JP2016538376A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016538376A5 JP2016538376A5 JP2016526854A JP2016526854A JP2016538376A5 JP 2016538376 A5 JP2016538376 A5 JP 2016538376A5 JP 2016526854 A JP2016526854 A JP 2016526854A JP 2016526854 A JP2016526854 A JP 2016526854A JP 2016538376 A5 JP2016538376 A5 JP 2016538376A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- polymer
- chain
- isocyanate
- imide
- 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.)
- Granted
Links
- 229920000642 polymer Polymers 0.000 claims description 89
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 40
- 125000005462 imide group Chemical group 0.000 claims description 37
- 229920000728 polyester Polymers 0.000 claims description 34
- 229920000098 polyolefin Polymers 0.000 claims description 34
- 229920000570 polyether Polymers 0.000 claims description 33
- 239000000203 mixture Substances 0.000 claims description 30
- 229920000058 polyacrylate Polymers 0.000 claims description 28
- 229920001228 polyisocyanate Polymers 0.000 claims description 26
- 239000005056 polyisocyanate Substances 0.000 claims description 26
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 23
- 230000003381 solubilizing effect Effects 0.000 claims description 20
- 239000002904 solvent Substances 0.000 claims description 20
- 239000004814 polyurethane Substances 0.000 claims description 19
- 229920002635 polyurethane Polymers 0.000 claims description 19
- 125000003118 aryl group Chemical group 0.000 claims description 18
- 239000002609 medium Substances 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 14
- 125000000524 functional group Chemical group 0.000 claims description 13
- 239000012948 isocyanate Substances 0.000 claims description 11
- 150000002513 isocyanates Chemical class 0.000 claims description 11
- 239000012736 aqueous medium Substances 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- -1 hydrocarbylene Motoma Chemical compound 0.000 claims description 8
- 125000001624 naphthyl group Chemical group 0.000 claims description 8
- 125000000743 hydrocarbylene group Chemical group 0.000 claims description 7
- 125000003636 chemical group Chemical group 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000003607 modifier Substances 0.000 claims description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 239000003973 paint Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- KZMAWJRXKGLWGS-UHFFFAOYSA-N 2-chloro-n-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]-n-(3-methoxypropyl)acetamide Chemical compound S1C(N(C(=O)CCl)CCCOC)=NC(C=2C=CC(OC)=CC=2)=C1 KZMAWJRXKGLWGS-UHFFFAOYSA-N 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 150000003949 imides Chemical class 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 239000011343 solid material Substances 0.000 claims 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical group Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- HNJJXZKZRAWDPF-UHFFFAOYSA-N methapyrilene Chemical group C=1C=CC=NC=1N(CCN(C)C)CC1=CC=CS1 HNJJXZKZRAWDPF-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 4
- 0 **(C(N1C*I(=C)=I)=O)C1=O Chemical compound **(C(N1C*I(=C)=I)=O)C1=O 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361898670P | 2013-11-01 | 2013-11-01 | |
| US61/898,670 | 2013-11-01 | ||
| PCT/US2014/062132 WO2015065831A1 (en) | 2013-11-01 | 2014-10-24 | Dispersants with multiple aromatic imide anchor groups |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016538376A JP2016538376A (ja) | 2016-12-08 |
