CA2472355C - Procede d'impression par jet d'encre - Google Patents

Procede d'impression par jet d'encre Download PDF

Info

Publication number: CA2472355C
Authority: CA; Canada
Prior art keywords: composition; ink; color; ink jet; reacting
Prior art date: 1998-09-11
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

Application number

CA002472355A

Other languages

English (en)

Other versions

CA2472355A1 (fr

Inventor

Thomas W. Smith

Kathleen M. Mcgrane

David J. Luca

William W. Limburg

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Xerox Corp

Original Assignee

Xerox Corp

Priority date (The priority date 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 date listed.)

1998-09-11

Filing date

1999-08-05

Publication date

2008-01-08

1998-09-11 Priority claimed from US09/152,100 external-priority patent/US6312121B1/en

1999-08-05 Application filed by Xerox Corp filed Critical Xerox Corp

1999-08-05 Priority claimed from CA002439739A external-priority patent/CA2439739C/fr

2000-03-11 Publication of CA2472355A1 publication Critical patent/CA2472355A1/fr

2008-01-08 Application granted granted Critical

2008-01-08 Publication of CA2472355C publication Critical patent/CA2472355C/fr

2019-08-05 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 91
230000008569 process Effects 0.000 title claims abstract description 84
238000007641 inkjet printing Methods 0.000 title claims abstract description 58
239000000203 mixture Substances 0.000 claims abstract description 288
239000007788 liquid Substances 0.000 claims abstract description 80
239000000758 substrate Substances 0.000 claims abstract description 59
239000000463 material Substances 0.000 claims abstract description 27
239000003795 chemical substances by application Substances 0.000 claims abstract description 19
238000004040 coloring Methods 0.000 claims description 52
230000001590 oxidative effect Effects 0.000 claims description 51
239000000975 dye Substances 0.000 claims description 49
239000007800 oxidant agent Substances 0.000 claims description 23
229910052751 metal Inorganic materials 0.000 claims description 5
239000002184 metal Substances 0.000 claims description 5
239000000984 vat dye Substances 0.000 claims description 4
LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 claims description 3
150000008442 polyphenolic compounds Chemical class 0.000 claims description 2
239000000976 ink Substances 0.000 description 203
238000007639 printing Methods 0.000 description 47
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
125000004432 carbon atom Chemical group C* 0.000 description 29
-1 and the like Substances 0.000 description 28
229910001868 water Inorganic materials 0.000 description 27
239000012530 fluid Substances 0.000 description 18
238000000151 deposition Methods 0.000 description 17
125000000217 alkyl group Chemical group 0.000 description 16
230000008021 deposition Effects 0.000 description 16
238000003491 array Methods 0.000 description 13
239000000834 fixative Substances 0.000 description 13
239000000654 additive Substances 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 12
239000002585 base Substances 0.000 description 9
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 9
239000003086 colorant Substances 0.000 description 9
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 8
125000001424 substituent group Chemical group 0.000 description 8
230000000996 additive effect Effects 0.000 description 7
150000002170 ethers Chemical class 0.000 description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 7
239000001043 yellow dye Substances 0.000 description 7
238000005859 coupling reaction Methods 0.000 description 6
LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 6
238000004519 manufacturing process Methods 0.000 description 6
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 5
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
125000003118 aryl group Chemical group 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
239000006184 cosolvent Substances 0.000 description 5
230000006870 function Effects 0.000 description 5
150000002334 glycols Chemical class 0.000 description 5
238000010438 heat treatment Methods 0.000 description 5
239000003906 humectant Substances 0.000 description 5
239000004615 ingredient Substances 0.000 description 5
238000002156 mixing Methods 0.000 description 5
230000003381 solubilizing effect Effects 0.000 description 5
150000003457 sulfones Chemical class 0.000 description 5
235000011149 sulphuric acid Nutrition 0.000 description 5
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 4
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
239000000010 aprotic solvent Substances 0.000 description 4
239000008367 deionised water Substances 0.000 description 4
229910021641 deionized water Inorganic materials 0.000 description 4
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 4
