JP2002194252A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2002194252A5 JP2002194252A5 JP2001325176A JP2001325176A JP2002194252A5 JP 2002194252 A5 JP2002194252 A5 JP 2002194252A5 JP 2001325176 A JP2001325176 A JP 2001325176A JP 2001325176 A JP2001325176 A JP 2001325176A JP 2002194252 A5 JP2002194252 A5 JP 2002194252A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- aryl
- fluid composition
- printing fluid
- 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
- 239000000203 mixture Substances 0.000 claims 75
- 239000012530 fluid Substances 0.000 claims 73
- 125000003118 aryl group Chemical group 0.000 claims 49
- 125000000217 alkyl group Chemical group 0.000 claims 48
- 239000000178 monomer Substances 0.000 claims 47
- 125000000547 substituted alkyl group Chemical group 0.000 claims 39
- 125000003107 substituted aryl group Chemical group 0.000 claims 34
- 125000002947 alkylene group Chemical group 0.000 claims 25
- 229910052736 halogen Inorganic materials 0.000 claims 22
- 150000002367 halogens Chemical class 0.000 claims 22
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 19
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 19
- 125000000732 arylene group Chemical group 0.000 claims 19
- -1 aroxy Chemical group 0.000 claims 15
- 125000003545 alkoxy group Chemical group 0.000 claims 12
- 229910052760 oxygen Inorganic materials 0.000 claims 12
- 125000002877 alkyl aryl group Chemical group 0.000 claims 9
- 229910052739 hydrogen Inorganic materials 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 9
- 239000000463 material Substances 0.000 claims 9
- 150000002431 hydrogen Chemical class 0.000 claims 8
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 7
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 7
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims 7
- 229920006395 saturated elastomer Polymers 0.000 claims 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 5
- 229910019142 PO4 Inorganic materials 0.000 claims 5
- 229920006243 acrylic copolymer Polymers 0.000 claims 5
- 150000002148 esters Chemical class 0.000 claims 5
- 230000002209 hydrophobic effect Effects 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 235000021317 phosphate Nutrition 0.000 claims 5
- 150000003839 salts Chemical class 0.000 claims 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 4
- 229940048053 acrylate Drugs 0.000 claims 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims 4
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims 4
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 3
- 239000002202 Polyethylene glycol Substances 0.000 claims 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 239000011248 coating agent Substances 0.000 claims 3
- 238000000576 coating method Methods 0.000 claims 3
- 229920001427 mPEG Polymers 0.000 claims 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 3
- 239000011976 maleic acid Substances 0.000 claims 3
- 239000010452 phosphate Substances 0.000 claims 3
- 229920001223 polyethylene glycol Polymers 0.000 claims 3
- 238000006116 polymerization reaction Methods 0.000 claims 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 3
