US20020139281A1 - Use of hydrolyzed reactive red 23 - Google Patents
Use of hydrolyzed reactive red 23 Download PDFInfo
- Publication number
- US20020139281A1 US20020139281A1 US09/772,255 US77225501A US2002139281A1 US 20020139281 A1 US20020139281 A1 US 20020139281A1 US 77225501 A US77225501 A US 77225501A US 2002139281 A1 US2002139281 A1 US 2002139281A1
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- ink
- reactive red
- hydrolyzed
- jet
- inks
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- SOFRHZUTPGJWAM-UHFFFAOYSA-N 3-hydroxy-4-[(2-methoxy-5-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound COc1ccc(cc1N=Nc1c(O)c(cc2ccccc12)C(=O)Nc1cccc(c1)[N+]([O-])=O)[N+]([O-])=O SOFRHZUTPGJWAM-UHFFFAOYSA-N 0.000 title claims abstract description 32
- 239000000976 ink Substances 0.000 claims description 34
- 239000000975 dye Substances 0.000 claims description 21
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 18
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 12
- 238000007641 inkjet printing Methods 0.000 claims description 7
- 230000003301 hydrolyzing effect Effects 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 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 claims description 2
- 239000001043 yellow dye Substances 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 101150048251 RR23 gene Proteins 0.000 description 10
- FBBPTVMIVIHZBI-UHFFFAOYSA-F C=CCC1=CC2=C(C=C1)O[Cu-]1OC3=C(N=[N+]21)C1=C(C=C(S(=O)(=O)O[Na])C=C1)C=C3S(=O)(=O)O[Na].O=S(=O)(O[Na])C1=CC2=C(C=C1)C1=C(O[Cu-]3OC4=C(C=C(SOOCCO)C=C4)[N+]3=N1)C(S(=O)(=O)O[Na])=C2 Chemical compound C=CCC1=CC2=C(C=C1)O[Cu-]1OC3=C(N=[N+]21)C1=C(C=C(S(=O)(=O)O[Na])C=C1)C=C3S(=O)(=O)O[Na].O=S(=O)(O[Na])C1=CC2=C(C=C1)C1=C(O[Cu-]3OC4=C(C=C(SOOCCO)C=C4)[N+]3=N1)C(S(=O)(=O)O[Na])=C2 FBBPTVMIVIHZBI-UHFFFAOYSA-F 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 3
- 238000002161 passivation Methods 0.000 description 3
- 235000001892 vitamin D2 Nutrition 0.000 description 3
- KRUHIXJOUBAHKJ-UHFFFAOYSA-A C=CSOOC1=CC2=C(C=C1)O[Cu]OC1=C(N=N2)C2=C(C=C(S(=O)(=O)O[Na])C=C2)C=C1S(=O)(=O)O[Na].O=S(=O)(O[Na])C1=CC2=C(C=C1)C1=C(O[Cu]OC3=C(C=C(SOOCCO)C=C3)N=N1)C(S(=O)(=O)O[Na])=C2.O=S(CCOOSC1=CC2=C(C=C1)O[Cu]OC1=C(N=N2)C2=C(C=C(S(=O)(=O)O[Na])C=C2)C=C1S(=O)(=O)O[Na])OOO[Na] Chemical compound C=CSOOC1=CC2=C(C=C1)O[Cu]OC1=C(N=N2)C2=C(C=C(S(=O)(=O)O[Na])C=C2)C=C1S(=O)(=O)O[Na].O=S(=O)(O[Na])C1=CC2=C(C=C1)C1=C(O[Cu]OC3=C(C=C(SOOCCO)C=C3)N=N1)C(S(=O)(=O)O[Na])=C2.O=S(CCOOSC1=CC2=C(C=C1)O[Cu]OC1=C(N=N2)C2=C(C=C(S(=O)(=O)O[Na])C=C2)C=C1S(=O)(=O)O[Na])OOO[Na] KRUHIXJOUBAHKJ-UHFFFAOYSA-A 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- HKQAWDQBKHGZPE-UHFFFAOYSA-B C=CSOOC1=CC2=C(C=C1)O[Cu]OC1=C(N=N2)C2=C(C=C(C)C=C2)C=C1S(=O)(=O)O[Na].O=S(=O)(O[Na])C1=CC2=C(C=C1)C1=C(O[Cu]OC3=C(C=C(SOOCCO)C=C3)N=N1)C(S(=O)(=O)O[Na])=C2.O=S(CCOOSC1=CC2=C(C=C1)O[Cu]OC1=C(N=N2)C2=C(C=C(S(=O)(=O)O[Na])C=C2)C=C1S(=O)(=O)O[Na])OOO[Na] Chemical compound C=CSOOC1=CC2=C(C=C1)O[Cu]OC1=C(N=N2)C2=C(C=C(C)C=C2)C=C1S(=O)(=O)O[Na].O=S(=O)(O[Na])C1=CC2=C(C=C1)C1=C(O[Cu]OC3=C(C=C(SOOCCO)C=C3)N=N1)C(S(=O)(=O)O[Na])=C2.O=S(CCOOSC1=CC2=C(C=C1)O[Cu]OC1=C(N=N2)C2=C(C=C(S(=O)(=O)O[Na])C=C2)C=C1S(=O)(=O)O[Na])OOO[Na] HKQAWDQBKHGZPE-UHFFFAOYSA-B 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 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
