JP2000290567A5 - - Google Patents
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- Publication number
- JP2000290567A5 JP2000290567A5 JP2000064481A JP2000064481A JP2000290567A5 JP 2000290567 A5 JP2000290567 A5 JP 2000290567A5 JP 2000064481 A JP2000064481 A JP 2000064481A JP 2000064481 A JP2000064481 A JP 2000064481A JP 2000290567 A5 JP2000290567 A5 JP 2000290567A5
- Authority
- JP
- Japan
- Prior art keywords
- aryl
- alkyl
- alkylene
- embedded image
- substituted alkyl
- 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
- 125000003118 aryl group Chemical group 0.000 description 61
- 125000000217 alkyl group Chemical group 0.000 description 32
- 125000002947 alkylene group Chemical group 0.000 description 28
- 125000000547 substituted alkyl group Chemical group 0.000 description 23
- 125000003545 alkoxy group Chemical group 0.000 description 18
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 16
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 15
- 125000000732 arylene group Chemical group 0.000 description 15
- 229910052736 halogen Inorganic materials 0.000 description 15
- 150000002367 halogens Chemical class 0.000 description 15
- 239000000203 mixture Substances 0.000 description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- 150000001412 amines Chemical class 0.000 description 10
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- 239000001257 hydrogen Substances 0.000 description 10
- 150000002431 hydrogen Chemical class 0.000 description 9
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 8
- 230000002209 hydrophobic effect Effects 0.000 description 8
- 238000007641 inkjet printing Methods 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 7
- DOMLXBPXLNDFAB-UHFFFAOYSA-N ethoxyethane;methyl prop-2-enoate Chemical compound CCOCC.COC(=O)C=C DOMLXBPXLNDFAB-UHFFFAOYSA-N 0.000 description 6
- 229920001427 mPEG Polymers 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000000178 monomer Substances 0.000 description 5
- 229920005596 polymer binder Polymers 0.000 description 5
- 239000002491 polymer binding agent Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000004816 latex Substances 0.000 description 4
- 229920000126 latex Polymers 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- 229910015892 BF 4 Inorganic materials 0.000 description 3
- 229910020366 ClO 4 Inorganic materials 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- CBECDWUDYQOTSW-UHFFFAOYSA-N 2-ethylbut-3-enal Chemical compound CCC(C=C)C=O CBECDWUDYQOTSW-UHFFFAOYSA-N 0.000 description 2
- OBWGMYALGNDUNM-UHFFFAOYSA-N 3,3-dimethoxyprop-1-ene Chemical compound COC(OC)C=C OBWGMYALGNDUNM-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 0 CC*(C)N1CC1 Chemical compound CC*(C)N1CC1 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- -1 aroxy Chemical group 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-O diethylammonium Chemical compound CC[NH2+]CC HPNMFZURTQLUMO-UHFFFAOYSA-O 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- JTHNLKXLWOXOQK-UHFFFAOYSA-N n-propyl vinyl ketone Natural products CCCC(=O)C=C JTHNLKXLWOXOQK-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 2
