USRE39700E1 - Ink additives for improved ink-jet performance - Google Patents

Ink additives for improved ink-jet performance Download PDF

Info

Publication number
USRE39700E1
USRE39700E1 US11/258,587 US25858705A USRE39700E US RE39700 E1 USRE39700 E1 US RE39700E1 US 25858705 A US25858705 A US 25858705A US RE39700 E USRE39700 E US RE39700E
Authority
US
United States
Prior art keywords
ink
phosphate
anions
diphosphate
vehicle
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US11/258,587
Inventor
David J. Halko
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.)
HP Inc
Original Assignee
Hewlett Packard Co
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.)
Filing date
Publication date
Application filed by Hewlett Packard Co filed Critical Hewlett Packard Co
Priority to US11/258,587 priority Critical patent/USRE39700E1/en
Application granted granted Critical
Publication of USRE39700E1 publication Critical patent/USRE39700E1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D11/00Inks
    • C09D11/30Inkjet printing inks
    • C09D11/38Inkjet printing inks characterised by non-macromolecular additives other than solvents, pigments or dyes

Definitions

  • the present invention relates to inks used in ink-jet printers, and, more particularly, to an ink used in thermal ink-jet printers having improved kogation properties.
  • Thermal ink-jet printers offer a low cost, high quality, and comparatively noise-free option to other types of printers commonly used with computers.
  • Such printers employ a resistor element in a chamber provided with an egress for ink to enter from a plenum.
  • the plenum is connected to a reservoir for storing the ink.
  • a plurality of such resistor elements are arranged in a particular pattern, called a primitive, in a printhead.
  • Each resistor element is associated with a nozzle in a nozzle plate, through which ink is expelled toward a print medium.
  • the entire assembly of printhead and reservoir comprise an ink-jet pen.
  • each resistor element is connected via a conductive trace to microprocessor, where current-carrying signals cause one or more selected elements to heat up.
  • the heating creates a bubble of ink in the chamber, which is expelled through the nozzle toward the print medium.
  • firing of a plurality of such resistor elements in a particular order in a given primitive forms alphanumeric characters, performs area-fill, and provides other print capabilities on the medium.
  • oxo anions serve as additives, and in the case of cationic dyes, may serve as replacement counter-ions, for use in thermal ink-jet inks to reduce kogation significantly.
  • the oxo anions of the invention may be singly or multiply charged.
  • additives essentially eliminates kogation for the life of ink pens, such as those used in Hewlett-Packard's DeskJet printer. Further, such additives will prevent kogation for inks containing dyes with negatively-charged water-solubilizing groups, such as sulfonate and carboxylate.
  • FIG. 1 on coordinates of weight (in nanograms, ng) and number of cycles (resistor firings), is a plot of drop weight versus cycles for three different energies of an ink not including the additive of the invention, depicting the effect of kogation on drop weight out to 5 million cycles;
  • FIG. 2 is a plot similar to that of FIG. 1 , but for an ink containing the additive of the invention, depicting essentially no kogation out to 10 million cycles.
  • Inks benefitted by the practice of the invention comprise a vehicle and a dye.
  • the vehicle typically comprises one or more water-miscible organic compounds, such as a glycol or glycol ether and water.
  • the dye may be any of the anionic or cationic dyes.
  • the dye is typically present in an amount ranging from about 1 to 12% (by weight), although more or less dye may be used, depending on the vehicle/dye system, the desired optical density, etc. Typically, the dye concentration is about 2 to 6% (by weight). All amounts herein are by weight, unless otherwise indicated.
  • ICI dyes 286 and 287 Particularly employed as inks herein are ICI dyes 286 and 287, preferably in a 50—50 mixture. However, any of the well-known dyes may alternately be used.
  • the particular water-miscible organic compounds and their concentration does not form a part of this invention.
  • examples of such compounds include glycols such as ethylene glycol, diethylene glycol, propylene glycol, polyethylene glycol, etc., and pyrrolidones, such as 2-pyrrolidone.
  • glycol is present in an amount up to about 50%, and more typically up to about 10%, with the balance water.
  • pyrrolidine is usually present in an amount of about 7 to 10%, with the balance water.
  • additives may be added to the ink, such as fungicides, bactericides, pH adjusters, and the like, as is well-known.
  • Such additives, and the materials comprising the vehicle and dye are of a purity commonly found in normal commercial practice.
  • a compound containing an oxo anion significantly reduces kogation, and may even eliminate it entirely.
  • oxo anions include phosphates (both PO 4 3 ⁇ and P 2 O 7 4 ⁇ ) and phosphate esters (both mono-organo, ROPO 3 2 ⁇ , and di-organo, (RO) 2 PO 2 ⁇ ).
  • phosphate esters both mono-organo, ROPO 3 2 ⁇ , and di-organo, (RO) 2 PO 2 ⁇ .
  • R is an alkyl or aromatic group.
  • the R groups for the di-organo phosphates may be the same or different.
  • the organic R group can also be substituted with various functional groups.
  • oxo anions beneficially employed in the practice of the invention include, in descending order of preference, arsenate (AsO 4 3 ⁇ ), molybdate (Mo 7 O 24 6 ⁇ ), sulfate (SO 4 2 ⁇ ), sulfite (SO 3 2 ⁇ ), and oxalate (C 2 O 4 2 ⁇ ).
  • Anions other than these may not have a beneficial effect.
  • nitrate and thiocyanate anions are ineffective with the ICI dyes mentioned above.
  • an oxo anion is a class of anions in which various elements are bound to oxygen and which bear an overall negative charge in aqueous solution.
  • phosphate salts added either as dibasic (HPO 4 2 ⁇ ) monobasic (H 2 PO 4 ⁇ ), polyphosphates such as diphosphate (P 2 O 7 4 ⁇ ), or phosphate esters.
  • the phosphate species in solution is determined by the pH of the ink. In the pH range of 8 to 9 (typical for inks containing ICI dyes), the predominate species for both mono and dibasic phosphate is HPO 4 2 ⁇ .
  • FIG. 1 depicts a measure of kogation from an ink comprising a vehicle of 10% 2-pyrrolidone and 0.2% sodium borate, the balance water, and 2.2% of a 50—50 mixture of ICI 286/287 dyes (NH 4 + form). The pH was adjusted to 8.5 with NH 4 OH. In this ink, no additive was used, and it is clear that there is a large decrease in drop volume (determination is by weight) with this ink, beginning almost immediately.
  • the selection of the counter-ion is not critical, other than it not adversely interfere with the reduction in kogation.
  • suitable cations include alkali metals, ammonium, and alkyl ammonium.
  • An especially efficacious compound is ammonium phosphate.
  • Phosphate ion can also be added as phosphoric acid (H 3 PO 4 ), along with neutralization with an appropriate base.
  • the concentration of the kogatin-reducing additive (anions) of the invention ranges from about 9 mg/L to 14 wt%, based on the oxo anion. Less than about 9 mg/L, while effective, is not enough to yield stable drop volumes out to several million firings. Greater than about 14 wt% provides no further benefit. Preferably, the concentration of the oxo anion ranges from about 0.01 to 1 wt%.
  • kogation degrades pen performance.
  • a decrease in pen performance can be monitored by measuring (weighing) drops fired from a pen.
  • a change in drop volume indicates the formation of resistor residues.
  • the kogation effect is due to adsorption of dye and/or decomposition products of ink on the resistor surface.
  • the appearance and increase in adsorbed dye or decomposition products apparently reduces the volume of ink fired.
  • the additive of the invention is believed to eliminate or reduce the adsorption process.
  • ammonium phosphate to inks at relatively low concentrations (0.02 to 0.5%) yields inks which have constant drop volumes out to many million drops.
  • inks containing such amounts of ammonium phosphate have shown that ink volumes remain constant to at least 30 million drops.
  • the same inks without ammonium phosphate do not have constant drop volumes, as indicated earlier with reference to FIGS. 1 and 2 .
  • Auger Electron Spectroscopy has determined that the resistor residue primarily comprises carbon. Other elements, such as nitrogen, oxygen, and sulfur are at relatively lower concentrations.
  • the resistor surfaces exposed to non-phosphate containing inks have a thick carbon layer (corresponding to adsorbed dye and/or ink decomposition products), whereas the resistor surfaces exposed to phosphate-containing inks have only a very thin carbon layer, together with some phosphorus.
  • phosphate is being adsorbed on the resistor surface, and prevents the adsorption of dye and/or ink decomposition products thereon.
  • the pH of the inks is adjusted to be within the range of about 3 to 10, and preferably about 8 to 9 for the ICI dye examples discussed herein, using commonly-employed pH adjusters.
  • the oxo anion additive of the invention is expected to find use in inks used in thermal ink-jet printers.
  • the ink comprised a vehicle of 10% 2-pyrrolidone, 0.2% sodium borate as a pH buffer, and the balance deionized water and 2.2% of 50—50 ICI 287/287 dye.
  • Monobasic ammonium phosphate (NH 4 H 2 PO 4 ) was added to the foregoing ink to provide a concentration of 0.1 wt% therein.
  • the initial pH was adjusted to 8.5 with concentrated NH 4 OH.
  • Example 1 The ink from Example 1 was tested for kogation out to 10 million cycles.
  • the parameter which has been used to evaluate the effectiveness of an additive is drop volume.
  • droplets ejected from a pen are collected and weighed in a pan on an analytical balance. An average weight is obtained and is commonly referred to as drop volume in picoliters (pL).
  • the current test operates at three different energies (15%, 30%, and 45%) over (OE) that required to fire a droplet from a nozzle in order to obtain a range of performance. In a given printer and a given pen under normal operating conditions, a pen will be operating at a single energy.
  • the dashed line represents 15% OE
  • the heavy solid line represents 30% OE
  • the light solid line represents 45% OE.
  • Example 2 For comparison, the same ink as in Example 1 was prepared, but omitting the ammonium phosphate. The ink was tested as in Example 2. The results are depicted in FIG. 1 , as discussed above.
  • the ink without ammonium phosphate is seen to exhibit kogation within a very short number of cycles, while the ink containing ammonium phosphate is stable against kogation out to at least 10 million cycles.
  • a mixture of dimethyl phosphate (55%) and monomethyl phosphate (45%) was added to an ink which was the same as in Example 3, except that the amount of pyrrolidone in the vehicle was 7.5%.
  • the total phosphate ester concentration was 0.5 wt% and the pH of the ink was adjusted to 8.5. This ink had stable drop volumes when tested to 4.8 million cycles.

