WO1997049774A2 - Waterfast pigmented ink jet inks - Google Patents
Waterfast pigmented ink jet inks Download PDFInfo
- Publication number
- WO1997049774A2 WO1997049774A2 PCT/US1997/011571 US9711571W WO9749774A2 WO 1997049774 A2 WO1997049774 A2 WO 1997049774A2 US 9711571 W US9711571 W US 9711571W WO 9749774 A2 WO9749774 A2 WO 9749774A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ink
- dendrimer
- glycol
- grams
- surfactant
- Prior art date
Links
- 239000000976 ink Substances 0.000 title abstract description 59
- 239000000412 dendrimer Substances 0.000 claims abstract description 26
- 229920000736 dendritic polymer Polymers 0.000 claims abstract description 26
- 239000000049 pigment Substances 0.000 claims abstract description 23
- 229920000962 poly(amidoamine) Polymers 0.000 claims abstract description 17
- 239000004094 surface-active agent Substances 0.000 claims abstract description 13
- 239000003139 biocide Substances 0.000 claims abstract description 9
- 239000003906 humectant Substances 0.000 claims abstract description 9
- 239000003922 charged colloid Substances 0.000 claims abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 15
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 15
- 241000284156 Clerodendrum quadriloculare Species 0.000 claims description 14
- 239000008213 purified water Substances 0.000 claims description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- 239000002202 Polyethylene glycol Substances 0.000 claims description 12
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 12
- 229920001223 polyethylene glycol Polymers 0.000 claims description 12
- SENLDUJVTGGYIH-UHFFFAOYSA-N n-(2-aminoethyl)-3-[[3-(2-aminoethylamino)-3-oxopropyl]-[2-[bis[3-(2-aminoethylamino)-3-oxopropyl]amino]ethyl]amino]propanamide Chemical compound NCCNC(=O)CCN(CCC(=O)NCCN)CCN(CCC(=O)NCCN)CCC(=O)NCCN SENLDUJVTGGYIH-UHFFFAOYSA-N 0.000 claims description 10
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 8
- 239000006229 carbon black Substances 0.000 claims description 8
- 239000000084 colloidal system Substances 0.000 claims description 8
- -1 nitrogen containing cyclic compounds Chemical class 0.000 claims description 8
- 230000003115 biocidal effect Effects 0.000 claims description 7
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 7
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 5
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 claims description 4
- 150000005846 sugar alcohols Polymers 0.000 claims description 4
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 claims description 4
- 229950006389 thiodiglycol Drugs 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000000654 additive Substances 0.000 abstract 1
- 239000008135 aqueous vehicle Substances 0.000 abstract 1
- 238000005516 engineering process Methods 0.000 abstract 1
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 13
- 239000001913 cellulose Substances 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 239000000975 dye Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 239000008365 aqueous carrier Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 238000007639 printing Methods 0.000 description 4
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005189 flocculation Methods 0.000 description 3
- 230000016615 flocculation Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000001041 dye based ink Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000007641 inkjet printing Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].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 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 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
- C09D11/324—Inkjet printing inks characterised by colouring agents containing carbon black
Definitions
- Ink jet printing is a non-impact method in which in response to a digitally produced signal, a drop of ink is ejected form a small orifice onto a substrate. Each drop produces one picture element (pixel) of the printed image.
- These small orifices being only 10 to 60 micrometers in diameter are very susceptible to clogging, which destroys the functionality of the entire printer. If the ink is not completely stable,
- the aqueous carrier can move, or migrate, upon application of the ink to a printing medium, such as paper.
- pigments In contrast to dyes, pigments give desired image qualities because they are
- pigments Since the pigment does not migrate on or in the media, image quality will not vary from one quality of media to the next. Also, pigments, being larger particles, are typically more opaque and denser than dyes. While these qualities may not always be wanted for colored inks, these qualities promote high quality black ink image qualities.
- pigments are held in aqueous suspension with the aid of surfactants, polymers, or polyelectrolytes.
- These pigmented inks may also be formulated with binders which adhere the pigment to the substrate and improve the waterfastness of the
- the present invention provides an aqueous, pigmented ink jet ink composition with low viscosity, high surface tension, waterfastness, and good latency.
- aqueous, pigmented ink jet ink composition with low viscosity, high surface tension, waterfastness, and good latency.