- QPKNDHZQPGMLCJ-UHFFFAOYSA-N 1-(3-aminophenyl)ethanol Chemical compound CC(O)C1=CC=CC(N)=C1 QPKNDHZQPGMLCJ-UHFFFAOYSA-N 0.000 description 1
- MEYJGUROSKBIDE-UHFFFAOYSA-N 1-(butoxyamino)ethanol Chemical compound CCCCONC(C)O MEYJGUROSKBIDE-UHFFFAOYSA-N 0.000 description 1
- RPPCFYFWGVIQFS-UHFFFAOYSA-N 1-(dimethylamino)butan-1-ol Chemical compound CCCC(O)N(C)C RPPCFYFWGVIQFS-UHFFFAOYSA-N 0.000 description 1
- CBYIMFCIPMCLQF-UHFFFAOYSA-N 1-(dipropylamino)propane-1,1-diol Chemical compound CCCN(CCC)C(O)(O)CC CBYIMFCIPMCLQF-UHFFFAOYSA-N 0.000 description 1
- ZGCHLAJIRWDGFE-UHFFFAOYSA-N 1-aminopropane-1,1-diol Chemical compound CCC(N)(O)O ZGCHLAJIRWDGFE-UHFFFAOYSA-N 0.000 description 1
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 description 1
- KKFDCBRMNNSAAW-UHFFFAOYSA-N 2-(morpholin-4-yl)ethanol Chemical compound OCCN1CCOCC1 KKFDCBRMNNSAAW-UHFFFAOYSA-N 0.000 description 1
- KZTWONRVIPPDKH-UHFFFAOYSA-N 2-(piperidin-1-yl)ethanol Chemical compound OCCN1CCCCC1 KZTWONRVIPPDKH-UHFFFAOYSA-N 0.000 description 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
- GPLIMIJPIZGPIF-UHFFFAOYSA-N 2-hydroxy-1,4-benzoquinone Chemical compound OC1=CC(=O)C=CC1=O GPLIMIJPIZGPIF-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- PTHDBHDZSMGHKF-UHFFFAOYSA-N 2-piperidin-2-ylethanol Chemical compound OCCC1CCCCN1 PTHDBHDZSMGHKF-UHFFFAOYSA-N 0.000 description 1
- TYPCBYZRJIFWEI-UHFFFAOYSA-N 3-(2-hydroxyethylamino)-5,5-dimethylcyclohex-2-en-1-one Chemical compound CC1(C)CC(=O)C=C(NCCO)C1 TYPCBYZRJIFWEI-UHFFFAOYSA-N 0.000 description 1
- PYSGFFTXMUWEOT-UHFFFAOYSA-N 3-(dimethylamino)propan-1-ol Chemical compound CN(C)CCCO PYSGFFTXMUWEOT-UHFFFAOYSA-N 0.000 description 1
- XUSNPFGLKGCWGN-UHFFFAOYSA-N 3-[4-(3-aminopropyl)piperazin-1-yl]propan-1-amine Chemical group NCCCN1CCN(CCCN)CC1 XUSNPFGLKGCWGN-UHFFFAOYSA-N 0.000 description 1
- VZBNUEHCOOXOHR-UHFFFAOYSA-N 3-morpholin-4-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCOCC1 VZBNUEHCOOXOHR-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical group COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- 229910004013 NO 2 Inorganic materials 0.000 description 1
- 229910021115 PF 6 Inorganic materials 0.000 description 1
- 229910018287 SbF 5 Inorganic materials 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- 229940043276 diisopropanolamine Drugs 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002373 hemiacetals Chemical class 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- ZYWUVGFIXPNBDL-UHFFFAOYSA-N n,n-diisopropylaminoethanol Chemical compound CC(C)N(C(C)C)CCO ZYWUVGFIXPNBDL-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- VUNPWIPIOOMCPT-UHFFFAOYSA-N piperidin-3-ylmethanol Chemical compound OCC1CCCNC1 VUNPWIPIOOMCPT-UHFFFAOYSA-N 0.000 description 1
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US265185 | 1988-10-31 | ||
| US26518599A | 1999-03-09 | 1999-03-09 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2000290567A JP2000290567A (ja) | 2000-10-17 |
| JP2000290567A5 true JP2000290567A5 (enExample) | 2006-11-30 |
| JP5053476B2 JP5053476B2 (ja) | 2012-10-17 |
Family