Abstract

Oxo anions (both singly and multiply charged), such as phosphates, polyphosphates, and phosphate esters, serve as additives, and in the case of cationic dyes, may serve as replacement counter-ions, for use in thermal ink-jet inks to reduce kogation significantly. The addition of such additive essentially eliminates kogation for the life of ink pens. Further, such additives will prevent kogation for inks containing dyes with negatively-charged water-solubilizing groups, such as sulfonate and carboxylate.

Description

TECHNICAL FIELD
The present invention relates to inks used in ink-jet printers, and, more particularly, to an ink used in thermal ink-jet printers having improved kogation properties.
BACKGROUND ART
Thermal ink-jet printers offer a low cost, high quality, and comparatively noise-free option to other types of printers commonly used with computers. Such printers employ a resistor element in a chamber provided with an egress for ink to enter from a plenum. The plenum is connected to a reservoir for storing the ink. A plurality of such resistor elements are arranged in a particular pattern, called a primitive, in a printhead. Each resistor element is associated with a nozzle in a nozzle plate, through which ink is expelled toward a print medium. The entire assembly of printhead and reservoir comprise an ink-jet pen.
In operation, each resistor element is connected via a conductive trace to microprocessor, where current-carrying signals cause one or more selected elements to heat up. The heating creates a bubble of ink in the chamber, which is expelled through the nozzle toward the print medium. In this way, firing of a plurality of such resistor elements in a particular order in a given primitive forms alphanumeric characters, performs area-fill, and provides other print capabilities on the medium.
A problem with inks used in such thermal ink-jet printers is that the repeated heating of the resistor element over several hundreds of thousand or over millions of firings can cause breakdown of the ink, with consequent fouling of the surface of the resistor element. This process has been termed “kogation”, which is defined as the build-up of residue (koga) on the resistor surface. The build-up of residue degrades pen performance.
Various ink compositions and processes have been developed in an effort to reduce kogation. For example, in the anionic dyes (sulfonate or carboxylate) commonly employed in aqueous inks used in thermal ink-jet printing, sodium is generally the counter-ion used. However, while dyes containing sodium counter-ions generally provide good print quality, sodium counter-ions have been found to contribute to the kogation problem.
One solution has been to partially or totally eliminate sodium. Successful replacement counter-ions are lithium and tetramethylammonium.
The need remains for the development of inks having reduced kogation, and hence longer life, using low cost chemicals with minimal additional processing.
DISCLOSURE OF INVENTION
In accordance with the invention, oxo anions serve as additives, and in the case of cationic dyes, may serve as replacement counter-ions, for use in thermal ink-jet inks to reduce kogation significantly. The oxo anions of the invention may be singly or multiply charged.
The addition of such additive essentially eliminates kogation for the life of ink pens, such as those used in Hewlett-Packard's DeskJet printer. Further, such additives will prevent kogation for inks containing dyes with negatively-charged water-solubilizing groups, such as sulfonate and carboxylate.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1, on coordinates of weight (in nanograms, ng) and number of cycles (resistor firings), is a plot of drop weight versus cycles for three different energies of an ink not including the additive of the invention, depicting the effect of kogation on drop weight out to 5 million cycles; and
FIG. 2 is a plot similar to that of FIG. 1, but for an ink containing the additive of the invention, depicting essentially no kogation out to 10 million cycles.
BEST MODES FOR CARRYING OUT THE INVENTION
Inks benefitted by the practice of the invention comprise a vehicle and a dye. The vehicle typically comprises one or more water-miscible organic compounds, such as a glycol or glycol ether and water. The dye may be any of the anionic or cationic dyes. The dye is typically present in an amount ranging from about 1 to 12% (by weight), although more or less dye may be used, depending on the vehicle/dye system, the desired optical density, etc. Typically, the dye concentration is about 2 to 6% (by weight). All amounts herein are by weight, unless otherwise indicated.
Particularly employed as inks herein are ICI dyes 286 and 287, preferably in a 50—50 mixture. However, any of the well-known dyes may alternately be used.
The particular water-miscible organic compounds and their concentration does not form a part of this invention. However, examples of such compounds include glycols such as ethylene glycol, diethylene glycol, propylene glycol, polyethylene glycol, etc., and pyrrolidones, such as 2-pyrrolidone. Usually, the glycol is present in an amount up to about 50%, and more typically up to about 10%, with the balance water. The pyrrolidine is usually present in an amount of about 7 to 10%, with the balance water.
Other additives may be added to the ink, such as fungicides, bactericides, pH adjusters, and the like, as is well-known. Such additives, and the materials comprising the vehicle and dye are of a purity commonly found in normal commercial practice.
In accordance with the invention, the addition of a compound containing an oxo anion significantly reduces kogation, and may even eliminate it entirely. Examples of such oxo anions include phosphates (both PO4 3− and P2O7 4−) and phosphate esters (both mono-organo, ROPO3 2−, and di-organo, (RO)2PO2 ). For the phosphate esters, R is an alkyl or aromatic group. The R groups for the di-organo phosphates may be the same or different. The organic R group can also be substituted with various functional groups.) Further examples of oxo anions beneficially employed in the practice of the invention include, in descending order of preference, arsenate (AsO4 3−), molybdate (Mo7O24 6−), sulfate (SO4 2−), sulfite (SO3 2−), and oxalate (C2O4 2−). Anions other than these may not have a beneficial effect. For example, nitrate and thiocyanate anions are ineffective with the ICI dyes mentioned above. As used herein, an oxo anion is a class of anions in which various elements are bound to oxygen and which bear an overall negative charge in aqueous solution.
The most effective additive to date are phosphate salts; added either as dibasic (HPO4 2−) monobasic (H2PO4 ), polyphosphates such as diphosphate (P2O7 4−), or phosphate esters.
The phosphate species in solution is determined by the pH of the ink. In the pH range of 8 to 9 (typical for inks containing ICI dyes), the predominate species for both mono and dibasic phosphate is HPO4 2−.
FIG. 1 depicts a measure of kogation from an ink comprising a vehicle of 10% 2-pyrrolidone and 0.2% sodium borate, the balance water, and 2.2% of a 50—50 mixture of ICI 286/287 dyes (NH4 + form). The pH was adjusted to 8.5 with NH4OH. In this ink, no additive was used, and it is clear that there is a large decrease in drop volume (determination is by weight) with this ink, beginning almost immediately.