- the percent solids of the Cabot CSX-440 used is 2% to 10%, or preferably from 3% to 7% , based on total weight of the ink. Concentrations greater than these do not increase print density, but do increase the likelihood of pigment flocculation while concentrations less than these do not provide for suitable densities.
- a biocide is added to the ink to extend its
- the final ink formulation is filtered down to
- a surface acting agent surfactant
- surfactants are generally used in very low percentages
- Anionic, cationic, or non-ionic surfactants may be used in this invention, preferably non-ionic because these are less likely to destabilize the negatively charged colloid pigment.
- a humectant is added to the ink to keep the jet orifices from clogging when the water carrier starts to evaporate.
- These water soluble organic solvents may be used in weight percentages from 0.5% to 50% as well as being used in varying combinations.
- Representative examples of water soluble organic solvents that may be used with this invention are polyhydric alcohols, such as
- ethylene glycol diethylene glycol, triethylene glycol, propylene glycol, tetraethylene glycol, polyethylene glycol, glycerol, and thiodiglycol; and nitrogen-containing cyclic compounds such as 2-pyrrolidinone, and N-methyl-2-pyrrolidinone.
- nitrogen-containing cyclic compounds such as 2-pyrrolidinone, and N-methyl-2-pyrrolidinone.
- polyethylene glycol w Avg. molecular weight 200
- 2- pyrrolidinone and preferably 2-pyrrolidinone exhibit the best anti-clogging properties.
- Example 1 To 87.8 grams of purified water, 0.2 grams of Proxel G.X.L. were added. Further, 6.0 grams of diethylene glycol were added, and these components were then mixed to evenly distribute them through the solution. Then 6.0 grams of
- Cabot CSX 440 was added and then further mixed for 15 minutes. This ink was then filtered down through a 0.22 micron filter.
- Example 2 To 87.8 grams of purified water, 0.2 grams of Proxel G.X.L. were added. Further, 6.0 grams of glycerol were added, and these components were then mixed to evenly distribute them through the solution. Then 6.0 grams of Cabot CSX
- Example 3 To 87.8 grams of purified water, 0.2 grams of Proxel G.X.L. were added. Further, 6.0 grams of triethylene glycol were added, and these components were then mixed to evenly distribute them through the solution. Then 6.0 grams of Cabot CSX 440 was added and then further mixed for 15 minutes. This ink was then filtered down through a 0.22 micron filter.
- Example 4 To 87.8 grams of purified water, 0.2 &rams of Proxel G.X.L. were
- Example 5 To 87.8 grams of purified water, 0.2 grams of Proxel G.X.L. were added. Further, 6.0 grams of polyethylene glycol (200) were added, and these components were then mixed to evenly distribute them through the solution. Then 6.0 grams of Cabot CSX 440 was added and then further mixed for 15 minutes. This ink
- an accelerated latency test can be
- This base formulation can be further modified by adding a dendritic polymer to
- this ink improves water resistance of this ink and preferably a radial dendrimer and more preferably a STARBURST PAMAM (polyamidoamine) dendrimer dendrimer (DENDRITECH, Inc., Midland, NE), and still more preferably a STARBURST PAMAM (polyamidoamine) dendrimer of the 1 " generation.
- a radial dendrimer and more preferably a STARBURST PAMAM (polyamidoamine) dendrimer dendrimer (DENDRITECH, Inc., Midland, NE) and still more preferably a STARBURST PAMAM (polyamidoamine) dendrimer of the 1 " generation.
- the number of surface groups of a STARBURST PAMAM double with each generation. And with each generation the molecular weight of the dendrimer more than doubles.
- the larger dendrimer molecules crosslink enough pigment particles to
- STARBURST PAMAM dendrimer by roughly doubling the weight percentage used in the from the next higher generation STARBURST PAMAM dendrimer: and that these lower generation dendrimers while exhibiting equal or better waterfastness yield better cartridge latency times.
- Example 1 To 69.6 grams of purified water, 0.2 grams of Proxel G.X.L. were
- Example 2 To 69.5 gams of purified water, 0.2 grams of Proxel G.X.L. were added. Further, 18.0 grams of polyethylene glycol (200) were added, further 0.1 grams of
- Example 3 To 69.2 grams of purified water, 0.2 grams of Proxel G.X.L. were added, and then these components were mixed to evenly distribute them throughout the solution. Then 12.0 grams of Cabot CSX 440 was added and then further mixed for 15 minutes. This ink was then filtered down through a filter ladder to a final filter size of 0.22 microns. Upon which all 100 grams passed through a single 47mm mixed cellulose 0.22 micron filter.
