JP5319864B2 - 画像安定化剤の組み込まれたラテックス粒子 - Google Patents
画像安定化剤の組み込まれたラテックス粒子 Download PDFInfo
- Publication number
- JP5319864B2 JP5319864B2 JP2003408985A JP2003408985A JP5319864B2 JP 5319864 B2 JP5319864 B2 JP 5319864B2 JP 2003408985 A JP2003408985 A JP 2003408985A JP 2003408985 A JP2003408985 A JP 2003408985A JP 5319864 B2 JP5319864 B2 JP 5319864B2
- Authority
- JP
- Japan
- Prior art keywords
- latex particles
- latex
- stabilizing agent
- stabilizer
- ink
- 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.)
- Expired - Fee Related
Links
- 239000003381 stabilizer Substances 0.000 title claims abstract description 175
- 239000004816 latex Substances 0.000 title claims abstract description 148
- 229920000126 latex Polymers 0.000 title claims abstract description 148
- 239000002245 particle Substances 0.000 title claims abstract description 101
- 239000000178 monomer Substances 0.000 claims abstract description 73
- 239000000203 mixture Substances 0.000 claims abstract description 40
- 239000002243 precursor Substances 0.000 claims abstract description 38
- 238000000034 method Methods 0.000 claims abstract description 25
- 230000008878 coupling Effects 0.000 claims abstract description 5
- 238000010168 coupling process Methods 0.000 claims abstract description 5
- 238000005859 coupling reaction Methods 0.000 claims abstract description 5
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 4
- 150000001412 amines Chemical class 0.000 claims description 37
- 125000000524 functional group Chemical group 0.000 claims description 23
- 230000000087 stabilizing effect Effects 0.000 claims description 23
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 19
- WARQUFORVQESFF-UHFFFAOYSA-N isocyanatoethene Chemical compound C=CN=C=O WARQUFORVQESFF-UHFFFAOYSA-N 0.000 claims description 11
- -1 alkylidene bisphenol Chemical compound 0.000 claims description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical group OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 8
- 230000006870 function Effects 0.000 claims description 8
- 238000007641 inkjet printing Methods 0.000 claims description 7
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 6
- 239000003112 inhibitor Substances 0.000 claims description 6
- 150000002989 phenols Chemical class 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 3
- 238000006482 condensation reaction Methods 0.000 claims description 3
- PZMWHOITXWIHBP-UHFFFAOYSA-N 3-[hydroxy(phenyl)methoxy]-3-oxopropanoic acid Chemical compound OC(=O)CC(=O)OC(O)C1=CC=CC=C1 PZMWHOITXWIHBP-UHFFFAOYSA-N 0.000 claims description 2
- 229930185605 Bisphenol Natural products 0.000 claims description 2
- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical compound NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 claims description 2
- WAKMOVBCOYGSDK-UHFFFAOYSA-N phenol;triazine Chemical compound C1=CN=NN=C1.OC1=CC=CC=C1 WAKMOVBCOYGSDK-UHFFFAOYSA-N 0.000 claims description 2
- 229930003799 tocopherol Natural products 0.000 claims description 2
- 239000011732 tocopherol Substances 0.000 claims description 2
- 238000006385 ozonation reaction Methods 0.000 claims 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims 2
- OGBVRMYSNSKIEF-UHFFFAOYSA-L benzyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)CC1=CC=CC=C1 OGBVRMYSNSKIEF-UHFFFAOYSA-L 0.000 claims 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims 1
- 229960001295 tocopherol Drugs 0.000 claims 1
- 235000010384 tocopherol Nutrition 0.000 claims 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 claims 1
- 239000000976 ink Substances 0.000 description 61
- 239000012948 isocyanate Substances 0.000 description 45
- 150000002513 isocyanates Chemical class 0.000 description 45
- 238000006243 chemical reaction Methods 0.000 description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 35
- 229920000642 polymer Polymers 0.000 description 28
- 238000006116 polymerization reaction Methods 0.000 description 20