For comparison, kogation results for the same base ink composition with 0.1 wt% ammonium phosphate are depicted in FIG. 2. The addition of ammonium phosphate clearly yields an ink with constant drop volume. This ink evidence substantially flat behavior even out to 30 million cycles.
The selection of the counter-ion is not critical, other than it not adversely interfere with the reduction in kogation. Examples of suitable cations include alkali metals, ammonium, and alkyl ammonium. An especially efficacious compound is ammonium phosphate. Phosphate ion can also be added as phosphoric acid (H3PO4), along with neutralization with an appropriate base.
The concentration of the kogatin-reducing additive (anions) of the invention ranges from about 9 mg/L to 14 wt%, based on the oxo anion. Less than about 9 mg/L, while effective, is not enough to yield stable drop volumes out to several million firings. Greater than about 14 wt% provides no further benefit. Preferably, the concentration of the oxo anion ranges from about 0.01 to 1 wt%.
As indicated earlier, kogation degrades pen performance. A decrease in pen performance can be monitored by measuring (weighing) drops fired from a pen. A change in drop volume indicates the formation of resistor residues.
Without subscribing to any particular theory, it appears that the kogation effect is due to adsorption of dye and/or decomposition products of ink on the resistor surface. The appearance and increase in adsorbed dye or decomposition products apparently reduces the volume of ink fired. The additive of the invention is believed to eliminate or reduce the adsorption process.
The addition of ammonium phosphate to inks at relatively low concentrations (0.02 to 0.5%) yields inks which have constant drop volumes out to many million drops. For example, inks containing such amounts of ammonium phosphate have shown that ink volumes remain constant to at least 30 million drops. The same inks without ammonium phosphate do not have constant drop volumes, as indicated earlier with reference to FIGS. 1 and 2.
Examination of the resistors from inks without and with the addition of ammonium phosphate shows that there is a large amount of residue (koga) on resistors for inks without phosphate fired only to 5 million cycles and essentially clean resistor surfaces for inks containing phosphate when fired twice that number of cycles (10 million).
Auger Electron Spectroscopy has determined that the resistor residue primarily comprises carbon. Other elements, such as nitrogen, oxygen, and sulfur are at relatively lower concentrations. The resistor surfaces exposed to non-phosphate containing inks have a thick carbon layer (corresponding to adsorbed dye and/or ink decomposition products), whereas the resistor surfaces exposed to phosphate-containing inks have only a very thin carbon layer, together with some phosphorus. Apparently, phosphate is being adsorbed on the resistor surface, and prevents the adsorption of dye and/or ink decomposition products thereon.
Interestingly, the foregoing suggests that the process of kogation is reversible. Indeed, pens have been kogated by firing with an ink that does not contain phosphate to several million cycles until the drop volumes decrease considerably. Refilling these pens with a phosphate-containing ink yields complete recovery of the pen. That is, the drop volumes rise to a “normal level” of about 140 pL.
The pH of the inks is adjusted to be within the range of about 3 to 10, and preferably about 8 to 9 for the ICI dye examples discussed herein, using commonly-employed pH adjusters.
INDUSTRIAL APPLICABILITY
The oxo anion additive of the invention is expected to find use in inks used in thermal ink-jet printers.
EXAMPLES Example 1
In this example, the preparation of an ink containing phosphate is described.
The ink comprised a vehicle of 10% 2-pyrrolidone, 0.2% sodium borate as a pH buffer, and the balance deionized water and 2.2% of 50—50 ICI 287/287 dye. Monobasic ammonium phosphate (NH4H2PO4) was added to the foregoing ink to provide a concentration of 0.1 wt% therein. The initial pH was adjusted to 8.5 with concentrated NH4OH.
Example 2
The ink from Example 1 was tested for kogation out to 10 million cycles. The parameter which has been used to evaluate the effectiveness of an additive is drop volume. In this test, droplets ejected from a pen are collected and weighed in a pan on an analytical balance. An average weight is obtained and is commonly referred to as drop volume in picoliters (pL). The current test operates at three different energies (15%, 30%, and 45%) over (OE) that required to fire a droplet from a nozzle in order to obtain a range of performance. In a given printer and a given pen under normal operating conditions, a pen will be operating at a single energy.
The results are depicted in FIG. 2, as discussed above. In FIG. 2 (and in FIG. 1), the dashed line represents 15% OE, the heavy solid line represents 30% OE, and the light solid line represents 45% OE.
Example 3
For comparison, the same ink as in Example 1 was prepared, but omitting the ammonium phosphate. The ink was tested as in Example 2. The results are depicted in FIG. 1, as discussed above.
Clearly, the ink without ammonium phosphate is seen to exhibit kogation within a very short number of cycles, while the ink containing ammonium phosphate is stable against kogation out to at least 10 million cycles.
Example 4
A mixture of dimethyl phosphate (55%) and monomethyl phosphate (45%) was added to an ink which was the same as in Example 3, except that the amount of pyrrolidone in the vehicle was 7.5%. The total phosphate ester concentration was 0.5 wt% and the pH of the ink was adjusted to 8.5. This ink had stable drop volumes when tested to 4.8 million cycles.
Example 5
Addition of 0.2% ammonium phosphate to an ink prepared with the sodium form of Direct Black 168 (1.9 wt%) in a vehicle of 5.5% diethylene glycol, balance water, yielded excellent results. The drop volumes were constant when tested to 9 million cycles.
Example 6
Addition of 0.5% of a mixture of dimethyl phosphate (55%) and monomethyl phosphate (45%) to an ink prepared with the lithium form of Acid Red 27 (3 wt%), a magenta dye, in a vehicle of 5.5 wt% diethylene glycol, balance water, yielded stable drop volumes for all energies when tested to 4.8 million cycles.
Example 7
Addition of 0.2% ammonium phosphate to an ink prepared with Acid Red 27 (3 wt%) in a vehicle of 5.5 wt% diethylene glycol, balance water, yielded stable drop volumes for all energies for all energies (15%, 30%, 45% OE) after an initial rise, which converged at approximately 160 pL. Each OE curve rose at a different rate and was stable after 0.4 million for 45% OE, 1.4 million for 30% OE, and approximately 3 million for 15% OE. This demonstrates that after some initial “break-in period”, phosphate stabilized the drop volumes at a high level, giving excellent results.
Thus, there has been disclosed an additive for reduction or eliminating kogation in inks used in thermal ink-jet printers. It will be readily apparent to those skilled in this art that various changes and modifications of an obvious nature may be made, and all such changes and modifications are considered to fall within the scope of the invention as defined by the appended claims.

