scholarly journals Synthesis and Structural-reactivity Studies of Bifunctional MCT/SES (Monochlorotriazine/ Sulphatoethylsulphone) Azo Reactive Disperse Dyes Applied to Wool and Polyester Fabric

Author(s):  
Ishegbe Joyce Eko ◽  
Bello Kasali Ademola ◽  
Nkeonye Peter Obinna ◽  
A. A. Kogo

Reactive disperse dyes containing monochlorotriazine/sulphatoethylsulphone reactive moieties were synthesized by condensing aniline with cyanuric chloride and further reacting it with a series of monoazo dyes obtained by diazotising 1-aminobenzene-4-β-sulphatoethylsulphone and coupling with various substituted 2-amino-4-phenylthiazole derivatives. The dyeing performance of the dyes was evaluated on polyester and wool fabrics. The dyes obtained gave various shades ranging from reddish to bright red colours. They had good depth and good levelling properties. They dyed fabrics showed moderate to good light fastness properties and very good to excellent fastness to washing and perspiration. The dye bath exhaustion on the polyester and wool fabrics were found to be very good and their fixation values were moderate.

2021 ◽  
Vol 18 ◽  
Author(s):  
Fatma A. Mohamed ◽  
Shaban Elkhabiry ◽  
Ismail A. Ismail ◽  
Attia O. Attia

: The dyes are synthesized by 3-Amino-2-thioxo-4thiazolidinone (N-Amino rhodanine) with glutaraldehyde or Terephthalaldehyde by 2:1 mole to form a and b then coupled with diazonium salts p-Amino benzenesulfonic acid and 4-Amino 3,4 disulfoazobenzeneazobenzene by 2:1 to form new different bis monoazo a1, b1 and diazo a2 and b2 acid dyes. Therefore, the synthesized dyes were applied to both silk and wool fabric materials. We also evaluated the antimicrobial activity for these dyed fabrics against two model gram-negative and gram-positive bacteria. Further, the chemical composition of these dyes is emphasized by elemental analysis Aims: This paper aims to synthesize, apply dye and antimicrobial to four new acid dyes based on derivatives of N-Amino rodanine as a chromophoric group. These dyes are used in dyeing silk and wool with the good lightfastness and are also excellent for washing, rubbing, and sweating fastness. Also, we measure antimicrobial activity for silk and wool fabrics toward Gram-negative, Gram-positive. Background: The search for a synthesis of new acid dyes has antimicrobial for gram-negative and gram-positive. These dyes are mainly used on silk and wool fabrics which have excellent for light fastness, washing, rubbing, and sweating fastness. Objective: The present studies were aimed at synthesis, characterization and antimicrobial toward gram- negative and gram-positive. Methods: The infra-red spectrum was recorded using an Infra-red spectrometer, Perkin Elmer/1650 FT-IR. The 1H-NMR spectra were recorded using a Varian 400MHz spectrometer. The absorbance of the dyes was measured in the ultraviolet-visible region between 300 and 700 nm by a UNICAM UV spectrophotometer. The dye uptake by wool and silk fabrics was measured using a Shimadzu UV-2401PC (UV/V is spectrophotometer at λmax) before and after dyeing. The produced dyes were found to have good antimicrobial activity against a variety of bacteria. Results and Discussion: The compounds a1, b1, a2 &b2 shows good antimicrobial activity toward gram-negative (E. coli), gram-positive (S. aurous). The data showed that exhaustion and the fastness properties of silk and wool dyed fabrics were both very high. Conclusion: This work prepares newly synthesized acid dyes based on 3-Amino-2-thioxo-4thiazolidinone derivatives and uses them for dyeing wool and silk fabrics. Both synthetic dyes have good light fastness and fastness properties. Also, all dyes have a good antimicrobial effect.


