JPH0343313B2 - - Google Patents

Info

Publication number: JPH0343313B2
Authority: JP; Japan
Prior art keywords: ink; recording; paper; water; present
Prior art date: 1985-10-16
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 - Lifetime

Application number

JP60228922A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6289776A (ja

Inventor

Shoji Koike

Kazuo Iwata

Shinichi Tochihara

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.)

Canon Inc

Original Assignee

Canon Inc

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.)

1985-10-16

Filing date

1985-10-16

Publication date

1991-07-02

1985-10-16 Application filed by Canon Inc filed Critical Canon Inc

1985-10-16 Priority to JP60228922A priority Critical patent/JPS6289776A/ja

1986-08-06 Priority to DE3626567A priority patent/DE3626567C3/de

1986-08-06 Priority to GB8619192A priority patent/GB2180252B/en

1987-04-24 Publication of JPS6289776A publication Critical patent/JPS6289776A/ja

1988-03-03 Priority to US07/168,593 priority patent/US4923515A/en

1990-02-07 Priority to US07/478,580 priority patent/US5099255A/en

1991-07-02 Publication of JPH0343313B2 publication Critical patent/JPH0343313B2/ja

1991-08-29 Priority to HK689/91A priority patent/HK68991A/xx

1991-10-22 Priority to SG889/91A priority patent/SG88991G/en

Status Granted legal-status Critical Current

Links

238000000034 method Methods 0.000 claims description 33
150000001875 compounds Chemical class 0.000 claims description 24
239000007788 liquid Substances 0.000 claims description 12
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
239000000976 ink Substances 0.000 description 89
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
230000000052 comparative effect Effects 0.000 description 12
239000000975 dye Substances 0.000 description 12
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
238000001035 drying Methods 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 8
239000000463 material Substances 0.000 description 8
239000003960 organic solvent Substances 0.000 description 8
239000004094 surface-active agent Substances 0.000 description 7
239000000203 mixture Substances 0.000 description 6
238000001454 recorded image Methods 0.000 description 5
230000000740 bleeding effect Effects 0.000 description 4
230000000694 effects Effects 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
235000011187 glycerol Nutrition 0.000 description 4
239000002245 particle Substances 0.000 description 4
150000005846 sugar alcohols Polymers 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-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
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
230000008859 change Effects 0.000 description 3
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 3
235000019441 ethanol Nutrition 0.000 description 3
239000000049 pigment Substances 0.000 description 3
-1 polyoxyethylene chain Polymers 0.000 description 3
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
230000009471 action Effects 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000005215 alkyl ethers Chemical class 0.000 description 2
229920001400 block copolymer Polymers 0.000 description 2
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000000982 direct dye Substances 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
239000012046 mixed solvent Substances 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
238000003825 pressing Methods 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
LXOFYPKXCSULTL-UHFFFAOYSA-N 2,4,7,9-tetramethyldec-5-yne-4,7-diol Chemical compound CC(C)CC(C)(O)C#CC(C)(O)CC(C)C LXOFYPKXCSULTL-UHFFFAOYSA-N 0.000 description 1
WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
IHZXTIBMKNSJCJ-UHFFFAOYSA-N 3-{[(4-{[4-(dimethylamino)phenyl](4-{ethyl[(3-sulfophenyl)methyl]amino}phenyl)methylidene}cyclohexa-2,5-dien-1-ylidene)(ethyl)azaniumyl]methyl}benzene-1-sulfonate Chemical compound C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S(O)(=O)=O)=C1 IHZXTIBMKNSJCJ-UHFFFAOYSA-N 0.000 description 1
AVERNFJXXRIVQN-XSDYUOFFSA-N 5-[(4-ethoxyphenyl)diazenyl]-2-[(e)-2-[4-[(4-ethoxyphenyl)diazenyl]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C1=CC(OCC)=CC=C1N=NC(C=C1S(O)(=O)=O)=CC=C1\C=C\C1=CC=C(N=NC=2C=CC(OCC)=CC=2)C=C1S(O)(=O)=O AVERNFJXXRIVQN-XSDYUOFFSA-N 0.000 description 1
STOOUUMSJPLRNI-UHFFFAOYSA-N 5-amino-4-hydroxy-3-[[4-[4-[(4-hydroxyphenyl)diazenyl]phenyl]phenyl]diazenyl]-6-[(4-nitrophenyl)diazenyl]naphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC2=CC(S(O)(=O)=O)=C(N=NC=3C=CC(=CC=3)C=3C=CC(=CC=3)N=NC=3C=CC(O)=CC=3)C(O)=C2C(N)=C1N=NC1=CC=C([N+]([O-])=O)C=C1 STOOUUMSJPLRNI-UHFFFAOYSA-N 0.000 description 1
CQPFMGBJSMSXLP-ZAGWXBKKSA-M Acid orange 7 Chemical compound OC1=C(C2=CC=CC=C2C=C1)/N=N/C1=CC=C(C=C1)S(=O)(=O)[O-].[Na+] CQPFMGBJSMSXLP-ZAGWXBKKSA-M 0.000 description 1
HMEKVHWROSNWPD-UHFFFAOYSA-N Erioglaucine A Chemical compound [NH4+].[NH4+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 HMEKVHWROSNWPD-UHFFFAOYSA-N 0.000 description 1
229930194542 Keto Natural products 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
GRPFBMKYXAYEJM-UHFFFAOYSA-M [4-[(2-chlorophenyl)-[4-(dimethylamino)phenyl]methylidene]cyclohexa-2,5-dien-1-ylidene]-dimethylazanium;chloride Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C(=CC=CC=1)Cl)=C1C=CC(=[N+](C)C)C=C1 GRPFBMKYXAYEJM-UHFFFAOYSA-M 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000980 acid dye Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
