Dye having hydrophobic substituent and aqueous ink

Information

  • Patent Grant
  • 5494507
  • Patent Number
    5,494,507
  • Date Filed
    Monday, December 19, 1994
    29 years ago
  • Date Issued
    Tuesday, February 27, 1996
    28 years ago
Abstract
A dye having a representative formula as follows and an ink providing waterfast printing having the dye, in which a surfactant is not essential: ##STR1##
Description

TECHNICAL FIELD
This invention relates to aqueous ink jet inks which are stable during storage and use and waterfast after printing. More specifically, this invention relates to dye molecules which provide the color or hue in final printing, which are waterfast when printed and which are soluble or dispersible in aqueous ink with little or no dispersants added to the ink.
BACKGROUND OF THE INVENTION
U.S. Pat. No. 5,106,416 to Moffatt et al is directed to cationic dyes in aqueous ink jet inks which are dissolved or dispersed using surfactants or amphiphiles to form micelles. U.S. Pat. No. 5,275,647 to Winnik is directed to surfactant micelles colored with dyes covalently attached in aqueous ink jet inks. The dyes of this invention are believed to be dissolved or dispersed through the formation of micelles, but not with the essential aid of any additive. The jet ink is therefore potentially inexpensive in manufacture and cost of ingredients.
DISCLOSURE OF THE INVENTION
This invention is an ink jet ink having a dye molecule of the following formula and the dye molecules themselves.
The dye molecule is the following: ##STR2## Wherein: R.sub.1 is an alkyl group having from 6 to 16 carbon atoms;
R.sub.2 is: ##STR3## R.sub.5 is: --H, --lower alkyl, --lower alkoxyl; R.sub.6 is: --H--lower alkyl, --lower alkoxyl;
R.sub.7 is: --lower alkyl, --lower hydroxyalkyl, --CH.sub.2 CH.sub.2 CO.sub.2 M;
R.sub.8 is: --lower hydroxyalkyl, --CH.sub.2 CH.sub.2 CO.sub.2 M. ##STR4## M is --H, --NH.sub.4, --Li, --Na, --K.
The foregoing dye is magenta when R.sub.1 is C.sub.12 H.sub.25 and R.sub.2 is ##STR5##
The foregoing dye is black when R.sub.1 is C.sub.12 H.sub.25 and R.sub.2 is ##STR6##
The foregoing dye is yellow when R.sub.1 is C.sub.12 H.sub.25 and R.sub.2 is ##STR7##
The foregoing dye is black when R.sub.1 is C.sub.12 H.sub.25 and R.sub.2 is ##STR8##
The foregoing dye is black when R.sub.1 is C.sub.12 H.sub.25 and R.sub.2 is ##STR9##
The foregoing dye is black when R.sub.1 is C.sub.12 H.sub.25 and R.sub.2 is ##STR10##
An effective ink comprises at least 1% by weight of said dye dissolved or dispersed in a polar vehicle such as water or a water and alcohol mixture.
These dyes are believed to form micelles in the vehicle by action of the carboxylic group but to be highly hydrophobic and therefore waterfast when printed by action of the R group.





