KR101292385B1 - 경화성 수지 조성물 - Google Patents
경화성 수지 조성물 Download PDFInfo
- Publication number
- KR101292385B1 KR101292385B1 KR1020060084412A KR20060084412A KR101292385B1 KR 101292385 B1 KR101292385 B1 KR 101292385B1 KR 1020060084412 A KR1020060084412 A KR 1020060084412A KR 20060084412 A KR20060084412 A KR 20060084412A KR 101292385 B1 KR101292385 B1 KR 101292385B1
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- KR
- South Korea
- Prior art keywords
- resin composition
- curable resin
- group
- color filter
- monomer
- 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.)
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Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
-
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/06—Polystyrene
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
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- 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
- G02F1/133509—Filters, e.g. light shielding masks
- G02F1/133514—Colour filters
- G02F1/133519—Overcoatings
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Abstract
Description
바인더 폴리머 | 모노머 | 열잠재성 개시제 | 계면활성제 | 용매 | |||||
성 분 | 비율 | 함량 (중량부) |
성 분 | 함량(중량부) | 함량(중량부) | 성 분 | 함량(중량부) | 성분 | |
실시예1 | (A)-(a) (A)-(b) |
0.5 0.5 |
100 | 비스페놀-A | 50 | 4 | SH-8400 | 0.1 | PGMEA |
실시예2 | (A)-(a) (A)-(b) |
0.5 0.5 |
100 | YH-300 | 50 | 4 | SH-8400 | 0.1 | PGMEA |
실시예3 | (A)-(a) (A)-(b) |
0.5 0.5 |
100 | 옥세탄 | 50 | 4 | SH-8400 | 0.1 | PGMEA |
실시예4 | (A)-(a) (A)-(b) |
0.5 0.5 |
100 | YH-300 옥세탄 |
25 25 |
4 | PGMEA | ||
실시예5 | (A)-(a) (A)-(b) |
0.5 0.5 |
100 | YH-300 Epi-B 4400 |
70 20 |
4 | PGMEA / GBL |
||
실시예6 | (A)-(a) (A)-(b) |
0.33 0.67 |
100 | 비스페놀-A | 50 | 4 | SH-8400 | 0.1 | PGMEA |
실시예7 | (A)-(a) (A)-(b) |
0.33 0.67 |
100 | YH-300 | 50 | 4 | SH-8400 | 0.1 | PGMEA |
실시예8 | (A)-(a) (A)-(b) |
0.33 0.67 |
100 | 옥세탄 | 50 | 4 | SH-8400 | 0.1 | PGMEA |
실시예9 | (A)-(a) (A)-(b) |
0.33 0.67 |
100 | YH-300 옥세탄 |
25 25 |
4 | PGMEA | ||
실시예10 | (A)-(a) (A)-(b) |
0.33 0.67 |
100 | YH-300 Epi-B 4400 |
70 20 |
4 | PGMEA / GBL |
||
비교예1 | 공중합체-1 | 100 | 비스페놀-A | 50 | 4 | SH-8400 | 0.1 | PGMEA |
평가항목 | 사용 화학액 | 온도(℃) | 침지시간 |
내산성 | MA-SO2 (동우화인켐사 제조 ITO Etchant) |
45 | 15분 |
내알칼리성 | 5% 수산화나트륨 수용액 | 30 | 30분 |
내용제성 | N-메틸-2-피롤리돈(NMP) | 40 | 40분 |
내박리액성 | PRS-2000 (동우화인켐사 제조 포토레지스트 박리액) |
70 | 10분 |
평가항목 | 실시예 1 |
실시예 2 |
실시예 3 |
실시예 4 |
실시예 5 |
실시예 6 |
실시예 7 |
실시예 8 |
실시예 9 |
실시예10 | 비교예 1 |
|
투과율 | 포스트 베이크후 | 96% | 96% | 96% | 97% | 97% | 96% | 99% | 99% | 99% | 97% | 94% |
250℃, 1시간후 | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | |
내열성 | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | △ | |
내화학성 | 내산성 | △ | △ | △ | △ | △ | △ | ○ | ○ | ○ | ○ | △ |
내알칼리성 | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | △ | |
내용제성 | △ | △ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | |
내박리액성 | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | |
밀착성 | 내산성 | △ | △ | △ | △ | △ | △ | ○ | ○ | ○ | ○ | △ |
내알칼리성 | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | △ | |
내용제성 | △ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | |
내박리액성 | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | |
표면경도 | 7H | 7H | 7H | 7H | 7H | 7H | 7H | 7H | 7H | 7H | 7H | |
보존안정성 | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ | ○ |
Claims (10)
- [A] (a) 주쇄에 무수물 구조를 중합시킨 구조를 갖는 단량체 및 (b)스티렌계 단량체를 부가중합시켜 수득되는 중합체를 포함하는 800이상의 분자량을 갖는 경화성 수지 35 내지 90 중량%;[B] 무수물과 반응할 수 있는 경화제로써, 에폭시 관능기를 가진 단량체 또는 수지, 및 옥세탄 관능기를 가진 단량체 또는 수지로 이루어진 군으로부터 선택되는 1종 이상 5 내지 60중량%; 및[C] 열에 의해 이온을 발생하는 열잠재성 개시제 0.1 내지 10중량%를 포함하며,상기 성분 [C]는 하기 화학식 3-(b) 및 화학식 3-(c)로 이루어진 군으로부터 선택되는 1종 이상인 것임을 특징으로 하는 디스플레이 칼라필터 보호막용 경화성 수지 조성물.[화학식 3-(b)][화학식 3-(c)]상기 식에서,R1,R2,R3,R4 및 R5는 각각 수소원자 또는 탄소수 1~4개를 포함하는 알킬기이며,X1은 질소이고, X3는 질소이다.
