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Journal articles on the topic 'Reactive triazine dyes'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

HLADÍK, VLADIMÍR, and ZBYŇĚK ŠVEC. "Photochemical Decomposition of Some Triazine Reactive Dyes." Journal of the Society of Dyers and Colourists 95, no. 4 (2008): 147–51. http://dx.doi.org/10.1111/j.1478-4408.1979.tb03468.x.

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2

He, Pengshuang, Chaohong Dong, Xiaoyan Chen, et al. "Flame Retardant Finishing and Dyeing of Cotton Fabric in One Bath." AATCC Journal of Research 7, no. 4 (2020): 9–14. http://dx.doi.org/10.14504/ajr.7.4.2.

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Flame resistant cotton fabric is usually dyed first, and is then treated with a flame retardant by the pad-dry-cure technique. In this research, cotton fabric was treated with 2-(2-aminoethyl hydrogen phosphite)-4,6-dichloro-1,3,5-triazine (APDCT). APDCT contains s-triazine groups, which are the same used by reactive dyes. This process allows cotton fabric dyeing and flame retardant treatment to occur simultaneously, while decreasing treatment temperature, improving efficiency, and saving energy. Optimal treatment was determined by the percent dye uptake, fixation, and fabric flame resistance.

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3

Konstantinova, T., and P. Petrova. "On the synthesis of some bifunctional reactive triazine dyes." Dyes and Pigments 52, no. 2 (2002): 115–20. http://dx.doi.org/10.1016/s0143-7208(01)00080-8.

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4

Arora, Taruna, Pankaj Patel, and K. Muralidhar. "Assessment of Pseudoaffinity Chromatography Using Textile Dyes for Isolation of Buffalo Pituitary Luteinizing Hormone." ISRN Chromatography 2012 (December 16, 2012): 1–8. http://dx.doi.org/10.5402/2012/639514.

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Extensive investigation has been carried out to elucidate the mechanisms involved in pseudoligand affinity chromatography using textile dyes, and, empirically, it has been attributed to the chemical and steric structures of dye and protein. Possibly, a variety of interactions especially ionic and/or hydrophobic influence with a varying share in the binding and differ from protein to protein and from dye to dye. In this study, we have attempted to understand the effect of various biophysical parameters like the nature of the eluant, pH, and ionic strength on the binding of crude luteinizing hor

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5

Palanisamy, Sakthisharmila, Palanisamy Nachimuthu, Mukesh Kumar Awasthi, et al. "Application of electrochemical treatment for the removal of triazine dye using aluminium electrodes." Journal of Water Supply: Research and Technology-Aqua 69, no. 4 (2020): 345–54. http://dx.doi.org/10.2166/aqua.2020.109.

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Abstract Textile effluents contain triazine-substituted reactive dyes that cause health problems such as cancer, birth defects, and hormone damage. An electrochemical process was employed effectively to degrade azo reactive dye with the aim of reducing the production of carcinogenic chemicals during biodegradation. Textile dye C.I. Reactive Red 2 (RR2), a model pollutant that contains dichloro triazine ring, was subjected to the electrocoagulation process using aluminium (Al) electrodes. A maximum of 97% of colour and 72% of chemical oxygen demand (COD) removal efficiencies were achieved and 9

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6

Wei, Xiong, Ma Wei, and Zhang Shufen. "A new way to improve the light-fastness of azo reactive dyes through the introduction of benzene sulfonamide derivatives into the triazine ring." RSC Advances 9, no. 31 (2019): 17658–63. http://dx.doi.org/10.1039/c9ra02108f.

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7

Raman, Chandra Devi, Kanmani Sellappa, and Martin Mkandawire. "Facile one step green synthesis of iron nanoparticles using grape leaves extract: textile dye decolorization and wastewater treatment." Water Science and Technology 83, no. 9 (2021): 2242–58. http://dx.doi.org/10.2166/wst.2021.140.