238000009472 formulation Methods 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
150000002430 hydrocarbons Chemical class 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
150000002978 peroxides Chemical class 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
229920000233 poly(alkylene oxides) Polymers 0.000 description 4
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 4
150000004040 pyrrolidinones Chemical class 0.000 description 4
230000005855 radiation Effects 0.000 description 4
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 description 3
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 3
WSEFOZIMAJPJHW-UHFFFAOYSA-N 4-amino-2-(hydroxymethyl)phenol Chemical compound NC1=CC=C(O)C(CO)=C1 WSEFOZIMAJPJHW-UHFFFAOYSA-N 0.000 description 3
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
230000009471 action Effects 0.000 description 3
125000002877 alkyl aryl group Chemical group 0.000 description 3
XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 3
238000009835 boiling Methods 0.000 description 3
PBAYDYUZOSNJGU-UHFFFAOYSA-N chelidonic acid Natural products OC(=O)C1=CC(=O)C=C(C(O)=O)O1 PBAYDYUZOSNJGU-UHFFFAOYSA-N 0.000 description 3
239000003153 chemical reaction reagent Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
229940074391 gallic acid Drugs 0.000 description 3
235000004515 gallic acid Nutrition 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
239000011976 maleic acid Substances 0.000 description 3
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
230000007246 mechanism Effects 0.000 description 3
239000000049 pigment Substances 0.000 description 3
229920001223 polyethylene glycol Polymers 0.000 description 3
229910000027 potassium carbonate Inorganic materials 0.000 description 3
230000009257 reactivity Effects 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 3
125000000547 substituted alkyl group Chemical group 0.000 description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
WXTMDXOMEHJXQO-UHFFFAOYSA-N 2,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC=C1O WXTMDXOMEHJXQO-UHFFFAOYSA-N 0.000 description 2
LAQYHRQFABOIFD-UHFFFAOYSA-N 2-methoxyhydroquinone Chemical compound COC1=CC(O)=CC=C1O LAQYHRQFABOIFD-UHFFFAOYSA-N 0.000 description 2
GCABLKFGYPIVFC-UHFFFAOYSA-N 3-(1-benzofuran-2-yl)-3-oxopropanenitrile Chemical compound C1=CC=C2OC(C(CC#N)=O)=CC2=C1 GCABLKFGYPIVFC-UHFFFAOYSA-N 0.000 description 2
ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 2
NTDRZJLMIOFNLK-UHFFFAOYSA-N 5-(4-nitroanilino)-2-(2,4,6-trichlorophenyl)-4h-pyrazol-3-one Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC1=NN(C=2C(=CC(Cl)=CC=2Cl)Cl)C(=O)C1 NTDRZJLMIOFNLK-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
101100285903 Drosophila melanogaster Hsc70-2 gene Proteins 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
229910006069 SO3H Inorganic materials 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
MPLZNPZPPXERDA-UHFFFAOYSA-N [4-(diethylamino)-2-methylphenyl]azanium;chloride Chemical compound [Cl-].CC[NH+](CC)C1=CC=C(N)C(C)=C1 MPLZNPZPPXERDA-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
125000004104 aryloxy group Chemical group 0.000 description 2
235000010323 ascorbic acid Nutrition 0.000 description 2
229960005070 ascorbic acid Drugs 0.000 description 2
239000011668 ascorbic acid Substances 0.000 description 2
230000008901 benefit Effects 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
235000013877 carbamide Nutrition 0.000 description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
125000002091 cationic group Chemical group 0.000 description 2
239000003638 chemical reducing agent Substances 0.000 description 2
239000002131 composite material Substances 0.000 description 2
229920001577 copolymer Chemical compound 0.000 description 2
230000008878 coupling Effects 0.000 description 2
238000010168 coupling process Methods 0.000 description 2
238000011161 development Methods 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000001914 filtration Methods 0.000 description 2
235000011187 glycerol Nutrition 0.000 description 2
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
239000012943 hotmelt Substances 0.000 description 2
150000002505 iron Chemical class 0.000 description 2
239000011159 matrix material Substances 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000007645 offset printing Methods 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
150000004986 phenylenediamines Chemical class 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000000276 potassium ferrocyanide Substances 0.000 description 2
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
239000000843 powder Substances 0.000 description 2
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
230000000452 restraining effect Effects 0.000 description 2
229910052709 silver Inorganic materials 0.000 description 2
239000004332 silver Substances 0.000 description 2
