CN1962748B - 固化性树脂组合物及防反射膜 - Google Patents
固化性树脂组合物及防反射膜 Download PDFInfo
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- CN1962748B CN1962748B CN200610144514XA CN200610144514A CN1962748B CN 1962748 B CN1962748 B CN 1962748B CN 200610144514X A CN200610144514X A CN 200610144514XA CN 200610144514 A CN200610144514 A CN 200610144514A CN 1962748 B CN1962748 B CN 1962748B
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- 239000011342 resin composition Substances 0.000 title claims abstract description 64
- 150000001875 compounds Chemical class 0.000 claims abstract description 147
- -1 (methyl) acryloyl Chemical group 0.000 claims abstract description 123
- 239000003960 organic solvent Substances 0.000 claims abstract description 29
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 23
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 23
- 239000011737 fluorine Substances 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims description 108
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 84
- 239000002245 particle Substances 0.000 claims description 67
- 229920002313 fluoropolymer Polymers 0.000 claims description 60
- 239000004811 fluoropolymer Substances 0.000 claims description 60
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 57
- 239000000377 silicon dioxide Substances 0.000 claims description 35
- 238000006243 chemical reaction Methods 0.000 claims description 32
- 235000012239 silicon dioxide Nutrition 0.000 claims description 29
- 229960001866 silicon dioxide Drugs 0.000 claims description 28
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- 239000011324 bead Substances 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 238000007711 solidification Methods 0.000 claims description 5
- 230000008023 solidification Effects 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 abstract description 18
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- 239000010408 film Substances 0.000 description 104
- 239000002585 base Substances 0.000 description 75
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 48
- 239000000463 material Substances 0.000 description 28
- 150000002894 organic compounds Chemical class 0.000 description 28
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- 238000004519 manufacturing process Methods 0.000 description 22
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- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 20
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 20
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 20
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 15
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- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 14
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
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- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 10
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- 229940059574 pentaerithrityl Drugs 0.000 description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 9
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 239000004205 dimethyl polysiloxane Substances 0.000 description 8
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
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- 238000012216 screening Methods 0.000 description 7
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 6
- LDHQCZJRKDOVOX-UHFFFAOYSA-N 2-butenoic acid Chemical compound CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 238000007259 addition reaction Methods 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 229910000077 silane Inorganic materials 0.000 description 6
- 238000005303 weighing Methods 0.000 description 6
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 5
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 5
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 150000001335 aliphatic alkanes Chemical class 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
- 125000005442 diisocyanate group Chemical group 0.000 description 5
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- 239000010954 inorganic particle Substances 0.000 description 5
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 5
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- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 description 4
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
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- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 4
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 4
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JP2006273925A JP5045052B2 (ja) | 2005-11-10 | 2006-10-05 | 硬化性樹脂組成物及び反射防止膜 |
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JP4678399B2 (ja) * | 2006-12-01 | 2011-04-27 | Jsr株式会社 | 反射防止膜 |
JP2009143048A (ja) * | 2007-12-12 | 2009-07-02 | Tdk Corp | ハードコート層および光透過層を有する積層体およびその製造方法 |
JP5672661B2 (ja) * | 2008-04-25 | 2015-02-18 | 日立化成株式会社 | 樹脂組成物及びその硬化物を用いた光学部材 |
JP2009292898A (ja) * | 2008-06-03 | 2009-12-17 | Kaneka Corp | 硬化性組成物およびその硬化物 |
JP5441056B2 (ja) * | 2008-11-28 | 2014-03-12 | 日東電工株式会社 | ハードコート層形成用組成物、ハードコートフィルム、光学素子および画像表示装置 |
CN102473480B (zh) | 2009-07-08 | 2014-10-08 | 日东电工株式会社 | 透明导电性膜、电子设备及触摸面板 |
JP6128576B2 (ja) | 2011-04-22 | 2017-05-17 | 日東電工株式会社 | 光学積層体 |
JP2012234164A (ja) * | 2011-04-22 | 2012-11-29 | Nitto Denko Corp | 光学積層体 |
CN104245766A (zh) * | 2012-04-13 | 2014-12-24 | 横滨橡胶株式会社 | 光硬化性树脂组合物 |
CN105431490B (zh) * | 2013-08-02 | 2017-09-01 | 大金工业株式会社 | 包含含有选自由聚合性官能团和交联性官能团组成的组中的至少一种基团的含氟聚合物的组成物和涂装物品 |
CN104007618B (zh) * | 2014-06-18 | 2017-09-29 | 杭州福斯特应用材料股份有限公司 | 一种pcb用高粘附力感光干膜 |
US10471692B2 (en) * | 2015-08-06 | 2019-11-12 | Sharp Kabushiki Kaisha | Optical member and polymerizable composition for nanoimprinting |
CN106009021B (zh) * | 2016-05-18 | 2019-03-12 | 西南科技大学 | 一种适合塑料基材的减反射、防指纹涂覆膜的制备方法 |
KR102753467B1 (ko) * | 2020-05-14 | 2025-01-10 | 삼성에스디아이 주식회사 | 경화형 수지 조성물, 그로부터 형성된 경화막, 및 상기 경화막을 갖는 전자 장치 |
US20230279230A1 (en) * | 2020-05-14 | 2023-09-07 | Samsung Sdi Co., Ltd. | Curable resin composition, cured film formed therefrom, and electronic device having cured film |
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JPH0729232A (ja) * | 1993-07-14 | 1995-01-31 | Kuraray Co Ltd | 光磁気記録媒体 |
JP3118389B2 (ja) * | 1995-02-28 | 2000-12-18 | 株式会社クラレ | 含水性眼用レンズ材料 |
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JP5045052B2 (ja) | 2012-10-10 |
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TWI471376B (zh) | 2015-02-01 |
KR20070050372A (ko) | 2007-05-15 |
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