TWI724291B - 改質樹脂及含有其之硬化性樹脂組成物 - Google Patents
改質樹脂及含有其之硬化性樹脂組成物 Download PDFInfo
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- TWI724291B TWI724291B TW107111229A TW107111229A TWI724291B TW I724291 B TWI724291 B TW I724291B TW 107111229 A TW107111229 A TW 107111229A TW 107111229 A TW107111229 A TW 107111229A TW I724291 B TWI724291 B TW I724291B
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- OEBXWWBYZJNKRK-UHFFFAOYSA-N 1-methyl-2,3,4,6,7,8-hexahydropyrimido[1,2-a]pyrimidine Chemical compound C1CCN=C2N(C)CCCN21 OEBXWWBYZJNKRK-UHFFFAOYSA-N 0.000 description 4
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- 238000006213 oxygenation reaction Methods 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-N pent-4-enoic acid Chemical compound OC(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical compound OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 description 1
- NIXKBAZVOQAHGC-UHFFFAOYSA-N phenylmethanesulfonic acid Chemical class OS(=O)(=O)CC1=CC=CC=C1 NIXKBAZVOQAHGC-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical class C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- KCTAHLRCZMOTKM-UHFFFAOYSA-N tripropylphosphane Chemical compound CCCP(CCC)CCC KCTAHLRCZMOTKM-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
- C08G59/1455—Monocarboxylic acids, anhydrides, halides, or low-molecular-weight esters thereof
- C08G59/1461—Unsaturated monoacids
- C08G59/1466—Acrylic or methacrylic acids
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
-
- 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
- G02F1/1339—Gaskets; Spacers; Sealing of cells
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nonlinear Science (AREA)
- General Chemical & Material Sciences (AREA)
- Optics & Photonics (AREA)
- General Physics & Mathematics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mathematical Physics (AREA)
- Emergency Medicine (AREA)
- Epoxy Resins (AREA)
- Liquid Crystal (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2017070658A JP6601634B2 (ja) | 2017-03-31 | 2017-03-31 | 変性樹脂及びそれを含む硬化性樹脂組成物 |
| JP2017-070658 | 2017-03-31 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201902680A TW201902680A (zh) | 2019-01-16 |
| TWI724291B true TWI724291B (zh) | 2021-04-11 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW107111229A TWI724291B (zh) | 2017-03-31 | 2018-03-30 | 改質樹脂及含有其之硬化性樹脂組成物 |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JP6601634B2 (enrdf_load_stackoverflow) |
| KR (1) | KR102220144B1 (enrdf_load_stackoverflow) |
| CN (1) | CN110366571B (enrdf_load_stackoverflow) |
| TW (1) | TWI724291B (enrdf_load_stackoverflow) |
| WO (1) | WO2018181649A1 (enrdf_load_stackoverflow) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6601633B2 (ja) * | 2017-03-31 | 2019-11-06 | 協立化学産業株式会社 | （メタ）アクリレート樹脂及びそれを含む硬化性樹脂組成物 |
| JP7730763B2 (ja) * | 2019-11-27 | 2025-08-28 | 大阪有機化学工業株式会社 | （メタ）アクリレート、硬化性樹脂組成物、及び硬化物 |
| JPWO2024024331A1 (enrdf_load_stackoverflow) * | 2022-07-26 | 2024-02-01 |