Claims (27)

1. An ink for thermal ink-jet printing comprising a vehicle and an anionic dye, characterized by the presence of at least one oxo anion therein, said at least one oxo anion selected from the group consisting of phosphates, polyphosphates, phosphate esters, arsenate, molybdate, sulfate, sulfite, and oxalate and present in an amount ranging from about 9 mg/L to 14 wt%,
wherein said ink further comprises ammonium (NH 4 +) cations, and
wherein said at least one oxo anion is selected from monobasic phosphate (H 2PO4 ), dibasic phosphate (HPO 4 2−), or diphosphate (P 2O7 4−) anions or combinations thereof.
2. The ink of claim 1 wherein said vehicle comprises at least one glycol and the balance water.
3. The ink of claim 2 wherein said vehicle comprises up to about 10 wt% diethylene glycol and the balance water.
4. The ink of claim 1 wherein said vehicle comprises at least one pyrrolidone and the balance water.
5. The ink of claim 4 wherein said vehicle comprises up to about 10 wt% 2-pyrrolidone and the balance water.
6. The ink of claim 1 comprising about 1 to 12 wt% of said dye.
7. The ink of claim 1 wherein said phosphate is in the form of dibasic, monobasic, or diphosphate anions.
8. The ink of claim 1 wherein said phosphate ester is selected from the group consisting of mono-organo and di-organo phosphate esters.
9. The ink of claim 1 wherein said at least one oxo anion is present in an amount ranging from about 0.01 to 1 wt%.
10. An ink for thermal ink-jet printing comprising a vehicle and an anionic dye, characterized by the presence of anions selected from the group consisting of phosphates, polyphosphates, and phosphate esters, said anions present in an amount ranging from about 9 mg/L to 14 wt%,
wherein said ink further comprises ammonium (NH 4 +) cations,
wherein said anions are selected from monobasic phosphate (H 2PO4 ), dibasic phosphate (HPO 4 2−), or diphosphate (P 2O7 4−) anions or combinations thereof, and
wherein the ink provides substantially constant drop volume through 5 million resistor firings.
11. The ink of claim 10 wherein said vehicle comprises at least one glycol and the balance water.
12. The ink of claim 11 wherein said vehicle comprises up to about 10 wt% diethylene glycol and the balance water.
13. The ink of claim 10 wherein said vehicle comprises at least one pyrrolidone and the balance water.
14. The ink of claim 13 wherein said vehicle comprises up to about 10 wt% 2-pyrrolidone and the balance water.
15. The ink of claim 10 comprising about 1 to 12 wt% of said dye.
16. The ink of claim 18 wherein said phosphate anion is in the form of dibasic, monobasic, or diphosphate anions.
17. The ink of claim 10 wherein said phosphate ester is selected from the group consisting of mono-organo and di-organo phosphate esters.
18. The ink of claim 12 wherein said phosphate anion is present in an amount ranging from about 0.01 to 1 wt%.
19. A method of reducing kogation in an ink used in thermal ink-jet printers, said ink comprising a vehicle and an anionic dye, characterized in that at least one salt containing at least one oxo anion is added thereto, said at least one oxo anion selected from the group consisting of phosphates, polyphosphates, phosphate esters, arsenate, molybdate, sulfate, sulfite, and oxalate and present in an amount ranging from about 9 mg/L to 14 wt%,
wherein said ink further comprises ammonium (NH 4 +) cations, and
wherein said at least one oxo anion is selected from monobasic phosphate (H 2PO4 ), dibasic phosphate (HPO 4 2−), or diphosphate (P 2O7 4−) anions or combinations thereof.
20. The method of claim 19 wherein said at least one oxo anion is added in an amount of 0.01 to 1 wt%.
21. The method of claim 19 wherein said phosphate is in the form of dibasic, monobasic, or diphosphate anions.
22. The method of claim 19 wherein said phosphate ester is selected from the group consisting of mono-organic and di-organic phosphate esters.
23. A method of reducing kogation in an ink used in thermal ink-jet printers, said ink comprising a vehicle and an anionic dye, characterized in that from about 9 mg/L to 14 wt% of a salt containing an anion selected from the group consisting of phosphate, polyphosphates, and phosphate esters is added thereto,
wherein said ink further comprises ammonium (NH 4 +) cations, and
wherein said anion is selected from monobasic phosphate (H 2PO4 ), dibasic phosphate (HPO 4 2−), or diphosphate (P 2O7 4−) anions or combinations thereof, and
wherein the ink provides substantially constant drop volume through 5 million resistor firings.
24. The method of claim 23 wherein said phosphate is in the form of dibasic, monobasic, or diphosphate anions.
25. The method of claim 23 wherein said phosphate is in the form of dibasic, monobasic, or diphosphate anions.
26. The method of claim 23 wherein said phosphate ester is selected from the group consisting of mono-organic and di-organic diphosphate esters.
27. An ink for thermal ink-jet printing comprising a vehicle and an anionic dye, characterized by the presence of at least one oxo anion therein, said at least one oxo anion selected from the group consisting of phosphates, polyphosphates, phosphate esters, arsenate, molybdate, sulfate, sulfite, and oxalate and present in an amount ranging from about 9 mg/L to 14 wt%, wherein said ink further comprises ammonium (NH 4 +) cations.
US11/258,587 1989-10-27 2005-10-26 Ink additives for improved ink-jet performance Expired - Lifetime USRE39700E1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/258,587 USRE39700E1 (en) 1989-10-27 2005-10-26 Ink additives for improved ink-jet performance

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US07/428,282 US5062892A (en) 1989-10-27 1989-10-27 Ink additives for improved ink-jet performance
US11/258,587 USRE39700E1 (en) 1989-10-27 2005-10-26 Ink additives for improved ink-jet performance

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US07/428,282 Reissue US5062892A (en) 1989-10-27 1989-10-27 Ink additives for improved ink-jet performance

Publications (1)

Publication Number Publication Date
USRE39700E1 true USRE39700E1 (en) 2007-06-26

Family

ID=23698243

Family Applications (2)

Application Number Title Priority Date Filing Date
US07/428,282 Ceased US5062892A (en) 1989-10-27 1989-10-27 Ink additives for improved ink-jet performance
US11/258,587 Expired - Lifetime USRE39700E1 (en) 1989-10-27 2005-10-26 Ink additives for improved ink-jet performance

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US07/428,282 Ceased US5062892A (en) 1989-10-27 1989-10-27 Ink additives for improved ink-jet performance

Country Status (5)

Country Link
US (2) US5062892A (en)
EP (1) EP0425150B1 (en)
JP (1) JP3148228B2 (en)
DE (1) DE69018006T2 (en)
HK (1) HK117495A (en)

