Hierarchical N‐doped carbons from designed N‐rich polymer: Adsorbents with a record‐high capacity for desulfurization
The removal of 4,6‐dimethyldibenzothiophene is quite challenging in petroleum refining process. Adsorptive desulfurization is an efficient technique but the capacities and/or poor stability of current adsorbents need to be improved. Here, the fabrication of hierarchical N‐doped carbons (NCs) derived...
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Published in | AIChE journal Vol. 64; no. 11; pp. 3786 - 3793 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.11.2018
American Institute of Chemical Engineers |
Subjects | |
Online Access | Get full text |
ISSN | 0001-1541 1547-5905 |
DOI | 10.1002/aic.16357 |
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Summary: | The removal of 4,6‐dimethyldibenzothiophene is quite challenging in petroleum refining process. Adsorptive desulfurization is an efficient technique but the capacities and/or poor stability of current adsorbents need to be improved. Here, the fabrication of hierarchical N‐doped carbons (NCs) derived from carbonizing the polymerization of 2,4,6‐tris(chloromethyl)mesitylene and p‐phenylenediamine is reported. The results show that the NCs have developed micropores (0.34–0.93 cm3 g−1) and mesopores (0.15–0.47 cm3 g−1), and their surfaces have abundant pyrrole‐like/graphitic N and topological defects and vacancies, and high cycle stability (6 cycles). The typical adsorbent NC‐700 shows a record‐high capacity of 2.91 mmol g−1 under ambient conditions. The computational results show that the doped N is capable of promoting adsorptive strength by 0.055–0.178 eV. In conclusion, the obtained materials exhibit excellent performance for deep desulfurization, and this work may open up new avenues for the development of efficient adsorbents. © 2018 American Institute of Chemical Engineers AIChE J, 64: 3786–3793, 2018 |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 0001-1541 1547-5905 |
DOI: | 10.1002/aic.16357 |