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/328—Inkjet printing inks characterised by colouring agents characterised by dyes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0046—Mixtures of two or more azo dyes
- C09B67/0051—Mixtures of two or more azo dyes mixture of two or more monoazo dyes
- C09B67/0052—Mixtures of two or more reactive monoazo dyes
- C09B67/0054—Mixtures of two or more reactive monoazo dyes all the reactive groups not being directly attached to a heterocyclic system
Definitions
- the present invention generally relates to ink-jet printing, and in particular to a specific form of Reactive Red 23 magenta dye which is hydrolyzed to produce a passivated form with better pH stability thus improving kogation, decap and lightfastness.
- ink-jet printing systems have grown dramatically in recent years. This growth may be attributed to substantial improvements in print resolution and overall print quality coupled with appreciable reduction in cost.
- Today's ink-jet printers offer acceptable print quality for many commercial, business, and household applications at costs fully an order of magnitude lower than comparable products available just a few years ago. Notwithstanding their recent success, intensive research and development efforts continue toward improving ink-jet print quality. In general, ink-jet print quality still falls short of that produced by more expensive technologies such as photography and offset or gravure printing.
- a surge in interest in ink-jet imaging e.g., the rendition of pictures
- the challenge remains to further improve the image quality and lightfastness of ink-jet printed images, especially images containing skin tones, without increasing their cost.
- a successful ink set for color ink-jet printing must be compatible with the ink-jet pen and printing system.
- Some of the required properties for the ink-jet ink include: good crusting resistance, good stability, the proper viscosity, the proper surface tension, little color-to-color bleed, rapid dry time, no negative reaction with the vehicle, high solubility of the dyes in the vehicle, consumer safety, low strike through, high color saturation, and good dot gain.
- Color ink-jet printers typically use three inks of differing hues: magenta, yellow, and cyan. Optionally black is also used.
- EP 662499 and EP 366121 both assigned to Canon disclose the use of Reactive Red 23 in inkjet ink.
- the present invention relates to a high lightfastness magenta dye comprising hydrolyzed Reactive Red 23 with from 0 to 100% hydroxy form and from 0 to 100% vinyl form:
- the present invention further relates to a set of ink-jet inks for ink-jet printing, at least one of the inks being a magenta ink comprising a high lightfastness magenta dye, the high lightfastness magenta dye comprising hydrolyzed Reactive Red 23 with from 0 to 100% hydroxy form and from 0 to 100% vinyl form:
- the present invention additionally relates to a method of making a passivated form of Reactive Red 23 comprising
- the present invention described herein is directed to ink-jet inks for printing ink-jet images using commercially available ink-jet printers such as, for example but not limited to, HP DeskJet® printers, manufactured by Hewlett-Packard Company, of Palo Alto, Calif.