Families Citing this family (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5164232A (en) * 1991-02-11 1992-11-17 Xerox Corporation Ink compositions
DE4227591A1 (en) * 1992-08-20 1994-02-24 Basf Ag Use of liquid dye preparations containing a disazo dye in the ink-jet process and disazo dye
MY109293A (en) * 1991-12-18 1996-12-31 Gillette Co Fiber marker including an erasable ink
US5599853A (en) * 1993-01-29 1997-02-04 The Gillette Company Erasable inks
JPH0616985A (en) * 1992-04-22 1994-01-25 Lexmark Internatl Inc Jet ink that does not solidify
US5338793A (en) * 1992-06-02 1994-08-16 The Gillette Company Erasable ink
US5462592A (en) * 1992-06-09 1995-10-31 Ricoh Company, Ltd. Aqueous ink composition
JPH06126973A (en) * 1992-08-31 1994-05-10 Xerox Corp Method for removing foreign particle on heating means of thermal ink jet printer
US5389131A (en) * 1992-12-17 1995-02-14 Xerox Corporation Ink compositions and preparation processes thereof
US5554213A (en) * 1992-12-17 1996-09-10 Xerox Corporation Ink compositions for ink jet printing
US5389133A (en) * 1992-12-17 1995-02-14 Xerox Corporation Ink compositions for ink jet printing
US5258064A (en) * 1992-12-17 1993-11-02 Xerox Corporation Ink compositions and preparation processes thereof
JP3666895B2 (en) * 1993-01-13 2005-06-29 キヤノン株式会社 Ink jet textile printing ink, textile printing method, equipment using such ink, and printed matter obtained
JP3194307B2 (en) * 1993-01-27 2001-07-30 富士ゼロックス株式会社 Thermal inkjet ink
US5451251A (en) * 1993-02-26 1995-09-19 Canon Kabushiki Kaisha Ink, and ink-jet recording method and instrument using the same
EP0699723A3 (en) * 1994-08-31 1997-07-02 Canon Kk Ink-jet ink
WO1996026248A1 (en) * 1995-02-20 1996-08-29 Kao Corporation Water-base pigment ink
US5562762A (en) * 1995-05-17 1996-10-08 Lexmark International, Inc. Jet ink with amine surfactant
JP3466800B2 (en) * 1995-11-30 2003-11-17 キヤノン株式会社 Ink jet ink, ink jet recording method and ink jet device
US5725641A (en) * 1996-10-30 1998-03-10 Macleod; Cheryl A. Lightfast inks for ink-jet printing
EP0859033B1 (en) * 1997-02-13 1999-06-23 ILFORD Imaging Switzerland GmbH Dyes for ink jet printing
DE59702018D1 (en) * 1997-11-20 2000-08-17 Ilford Imaging Ch Gmbh Azo dyes, their production and use
US6398355B1 (en) 1998-03-03 2002-06-04 Canon Kabushiki Kaisha Ink, ink set, ink cartridge, recording unit, image recording method and image recording apparatus
GB9812119D0 (en) 1998-06-05 1998-08-05 Zeneca Ltd Composition
US6048388A (en) * 1998-06-29 2000-04-11 Schwarz; William M. Ink compositions containing ionic liquid solvents
DE69801818T2 (en) 1998-08-19 2002-04-11 Ilford Imaging Ch Gmbh Metal complex disazo dyes, their production and use
EP1029680B1 (en) 1999-02-19 2006-08-23 Canon Kabushiki Kaisha Method of reducing kogation on heater of ink-jet recording head, ink-jet recording process, ink-jet recording apparatus, recording unit, and method for lengthening the life of recording head
DE59903965D1 (en) 1999-02-23 2003-02-13 Ilford Imaging Ch Gmbh Monoazo dyes, their production and use
US6394594B1 (en) * 1999-02-26 2002-05-28 Canon Kabushiki Kaisha Ink, method of reducing kogation on heater of ink-jet recording head, ink-jet recording process, ink-jet recording apparatus, recording unit, and method for lengthening the life of recording head
US6425659B1 (en) 1999-02-26 2002-07-30 Canon Kabushiki Kaisha Method for alleviating kogation on surface of heater of ink-jet recording head, method for ink-jet recording, ink-jet recording apparatus, recording unit, and method for prolonging ink-jet recording head life
US6514920B1 (en) 1999-06-03 2003-02-04 Canon Kabushiki Kaisha Liquid composition, method of cleaning ink-jet recording head, ink-jet recording apparatus, cartridge, and method of regenerating ink-jet recording head
JP2001171126A (en) 1999-10-05 2001-06-26 Canon Inc Substrate for ink-jet head with heating resistance element, ink-jet head using the same, ink-jet apparatus and recording method
US7048375B2 (en) 1999-11-01 2006-05-23 Praful Doshi Tinted lenses and methods of manufacture
US7267846B2 (en) 1999-11-01 2007-09-11 Praful Doshi Tinted lenses and methods of manufacture
JP2003515787A (en) 1999-11-01 2003-05-07 ドーシ,プレイフール Lightly colored lens and method of making same
US6880932B2 (en) 1999-11-01 2005-04-19 Praful Doshi Tinted lenses and methods of manufacture
US6604809B2 (en) 1999-12-14 2003-08-12 Canon Kabushiki Kaisha Cleaning ink-jet recording head with liquid composition
EP1125991B1 (en) * 2000-02-10 2006-01-25 Canon Kabushiki Kaisha Method of reducing kogation of heater of ink-jet recording head, ink-jet recording apparatus and method of prolonging service life of recording head
DE60137809D1 (en) * 2000-02-17 2009-04-16 Canon Kk An ink-jet ink, a method for reducing deposits on the heaters of ink-jet recording heads, ink-jet recording method, and ink-jet recording apparatus
US6610129B1 (en) * 2000-04-05 2003-08-26 Hewlett-Packard Development Company Ink-jet inks which prevent kogation and prolong resistor life in ink-jet pens
SG164272A1 (en) * 2000-04-26 2010-09-29 Canon Kk Ink, ink-jet ink, method for reducing kogation on surface of heater of ink- jet recording head, method for ink-jet recording, ink-jet recording apparatus, recording unit and method for prolonging ink-jet recording head life
ATE213759T1 (en) 2000-05-30 2002-03-15 Ilford Imaging Ch Gmbh AZO DYES, THEIR PRODUCTION AND USE
