Paper Titles

Morphology Control and Upconversion Enhancement in NaYF₄:Yb³⁺,Er³⁺ Crystals via Ca²⁺ Ions Doping
p.242

Surface Modification of Nano-Al₂O₃ with Stearic Acid
p.246

The Influence of Geology Factor on Alkaline Surfactant Polymer Flood Effect and the Corresponding Strategy
p.251

Study on the Synthesis of Waterborne UV Curable Polyurethane Acrylate
p.256

Structure and Properties of Dyes in Coloration of Textiles: Application of Fragment Approach
p.261

One-Pot, Low-Temperature Preparation of Pyrochlore-Like Na₂Ta₂O₆ Nanocrystals by Solvothermal Synthesis
p.267

Synthesis and Property of Polyurethane Acrylates Modified Graphene Oxide
p.273

Preparation and Characteristics of Highly Expandable Graphite Intercalation Compounds by Two-Step Chemical Intercalation
p.278

Research on the Preparation and Properties of UV-Curable Organic Silicon Nanomaterials
p.284

HomeKey Engineering MaterialsKey Engineering Materials Vol. 703Structure and Properties of Dyes in Coloration of...

Structure and Properties of Dyes in Coloration of Textiles: Application of Fragment Approach

Article Preview

Abstract:

The paper reports the results of QSPR analysis of several problems of coloration of textiles, including light fastness of azo benzothiazole and indigoid dyes, ionization of hydroxyl groups in mordant dyes forming complexes with polyvalent metal ions and rate reactions of organic substances with OH radical during catalytic oxidizing of pollutants. Multiple linear regression models are built with the use of fragment descriptors. The role of different molecular fragments is discussed emphasizing the mechanism of the phenomena and ways of application in coloration technology.

You might also be interested in these eBooks

Advanced Materials and Engineering Materials V

Info:

Periodical:

Key Engineering Materials (Volume 703)

Pages:

261-266

DOI:

https://doi.org/10.4028/www.scientific.net/KEM.703.261

Citation:

Cite this paper

Online since:

August 2016

Authors:

Felix Y. Telegin*, Jian Hua Ran, Mainul Morshed, Md. Nahid Pervez, Li Sun, Cong Zhang, Viktoriia G. Priazhinikova

Keywords:

Disperse Dye, Fragment Approach, Indigoid Dyes, Mordant Dyes, Organic Pollutant, QSPR Study

Export:

RIS, BibTeX

Price:

Permissions:

Request Permissions

* - Corresponding Author

[1] Vickerstaff T. The Physical Chemistry of Dyeing. 2-nd ed. London-Edinburgh: Oliver and Boyd, 1954. 514 pp.

[2] Giles C.H., Duff D.G., Sinclair R.S. Relation between the molecular structure of dyes and their technical properties. Chapter VII. In: The Chemistry of Synthetic Dyes. Vol. 8. Ed. by K. Venkataraman. New York-London: Academic Press, 1978. 279-329.

DOI: 10.1016/b978-0-12-717008-4.50016-1

[3] Katritzky A.R., Karelson M; Lobanov V. S. (1997) QSPR as a means of predicting and understanding chemical and physical properties in terms of structure, Pure and Applied Chemistry 69 (2) 245-248.

DOI: 10.1351/pac199769020245

[4] Baskin, I, Varnek, A. (2008).

[5] Vorberg S., Tetko I.V. (2014) Modeling the Biodegradability of Chemical Compounds Using the Online CHEmical Modeling Environment (OCHEM), Mol. Inf. 33 (1) 73–85.

DOI: 10.1002/minf.201300030

[6] Timofei S., Schmidt W., Kurunczi L., Simon Z. (2000) A review of QSAR for dye affinity for cellulose fibres, Dyes and Pigment 47, No. 1-2. P. 5-16.