- JLIDVCMBCGBIEY-UHFFFAOYSA-N 1-penten-3-one Chemical compound CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 claims 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical group NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical group CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 2
- 108010010803 Gelatin Proteins 0.000 claims 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 125000005250 alkyl acrylate group Chemical group 0.000 claims 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims 2
- 125000005626 carbonium group Chemical group 0.000 claims 2
- HPNMFZURTQLUMO-UHFFFAOYSA-O diethylammonium Chemical compound CC[NH2+]CC HPNMFZURTQLUMO-UHFFFAOYSA-O 0.000 claims 2
- DUDCYUDPBRJVLG-UHFFFAOYSA-N ethoxyethane methyl 2-methylprop-2-enoate Chemical compound CCOCC.COC(=O)C(C)=C DUDCYUDPBRJVLG-UHFFFAOYSA-N 0.000 claims 2
- DOMLXBPXLNDFAB-UHFFFAOYSA-N ethoxyethane;methyl prop-2-enoate Chemical compound CCOCC.COC(=O)C=C DOMLXBPXLNDFAB-UHFFFAOYSA-N 0.000 claims 2
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims 2
- 229920000159 gelatin Polymers 0.000 claims 2
- 239000008273 gelatin Substances 0.000 claims 2
- 235000019322 gelatine Nutrition 0.000 claims 2
- 235000011852 gelatine desserts Nutrition 0.000 claims 2
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 claims 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 2
- 229920001451 polypropylene glycol Polymers 0.000 claims 2
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 claims 2
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 claims 2
- 239000007787 solid Substances 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 claims 2
- GWYSWOQRJGLJPA-UHFFFAOYSA-N 1,1,2,2-tetrafluoropropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(F)(F)C(C)(F)F GWYSWOQRJGLJPA-UHFFFAOYSA-N 0.000 claims 1
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical group CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 claims 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims 1
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 claims 1
- XIRPMPKSZHNMST-UHFFFAOYSA-N 1-ethenyl-2-phenylbenzene Chemical group C=CC1=CC=CC=C1C1=CC=CC=C1 XIRPMPKSZHNMST-UHFFFAOYSA-N 0.000 claims 1
- LWWJIQWIJBMGKE-UHFFFAOYSA-N 1-ethenyl-4-methylpyrrolidin-2-one Chemical compound CC1CN(C=C)C(=O)C1 LWWJIQWIJBMGKE-UHFFFAOYSA-N 0.000 claims 1
- KNXAJSDVPFIKRN-UHFFFAOYSA-N 1-ethenyl-4-phenylpyrrolidin-2-one Chemical compound C1C(=O)N(C=C)CC1C1=CC=CC=C1 KNXAJSDVPFIKRN-UHFFFAOYSA-N 0.000 claims 1
- UVHXEHGUEKARKZ-UHFFFAOYSA-N 1-ethenylanthracene Chemical compound C1=CC=C2C=C3C(C=C)=CC=CC3=CC2=C1 UVHXEHGUEKARKZ-UHFFFAOYSA-N 0.000 claims 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical group C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims 1
- WPMHMYHJGDAHKX-UHFFFAOYSA-N 1-ethenylpyrene Chemical compound C1=C2C(C=C)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 WPMHMYHJGDAHKX-UHFFFAOYSA-N 0.000 claims 1
- KZCSJWFLPQFDNW-UHFFFAOYSA-N 1-ethenylpyrrole-2,5-dione Chemical compound C=CN1C(=O)C=CC1=O KZCSJWFLPQFDNW-UHFFFAOYSA-N 0.000 claims 1
- OYLCUJRJCUXQBQ-UHFFFAOYSA-N 1-hepten-3-one Chemical compound CCCCC(=O)C=C OYLCUJRJCUXQBQ-UHFFFAOYSA-N 0.000 claims 1
- FBPVUBVZRPURIU-UHFFFAOYSA-N 1-hexylpyrrole-2,5-dione Chemical compound CCCCCCN1C(=O)C=CC1=O FBPVUBVZRPURIU-UHFFFAOYSA-N 0.000 claims 1
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 claims 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 claims 1