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Abstract The existing knowledge on the reactivity of green iron particles on textile dye and wastewater decolorization is very limited. In this study, the potential of green iron particles synthesized using grape leaves extract on reactive dye (reactive red 195, reactive yellow 145, reactive blue 4 and reactive black 5) decolorization were investigated. 95–98% of decolorization was achieved for all reactive dyes at 1.4–2.0 g/L of green iron. Maximum decolorization was attained at lower dye concentration and showed very little impact on decolorization when pH was increased from 3 to 11. The pse

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8

Qadri, Firdausi. "The reactive triazine dyes: Their usefulness and limitations in protein purifications." Trends in Biotechnology 3, no. 1 (1985): 7–12. http://dx.doi.org/10.1016/0167-7799(85)90069-1.

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9

Yu, Sheng Fei, Yuan Liu, Xian Jun Li, and Wu Sheng Luo. "Studies on Poplar Veneer Dyeing with Reactive Yellow Dyes." Advanced Materials Research 1049-1050 (October 2014): 118–22. http://dx.doi.org/10.4028/www.scientific.net/amr.1049-1050.118.

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In this paper, the relationship is studied by spectrophotometric method between the structure of reactive yellow X-R, reactive yellow K-6G, reactive yellow KN-GR, reactive yellow M-5G, reactive yellow M-3RE, reactive yellow EF-3R and their colors, poplar veneer dyeing characteristic parameters S, E, R, F values, exhaustion curves and fixation curves. The results showed that longer conjugated system and better coordination of electron donor and acceptor group and smaller steric hindrance generates longer absorbance wavelength. The S value of six active dyes is reactive yellow X-R> reactive y

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10

Dongzhi, Liu, Gao Kunyu, and Cheng Lubai. "The hydrolysis kinetics and dyeing properties of 3′-carboxypyridino-triazine reactive dyes." Dyes and Pigments 33, no. 2 (1997): 87–96. http://dx.doi.org/10.1016/s0143-7208(96)00042-3.

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11

Klančnik, Maja, and Marija Gorenšek. "Kinetics of hydrolysis of monofunctional and bifunctional monochloro-s-triazine reactive dyes." Dyes and Pigments 33, no. 4 (1997): 337–50. http://dx.doi.org/10.1016/s0143-7208(96)00054-x.

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12

Kusic, Hrvoje, Natalija Koprivanac, and Ana Loncaric Bozic. "Environmental aspects on the photodegradation of reactive triazine dyes in aqueous media." Journal of Photochemistry and Photobiology A: Chemistry 252 (January 2013): 131–44. http://dx.doi.org/10.1016/j.jphotochem.2012.11.018.

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13

Xie, Kongliang, Yan Sun, and Aiqin Hou. "Diffusion properties of reactive dyes into net modified cotton cellulose with triazine derivative." Journal of Applied Polymer Science 103, no. 4 (2006): 2166–71. http://dx.doi.org/10.1002/app.25097.

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14

Xie, Kongliang, Hongdong Liu, and Xiaojun Wang. "Surface modification of cellulose with triazine derivative to improve printability with reactive dyes." Carbohydrate Polymers 78, no. 3 (2009): 538–42. http://dx.doi.org/10.1016/j.carbpol.2009.05.013.

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15

Rosu, Liliana, Dan Rosu, Cristian-Catalin Gavat, and Cristian-Dragos Varganici. "Photochemical stability of cellulose textile surfaces painted with some reactive azo-triazine dyes." Journal of Materials Science 49, no. 13 (2014): 4469–80. http://dx.doi.org/10.1007/s10853-014-8144-0.

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16

Barek, Jir̆í, Arnold G. Fogg, Josino C. Moreira, M. Valnice B. Zanoni, and Jir̆í Zima. "Polarographic and voltammetric determination of selected triazine-based azo dyes with different reactive groups." Analytica Chimica Acta 320, no. 1 (1996): 31–42. http://dx.doi.org/10.1016/0003-2670(95)00520-x.

