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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Bibliographic Details
Published in:International journal of hydrogen energy Vol. 36; no. 13; pp. 7937 - 7943
Main Authors: Armandi, M., Bonelli, B., Cho, K., Ryoo, R., Garrone, E.
Format: Journal Article Conference Proceeding
Language:English
Published: Kidlington Elsevier Ltd 01-07-2011
Elsevier
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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].
Bibliography:ObjectType-Article-2
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content type line 23
ISSN:0360-3199
1879-3487
DOI:10.1016/j.ijhydene.2011.01.049