- PKNHMUUNDHSGKI-UHFFFAOYSA-N 12-aminododecyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCCCCCCCN PKNHMUUNDHSGKI-UHFFFAOYSA-N 0.000 claims 1
- UKGQUCAKWDITNO-UHFFFAOYSA-N 12-aminododecyl prop-2-enoate Chemical compound NCCCCCCCCCCCCOC(=O)C=C UKGQUCAKWDITNO-UHFFFAOYSA-N 0.000 claims 1
- NKYRAXWYDRHWOG-UHFFFAOYSA-N 12-hydroxydodecyl prop-2-enoate Chemical compound OCCCCCCCCCCCCOC(=O)C=C NKYRAXWYDRHWOG-UHFFFAOYSA-N 0.000 claims 1
- BQBCWCQUNGRXLG-UHFFFAOYSA-N 18-aminooctadecyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCCCCCCCCCCCCCN BQBCWCQUNGRXLG-UHFFFAOYSA-N 0.000 claims 1
- GCNLVJHOXZVCPK-UHFFFAOYSA-N 18-aminooctadecyl prop-2-enoate Chemical compound NCCCCCCCCCCCCCCCCCCOC(=O)C=C GCNLVJHOXZVCPK-UHFFFAOYSA-N 0.000 claims 1
- HZDCCHQSZMIRHG-UHFFFAOYSA-N 18-hydroxyoctadecyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCCCCCCCCCCCCCO HZDCCHQSZMIRHG-UHFFFAOYSA-N 0.000 claims 1
- JHGWYTWADRWKPW-UHFFFAOYSA-N 18-hydroxyoctadecyl prop-2-enoate Chemical compound OCCCCCCCCCCCCCCCCCCOC(=O)C=C JHGWYTWADRWKPW-UHFFFAOYSA-N 0.000 claims 1
- VIEHKBXCWMMOOU-UHFFFAOYSA-N 2,2,3,3,4,4,4-heptafluorobutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(F)(F)C(F)(F)C(F)(F)F VIEHKBXCWMMOOU-UHFFFAOYSA-N 0.000 claims 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 claims 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims 1
- QLIBJPGWWSHWBF-UHFFFAOYSA-N 2-aminoethyl methacrylate Chemical compound CC(=C)C(=O)OCCN QLIBJPGWWSHWBF-UHFFFAOYSA-N 0.000 claims 1
- UGIJCMNGQCUTPI-UHFFFAOYSA-N 2-aminoethyl prop-2-enoate Chemical group NCCOC(=O)C=C UGIJCMNGQCUTPI-UHFFFAOYSA-N 0.000 claims 1
- GEPVYUYZXJFYDI-UHFFFAOYSA-N 2-aminopropan-2-yl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)N GEPVYUYZXJFYDI-UHFFFAOYSA-N 0.000 claims 1
- GSDBRJGLFJCCIT-UHFFFAOYSA-N 2-aminopropan-2-yl prop-2-enoate Chemical compound CC(C)(N)OC(=O)C=C GSDBRJGLFJCCIT-UHFFFAOYSA-N 0.000 claims 1
- ZXMSEKZWSHOVQW-UHFFFAOYSA-N 2-but-2-enyloxirane Chemical group CC=CCC1CO1 ZXMSEKZWSHOVQW-UHFFFAOYSA-N 0.000 claims 1
- NQIJAAURIDJBPB-UHFFFAOYSA-N 2-cyclopentyloxyethoxycyclopentane Chemical compound C1CCCC1OCCOC1CCCC1 NQIJAAURIDJBPB-UHFFFAOYSA-N 0.000 claims 1
- FVCDMHWSPLRYAB-UHFFFAOYSA-N 2-ethenyl-2-methyloxirane Chemical compound C=CC1(C)CO1 FVCDMHWSPLRYAB-UHFFFAOYSA-N 0.000 claims 1
- FJFXQAXZWRDDOO-UHFFFAOYSA-N 2-ethenyl-5-methyl-1h-imidazole Chemical compound CC1=CNC(C=C)=N1 FJFXQAXZWRDDOO-UHFFFAOYSA-N 0.000 claims 1
- TZAAXWSIBQAITB-UHFFFAOYSA-N 2-ethenyl-5-phenyl-1h-imidazole Chemical compound N1C(C=C)=NC=C1C1=CC=CC=C1 TZAAXWSIBQAITB-UHFFFAOYSA-N 0.000 claims 1
- IGDLZDCWMRPMGL-UHFFFAOYSA-N 2-ethenylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(C=C)C(=O)C2=C1 IGDLZDCWMRPMGL-UHFFFAOYSA-N 0.000 claims 1
- YYPLPZPLLWYWKD-UHFFFAOYSA-N 2-ethenylpyridin-1-ium;chloride Chemical compound Cl.C=CC1=CC=CC=N1 YYPLPZPLLWYWKD-UHFFFAOYSA-N 0.000 claims 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 claims 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 1
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical compound CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 claims 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 claims 1
- ILZXXGLGJZQLTR-UHFFFAOYSA-N 2-phenylethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC1=CC=CC=C1 ILZXXGLGJZQLTR-UHFFFAOYSA-N 0.000 claims 1
