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Pyrolysis of Porous Organic Polymers under a Chlorine Atmosphere to Produce Heteroatom-Doped Microporous Carbons

Three types of cross-linked porous organic polymers (either oxygen-, nitrogen-, or sulfur-doped) were carbonized under a chlorine atmosphere to obtain chars in the form of microporous heteroatom-doped carbons. The studied organic polymers constitute thermosetting resins obtained via sol-gel polycond...

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Autores principales: Kiciński, Wojciech, Dyjak, Sławomir, Gratzke, Mateusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232777/
https://www.ncbi.nlm.nih.gov/pubmed/34203962
http://dx.doi.org/10.3390/molecules26123656
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author Kiciński, Wojciech
Dyjak, Sławomir
Gratzke, Mateusz
author_facet Kiciński, Wojciech
Dyjak, Sławomir
Gratzke, Mateusz
author_sort Kiciński, Wojciech
collection PubMed
description Three types of cross-linked porous organic polymers (either oxygen-, nitrogen-, or sulfur-doped) were carbonized under a chlorine atmosphere to obtain chars in the form of microporous heteroatom-doped carbons. The studied organic polymers constitute thermosetting resins obtained via sol-gel polycondensation of resorcinol and five-membered heterocyclic aldehydes (either furan, pyrrole, or thiophene). Carbonization under highly oxidative chlorine (concentrated and diluted Cl(2) atmosphere) was compared with pyrolysis under an inert helium atmosphere. All pyrolyzed samples were additionally annealed under NH(3). The influence of pyrolysis and additional annealing conditions on the carbon materials’ porosity and chemical composition was elucidated.
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spelling pubmed-82327772021-06-26 Pyrolysis of Porous Organic Polymers under a Chlorine Atmosphere to Produce Heteroatom-Doped Microporous Carbons Kiciński, Wojciech Dyjak, Sławomir Gratzke, Mateusz Molecules Article Three types of cross-linked porous organic polymers (either oxygen-, nitrogen-, or sulfur-doped) were carbonized under a chlorine atmosphere to obtain chars in the form of microporous heteroatom-doped carbons. The studied organic polymers constitute thermosetting resins obtained via sol-gel polycondensation of resorcinol and five-membered heterocyclic aldehydes (either furan, pyrrole, or thiophene). Carbonization under highly oxidative chlorine (concentrated and diluted Cl(2) atmosphere) was compared with pyrolysis under an inert helium atmosphere. All pyrolyzed samples were additionally annealed under NH(3). The influence of pyrolysis and additional annealing conditions on the carbon materials’ porosity and chemical composition was elucidated. MDPI 2021-06-15 /pmc/articles/PMC8232777/ /pubmed/34203962 http://dx.doi.org/10.3390/molecules26123656 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kiciński, Wojciech
Dyjak, Sławomir
Gratzke, Mateusz
Pyrolysis of Porous Organic Polymers under a Chlorine Atmosphere to Produce Heteroatom-Doped Microporous Carbons
title Pyrolysis of Porous Organic Polymers under a Chlorine Atmosphere to Produce Heteroatom-Doped Microporous Carbons
title_full Pyrolysis of Porous Organic Polymers under a Chlorine Atmosphere to Produce Heteroatom-Doped Microporous Carbons
title_fullStr Pyrolysis of Porous Organic Polymers under a Chlorine Atmosphere to Produce Heteroatom-Doped Microporous Carbons
title_full_unstemmed Pyrolysis of Porous Organic Polymers under a Chlorine Atmosphere to Produce Heteroatom-Doped Microporous Carbons
title_short Pyrolysis of Porous Organic Polymers under a Chlorine Atmosphere to Produce Heteroatom-Doped Microporous Carbons
title_sort pyrolysis of porous organic polymers under a chlorine atmosphere to produce heteroatom-doped microporous carbons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232777/
https://www.ncbi.nlm.nih.gov/pubmed/34203962
http://dx.doi.org/10.3390/molecules26123656
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