JP5790155B2 - 硬化性樹脂組成物 - Google Patents
硬化性樹脂組成物 Download PDFInfo
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- JP5790155B2 JP5790155B2 JP2011120422A JP2011120422A JP5790155B2 JP 5790155 B2 JP5790155 B2 JP 5790155B2 JP 2011120422 A JP2011120422 A JP 2011120422A JP 2011120422 A JP2011120422 A JP 2011120422A JP 5790155 B2 JP5790155 B2 JP 5790155B2
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- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- UUQQGGWZVKUCBD-UHFFFAOYSA-N [4-(hydroxymethyl)-2-phenyl-1h-imidazol-5-yl]methanol Chemical compound N1C(CO)=C(CO)N=C1C1=CC=CC=C1 UUQQGGWZVKUCBD-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- IPTNXMGXEGQYSY-UHFFFAOYSA-N acetic acid;1-methoxybutan-1-ol Chemical compound CC(O)=O.CCCC(O)OC IPTNXMGXEGQYSY-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 description 1
- HDFRDWFLWVCOGP-UHFFFAOYSA-N carbonothioic O,S-acid Chemical compound OC(S)=O HDFRDWFLWVCOGP-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000013035 low temperature curing Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229940057867 methyl lactate Drugs 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 125000005369 trialkoxysilyl group Chemical group 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- 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
- C08G59/40—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 curing agents used
- C08G59/66—Mercaptans
-
- C—CHEMISTRY; METALLURGY
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
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JP2011120422A JP5790155B2 (ja) | 2011-05-30 | 2011-05-30 | 硬化性樹脂組成物 |
KR1020137033163A KR101528737B1 (ko) | 2011-05-30 | 2012-05-22 | 경화성 수지 조성물 |
CN201280000439.3A CN102985461B (zh) | 2011-05-30 | 2012-05-22 | 固化性树脂组合物 |
PCT/JP2012/003334 WO2012164870A1 (fr) | 2011-05-30 | 2012-05-22 | Composition de résine durcissable |
TW101118125A TWI481660B (zh) | 2011-05-30 | 2012-05-22 | A curable resin composition |
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KR (1) | KR101528737B1 (fr) |
CN (1) | CN102985461B (fr) |
TW (1) | TWI481660B (fr) |
WO (1) | WO2012164870A1 (fr) |
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JP5772229B2 (ja) * | 2011-05-30 | 2015-09-02 | 日油株式会社 | 硬化性樹脂組成物 |
KR101252063B1 (ko) | 2011-08-25 | 2013-04-12 | 한국생산기술연구원 | 알콕시실릴기를 갖는 에폭시 화합물, 이의 제조 방법, 이를 포함하는 조성물과 경화물 및 이의 용도 |
CN103906624B (zh) | 2011-09-26 | 2016-02-10 | 富士胶片株式会社 | 屏障积层体与其制造方法与其用途、屏障装置的制造方法、可聚合化合物与可聚合组合物 |
JP5732362B2 (ja) * | 2011-09-26 | 2015-06-10 | 富士フイルム株式会社 | 重合性化合物および重合性組成物 |
JP2015502919A (ja) * | 2011-11-01 | 2015-01-29 | コリア インスティチュート オブ インダストリアル テクノロジー | アルコキシシリル基を有するイソシアヌレートエポキシ化合物、その製造方法、それを含む組成物、該組成物の硬化物及び該組成物の用途 |
US9902803B2 (en) | 2012-03-14 | 2018-02-27 | Korea Institute Of Industrial Technology | Epoxy compound having alkoxy silyl group, composition comprising same, cured product, use thereof and method for preparing epoxy compound having alkoxy silyl group |