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17

Zhang, Qiushui, Wei Xiong, Shufen Zhang, Wei Ma, and Bingtao Tang. "Synthesis and application of KM‐type reactive dyes containing 2‐ethoxy‐4‐chloro‐ s ‐triazine." Coloration Technology 135, no. 5 (2019): 335–48. http://dx.doi.org/10.1111/cote.12424.

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18

Lewis, D. M., and A. A. Siddique. "Synthesis of reactive dyes based on the bis-(N-carboxymethylamino)monoquaternary-triazine-bis-ethylsulphone reactive group. Part 1: Application to cotton cellulose." Coloration Technology 122, no. 4 (2006): 217–26. http://dx.doi.org/10.1111/j.1478-4408.2006.00031.x.

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19

Kampyli, V., D. A. S. Phillips, and A. H. M. Renfrew. "Reactive dyes containing a 4-m-carboxypyridinium-1,3,5-triazine-2-oxide reactive group: exhaust dyeing of cotton under alkaline and neutral fixation conditions." Dyes and Pigments 61, no. 2 (2004): 165–75. http://dx.doi.org/10.1016/j.dyepig.2003.10.001.

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20

Bone, J. A., T. T. Le, D. A. S. Phillips, and J. A. Taylor. "One-bath dyeing of polyester/cotton blends with disperse and bis-3-carboxypyridinium-s-triazine reactive dyes. Part 2: Application of substantive reactive dyes to cotton at 130 °C and neutral pH." Coloration Technology 124, no. 2 (2008): 117–26. http://dx.doi.org/10.1111/j.1478-4408.2008.00131.x.

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21

Xu, Le, Rodney V. Jones, and Gerhard Meissner. "Activation of the skeletal muscle Ca2+ release channel by the triazine dyes Cibacron Blue F3A-G and reactive Red 120." Archives of Biochemistry and Biophysics 274, no. 2 (1989): 609–16. http://dx.doi.org/10.1016/0003-9861(89)90476-1.

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22

Fogg, Arnold G., M. V. B. Zanoni, A. Rahim H. M. Yusoff, Rahmalan Ahmad, Jiři Barek, and Jiři Zima. "Polarographic and voltammetric determination of triazine-based reactive azo dyes with 4-carboxypyridyl and 1,4-diazabicyclo[2,2,2]octanyl (DABCO) leaving groups." Analytica Chimica Acta 362, no. 2-3 (1998): 235–40. http://dx.doi.org/10.1016/s0003-2670(98)00056-7.

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23

Hou, Aiqin, Minge Zhou, and Xiaojun Wang. "Modifying Cellulose with the Emulsion of the Triazine Derivative Containing the Tertiary Amino Group to Improve the Reactivity with Reactive Dyes." Journal of Dispersion Science and Technology 30, no. 5 (2009): 643–48. http://dx.doi.org/10.1080/01932690802598770.

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24

Patel, Manoj J., and R. C. Tandel. "Synthesis of reactive dyes by the introduction of Phenyl Urea derivatives into the triazine ring and their application on different fibers." Materials Today: Proceedings 46 (2021): 6459–64. http://dx.doi.org/10.1016/j.matpr.2021.03.575.

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25

Bone, J. A., T. T. Le, D. A. S. Phillips, and J. A. Taylor. "One-bath dyeing of polyester/cotton with disperse and bis-3-carboxypyridinium-s-triazine reactive dyes. Part 1: Factors limiting production of heavy shades." Coloration Technology 123, no. 3 (2007): 152–62. http://dx.doi.org/10.1111/j.1478-4408.2007.00077.x.

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26

Lewis, D. M., and Y. C. Ho. "Improved fixation of dyes on polyamide fibres. Part 2: Use of the reactive crosslinking agent, 2-chloro-4,6-di(aminobenzene-4′-sulphatoethylsulphone)-s-triazine (XLC)." Dyes and Pigments 28, no. 4 (1995): 237–59. http://dx.doi.org/10.1016/0143-7208(95)00015-8.