US6471350B2 (en) * 2000-08-09 2002-10-29 Canon Kabushiki Kaisha Method of protecting heater surface of ink-jet printer, ink-jet recording apparatus, recording unit and method of prolonging service life of ink-jet recording head
ATE272502T1 (en) 2000-12-07 2004-08-15 Avecia Ltd GUANIDINE-BASED COATING COMPOSITIONS AND RECORDING MATERIALS CONTAINING THESE COMPOSITIONS
US6503308B2 (en) 2000-12-20 2003-01-07 Hewlett-Packard Company Black ink compositions for inkjet printing
DE50001223D1 (en) 2000-12-21 2003-03-13 Ilford Imaging Ch Gmbh Monoazo dyes, their production and use
US6533851B2 (en) 2001-02-12 2003-03-18 Hewlett-Packard Company Kogation reducing ink
US20030072717A1 (en) * 2001-02-23 2003-04-17 Vapotronics, Inc. Inhalation device having an optimized air flow path
US6524378B2 (en) * 2001-02-27 2003-02-25 Eastman Kodak Company Ink jet printing method
US6527844B2 (en) * 2001-02-27 2003-03-04 Eastman Kodak Company Metal complex for ink jet ink
GB0106343D0 (en) 2001-03-14 2001-05-02 Avecia Ltd Compounds compositions and processes
GB0108318D0 (en) 2001-04-03 2001-05-23 Clariant Int Ltd Organic compounds
CA2448022C (en) * 2001-05-21 2013-11-12 Injet Digital Aerosols Limited Compositions for protein delivery via the pulmonary route
GB0126103D0 (en) 2001-10-31 2002-01-02 Avecia Ltd Ink compositions
GB0130316D0 (en) * 2001-12-19 2002-02-06 Clariant Int Ltd Composition for printing recording materials
MXPA04003489A (en) 2001-12-19 2004-07-30 Clariant Finance Bvi Ltd Use of a dyestuff for ink jet printing recording materials .
DE50200372D1 (en) 2002-05-27 2004-05-27 Ilford Imaging Ch Gmbh Monoazo dyes, their production and use
US7481522B2 (en) 2002-06-07 2009-01-27 Fujifilm Imaging Colorants Limited Compositions and inks containing disazo dyes
GB0213011D0 (en) 2002-06-07 2002-07-17 Avecia Ltd Compounds
EP1403328B1 (en) 2002-09-26 2006-10-25 ILFORD Imaging Switzerland GmbH Copper complex monoazo dyes, their preparation and their use
ES2268408T3 (en) * 2002-10-18 2007-03-16 Clariant Finance (Bvi) Limited AZOIC COMPOUNDS.
EP1563011B1 (en) * 2002-11-13 2009-01-14 Clariant Finance (BVI) Limited Mono azo dyes
US7621631B2 (en) * 2004-02-04 2009-11-24 Hewlett-Packard Development Company, L.P. Enhancing color space of reactive ink using heat
US7388040B2 (en) * 2004-04-08 2008-06-17 Hewlett-Packard Development Company, L.P. Anti-kogation additives compatible with cationic polymers for fixer-based printing systems
TW200628556A (en) 2004-12-10 2006-08-16 Clariant Int Ltd Azo compounds
CN100362056C (en) * 2005-02-05 2008-01-16 明德国际仓储贸易(上海)有限公司 Blank ink dye composition
US7763668B2 (en) * 2005-03-23 2010-07-27 Imtech, Inc. Curable thermally ejectable printing fluid
CN100413927C (en) * 2005-09-05 2008-08-27 明德国际仓储贸易(上海)有限公司 Disazo dyes compounds and application thereof
ATE526367T1 (en) 2006-06-13 2011-10-15 Ilford Imaging Ch Gmbh PHTHALOCYANINE DYES, THEIR PRODUCTION AND USE
EP1882723B1 (en) 2006-07-27 2009-03-25 ILFORD Imaging Switzerland GmbH Bisazo dyes, their preparation and their use
GB0620774D0 (en) 2006-10-19 2006-11-29 Fujifilm Imaging Colorants Ltd Improvements in and relating to azo compounds and their use in printing
US8163075B2 (en) 2006-10-31 2012-04-24 Sensient Colors Llc Inks comprising modified pigments and methods for making and using the same
US7846245B2 (en) * 2006-11-02 2010-12-07 Hewlett-Packard Development Company, L.P. Ink-jet inks for neutral gray and black printing
CN101235219B (en) * 2007-02-01 2010-09-08 明德国际仓储贸易(上海)有限公司 Black dyestuff composition and ink composition applied for textile number printing and dyeing
CN101289579B (en) 2007-04-16 2011-03-30 明德国际仓储贸易(上海)有限公司 Black dye composition and black ink composition
EP3483222A3 (en) 2007-08-23 2019-08-07 Sensient Colors LLC Self-dispersed pigments and methods for making and using the same
CN102131875A (en) 2008-08-22 2011-07-20 富士胶片映像着色有限公司 Phthalocyanines and their use in ink-jet printing
EP2169009B1 (en) 2008-09-24 2011-05-25 ILFORD Imaging Switzerland GmbH Anthrapyridone dyes, their preparation and their use
CA2757928A1 (en) 2009-04-07 2010-10-14 Sensient Colors Inc. Self-dispersing particles and methods for making and using the same
TWI444437B (en) 2010-06-18 2014-07-11 Everlight Chem Ind Corp Blue, red, and yellow dye compounds, and black ink composition comprising the same
CN102892846A (en) * 2010-08-16 2013-01-23 Lg化学株式会社 Printing composition and a printing method using the same
BR112013004057A2 (en) * 2010-09-24 2020-08-25 Hewlett-Packard Development Company,L.P. produce the dry ink deposition antiforming agent and method for forming printed images on a substrate-medium
EP2468822B1 (en) 2010-12-22 2015-06-10 Rex-Tone Industries Ltd Black trisazo dyes, their preparation and their use
GB201117187D0 (en) 2011-10-06 2011-11-16 Fujifilm Imaging Colorants Ltd A process for preparing a dispersion, dispersion, use and method
PT3126452T (en) 2014-04-01 2020-07-15 Archroma Ip Gmbh Bisazo dyes and mixtures thereof
KR200479808Y1 (en) 2014-06-17 2016-03-09 주식회사 동경모드 Funtional brassiere
WO2017092872A1 (en) 2015-12-02 2017-06-08 Damien Moigno Anthrapyridone azo dyes, their preparation and use
WO2019073030A1 (en) 2017-10-13 2019-04-18 Archroma Ip Gmbh Mixtures of fibre-reactive azo dyes, their preparation and their use
JP7364675B2 (en) 2018-11-17 2023-10-18 インターナショナル イメージング マテリアルズ, インコーポレーテッド Outdoor durable inkjet ink

