JP2016538377A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016538377A5 JP2016538377A5 JP2016526858A JP2016526858A JP2016538377A5 JP 2016538377 A5 JP2016538377 A5 JP 2016538377A5 JP 2016526858 A JP2016526858 A JP 2016526858A JP 2016526858 A JP2016526858 A JP 2016526858A JP 2016538377 A5 JP2016538377 A5 JP 2016538377A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- polymer
- imide
- amino
- pendant
- 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 47
- 239000000203 mixture Substances 0.000 claims description 45
- 125000005462 imide group Chemical group 0.000 claims description 31
- 125000003277 amino group Chemical group 0.000 claims description 27
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 26
- 229920000570 polyether Polymers 0.000 claims description 25
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 23
- 229920000728 polyester Polymers 0.000 claims description 22
- 239000012948 isocyanate Substances 0.000 claims description 19
- 150000002513 isocyanates Chemical class 0.000 claims description 19
- -1 imide compound Chemical class 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 150000001735 carboxylic acids Chemical class 0.000 claims description 12
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 12
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 claims description 11
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
- 150000003949 imides Chemical class 0.000 claims description 10
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 9
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 150000002924 oxiranes Chemical group 0.000 claims description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- 150000008064 anhydrides Chemical class 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 150000002596 lactones Chemical class 0.000 claims description 8
- 229920000647 polyepoxide Polymers 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 8
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 7
- 125000003700 epoxy group Chemical group 0.000 claims description 6
- 150000001414 amino alcohols Chemical class 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 4
- 238000012644 addition polymerization Methods 0.000 claims description 4
- 239000002168 alkylating agent Substances 0.000 claims description 4
- 229940100198 alkylating agent Drugs 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000005660 chlorination reaction Methods 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 150000005676 cyclic carbonates Chemical class 0.000 claims description 4
- 239000002270 dispersing agent Substances 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 125000000743 hydrocarbylene group Chemical group 0.000 claims description 4
- 239000002609 medium Substances 0.000 claims description 4
- 150000007522 mineralic acids Chemical class 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 235000011007 phosphoric acid Nutrition 0.000 claims description 4
- 150000003016 phosphoric acids Chemical class 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 239000011574 phosphorus Substances 0.000 claims description 4
- 239000013460 polyoxometalate Substances 0.000 claims description 4
- 229920000137 polyphosphoric acid Polymers 0.000 claims description 4
- 238000005956 quaternization reaction Methods 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 150000001261 hydroxy acids Chemical class 0.000 claims description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
- 239000012736 aqueous medium Substances 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- XJHABGPPCLHLLV-UHFFFAOYSA-N benzo[de]isoquinoline-1,3-dione Chemical compound C1=CC(C(=O)NC2=O)=C3C2=CC=CC3=C1 XJHABGPPCLHLLV-UHFFFAOYSA-N 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 125000005647 linker group Chemical group 0.000 claims description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 239000003973 paint Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 4
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical group Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- IUMNWHADVMZBJV-UHFFFAOYSA-N 6-nitrobenzo[de]isoquinoline-1,3-dione Chemical compound O=C1NC(=O)C2=CC=CC3=C2C1=CC=C3[N+](=O)[O-] IUMNWHADVMZBJV-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361898714P | 2013-11-01 | 2013-11-01 | |