- Example 3 To 69.2 grams of purified water, 0.2 grams of Proxel G.X.L. were added, and then these components were mixed to evenly distribute them throughout the solution. Then 12.0 grams of Cabot CSX 440 was added and then further mixed for 15 minutes. This ink was then filtered down through a filter ladder to a final filter size of 0.22 microns. Upon which all 100 grams passed through a single 47mm mixed cellulose 0.22 micron filter.
- Example 3 To 69.2 grams of purified water, 0.2 grams of Proxe
- Example 4 To 64.8 grams of purified water, 0.2 grams of Proxel G.X.L. were
- Example 5 To 64.8 gams of purified water, 0.2 grams of Proxel G.X.L. were added.
- Example 6 To 87.3 grams of purified water, 0.2 grams of Proxel G.X.L. were added. Further, 10.0 grams of polyethylene glycol (200) were added, further 0.5 grams of STARBURST PAMAM dendrimer (2- generation) were added, and then
- Examples 1, 2, and 3 support the claim that a generation of dendrimers exhibit
- Examples 4, 5, and 6 support the uniqueness of this invention. Examples 4 and 5
- Example 6 shows the inability of the STARBURST PAMAM dendrimer to promote waterfastness in other ink systems.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU38801/97A AU3880197A (en) | 1996-06-27 | 1997-06-27 | Waterfast pigmented ink jet inks |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US2196796P | 1996-06-27 | 1996-06-27 | |
US60/021,967 | 1996-06-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1997049774A2 true WO1997049774A2 (en) | 1997-12-31 |
WO1997049774A3 WO1997049774A3 (en) | 1998-02-05 |
Family
ID=21807126
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1997/011571 WO1997049774A2 (en) | 1996-06-27 | 1997-06-27 | Waterfast pigmented ink jet inks |
Country Status (2)
Country | Link |
---|---|
AU (1) | AU3880197A (en) |
WO (1) | WO1997049774A2 (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0859037A1 (en) * | 1997-02-17 | 1998-08-19 | Seiko Epson Corporation | Ink jet recording ink and ink jet recording apparatus |
WO2000037542A1 (en) * | 1998-12-18 | 2000-06-29 | 3M Innovative Properties Company | Dendritic polymer dispersants for hydrophobic particles in water-based systems |
WO2001012725A1 (en) * | 1999-08-11 | 2001-02-22 | Neste Chemicals Oy | Curable antimicrobial hyperbranched polymer compositions |
US6262207B1 (en) | 1998-12-18 | 2001-07-17 | 3M Innovative Properties Company | ABN dispersants for hydrophobic particles in water-based systems |
US6395804B1 (en) | 1998-12-18 | 2002-05-28 | 3M Innovative Properties Company | Polyelectrolyte dispersants for hydrophobic particles in water-based systems |
US6402825B1 (en) | 2001-07-27 | 2002-06-11 | Lexmark International, Inc | Surface modified carbon black |
US6852156B2 (en) | 2000-06-05 | 2005-02-08 | E.I. Du Pont De Nemours And Company | Self-dispersing pigment and process of making and use of same |
EP1187622A4 (en) * | 1999-06-01 | 2005-06-22 | Univ California | STERILIZATION TECHNOLOGY |
US7151153B2 (en) | 2000-10-31 | 2006-12-19 | Basf Aktiengesellschaft | Use of hyperbranched polyurethanes for producing printing inks |
US7226609B2 (en) | 1997-02-21 | 2007-06-05 | The Regents Of The University Of California | Sodium dodecyl sulfate compositions for inactivating prions |
US7511085B2 (en) | 2000-10-31 | 2009-03-31 | Basf Aktiengesellschaft | Liquid printing inks for flexographic and/or intaglio printing comprising hyperbranched polymers as the vehicle |
JP2011127065A (en) * | 2009-12-21 | 2011-06-30 | Kao Corp | Aqueous ink for inkjet recording |
