2000
DOI: 10.1016/s0143-7208(00)00058-9
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A review of QSAR for dye affinity for cellulose fibres

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Cited by 65 publications
(70 citation statements)
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“…In accordance with Akar et al [35] and Rizzi et al [15], the reported spectrum provided evidence of the presence of the main components of olive pomace [15,36,37]. Bands were observed in the wavenumbers region between 3600-2800 cm −1 and 1800-800 cm −1 .…”
Section: Ftir-atr Spectroscopic Measurementssupporting
confidence: 89%
See 1 more Smart Citation
“…In accordance with Akar et al [35] and Rizzi et al [15], the reported spectrum provided evidence of the presence of the main components of olive pomace [15,36,37]. Bands were observed in the wavenumbers region between 3600-2800 cm −1 and 1800-800 cm −1 .…”
Section: Ftir-atr Spectroscopic Measurementssupporting
confidence: 89%
“…As already observed for the disperse blue dye [15], these findings suggested the presence of interaction between DO and DR and OPP via hydrogen bonds and van der Waals forces involving the main components of olive pomace and dye molecules. The interaction with cellulose or cellulose-like structure was thus suggested [36]; in fact, not surprisingly, disperse dyes are used to color cellulose fibers [35][36][37][38][39]. The absence of the main IR bands in OPP + dyes spectra suggested that the dye molecules were blocked inside olive pomace matrix, deshielding them from detection [15,39].…”
Section: Ftir-atr Spectroscopic Measurementsmentioning
confidence: 97%
“…A wide range of reactive groups have been investigated, with 20-30 used commercially and over 200 patented. These have been described in detail elsewhere (20,51). Because these reactive groups differ chemically, the activation of the reactive systems is different as are the rates of reaction with cellulose, from one reactive system to another.…”
Section: Fiber-reactive Dyesmentioning
confidence: 99%
“…In practice, the appropriate HOMO-LUMO gaps are found in conjugated aromatic systems that contain electron donor groups (eg, amino, substituted amino, and hydroxy) and acceptor groups (eg, nitro and cyano), the socalled donor-acceptor colorants (19). Sophisticated molecular modeling has allowed some success in predicting the color of a given structure, but the accuracy of prediction is not at the point where dyestuff synthesis is a paper exercise; the prediction of the dyeing properties of a dye and substantivity for a fiber from its chemical structure is even further away, although some initial efforts at quantitative structure-activity relationships (QSAR) of dyes and fibers, largely based on those that predict the activity of pharmaceuticals, have been made (20).Correlation between classifications according to chemical type and application properties is limited. Application-based classifications are of most practical usefulness to the dyer, and therefore the chemical constitutions of dyes are described here only briefly.…”
mentioning
confidence: 99%
“…This leads to favorable properties, such as wash fastness. Furthermore, unfix dye reacts with water to form hydrolyzed or oxy-dye that has lost its bonding capacity, and thus cannot be reused [10,11]. The dyes for this research were selected from Novacron series reactive dyes by Huntsman.…”
Section: Introductionmentioning
confidence: 99%