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3853913A (en) 1971-06-08 1974-12-10 Benz-{8 c,d{9 -indolium dyestuffs
US4239543A (en) 1979-02-09 1980-12-16 Gould Inc. Non-crusting jet ink and method of making same
US4285727A (en) 1978-12-18 1981-08-25 Konishiroku Photo Industry Co., Ltd. Ink compositions for ink jet recoding
US4286989A (en) 1980-09-30 1981-09-01 International Business Machines Corporation Formulations for ink jet printing
US4299630A (en) 1977-04-27 1981-11-10 The Mead Corporation Infrared absorptive jet printing ink
JPS5736170A (en) 1980-08-14 1982-02-26 Fuji Photo Film Co Ltd Water-based ink for ink-jet printing
US4373954A (en) 1980-05-06 1983-02-15 Canon Kabushiki Kaisha Recording liquid and method for producing the same
JPS5951960A (en) 1982-09-17 1984-03-26 Dainippon Toryo Co Ltd Ink for ink jet recording
US4592756A (en) 1984-02-09 1986-06-03 Taoka Chemical Company, Limited Dye solution composition
US4685968A (en) 1985-12-05 1987-08-11 Hewlett-Packard Company Process for preparing ink compositions for ink-jets printers
US4724001A (en) 1985-05-14 1988-02-09 Canon Kabushiki Kaisha Disazoic dye and recording liquid containing the same
US4786288A (en) 1983-10-07 1988-11-22 Toray Industries Incorporated Fabric treating method to give sharp colored patterns
US4810292A (en) 1985-12-05 1989-03-07 Hewlett-Packard Company Ink compositions for ink-jet printers
US4853037A (en) 1987-10-30 1989-08-01 Hewlett-Packard Company Low glycol inks for plain paper printing
US4935059A (en) 1988-06-23 1990-06-19 Basf Aktiengesellschaft Basic rhodamine dyes
US4975118A (en) 1988-01-29 1990-12-04 Basf Aktiengesellschaft Recording fluid containing phenyl azo naphthalene dyes for the ink jet process

