Microwave assisted synthesis of some azo disperse dyes part 2: Eco-friendly dyeing of polyester fabrics by using microwave irradiation

Mohamed Osman Saleh; Morsy Ahmed El-Apasery; Abdelhaleem Mostafa Hussein; Abu-Bakr Abdelhady El-Adasy; Magda Mohamed Kamel

doi:10.5155/eurjchem.12.1.64-68.2059

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Published: Mar 31, 2021

DOI: https://doi.org/10.5155/eurjchem.12.1.64-68.2059

Keywords:

Disperse dyes, Polyester fabrics, Microwave heating, Fastness properties, Dyeing performance, Conventional dyeing

Section

Research Article

Issue

Vol. 12 No. 1 (2021): March 2021

Dates

Received 2021-01-04
Accepted 2021-02-20
Published 2021-03-31

Mohamed Osman Saleh

Department of Chemistry, Faculty of Science, Al Azhar University, Assiut 71524, Egypt

https://orcid.org/0000-0001-9111-6006

Morsy Ahmed El-Apasery

Dyeing, Printing and Auxiliaries Department, Textile Industries Research Division, National Research Centre, Cairo 12622, Egypt

https://orcid.org/0000-0002-4686-2007

Abdelhaleem Mostafa Hussein

Department of Chemistry, Faculty of Science, Al Azhar University, Assiut 71524, Egypt

https://orcid.org/0000-0003-2496-2696

Abu-Bakr Abdelhady El-Adasy

Department of Chemistry, Faculty of Science, Al Azhar University, Assiut 71524, Egypt

https://orcid.org/0000-0002-5828-4750

Magda Mohamed Kamel

Dyeing, Printing and Auxiliaries Department, Textile Industries Research Division, National Research Centre, Cairo 12622, Egypt

https://orcid.org/0000-0002-7772-9970

Abstract

This study aimed to use microwave irradiation as a green technique, not only to enhance the dyeing efficiency of disperse-colored polyester fabrics, but also to conserve resources and minimize the environmental effects. Arylazopyrazolopyrimidinones dyes 1-9 were applied to polyester fabrics at 2% shade using conventional method and microwave at 100 °C. Both the color intensity expressed as dye absorption and the fastness characteristics of the dyed fabric were investigated. The K/S values are increased by increasing the time of irradiation from 10-60 minutes. The dyed substrate displayed good light fastness, and very good fastness levels to rubbing, perspiration washing, and sublimation, respectively.

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How to Cite

(1)

Saleh, M. O.; El-Apasery, M. A.; Hussein, A. M.; El-Adasy, A.-B. A.; Kamel, M. M. Microwave Assisted Synthesis of Some Azo Disperse Dyes Part 2: Eco-Friendly Dyeing of Polyester Fabrics by Using Microwave Irradiation. Eur. J. Chem. 2021, 12, 64-68.

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References

[1]. Corsaro, A.; Chiacchio, U.; Pistara, V.; Romeo, G. Curr. Org. Chem. 2004, 8 (6), 511-538.
https://doi.org/10.2174/1385272043485828

[2]. de la Hoz, A.; Diaz-Ortiz, A.; Moreno, A. Chem. Soc. Rev. 2005, 34 (2), 164-178.
https://doi.org/10.1039/B411438H

[3]. Oliver Kappe, C. Chem. Soc. Rev. 2008, 37 (6), 1127-1139.
https://doi.org/10.1039/b803001b

[4]. Kappe, C. O. Chem. Soc. Rev. 2013, 42 (12), 4977-4990.
https://doi.org/10.1039/c3cs00010a

[5]. Krstenansky, J. L.; Cotterill, I. ChemInform 2000, 31 (49), 454-461.
https://doi.org/10.1002/chin.200049266

[6]. Oner, E.; Buyukakinci, Y.; Sokmen, N. Coloration. Technol. 2013, 129 (2), 125-130.
https://doi.org/10.1111/cote.12014

[7]. Haggag, K.; Hanna, H. L.; Youssef, B. M.; El-Shimy, N. S. Amer. Dyest. Rep. 1995, 84, 22-36.

[8]. Kale, M. J.; Bhat, N. V. Coloration Technol. 2011, 127 (6), 365-371.
https://doi.org/10.1111/j.1478-4408.2011.00332.x

[9]. Al-Mousawi, S. M.; El-Apasery, M. A.; Mahmoud, H. M. Molecules 2012, 17 (10), 11495-11506.
https://doi.org/10.3390/molecules171011495

[10]. Chiao-Cheng, J. H.; Reagan, B. M. Chem. Color. 1983, 15, 29-36.

[11]. Yigit, E. A.; Teker, M. Polym. Polym. Compos. 2011, 19 (8), 711-716.
https://doi.org/10.1177/096739111101900812

[12]. Al-Etaibi, A. M.; Al-Awadi, N. A.; El-Apasery, M. A.; Ibrahim, M. R. Molecules 2011, 16 (6), 5182-5193.
https://doi.org/10.3390/molecules16065182

[13]. Al-Etaibi, A. M.; El-Apasery, M. A.; Mahmoud, H. M.; Al-Awadi, N. A. Molecules 2012, 17 (4), 4266-4280.
https://doi.org/10.3390/molecules17044266

[14]. Al-Mousawi, S. M.; El-Apasery, M. A. Molecules 2012, 17 (6), 6547-6556.
https://doi.org/10.3390/molecules17066547

[15]. El-Apasery, M. A.; Al-Qalaf, F.; Almohammad, K.; Mahmoud, H. Eur. J. Chem. 2013, 4 (3), 211-215.
https://doi.org/10.5155/eurjchem.4.3.211-215.783

[16]. El-Apasery, M. A. Pol. J. Appl. Chem. 2006, 50, 75-81.

[17]. Al-Mousawi, S.; El-Apasery, M.; Elnagdi, M. Molecules 2013, 18 (9), 11033-11043.
https://doi.org/10.3390/molecules180911033

[18]. Elapasery, M.; Hussein, A.; Eladasy, A.; Saleh, M.; Kamel, M. Egypt. J. Chem. 2019, 62,1253-1259.

[19]. Ashkar, S. M.; El-Apasery, M. A.; Touma, M. M.; Elnagdi, M. H. Molecules 2012, 17 (8), 8822-8831.
https://doi.org/10.3390/molecules17088822

[20]. Al-Etaibi, A. M.; El-Apasery, M. A. Inter. J. Environ. Res. Public Health 2019, 16 (23), 4603, 1-8.
https://doi.org/10.3390/ijerph16234603

[21]. Haggag, K.; El-Molla, M.; Ahmed, K. Inter. Res. J. Pure Appl. Chem. 2015, 8 (2), 103-111.
https://doi.org/10.9734/IRJPAC/2015/17922

[22]. Al-Mousawi, S.; El-Apasery, M.; Mahmoud, H. Molecules 2013, 18 (6), 7081-7092.
https://doi.org/10.3390/molecules18067081

[23]. El-Adasy, A. A. A. M.; Kamel M. M.; Saleh, M. O.; Hussein, A. M.; El-Apasery, M. A. Inter. J. Chem. Tech. Res. 2016, 9, 31-38.

[24]. Maradiya, H., Raghav; Patel, V., Soma. J. Serb. Chem. Soc. 2001, 66 (6), 367-376.
https://doi.org/10.2298/JSC0106367M

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