JP2017519056A5 - - Google Patents
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- JP2017519056A5 JP2017519056A5 JP2016561378A JP2016561378A JP2017519056A5 JP 2017519056 A5 JP2017519056 A5 JP 2017519056A5 JP 2016561378 A JP2016561378 A JP 2016561378A JP 2016561378 A JP2016561378 A JP 2016561378A JP 2017519056 A5 JP2017519056 A5 JP 2017519056A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- polyether chain
- alkylene oxide
- amine
- derived
- 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.)
- Pending
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- 239000000203 mixture Substances 0.000 claims description 89
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 34
- 229920000570 polyether Polymers 0.000 claims description 34
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 28
- 125000000743 hydrocarbylene group Chemical group 0.000 claims description 27
- 150000001875 compounds Chemical class 0.000 claims description 22
- 229910052757 nitrogen Inorganic materials 0.000 claims description 22
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- 229910003455 mixed metal oxide Inorganic materials 0.000 claims description 21
- 239000000049 pigment Substances 0.000 claims description 20
- 150000001412 amines Chemical class 0.000 claims description 19
- -1 Cl and Br Chemical class 0.000 claims description 18
- 125000002947 alkylene group Chemical group 0.000 claims description 18
- 125000003277 amino group Chemical group 0.000 claims description 18
- 125000005842 heteroatoms Chemical group 0.000 claims description 18
- 239000002270 dispersing agent Substances 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 16
- 150000008064 anhydrides Chemical group 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 15
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 13
- 239000000919 ceramic Substances 0.000 claims description 13
- 229910052736 halogen Inorganic materials 0.000 claims description 13
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 11
- 229910044991 metal oxide Inorganic materials 0.000 claims description 11
- 150000004706 metal oxides Chemical class 0.000 claims description 11
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims description 11
- 229910052782 aluminium Inorganic materials 0.000 claims description 10
- 229910052791 calcium Inorganic materials 0.000 claims description 10
- 150000001735 carboxylic acids Chemical class 0.000 claims description 10
- 125000002091 cationic group Chemical group 0.000 claims description 10
- 229910052804 chromium Inorganic materials 0.000 claims description 10
- 229910052803 cobalt Inorganic materials 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 10
- 229910052742 iron Inorganic materials 0.000 claims description 10
- 229910052748 manganese Inorganic materials 0.000 claims description 10
- 238000003801 milling Methods 0.000 claims description 10
- 229910052718 tin Inorganic materials 0.000 claims description 10
- 229910052719 titanium Inorganic materials 0.000 claims description 10
- 229910052725 zinc Inorganic materials 0.000 claims description 10
- 229910052726 zirconium Inorganic materials 0.000 claims description 10
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 claims description 9
- 238000006845 Michael addition reaction Methods 0.000 claims description 9
- 230000002378 acidificating Effects 0.000 claims description 9
- HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 9
- 125000003368 amide group Chemical group 0.000 claims description 9
- 150000001408 amides Chemical class 0.000 claims description 9
- 125000004429 atoms Chemical group 0.000 claims description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 230000001808 coupling Effects 0.000 claims description 9
- 238000010168 coupling process Methods 0.000 claims description 9
