JP2011099919A

JP2011099919A - 着色樹脂組成物、カラーフィルタ、液晶表示装置及び有機ｅｌディスプレイ

着色樹脂組成物、カラーフィルタ、液晶表示装置及び有機ｅｌディスプレイ Download PDF

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Publication number: JP2011099919A
Authority: JP; Japan
Prior art keywords: group; meth; acid; resin composition; resin
Prior art date: 2009-11-04
Legal status : Pending

Application number

JP2009253201A

Other languages

English (en)

Japanese (ja)

Other versions

JP2011099919A5 (enExample

Inventor

Tatsuhiro Ohata

達寛大畑

Toshiyuki Tanaka

俊行田中

Current Assignee

Mitsubishi Chemical Corp

Original Assignee

Mitsubishi Chemical Corp

Priority date

2009-11-04

Filing date

2009-11-04

Publication date

2011-05-19

2009-11-04 Application filed by Mitsubishi Chemical Corp filed Critical Mitsubishi Chemical Corp

2009-11-04 Priority to JP2009253201A priority Critical patent/JP2011099919A/ja

2011-05-19 Publication of JP2011099919A publication Critical patent/JP2011099919A/ja

2013-02-28 Publication of JP2011099919A5 publication Critical patent/JP2011099919A5/ja

Status Pending legal-status Critical Current

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239000011342 resin composition Substances 0.000 title claims abstract description 137
239000004973 liquid crystal related substance Substances 0.000 title claims description 44
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229920005989 resin Polymers 0.000 claims abstract description 181
239000011347 resin Substances 0.000 claims abstract description 181
239000000049 pigment Substances 0.000 claims abstract description 107
239000011230 binding agent Substances 0.000 claims abstract description 62
125000006267 biphenyl group Chemical group 0.000 claims abstract description 26
239000000178 monomer Substances 0.000 claims description 115
239000002270 dispersing agent Substances 0.000 claims description 60
150000001875 compounds Chemical class 0.000 claims description 59
239000003999 initiator Substances 0.000 claims description 25
239000003822 epoxy resin Substances 0.000 claims description 22
229920000647 polyepoxide Polymers 0.000 claims description 22
150000007519 polyprotic acids Polymers 0.000 claims description 19
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 18
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 18
238000012719 thermal polymerization Methods 0.000 claims description 17
150000008064 anhydrides Chemical class 0.000 claims description 14
239000003505 polymerization initiator Substances 0.000 claims description 14
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 11
239000004305 biphenyl Substances 0.000 claims description 9
235000010290 biphenyl Nutrition 0.000 claims description 9
125000003118 aryl group Chemical group 0.000 claims description 7
238000004040 coloring Methods 0.000 claims description 7
125000005843 halogen group Chemical group 0.000 claims description 6
239000007795 chemical reaction product Substances 0.000 claims description 5
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 3
125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 3
238000002834 transmittance Methods 0.000 abstract description 12
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 96
238000000034 method Methods 0.000 description 87
239000002253 acid Substances 0.000 description 78
239000010408 film Substances 0.000 description 72
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239000002904 solvent Substances 0.000 description 54
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239000000758 substrate Substances 0.000 description 40
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CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 25
230000015572 biosynthetic process Effects 0.000 description 25
239000011159 matrix material Substances 0.000 description 24
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125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 23
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238000006243 chemical reaction Methods 0.000 description 20
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238000004519 manufacturing process Methods 0.000 description 18
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125000004432 carbon atom Chemical group C* 0.000 description 14
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125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 10
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239000004793 Polystyrene Substances 0.000 description 9
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150000003751 zinc Chemical class 0.000 description 9
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GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 7
238000002347 injection Methods 0.000 description 7
239000007924 injection Substances 0.000 description 7
239000011164 primary particle Substances 0.000 description 7
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239000000243 solution Substances 0.000 description 7
125000001424 substituent group Chemical group 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
125000002723 alicyclic group Chemical group 0.000 description 6
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 6
150000002170 ethers Chemical class 0.000 description 6
239000001056 green pigment Substances 0.000 description 6
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
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125000006850 spacer group Chemical group 0.000 description 6
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238000010550 living polymerization reaction Methods 0.000 description 5
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238000001179 sorption measurement Methods 0.000 description 5
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238000004448 titration Methods 0.000 description 5
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