| US61/898,714 | 2013-11-01 | ||
| PCT/US2014/061456 WO2015065753A1 (en) | 2013-11-01 | 2014-10-21 | Aromatic dispersant composition |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019124466A Division JP2019167550A (ja) | 2013-11-01 | 2019-07-03 | 芳香族分散剤組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016538377A JP2016538377A (ja) | 2016-12-08 |
| JP2016538377A5 true JP2016538377A5 (enExample) | 2017-11-16 |
| JP6577946B2 JP6577946B2 (ja) | 2019-09-18 |
Family
ID=51842922
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016526858A Active JP6577946B2 (ja) | 2013-11-01 | 2014-10-21 | 芳香族分散剤組成物 |
| JP2019124466A Withdrawn JP2019167550A (ja) | 2013-11-01 | 2019-07-03 | 芳香族分散剤組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019124466A Withdrawn JP2019167550A (ja) | 2013-11-01 | 2019-07-03 | 芳香族分散剤組成物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10113031B2 (enExample) |
| EP (1) | EP3063204B1 (enExample) |
| JP (2) | JP6577946B2 (enExample) |
| KR (1) | KR102247503B1 (enExample) |
| CN (1) | CN105899578B (enExample) |
| TW (1) | TWI667268B (enExample) |
| WO (1) | WO2015065753A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3606981B1 (de) * | 2017-04-05 | 2021-02-24 | BYK-Chemie GmbH | Monoepoxid-monoamin-addukte als netz- und dispergiermittel |
| HUE062347T2 (hu) * | 2017-06-28 | 2023-10-28 | Huntsman Petrochemical Llc | Tetrahidrofurfuril-alkohollal iniciált poliéteraminok és alkalmazásuk |
| CN107983264B (zh) * | 2017-10-30 | 2020-03-17 | 珠海市金团化学品有限公司 | 一种环保型水油两用高分子分散剂及其制备方法 |
| PL3802665T3 (pl) * | 2018-06-06 | 2024-01-03 | Basf Se | Alkoksylowane poliamidoaminy jako środki dyspergujące |
| EP3840870B1 (en) * | 2018-08-22 | 2026-06-24 | Lubrizol Advanced Materials, Inc. | Aromatic amide dispersant |
| CN112584922B (zh) * | 2018-08-22 | 2023-01-24 | 路博润先进材料公司 | 芳香族酰胺分散剂 |
| US12202937B2 (en) * | 2018-09-25 | 2025-01-21 | Huntsman Petrochemical Llc | Cyclic amide initialized polyetheramine and uses thereof |
| PT3670618T (pt) | 2018-12-20 | 2023-06-15 | Henkel Ag & Co Kgaa | Método de produção de poliésteres funcionalizados |
| WO2020186126A1 (en) * | 2019-03-14 | 2020-09-17 | Lubrizol Advanced Materials, Inc. | Multi-amine polyester dispersant made via an anhydride intermediate |
| EP4031600A1 (en) * | 2019-09-20 | 2022-07-27 | Basf Se | Polyalkyleneimine-based polymers containing polyether chains |
| EP4031599B1 (en) | 2019-09-20 | 2026-04-01 | Basf Se | Polyalkyleneimine-based polymer containing polyether chains |
| CN112778514B (zh) * | 2019-11-07 | 2023-07-07 | 长春人造树脂厂股份有限公司 | 化合物、包含该化合物的水性环氧树脂组合物及包含该水性环氧树脂组合物的涂料组合物 |
| CN110845906A (zh) * | 2019-12-20 | 2020-02-28 | 江苏正红彩印有限公司 | 一种环保水性柔印uv油墨 |
| CN110982329A (zh) * | 2019-12-20 | 2020-04-10 | 江苏正红彩印有限公司 | 一种低voc高亮耐磨水性环保油墨 |
| WO2023008359A1 (ja) * | 2021-07-29 | 2023-02-02 | 富士フイルム株式会社 | 磁気粘性流体および磁気粘性流体デバイス |
| DE102023120315A1 (de) | 2023-07-31 | 2025-02-06 | Rheinisch-Westfälische Technische Hochschule Aachen, abgekürzt RWTH Aachen, Körperschaft des öffentlichen Rechts | Verfahren zur Herstellung von Pyrrolidon-substituierten Polyolen |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2140087B1 (enExample) * | 1971-06-03 | 1978-03-17 | Basf Ag | |
| US5424346A (en) | 1988-08-08 | 1995-06-13 | Ecopol, Llc | Biodegradable replacement of crystal polystyrene |
| US5128393A (en) | 1989-07-12 | 1992-07-07 | E. I. Du Pont De Nemours And Company | Imidazoline amine-epoxy adduct as a pigment dispersant |
| US4992204A (en) * | 1989-08-22 | 1991-02-12 | Miliken Research Corporation | Irradiation detection and identification method and compositions useful therein |
| FR2696736B1 (fr) | 1992-10-12 | 1994-12-30 | Chryso | Fluidifiants pour suspensions aqueuses de particules minérales et pâtes de liant hydraulique. |
| US5324756A (en) | 1993-05-05 | 1994-06-28 | E. I. Du Pont De Nemours And Company | Pigment dispersant for cathodic electrocoating compositions |
| US5424364A (en) * | 1994-05-17 | 1995-06-13 | E. I. Du Pont De Nemours & Company | Comb pigment dispersants |
| US5688312A (en) | 1996-03-29 | 1997-11-18 | Xerox Corporation | Ink compositions |
