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Process for trichromatic dyeing or printing
| Details |
Inventors: Lehmann, Urs; Hoegerle, Karl;
Assignee: Ciba-Geigy Corporation (Ardsley, NY)
Primary Examiner: Clingman; A. Lionel
Assistant Examiner: Darland; J.
Attorney, Agent or Firm: Dohmann; George P., Roberts; Edward McC.
In the process for the trichromatic dyeing or printing of natural and synthetic polyamide fibre materials, mixtures of reactive dyes, wherein blue-dyeing reactive dyes of the formula ##STR1## in which X is halogen, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, cyano or nitro, n is the number 0, 1 or 2, q is the number 0 or 1, m is the number 1, 2 or 3, Z is halogen and Y is a CN, CHO or S(O).sub.p R group in which p is the number 0, 1 or 2 and R is substituted or unsubstituted C.sub.1 -C.sub.8 alkyl or phenyl, are used together with sulfo-containing yellow- or orange-dyeing reactive dyes and sulfo-containing red-dyeing reactive dyes, have a uniform color build-up in combination with shade constancy in different concentrations and good compatibility. |
|
DETAILED DESCRIPTION What is claimed is: 1.
A process for the trichromatic dyeing or printing of natural and synthetic polyamide fibre material by means of mixtures of reactive dyes, which comprises treating these fibre materials with a dye liquor or printing paste which contains a blue-dyeing reactive dye of the formula ##STR79## in which X is halogen, C.
sub.
1 -C.
sub.
4 alkyl, C.
sub.
1 -C.
sub.
4 alkoxy, cyano or nitro, n is the number 0, 1 or 2, q is the number 0 or 1, m is the number 1, 2 or 3, Z is halogen and Y is a CN, CHO or S(O).
sub.
p R group in which p is the number 0, 1 or 2 and R is phenyl or C.
sub.
1 -C.
sub.
8 alkyl which is unsubstituted or substituted by halogen or phenyl, together with at least one yellow- or orange-dyeing sulfo-containing reactive dye of the formulae ##STR80## and at least one red-dyeing sulfo-containing reactive dye of the formulae ##STR81## in which acyl is acetyl or benzoyl, R' is difluorochloropyrimidinyl, .
alpha.
,.
beta.
-dihalogenopropionyl or .
alpha.
-halogenoacryloyl, and the fused rings indicated by dots represent naphthalene systems which are a possible alternative.
2.
A process according to claim 1, wherein R' is 2,4-difluoro-5-chloropyrimidin-6-yl, .
alpha.
,.
beta.
-dibromopropionyl or .
alpha.
-bromoacryloyl.
3.
An aqueous dye liquor or printing paste, which contains yellow- or orange-, red- and blue-dyeing reactive dyes according to claim 1 in amounts of 0.
01 to 10% by weight, relative to the fibre material to be dyed or relative to the printing paste.
4.
A process according to claim 1, wherein the fibre material used is natural or synthetic polyamide material.
5.
The natural or synthetic polyamide fibre material dyed or printed by the process according to claim 1.
6.
A process according to claim 1, wherein q is the number 1, n is the number 0 and m is the number 2.
7.
A process according to claim 1, wherein Z is fluorine or chlorine.
8.
A process according to claim 1, wherein Y is a S(O).
sub.
p R group, in which R is phenyl or C.
sub.
1 -C.
sub.
4 alkyl which is unsubstituted or substituted by halogen or phenyl and p is the number 0, 1 or 2
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