Claims
- 1. A dye of the formula: ##STR17## wherein: M.sup.+ is Na.sup.+, Li.sup.+, K.sup.+, NH.sub.4.sup.+, or hydroxyalkylammonium of the formula [H--(OCH.sub.2 CH.sub.2).sub.n ].sub.p NH.sub.m, where n is 1 to 5, p is 1 to 3, and p+m is 4;
- R.sub.1 is hydrogen, a metal ion, an alkyl of C.sub.1-4, or hydroxyalkyl of C.sub.1-4, and combinations thereof; and
- R.sub.2 is a phenyl group substituted with at least one member selected from the group consisting of: alkyl; alkoxy; hydroxyalkoxy; halogen; hydroxyl; C.sub.2 -C.sub.6 acylamino, perfluoroalkyl, substituted or unsubstituted benzoylamino;
- HO.sub.3 SOCH.sub.2 CH.sub.2 SO.sub.2.sup.- ; vinyl sulfone or moiety that can undergo elimination to form the vinyl sulfone structure; amino substituted with an alkyl of C.sub.1-4, a dialkyl of C.sub.1 -C.sub.4, substituted or unsubstituted phenyl, diphenyl, or combinations thereof; and combinations thereof.
- 2. The dye of claim 1 wherein R.sub.2 is a phenyl group with a methoxy group para to the azo group.
- 3. The dye of claim 1 wherein R.sub.2 is a phenyl group with an ethoxy group para to the azo group.
- 4. The dye of claim 1 wherein R.sub.2 is a phenyl group with a 2-hydroxypropoxy-group para to the azo group.
- 5. The dye of claim 1 wherein R.sub.2 is a phenyl group with a 2-hydroxybutoxy-group para to the azo group.
- 6. The dye of claim 2 wherein M.sup.+ is Na.sup.+.
- 7. The dye of claim 3 wherein M.sup.+ is Na.sup.+.
- 8. The dye of claim 4 wherein M.sup.+ is Na.sup.+.
- 9. The dye of claim 5 wherein M.sup.+ is Na.sup.+.
- 10. The dye of claim 1 wherein R.sub.2 is a phenyl group substituted with an ethoxy group and a halogen.
- 11. The dye of claim 1 wherein R.sub.2 is a phenyl group substituted with a methoxy group and a halogen.
- 12. The dye of claim 1 wherein R.sub.1 is a member selected from the group consisting of hydrogen, methyl, ethyl, and mixtures thereof.
- 13. The dye of claim 1 having the structure: ##STR18##
- 14. The dye of claim 1 having the structure:
- 15. The dye of claim 1 having the structure:
- 16. The dye of claim 1 having the structure:
- 17. A dye composition comprising a plurality of dyes of the formula: wherein:
- M.sup.+ is Na.sup.+, Li.sup.+, K.sup.+, NH.sub.4.sup.+, or hydroxyalkylammonium of the formula [H--(OCH.sub.2 CH.sub.2).sub.n ].sub.p NH.sub.m, where n is 1 to 5, p is 1 to 3, and p+m is 4;
- R.sub.1 is hydrogen, a metal ion, an alkyl of C.sub.1-4, or hydroxyalkyl of C.sub.1-4, and combinations thereof; and
- R.sub.2 is a phenyl group substituted with at least one member selected from the group consisting of: alkyl; alkoxy; hydroxyalkoxy; halogen; hydroxyl; C.sub.2 -C.sub.6 acylamino, perfluoroalkyl, substituted or unsubstituted benzoylamino; HO.sub.3 SOCH.sub.2 CH.sub.2 SO.sub.2.sup.- ; vinyl sulfone or moiety that can undergo elimination to form the vinyl sulfone structure; amino substituted with an alkyl of C.sub.1-4, a dialkyl of C.sub.1-4, substituted or unsubstituted phenyl, diphenyl, or combinations thereof; and combinations thereof.
- 18. The dye composition of claim 12 wherein R.sub.2 of at least one of said dyes is a phenyl group with a methoxy group para to the azo group.
- 19. The dye composition of claim 12 wherein R.sub.2 of at least one of said dyes is a phenyl group with an ethoxy group para to the azo group.
- 20. The dye composition of claim 12 wherein R.sub.2 of at least one of said dyes is a phenyl group with a 2-hydroxypropoxy-group para to the azo group.
- 21. The dye composition of claim 12 wherein R.sub.2 of at least one of said dyes is a phenyl group with a 2-hydroxybutoxy-group para to the azo group.
- 22. The dye composition of claim 18 wherein M.sup.+ of at least one of said dyes is Na.sup.+.
- 23. The dye composition of claim 19 wherein M.sup.+ of at least one of said dyes is Na.sup.+.
- 24. The dye composition of claim 20 wherein M.sup.+ of at least one of said dyes is Na.sup.+.
- 25. The dye composition of claim 21 wherein M.sup.+ of at least one of said dyes is Na.sup.+.
- 26. The dye composition of claim 17 wherein R.sub.2 of at least one of said dyes is a phenyl group substituted with an ethoxy group and a halogen.
- 27. The dye composition of claim 17 wherein R.sub.2 of at least one of said dyes is a phenyl group substituted with a methoxy group and a halogen.