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| JP2004043575A (ja) * | 2002-07-10 | 2004-02-12 | Sumitomo Chem Co Ltd | 樹脂組成物 |
| CN103140535A (zh) * | 2010-10-01 | 2013-06-05 | 协立化学产业株式会社 | 低溶出性环氧树脂及其部分酯化环氧树脂、它们的制造方法以及含有它们的固化性树脂组合物 |
| JP2017002204A (ja) * | 2015-06-11 | 2017-01-05 | 協立化学産業株式会社 | エポキシ化合物及びその部分エステル化エポキシ化合物、その製造方法、並びにそれを含む硬化性組成物 |
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| JPS5512043B2 (enrdf_load_stackoverflow) * | 1972-10-28 | 1980-03-29 | ||
| JPS5910726B2 (ja) * | 1979-10-12 | 1984-03-10 | 日立化成工業株式会社 | 水希釈可能な自己硬化性樹脂の製造法 |
| JPS5659819A (en) * | 1979-10-18 | 1981-05-23 | Hitachi Chem Co Ltd | Production of epoxy-modified copolymer |
| JPS62184014A (ja) * | 1986-02-10 | 1987-08-12 | Nippon Shokubai Kagaku Kogyo Co Ltd | 耐熱性，電気絶縁性にすぐれた硬化物を与える樹脂組成物 |
| JP3543409B2 (ja) * | 1995-03-24 | 2004-07-14 | 大日本インキ化学工業株式会社 | 活性エネルギ−線硬化型エポキシアクリレ−ト樹脂組成物 |
| JPH08333356A (ja) * | 1995-06-09 | 1996-12-17 | Asahi Chiba Kk | 新規グリシジル化合物およびその製法ならびに該化合物を含有する硬化性組成物 |
| JP3605452B2 (ja) * | 1995-10-04 | 2004-12-22 | 三菱レイヨン株式会社 | 水性塗料用樹脂及びこれを用いた水性塗料 |
| JP2003107693A (ja) * | 2001-09-27 | 2003-04-09 | Sumitomo Chem Co Ltd | 樹脂組成物 |
| CN100418995C (zh) * | 2003-07-31 | 2008-09-17 | 日立化成工业株式会社 | 感光性树脂组合物及感光性元件 |
| US20070096056A1 (en) * | 2003-11-26 | 2007-05-03 | Mitsui Chemicals, Inc. | One component resin composition curable with combination of light and heat and use of the same |
| JP5184361B2 (ja) * | 2006-09-07 | 2013-04-17 | 三井化学株式会社 | 液晶シール剤、およびそれを用いた液晶表示パネルの製造方法、ならびに液晶表示パネル |
| JP5172321B2 (ja) | 2006-12-26 | 2013-03-27 | 三井化学株式会社 | 液晶シール剤 |
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| JP6601633B2 (ja) * | 2017-03-31 | 2019-11-06 | 協立化学産業株式会社 | （メタ）アクリレート樹脂及びそれを含む硬化性樹脂組成物 |
-
2017
- 2017-03-31 JP JP2017070658A patent/JP6601634B2/ja active Active
-
2018
- 2018-03-29 KR KR1020197028437A patent/KR102220144B1/ko active Active
- 2018-03-29 CN CN201880014530.8A patent/CN110366571B/zh active Active
- 2018-03-29 WO PCT/JP2018/013093 patent/WO2018181649A1/ja active Application Filing
- 2018-03-30 TW TW107111229A patent/TWI724291B/zh active
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| JP2004043575A (ja) * | 2002-07-10 | 2004-02-12 | Sumitomo Chem Co Ltd | 樹脂組成物 |
| CN103140535A (zh) * | 2010-10-01 | 2013-06-05 | 协立化学产业株式会社 | 低溶出性环氧树脂及其部分酯化环氧树脂、它们的制造方法以及含有它们的固化性树脂组合物 |
| CN103140535B (zh) | 2010-10-01 | 2015-09-02 | 协立化学产业株式会社 | 低溶出性环氧树脂及其部分酯化环氧树脂、它们的制造方法以及含有它们的固化性树脂组合物 |
| JP2017002204A (ja) * | 2015-06-11 | 2017-01-05 | 協立化学産業株式会社 | エポキシ化合物及びその部分エステル化エポキシ化合物、その製造方法、並びにそれを含む硬化性組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2018181649A1 (ja) | 2018-10-04 |
| KR102220144B1 (ko) | 2021-02-25 |
| CN110366571B (zh) | 2020-09-18 |
| JP2018172484A (ja) | 2018-11-08 |
| TW201902680A (zh) | 2019-01-16 |
| JP6601634B2 (ja) | 2019-11-06 |
| KR20190131045A (ko) | 2019-11-25 |
| CN110366571A (zh) | 2019-10-22 |
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