DOI: 10.1016/s0143-7208(00)00058-9

[7] Churchley J.H., Greaves A.J., Hutchings M.G., Phillips D.A.S. and Taylor J.A. A chemometric approach to understanding the bioelimination of anionic, water soluble dyes by a biomass. Part 2: Acid dyes, J. Soc. Dyers Colour. 2000, 116, No. 7/8. P. 222-228; Part 3: Direct dyes, J. Soc. Dyers Colour. 2000, 116, No. 9. P. 279-284; Part 4: Reactive dyes, J. Soc. Dyers Colour. 2000, 116, No. 1. P. 323-329.

DOI: 10.1111/j.1478-4408.2000.tb00009.x

[8] Egorova, L.P., Kobrakov, K.I. Study of the relationship between electronic structure and properties of direct azo dyes, Book of Papers of Moscow State Textile University, 2003, issue 6. 35-39.

[9] Telegin F., Shushina I. Ran J.H., Biba Y., Mikhaylov A., Priazhnikova V. Structure – Property Relationships for Dyes of Different Nature, Advanced Materials Research, Vols. 821-822 (2013) pp.488-492.

DOI: 10.4028/www.scientific.net/amr.821-822.488

[10] Zhokhova N I, Baskin I I, Palyulin V A et al. (2005), A Study of the Affinity of Dyes for Cellulose Fiber within the Framework of a Fragment Approach in QSPR. Russ J Appl Chem 78(6): 1013–1017.

DOI: 10.1007/s11167-005-0439-0

[11] Chemical software JChem. www. chemaxon. com/jchem. Program is licensed to ISUCT.

[12] Peters, A. T. (1988) Substituent effects on the colour, dyeing and fastness properties of 4-phenylazo-1-naphthylamines and of 2-acetylamino-5-methoxy-4-N-ß-cyanoethyl-N-ß-hydroxyethylaminoazobenzene. J. Soc. Dyers and Colour. 104 (9), 344–348.

DOI: 10.1111/j.1478-4408.1988.tb01177.x

[13] Peters, A. T.; Gbadamosi, N.M.A. (1992) 5, 6-(6, 7-)dichlorobenzothiazolylazo dyes for synthetic-polymer fibres. Dyes and Pigments 18 (2), 115–123.

DOI: 10.1016/0143-7208(92)80011-b

[14] Peters, A. (1992) Hetarylazo disperse dyes derived from 5, 6-dichloro-and 6, 7-dichloro-2 aminobenzothiazoles. Dyes and Pigments 20 (1), 41–51.

DOI: 10.1016/0143-7208(92)80039-p

[15] Peters, A. T.; Taebi, A.; Yang, S. S. (1993) Disperse dyes. Hetarylazo derivatives from dichloro-2-aminobenzothiazoles. J Soc. Dyers and Colour. 109 (12), 397–401.

DOI: 10.1111/j.1478-4408.1993.tb01525.x

[16] Peters, A. T.; Yang, S. S. (1996) Monoazo disperse dyes derived from mononitro-dichloro-2-aminobenzothiazoles. Dyes and Pigments 30 (4), 291–299.

DOI: 10.1016/0143-7208(95)00064-x

[17] Peters, A. (1995) Monoazo disperse dyes derived from nitro-2-aminobenzothiazoles. Dyes and Pigments 28 (3), 151–164.

DOI: 10.1016/0143-7208(95)00012-5

[18] World Dye Variety, www. worlddyevariety. com, 2015-01-05.

[19] Ran J.H., Shushina I. Priazhnikova V. and Telegin F. (2013) Inhibition of Mordant Dyes Destruction in Fenton Reaction, Advanced Materials Research, Vols. 821-822, 493-496.

DOI: 10.4028/www.scientific.net/amr.821-822.493

[20] Hilal, S H; Carreira, A; Baughman, G L; Karickhoff, S W. (1994) Estimation of ionization constants of azo dyes and related aromatic amines: Environmental implication. J Phys Org Chem, 7, 122-141.

DOI: 10.1002/poc.610070304

[21] Kušić, H; Rasulev, B; Leszczynska, et al. (2009): Prediction of rate constants for radical degradation of aromatic pollutants in water matrix. A QSAR study. Chemosphere 75 (8), p.1128–1134.

DOI: 10.1016/j.chemosphere.2009.01.019