ID=23009378
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000064481A Expired - Fee Related JP5053476B2 (ja) | 1999-03-09 | 2000-03-09 | 優れた耐汚れ堅牢性を有するインクジェット印刷用インク組成物 |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP1035179B1 (enExample) |
| JP (1) | JP5053476B2 (enExample) |
| DE (1) | DE60026113T2 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1201720B1 (en) * | 2000-10-23 | 2004-09-15 | Hewlett-Packard Company | Printing fluid additives promoting overcoat adhesion |
| US20030055135A1 (en) * | 2001-09-17 | 2003-03-20 | Westvaco Corporation | Pigmented ink jet inks |
| JP4296750B2 (ja) * | 2002-03-29 | 2009-07-15 | セイコーエプソン株式会社 | インクセット、及びこれを用いたインクジェット記録物の製造方法 |
| US6779882B2 (en) | 2002-10-08 | 2004-08-24 | Hewlett-Packard Development Company, L.P. | Ink-jet printing systems and methods for extending air fade resistance of ink-jet prints |
| US7153350B2 (en) | 2003-12-10 | 2006-12-26 | Pitney Bowes Inc. | Water soluble colorants for ink jet printing |
| US7847027B2 (en) * | 2006-12-29 | 2010-12-07 | Eastman Kodak Company | Encapsulated mordant particle dispersion and method of preparing |
| US7833591B2 (en) | 2006-12-29 | 2010-11-16 | Eastman Kodak Company | Image recording element comprising encapsulated mordant particles |
| US10072166B2 (en) | 2014-07-30 | 2018-09-11 | Hewlett-Packard Development Company, L.P. | Inks with latex polymers having improved printing performance |
| JP6833339B2 (ja) * | 2015-05-21 | 2021-02-24 | キヤノン株式会社 | 水性インク、インクカートリッジ、及びインクジェット記録方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6042832B2 (ja) * | 1977-10-18 | 1985-09-25 | 富士写真フイルム株式会社 | インクジエツト記録用インク組成物 |
| JPS582366A (ja) * | 1981-06-30 | 1983-01-07 | Konishiroku Photo Ind Co Ltd | インクジエツト記録用インク組成物 |
| US5160372A (en) * | 1991-06-13 | 1992-11-03 | E. I. Du Pont De Nemours And Company | Aqueous ink jet inks containing ester diol and amide diol cosolvents |
| JP3642358B2 (ja) * | 1995-12-06 | 2005-04-27 | 東洋紡績株式会社 | ポリエステル系樹脂水分散体およびその製法 |
| JP3257391B2 (ja) * | 1996-03-18 | 2002-02-18 | 東洋インキ製造株式会社 | インクジェット記録液 |
| JP3859260B2 (ja) * | 1996-04-09 | 2006-12-20 | 三菱化学株式会社 | 水性着色樹脂分散体、水性インク及びインクジェット用記録液 |
| US6020400A (en) * | 1996-12-27 | 2000-02-01 | E. I. Du Pont De Nemours And Company | Ink jet inks containing emulsion polymer additives stabilized with structured polymers |
| JP3322830B2 (ja) * | 1997-02-07 | 2002-09-09 | 花王株式会社 | インクジェット記録用水系インク |
| JPH10279854A (ja) * | 1997-04-07 | 1998-10-20 | Seiko Epson Corp | 耐光性に優れた画像を実現するインク組成物 |
| JPH1143638A (ja) * | 1997-05-28 | 1999-02-16 | Fuji Photo Film Co Ltd | インクジェット式製版用油性インクおよびインクジェット式製版印刷版の作成方法 |
| US6329446B1 (en) * | 1997-06-05 | 2001-12-11 | Xerox Corporation | Ink composition |
| WO1999023183A1 (en) * | 1997-10-31 | 1999-05-14 | Hewlett-Packard Company | Printing ink compositions having superior smear-fastness |
-
2000
- 2000-02-22 DE DE2000626113 patent/DE60026113T2/de not_active Expired - Lifetime
- 2000-02-22 EP EP20000301396 patent/EP1035179B1/en not_active Expired - Lifetime
- 2000-03-09 JP JP2000064481A patent/JP5053476B2/ja not_active Expired - Fee Related
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