Claims
- 1. A process for dyeing or printing synthetic polyamide fibres by a rapid fixation method, which process comprises dyeing or printing synthetic polyamide fibers with a dye or a mixture of dyes selected from the dyes of the formulae ##STR41## wherein (R.sub.1).sub.0-2 represents 0 to 2 substituents R.sub.1 which may each independently be C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, halogen, nitro, sulfamoyl, N--C.sub.1 -C.sub.4 alkylsulfamoyl, N--C.sub.1 -C.sub.2 alkoxy-C.sub.1 -C.sub.2 alkylsulfamoyl, phenylaminosulfonyl, carboxyphenylamoinosulfonyl, C.sub.1 -C.sub.4 alkylsulfonyl or acetylamino; ##STR42## wherein (R.sub.2).sub.0-2 represents 0 to 2 substituents R.sub.2 which may each independently be C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, halogen, nitro, sulfamoyl, N--C.sub.1 -C.sub.4 alkylsulfamoyl, N--C.sub.1 -C.sub.2 alkoxy-C.sub.1 -C.sub.3 alkylsulfamoyl, phenylaminosulfonyl, carboxyphenylaminosulfonyl, C.sub.1 -C.sub.4 alkylsulfonyl or acetylamino, and (R.sub.3).sub.0-2 represents 0 to 2 substituents R.sub.3 which may each independently be halogen, C.sub.1 -C.sub.4 alkyl, cyano or sulfamoyl; 1:2 cobalt complex of the dyes of the formula (2), wherein R.sub.2 has the same meaning as in the 1:2 chromium complexes and (R.sub.3).sub.0-2 represents 0 to 2 substituents R.sub.3 which may each independently be halogen, cyano or sulfamoyl; ##STR43## wherein R.sub.4 has the same meaning as R.sub.1 in formula (1), and R.sub.5 is hydrogen, acetylamino, methoxycarbonylamino or methylsulfonylamino; ##STR44## wherein R.sub.6 has the same meaning as R.sub.1 in formula (1), and (R.sub.7).sub.1-2 represents 1 to 2 substituents R.sub.7 which may each independently be halogen, methyl, methoxy or sulfo, or wherein 2 adjacent substituents R.sub.7 are able to form a closed bridge member --SO.sub.2 --CH.sub.2 --O--; ##STR45## wherein (R.sub.8).sub.1-2 represents 1 to 2 substituents R.sub.8 which may each independently be sulfo or nitro and R.sub.9 is hydrogen or hydroxy; ##STR46## wherein Z is the radical of the formula ##STR47## wherein X is the --O--SO.sub.2 --, --NH--SO.sub.2 or --NH--CO-- group and X' is oxygen or sulfur, R.sub.10 is hydrogen or C.sub.1 -C.sub.4 alkyl, Y is an unsubstituted or substituted aryl radical, n is 1, 2 or 3, the benzene ring A may be substituted by halogen and the benzene rings B and D may each independently be substituted by halogen, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy or by a radical of the formula --O--CH.sub.2 CH.sub.2 --O--R.sub.11, wherein R.sub.11 is hydrogen, methyl or ethyl; ##STR48## wherein R.sub.12 has the same meaning as R.sub.1 in formula (1), and R.sub.13 is hydrogen or phenyl; ##STR49## wherein (R.sub.14).sub.0-2 represents 0 to 2 substituents R.sub.14, which may each independently be C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, halogen, carboxy or sulfo; and a mixture of the 1:2-chromium complexes of formula (10), (10a) and (10b) ##STR50## wherein (R.sub.15).sub.1-2 represents 1 to 2 substituents R.sub.15, which may each independently be sulfo or nitro, (R.sub.16).sub.1-2 represents 1 to 2 substituents R.sub.16, which may each independently be nitro, halogen, methyl or acetylamino, R.sub.17 has the same meaning as R.sub.16, independently thereof, R.sub.18 has the same meaning as R.sub.16, independently thereof, and R.sub.19 is acetylamino, methoxycarbonylamino, ethoxycarbonylamino, methylsulfonylamino or N,N-dimethylaminosulfonyl; 1:2 cobalt mixed complexes of the dyes of the formulae (2) and (3) or (4) and (8); in a continuous dyeing process or printing method, and fixing the dyeings or prints by steaming for less than 3 minutes, during which time at least 95% fixation of the dyes is achieved.