- 239000000049 pigment Substances 0.000 description 15
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000003086 colorant Substances 0.000 description 12
- 238000010511 deprotection reaction Methods 0.000 description 12
- 150000003141 primary amines Chemical class 0.000 description 12
- 150000003254 radicals Chemical class 0.000 description 12
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 10
- 239000003223 protective agent Substances 0.000 description 10
- 238000007639 printing Methods 0.000 description 9
- 229920002554 vinyl polymer Polymers 0.000 description 9
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 239000007795 chemical reaction product Substances 0.000 description 7
- 238000011065 in-situ storage Methods 0.000 description 7
- 239000004611 light stabiliser Substances 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 6
- 238000000926 separation method Methods 0.000 description 6
- 239000003973 paint Substances 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000001721 carbon Chemical group 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000010526 radical polymerization reaction Methods 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 150000003335 secondary amines Chemical class 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- WWYFPDXEIFBNKE-UHFFFAOYSA-M 4-carboxybenzyl alcohol Chemical compound OCC1=CC=C(C([O-])=O)C=C1 WWYFPDXEIFBNKE-UHFFFAOYSA-M 0.000 description 3
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 239000000539 dimer Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- YIDSTEJLDQMWBR-UHFFFAOYSA-N 1-isocyanatododecane Chemical compound CCCCCCCCCCCCN=C=O YIDSTEJLDQMWBR-UHFFFAOYSA-N 0.000 description 2
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000006957 Michael reaction Methods 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000003636 chemical group Chemical group 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 230000002860 competitive effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 2
- 229920001600 hydrophobic polymer Polymers 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
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- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
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- 238000002360 preparation method Methods 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
- VDVUCLWJZJHFAV-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1 VDVUCLWJZJHFAV-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- DVEUHJOFXAVILY-UHFFFAOYSA-N 4-(2-but-2-enoyloxyethoxy)-4-oxobutanoic acid Chemical compound CC=CC(=O)OCCOC(=O)CCC(O)=O DVEUHJOFXAVILY-UHFFFAOYSA-N 0.000 description 1
- ZEWLHMQYEZXSBH-UHFFFAOYSA-N 4-[2-(2-methylprop-2-enoyloxy)ethoxy]-4-oxobutanoic acid Chemical compound CC(=C)C(=O)OCCOC(=O)CCC(O)=O ZEWLHMQYEZXSBH-UHFFFAOYSA-N 0.000 description 1
- IUNVCWLKOOCPIT-UHFFFAOYSA-N 6-methylheptylsulfanyl 2-hydroxyacetate Chemical compound CC(C)CCCCCSOC(=O)CO IUNVCWLKOOCPIT-UHFFFAOYSA-N 0.000 description 1
- 0 CC(C(OCCNC(Oc1ccc(*)cc1)=O)=O)=C Chemical compound CC(C(OCCNC(Oc1ccc(*)cc1)=O)=O)=C 0.000 description 1
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- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
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- 238000005481 NMR spectroscopy Methods 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
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- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 1
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- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
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- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
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- 230000004044 response Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000012619 stoichiometric conversion Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000006557 surface reaction Methods 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/10—Encapsulated ingredients