235000010265 sodium sulphite Nutrition 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000003107 substituted aryl group Chemical group 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
XOGGUFAVLNCTRS-UHFFFAOYSA-N tetrapotassium;iron(2+);hexacyanide Chemical compound [K+].[K+].[K+].[K+].[Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] XOGGUFAVLNCTRS-UHFFFAOYSA-N 0.000 description 2
125000005000 thioaryl group Chemical group 0.000 description 2
QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 1
KDGNCLDCOVTOCS-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy propan-2-yl carbonate Chemical compound CC(C)OC(=O)OOC(C)(C)C KDGNCLDCOVTOCS-UHFFFAOYSA-N 0.000 description 1
GVEYRUKUJCHJSR-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C(C)=C1 GVEYRUKUJCHJSR-UHFFFAOYSA-N 0.000 description 1
KAJALVWKFPQZOO-UHFFFAOYSA-N (4-azaniumylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C=C1 KAJALVWKFPQZOO-UHFFFAOYSA-N 0.000 description 1
QDNPCYCBQFHNJC-UHFFFAOYSA-N 1,1'-biphenyl-3,4-diol Chemical compound C1=C(O)C(O)=CC=C1C1=CC=CC=C1 QDNPCYCBQFHNJC-UHFFFAOYSA-N 0.000 description 1
XBYRMPXUBGMOJC-UHFFFAOYSA-N 1,2-dihydropyrazol-3-one Chemical compound OC=1C=CNN=1 XBYRMPXUBGMOJC-UHFFFAOYSA-N 0.000 description 1
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
RKMZJVBSOAVGQS-UHFFFAOYSA-N 1-methylsulfonylethanol Chemical compound CC(O)S(C)(=O)=O RKMZJVBSOAVGQS-UHFFFAOYSA-N 0.000 description 1
XIROXSOOOAZHLL-UHFFFAOYSA-N 2',3',4'-Trihydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C(O)=C1O XIROXSOOOAZHLL-UHFFFAOYSA-N 0.000 description 1
KJSVAEGLTPBKAA-UHFFFAOYSA-N 2,2-dichloro-n-phenylacetamide Chemical compound ClC(Cl)C(=O)NC1=CC=CC=C1 KJSVAEGLTPBKAA-UHFFFAOYSA-N 0.000 description 1
XTNHVTIXTMOWGU-UHFFFAOYSA-N 2,3,4-triaminophenol Chemical compound NC1=CC=C(O)C(N)=C1N XTNHVTIXTMOWGU-UHFFFAOYSA-N 0.000 description 1
GLDQAMYCGOIJDV-UHFFFAOYSA-N 2,3-dihydroxybenzoic acid Chemical class OC(=O)C1=CC=CC(O)=C1O GLDQAMYCGOIJDV-UHFFFAOYSA-N 0.000 description 1
WZPLEIAOQJXZJX-UHFFFAOYSA-N 2,3-dihydroxynaphthalene-1-carboxylic acid Chemical class C1=CC=C2C(C(=O)O)=C(O)C(O)=CC2=C1 WZPLEIAOQJXZJX-UHFFFAOYSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
VYHSWZULFYFDMO-UHFFFAOYSA-N 2-(2-hydroxyethylamino)phenol Chemical compound OCCNC1=CC=CC=C1O VYHSWZULFYFDMO-UHFFFAOYSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
GTOOAPLRWMOITA-UHFFFAOYSA-N 2-(4-amino-n-ethyl-3-methylanilino)ethyl hydrogen sulfate Chemical compound OS(=O)(=O)OCCN(CC)C1=CC=C(N)C(C)=C1 GTOOAPLRWMOITA-UHFFFAOYSA-N 0.000 description 1
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 description 1
YTBVROFMBPPMCW-UHFFFAOYSA-N 2-amino-4-[(4-hydroxyphenyl)methylamino]phenol Chemical compound C1=C(O)C(N)=CC(NCC=2C=CC(O)=CC=2)=C1 YTBVROFMBPPMCW-UHFFFAOYSA-N 0.000 description 1
REFDOIWRJDGBHY-UHFFFAOYSA-N 2-bromobenzene-1,4-diol Chemical compound OC1=CC=C(O)C(Br)=C1 REFDOIWRJDGBHY-UHFFFAOYSA-N 0.000 description 1
JYHNNCBQCSLFQM-UHFFFAOYSA-N 3,6-dihydroxybenzonorbornane Chemical compound OC1=CC=C(O)C2=C1C1CCC2C1 JYHNNCBQCSLFQM-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
XRZDIHADHZSFBB-UHFFFAOYSA-N 3-oxo-n,3-diphenylpropanamide Chemical compound C=1C=CC=CC=1NC(=O)CC(=O)C1=CC=CC=C1 XRZDIHADHZSFBB-UHFFFAOYSA-N 0.000 description 1
ZBZRXHXMLGRAOE-UHFFFAOYSA-N 4-(2-hydroxyethylamino)-3-methylphenol Chemical compound CC1=CC(O)=CC=C1NCCO ZBZRXHXMLGRAOE-UHFFFAOYSA-N 0.000 description 1
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235000019394 potassium persulphate Nutrition 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
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239000000377 silicon dioxide Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
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229910000162 sodium phosphate Inorganic materials 0.000 description 1
IQNDCJMEVJJWQL-UHFFFAOYSA-M sodium;5-amino-6-hydroxynaphthalene-2-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=C2C(N)=C(O)C=CC2=C1 IQNDCJMEVJJWQL-UHFFFAOYSA-M 0.000 description 1
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RAHZWNYVWXNFOC-UHFFFAOYSA-N sulfur dioxide Inorganic materials O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
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235000015523 tannic acid Nutrition 0.000 description 1
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CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
239000004753 textile Substances 0.000 description 1
CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 1
JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical class [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
238000009834 vaporization Methods 0.000 description 1
230000008016 vaporization Effects 0.000 description 1
239000002966 varnish Substances 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
239000002023 wood Substances 0.000 description 1