2021 ◽  
pp. 54-57
Author(s):  
Navinkumar A. Kucha ◽  
Manishkumar J. Tank ◽  
G. M. Malik

In this paper synthesis of some new mono azo disperse dyes based on 2-amino 5-(4'-nitro phenyl) 1,3,4-thiadiazole moiety has been reported. Preparation of mono azo disperse dyes via condensation and nally diazotization of substituted primary amine and condensed with N-(4-(4'-chlorophenyl)thiazol-2-yl)-2-((5-(4'-nitrophenyl)-1,3,4-thiadiazol-2-yl)amino)acetamide (RR) to 1 give a series of mono azo dyes (RR -RR ). All the dyes were characterized by IR, H NMR, UV-Visible and elemental analysis and their dyeing 1 15 performance evaluated using High Temperature High Pressure method (HTHP) at 130°C on polyester fabric. All dyes gave good to excellent fastness properties.


2011 ◽  
Vol 8 (3) ◽  
pp. 1218-1225 ◽  
Author(s):  
B. C. Dixit ◽  
D. M. Patel

Novel bisazo-bisazomethine disperse dyes were prepared by the coupling of diazotized solutions of various aromatic amines with 2,2'-{sulfonylbis [4,1-phenylene nitrilomethylylidene]} diphenol (SB). Above Schiff base was prepared by the condensation of 2-hydroxybenzaldehyde with 4,4’-sulphonyl- dianiline (Dapson). The resultant dyes were characterized by elemental analysis, IR and1H NMR spectral studies. The UV Visible absorption spectral data were investigated in dimethylformamide (DMF) and are discussed in terms of structural property relationship. Their dyeing performance as disperse dyes has been assessed on polyester fabrics. The results show that a better hue was obtained on polyester fabrics and have mild to moderate fastness properties.


2021 ◽  
pp. 004051752110246
Author(s):  
Seham A Ibrahim ◽  
Hala F Rizk

Eight azomethine pyrazolone magenta dyes with iminodiethanol groups have been synthesized from 1,3-disubstituted- 1H-pyrazol-5( 4H)-ones in good yield. The newly synthesized dyes were characterized using spectroscopic data and elemental analyses techniques. All dyes have been successfully applied to polyester fabrics as disperse dyes where their dyeing performances have been discussed and evaluated in detail. The shades of these dyes ranged from red violet, purple and dark purple colors with good depth, brightness and good leveling properties. Multifunctional properties such as color representation, colorimetric data (L*, a*, b*, C*, h*, K/S), fastness properties of the dyed samples with respect to washing, perspiration, rubbing and light fastness have been discussed and evaluated in detail. The degree of exhaustion and fixation was also achieved after establishing the optimal dyeing conditions at 130°C, high pressure, 2% shade, and pH ≈5. As well, the influence of the dye bath pH on the K/S percentage and color intensity was estimated and discussed. Furthermore, the dyed fabrics were tested for ultraviolet protection factor and the results showed that these dyes gave excellent ultraviolet protection.


2002 ◽  
Vol 67 (11) ◽  
pp. 709-718 ◽  
Author(s):  
Harir Maradiya

A series of monoazo disperse dyes based on 2-amino-5-mercapto-1,3,4-thiadiazole was prepared by coupling with various N-arylmaleimides. The dyeing performance of these dyes was assessed on nylon fabric. The dyes were found to give yellow to brown colour shades on dyeing with good depth and levelness on nylon fabric. The dyebath exhaustion fixation and fastness properties of the dyes were also determined. The dyed fabric showed moderate to good light fastness and very good to excellent fastness to washing, rubbing, perspiration and sublimation. The IR and visible range spectral properties of the dyes were also determined.