125000005233 alkylalcohol group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
VJDDAARZIFHSQY-UHFFFAOYSA-N basic black 2 Chemical compound [Cl-].C=1C2=[N+](C=3C=CC=CC=3)C3=CC(N(CC)CC)=CC=C3N=C2C=CC=1NN=C1C=CC(=O)C=C1 VJDDAARZIFHSQY-UHFFFAOYSA-N 0.000 description 1
239000000981 basic dye Substances 0.000 description 1
230000008901 benefit Effects 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
230000001934 delay Effects 0.000 description 1
DHQJMKJYFOHOSY-UHFFFAOYSA-L disodium 4-amino-3-[[4-[4-[(2,4-diaminophenyl)diazenyl]-3-methylphenyl]-2-methylphenyl]diazenyl]-5-oxido-6-phenyldiazenyl-7-sulfonaphthalene-2-sulfonate Chemical compound [Na+].[Na+].Cc1cc(ccc1N=Nc1ccc(N)cc1N)-c1ccc(N=Nc2c(N)c3c(O)c(N=Nc4ccccc4)c(cc3cc2S([O-])(=O)=O)S([O-])(=O)=O)c(C)c1 DHQJMKJYFOHOSY-UHFFFAOYSA-L 0.000 description 1
AOMZHDJXSYHPKS-UHFFFAOYSA-L disodium 4-amino-5-hydroxy-3-[(4-nitrophenyl)diazenyl]-6-phenyldiazenylnaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(N=NC=3C=CC=CC=3)C(O)=C2C(N)=C1N=NC1=CC=C([N+]([O-])=O)C=C1 AOMZHDJXSYHPKS-UHFFFAOYSA-L 0.000 description 1
YCMOBGSVZYLYBZ-UHFFFAOYSA-L disodium 5-[[4-[4-[(2-amino-8-hydroxy-6-sulfonatonaphthalen-1-yl)diazenyl]phenyl]phenyl]diazenyl]-2-hydroxybenzoate Chemical compound NC1=CC=C2C=C(C=C(O)C2=C1N=NC1=CC=C(C=C1)C1=CC=C(C=C1)N=NC1=CC=C(O)C(=C1)C(=O)O[Na])S(=O)(=O)O[Na] YCMOBGSVZYLYBZ-UHFFFAOYSA-L 0.000 description 1
FPVGTPBMTFTMRT-UHFFFAOYSA-L disodium;2-amino-5-[(4-sulfonatophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-UHFFFAOYSA-L 0.000 description 1
239000000986 disperse dye Substances 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
230000005684 electric field Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000005284 excitation Effects 0.000 description 1
235000019233 fast yellow AB Nutrition 0.000 description 1
239000000576 food coloring agent Substances 0.000 description 1
229940051250 hexylene glycol Drugs 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229940035429 isobutyl alcohol Drugs 0.000 description 1
ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical group C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000002609 medium Substances 0.000 description 1
239000012528 membrane Substances 0.000 description 1
239000003607 modifier Substances 0.000 description 1
JQZWHMOVSQRYRN-UHFFFAOYSA-M n-(2-chloroethyl)-n-ethyl-3-methyl-4-[2-(1,3,3-trimethylindol-1-ium-2-yl)ethenyl]aniline;chloride Chemical compound [Cl-].CC1=CC(N(CCCl)CC)=CC=C1C=CC1=[N+](C)C2=CC=CC=C2C1(C)C JQZWHMOVSQRYRN-UHFFFAOYSA-M 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
230000035699 permeability Effects 0.000 description 1
239000002985 plastic film Substances 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229940068886 polyethylene glycol 300 Drugs 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000000985 reactive dye Substances 0.000 description 1
230000004044 response Effects 0.000 description 1
BQHRKYUXVHKLLZ-UHFFFAOYSA-M sodium 7-amino-2-[[4-[(4-aminophenyl)diazenyl]-2-methoxy-5-methylphenyl]diazenyl]-3-sulfonaphthalen-1-olate Chemical compound [Na+].COc1cc(N=Nc2ccc(N)cc2)c(C)cc1N=Nc1c(O)c2cc(N)ccc2cc1S([O-])(=O)=O BQHRKYUXVHKLLZ-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
235000012756 tartrazine Nutrition 0.000 description 1
UJMBCXLDXJUMFB-GLCFPVLVSA-K tartrazine Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-GLCFPVLVSA-K 0.000 description 1
239000004149 tartrazine Substances 0.000 description 1
UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
BZJNMKDNHPKBHE-UHFFFAOYSA-J tetrasodium 3-amino-5-oxido-7-sulfo-6-[[7-sulfonato-4-[(4-sulfonatophenyl)diazenyl]naphthalen-1-yl]diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C=1C=C2C=C(S([O-])(=O)=O)C(N)=CC2=C(O)C=1N=NC(C1=CC(=CC=C11)S([O-])(=O)=O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 BZJNMKDNHPKBHE-UHFFFAOYSA-J 0.000 description 1
GMMAPXRGRVJYJY-UHFFFAOYSA-J tetrasodium 4-acetamido-5-hydroxy-6-[[7-sulfonato-4-[(4-sulfonatophenyl)diazenyl]naphthalen-1-yl]diazenyl]naphthalene-1,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].OC1=C2C(NC(=O)C)=CC=C(S([O-])(=O)=O)C2=CC(S([O-])(=O)=O)=C1N=NC(C1=CC(=CC=C11)S([O-])(=O)=O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 GMMAPXRGRVJYJY-UHFFFAOYSA-J 0.000 description 1
MPCYPRXRVWZKGF-UHFFFAOYSA-J tetrasodium 5-amino-3-[[4-[4-[(8-amino-1-hydroxy-3,6-disulfonatonaphthalen-2-yl)diazenyl]phenyl]phenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(N=NC3=CC=C(C=C3)C3=CC=C(C=C3)N=NC3=C(C=C4C=C(C=C(C4=C3O)N)S([O-])(=O)=O)S([O-])(=O)=O)=C(O)C2=C1N MPCYPRXRVWZKGF-UHFFFAOYSA-J 0.000 description 1
YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
229950006389 thiodiglycol Drugs 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 1
VRVDFJOCCWSFLI-UHFFFAOYSA-K trisodium 3-[[4-[(6-anilino-1-hydroxy-3-sulfonatonaphthalen-2-yl)diazenyl]-5-methoxy-2-methylphenyl]diazenyl]naphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].[Na+].COc1cc(N=Nc2cc(c3cccc(c3c2)S([O-])(=O)=O)S([O-])(=O)=O)c(C)cc1N=Nc1c(O)c2ccc(Nc3ccccc3)cc2cc1S([O-])(=O)=O VRVDFJOCCWSFLI-UHFFFAOYSA-K 0.000 description 1
239000004034 viscosity adjusting agent Substances 0.000 description 1