EP3375827A1 (en) | 2017-03-17 | 2018-09-19 | TIGER Coatings GmbH & Co. KG | Laminate ink |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5281261A (en) * | 1990-08-31 | 1994-01-25 | Xerox Corporation | Ink compositions containing modified pigment particles |
US5120361A (en) * | 1991-06-27 | 1992-06-09 | Xerox Corporation | Ink compositions |
US5531818A (en) * | 1994-12-01 | 1996-07-02 | Xerox Corporation | Ink jet ink compositions and printing processes |
US5596027A (en) * | 1995-07-13 | 1997-01-21 | Videojet Systems International, Inc. | Condensation and water resistant jet ink |
-
1997
- 1997-06-27 AU AU38801/97A patent/AU3880197A/en not_active Abandoned
- 1997-06-27 WO PCT/US1997/011571 patent/WO1997049774A2/en active Application Filing
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0859037A1 (en) * | 1997-02-17 | 1998-08-19 | Seiko Epson Corporation | Ink jet recording ink and ink jet recording apparatus |
US6737449B1 (en) | 1997-02-17 | 2004-05-18 | Seiko Epson Corporation | Ink jet recording ink and ink jet recording apparatus |
US7307103B2 (en) | 1997-02-21 | 2007-12-11 | The Regents Of The University Of California | Sodium dodecyl sulfate compositions for inactivating prions |
US7226609B2 (en) | 1997-02-21 | 2007-06-05 | The Regents Of The University Of California | Sodium dodecyl sulfate compositions for inactivating prions |
WO2000037542A1 (en) * | 1998-12-18 | 2000-06-29 | 3M Innovative Properties Company | Dendritic polymer dispersants for hydrophobic particles in water-based systems |
US6258896B1 (en) | 1998-12-18 | 2001-07-10 | 3M Innovative Properties Company | Dendritic polymer dispersants for hydrophobic particles in water-based systems |
US6262207B1 (en) | 1998-12-18 | 2001-07-17 | 3M Innovative Properties Company | ABN dispersants for hydrophobic particles in water-based systems |
US6395804B1 (en) | 1998-12-18 | 2002-05-28 | 3M Innovative Properties Company | Polyelectrolyte dispersants for hydrophobic particles in water-based systems |
US6518370B2 (en) | 1998-12-18 | 2003-02-11 | 3M Innovative Properties Company | Dendritic polymer dispersants for hydrophobic particles in water-based systems |
EP1187622A4 (en) * | 1999-06-01 | 2005-06-22 | Univ California | STERILIZATION TECHNOLOGY |
WO2001012725A1 (en) * | 1999-08-11 | 2001-02-22 | Neste Chemicals Oy | Curable antimicrobial hyperbranched polymer compositions |
US6852156B2 (en) | 2000-06-05 | 2005-02-08 | E.I. Du Pont De Nemours And Company | Self-dispersing pigment and process of making and use of same |
US7151153B2 (en) | 2000-10-31 | 2006-12-19 | Basf Aktiengesellschaft | Use of hyperbranched polyurethanes for producing printing inks |
US7511085B2 (en) | 2000-10-31 | 2009-03-31 | Basf Aktiengesellschaft | Liquid printing inks for flexographic and/or intaglio printing comprising hyperbranched polymers as the vehicle |
US7939583B2 (en) | 2000-10-31 | 2011-05-10 | Basf Se | Liquid printing inks for flexographic and/or gravure printing using hyperbranched polymers as binders |
US6402825B1 (en) | 2001-07-27 | 2002-06-11 | Lexmark International, Inc | Surface modified carbon black |
JP2011127065A (en) * | 2009-12-21 | 2011-06-30 | Kao Corp | Aqueous ink for inkjet recording |
EP3375827A1 (en) | 2017-03-17 | 2018-09-19 | TIGER Coatings GmbH & Co. KG | Laminate ink |
WO2018167250A1 (en) | 2017-03-17 | 2018-09-20 | Tiger Coatings Gmbh & Co. Kg | Laminate ink |
US11161992B2 (en) | 2017-03-17 | 2021-11-02 | Tiger Coatings Gmbh & Co. Kg | Laminate ink |
Also Published As
Publication number | Publication date |
---|---|
AU3880197A (en) | 1998-01-14 |
WO1997049774A3 (en) | 1998-02-05 |
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