- the inks enable production of near photographic images having little or no coalescence, excellent waterfastness, and reduced dry time, on a range of print media, in particular, for example but not limited to, plain white, 8 1 ⁇ 2′′ ⁇ 11′′, 20 lb. weight, printer paper conventionally used for office and home computers.
- RR23 is a very lightfast dye.
- the reactive portion of this dye molecule will hydrolyze over time in an aqueous solution. It is known that when the reactive group of other inkjet dyes (Reactive Red 180 and Reactive Black 31) is hydrolyzed over time, pH instability over the life of the ink has resulted. The pH change and salts formed during hydrolysis over time increase the occurrence of kogation, decap and lightfastness problems in an ink containing a reactive dye .
- the present inventor has found that when RR23 is passivated initially by hydrolyzing the reactive sulfate group of the dye that a more stable dye results with better characteristics of pH stability, kogation, decap and lightfastness.
- the passivation can occur under acid or alkaline conditions. In a preferred embodiment the passivation occurs under alkaline conditions and in a more preferred embodiment the passivation occurs at a pH of at least 9.
- the present invention relates to a high lightfastness magenta dye comprising hydrolyzed Reactive Red 23 with from 0 to 100% hydroxy form and from 0 to 100% vinyl form:
- At least 50% of the hydrolyzed Reactive Red 23 is the hydroxy form.
- the present invention relates to a set of inkjet inks for ink-jet printing, at least one of the inks being a magenta ink comprising a high lightfastness magenta dye, the high lightfastness magenta dye comprising hydrolyzed Reactive Red 23 with from 0 to 100% hydroxy form and from 0 to 100% vinyl form:
- At least 50% of the hydrolyzed Reactive Red 23 is the hydroxy form.
- At least one of the inks is a cyan ink comprising a cyan dye; and at least one of the inks is a yellow ink comprising a yellow dye.
- the present invention relates to a method of making a passivated form of Reactive Red 23 comprising
- hydrolyzing the Reactive Red 23 is conducted at a pH of at least 9.
- At least 50% of the hydrolyzed Reactive Red 23 is the hydroxy form.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
Abstract
Description
- The present invention generally relates to ink-jet printing, and in particular to a specific form of Reactive Red 23 magenta dye which is hydrolyzed to produce a passivated form with better pH stability thus improving kogation, decap and lightfastness.
- The use of ink-jet printing systems has grown dramatically in recent years. This growth may be attributed to substantial improvements in print resolution and overall print quality coupled with appreciable reduction in cost. Today's ink-jet printers offer acceptable print quality for many commercial, business, and household applications at costs fully an order of magnitude lower than comparable products available just a few years ago. Notwithstanding their recent success, intensive research and development efforts continue toward improving ink-jet print quality. In general, ink-jet print quality still falls short of that produced by more expensive technologies such as photography and offset or gravure printing. A surge in interest in ink-jet imaging (e.g., the rendition of pictures) has resulted in the need to produce near photographic quality printed images at a reasonable cost. The challenge remains to further improve the image quality and lightfastness of ink-jet printed images, especially images containing skin tones, without increasing their cost.
- If such an ink is to be used in an ink-jet printing device, characteristics such as crusting, long-term stability, and materials compatibility must also be addressed. If the ink is to be used in a thermal ink-jet printer, the further constraint of being thermally stable (kogation-resistant) is added.
- In general, a successful ink set for color ink-jet printing must be compatible with the ink-jet pen and printing system. Some of the required properties for the ink-jet ink include: good crusting resistance, good stability, the proper viscosity, the proper surface tension, little color-to-color bleed, rapid dry time, no negative reaction with the vehicle, high solubility of the dyes in the vehicle, consumer safety, low strike through, high color saturation, and good dot gain. Color ink-jet printers typically use three inks of differing hues: magenta, yellow, and cyan. Optionally black is also used. EP 662499 and EP 366121 both assigned to Canon disclose the use of Reactive Red 23 in inkjet ink.