- 238000005859 coupling reaction Methods 0.000 claims description 9
- 125000004185 ester group Chemical group 0.000 claims description 9
- 239000011521 glass Substances 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 125000005462 imide group Chemical group 0.000 claims description 9
- 150000003949 imides Chemical class 0.000 claims description 9
- 125000005647 linker group Chemical group 0.000 claims description 9
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 8
- 229910052787 antimony Inorganic materials 0.000 claims description 7
- 229910052793 cadmium Inorganic materials 0.000 claims description 7
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 7
- 239000000194 fatty acid Substances 0.000 claims description 7
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 7
- 229910052738 indium Inorganic materials 0.000 claims description 7
- 229910052749 magnesium Inorganic materials 0.000 claims description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 7
- 229910052720 vanadium Inorganic materials 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 235000019864 coconut oil Nutrition 0.000 claims description 6
- 239000003240 coconut oil Substances 0.000 claims description 6
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 238000010304 firing Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000010419 fine particle Substances 0.000 claims description 5
- OPJWPPVYCOPDCM-UHFFFAOYSA-N 2-ethylhexyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC OPJWPPVYCOPDCM-UHFFFAOYSA-N 0.000 claims description 4
- IJWIRZQYWANBMP-UHFFFAOYSA-N 4-[2-(4-hydroxy-3-propan-2-ylphenyl)propan-2-yl]-2-propan-2-ylphenol Chemical compound C1=C(O)C(C(C)C)=CC(C(C)(C)C=2C=C(C(O)=CC=2)C(C)C)=C1 IJWIRZQYWANBMP-UHFFFAOYSA-N 0.000 claims description 4
- SAOKZLXYCUGLFA-UHFFFAOYSA-N Bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 claims description 4
- UJPPXNXOEVDSRW-UHFFFAOYSA-N Isopropyl_laurate Chemical compound CCCCCCCCCCCC(=O)OC(C)C UJPPXNXOEVDSRW-UHFFFAOYSA-N 0.000 claims description 4
- 229940057007 Petroleum distillate Drugs 0.000 claims description 4
- 229920002367 Polyisobutene Polymers 0.000 claims description 4
- 239000011324 bead Substances 0.000 claims description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 229940033357 isopropyl laurate Drugs 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 239000012454 non-polar solvent Substances 0.000 claims description 4
- 239000001301 oxygen Chemical group 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 239000011236 particulate material Substances 0.000 claims description 4
- 239000003209 petroleum derivative Substances 0.000 claims description 4
- OVYMWJFNQQOJBU-UHFFFAOYSA-N 1-octanoyloxypropan-2-yl octanoate Chemical compound CCCCCCCC(=O)OCC(C)OC(=O)CCCCCCC OVYMWJFNQQOJBU-UHFFFAOYSA-N 0.000 claims description 3
- OBETXYAYXDNJHR-UHFFFAOYSA-M 2-ethylhexanoate Chemical compound CCCCC(CC)C([O-])=O OBETXYAYXDNJHR-UHFFFAOYSA-M 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- DUFKCOQISQKSAV-UHFFFAOYSA-N 2-(2-hydroxypropoxy)propan-1-ol Chemical compound CC(O)COC(C)CO DUFKCOQISQKSAV-UHFFFAOYSA-N 0.000 claims description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N Dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 1
- 238000000137 annealing Methods 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 238000005496 tempering Methods 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 description 4
- 239000000976 ink Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 240000007170 Cocos nucifera Species 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000015096 spirit Nutrition 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- KLXCNZMCHQCWKK-UHFFFAOYSA-N CCCCC(CC)C(O)=O.CC(O)COC(C)COC(C)CO Chemical compound CCCCC(CC)C(O)=O.CC(O)COC(C)COC(C)CO KLXCNZMCHQCWKK-UHFFFAOYSA-N 0.000 description 1
