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Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones
A series of wholly aromatic polyketones bearing benzimidazolone moieties (PK-BI) were synthesized via N–C coupling polycondensation. Calcium carbonate coupled with potassium carbonate was used for the first time to achieve a high molecular weight, with T(g) of the polymer as high as 299 °C. The poly...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694728/ https://www.ncbi.nlm.nih.gov/pubmed/35423105 http://dx.doi.org/10.1039/d0ra09831k |
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author | Gu, Xinming Wang, Zhipeng Wang, Honghua Zhou, Guangyuan Zhou, Yanmin |
author_facet | Gu, Xinming Wang, Zhipeng Wang, Honghua Zhou, Guangyuan Zhou, Yanmin |
author_sort | Gu, Xinming |
collection | PubMed |
description | A series of wholly aromatic polyketones bearing benzimidazolone moieties (PK-BI) were synthesized via N–C coupling polycondensation. Calcium carbonate coupled with potassium carbonate was used for the first time to achieve a high molecular weight, with T(g) of the polymer as high as 299 °C. The polymer structure was confirmed by solid state (13)C NMR and FT-IR. The thermal stability of wholly aromatic polyketones with a benzimidazolone unit in the main chain was significantly improved, being higher than those of PEEKs and other amorphous PAEKs, proved by thermogravimetric analysis (TGA) and derivative thermogravimetric (DTG) analysis. The degradation activation energy (E(k)) values estimated by Flynn–Wall–Ozawa (FWO) and Kissinger methods were 260.33 kJ mol(−1) and 282.57 kJ mol(−1), respectively, which are higher than those of PEEKs. |
format | Online Article Text |
id | pubmed-8694728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86947282022-04-13 Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones Gu, Xinming Wang, Zhipeng Wang, Honghua Zhou, Guangyuan Zhou, Yanmin RSC Adv Chemistry A series of wholly aromatic polyketones bearing benzimidazolone moieties (PK-BI) were synthesized via N–C coupling polycondensation. Calcium carbonate coupled with potassium carbonate was used for the first time to achieve a high molecular weight, with T(g) of the polymer as high as 299 °C. The polymer structure was confirmed by solid state (13)C NMR and FT-IR. The thermal stability of wholly aromatic polyketones with a benzimidazolone unit in the main chain was significantly improved, being higher than those of PEEKs and other amorphous PAEKs, proved by thermogravimetric analysis (TGA) and derivative thermogravimetric (DTG) analysis. The degradation activation energy (E(k)) values estimated by Flynn–Wall–Ozawa (FWO) and Kissinger methods were 260.33 kJ mol(−1) and 282.57 kJ mol(−1), respectively, which are higher than those of PEEKs. The Royal Society of Chemistry 2021-01-29 /pmc/articles/PMC8694728/ /pubmed/35423105 http://dx.doi.org/10.1039/d0ra09831k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Gu, Xinming Wang, Zhipeng Wang, Honghua Zhou, Guangyuan Zhou, Yanmin Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones |
title | Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones |
title_full | Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones |
title_fullStr | Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones |
title_full_unstemmed | Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones |
title_short | Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones |
title_sort | synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694728/ https://www.ncbi.nlm.nih.gov/pubmed/35423105 http://dx.doi.org/10.1039/d0ra09831k |
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