-
- The present invention further relates to a set of ink-jet inks for ink-jet printing, at least one of the inks being a magenta ink comprising a high lightfastness magenta dye, the high lightfastness magenta dye comprising hydrolyzed Reactive Red 23 with from 0 to 100% hydroxy form and from 0 to 100% vinyl form:
- The present invention additionally relates to a method of making a passivated form of Reactive Red 23 comprising
-
- The present invention described herein is directed to ink-jet inks for printing ink-jet images using commercially available ink-jet printers such as, for example but not limited to, HP DeskJet® printers, manufactured by Hewlett-Packard Company, of Palo Alto, Calif. The inks enable production of near photographic images having little or no coalescence, excellent waterfastness, and reduced dry time, on a range of print media, in particular, for example but not limited to, plain white, 8 ½″×11″, 20 lb. weight, printer paper conventionally used for office and home computers.
- RR23 is a very lightfast dye. The reactive portion of this dye molecule will hydrolyze over time in an aqueous solution. It is known that when the reactive group of other inkjet dyes (Reactive Red 180 and Reactive Black 31) is hydrolyzed over time, pH instability over the life of the ink has resulted. The pH change and salts formed during hydrolysis over time increase the occurrence of kogation, decap and lightfastness problems in an ink containing a reactive dye .
- The present inventor has found that when RR23 is passivated initially by hydrolyzing the reactive sulfate group of the dye that a more stable dye results with better characteristics of pH stability, kogation, decap and lightfastness. The passivation can occur under acid or alkaline conditions. In a preferred embodiment the passivation occurs under alkaline conditions and in a more preferred embodiment the passivation occurs at a pH of at least 9.
-
- In a preferred embodiment of the high lightfastness magenta dye of the present invention, at least 50% of the hydrolyzed Reactive Red 23 is the hydroxy form.
- In another embodiment, the present invention relates to a set of inkjet inks for ink-jet printing, at least one of the inks being a magenta ink comprising a high lightfastness magenta dye, the high lightfastness magenta dye comprising hydrolyzed Reactive Red 23 with from 0 to 100% hydroxy form and from 0 to 100% vinyl form:
- In a preferred embodiment of the set of ink-jet inks of the present invention, at least 50% of the hydrolyzed Reactive Red 23 is the hydroxy form.
- In another preferred embodiment of the set of ink-jet inks of the present invention, at least one of the inks is a cyan ink comprising a cyan dye; and at least one of the inks is a yellow ink comprising a yellow dye.
- In yet another embodiment, the present invention relates to a method of making a passivated form of Reactive Red 23 comprising
-
- In a preferred embodiment of the method of the present invention, hydrolyzing the Reactive Red 23 is conducted at a pH of at least 9.
- In another preferred embodiment of the method of the present invention, at least 50% of the hydrolyzed Reactive Red 23 is the hydroxy form.
- The extent of real time fade of inkjet printed samples of passivated Reactive Red 23 was compared directly to similar inkjet printed samples of Magenta 377. Real time fade was measured by determining the original optical density of the inkjet printed samples and the faded optical density of the samples after 7.5 months of exposure to office light. The results are shown in the following table. Reactive red 23 was shown to fade 37% in 7.5 months, while Magenta 377 faded 86% under the same conditions.
TABLE 1 Fade after 7.5 months of office light Sample Original OD after fade OD % fade M377 1.76 0.24 86% RR23 1.27 0.8 37% - The extent of accelerated fade of inkjet printed samples of passivated Reactive Red 23 was compared directly to similar inkjet printed samples of Magenta 377 and Pro-Jet™ Fast Magenta 2. Accelerated fade was measured by determining the % optical density fade of the inkjet-printed samples at 3 months and 6 months accelerated fade. The results are shown in the following Table 2. Reactive red 23 was shown to fade 37% in 7.5 months, while Magenta 377 faded 86% under the same conditions.
TABLE 2 Accelerated Fade after 3 and 6 months of office light Sample 3 month fade OD 6 month fade M377 6% 7% Pro-jet ™ Fast 30% 43% Magenta 2 RR23 1% 4% - Samples of RR23 were prepared under various conditions of pH and temperature. The area count @ 530 nm was measured at 1.2 minutes, 3.3 minutes and 5.4 minutes for the samples under the various conditions and from the Area Count measurements the percentages in each sample of Reactive Form (MW 673), Hydroxy Form (MW 593) and Vinyl Form (MW 575) were determined at the various conditions. The results are given below in Table 3.