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2989—Microcapsule with solid core [includes liposome]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/322032 | 2002-12-17 | ||
| US10/322,032 US7358301B2 (en) | 2002-12-17 | 2002-12-17 | Latex particles having incorporated image stabilizers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004197090A JP2004197090A (ja) | 2004-07-15 |
| JP2004197090A5 JP2004197090A5 (enExample) | 2006-11-16 |
| JP5319864B2 true JP5319864B2 (ja) | 2013-10-16 |
Family
ID=32393009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003408985A Expired - Fee Related JP5319864B2 (ja) | 2002-12-17 | 2003-12-08 | 画像安定化剤の組み込まれたラテックス粒子 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US7358301B2 (enExample) |
| EP (1) | EP1431339B1 (enExample) |
| JP (1) | JP5319864B2 (enExample) |
| CN (1) | CN100365078C (enExample) |
| DE (1) | DE60331402D1 (enExample) |
| TW (1) | TWI285213B (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7705070B2 (en) | 2003-02-06 | 2010-04-27 | Hewlett-Packard Development Company, L.P. | Ink-jet compatible latexes |
| US7402617B2 (en) * | 2003-02-06 | 2008-07-22 | Hewlett-Packard Development Company, L.P. | Low bulk density, low surface dielectric constant latex polymers for ink-jet ink applications |
| US7544418B2 (en) * | 2006-07-31 | 2009-06-09 | Hewlett-Packard Development Company, L.P. | Polymer-encapsulated pigments and associated methods |
| US20080126703A1 (en) * | 2006-10-05 | 2008-05-29 | Holt John M | Cyclic redundant multiple computer architecture |
| US20080182932A1 (en) * | 2007-01-25 | 2008-07-31 | Zhang-Lin Zhou | Biocatalytic polymerization of anti-oxidant-modified latex particulates |
| US9156956B2 (en) | 2007-01-31 | 2015-10-13 | Hewlett-Packard Development Company, L.P. | Surface-crosslinked latex particulates |
| KR20100099287A (ko) * | 2007-12-14 | 2010-09-10 | 휴렛-팩커드 디벨롭먼트 컴퍼니, 엘.피. | 첨가된 라텍스에 의해 개선된 색 및 내구성을 갖는 잉크젯 잉크 세트 |
| GB0906211D0 (en) | 2009-04-09 | 2009-05-20 | Andergauge Ltd | Under-reamer |
| US8246754B2 (en) * | 2009-09-25 | 2012-08-21 | Hewlett-Packard Development Company, L.P. | Process for removing ink from printed substrate |
| US20110184095A1 (en) * | 2010-01-25 | 2011-07-28 | Tom Howard S | Light fast encapsulated pigment |
| GB2484453B (en) | 2010-08-05 | 2016-02-24 | Nov Downhole Eurasia Ltd | Lockable reamer |
| GB2486898A (en) | 2010-12-29 | 2012-07-04 | Nov Downhole Eurasia Ltd | A downhole tool with at least one extendable offset cutting member for reaming a bore |
| JP5717134B2 (ja) | 2011-03-15 | 2015-05-13 | 大日精化工業株式会社 | エマルジョンバインダー及びそれを含有するインクジェット用水性顔料インク、並びにエマルジョンバインダーの製造方法 |
| GB201117800D0 (en) | 2011-10-14 | 2011-11-30 | Nov Downhole Eurasia Ltd | Downhole tool actuator |
| GB201201652D0 (en) | 2012-01-31 | 2012-03-14 | Nov Downhole Eurasia Ltd | Downhole tool actuation |
| WO2014035528A2 (en) * | 2012-06-15 | 2014-03-06 | Tufts University | Paint-on approach for fabrication of electrically active structures |
| AU2014258546B2 (en) | 2013-04-22 | 2016-09-22 | Dainichiseika Color & Chemicals Mfg. Co., Ltd. | Aqueous emulsion solution, coloring agent composition containing said aqueous solution, aqueous inkjet ink, and method for producing aqueous emulsion solution |
| CA2857841C (en) | 2013-07-26 | 2018-03-13 | National Oilwell DHT, L.P. | Downhole activation assembly with sleeve valve and method of using same |
| GB2550255B (en) | 2014-06-26 | 2018-09-19 | Nov Downhole Eurasia Ltd | Downhole under-reamer and associated methods |
| JP6820429B2 (ja) * | 2017-08-29 | 2021-01-27 | 富士フイルム株式会社 | インク組成物及びその製造方法、並びに画像形成方法 |
| JP6886062B1 (ja) | 2020-08-25 | 2021-06-16 | 大日精化工業株式会社 | Ａ−ｂブロックコポリマー、ポリマーエマルジョン、及び水性インクジェットインク |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4593064A (en) * | 1979-04-06 | 1986-06-03 | Rohm Gmbh | Method for polymerizing methyl methacrylate |