- HPSGLFKWHYAKSF-UHFFFAOYSA-N 2-phenylethyl prop-2-enoate Chemical compound C=CC(=O)OCCC1=CC=CC=C1 HPSGLFKWHYAKSF-UHFFFAOYSA-N 0.000 claims 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 1
- HKADMMFLLPJEAG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-enylbenzene Chemical compound FC(F)(F)C=CC1=CC=CC=C1 HKADMMFLLPJEAG-UHFFFAOYSA-N 0.000 claims 1
- JBDMKOVTOUIKFI-UHFFFAOYSA-N 3-[methoxy(dimethyl)silyl]propyl 2-methylprop-2-enoate Chemical compound CO[Si](C)(C)CCCOC(=O)C(C)=C JBDMKOVTOUIKFI-UHFFFAOYSA-N 0.000 claims 1
- SNCMCDMEYCLVBO-UHFFFAOYSA-N 3-aminopropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCN SNCMCDMEYCLVBO-UHFFFAOYSA-N 0.000 claims 1
- OTKLRHWBZHQJOP-UHFFFAOYSA-N 3-aminopropyl prop-2-enoate Chemical compound NCCCOC(=O)C=C OTKLRHWBZHQJOP-UHFFFAOYSA-N 0.000 claims 1
- WSUIRDORMCYOBS-UHFFFAOYSA-N 3-chloro-2-methylprop-2-enoic acid Chemical compound ClC=C(C)C(O)=O WSUIRDORMCYOBS-UHFFFAOYSA-N 0.000 claims 1
- IZUVGRMMRWJVKU-UHFFFAOYSA-N 3-ethoxycarbonylbut-3-enoic acid Chemical compound CCOC(=O)C(=C)CC(O)=O IZUVGRMMRWJVKU-UHFFFAOYSA-N 0.000 claims 1
- BESKSSIEODQWBP-UHFFFAOYSA-N 3-tris(trimethylsilyloxy)silylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C BESKSSIEODQWBP-UHFFFAOYSA-N 0.000 claims 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 claims 1
- AOIUPKVEPBMRDZ-UHFFFAOYSA-N 4-aminobutyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCN AOIUPKVEPBMRDZ-UHFFFAOYSA-N 0.000 claims 1
- IEOMKERTJQIKKF-UHFFFAOYSA-N 4-aminobutyl prop-2-enoate Chemical compound NCCCCOC(=O)C=C IEOMKERTJQIKKF-UHFFFAOYSA-N 0.000 claims 1
- PGXIJLSNAVMTTA-UHFFFAOYSA-N 6-aminohexyl prop-2-enoate Chemical compound NCCCCCCOC(=O)C=C PGXIJLSNAVMTTA-UHFFFAOYSA-N 0.000 claims 1
- XFOFBPRPOAWWPA-UHFFFAOYSA-N 6-hydroxyhexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCO XFOFBPRPOAWWPA-UHFFFAOYSA-N 0.000 claims 1
- OCIFJWVZZUDMRL-UHFFFAOYSA-N 6-hydroxyhexyl prop-2-enoate Chemical compound OCCCCCCOC(=O)C=C OCIFJWVZZUDMRL-UHFFFAOYSA-N 0.000 claims 1
- NQSLZEHVGKWKAY-UHFFFAOYSA-N 6-methylheptyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C(C)=C NQSLZEHVGKWKAY-UHFFFAOYSA-N 0.000 claims 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 1
- QKWQAGQPDZNXFV-UHFFFAOYSA-M C(CC)S(=O)(=O)[O-].C(C(=C)C)(=O)N.[Na+] Chemical compound C(CC)S(=O)(=O)[O-].C(C(=C)C)(=O)N.[Na+] QKWQAGQPDZNXFV-UHFFFAOYSA-M 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- XLYMOEINVGRTEX-ARJAWSKDSA-N Ethyl hydrogen fumarate Chemical compound CCOC(=O)\C=C/C(O)=O XLYMOEINVGRTEX-ARJAWSKDSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 1
- 229910018287 SbF 5 Inorganic materials 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- GYKFOCBYAQDOCU-UHFFFAOYSA-N [2-(2-aminoethyl)phenyl] prop-2-enoate Chemical compound NCCC1=CC=CC=C1OC(=O)C=C GYKFOCBYAQDOCU-UHFFFAOYSA-N 0.000 claims 1
- LGICNCFHCOAIAD-UHFFFAOYSA-N [Cl-].C(C)[NH+](CC)CC.CCC.C(C(=C)C)(=O)N Chemical compound [Cl-].C(C)[NH+](CC)CC.CCC.C(C(=C)C)(=O)N LGICNCFHCOAIAD-UHFFFAOYSA-N 0.000 claims 1
- GGSVHHHZFRLTDA-UHFFFAOYSA-N [Cl-].C(C)[NH+](CC)CC.CCC.C(C=C)(=O)N Chemical group [Cl-].C(C)[NH+](CC)CC.CCC.C(C=C)(=O)N GGSVHHHZFRLTDA-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000002318 adhesion promoter Substances 0.000 claims 1
