Trizane functionalized inverse vulcanized copolymer prepared using one-pot method

Trizane functionalized inverse vulcanized copolymer prepared using one-pot method

ALI SHAAN MANZOOR Ghumman, RASHID Shamsuddin, MUHAMMAD Ayoub, THE Men Qi

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Abstract. Inverse vulcanized copolymers have emerged as a promising adsorbent for mercury remediation due the presence of S-S chain in their structure. However, these adsorbents are still suffering from low selectivity, adsorption capacity due to their hydrophobic nature and less functionality. Herein we reported the synthesis of Trizane functionalized inverse vulcanized copolymer using one-pot method by reacting sulfur and 2,4,6-triallyl-1,3,5-trizane and DIB (crosslinker) at 163 oC. Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) were used to characterize the resultant copolymers. FTIR spectra of all copolymers shows the absence of C=C bond and C-C=C as there were no peak observed at 1660 and 3005 cm-1. TGA revealed that the produced copolymers are thermally stable and only started to degrade at 200 oC. It can be concluded here that TAC and DIB can react successfully with sulfur to form trizane containing copolymer.

Keywords
Heavy Metal Removal, Trizane, Inverse Vulcanized Copolymers, Sulfur Enriched Polymers

Published online 5/20/2023, 6 pages
Copyright © 2023 by the author(s)
Published under license by Materials Research Forum LLC., Millersville PA, USA

Citation: ALI SHAAN MANZOOR Ghumman, RASHID Shamsuddin, MUHAMMAD Ayoub, THE Men Qi, Trizane functionalized inverse vulcanized copolymer prepared using one-pot method, Materials Research Proceedings, Vol. 29, pp 66-71, 2023

DOI: https://doi.org/10.21741/9781644902516-9

The article was published as article 9 of the book Sustainable Processes and Clean Energy Transition

Content from this work may be used under the terms of the Creative Commons Attribution 3.0 license. Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI.

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