Synthesis and Characterization of Some Mono Azo Reactive Dyes Derive from Quinazolinone and their Application on Cotton Fabric
Abstract
Various monoazo reactive dyes with quinazolinone moiety was synthesized starting with the preparation of 6,7-dimethoxy-2-phenyl-4H-benzo[d][1,3]oxazin-4-one from 2-amino-4,5-dimethoxybenzoic acid and fusing with different di-amino compounds to give dye intermediates B, 4-amino-4'-(6,7-dimethoxy-4-oxo-2-phenylquinazolin-3(4H)-yl)-[1,1'-biphenyl]-2,2'-disulfonic acid (B), which was diazotized, followed by azo coupling with various cyanurated coupling components such as H-acid, gamma acid and J-acid. All the reactive dyes were characterized by their percentage yield, UV-Vis spectroscopy, IR spectroscopy and dyeing performance on cotton fabric have been assessed. The UV-visible spectrophotometric investigation of the synthesized dyes was carried out in different solvents to obtain the absorption maxima, molar coefficients and solvatochromic effects of the dyes. The synthesized reactive dyes were applied on cotton the percentage exhaustion and fixation of the dyes were evaluated and usage properties of the dyes were also examined. The percentage of dye bath exhaustion on the fibre is reasonably good and acceptable. The dyeing performance of all dyes on cotton fabric gave moderate to good light fastness, good to very good wash fastness and fair to very good fastness to perspiration – acid and alkaline. The dyes gave colour ranges from purple to red to pink shade
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Taylor J.A (2000). Recent development in reactive dyes Rev. Prog. Color, 30 pp 93-107.
Freeman and Sokolowska, (1999) New methods for improving the dyeability of cellulose fibres with reactive dyes Rev. prog. Color, 29 pp.8-22
Zollinger, H. 2003. Color Chemistry. Syntheses, Properties, Application of Organic Dyes and Pigments.Third revised edition.Wiley-VCH.
Seferoglu, Z. 2009. A study on tautomericequilibria of new hetarylazo-6-aminouracils.ARKIVOC, (viii) 42-57.
Sekar, N. and Deulgaonkar, D.S. (2006). Recent developments in azo reactive dyes for wool. Colouration Technology, 53(1), 82. Retrieved August 29, 2014 from http://www.Connection.ebscohost.eom/c/articles/l 9966984/recent- devlopmemts-zo-reactive-dyes-wool
Sekar, N. and Deulgaonkar, D.S. (2007). Synthesis of azo reactive dyes containing Aldehyde group. Asian journal of chemistry, 19(4), 2565-2573. Retrieved March 22, 2015 from http://www.asianiournalof chemistry.co.in/u...
David, w. and Geoffrey, H. (1994). Chemistry and Application of Dyes. Plenum Press, New York, PP. 12-31.
John, C. (2000). A Practical Approach of Interpretation of Infrared Spectra. Encyclopedia of Analytical Chemistry, John Wiley & Sons Ltd Chichester, pp.10815-10837.
John, S.(2002) Colourant and auxiliaries organic chemistry and application properties. England: Society of dyers and colourist, Perkin House Brandford pp 205-225.
Kanik, M. and Hauser, P.J. (2002). Dyeing of cotton with reactive dyes. Coloration Technology 118(6):300-306.
Kamel, M.M., Youssef, Y.A., Ali, N.F and Abdelmegiede, A. (2014). Synthesis and application of novel bi-functional pyrazol (1,5-9) pyrimidine reactive dyes. International journal of current microbiology and applied science. 3(10), pp519-530. .
Karci, F., (2005). Synthesis of diazo dyes derived from heterocyclic components. Coloratin Technol., 121: pp275-280. Synthesis of monoazo reactive dyes and their dyeing performance on various fibres International journal applied science.
Maradiya, H.R and Patel, V.S. (2001). Synthesis and Dyeing Performance of Some novel heterocyclic azo disperse dyes. Journal of Brazil Chemical Society. 12(6), pp.710-714.
Taylor, J.A. (2000). Recent Developments in Reactive Dyes. Review of Progress in Coloration and Related Topics, 30(1): 93 108.doi: 10.1111/j.1478-4408.2000.tb03785.x
Yusuf ,Y. L., Nkeonye, P. O., Bello, K. A., Yakubu, M. K. and Lawal A. O. (2014). Synthesis of Malononitrile-Condensed Disperse Dyes and Application on Polyester and Nylon Fabrics. Journal of Textiles Volume 2014 Article ID 460794, 8 pages http://dx.doi.org/10.1155/2014/460794
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