- 125000005192 alkyl ethylene group Chemical group 0.000 claims 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- WPKYZIPODULRBM-UHFFFAOYSA-N azane;prop-2-enoic acid Chemical compound N.OC(=O)C=C WPKYZIPODULRBM-UHFFFAOYSA-N 0.000 claims 1
- DZGUJOWBVDZNNF-UHFFFAOYSA-N azanium;2-methylprop-2-enoate Chemical compound [NH4+].CC(=C)C([O-])=O DZGUJOWBVDZNNF-UHFFFAOYSA-N 0.000 claims 1
- 230000004888 barrier function Effects 0.000 claims 1
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 claims 1
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 claims 1
- GWVIABVICWKUMR-UHFFFAOYSA-L disodium;dioxido-oxo-prop-1-en-2-yl-$l^{5}-phosphane Chemical compound [Na+].[Na+].CC(=C)P([O-])([O-])=O GWVIABVICWKUMR-UHFFFAOYSA-L 0.000 claims 1
- CGQZIFGCHVCAHE-UHFFFAOYSA-L disodium;ethenyl-dioxido-oxo-$l^{5}-phosphane Chemical group [Na+].[Na+].[O-]P([O-])(=O)C=C CGQZIFGCHVCAHE-UHFFFAOYSA-L 0.000 claims 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 claims 1
- YCUBDDIKWLELPD-UHFFFAOYSA-N ethenyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC=C YCUBDDIKWLELPD-UHFFFAOYSA-N 0.000 claims 1
- WBZPMFHFKXZDRZ-UHFFFAOYSA-N ethenyl 6,6-dimethylheptanoate Chemical compound CC(C)(C)CCCCC(=O)OC=C WBZPMFHFKXZDRZ-UHFFFAOYSA-N 0.000 claims 1
- TVFJAZCVMOXQRK-UHFFFAOYSA-N ethenyl 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC(=O)OC=C TVFJAZCVMOXQRK-UHFFFAOYSA-N 0.000 claims 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 claims 1
- SLZIQIZBQKIOGN-UHFFFAOYSA-N ethenyl morpholine-4-sulfonate;sodium Chemical compound [Na].C=COS(=O)(=O)N1CCOCC1 SLZIQIZBQKIOGN-UHFFFAOYSA-N 0.000 claims 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical group CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims 1
- CALBZAJAQLUBHG-UHFFFAOYSA-N ethenylsulfamic acid Chemical compound OS(=O)(=O)NC=C CALBZAJAQLUBHG-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 1
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 230000009477 glass transition Effects 0.000 claims 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims 1
- MDNFYIAABKQDML-UHFFFAOYSA-N heptyl 2-methylprop-2-enoate Chemical compound CCCCCCCOC(=O)C(C)=C MDNFYIAABKQDML-UHFFFAOYSA-N 0.000 claims 1
- SCFQUKBBGYTJNC-UHFFFAOYSA-N heptyl prop-2-enoate Chemical compound CCCCCCCOC(=O)C=C SCFQUKBBGYTJNC-UHFFFAOYSA-N 0.000 claims 1
- JTHNLKXLWOXOQK-UHFFFAOYSA-N hex-1-en-3-one Chemical compound CCCC(=O)C=C JTHNLKXLWOXOQK-UHFFFAOYSA-N 0.000 claims 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 claims 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- 125000005439 maleimidyl group Chemical group C1(C=CC(N1*)=O)=O 0.000 claims 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- WFKDPJRCBCBQNT-UHFFFAOYSA-N n,2-dimethylprop-2-enamide Chemical compound CNC(=O)C(C)=C WFKDPJRCBCBQNT-UHFFFAOYSA-N 0.000 claims 1
- JWAJUTZQGZBKFS-UHFFFAOYSA-N n,n-diethylprop-2-en-1-amine Chemical compound CCN(CC)CC=C JWAJUTZQGZBKFS-UHFFFAOYSA-N 0.000 claims 1
- OVHHHVAVHBHXAK-UHFFFAOYSA-N n,n-diethylprop-2-enamide Chemical compound CCN(CC)C(=O)C=C OVHHHVAVHBHXAK-UHFFFAOYSA-N 0.000 claims 1
- ZLSJVVLETDAEQY-UHFFFAOYSA-N n,n-dihexylprop-2-enamide Chemical group CCCCCCN(C(=O)C=C)CCCCCC ZLSJVVLETDAEQY-UHFFFAOYSA-N 0.000 claims 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 claims 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims 1