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27

Frank, H. G. "Mechanisms and products of azo coupling in histochemical protease procedures based on primary aromatic amines as unspecific moieties." Journal of Histochemistry & Cytochemistry 38, no. 9 (1990): 1295–300. http://dx.doi.org/10.1177/38.9.2201736.

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It is presumed that the azo dyes generated by histochemical protease reactions are formed by substitution of a reactive aromatic carbon. They are referred to as dyes of the C-azo series. To confirm this assumption, the absorption spectra between 330 and 630 nm of azo dyes resulting from coupling between various aromatic amines of the aniline and naphthylamine series and the diazonium salts Fast Blue B and Fast Garnet GBC were studied in test tube experiments. Some of the amines were blocked by methylation to prevent coupling either at the amino group (N-methylated) or at the aromatic nucleus (

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28

Iglesias, Bernardo A., Manfredo Hörner, Henrique E. Toma, and Koiti Araki. "5-(1-(4-phenyl)-3-(4-nitrophenyl)triazene)-10,15,20-triphenylporphyrin: a new triazene-porphyrin dye and its spectroelectrochemical properties." Journal of Porphyrins and Phthalocyanines 16, no. 02 (2012): 200–209. http://dx.doi.org/10.1142/s1088424612004501.

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The new triazene-porphyrin dye 5-(1-(4-phenyl)-3-(4-nitrophenyl)triazene)-10,15,20-triphenylporphyrin, encompassing a reactive protonated triazene moiety, was prepared starting from meso-tetraphenylporphyrin ( H2TPP ), first converting it to the 5-(4-nitrophenyl)-10,15,20-triphenylporphyrin, then reducing to the 5-(4-aminophenyl)-10,15,20-tri(phenyl)porphyrin intermediate, and reacting with the diazonium salt of 4-nitroaniline; and characterized by spectroscopic and electrochemical methods. The absorption spectrum of the neutral species resembled the sum of H2TPP and of 1,3-bis(4-nitrophenyl)t

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29

Abrar, Shazia, Kazim Raza Naqvi, Sadia Javed, Shumaila Kiran, and Tahsin Gulzar. "Synthesis of a Fluorescent Whitening Molecule and its Application to Wool Fibres." Current Organic Synthesis 16, no. 2 (2019): 314–18. http://dx.doi.org/10.2174/1570179416666190206141751.

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Aim and Objective: Reactive dye molecules are commonly employed to dye or modify colour characteristics of wool fibres. Yellowness of wool fibres poses a challenge and here, we report synthesis of a reactive fluorescent molecule and its application to wool fibres to reduce yellowness of the wool fibre and improve its colour features. Material and Methods: The new molecule was based upon 7-amino-4-methylcoumarin (AMC) and 2,4,6- trichloro-1,3,5-triazine (TZT). The synthesis involved a two-step chemical reaction, initiated by the nucleophilic substitution of a chloro group on the triazine ring w

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30

Hickmott, P. W. "Reactive dyes: Preparation of substituted styrylpyrimidines and styryl-s-triazines." Journal of Applied Chemistry 16, no. 8 (2007): 227–29. http://dx.doi.org/10.1002/jctb.5010160803.

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31

Li, Lin Feng, and Hong Yao Xu. "The Preparation and Characterization of Novel Nonlinear Optical Active Dye." Advanced Materials Research 750-752 (August 2013): 899–902. http://dx.doi.org/10.4028/www.scientific.net/amr.750-752.899.

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A novel nonlinear optical active triazine dye 2-(4-methyl-4-amino-azobenzene )-4-sodium sulfanilate-6-chloro-1,3,5-triazine was synthesized by condensation reaction and characterized by FTIR, 1HNMR, respectively. Their nonlinear optical properties were investigated using 5 ns pulse at 532 nm, which showed excellent nonlinear optical property.

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32

PIERCE, J. H., and I. D. RATTEE. "Acid-catalysed Hydrolysis of Type 3 Dye-Fibre Bonds between Cellulose and Triazinyl Reactive Dyes." Journal of the Society of Dyers and Colourists 83, no. 9 (2008): 361–68. http://dx.doi.org/10.1111/j.1478-4408.1967.tb02776.x.