- 청구항 1에 있어서, 경화제로 카르복실산 무수물기를 가진 단량체를 추가로 포함하는 경화성 수지 조성물.
- 청구항 3에 있어서, 스티렌계 단량체가 스티렌, α-메틸스티렌 및 하이드록실 벤젠으로 이루어진 군에서 선택된 1종 이상인 것을 특징으로 하는 경화성 수지 조성물.
- 청구항 1에 있어서, 성분 [B]가 레소신 타입 옥세탄 수지, 3관능 또는 4관능성 에폭시 수지, 비스페놀 A형 에폭시 수지, 비스페놀 F형 에폭시 수지, 노볼락형 에폭시 수지, 이소시아네이트, 에폭시, 말레인산, 디카르복실산, 무수말레인산, 아크릴산, 말레인산 모노메틸 에스테르 및 말레인산 모노에틸 에스테르로 이루어진 군 중에서 선택된 1종 이상임을 특징으로 하는 경화성 수지 조성물.
- 삭제
- 청구항 1에 있어서, 계면활성제를 추가로 함유하는 것을 특징으로 하는 경화성 수지 조성물.
- 청구항 7에 있어서, 상기 계면활성제가 실리콘계 계면활성제, 불소계 계면활성제 및 불소원자를 갖는 실리콘계 계면활성제로 이루어진 그룹으로부터 선택되는 1종 이상인 것을 특징으로 하는 경화성 수지 조성물.
- 청구항 1의 경화성 수지 조성물에 의하여 형성된 것을 특징으로 하는 칼라필터 보호막.
- 청구항 1의 경화성 수지 조성물에 의하여 형성된 칼라필터 보호막을 포함하는 디스플레이.
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH06321915A (ja) * | 1993-05-11 | 1994-11-22 | Nippon Soda Co Ltd | 新規ピラジニウム塩化合物および重合開始剤 |
JPH07110577A (ja) * | 1993-08-16 | 1995-04-25 | Fuji Photo Film Co Ltd | 光重合性組成物、それを用いたカラーフィルター及びその製造方法 |
JPH07325296A (ja) * | 1994-05-31 | 1995-12-12 | Fuji Photo Film Co Ltd | 液晶表示パネル用プラスチック基板 |
KR0131137B1 (ko) * | 1994-01-10 | 1998-04-13 | 강박광 | 열중합용 양이온 중합성 조성물, 중합촉매 및 중합방법 |
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Publication number | Priority date | Publication date | Assignee | Title |
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JPH06321915A (ja) * | 1993-05-11 | 1994-11-22 | Nippon Soda Co Ltd | 新規ピラジニウム塩化合物および重合開始剤 |
JPH07110577A (ja) * | 1993-08-16 | 1995-04-25 | Fuji Photo Film Co Ltd | 光重合性組成物、それを用いたカラーフィルター及びその製造方法 |
KR0131137B1 (ko) * | 1994-01-10 | 1998-04-13 | 강박광 | 열중합용 양이온 중합성 조성물, 중합촉매 및 중합방법 |
JPH07325296A (ja) * | 1994-05-31 | 1995-12-12 | Fuji Photo Film Co Ltd | 液晶表示パネル用プラスチック基板 |
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