- 2. A process according to claim 1, which comprises the use of dyes or mixtures of dyes of the formulae
- (1) 1:2 cobalt complex, wherein R.sub.1 is nitro, sulfamoyl, N-methylsulfamoyl, methylsulfonyl, carboxyphenylaminosulfonyl or N-(.beta.-methoxyethyl)sulfamoyl;
- (2) 1:2 chromium complex, wherein R.sub.2 is chlorine, nitro, sulfamoyl or N-methylsulfamoyl, and R.sub.3 is chlorine, methyl or sulfamoyl;
- (2) 1:2 cobalt complex, wherein R.sub.2 is chlorine, nitro, sulfamoyl or N-methylsulfamoyl, and R.sub.3 is chlorine, cyano or sulfamoyl;
- (3) 1:2 cobalt or 1:2 chromium complex, wherein R.sub.4 is methyl, methoxy, chlorine, nitro, sulfo, sulfamoyl, N--C.sub.1 -C.sub.3 alkylsulfamoyl, N-.beta.-methoxyethylsulfamoyl, phenylaminosulfonyl, methylsulfonyl or acetylamino, and R.sub.5 is hydrogen, acetylamino, methoxycarbonylamino or methylsulfonylamino;
- (4) 1:2 chromium complex;
- (5) 1:2 chromium or 1:2 cobalt complex, wherein R.sub.6 is nitro, chlorine, sulfamoyl, N-methylsulfamoyl or N-ethylsulfamoyl, and R.sub.7 is chlorine, methyl, methoxy or sulfo, or wherein 2 adjacent substituents R.sub.7 are able to form a closed bridge member --SO.sub.2 --CH.sub.2 --O--;
- (6) 1:2 cobalt or 1:2 chromium complex, wherein R.sub.8 is as defined in claim 1 and R.sub.9 is hydrogen;
- (7) wherein X is as defined in claim 1, the benzene ring A is unsubstituted and the benzene ring B can be substituted by methyl or methoxy, or wherein X' is oxygen, R.sub.10 is hydrogen, Y is phenyl, and n is 1 or 2, the benzene ring A is unsubstituted and the benzene rings B and D can each independently be substituted by chlorine, methyl or methoxy.
- (8) 1:2 cobalt complex, wherein R.sub.12 is methoxy, chlorine, nitro, sulfo or sulfamoyl;
- (9) wherein R.sub.14 is methyl, methoxy, ethoxy, chlorine, carboxy or sulfo;
- (10) 1:2 chromium mixed complex, wherein R.sub.15 is as defined in claim 1, R.sub.16, R.sub.17 and R.sub.18 are each independently nitro, chlorine, methyl or acetylamino, and R.sub.19 is as defined in claim 1; or
- 1:2 cobalt mixed complexes of dyes of the formulae (2) and (3) or (4) and (8).
- 3. A process according to claim 2, which comprises the use of dyes or mixtures of dyes of the formulae ##STR51## a mixture of the 1:2-chromium complexes of formulae (50), (50a) and (50b) ##STR52## or the 1:2 cobalt mixed complex of the dyes of the formulae (31), (32) and (33).
- 4. A process according to claim 1 for producing combination shades, which comprises the use of a mixture comprising 3 or 4 dyes selected from the group consisting of the dyes of the formulae (1) to (10).
- 5. A process according to claim 1 for trichromatic dyeing or printing, which comprises the use of a mixture of 3 or 4 suitable yellow or orange, red and blue dyes selected from the group consisting of the dyes of the formulae (1) to (10).
- 6. A process according to claim 5, which comprises the use of a mixture which contains a dye of the formula (7).
- 7. A process according to claim 1, wherein the dyes or mixtures of dyes are used in aqueous dye liquors or printing pastes which optionally contain further ingredients.
- 8. A process according to claim 7, wherein the dyes or mixtures of dyes are used in short liquors.
- 9. A process according to claim 1, wherein the dyes or mixtures of dyes are used in the continuous foam dyeing method.
- 10. A process according to claim 1, wherein the dyes are fixed by steaming for 1 to 2 minutes.
- 11. A process according to claim 3, which comprises the use of 1:2 cobalt complexes of the formulae (11), (13), (20), (32), (33), (34) or (35), 1:2 chromium complexes of the formulae (19), (49) or (50), or 1:2 cobalt mixed complexes of the formulae (31), (32) and (33).
- 12. A process according to claim 1 for dyeing or printing polyamide carpeting material.
- 13. An aqueous dye liquor or printing paste which contains a mixture of 3 or 4 dyes selected from the group consisting of the dyes of the formulae (11) to (50).
- 14. An aqueous dye liquor or printing paste according to claim 13 which contains a dye of the formula (40).
Priority Claims (1)
Number |
Date |
Country |
Kind |
176/83 |
Jan 1983 |
CHX |
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CROSS REFERENCE TO RELATED APPLICATION
This is a continuation-in-part of our copending application Ser. No. 470,493 filed Feb. 28, 1983 (now abandoned).
US Referenced Citations (8)
Foreign Referenced Citations (10)
Number |
Date |
Country |
55808 |
Jul 1982 |
EPX |
61670 |
Oct 1982 |
EPX |
2918633 |
Nov 1980 |
DEX |
3023664 |
Jan 1982 |
DEX |
3200146 |
Oct 1982 |
DEX |
930429 |
Jul 1963 |
GBX |
1137748 |
Dec 1968 |
GBX |
1206295 |
Sep 1970 |
GBX |
1214194 |
Dec 1970 |
GBX |
2041010 |
Sep 1980 |
GBX |
Non-Patent Literature Citations (2)
Entry |
American Dyestuff Reporter, vol. 67 (Jun. 1978), pp. 27, 30, 31 and 34. |
Journal of the Society of Dyers and Colourists, vol. 97, pp. 262-274. |
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
470493 |
Feb 1983 |
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