TABLE 3 Area Count @ 530 nm Percentage (%) Reactive Hydroxy Reactive Hydroxy Sample ID Form (MW Form (MW Vinyl Form Form (MW Form (MW Vinyl Form RR 23 673) 593) (MW 575) 673) 593) (MW 575) Retention 1.2 3.3 5.4 Time (min) Starting 9196 428 2694 74.7 3.5 21.9 Dye (powder) pH = 7 8121 932 9862 42.9 4.9 52.1 ambient 2 weeks pH = 7 ASL 0 2105 17253 0.0 10.9 89.1 2 weeks pH = 4 ASL 12633 572 4177 72.7 3.3 24.0 2 weeks pH = 9 ASL 3322 14978 262 17.9 80.7 1.4 2 weeks - Inkjet inks of RR23 and M377 were printed on HP Professional Brochure paper. Percent fade was measured after 2 years. Results are given below in Table 4.
TABLE 4 % Fade at 2 years on HP Professional Brochure paper RR23 5% M377 38% - Two digital colored photographs were printed on HP Premium Photoglossy paper. The only difference in the two photographs was with the dark magenta ink that was used. The dark magenta ink used in the photographs was either dark magenta of M377 or of RR23. Years of life for magenta, neutral patch, red and blue were measured in each photograph and shown below in Table 5.
TABLE 5 Years of life using dark magenta (M377 and RR23) on HP Premium Photoglossy Magenta Neutral patch Red Blue M377 5.5 5.5 5.5 4.8 RR23 7.5 7.5 9 7.5 - While the foregoing invention has been described in some detail for purposes of clarity and understanding, it will be clear to one skilled in the art from the reading of this disclosure that various changes in form and detail can be made without departing from the true scope of the invention.
Claims (8)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/772,255 US6458195B1 (en) | 2001-01-26 | 2001-01-26 | Use of hydrolyzed Reactive Red 23 |
JP2002002947A JP2002302622A (en) | 2001-01-26 | 2002-01-10 | Magenta dye |
EP02250342A EP1229084B1 (en) | 2001-01-26 | 2002-01-18 | Use of hydrolyzed "reactive red 23" (RR23) as dye for ink-jet printing |
DE60200841T DE60200841T2 (en) | 2001-01-26 | 2002-01-18 | Use of hydrolyzed "reactive red 23" (RR23) as a dye for inkjet printers |
HK02109284.4A HK1047759B (en) | 2001-01-26 | 2002-12-23 | Use of hydrolyzed "reactive red 23" (rr23) as dye for ink-jet printing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/772,255 US6458195B1 (en) | 2001-01-26 | 2001-01-26 | Use of hydrolyzed Reactive Red 23 |
Publications (2)
Publication Number | Publication Date |
---|---|
US6458195B1 US6458195B1 (en) | 2002-10-01 |
US20020139281A1 true US20020139281A1 (en) | 2002-10-03 |
Family
ID=25094457
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/772,255 Expired - Lifetime US6458195B1 (en) | 2001-01-26 | 2001-01-26 | Use of hydrolyzed Reactive Red 23 |
Country Status (5)
Country | Link |
---|---|
US (1) | US6458195B1 (en) |
EP (1) | EP1229084B1 (en) |
JP (1) | JP2002302622A (en) |
DE (1) | DE60200841T2 (en) |
HK (1) | HK1047759B (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050211133A1 (en) * | 2004-03-23 | 2005-09-29 | Benq Corporation | Red colorant composition and magenta inkjet ink composition with stable pH |
US20050277765A1 (en) * | 2004-06-10 | 2005-12-15 | Eastman Kodak Company | Multimetallic polymeric azo colorants |
US20050282926A1 (en) * | 2004-06-10 | 2005-12-22 | Eastman Kodak Company | Ink jet ink containing multimetallic polymeric colorants |