Landscapes

Ink Jet (AREA)
Ink Jet Recording Methods And Recording Media Thereof (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)

JP60228922A 1985-08-06 1985-10-16 記録液及びこれを用いたインクジェット記録方法 Granted JPS6289776A (ja)

Priority Applications (7)

Application Number	Priority Date	Filing Date	Title
JP60228922A JPS6289776A (ja)	1985-10-16	1985-10-16	記録液及びこれを用いたインクジェット記録方法
DE3626567A DE3626567C3 (de)	1985-08-06	1986-08-06	Aufzeichnungsflüssigkeit und deren Verwendung in Schreibgeräten, Druckern und Tintenstrahldruckgeräten
GB8619192A GB2180252B (en)	1985-08-06	1986-08-06	Recording liquid and recording method by use thereof
US07/168,593 US4923515A (en)	1985-08-06	1988-03-03	Recording liquid having organic solvent with plural (C2 H4 O) moieties and recording method using the same
US07/478,580 US5099255A (en)	1985-08-06	1990-02-07	Recording method using recording liquid having organic solvent with plural (C2 H4 O) moieties
HK689/91A HK68991A (en)	1985-08-06	1991-08-29	Recording liquid and recording method by use thereof
SG889/91A SG88991G (en)	1985-08-06	1991-10-22	Recording liquid and recording method by use thereof

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP60228922A JPS6289776A (ja)	1985-10-16	1985-10-16	記録液及びこれを用いたインクジェット記録方法

Publications (2)

Publication Number	Publication Date
JPS6289776A JPS6289776A (ja)	1987-04-24
JPH0343313B2 true JPH0343313B2 (de)	1991-07-02