| JP2016538376A5 true JP2016538376A5 (enExample) | 2017-11-24 |
| JP6600306B2 JP6600306B2 (ja) | 2019-10-30 |
Family
ID=51951996
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016526854A Active JP6600306B2 (ja) | 2013-11-01 | 2014-10-24 | 複数の芳香族イミドアンカー基を有する分散剤 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10308836B2 (enExample) |
| EP (1) | EP3063239B1 (enExample) |
| JP (1) | JP6600306B2 (enExample) |
| KR (1) | KR102236881B1 (enExample) |
| CN (1) | CN105874019B (enExample) |
| TW (1) | TWI664208B (enExample) |
| WO (1) | WO2015065831A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015065829A1 (en) * | 2013-11-01 | 2015-05-07 | Lubrizol Advanced Materials, Inc. | Dispersants with multiple aromatic imide anchor groups |
| JP6712607B2 (ja) * | 2016-01-29 | 2020-06-24 | 富士フイルム株式会社 | 感光性樹脂組成物、硬化膜、積層体、硬化膜の製造方法、積層体の製造方法、および半導体デバイス |
| WO2020041433A1 (en) * | 2018-08-22 | 2020-02-27 | Lubrizol Advanced Materials, Inc. | Aromatic amide dispersant |
| US20210198500A1 (en) * | 2018-08-22 | 2021-07-01 | Lubrizol Advanced Materials, Inc. | Aromatic Amide Dispersant |
| WO2020140909A1 (zh) * | 2018-12-31 | 2020-07-09 | 博尔金海伦 | 一种酰亚胺末端的预聚物及其制备方法、可固化树脂组合物、其用途和双重固化方法 |
| WO2025108371A1 (zh) * | 2023-11-24 | 2025-05-30 | 元素驱动(杭州)生物科技有限公司 | 一种强度提高的共聚物及其制备方法 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3510453A (en) * | 1967-07-19 | 1970-05-05 | Universal Oil Prod Co | Polymeric composition of matter containing hydroxyalkyl - substituted polyalkylenepolyamino imides of polyhalopolyhydromethano - naphthalene dicarboxylic acids |
| US4585806A (en) * | 1981-09-17 | 1986-04-29 | Ethyl Corporation | Flame retardant, self-extinguishing polyurethanes and polyurethane foams |
| US4794147A (en) | 1987-07-24 | 1988-12-27 | Basf Corporation, Inmont Division | Novel non-ionic polyurethane resins having polyether backbones in water-dilutable basecoats |
| EP0317258B1 (en) | 1987-11-18 | 1994-06-29 | Zeneca Limited | Aqueous polyurethane dispersions |
| US5336314A (en) * | 1993-07-30 | 1994-08-09 | Ppg Industries, Inc. | Polymers for pigment flushing |
| US5688312A (en) | 1996-03-29 | 1997-11-18 | Xerox Corporation | Ink compositions |
| US6037414A (en) * | 1998-09-02 | 2000-03-14 | E. I. Du Pont Nemours And Company | Polymeric pigment dispersant having an acrylic backbone, polyester side chains, cyclic imide groups and quaternary ammonium groups |
| US6596899B1 (en) | 2000-02-16 | 2003-07-22 | Noveon Ip Holdings Corp. | S,S′BIS-(α, α′-DISUBSTITUTED-α″-ACETIC ACID)- TRITHIOCARBONATES AND DERIVATIVES AS INITIATOR-CHAIN TRANSFER AGENT-TERMINATOR FOR CONTROLLED RADICAL POLYMERIZATIONS AND THE PROCESS FOR MAKING THE SAME |
| US6440207B1 (en) | 2000-03-03 | 2002-08-27 | Bayer Corporation | Method for preparing organic pigments |
| GB0009798D0 (en) | 2000-04-20 | 2000-06-07 | Avecia Ltd | Dispersants |
| US7265197B2 (en) | 2003-12-05 | 2007-09-04 | Sun Chemical Corporation | Polymeric dispersant |
| WO2006020281A1 (en) | 2004-08-06 | 2006-02-23 | Noveon, Inc. | Polyurethanes and urethane acrylics made from hydroxyl-terminated thiocarbonate containing compounds |
| KR101358658B1 (ko) * | 2005-06-07 | 2014-02-06 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 반응성 이중 결합을 함유하는 폴리우레탄 기재 안료 분산제 |
| WO2007139980A2 (en) | 2006-05-25 | 2007-12-06 | Sun Chemical Corporation | Polymeric dispersants |
| EP2514744A1 (en) | 2006-09-07 | 2012-10-24 | Lubrizol Limited | Novel compounds and compositions thereof |