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33

Fernandez Cid, M. V., J. van Spronsen, M. van der Kraan, W. J. T. Veugelers, G. F. Woerlee, and G. J. Witkamp. "Acid-catalysed methanolysis reaction of non-polar triazinyl reactive dyes in supercritical carbon dioxide." Journal of Supercritical Fluids 39, no. 3 (2007): 389–98. http://dx.doi.org/10.1016/j.supflu.2006.02.010.

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34

Alsberg, Fred R. "Reactive Dyes in Textile Printing with Special Reference to Chloro-s-triazinyl Dyes." Review of Progress in Coloration and Related Topics 12, no. 1 (2008): 66–72. http://dx.doi.org/10.1111/j.1478-4408.1982.tb00227.x.

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35

Croft, S. N., D. M. Lewis, R. Orita, and T. Sugimoto. "Neutral-fixing reactive dyes for cotton. Part 1 -synthesis and application of quaternised S-triazinyl reactive dyes." Journal of the Society of Dyers and Colourists 108, no. 4 (2008): 195–99. http://dx.doi.org/10.1111/j.1478-4408.1992.tb01439.x.

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36

Benkovics, Gábor, Damien Afonso, András Darcsi та ін. "Novel β-cyclodextrin–eosin conjugates". Beilstein Journal of Organic Chemistry 13 (15 березня 2017): 543–51. http://dx.doi.org/10.3762/bjoc.13.52.

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Eosin B (EoB) and eosin Y (EoY), two xanthene dye derivatives with photosensitizing ability were prepared in high purity through an improved synthetic route. The dyes were grafted to a 6-monoamino-β-cyclodextrin scaffold under mild reaction conditions through a stable amide linkage using the coupling agent 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride. The molecular conjugates, well soluble in aqueous medium, were extensively characterized by 1D and 2D NMR spectroscopy and mass spectrometry. Preliminary spectroscopic investigations showed that the β-cyclodextrin–EoY conjug

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37

Goward, C. R., M. D. Scawen, and T. Atkinson. "The inhibition of glucokinase and glycerokinase from Bacillus stearothermophilus by the triazine dye Procion Blue MX-3G." Biochemical Journal 246, no. 1 (1987): 83–88. http://dx.doi.org/10.1042/bj2460083.

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Glucokinase from Bacillus stearothermophilus was irreversibly inactivated by the reactive dichlorotriazinyl dye Procion Blue MX-3G at pH 8.0. The enzyme was protected from inactivation by the substrate MgATP. Kinetic data implied that the dye occupied the MgATP-binding site. The apparent Km values for MgATP and D-glucose were found to be 70 microM and 210 microM respectively, and the Kd of the pure reactive dye was 16 microM; 1 mol of the pure reactive dye bound to 1 mol of glucokinase subunit. The dye was shown to have potential as an affinity probe for glucokinase. Glycerokinase from the sam

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38

Taylor, J. A., and A. H. M. Renfrew. "Reactive dyes for cellulose. An unexpected hydrolysis product of a triazinyl reactive dye with a 3-carboxypyridine (nicotinic acid) leaving group." Journal of the Society of Dyers and Colourists 106, no. 7-8 (2008): 230–34. http://dx.doi.org/10.1111/j.1478-4408.1990.tb01259.x.

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39

Cai, Yingjie, Yingya Huang, Fan Liu, Linwei He, Lina Lin, and Qingfu Zeng. "Liquid ammonia dyeing of cationic ramie yarn with triazinyl reactive dyes." Cellulose 21, no. 5 (2014): 3841–49. http://dx.doi.org/10.1007/s10570-014-0393-1.

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40

Johnston, Jan E., and Ian D. Rattee. "Further Studies of the Acid-catalysed Hydrolysis of Type 3 Dye-Fibre Bonds between Cellulose and Triazinyl Reactive Dyes." Journal of the Society of Dyers and Colourists 89, no. 3 (2008): 89–94. http://dx.doi.org/10.1111/j.1478-4408.1973.tb03134.x.