| US4264748A (en) * | 1980-01-28 | 1981-04-28 | The Dow Chemical Company | Epoxy resin coating compositions |
| US4495229A (en) * | 1982-06-08 | 1985-01-22 | Chemische Werke Huls A.G. | One-component, heat-curing polyurethane-coatings, stable in storage |
| US4742097A (en) * | 1984-12-03 | 1988-05-03 | The Glidden Company | Acrylic and acrylic/epoxy copolymer composition as self-curing cathodic electrocoating vehicles |
| US5355245A (en) * | 1988-02-12 | 1994-10-11 | Donnelly Corporation | Ultraviolet protected electrochemichromic rearview mirror |
| TW267179B (enExample) * | 1993-07-13 | 1996-01-01 | Ciba Geigy | |
| DE4433437A1 (de) * | 1994-09-20 | 1996-03-21 | Bayer Ag | Vernetzer für Textildruck-Bindemittel |
| AU2355997A (en) * | 1996-05-22 | 1997-11-27 | H.B. Fuller Licensing And Financing Inc. | A structural reactive latex |
| US5981076A (en) * | 1996-12-09 | 1999-11-09 | 3M Innovative Properties Company | UV protected syndiotactic polystyrene overlay films |
| WO1998045348A1 (en) * | 1997-04-04 | 1998-10-15 | Cook Composites And Polymers Company | Low voc acrylic polymer blocked isocyanate coating systems and a process for their preparation |
| JP4168477B2 (ja) * | 1997-04-28 | 2008-10-22 | セイコーエプソン株式会社 | 耐光性に優れた画像を実現するインク組成物 |
| US6590012B2 (en) * | 1997-04-28 | 2003-07-08 | Seiko Epson Corporation | Ink composition capable of realizing light fast image |
| WO1999023183A1 (en) * | 1997-10-31 | 1999-05-14 | Hewlett-Packard Company | Printing ink compositions having superior smear-fastness |
| US6417249B1 (en) * | 1997-10-31 | 2002-07-09 | Hewlett-Packard Company | Ink-jet printing ink compositions having superior smear-fastness |
| SE9704031D0 (sv) | 1997-11-05 | 1997-11-05 | Astra Ab | Novel formulation |
| TW457403B (en) * | 1998-07-03 | 2001-10-01 | Clariant Int Ltd | Composition for forming a radiation absorbing coating containing blocked isocyanate compound and anti-reflective coating formed therefrom |
| JP2000160072A (ja) * | 1998-11-24 | 2000-06-13 | Ricoh Co Ltd | 記録用インク |
| US7040747B2 (en) * | 1999-07-30 | 2006-05-09 | Seiko Epson Corporation | Recording method for printing using two liquids on recording medium |
| JP3622910B2 (ja) * | 1999-07-30 | 2005-02-23 | セイコーエプソン株式会社 | 記録媒体に二液を用いて印刷する記録方法 |
| JP3630089B2 (ja) * | 1999-09-29 | 2005-03-16 | セイコーエプソン株式会社 | インク組成物およびそれを用いたインクジェット記録方法 |
| US6361916B1 (en) | 1999-12-14 | 2002-03-26 | Eastman Kodak Company | Loaded latex compositions with dye and stabilizer |
| US6340719B1 (en) * | 1999-12-29 | 2002-01-22 | 3M-Innovative Properties Company | Crosslinking process |
| HK1054355A1 (zh) * | 2000-10-02 | 2003-11-28 | Kimberly-Clark Worldwide, Inc. | 基於纳米粒子的油墨及其制造方法 |
| JP2002265828A (ja) * | 2001-03-09 | 2002-09-18 | Fuji Photo Film Co Ltd | インクジェット記録用インクおよびインクジェット画像形成方法 |
-
2002
- 2002-12-17 US US10/322,032 patent/US7358301B2/en not_active Expired - Fee Related
-
2003
- 2003-06-27 TW TW092117600A patent/TWI285213B/zh not_active IP Right Cessation
- 2003-09-17 CN CNB031586171A patent/CN100365078C/zh not_active Expired - Fee Related
- 2003-12-08 JP JP2003408985A patent/JP5319864B2/ja not_active Expired - Fee Related
- 2003-12-10 EP EP03257750A patent/EP1431339B1/en not_active Expired - Lifetime
- 2003-12-10 DE DE60331402T patent/DE60331402D1/de not_active Expired - Lifetime
-
2007
- 2007-11-06 US US11/983,158 patent/US8148461B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20040116596A1 (en) | 2004-06-17 |
| JP2004197090A (ja) | 2004-07-15 |
| US7358301B2 (en) | 2008-04-15 |
| DE60331402D1 (de) | 2010-04-08 |
| CN1508202A (zh) | 2004-06-30 |
| US20080070038A1 (en) | 2008-03-20 |
| TW200411023A (en) | 2004-07-01 |
| CN100365078C (zh) | 2008-01-30 |
| EP1431339B1 (en) | 2010-02-24 |
| US8148461B2 (en) | 2012-04-03 |
| TWI285213B (en) | 2007-08-11 |
| EP1431339A1 (en) | 2004-06-23 |
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