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Synthesis of Hydrogenated Natural Rubber Having Epoxide Groups Using Diimide
[Image: see text] Epoxidized natural rubber (ENR) with 50% mol of epoxide groups was synthesized using performic acid generated from the reaction of formic acid/hydrogen peroxide in latex form followed by hydrogenation using diimide generated from hydrazine (N(2)H(4)) and hydrogen peroxide (H(2)O(2)...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245146/ https://www.ncbi.nlm.nih.gov/pubmed/35785283 http://dx.doi.org/10.1021/acsomega.2c01011 |
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author | Ngudsuntear, Kitnipat Limtrakul, Sunun Arayapranee, Wanvimon |
author_facet | Ngudsuntear, Kitnipat Limtrakul, Sunun Arayapranee, Wanvimon |
author_sort | Ngudsuntear, Kitnipat |
collection | PubMed |
description | [Image: see text] Epoxidized natural rubber (ENR) with 50% mol of epoxide groups was synthesized using performic acid generated from the reaction of formic acid/hydrogen peroxide in latex form followed by hydrogenation using diimide generated from hydrazine (N(2)H(4)) and hydrogen peroxide (H(2)O(2)) with boric acid (H(3)BO(3)) as a catalyst. The resulting products (hydrogenated epoxidized natural rubber, HENR) were characterized by proton nuclear magnetic resonance spectroscopy ((1)H-NMR), gel testing, transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The effects of reaction parameters such as N(2)H(4) amount, H(2)O(2) amount, H(3)BO(3) amount, gelatin amount, reaction time, and reaction temperature on the percentage of hydrogenation degree and gel content were investigated. The transmission electron micrographs of the particles confirmed a core/shell structure consisting of a highly unsaturated concentration region as the core encapsulated by a low carbon–carbon double bond concentration region as the shell, which indicated that the rubber particle seemed to be modified from the outer layer to the center of the rubber particle. Overall, the data showed that an increase in the amount of the individual chemicals, reaction time, and temperature increased the hydrogenation degree. However, a higher level of gelatin retarded an increase in the percentage of hydrogenation degree. As the hydrogenation degree increased, the gel content increased due to the ether linkage and the crosslinking reaction triggered through hydroxyl radicals. From DSC measurements, the glass transition temperatures of hydrogenated products increased above those of original rubbers. The thermal stability of hydrogenated products was improved, demonstrated by a decomposition temperature shift to a higher temperature than ENR, as shown by the results from the thermogravimetric analysis. Therefore, the hydrogenated ENR (HENR) exhibited good thermal stability, which could extend the applications of ENR in the automotive and oil industries. |
format | Online Article Text |
id | pubmed-9245146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92451462022-07-01 Synthesis of Hydrogenated Natural Rubber Having Epoxide Groups Using Diimide Ngudsuntear, Kitnipat Limtrakul, Sunun Arayapranee, Wanvimon ACS Omega [Image: see text] Epoxidized natural rubber (ENR) with 50% mol of epoxide groups was synthesized using performic acid generated from the reaction of formic acid/hydrogen peroxide in latex form followed by hydrogenation using diimide generated from hydrazine (N(2)H(4)) and hydrogen peroxide (H(2)O(2)) with boric acid (H(3)BO(3)) as a catalyst. The resulting products (hydrogenated epoxidized natural rubber, HENR) were characterized by proton nuclear magnetic resonance spectroscopy ((1)H-NMR), gel testing, transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The effects of reaction parameters such as N(2)H(4) amount, H(2)O(2) amount, H(3)BO(3) amount, gelatin amount, reaction time, and reaction temperature on the percentage of hydrogenation degree and gel content were investigated. The transmission electron micrographs of the particles confirmed a core/shell structure consisting of a highly unsaturated concentration region as the core encapsulated by a low carbon–carbon double bond concentration region as the shell, which indicated that the rubber particle seemed to be modified from the outer layer to the center of the rubber particle. Overall, the data showed that an increase in the amount of the individual chemicals, reaction time, and temperature increased the hydrogenation degree. However, a higher level of gelatin retarded an increase in the percentage of hydrogenation degree. As the hydrogenation degree increased, the gel content increased due to the ether linkage and the crosslinking reaction triggered through hydroxyl radicals. From DSC measurements, the glass transition temperatures of hydrogenated products increased above those of original rubbers. The thermal stability of hydrogenated products was improved, demonstrated by a decomposition temperature shift to a higher temperature than ENR, as shown by the results from the thermogravimetric analysis. Therefore, the hydrogenated ENR (HENR) exhibited good thermal stability, which could extend the applications of ENR in the automotive and oil industries. American Chemical Society 2022-06-13 /pmc/articles/PMC9245146/ /pubmed/35785283 http://dx.doi.org/10.1021/acsomega.2c01011 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Ngudsuntear, Kitnipat Limtrakul, Sunun Arayapranee, Wanvimon Synthesis of Hydrogenated Natural Rubber Having Epoxide Groups Using Diimide |
title | Synthesis of Hydrogenated Natural Rubber Having Epoxide
Groups Using Diimide |
title_full | Synthesis of Hydrogenated Natural Rubber Having Epoxide
Groups Using Diimide |
title_fullStr | Synthesis of Hydrogenated Natural Rubber Having Epoxide
Groups Using Diimide |
title_full_unstemmed | Synthesis of Hydrogenated Natural Rubber Having Epoxide
Groups Using Diimide |
title_short | Synthesis of Hydrogenated Natural Rubber Having Epoxide
Groups Using Diimide |
title_sort | synthesis of hydrogenated natural rubber having epoxide
groups using diimide |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245146/ https://www.ncbi.nlm.nih.gov/pubmed/35785283 http://dx.doi.org/10.1021/acsomega.2c01011 |
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