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41

Bae, Sook Hee, Motoko Komaki, and Toshinari Nakajima. "Solvent dyeing of silk with reactive triazinyl dyes from aqueous alcoholic dyebath." Sen'i Gakkaishi 48, no. 12 (1992): 704–10. http://dx.doi.org/10.2115/fiber.48.12_704.

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42

Goswami, Jyoti, Thakur Vikram Singh, Chhaya Bhatt, et al. "An Extractive Spectrophotometric Method for the Determination of Pymetrozine in Various Ecological Samples of Bilaspur District (C.G.)." Journal of Ravishankar University (PART-B) 33, no. 1 (2020): 65–72. http://dx.doi.org/10.52228/jrub.2020-33-1-9.

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Pesticides are designated mixture of substances for extenuating and destroying any group of pests such as insects and vegetation. Pymetrozine [6-methyl-4-[(E)-pyridin-3-ylmethylideneamino]-2, 5-dihydro-1, 2, 4-triazin-3-one] is a pyridine azomethine compound which represents a class of insecticide. A Spectrophotometric method has been developed on the modified Fujiwara reaction for the determination of pymetrozine. Pymetrozine directly reacts with chloroform the 45-500C turns out the violet color in the formation of Schiff’s Base (Glutaconic Aldehyde). In the present reaction, the violet color

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43

Pasha, Khalid, and John A. Taylor. "The synthesis and application of novel 2-chloro-4-alkylthio triazinyl reactive dyes." Dyes and Pigments 96, no. 2 (2013): 397–402. http://dx.doi.org/10.1016/j.dyepig.2012.08.016.

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44

Patel, Divyesh R., Bhavesh M. Patel, Naitik B. Patel, and Keshav C. Patel. "Application of newly synthesized bisazo dichloro-s-triazinyl reactive dyes bearing 1,3,4-oxadiazole molecule." Journal of Saudi Chemical Society 18, no. 3 (2014): 245–54. http://dx.doi.org/10.1016/j.jscs.2011.06.018.

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45

Phillips, D. A. S., R. Reisel, and A. H. M. Renfrew. "Influence of dichloro-s-triazinyl reactive dyes on the fibrillation propensity of lyocell fibres." Coloration Technology 124, no. 3 (2008): 173–79. http://dx.doi.org/10.1111/j.1478-4408.2008.00138.x.

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46

Dawson, T. L. "The Reaction Mechanism and Fixation of Monochloro-s-triazine Dyes on Cellulose Using Tertiary Amine Catalysts." Journal of the Society of Dyers and Colourists 80, no. 3 (2008): 134–43. http://dx.doi.org/10.1111/j.1478-4408.1964.tb02584.x.

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47

Wu Zuwang, Li Peng, Wang Shirong, and Lin Li. "A study on the relationship between steric effects and performance of some triazinyl reactive dyes." Dyes and Pigments 38, no. 1-3 (1998): 1–10. http://dx.doi.org/10.1016/s0143-7208(97)00109-5.

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48

Huang, Huei-Chin, and Chun-Guey Wu. "Synthesis and kinetic study of a series of chloro- and m-carboxypyridium triazinyl reactive dyes." Dyes and Pigments 188 (April 2021): 109147. http://dx.doi.org/10.1016/j.dyepig.2021.109147.

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49

Bates, I., R. Ibbett, R. Reisel, and A. H. M. Renfrew. "Protection of lyocell fibres against fibrillation; influence of dyeing with bis-monochloro-s-triazinyl reactive dyes." Coloration Technology 124, no. 4 (2008): 254–58. http://dx.doi.org/10.1111/j.1478-4408.2008.00149.x.

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50

MOKHTARI, J. "Synthesis and evaluation of a series of trisazo, monochloro-s-triazinyl (MCT) reactive dyes for cotton." Dyes and Pigments 63, no. 1 (2004): 51–63. http://dx.doi.org/10.1016/j.dyepig.2004.02.001.

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