- JRUSUOGPILMFBM-UHFFFAOYSA-N n,n-dioctylprop-2-enamide Chemical compound CCCCCCCCN(C(=O)C=C)CCCCCCCC JRUSUOGPILMFBM-UHFFFAOYSA-N 0.000 claims 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 claims 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- HILCQVNWWOARMT-UHFFFAOYSA-N non-1-en-3-one Chemical compound CCCCCCC(=O)C=C HILCQVNWWOARMT-UHFFFAOYSA-N 0.000 claims 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 claims 1
- FSAJWMJJORKPKS-UHFFFAOYSA-N octadecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C=C FSAJWMJJORKPKS-UHFFFAOYSA-N 0.000 claims 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 claims 1
- 229940065472 octyl acrylate Drugs 0.000 claims 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 claims 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical compound CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 claims 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 claims 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 claims 1
- 229940047670 sodium acrylate Drugs 0.000 claims 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 claims 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 claims 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 claims 1
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical group [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 claims 1
- CPJUXKYRSFYJPS-UHFFFAOYSA-M sodium;prop-1-ene-2-sulfonate Chemical compound [Na+].CC(=C)S([O-])(=O)=O CPJUXKYRSFYJPS-UHFFFAOYSA-M 0.000 claims 1
- JAXRXOLOMNDJGH-UHFFFAOYSA-M sodium;propane-1-sulfonate;prop-2-enamide Chemical compound [Na+].NC(=O)C=C.CCCS([O-])(=O)=O JAXRXOLOMNDJGH-UHFFFAOYSA-M 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000003831 tetrazolyl group Chemical group 0.000 claims 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims 1
- AFFZTFNQQHNSEG-UHFFFAOYSA-N trifluoromethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(F)(F)F AFFZTFNQQHNSEG-UHFFFAOYSA-N 0.000 claims 1
- ZESXUEKAXSBANL-UHFFFAOYSA-N trifluoromethyl prop-2-enoate Chemical compound FC(F)(F)OC(=O)C=C ZESXUEKAXSBANL-UHFFFAOYSA-N 0.000 claims 1
- ADDGAKQSFRASOV-UHFFFAOYSA-N undec-1-en-3-one Chemical compound CCCCCCCCC(=O)C=C ADDGAKQSFRASOV-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69472600A | 2000-10-23 | 2000-10-23 | |
| US09/694726 | 2000-10-23 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002194252A JP2002194252A (ja) | 2002-07-10 |
| JP2002194252A5 true JP2002194252A5 (enExample) | 2005-06-30 |
| JP4330831B2 JP4330831B2 (ja) | 2009-09-16 |
Family
ID=24790031
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001325176A Expired - Fee Related JP4330831B2 (ja) | 2000-10-23 | 2001-10-23 | オーバーコートの接着促進用印刷流体添加剤 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US6610412B2 (enExample) |
| EP (1) | EP1201720B1 (enExample) |
| JP (1) | JP4330831B2 (enExample) |
| DE (1) | DE60105522T2 (enExample) |
| HK (1) | HK1044014B (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| US7411011B2 (en) * | 2003-03-31 | 2008-08-12 | Hewlett-Packard Development Company, L.P. | Latex-based overcoat for ink-jet printing applications |
| JP4056929B2 (ja) * | 2003-05-21 | 2008-03-05 | シャープ株式会社 | インクジェット記録方法および記録物ならびにインクジェット記録装置 |
