Bleed alleviation using zwitterionic surfactants and cationic dyes

• US 5,106,416 A
• Filed: 08/28/1991
• Issued: 04/21/1992
• Est. Priority Date: 08/28/1991
• Status: Expired due to Term

• Current Assignee: Hewlett-Packard Company (HP Inc.)
• Original Assignee: Hewlett-Packard Company (HP Inc.)
• Inventors: Shields, James P., Moffatt, John R.
• Primary Examiner(s): Dixon, Jr., William R.
• Assistant Examiner(s): Saunders, Timothy
• Application Number:
  US07/751,369
• Time in Patent Office: 237 Days
• Field of Search: 106/20, 106/22, 106/23, 8/543, 260/31.85, 524/523
• US Class Current: 106/31.43
• CPC Class Codes: C09D 11/30 Inkjet printing inks

Abstract

Color bleed (the invasion of one color into another on the surface of the print medium) using ink-jet inks is alleviated by employing zwitterionic surfactants (ph-sensitive or pH-insensitive) or ionic or non-ionic amphiphiles. The inks of the invention comprise a vehicle and a cationic dye. The vehicle typically comprises a low viscosity, high boiling point solvent, one or two amphiphiles at concentrations above their critical micelle concentration (cmc), while the dye typically comprises any of the dyes commonly employed in ink-jet printing. The amount of surfactants/amphiphile is described in terms of its critical micelle concentration (cmc), which is a unique value for each amphiphile. Above the cmc, micelles form, which attract the dye molecule and thus control the color bleed. Below the cmc, there is no micelle formation, and thus no control of the color bleed.

Claims

1. A process for reducing color bleed in inks employed in ink-jet printing, comprising printing on a medium with an ink having the following composition:

(a) a vehicle; and

(b) about 0.1 to 10 wt % of at least one water-soluble cationic dye dissolved therein, wherein said vehicle comprises (1) at least one member selected from the group consisting of zwitterionic surfactants and non-ionic amphiphiles, present in an amount that is at least equal to its critical micelle concentration;

(2) about 0.5 to 20 wt % of at least one organic solvent which supports the micelle formation of said at least one member; and

(3) the balance water.

2. The process of claim 1 wherein said zwitterionic surfactants are selected from the group consisting of non-ionic compounds and ionic compounds.

3. The process of claim 2 wherein said non-ionic compounds are selected from the group consisting of (a) water-soluble amphiphile mimetics, (b) polyethers, polyethylene oxides, nonyl and octyl polyethylene oxides, and acetylenic backboned polyethylene oxides, and (c) amphoteric compounds.

4. The process of claim 3 wherein said mimetics are branched polyethylene amines.

5. The process of claim 3 wherein said polyethers are selected from the group consisting of ethylene glycol n-butyl ether, diethylene glycol n-butyl ether, diethylene col n-hexyl ether, triethylene glycol n-butyl ether, and propylene glycol isobutyl ether.

6. The process of claim 3 wherein said amphoteric surfactants are pH-sensitive surfactants selected from the group consisting of N,N-dimethyl-N-dodecyl amine oxide, N,N-dimethyl-N-tetradecyl amine oxide, N,N-dimethyl-N-hexadecyl amine oxide, N,N-dimethyl-N-octadecyl amine oxide, N,N-dimethyl-N-(Z-9-octadecenyl)-N-amine oxide, N-dodecyl-N,N-dimethyl glycine, phosphates, phosphites, phosphonates, lecithins, phosphate esters, phospatidylethanolamines, phosphatidylcholines, phosphatidyl serines, phosphatidylinositols, and B'"'"'-O-lysylphosphatidylglycerols.

7. The process of claim 3 wherein said amphoteric surfactants are pH-insensitive surfactants comprising sulfobetaines.

8. The process of claim 2 wherein said ionic surfactants are selected from the group consisting of cetyl trimethylammonium bromide, sodium dodecyl sulfate, sodium sulfonates, and cellusolves.

9. The process of claim 1 wherein said organic solvent is selected from the group consisting of glycols, diols, glycol esters, glycol ethers, mono and di glycol ethers, cellusolves, carbitols, long chain alcohols, esters, ketones, lactones, and glycerols, and derivatives thereof and mixtures thereof.

10. The process of claim 9 wherein said solvent is selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, polyethylene glycol, polypropylene glycol, and derivatives thereof;

butanediol, pentanediol, hexanediol, and homologous diols;

propylene glycol laurate;

ethylene glycol monobutyl ether, diethylene glycol mono ethyl ether, diethylene glycol mono butyl ether, diethylene glycol mono hexyl ether, propylene glycol ether, dipropylene glycol ether, and triethylene glycol ether;

butyl alcohol, pentyl alcohol, and homologous alcohols;

sulfolane, γ

-butyrolactone, N-pyrrolidone and N-(2-hydroxyethyl)pyrrolidone, and glycerols and their derivatives.

11. The process of claim 1 wherein said cationic dye is selected from the group consisting of C.I. Basic Violet 7, C.I. Basic Blue 3, Fastusol Yellow 32L, C.I. Basic Red 1, C.I. Basic Violet 10, C.I. Basic Red 3, C.I. Mordant Green 13, C.I. Basic Violet 23, C.I. Basic Yellow 9, C.I. Basic Yellow 11, C.I. Mordant Blue 14, and C.I. Basic Blue 9.

12. The process of claim 11 wherein said cationic dye is associated with an anion selected from the group consisting of Cl^-, Br^-, ZnCl₄^-, and NO₃^-.

13. The process of claim 1 wherein said ink consists essentially of:

about 0.9% N,N-dimethyl-N-(Z-9-octadecenyl)-N-amine oxide;

about 2% of an acetylenic polyethylene oxide surfactant;

about 5.5% diethylene glycol;

about 1 to 3% of said at least one cationic dye; and

the balance water.