BEST MODE FOR CARRYING OUT THE INVENTION
A representative and preferred aqueous ink has the following formula:
______________________________________Component Percent by Weight______________________________________Dye A (below) 22-pyrrolidinone (co-solvent) 10Tergitol NP-10 (trademark) 1-3(nonionic surfactant)Water, deionized Remainder (87-85)Dye A (Magenta) ##STR11##______________________________________
This is prepared by mixing the dye, water, 2-pyrolidinone, and Tergitol surfactant and then ultrasonically agitating for 10 minutes. The ink is then filtered through a 0.22 micron filter.
Where the dodecyl group (--C.sub.12 H.sub.25) is replaced by lower alkyl groups such as ethyl or butyl, the resulting dye molecules are soluble without the carboxylic group and the Tergitol surfactant. Dyes having R.sub.1 groups from hexyl to octyl are soluble with the surfactant, but not exceptionally waterfast. The foregoing dodecyl and carboxylic acid containing molecule is both soluble without the surfactant and highly waterfast (93%). This is summarized in the following table.
______________________________________Dye FunctionalGroups Water Tergitol Filter WaterfastR X Solubility Surfactant % Ability %______________________________________ethyl H yes 0 yes --ethyl H yes 1 yes 43butyl H yes 0 yes --butyl H yes 1 yes 52hexyl H no 0 no --hexyl H yes 1 yes 59Octyl H no 0 no --Octyl H yes 1 yes 76Dodecyl H no 0 no --Dodecyl H yes 2 yes 78Dodecyl COOH yes 0 yes 93______________________________________
Waterfastness is measured by controlled soaking in water of paper printed with the ink. The percent waterfastness is the percent of optical density retained after a five minute soak in deionized water, observed, for example, by an optical densitometer.
Claims
  • 1. A dye of the structural formula: ##STR12## Wherein: R.sub.1 is an alkyl group having from 6 to 16 carbon atoms;
  • R.sub.2 is one of the substitutents in the following list of substitutents: ##STR13## where, R.sub.4 is: --H, --lower alkyl, --lower alkoxyl;
  • R.sub.5 is: --H --lower alkyl, --lower alkoxyl;
  • R.sub.6 is: --lower alkyl, --lower hydroxyalkyl, --CH.sub.2 CH.sub.2 CO.sub.2 M;
  • R.sub.7 is: --lower hydroxylalkyl, --CH.sub.2 CH.sub.2 CO.sub.2 M; or ##STR14## M is --H, --NH.sub.4, --Li, --Na, --K.
  • 2. A magenta dye as in claim 1 having the structure: ##STR15##
  • 3. A black dye as in claim 1 having the structure: ##STR16##
  • 4. A yellow dye as in claim 1 having the structure: ##STR17##
  • 5. A black dye as in claim 1 having the structure: ##STR18##
  • 6. A black dye as in claim 1 having the structure: ##STR19##
  • 7. A black dye as in claim 1 having the structure: ##STR20##
  • 8. An ink comprising at least 1 percent by weight of dye dissolved in a polar vehicles, said dye being of the structural formula of claim 1.
  • 9. The ink as in claim 8 in which said dye is a magenta dye of the structure: ##STR21##
  • 10. The ink as in claim 8 in which said dye is a black dye of the structure: ##STR22##
  • 11. The ink as in claim 8 in which said dye is a yellow dye of the structure: ##STR23##
  • 12. The ink as in claim 8 in which said dye is a black dye of the structure: ##STR24##
  • 13. The ink as in claim 8 in which said dye is a black dye of the structure: ##STR25##
  • 14. The ink as in claim 8 in which said dye is a black dye of the structure: ##STR26##
  • 15. The ink of claim 14 also comprising 2-pyrrolidinone as a co-solvent.
  • 16. The ink of claim 8 also comprising 2-pyrrolidinone as a co-solvent.
  • 17. The ink of claim 9 also comprising 2-pyrrolidinone as a co-solvent.
  • 18. The ink of claim 10 also comprising 2-pyrrolidinone as a co-solvent.
  • 19. The ink of claim 11 also comprising 2-pyrrolidinone as a co-solvent.
  • 20. The ink of claim 12 also comprising 2-pyrrolidinone as a co-solvent.
  • 21. The ink of claim 13 also comprising 2-pyrrolidinone as a co-solvent.
US Referenced Citations (10)
Number Name Date Kind
4626284 Ohta et al. Dec 1986
4929277 Tanaka et al. May 1990
5074914 Shirota et al. Dec 1991
5106416 Moffatt et al. Apr 1992
5127947 Takimoto et al. Jul 1992
5135571 Shirota et al. Aug 1992
5213614 Eida et al. May 1993
5275647 Winnik Jan 1994
5281263 Gregory et al. Jan 1994
5429671 Yamamoto Jul 1995