| CA2546038C (en) * | 2003-11-17 | 2012-04-03 | Sun Chemical Corporation | Reactive hydroxylated and carboxylated polymers for use as adhesion promoters |
| US7696262B2 (en) * | 2003-12-19 | 2010-04-13 | Hewlett-Packard Development Company, L.P. | Wetting agent combinations for inkjet printing |
| US20050137282A1 (en) * | 2003-12-19 | 2005-06-23 | Cagle Phillip C. | Liquid vehicle systems for improving latex ink-jet ink frequency response |
| US8252409B2 (en) * | 2004-02-19 | 2012-08-28 | Hewlett-Packard Development Company, L.P. | Durable printed composite materials and associated methods |
| US20070075717A1 (en) * | 2005-09-14 | 2007-04-05 | Touchdown Technologies, Inc. | Lateral interposer contact design and probe card assembly |
| CN101676340B (zh) * | 2008-09-18 | 2011-08-17 | 浙江帝龙新材料股份有限公司 | 装饰纸专用水性油墨及其制造工艺 |
| EP2189847A3 (en) * | 2008-11-19 | 2010-07-21 | Rohm and Haas Electronic Materials LLC | Compositions comprising hetero-substituted carbocyclic aryl component and processes for photolithography |
| EP2189846B1 (en) * | 2008-11-19 | 2015-04-22 | Rohm and Haas Electronic Materials LLC | Process for photolithography applying a photoresist composition comprising a block copolymer |
| JP5771922B2 (ja) * | 2010-09-02 | 2015-09-02 | コニカミノルタ株式会社 | 水性インク |
| US9676932B2 (en) | 2012-08-02 | 2017-06-13 | Rohm And Haas Company | Adsorbing vinyl ester binders |
| JP5853988B2 (ja) * | 2013-05-14 | 2016-02-09 | コニカミノルタ株式会社 | 静電潜像用現像剤 |
| CN103665262B (zh) * | 2013-12-13 | 2016-05-11 | 山东大学 | 一种含氟改性n-乙烯基吡咯烷酮的水溶性共聚物及其制备方法 |
| US11084972B2 (en) | 2017-03-09 | 2021-08-10 | Saudi Arabian Oil Company | Surface charge modified nanosurfactants for reduced retention by reservoir rock |
| US11066594B2 (en) | 2017-03-09 | 2021-07-20 | Saudi Arabian Oil Company | Fluoropolymers to reduce retention of nanosurfactants to carbonate reservoir rock for applications in oil fields |
| US11066914B2 (en) | 2017-03-09 | 2021-07-20 | Saudi Arabian Oil Company | Foam from low cost petroleum sulfonate surfactants for fracturing along with wettability alteration |
| US11078405B2 (en) | 2017-03-09 | 2021-08-03 | Saudi Arabian Oil Company | 3 in 1 foam formulation for enhanced oil recovery including conformance control, ultra-low interfacial tension, and wettability alteration |
| US20210007964A1 (en) * | 2018-03-23 | 2021-01-14 | Shiseido Company, Ltd. | Raw material for cosmetic and oil-in-water emulsion cosmetic comprising core-corona polymer particle |
| CN109777378B (zh) * | 2019-02-21 | 2021-03-30 | 河南省新乡市第七化工有限公司 | 一种抗高温、抗盐钻井液用纳米乳液共聚物降滤失剂的制备方法 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3115532A1 (de) | 1980-04-17 | 1982-01-28 | Canon K.K., Tokyo | Tintenstrahl-aufzeichnungsverfahren und aufzeichnungstinte fuer die aufzeichnung auf einem bildempfangsmaterial |
| JPS6151391A (ja) | 1984-08-20 | 1986-03-13 | Toshiba Corp | 熱転写記録媒体と熱転写装置 |
| US5082757A (en) | 1990-08-31 | 1992-01-21 | Xerox Corporation | Encapsulated toner compositions |
| US5461125A (en) | 1993-04-30 | 1995-10-24 | Minnesota Mining And Manufacturing Company | Waterborne core-shell latex polymers |
| US5555011A (en) | 1994-01-26 | 1996-09-10 | Eastman Kodak Company | Lamination of a protective layer over an image produced by a thermal printer |
| JP3478647B2 (ja) | 1994-12-09 | 2003-12-15 | キヤノン株式会社 | 感圧転写性保護被覆材料及びこれを用いた画像の保護被覆方法 |