- VILAVOFMIJHSJA-UHFFFAOYSA-N Dicarbon monoxide Chemical class [C]=C=O VILAVOFMIJHSJA-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- DJNTZVRUYMHBTD-UHFFFAOYSA-N octyl octanoate Chemical compound CCCCCCCCOC(=O)CCCCCCC DJNTZVRUYMHBTD-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
Description
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Claims (20)
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WO2018107033A1 (en) * | 2016-12-09 | 2018-06-14 | Lubrizol Advanced Materials, Inc. | Aliphatic ceramic dispersant obtained by reaction of pibsa with non-polymeric amino ether/alcohol |
CN109810568A (zh) * | 2017-11-21 | 2019-05-28 | Tcléå¢è¡ä»œæéå ¬åž | æ æºçº³ç±³ææå°å·æ²¹å¢šåå ¶å¶å€æ¹æ³ååºçš |
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IT201800004985A1 (it) * | 2018-05-02 | 2019-11-02 | Composizione di inchiostro per la stampa a getto dâinchiostro. | |
BR112022004691A2 (pt) | 2019-09-17 | 2022-06-14 | Sun Inkjet Ceram S L | Composições para impressão a jato de tinta com base em solvente, processo para fornecer um artigo impresso, artigos impressos, uso de um ou mais compostos solúveis em água e uso de composição para impressão a jato de tinta à base de solvente |
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NL145565B (nl) | 1965-01-28 | 1975-04-15 | Shell Int Research | Werkwijze ter bereiding van een smeermiddelcompositie. |
US3574576A (en) | 1965-08-23 | 1971-04-13 | Chevron Res | Distillate fuel compositions having a hydrocarbon substituted alkylene polyamine |
US3755433A (en) | 1971-12-16 | 1973-08-28 | Texaco Inc | Ashless lubricating oil dispersant |
GB1434724A (en) | 1972-04-17 | 1976-05-05 | Rech Et Dapplications Scient S | Spasmolytic medicines comprising a vidiquil derivative |
DE3611230A1 (de) | 1986-04-04 | 1987-10-08 | Basf Ag | Polybutyl- und polyisobutylamine, verfahren zu deren herstellung und diese enthaltende kraft- und schmierstoffzusammensetzungen |
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DE4214810A1 (de) | 1992-05-04 | 1993-11-11 | Basf Ag | µ-Aminonitrile und N-Alkyl-1,3-propylendiamine sowie deren Verwendung als Kraft- und Schmierstoffadditive |
DE4309271A1 (de) | 1993-03-23 | 1994-09-29 | Basf Ag | Kraftstoffadditive, Verfahren zu ihrer Herstellung sowie Kraftstoffe fÃŒr Ottomotoren, enthaltend die Additive |
GB9421395D0 (en) * | 1994-10-24 | 1994-12-07 | Xaar Ltd | Ink jet ink composition |
US7265197B2 (en) | 2003-12-05 | 2007-09-04 | Sun Chemical Corporation | Polymeric dispersant |
US8530569B2 (en) | 2003-12-05 | 2013-09-10 | Sun Chemical Corporation | Polymeric dispersants and dispersions containing same |
WO2007102911A2 (en) | 2005-12-15 | 2007-09-13 | Lubrizol Limited | Novel dispersant and compositions thereof |
CN101410436B (zh) * | 2006-03-29 | 2013-10-16 | 西巎æ§è¡æéå ¬åž | èä¹ç¯äºèºåºé¢æåæ£å |
WO2007139980A2 (en) | 2006-05-25 | 2007-12-06 | Sun Chemical Corporation | Polymeric dispersants |
CN102532514B (zh) | 2006-09-07 | 2014-11-12 | è·¯å涊æéå ¬åž | æ°ååç©åå ¶ç»åç© |
TWI432472B (zh) | 2006-12-04 | 2014-04-01 | Lubrizol Advanced Mat Inc | èèºåºç²é žé ¯åæ£åãéæ°Žæ§çµæç©åå å«å ¶ä¹éæ°Žæ§ç 磚åºè³ªãå¡ææ墚氎 |
US7655082B2 (en) * | 2007-02-15 | 2010-02-02 | Sanford, L.P. | Ink compositions containing an emulsion |
JP5466612B2 (ja) | 2010-09-29 | 2014-04-09 | æ¥æ®è§Šåªåææ ªåŒäŒç€Ÿ | æš¹è被èŠéå±é žåç©ç²åæš¹èåæ£çµæç©ã®è£œé æ¹æ³ããã³éæ被èä»åºæ |
IT1404805B1 (it) * | 2011-02-10 | 2013-11-29 | Lamberti Spa | Disperdenti |
ITVA20110006A1 (it) | 2011-03-03 | 2012-09-04 | Lamberti Spa | Inchiostri ceramici per stampanti inkjet |
CN103184440B (zh) * | 2011-12-27 | 2015-12-02 | æ¯äºè¿ªè¡ä»œæéå ¬åž | äžç§è¡šé¢éæ©æ§éå±åçå¶ååå ¶å¶å€æ¹æ³ |
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