Family

ID=16883956

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP60228922A Granted JPS6289776A (ja)	1985-08-06	1985-10-16	記録液及びこれを用いたインクジェット記録方法

Country Status (1)

Country	Link
JP (1)	JPS6289776A (de)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2006299250A (ja) *	2005-03-24	2006-11-02	Canon Inc	インクジェット記録用インク、インクジェット記録方法及びインクジェット記録装置
WO2009066577A1 (ja)	2007-11-20	2009-05-28	Dic Corporation	水性顔料分散体、及びインクジェット記録用水性顔料インク

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JPH01230685A (ja) *	1988-03-11	1989-09-14	Canon Inc	インク
JPH0819877B2 (ja) *	1988-05-19	1996-02-28	株式会社ウオルブローフアーイースト	ロータリスロットル弁式気化器の始動操作機構
US5221334A (en) *	1990-04-11	1993-06-22	E. I. Du Pont De Nemours And Company	Aqueous pigmented inks for ink jet printers
JP2887939B2 (ja) *	1991-04-26	1999-05-10	富士ゼロックス株式会社	インクジェット記録用インク
US5382283A (en) *	1991-04-26	1995-01-17	Fuji Xerox Co., Ltd.	Ink containing propylene oxide/ethylene oxide block copolymers for ink jet recording

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JPS5710662A (en) *	1980-06-24	1982-01-20	Canon Inc	Recording liquid

1985
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Cited By (3)

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Publication number	Priority date	Publication date	Assignee	Title
JP2006299250A (ja) *	2005-03-24	2006-11-02	Canon Inc	インクジェット記録用インク、インクジェット記録方法及びインクジェット記録装置
WO2009066577A1 (ja)	2007-11-20	2009-05-28	Dic Corporation	水性顔料分散体、及びインクジェット記録用水性顔料インク
US8008391B2 (en)	2007-11-20	2011-08-30	Dic Corporation	Aqueous pigment dispersion and aqueous pigment ink for inkjet recording

Also Published As

Publication number	Publication date
JPS6289776A (ja)	1987-04-24

Publication	Publication Date	Title
US4973499A (en)	1990-11-27	Recording liquid having surface tension of at least 64 dyne/cm and viscosity of at most 2.5 cp at 25 degrees Celsius
US5221333A (en)	1993-06-22	Ink, inj-jet recording process, and instrument using the ink
JP3005059B2 (ja)	2000-01-31	インク、これを用いたインクジェット記録方法及び機器
US4923515A (en)	1990-05-08	Recording liquid having organic solvent with plural (C2 H4 O) moieties and recording method using the same
JP3862441B2 (ja)	2006-12-27	インクジェット記録用インク、インクセット、インクカートリッジ、記録ユニット、画像記録装置、画像記録方法、カラー画像の形成方法および画像の光学濃度向上方法
EP1433826B1 (de)	2010-09-08	Tintensatz für Tintenstrahl-Aufzeichnung, Tintenstrahl-Aufzeichnungsverfahren, Aufzeichnungseinheit, Aufzeichnungsgerät und Verfahren zur Reduzierung der Farbvermischung
US20060132568A1 (en)	2006-06-22	Aqueous ink, ink jet recording method, ink cartridge, recording unit, ink jet recording apparatus and image forming method
EP0376284A2 (de)	1990-07-04	Aufzeichnungs-Flüssigkeit und Tintenstrahlverfahren unter Verwendung dieser Flüssigkeit
JPH1112520A (ja)	1999-01-19	カール防止剤を含むインクジェットインク及び印刷プロセス
JPH0662000B2 (ja)	1994-08-17	インクジエツト記録方法
JP4981261B2 (ja)	2012-07-18	インクジェット用インク、インクジェット記録方法、インクカートリッジ、及びインクジェット記録装置
JPH0343313B2 (de)	1991-07-02
JP2000178490A (ja)	2000-06-27	水性インク及びインクジェット記録装置
JP4158303B2 (ja)	2008-10-01	インクジェット記録用水性顔料インキ
JP2003246949A (ja)	2003-09-05	インクジェット記録用水性インクセット
JPS62177079A (ja)	1987-08-03	記録液
JP4366558B2 (ja)	2009-11-18	インクジェット用水性インクセット及びインクジェット記録方法
JPH0621251B2 (ja)	1994-03-23	記録液
JP2000178489A (ja)	2000-06-27	水性インク及びインクジェット記録装置
JPS62177075A (ja)	1987-08-03	記録液
JPS62124166A (ja)	1987-06-05	記録方法
JP2980995B2 (ja)	1999-11-22	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機器
JP2003246952A (ja)	2003-09-05	インクジェット用インク
JP2004210902A (ja)	2004-07-29	インクジェット用インク
JP3004360B2 (ja)	2000-01-31	水系顔料インク

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2005-10-16	EXPY	Cancellation because of completion of term