EP2835373B1 (fr) | 2012-04-02 | 2019-09-11 | Korea Institute of Industrial Technology | Composé époxy présentant un groupe alcoxysilyle, composition et matériau durci le comprenant, son utilisation et procédé de préparation du composé époxy présentant un groupe alcoxysilyle |
KR101863111B1 (ko) | 2012-07-06 | 2018-06-01 | 한국생산기술연구원 | 노볼락계 에폭시 화합물, 이의 제조 방법, 이를 포함하는 조성물, 경화물 및 이의 용도 |
US9758615B2 (en) * | 2012-12-21 | 2017-09-12 | Dow Global Technologies Llc | Phase-segmented non-isocyanate elastomers |
JP5949674B2 (ja) * | 2013-06-12 | 2016-07-13 | 信越化学工業株式会社 | 新規有機ケイ素化合物、その製造方法及び密着向上剤 |
WO2015080141A1 (fr) * | 2013-11-28 | 2015-06-04 | Jnc株式会社 | Encre photodurcissable pour jet d'encre |
EP3083749B1 (fr) * | 2013-12-18 | 2020-01-22 | Dow Global Technologies LLC | Procédé de formation d'un polymère organique dans une réaction d'un polyène, d'une résine époxy et d'un mélange d'agents de durcissement thiol et amine |
EP3088436B1 (fr) | 2013-12-24 | 2019-04-24 | Bridgestone Corporation | Corps stratifié |
DE102014202609B4 (de) * | 2014-02-13 | 2020-06-04 | tooz technologies GmbH | Aminkatalysierte Thiolhärtung von Epoxidharzen |
JP6361212B2 (ja) * | 2014-03-26 | 2018-07-25 | 東洋インキScホールディングス株式会社 | 含硫黄エポキシ化合物、及びその製造方法 |
US20150322271A1 (en) * | 2014-05-09 | 2015-11-12 | Prc-Desoto International, Inc. | Chromate free pretreatment primer |
JP6710892B2 (ja) * | 2014-09-01 | 2020-06-17 | 日油株式会社 | 硬化性樹脂組成物 |
JP6359395B2 (ja) * | 2014-09-18 | 2018-07-18 | 東洋ゴム工業株式会社 | シラン化合物及びそれを用いたゴム組成物 |
KR102102692B1 (ko) * | 2018-04-25 | 2020-04-22 | 이아이씨티코리아 주식회사 | 자외선과 열 경화가 가능한 에폭시관능 아크릴레이트 수지 화합물, 이의 제조방법 및 경화성 수지 조성물 |
JP2021004229A (ja) * | 2019-06-25 | 2021-01-14 | 川口化学工業株式会社 | 新規なチオール基を有するイソシアヌレート化合物とその利用 |
KR102232340B1 (ko) | 2019-11-15 | 2021-03-26 | 한국생산기술연구원 | 알콕시실릴기를 갖는 에폭시 수지의 조성물 및 이의 복합체 |
JP7426608B2 (ja) * | 2020-04-17 | 2024-02-02 | パナソニックIpマネジメント株式会社 | 光硬化性組成物 |
JP7394011B2 (ja) * | 2020-04-17 | 2023-12-07 | パナソニックホールディングス株式会社 | 光硬化性樹脂組成物およびそれを用いた液晶表示装置 |
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JPH07242798A (ja) * | 1994-03-08 | 1995-09-19 | Sekisui Chem Co Ltd | 型内被覆成形用被覆組成物 |
KR100736240B1 (ko) * | 2003-11-26 | 2007-07-06 | 미쓰이 가가쿠 가부시키가이샤 | 1액형의 광 및 열병용 경화성 수지 조성물 및 그 용도 |
JP2006206642A (ja) * | 2005-01-25 | 2006-08-10 | Matsushita Electric Works Ltd | エポキシ系樹脂組成物及び電子部品 |
JP5009042B2 (ja) * | 2007-05-07 | 2012-08-22 | モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 | 室温硬化性ポリオルガノシロキサン組成物 |
JP2009173744A (ja) * | 2008-01-23 | 2009-08-06 | Shin Etsu Chem Co Ltd | アンダーフィル剤組成物 |
JP5671885B2 (ja) * | 2010-08-27 | 2015-02-18 | 日油株式会社 | 密着性向上剤 |
US9013069B2 (en) * | 2010-10-08 | 2015-04-21 | Panasonic Intellectual Property Management Co., Ltd. | Power generation system and power generating unit |
CN102666556B (zh) * | 2010-11-25 | 2015-02-18 | 日油株式会社 | 含硫醚的烷氧基硅烷衍生物及其应用 |
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TWI481660B (zh) | 2015-04-21 |
TW201247769A (en) | 2012-12-01 |
KR20140022912A (ko) | 2014-02-25 |
JP2012246422A (ja) | 2012-12-13 |
WO2012164870A1 (fr) | 2012-12-06 |
CN102985461B (zh) | 2016-04-27 |
KR101528737B1 (ko) | 2015-06-15 |
CN102985461A (zh) | 2013-03-20 |
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