Abstract
Three novel reactive azo disperse dyes were prepared using 7-acetamide-4-hydroxy-2-naphthalene sodium sulphate as the precursor. The structure of the dyes has the combined characteristics of reactive, disperse, and cationic dyes. Under alkaline conditions (pH 9), the dyes can be applied to cotton, silk, wool, and nylon. Under neutral conditions, they can be used to dye polyester. Under acidic conditions (pH 4.5), they can colour acrylic fabric after conversion of the tertiary amine group to the quaternary ammonium cation. The colour-fastness of the dyed fabrics were also evaluated.
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© 2013 Institute of Chemistry, Slovak Academy of Sciences
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Artikel in diesem Heft
- Analytical protocol for investigation of zinc speciation in plant tissue
- Assessment of waxy and non-waxy corn and wheat cultivars as starch substrates for ethanol fermentation
- Effect of quaternary ammonium silane coating on adhesive immobilization of industrial yeasts
- Modeling of supercritical fluid extraction of flavonoids from Calycopteris floribunda leaves
- Determination of limiting current density for different electrodialysis modules
- Dyeing of multiple types of fabrics with a single reactive azo disperse dye
- Physicochemical fractionation of americium, thorium, and uranium in Chernozem soil after sharp temperature change and soil drought
- Ultra-trace determination of Pb(II) and Cd(II) in drinking water and alcoholic beverages using homogeneous liquid-liquid extraction followed by flame atomic absorption spectrometry
- Synthesis, thermal stability, electronic features, and antimicrobial activity of phenolic azo dyes and their Ni(II) and Cu(II) complexes
- Inhibition of copper corrosion in acidic sulphate media by eco-friendly amino acid compound
- Formation of nanostructured polyaniline by dopant-free oxidation of aniline in a water/isopropanol mixture
- Total synthesis of cannabisin F
- Design and synthesis of novel thiopheno-4-thiazolidinylindoles as potent antioxidant and antimicrobial agents
- Microwave-assisted synthesis and antibacterial activity of derivatives of 3-[1-(4-fluorobenzyl)-1H-indol-3-yl]-5-(4-fluorobenzylthio)-4H-1,2,4-triazol-4-amine
- DFT study on [4+2] and [2+2] cycloadditions to [60] fullerene
- Efficient thioacetalisation of carbonyl compounds
- Trimerization of aldehydes with one α-hydrogen catalyzed by sodium hydroxide