TWI577709B - 光阻聚胺甲酸酯組成物 - Google Patents
光阻聚胺甲酸酯組成物 Download PDFInfo
- Publication number
- TWI577709B TWI577709B TW102114191A TW102114191A TWI577709B TW I577709 B TWI577709 B TW I577709B TW 102114191 A TW102114191 A TW 102114191A TW 102114191 A TW102114191 A TW 102114191A TW I577709 B TWI577709 B TW I577709B
- Authority
- TW
- Taiwan
- Prior art keywords
- polyisocyanate
- weight
- component
- ipdi
- isophorone diisocyanate
- Prior art date
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- 229920001228 polyisocyanate Polymers 0.000 claims description 131
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 102
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 99
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- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 39
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- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
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- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
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- 150000004984 aromatic diamines Chemical class 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- IBAHLNWTOIHLKE-UHFFFAOYSA-N cyano cyanate Chemical group N#COC#N IBAHLNWTOIHLKE-UHFFFAOYSA-N 0.000 description 3
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- 125000000524 functional group Chemical group 0.000 description 3
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- OONVMEUUWGEINX-UHFFFAOYSA-N n,n-dimethyl-2-piperidin-1-ylethanamine Chemical compound CN(C)CCN1CCCCC1 OONVMEUUWGEINX-UHFFFAOYSA-N 0.000 description 1
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- IUSOXUFUXZORBF-UHFFFAOYSA-N n,n-dioctyloctan-1-amine;hydrochloride Chemical compound [Cl-].CCCCCCCC[NH+](CCCCCCCC)CCCCCCCC IUSOXUFUXZORBF-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
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- MEYMMPIRYSIUTK-UHFFFAOYSA-N octyl 2-cyano-3,3-diphenylprop-2-enoate Chemical compound C=1C=CC=CC=1C(=C(C#N)C(=O)OCCCCCCCC)C1=CC=CC=C1 MEYMMPIRYSIUTK-UHFFFAOYSA-N 0.000 description 1
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- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
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- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 description 1
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- 238000010526 radical polymerization reaction Methods 0.000 description 1
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- 238000007142 ring opening reaction Methods 0.000 description 1
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
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- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
- VSLDMOKTYQLSAZ-UHFFFAOYSA-N tetrabutylphosphanium;hydrofluoride Chemical compound F.CCCC[P+](CCCC)(CCCC)CCCC VSLDMOKTYQLSAZ-UHFFFAOYSA-N 0.000 description 1
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
- UJJLJRQIPMGXEZ-UHFFFAOYSA-N tetrahydro-2-furoic acid Chemical compound OC(=O)C1CCCO1 UJJLJRQIPMGXEZ-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
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- 150000003609 titanium compounds Chemical class 0.000 description 1
- 238000012876 topography Methods 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
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- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
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- 238000005303 weighing Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/721—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
- C08G18/722—Combination of two or more aliphatic and/or cycloaliphatic polyisocyanates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/725—Combination of polyisocyanates of C08G18/78 with other polyisocyanates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
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- Polyurethanes Or Polyureas (AREA)
- Eyeglasses (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12165171 | 2012-04-23 |
Publications (2)
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| TW201348281A TW201348281A (zh) | 2013-12-01 |
| TWI577709B true TWI577709B (zh) | 2017-04-11 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| TW102114191A TWI577709B (zh) | 2012-04-23 | 2013-04-22 | 光阻聚胺甲酸酯組成物 |
Country Status (10)
| Country | Link |
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| US (2) | US9354355B2 (enExample) |
| EP (1) | EP2841970B1 (enExample) |
| JP (1) | JP6363994B2 (enExample) |
| KR (1) | KR102057746B1 (enExample) |
| CN (1) | CN104364675B (enExample) |
| CA (1) | CA2869851A1 (enExample) |
| HU (1) | HUE037949T2 (enExample) |
| MX (1) | MX2014012731A (enExample) |
| TW (1) | TWI577709B (enExample) |
| WO (1) | WO2013160226A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2841479B1 (de) * | 2012-04-23 | 2020-06-24 | Covestro Deutschland AG | Lichtechte polyurethanzusammensetzungen |
| EP3085720A1 (de) * | 2015-04-21 | 2016-10-26 | Covestro Deutschland AG | Hydrophil modifizierter polyisocyanuratkunststoff und verfahren zu dessen herstellung |
| JP2017025149A (ja) * | 2015-07-17 | 2017-02-02 | 三洋化成工業株式会社 | 非イオン性界面活性剤及びその製造方法 |
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- 2013-04-22 MX MX2014012731A patent/MX2014012731A/es unknown
- 2013-04-22 TW TW102114191A patent/TWI577709B/zh not_active IP Right Cessation
- 2013-04-22 KR KR1020147032398A patent/KR102057746B1/ko not_active Expired - Fee Related
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- 2013-04-22 HU HUE13723010A patent/HUE037949T2/hu unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| EP2841970B1 (de) | 2017-11-08 |
| JP6363994B2 (ja) | 2018-07-25 |
| US9733394B2 (en) | 2017-08-15 |
| HK1203635A1 (en) | 2015-10-30 |
| KR20150000509A (ko) | 2015-01-02 |
| CN104364675A (zh) | 2015-02-18 |
| EP2841970A1 (de) | 2015-03-04 |
| US9354355B2 (en) | 2016-05-31 |
| CN104364675B (zh) | 2018-06-12 |
| CA2869851A1 (en) | 2013-10-31 |
| MX2014012731A (es) | 2015-01-15 |
| KR102057746B1 (ko) | 2019-12-19 |
| US20150087774A1 (en) | 2015-03-26 |
| TW201348281A (zh) | 2013-12-01 |
| HUE037949T2 (hu) | 2018-09-28 |
| JP2015517017A (ja) | 2015-06-18 |
| US20160139301A1 (en) | 2016-05-19 |
| WO2013160226A1 (de) | 2013-10-31 |
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