Landscapes

Ink Jet (AREA)
Ink Jet Recording Methods And Recording Media Thereof (AREA)

CA002472355A 1998-09-11 1999-08-05 Procede d'impression par jet d'encre Expired - Fee Related CA2472355C (fr)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US09/152,100		1998-09-11
US09/152,100 US6312121B1 (en)	1998-09-11	1998-09-11	Ink jet printing process
CA002439739A CA2439739C (fr)	1998-09-11	1999-08-05	Procede d'impression par jet d'encre

Related Parent Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002439739A Division CA2439739C (fr)	1998-09-11	1999-08-05	Procede d'impression par jet d'encre

Publications (2)

Publication Number	Publication Date
CA2472355A1 CA2472355A1 (fr)	2000-03-11
CA2472355C true CA2472355C (fr)	2008-01-08

Family

ID=32870065

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CA002472726A Expired - Fee Related CA2472726C (fr)	1998-09-11	1999-08-05	Procede d'impression par jet d'encre
CA002472355A Expired - Fee Related CA2472355C (fr)	1998-09-11	1999-08-05	Procede d'impression par jet d'encre

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
CA002472726A Expired - Fee Related CA2472726C (fr)	1998-09-11	1999-08-05	Procede d'impression par jet d'encre

Country Status (1)

Country	Link
CA (2)	CA2472726C (fr)

1999
- 1999-08-05 CA CA002472726A patent/CA2472726C/fr not_active Expired - Fee Related
- 1999-08-05 CA CA002472355A patent/CA2472355C/fr not_active Expired - Fee Related

Also Published As

Publication number	Publication date
CA2472726A1 (fr)	2000-03-11
CA2472355A1 (fr)	2000-03-11
CA2472726C (fr)	2007-10-16

Legal Events

Date	Code	Title	Description
2004-07-20	EEER	Examination request
2017-09-18	MKLA	Lapsed	Effective date: 20170807

Publication	Publication Date	Title
CA2279695C (fr)	2004-09-21	Procede d'impression par jet d'encre
US6991327B2 (en)	2006-01-31	Inkjet recording method, inkjet recording apparatus, program and storage medium storing program code readable by computer
JPH04355157A (ja)	1992-12-09	インクジェット記録装置
JP3313963B2 (ja)	2002-08-12	インクジェットプリント方法およびプリント装置
JP2002283564A (ja)	2002-10-03	インクジェット記録装置、インク、及び記録方法
JPH08281931A (ja)	1996-10-29	インクジェットプリント装置およびインクジェットプリント方法
KR100204374B1 (ko)	1999-06-15	잉크젯 프린팅 장치
CA2472355C (fr)	2008-01-08	Procede d'impression par jet d'encre
CA2439739C (fr)	2005-12-27	Procede d'impression par jet d'encre
US6121370A (en)	2000-09-19	Color recording liquids, cartridges, recording methods and devices
JP3817388B2 (ja)	2006-09-06	インクジェット記録用インクセット、印刷方法、およびインクジェット記録用淡インク
JP3559637B2 (ja)	2004-09-02	画像形成方法、インクセット、インク、インクの調製方法及びカラー画像の異色境界滲みの低減方法
JPH07305013A (ja)	1995-11-21	インク、これを用いたインクジェット記録方法及びかかるインクを備えた機器
JPH08104000A (ja)	1996-04-23	インクジェットプリント方法およびインクジェットプリント装置
MXPA99008269A (en)	2000-06-05	Improved process for printing by it jet
WO2005002867A1 (fr)	2005-01-13	Procede d'impression a jet d'encre et imprimante a jet d'encre
JP3334037B2 (ja)	2002-10-15	インクジェット記録方法
JPH09272199A (ja)	1997-10-21	インクジェットプリント方法およびインクジェットプリント装置
JPH06228482A (ja)	1994-08-16	インク、これを用いたインクジェット記録方法及びかかるインクを用いた記録機器
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