JP2019195994A (ja) *	2018-05-08	2019-11-14	住友化学株式会社	積層体およびその製造方法
KR20200000359A (ko) *	2018-06-22	2020-01-02	스미또모 가가꾸 가부시키가이샤	수지 필름 및 그 제조 방법
JP2020001381A (ja) *	2018-06-22	2020-01-09	住友化学株式会社	透明樹脂フィルムの製造方法
JP2020001382A (ja) *	2018-06-22	2020-01-09	住友化学株式会社	樹脂フィルムロールの製造方法
JP2020189955A (ja) *	2018-09-28	2020-11-26	住友化学株式会社	光学フィルム
CN113429598A (zh) *	2020-03-18	2021-09-24	住友化学株式会社	光学膜及柔性显示装置

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP4957592B2 (ja)	2008-03-10	2012-06-20	新日本理化株式会社	ポリイミド樹脂組成物及びその成形体

2020
- 2020-03-18 JP JP2020048403A patent/JP2021148936A/ja not_active Withdrawn
2021
- 2021-03-15 TW TW110109108A patent/TW202200672A/zh unknown
- 2021-03-15 CN CN202110278578.3A patent/CN113493575A/zh active Pending
- 2021-03-16 KR KR1020210034310A patent/KR20210117963A/ko unknown

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20110311796A1 (en) *	2007-08-20	2011-12-22	Kolon Industries, Inc.	Polyimide film
KR20140005103A (ko) *	2012-07-03	2014-01-14	주식회사 엘지화학	폴리아믹산 고분자 복합체 및 이의 제조방법
WO2019208610A1 (ja) *	2018-04-27	2019-10-31	住友化学株式会社	光学フィルム、光学積層体及びフレキシブル画像表示装置
JP2019195994A (ja) *	2018-05-08	2019-11-14	住友化学株式会社	積層体およびその製造方法
KR20200000359A (ko) *	2018-06-22	2020-01-02	스미또모 가가꾸 가부시키가이샤	수지 필름 및 그 제조 방법
JP2020001381A (ja) *	2018-06-22	2020-01-09	住友化学株式会社	透明樹脂フィルムの製造方法
JP2020001382A (ja) *	2018-06-22	2020-01-09	住友化学株式会社	樹脂フィルムロールの製造方法
JP2020189955A (ja) *	2018-09-28	2020-11-26	住友化学株式会社	光学フィルム
CN113429598A (zh) *	2020-03-18	2021-09-24	住友化学株式会社	光学膜及柔性显示装置

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