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Carbazole-functionalized hyper-cross-linked polymers for CO(2) uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole
To systematically explore the effects of the synthesis conditions on the porosity of hyper-cross-linked polymers (HCPs), a series of 9-phenylcarbazole (9-PCz) HCPs (P1–P11) has been made by changing the molar ratio of cross-linker to monomer, the reaction temperature T(1), the used amount of catalys...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902873/ https://www.ncbi.nlm.nih.gov/pubmed/31839831 http://dx.doi.org/10.3762/bjoc.15.279 |
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author | Fang, Dandan Li, Xiaodong Zou, Meishuai Guo, Xiaoyan Zhang, Aijuan |
author_facet | Fang, Dandan Li, Xiaodong Zou, Meishuai Guo, Xiaoyan Zhang, Aijuan |
author_sort | Fang, Dandan |
collection | PubMed |
description | To systematically explore the effects of the synthesis conditions on the porosity of hyper-cross-linked polymers (HCPs), a series of 9-phenylcarbazole (9-PCz) HCPs (P1–P11) has been made by changing the molar ratio of cross-linker to monomer, the reaction temperature T(1), the used amount of catalyst and the concentration of reactants. Fourier transform infrared spectroscopy was utilized to characterize the structure of the obtained polymers. The TG analysis of the HCPs showed good thermal stability. More importantly, a comparative study on the porosity revealed that: the molar ratio of cross-linker to monomer was the main influence factor of the BET specific surface area. Increasing the reaction temperature T(1) or changing the used amount of catalyst could improve the total pore volume greatly but sacrificed a part of the BET specific surface area. Fortunately changing the concentration of reactants could remedy this situation. Slightly changing the concentration of reactants could simultaneously obtain a high surface area and a high total pore volume. The BET specific surface areas of P3 was up to 769 m(2) g(−1) with narrow pore size distribution and the CO(2) adsorption capacity of P11 was up to 52.4 cm(3) g(−1) (273 K/1.00 bar). |
format | Online Article Text |
id | pubmed-6902873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-69028732019-12-13 Carbazole-functionalized hyper-cross-linked polymers for CO(2) uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole Fang, Dandan Li, Xiaodong Zou, Meishuai Guo, Xiaoyan Zhang, Aijuan Beilstein J Org Chem Full Research Paper To systematically explore the effects of the synthesis conditions on the porosity of hyper-cross-linked polymers (HCPs), a series of 9-phenylcarbazole (9-PCz) HCPs (P1–P11) has been made by changing the molar ratio of cross-linker to monomer, the reaction temperature T(1), the used amount of catalyst and the concentration of reactants. Fourier transform infrared spectroscopy was utilized to characterize the structure of the obtained polymers. The TG analysis of the HCPs showed good thermal stability. More importantly, a comparative study on the porosity revealed that: the molar ratio of cross-linker to monomer was the main influence factor of the BET specific surface area. Increasing the reaction temperature T(1) or changing the used amount of catalyst could improve the total pore volume greatly but sacrificed a part of the BET specific surface area. Fortunately changing the concentration of reactants could remedy this situation. Slightly changing the concentration of reactants could simultaneously obtain a high surface area and a high total pore volume. The BET specific surface areas of P3 was up to 769 m(2) g(−1) with narrow pore size distribution and the CO(2) adsorption capacity of P11 was up to 52.4 cm(3) g(−1) (273 K/1.00 bar). Beilstein-Institut 2019-11-26 /pmc/articles/PMC6902873/ /pubmed/31839831 http://dx.doi.org/10.3762/bjoc.15.279 Text en Copyright © 2019, Fang et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Fang, Dandan Li, Xiaodong Zou, Meishuai Guo, Xiaoyan Zhang, Aijuan Carbazole-functionalized hyper-cross-linked polymers for CO(2) uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole |
title | Carbazole-functionalized hyper-cross-linked polymers for CO(2) uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole |
title_full | Carbazole-functionalized hyper-cross-linked polymers for CO(2) uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole |
title_fullStr | Carbazole-functionalized hyper-cross-linked polymers for CO(2) uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole |
title_full_unstemmed | Carbazole-functionalized hyper-cross-linked polymers for CO(2) uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole |
title_short | Carbazole-functionalized hyper-cross-linked polymers for CO(2) uptake based on Friedel–Crafts polymerization on 9-phenylcarbazole |
title_sort | carbazole-functionalized hyper-cross-linked polymers for co(2) uptake based on friedel–crafts polymerization on 9-phenylcarbazole |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902873/ https://www.ncbi.nlm.nih.gov/pubmed/31839831 http://dx.doi.org/10.3762/bjoc.15.279 |
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