2020 ◽  
Vol 85 (10) ◽  
pp. 1253-1264
Author(s):  
Umar Ameuru ◽  
Mohammed Yakubu ◽  
Kasali Bello ◽  
Peter Nkeonye ◽  
Azim Halimehjani

A series of monoazo disperse dyes were synthesized by coupling diazotized 4-amino-N-dodecyl-1,8-naphthalimide with N,N-dialkyl anilines and naphthol derivatives. The synthesized intermediates and the dyes were characterized using FTIR, 1H-NMR, 13C-NMR, mass spectroscopy and elemental analysis (CHN). Visible absorption spectra of the dyes were examined in solvents of different polarities. The electronic absorption spectra cover a wavelength (?max) range of 515-535 nm in DMF at uniformly absorption intensity between 1.59-3.00?104 L mol-1 cm-1. The dyes gave deep and bright intense hues of light violet, maroon, pink and neon red on polyester fabrics. The dyes generally showed good washing and perspiration rating but poor to moderate light fastness properties on woven polyester fabric and could be recommended for commercial outlets.


2005 ◽  
Vol 70 (11) ◽  
pp. 1249-1253 ◽  
Author(s):  
V.R. Kanetkar ◽  
R.R. Walavalkar

This paper describes the synthesis of 5-amino-6-cyano-2-phenylthieno[ 2,3-d]oxazole and its utilization for the preparation of a range of azo disperse dyes. These aryl azo disperse dyes were applied on polyester fabric and their fastness properties were evaluated. The dyes were characterized by NMR and IR spectroscopy. The visible absorption spectra of these dyes were Recorded.


Cotton leaves have been used to extract natural dye for dyeing of Egyptian cotton variety Giza 86 fabric and its blend with polyester 50:50, using different mordants such as iron (II) sulfate, copper (II) sulfate, and alum. The exhaust dyeing method was utilized using the pre-mordant technique. It is observed that both fabric samples can be dyed in different colors and depth of shades with Cotton leaves dye. Iron (II) sulfate ensures the best light fastness. Improved light fastness is obtained using abovementioned lower amounts of iron (II) sulfate and copper (II) sulfate. Alum is found to be less effective than iron (II) sulfate and copper (II) sulfate on the light fastness. As a novel alternative and potential natural dye, Cotton leaves extract solution can be used to get various colors and shades with satisfactory fastness properties. The mordanted and un-mordanted fabric samples were tested for their dyeing performance in terms of color parameters K/S, (L*), a*, b*, (C*) and (H*), and fastness properties (wash, perspiration, light and rubbing fastness) were studied. The samples showed high color strength, and high fastness properties. These results are very important for industrial application and with the production of a natural dye as an inexpensive source from cotton leaves as a by-product. Another objective is to increase the production of eco-textile garments with a good price for the Egyptian customers.


2008 ◽  
Vol 5 (s1) ◽  
pp. S987-S996
Author(s):  
Devang N. Wadia ◽  
Pravin M. Patel

A series of eight novel heterocyclic based monoazo acid dyes were synthesized using various substituted imidazol-4-one as diazo component and coupled with various amino-napthol sulphonic acids. The resultant dyes were characterized using standard spectroscopic methods and then dyeing performance on wool fabric was assessed. Final results concluded that exhaustion (%E) of the dyes on wool fibers increased with decreasing pH of application and that fixation (%F) of the dyes on wool fibers increased with increasing pH of application and the highest total fixation efficiency was achieved at pH 5. Wash and light fastness properties of prepared dyes showed encouraging results.


2001 ◽  
Vol 66 (6) ◽  
pp. 367-376 ◽  
Author(s):  
Hari Maradiya ◽  
Vithal Patel

A series of disperse dyes has been synthesized by diazotisation of 2,6-dibromo-4-nitroaniline and coupled with various N-arylmaleimides. The dyes were characterized by IR spectral studies, visible absorption spectroscopy and elemental analysis. All the dyes were applied as disperse dyes on nylon, cellulose triacetate and polyester fabrics. These dyeswere found to give yellowish orange to deep brown shades with very good depth, levelness and brightness on different fabrics. The percentage dye bath exhaustion and fixation on fabrics were found to be very good. The light, washing, rubbing, perspiration and sublimation fastness properties of the dyed fabrics were found to be good to excellent.


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