| US6258888B1 (en) | 1994-12-21 | 2001-07-10 | Zeneca Resins Bv | Aqueous polymer emulsions |
| US5656071A (en) | 1995-12-26 | 1997-08-12 | Lexmark International, Inc. | Ink compositions |
| US5906905A (en) | 1996-01-11 | 1999-05-25 | Xerox Corporation | Simulated photographic-quality prints using a transparent substrate containing a wrong reading image and a backing sheet containing an ultraviolet light absorber |
| US5612777A (en) | 1996-01-11 | 1997-03-18 | Xerox Corporation | Method and apparatus for applying a clear toner resin containing lightfastness material to toner images |
| JPH10298472A (ja) * | 1997-04-25 | 1998-11-10 | Fuji Photo Film Co Ltd | インクジェット式製版印刷版用油性インクおよびそれを用いた製版印刷版の作成方法 |
| US5847738A (en) | 1997-07-11 | 1998-12-08 | Eastman Kodak Company | Process for applying protective overcoat on printed media |
| US6057384A (en) * | 1997-10-31 | 2000-05-02 | Hewlett-Packard Company | Latex polymer blends for improving the permanence of ink-jet inks |
| WO1999023183A1 (en) * | 1997-10-31 | 1999-05-14 | Hewlett-Packard Company | Printing ink compositions having superior smear-fastness |
| DE69841533D1 (de) * | 1997-10-31 | 2010-04-15 | Hewlett Packard Co | Tintenstrahldrucktintenzusammensetzungen mit magnetischen eigenschaften |
| US6124376A (en) | 1998-08-24 | 2000-09-26 | Xerox Corporation | Ink composition for ink jet printing |
| DE60026113T2 (de) * | 1999-03-09 | 2007-02-15 | Hewlett-Packard Development Company, L.P., Houston | Tintenzusammensetzungen für Tintenstrahldrucker mit hoher Schmierfestigkeit |
-
2001
- 2001-10-17 EP EP01308824A patent/EP1201720B1/en not_active Expired - Lifetime
- 2001-10-17 DE DE60105522T patent/DE60105522T2/de not_active Expired - Lifetime
- 2001-10-23 JP JP2001325176A patent/JP4330831B2/ja not_active Expired - Fee Related
-
2002
- 2002-08-01 HK HK02105668.8A patent/HK1044014B/en not_active IP Right Cessation
- 2002-09-30 US US10/261,742 patent/US6610412B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2002194252A5 (enExample) | ||
| CN1832981B (zh) | 甲硅烷基酯共聚物组合物 | |
| CN100519671C (zh) | 成膜聚合物和防污漆 | |
| JP4185192B2 (ja) | 重合方法 | |
| JP2015523415A5 (enExample) | ||
| JPWO2021039960A5 (enExample) | ||
| EP1201720B1 (en) | Printing fluid additives promoting overcoat adhesion | |
| JPH11322866A (ja) | グラフトポリマー | |
| EP0542139B1 (en) | Aqueous emulsion composition of a silyl group-containing copolymer | |
| US6420505B1 (en) | Process for preparing thiosulfate salt polymers | |
| JP2005511289A5 (enExample) | ||
| JP4859437B2 (ja) | 被膜形成用樹脂組成物 | |
| CN111808228B (zh) | 超支化聚乙烯亚胺掺杂改性的丙烯酸乳液及其制备方法 | |
| US5262244A (en) | Hydrophilic copolymers and their use in reprography | |
| CA2047463A1 (en) | Hydrophilic copolymers and their use in reprography | |
| US20220269173A1 (en) | Surface treatment liquid and hydrophilizing treatment method | |
| JP5053476B2 (ja) | 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 | |
| JP2009531514A5 (enExample) | ||
| JP2000290567A5 (enExample) | ||
| JP4414056B2 (ja) | Ｎ−ビニル環状ラクタム系グラフト重合体およびその製造方法 | |
| JPH0476068A (ja) | 被覆用組成物 | |
| WO2017087446A1 (en) | Hydroxyethylpyrrolidone methacrylate/glycidyl methacrylate copolymers | |
| JP2000297105A (ja) | 水溶性共重合体の製造方法 | |
| JP3766053B2 (ja) | 製紙用ピッチ付着防止剤 | |
| JP2905248B2 (ja) | 表面紙力剤 |