US20060183046A1 (en) * | 2003-05-16 | 2006-08-17 | Canon Kabushiki Kaisha | Novel coloring compound and recording material using the same |
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DE10106682A1 (en) * | 2001-02-14 | 2002-08-29 | Clariant Gmbh | Colorant composition |
GB0222494D0 (en) * | 2002-09-27 | 2002-11-06 | Avecia Ltd | Compounds,compositions and processes |
US7387665B2 (en) * | 2006-04-12 | 2008-06-17 | E.I. Du Pont De Nemours And Company | Inkjet ink and ink set |
WO2008055244A2 (en) | 2006-10-31 | 2008-05-08 | Sensient Colors Inc. | Modified pigments and methods for making and using the same |
CA2697966C (en) | 2007-08-23 | 2018-11-06 | Sensient Colors Inc. | Self-dispersed pigments and methods for making and using the same |
CN102858886A (en) | 2009-04-07 | 2013-01-02 | 森馨颜色有限责任公司 | Self-dispersing particles and methods for making and using the same |
CN117327406A (en) * | 2023-09-27 | 2024-01-02 | 浙江亿得新材料股份有限公司 | Composite high-light fastness reactive red dye composition and application thereof |
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ES2185549T3 (en) | 1999-09-27 | 2003-05-01 | Ciba Sc Holding Ag | CARMESI RED COLOR INKS (MAGENTA) CONTAINING COPPER COMPLEX AZOIC COLORANTS BASED ON 1-NAFTOL-DI- OR -TRISULPHONIC ACIDS. |
ES2192516T3 (en) * | 1999-09-27 | 2003-10-16 | Ciba Sc Holding Ag | AZOIC COLORS OF COPPER COMPLEX, OBTAINING AND USING THEMSELVES. |
DE10032683A1 (en) | 2000-07-05 | 2002-01-17 | Clariant Gmbh | Colorant mixture |
-
2001
- 2001-01-26 US US09/772,255 patent/US6458195B1/en not_active Expired - Lifetime
-
2002
- 2002-01-10 JP JP2002002947A patent/JP2002302622A/en active Pending
- 2002-01-18 EP EP02250342A patent/EP1229084B1/en not_active Expired - Lifetime
- 2002-01-18 DE DE60200841T patent/DE60200841T2/en not_active Expired - Lifetime
- 2002-12-23 HK HK02109284.4A patent/HK1047759B/en not_active IP Right Cessation
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060183046A1 (en) * | 2003-05-16 | 2006-08-17 | Canon Kabushiki Kaisha | Novel coloring compound and recording material using the same |
US7598012B2 (en) | 2003-05-16 | 2009-10-06 | Canon Kabushiki Kaisha | Coloring compound and recording material using the same |
US20050211133A1 (en) * | 2004-03-23 | 2005-09-29 | Benq Corporation | Red colorant composition and magenta inkjet ink composition with stable pH |
US7125445B2 (en) * | 2004-03-23 | 2006-10-24 | Benq Corporation | Red colorant composition and magenta inkjet ink composition with stable pH |
US20050277765A1 (en) * | 2004-06-10 | 2005-12-15 | Eastman Kodak Company | Multimetallic polymeric azo colorants |
US20050282926A1 (en) * | 2004-06-10 | 2005-12-22 | Eastman Kodak Company | Ink jet ink containing multimetallic polymeric colorants |
US7119178B2 (en) | 2004-06-10 | 2006-10-10 | Eastman Kodak Company | Multimetallic polymeric azo colorants |
US7449500B2 (en) | 2004-06-10 | 2008-11-11 | Eastman Kodak Company | Ink jet ink containing multimetallic polymeric colorants |
Also Published As
Publication number | Publication date |
---|---|
JP2002302622A (en) | 2002-10-18 |
DE60200841T2 (en) | 2005-08-18 |
HK1047759B (en) | 2005-01-28 |
EP1229084A1 (en) | 2002-08-07 |
HK1047759A1 (en) | 2003-03-07 |
US6458195B1 (en) | 2002-10-01 |
EP1229084B1 (en) | 2004-08-04 |
DE60200841D1 (en) | 2004-09-09 |
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