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NMR and EPR Structural Analysis and Stability Study of Inverse Vulcanized Sulfur Copolymers
[Image: see text] Sulfur copolymers with high sulfur content find a broad range of applications from Li–S batteries to catalytic processes, self-healing materials, and the synthesis of nanoparticles. Synthesis of sulfur-containing polymers via the inverse vulcanization technique gained a lot of atte...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641320/ https://www.ncbi.nlm.nih.gov/pubmed/31458588 http://dx.doi.org/10.1021/acsomega.8b00031 |
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author | Shankarayya Wadi, Vijay Kumar Jena, Kishore K. Khawaja, Shahrukh Z. Yannakopoulou, Konstantina Fardis, Michael Mitrikas, George Karagianni, Marina Papavassiliou, Georgios Alhassan, Saeed M. |
author_facet | Shankarayya Wadi, Vijay Kumar Jena, Kishore K. Khawaja, Shahrukh Z. Yannakopoulou, Konstantina Fardis, Michael Mitrikas, George Karagianni, Marina Papavassiliou, Georgios Alhassan, Saeed M. |
author_sort | Shankarayya Wadi, Vijay Kumar |
collection | PubMed |
description | [Image: see text] Sulfur copolymers with high sulfur content find a broad range of applications from Li–S batteries to catalytic processes, self-healing materials, and the synthesis of nanoparticles. Synthesis of sulfur-containing polymers via the inverse vulcanization technique gained a lot of attention due to the feasibility of the reaction to produce copolymers with high sulfur content (up to 90 wt %). However, the interplay between the cross-linker and the structure of the copolymers has not yet been fully explored. In the present work, the effect of the amount of 1,3-diisopropenyl benzene (DIB) cross-linker on the structural stability of the copolymer was thoroughly investigated. Combining X-ray diffraction and differential scanning calorimetry, we demonstrated the partial depolymerization of sulfur in the copolymer containing low amount of cross-linker (<30 wt % DIB). On the other hand, by applying NMR and electron paramagnetic resonance techniques, we have shown that increasing the cross-linker content above 50 wt % leads to the formation of radicals, which may severely degrade the structural stability of the copolymer. Thus, an optimum amount of cross-linker is essential to obtain a stable copolymer. Moreover, we were able to detect the release of H(2)S gas during the cross-linking reaction as predicted based on the abstraction of hydrogen by the sulfur radicals and therefore we emphasize the need to take appropriate precautions while implementing the inverse vulcanization reaction. |
format | Online Article Text |
id | pubmed-6641320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66413202019-08-27 NMR and EPR Structural Analysis and Stability Study of Inverse Vulcanized Sulfur Copolymers Shankarayya Wadi, Vijay Kumar Jena, Kishore K. Khawaja, Shahrukh Z. Yannakopoulou, Konstantina Fardis, Michael Mitrikas, George Karagianni, Marina Papavassiliou, Georgios Alhassan, Saeed M. ACS Omega [Image: see text] Sulfur copolymers with high sulfur content find a broad range of applications from Li–S batteries to catalytic processes, self-healing materials, and the synthesis of nanoparticles. Synthesis of sulfur-containing polymers via the inverse vulcanization technique gained a lot of attention due to the feasibility of the reaction to produce copolymers with high sulfur content (up to 90 wt %). However, the interplay between the cross-linker and the structure of the copolymers has not yet been fully explored. In the present work, the effect of the amount of 1,3-diisopropenyl benzene (DIB) cross-linker on the structural stability of the copolymer was thoroughly investigated. Combining X-ray diffraction and differential scanning calorimetry, we demonstrated the partial depolymerization of sulfur in the copolymer containing low amount of cross-linker (<30 wt % DIB). On the other hand, by applying NMR and electron paramagnetic resonance techniques, we have shown that increasing the cross-linker content above 50 wt % leads to the formation of radicals, which may severely degrade the structural stability of the copolymer. Thus, an optimum amount of cross-linker is essential to obtain a stable copolymer. Moreover, we were able to detect the release of H(2)S gas during the cross-linking reaction as predicted based on the abstraction of hydrogen by the sulfur radicals and therefore we emphasize the need to take appropriate precautions while implementing the inverse vulcanization reaction. American Chemical Society 2018-03-20 /pmc/articles/PMC6641320/ /pubmed/31458588 http://dx.doi.org/10.1021/acsomega.8b00031 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Shankarayya Wadi, Vijay Kumar Jena, Kishore K. Khawaja, Shahrukh Z. Yannakopoulou, Konstantina Fardis, Michael Mitrikas, George Karagianni, Marina Papavassiliou, Georgios Alhassan, Saeed M. NMR and EPR Structural Analysis and Stability Study of Inverse Vulcanized Sulfur Copolymers |
title | NMR and EPR Structural Analysis and Stability Study
of Inverse Vulcanized Sulfur Copolymers |
title_full | NMR and EPR Structural Analysis and Stability Study
of Inverse Vulcanized Sulfur Copolymers |
title_fullStr | NMR and EPR Structural Analysis and Stability Study
of Inverse Vulcanized Sulfur Copolymers |
title_full_unstemmed | NMR and EPR Structural Analysis and Stability Study
of Inverse Vulcanized Sulfur Copolymers |
title_short | NMR and EPR Structural Analysis and Stability Study
of Inverse Vulcanized Sulfur Copolymers |
title_sort | nmr and epr structural analysis and stability study
of inverse vulcanized sulfur copolymers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641320/ https://www.ncbi.nlm.nih.gov/pubmed/31458588 http://dx.doi.org/10.1021/acsomega.8b00031 |
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