- 28. A dye composition comprising a first dye of the formula: ##STR19## and a second dye of the formula: ##STR20##
- 29. A process for dyeing a material comprising: selecting at least one first acid dye for said material;
- selecting at least one second acid dye, wherein said second acid dye is an acid yellow dye that is compatible on said material with said first acid dye and is of the formula: ##STR21##30.
- 30. The process of claim 29 wherein said effective dyeing temperature is between ambient temperature and about 205.degree. F.
- 31. The process of claim 29 wherein said sufficient time to exhaust said first acid dye and said second acid yellow dye is between about 2 minutes and about 20 minutes.
- 32. The process of claim 29 wherein two acid yellow dyes of the indicated Formula are selected wherein: R.sub.2 of the first acid yellow dye is a phenyl group substituted with a halogen and, optionally, at least one member selected from the group consisting of: alkyl; alkoxy; hydroxyalkoxy; halogen; hydroxyl; C.sub.2 -C.sub.6 acylamino, perfluoroalkyl, substituted or unsubstituted benzoylamino; HO.sub.3 SOCH.sub.2 CH.sub.2 SO.sub.2.sup.- ; vinyl sulfone or moiety that can undergo elimination to form the vinyl sulfone structure; amino substituted with an alkyl of C.sub.1-4, a dialkyl of C.sub.1-4, substituted or unsubstituted phenyl, diphenyl, or combinations thereof; and combinations thereof;
- R.sub.2 of the second acid yellow dye is a phenyl group substituted with at least one member selected from the group consisting of: alkyl; alkoxy; hydroxyalkoxy; halogen; hydroxyl; C.sub.2 -C.sub.6 acylamino, perfluoroalkyl, substituted or unsubstituted benzoylamino; HO.sub.3 SOCH.sub.2 CH.sub.2 SO.sub.2.sup.- ; vinyl sulfone or moiety that can undergo elimination to form the vinyl sulfone structure; amino substituted with an alkyl of C.sub.1-4, a dialkyl of C.sub.1-4, substituted or unsubstituted phenyl, diphenyl, or combinations thereof; and combinations thereof.
- 33. The process of claim 29 wherein two acid yellow dyes of the indicated Formula are selected and R.sub.2 for at least one of said acid yellow dyes is a phenyl group substituted para to the azo group with a member selected from the group consisting of a methoxy group, an ethoxy group, a 2-hydroxypropoxy-group, and a 2-hydroxybutoxy-group.
- 34. The process of claim 32 wherein M.sup.+ is Na.sup.+.
- 35. The process of claim 33 wherein M.sup.+ is Na.sup.+.
- 36. The process of claim 29 wherein the material is a polyamide.
- 37. The process of claim 36 wherein the polyamide material is a fiber.
- 38. The process of claim 36 wherein the polyamide material is a fabric.
- 39. A material dyed by a process comprising:
- selecting at least one first acid dye for said material;
- selecting at least one second acid dye, wherein said second acid dye is an acid yellow dye that is compatible on said material with said first acid dye and is of the formula: ##STR22## wherein: M.sup.+ is Na.sup.+, Li.sup.+, K.sup.+, NH.sub.4.sup.+, or hydroxyalkylammonium of the formula [H--(OCH.sub.2 CH.sub.2).sub.n ].sub.p NH.sub.m, where n is 1 to 5, p is 1 to 3, and p+m is 4;
- R.sub.1 is hydrogen, a metal ion, an alkyl of C.sub.1-4, hydroxyalkyl of C.sub.1-4, or combinations thereof; and
- R.sub.2 is a phenyl group substituted with at least one member selected from the group consisting of: alkyl; alkoxy; hydroxyalkoxy; halogen; hydroxyl; C.sub.2 -C.sub.6 acylamino; perfluoroalkyl; substituted or unsubstituted benzoylamino; HO.sub.3 SOCH.sub.2 CH.sub.2 SO.sub.2.sup.- ; vinyl sulfone or moiety that can undergo elimination to form the vinyl sulfone structure; amino substituted with an alkyl of C.sub.1-4 or a dialkyl of C.sub.1-4, substituted or unsubstituted phenyl, diphenyl, or combinations thereof; and combinations thereof;
- mixing said first acid dye with said second acid yellow dye at an effective dyeing temperature for said material;
- immersing said material into said heated mixture of said first acid dye and said second acid yellow dye for sufficient time to exhaust said first acid dye and said second acid yellow dye; and
- drying said dyed material.
- 40. The material of claim 39 wherein said material is a polyamide.
- 41. The material of claim 40 wherein said polyamide material is a fiber.
- 42. The material of claim 41 wherein said polyamide material is a fabric.
Parent Case Info
This application is a 371 of PCT/US97/21150, Nov. 18, 1997 which claims priority from U.S. provisional application 60/031,438 Nov. 20, 1996.
PCT Information
Filing Document |
Filing Date |
Country |
Kind |
102e Date |
371c Date |
PCT/US97/21150 |
11/18/1997 |
|
|
4/27/1999 |
4/27/1999 |
Publishing Document |
Publishing Date |
Country |
Kind |
WO98/22537 |
5/28/1998 |
|
|
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