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3853913A (en) 1971-06-08 1974-12-10 Benz-{8 c,d{9 -indolium dyestuffs
US4299630A (en) 1977-04-27 1981-11-10 The Mead Corporation Infrared absorptive jet printing ink
US4285727A (en) 1978-12-18 1981-08-25 Konishiroku Photo Industry Co., Ltd. Ink compositions for ink jet recoding
US4239543A (en) 1979-02-09 1980-12-16 Gould Inc. Non-crusting jet ink and method of making same
US4373954A (en) 1980-05-06 1983-02-15 Canon Kabushiki Kaisha Recording liquid and method for producing the same
JPS5736170A (en) 1980-08-14 1982-02-26 Fuji Photo Film Co Ltd Water-based ink for ink-jet printing
US4286989A (en) 1980-09-30 1981-09-01 International Business Machines Corporation Formulations for ink jet printing
JPS5951960A (en) 1982-09-17 1984-03-26 Dainippon Toryo Co Ltd Ink for ink jet recording
US4786288A (en) 1983-10-07 1988-11-22 Toray Industries Incorporated Fabric treating method to give sharp colored patterns
US4592756A (en) 1984-02-09 1986-06-03 Taoka Chemical Company, Limited Dye solution composition
US4724001A (en) 1985-05-14 1988-02-09 Canon Kabushiki Kaisha Disazoic dye and recording liquid containing the same
US4685968A (en) 1985-12-05 1987-08-11 Hewlett-Packard Company Process for preparing ink compositions for ink-jets printers
US4810292A (en) 1985-12-05 1989-03-07 Hewlett-Packard Company Ink compositions for ink-jet printers
US4853037A (en) 1987-10-30 1989-08-01 Hewlett-Packard Company Low glycol inks for plain paper printing
US4975118A (en) 1988-01-29 1990-12-04 Basf Aktiengesellschaft Recording fluid containing phenyl azo naphthalene dyes for the ink jet process
US4935059A (en) 1988-06-23 1990-06-19 Basf Aktiengesellschaft Basic rhodamine dyes

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
European Search Report for EP 90 31 1216 (corresponding to U.S. 5,062,892).
Gendler, P.L., et al., "Adverse Chemical Effects on the Plasma-Deposited Amorphous Carbide Passivation Layer of Thermal Ink-Jet Thin-Film Heaters," Advance Printing of Paper Summaries, Nov. 12-17, 1989, pp. 287-290, San Diego, California.
Halko, D. J., Adsorption from Solution at the Solid/Liquid Interface, G.D. Parfitt and C.H. Rochester, eds, p. 358-359, Academic Press, 1983.

Also Published As

Publication number Publication date
JP3148228B2 (en) 2001-03-19
EP0425150B1 (en) 1995-03-22
EP0425150A3 (en) 1992-06-17
EP0425150A2 (en) 1991-05-02
HK117495A (en) 1995-07-28
JPH03160070A (en) 1991-07-10
DE69018006T2 (en) 1995-07-20
US5062892A (en) 1991-11-05
DE69018006D1 (en) 1995-04-27

Similar Documents

Publication Publication Date Title
USRE39700E1 (en) Ink additives for improved ink-jet performance
EP0314485B1 (en) Low glycol inks for plain paper printing
US5026425A (en) Waterfastness of DB-168 ink by cation substitution
US5061316A (en) Ph-insensitive anti-kogating agent for ink-jet pens
EP0997505B1 (en) Ink-jet inks with improved performance
EP1085062B1 (en) Image recording method, method for improving quality of multicolor image, and method for forming monotone image
US5108503A (en) Smear resistant inks for ink-jet printers
EP0463737B1 (en) Use of ink formulations comprising mixtures of anionic waterfast dyes containing two or more carboxyl groups in thermal ink-jet printers to reduce nozzle clogging of the printer
EP1188804B1 (en) Ink set, bleed-alleviating method,and method for improving fixability of black image
EP1086997B1 (en) Ink, ink-set, and image recording process for improving density of ink-jet recorded image
US5389132A (en) Thermal ink-jet exhibiting reduced kogation
EP0651036A2 (en) Inks used in multi-color printing
EP1036830B1 (en) Ink containing a colouring material and an aqueous medium
US6533851B2 (en) Kogation reducing ink
US5108501A (en) Bile salts which control kogation in thermal ink-jet inks
JP2001010200A5 (en)
US6086198A (en) Bleed alleviation between two inks
US7288143B2 (en) Water-based ink, ink tank having the same, and ink-jet recording process
CA2023118A1 (en) Ink additives for improved ink-jet performance
EP0975700B1 (en) Ink additives