DYEING PROPERTIES OF BASIC AZO-DYES FROM 2-AMINO THIADIAZOLE

Citation
A. Arcoria et al., DYEING PROPERTIES OF BASIC AZO-DYES FROM 2-AMINO THIADIAZOLE, Dyes and pigments, 21(1), 1993, pp. 67-74
Citations number
9
Journal title
ISSN journal
01437208
Volume
21
Issue
1
Year of publication
1993
Pages
67 - 74
Database
ISI
SICI code
0143-7208(1993)21:1<67:DPOBAF>2.0.ZU;2-V
Abstract
Some new basic azo-dyes derived from thiadiazole were synthesized to e valuate the dyeing parameters on polyester fibre (PET) for optimizing the dyeing process. The kinetics of dyeing were performed at various t emperatures (80-degrees, 90-degrees and 100-degrees-C) in the absence and in the presence of phenol, benzoic acid and salicylic acid as carr iers. Thermodynamic affinities were also measured. The dyeing rate con stants increase on increasing the concentration of carrier, while low affinity values were observed for the dyes bearing hydroxyl groups, ow ing to increased solubility of the dye in the dyebath. This behaviour is less evident in the dyes bearing a methyl group in the thiadiazole ring. The dyes show good fastness to light, perspiration and dry clean ing.