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Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole

Using organic salts as precursors, heteroatom-doped porous carbons prepared by in situ activation had surface areas of up to 2703 m(2) g(−1). These porous carbons have been found to be effective adsorbents for adsorption of sulfamethoxazole (SMX) from water. The effects of precursor type, calcinatio...

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Detalles Bibliográficos
Autores principales: Zheng, Wei, Shi, Yawei, Liu, Guozhu, Zhao, Bin, Wang, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047560/
https://www.ncbi.nlm.nih.gov/pubmed/35494670
http://dx.doi.org/10.1039/c9ra09269b
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author Zheng, Wei
Shi, Yawei
Liu, Guozhu
Zhao, Bin
Wang, Liang
author_facet Zheng, Wei
Shi, Yawei
Liu, Guozhu
Zhao, Bin
Wang, Liang
author_sort Zheng, Wei
collection PubMed
description Using organic salts as precursors, heteroatom-doped porous carbons prepared by in situ activation had surface areas of up to 2703 m(2) g(−1). These porous carbons have been found to be effective adsorbents for adsorption of sulfamethoxazole (SMX) from water. The effects of precursor type, calcination temperature, pH and ionic strength as well as the regeneration properties were investigated. The different adsorption performances of porous carbons were related to their textural structures and chemical properties, and a reasonable adsorption mechanism was proposed. The effects of different heteroatom functional groups on the adsorption of SMX were also analyzed in detail. For potential practical applications, the performance of the porous carbon for removing SMX from real water was also tested.
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spelling pubmed-90475602022-04-28 Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole Zheng, Wei Shi, Yawei Liu, Guozhu Zhao, Bin Wang, Liang RSC Adv Chemistry Using organic salts as precursors, heteroatom-doped porous carbons prepared by in situ activation had surface areas of up to 2703 m(2) g(−1). These porous carbons have been found to be effective adsorbents for adsorption of sulfamethoxazole (SMX) from water. The effects of precursor type, calcination temperature, pH and ionic strength as well as the regeneration properties were investigated. The different adsorption performances of porous carbons were related to their textural structures and chemical properties, and a reasonable adsorption mechanism was proposed. The effects of different heteroatom functional groups on the adsorption of SMX were also analyzed in detail. For potential practical applications, the performance of the porous carbon for removing SMX from real water was also tested. The Royal Society of Chemistry 2020-01-08 /pmc/articles/PMC9047560/ /pubmed/35494670 http://dx.doi.org/10.1039/c9ra09269b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zheng, Wei
Shi, Yawei
Liu, Guozhu
Zhao, Bin
Wang, Liang
Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole
title Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole
title_full Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole
title_fullStr Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole
title_full_unstemmed Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole
title_short Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole
title_sort heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047560/
https://www.ncbi.nlm.nih.gov/pubmed/35494670
http://dx.doi.org/10.1039/c9ra09269b
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