Study of hydrogen physisorption on nanoporous carbon materials of different origin
Hydrogen adsorption capabilities of different nanoporous carbon, i.e. amorphous carbons obtained by chemical activation (with KOH) of a sucrose-derived char previously ground by ball milling and carbon replicas of NH 4-Y and mesocellular silica foam (MSU-F) inorganic templates, were measured and cor...
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Published in: | International journal of hydrogen energy Vol. 36; no. 13; pp. 7937 - 7943 |
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Main Authors: | , , , , |
Format: | Journal Article Conference Proceeding |
Language: | English |
Published: |
Kidlington
Elsevier Ltd
01-07-2011
Elsevier |
Subjects: | |
Online Access: | Get full text |
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Summary: | Hydrogen adsorption capabilities of different nanoporous carbon, i.e. amorphous carbons obtained by chemical activation (with KOH) of a sucrose-derived char previously ground by ball milling and carbon replicas of NH
4-Y and mesocellular silica foam (MSU-F) inorganic templates, were measured and correlated to their porous properties. The porous texture of the prepared carbon materials was studied by means of N
2 and CO
2 adsorption isotherms measured at −196
°C and 0
°C, respectively. Comparison with nanoporous carbons obtained without pre-grinding the sucrose-derived char
[12] shows that the ball milling procedure favours the formation of highly microporous carbon materials even at low KOH loadings, having a beneficial effect of the interaction between the char particles and the activating agent. Hydrogen adsorption isotherms at −196
°C were measured in the 0.0–1.1
MPa pressure range, and a maximum hydrogen adsorption capacity of 3.4 wt.% was obtained for the amorphous carbon prepared by activation at 900
°C with a KOH/char weight ratio of 2. Finally, a linear dependence was found between the maximum hydrogen uptake at 1.1
MPa and the samples microporous volume, confirming previous results obtained at −196
°C and sub-atmospheric pressure
[12]. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0360-3199 1879-3487 |
DOI: | 10.1016/j.ijhydene.2011.01.049 |