| TWI432472B (zh) * | 2006-12-04 | 2014-04-01 | Lubrizol Advanced Mat Inc | 聚胺基甲酸酯分散劑、非水性組成物及包含其之非水性研磨基質、塗料或墨水 |
| US20100132989A1 (en) * | 2007-04-19 | 2010-06-03 | Kan Fujihara | Novel polyimide precursor composition and use thereof |
| EP2281012B1 (en) * | 2008-05-30 | 2013-09-04 | Lubrizol Advanced Materials, Inc. | Dispersants from linear polyurethanes |
| JP5441464B2 (ja) * | 2009-03-23 | 2014-03-12 | 富士フイルム株式会社 | 顔料分散物、それを用いたインク組成物、硬化性組成物及び硬化性インク組成物 |
| US8436125B2 (en) * | 2010-05-27 | 2013-05-07 | Basf Se | Materials, methods for production thereof and components thereof |
| JP2013053200A (ja) | 2011-09-02 | 2013-03-21 | Tokai Carbon Co Ltd | 顔料水性分散体組成物および水性インキ組成物 |
| CN102658057B (zh) * | 2012-04-16 | 2014-09-10 | 王志军 | 一种新型聚氨酯分散剂及其制备方法 |
| US9540486B2 (en) | 2012-05-02 | 2017-01-10 | Lubrizol Advanced Materials, Inc. | Aromatic dispersant composition |
| WO2013165770A1 (en) | 2012-05-02 | 2013-11-07 | Lubrizol Advanced Materials, Inc. | Aromatic dispersant composition |
| WO2015065829A1 (en) * | 2013-11-01 | 2015-05-07 | Lubrizol Advanced Materials, Inc. | Dispersants with multiple aromatic imide anchor groups |
-
2014
- 2014-10-24 CN CN201480071428.3A patent/CN105874019B/zh active Active
- 2014-10-24 EP EP14802732.9A patent/EP3063239B1/en active Active
- 2014-10-24 KR KR1020167014522A patent/KR102236881B1/ko active Active
- 2014-10-24 US US15/032,792 patent/US10308836B2/en active Active
- 2014-10-24 JP JP2016526854A patent/JP6600306B2/ja active Active
- 2014-10-24 WO PCT/US2014/062132 patent/WO2015065831A1/en not_active Ceased
- 2014-10-31 TW TW103137732A patent/TWI664208B/zh active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2016538376A5 (enExample) | ||
| JP2016538375A5 (enExample) | ||
| JP2008169373A5 (enExample) | ||
| JP2016538377A5 (enExample) | ||
| JP2015516012A5 (enExample) | ||
| US8779155B2 (en) | 1,2,3-triazole based metal-organic framework as photo-active materials | |
| CN106459563A (zh) | 具有潜在增稠趋势的环氧树脂‑环氧固化体系 | |
| JP2009544834A5 (enExample) | ||
| CN106232698A (zh) | 用于流变控制的组合物 | |
| JP2014185333A5 (enExample) | ||
| RU2017123715A (ru) | Отверждаемые под действием влаги полимерные системы на основе смеси полисилилированных полиэфиров | |
| Risangud et al. | Hydrosilylation as an efficient tool for polymer synthesis and modification with methacrylates | |
| Wang et al. | Synthesis and properties of cyclic carbonates and non-isocyanate polyurethanes under atmospheric pressure | |
| Arslan et al. | POSS-based hybrid thermosets via photoinduced copper-catalyzed azide–alkyne cycloaddition click chemistry | |
| JP5700857B2 (ja) | コーティング組成物 | |
| Jin et al. | Aerobic cross-dehydrogenative coupling of terminal alkynes and tertiary amines by a combined catalyst of Zn 2+ and OMS-2 | |
| US11377553B2 (en) | Polymer suitable as a thickener | |
| JP2016536423A5 (enExample) | ||
| Jiang et al. | A bifunctionalized [3] rotaxane and its incorporation into a mechanically interlocked polymer | |
| NL1039698A (en) | Novel liquid curing agents and surfactants. | |
| Wołosz et al. | Sustainable associative thickeners based on hydrophobically modified ethoxylated poly (hydroxy-urethane) s end-capped by long alkyl chains | |
| JP2010526155A (ja) | ２つの隣接する水酸基を有するポリエーテルアミンマクロモノマーおよびポリウレタンを製造するためのその使用 | |
| Shin et al. | Facile Synthesis of Glycidyl Triazolyl Polymers in Water Using β-Cyclodextrin. | |
| JPH10324731A5 (enExample) | ||
| Lee et al. | Synthesis and characterization of TRITON™ X‐based surfactants with carboxylic or amino groups in the oxyethylene chain end |