| US5852123A (en) | 1996-10-17 | 1998-12-22 | E. I. Du Pont De Nemours And Company | Graft copolymer with a urea or imid functional group as a pigment dispersant |
| 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 |
| JP3993747B2 (ja) | 1999-02-02 | 2007-10-17 | ミリケン・アンド・カンパニー | アリールオキシ−ポリ（オキシアルキレン）ナフタルイミド誘導体着色剤 |
| US6440207B1 (en) | 2000-03-03 | 2002-08-27 | Bayer Corporation | Method for preparing organic pigments |
| DE10326147A1 (de) | 2003-06-06 | 2005-03-03 | Byk-Chemie Gmbh | Epoxid-Addukte und deren Salze als Dispergiermittel |
| US7265197B2 (en) * | 2003-12-05 | 2007-09-04 | Sun Chemical Corporation | Polymeric dispersant |
| KR101237170B1 (ko) | 2004-05-13 | 2013-02-25 | 헌츠만 페트로케미칼 엘엘씨 | 잉크 중의 빗-유사 폴리에테르알카놀아민 |
| WO2008018873A1 (en) | 2006-08-09 | 2008-02-14 | Huntsman Petrochemical Corporation | Comb-like polyetheralkanolamines in inks and coatings |
| JP5014984B2 (ja) | 2004-05-13 | 2012-08-29 | ハンツマン ペトロケミカル コーポレイション | インク中の櫛形ポリエーテルアルカノールアミン |
| US9238766B2 (en) | 2004-05-13 | 2016-01-19 | Huntsman Petrochemical Llc | Comb-like polyetheralkanolamines in inks and coatings |
| DE102004050955A1 (de) | 2004-10-20 | 2006-04-27 | Byk-Chemie Gmbh | Alkoxylierte Epoxyd-Amin-Addukte und deren Verwendung |
| EP2019849A4 (en) | 2006-05-25 | 2012-09-05 | Sun Chemical Corp | POLYMERIC DISPERSANTS |
| CN102532514B (zh) | 2006-09-07 | 2014-11-12 | 路博润有限公司 | 新化合物和其组合物 |
| DE102007005720A1 (de) | 2007-01-31 | 2008-08-07 | Byk-Chemie Gmbh | Epoxid-Amin-Addukte als Dispergier- und Netzmittel |
| AU2008338555B2 (en) | 2007-12-14 | 2013-05-02 | Coatings Foreign Ip Co. Llc | Organic solvent free pigment dispersant for waterborne electrocoating |
| TWI395806B (zh) | 2010-04-14 | 2013-05-11 | Ind Tech Res Inst | 封裝材料 |
| JP5520867B2 (ja) | 2011-03-30 | 2014-06-11 | 大日精化工業株式会社 | 顔料着色剤組成物及び該組成物を含有してなるカラーフィルター用顔料着色剤組成物 |
| 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 |
| JP6415428B2 (ja) * | 2012-05-02 | 2018-10-31 | ルブリゾル アドバンスド マテリアルズ， インコーポレイテッド | 芳香族分散剤組成物 |
| JP6642940B2 (ja) * | 2012-05-02 | 2020-02-12 | ルブリゾル アドバンスド マテリアルズ， インコーポレイテッド | 芳香族分散剤組成物 |
-
2014
- 2014-10-21 US US15/032,083 patent/US10113031B2/en active Active
- 2014-10-21 EP EP14790984.0A patent/EP3063204B1/en active Active
- 2014-10-21 JP JP2016526858A patent/JP6577946B2/ja active Active
- 2014-10-21 CN CN201480071274.8A patent/CN105899578B/zh active Active
- 2014-10-21 WO PCT/US2014/061456 patent/WO2015065753A1/en not_active Ceased
- 2014-10-21 KR KR1020167014516A patent/KR102247503B1/ko not_active Expired - Fee Related
- 2014-10-28 TW TW103137193A patent/TWI667268B/zh active
-
2019
- 2019-07-03 JP JP2019124466A patent/JP2019167550A/ja not_active Withdrawn
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FI96430B (fi) | Aminouretaaneja, niiden valmistusmenetelmä ja niiden käyttö | |
| KR102322812B1 (ko) | 잠복성 증점 경향이 있는 에폭시 수지-에폭시 경화 시스템 | |
| TWI629332B (zh) | 陽離子水可稀釋黏著劑、其製備方法及其應用 | |
| JP5351767B2 (ja) | イソシアネートモノアダクトをベースとする汎用湿潤分散剤 | |
| US2839495A (en) | Process for resinifying polyepoxides and resulting products | |
| US10155842B2 (en) | Titanium-based catalyst for vitrimer resins of epoxy/anhydride type | |
| JPH0649193A (ja) | ポリエーテル−ポリエステルブロックコポリマー及び分散剤としてのそれらの用途 | |
| RU2017138451A (ru) | Агрегирующие композиции, композиции модифицированных твердых частиц и способы их получения и применения | |
| JP4274691B2 (ja) | エポキシ樹脂用水混和性硬化剤 | |
| JP2014518909A (ja) | 多官能一級アミン、その調製方法、及びその使用 | |
| JP2004359956A6 (ja) | 湿潤剤又は分散剤用エポキシド付加物及びその塩 | |
| TW200427721A (en) | Epoxide adducts and their salts as dispersants | |
| JP2015516012A5 (enExample) | ||
| ATE20531T1 (de) | Wasserdispergierbare bindemittel fuer kationische elektrotauchlacke und verfahren zu ihrer herstellung. | |
| TW201221534A (en) | Water dispersible epoxy resin and production method thereof, water-based epoxy resin composition and curable articles thereof | |
| JPS58103527A (ja) | 予め触媒を添加したエポキシ樹脂組成物 | |
| CN111234182A (zh) | 快速固化的环氧体系 | |
| JP2015521216A5 (enExample) | ||
| JP2016538376A5 (enExample) | ||
| JPH01193317A (ja) | 熱硬化性液状組成物 | |
| US6258919B1 (en) | Curable epoxy resin compositions containing water-processable polyamine hardeners | |
| JP2005029797A (ja) | エポキシ樹脂組成物 | |
| CN106317381B (zh) | 一种水性环氧固化剂及其制备方法 | |
| JP6944518B2 (ja) | 熱硬化性樹脂組成物及びその製造方法 | |
| JP2004528423A (ja) | 高官能性ポリマー |