Preparation and characterization of activated CMK-1 with Zn and Ni species applied in hydrogen storage

Summary The aim of this work is to prepare CMK‐1 modified with Zn and Ni in order to improve its capacity in hydrogen storage. The approach that we have followed includes synthesis of nanostructures with the experimental study of its adsorption capacity and storage properties. We have shown that CMK...

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Published inInternational journal of energy research Vol. 39; no. 7; pp. 941 - 953
Main Authors Juárez, Juliana M., Gómez, Marcos B., Anunziata, Oscar A.
Format Journal Article
LanguageEnglish
Published Bognor Regis Blackwell Publishing Ltd 10.06.2015
Hindawi Limited
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Summary:Summary The aim of this work is to prepare CMK‐1 modified with Zn and Ni in order to improve its capacity in hydrogen storage. The approach that we have followed includes synthesis of nanostructures with the experimental study of its adsorption capacity and storage properties. We have shown that CMK‐1 ordered porous carbon modified with metals is a promising material for hydrogen storage. The incorporation of metals was performed by wetness impregnation. The samples were characterized by X‐ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscope, transmission electron microscopy, X‐ray photoelectron spectroscopy, and Brunauer–Emmett–Teller methods. The CMK‐1 modified with Zn showed the highest H2 uptake at 77 K and at low and high pressure (1.5 and 4.4 wt.% at 1 and 10 bar, respectively). The introduction of Ni into CMK‐1 does not increase hydrogen storage capacity at low pressure. However, at a higher pressure (10 bars), Ni‐CMK‐1 displays improved results in hydrogen uptake compared with those of CMK‐1 pristine, 2.4 and 2.1 wt.%, respectively. Copyright © 2015 John Wiley & Sons, Ltd. Scheme for the proposed mechanism of interaction between metal‐CMK‐1 and hydrogen.
Bibliography:Supporting info item
ark:/67375/WNG-T2JGVGGM-3
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ArticleID:ER3298
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0363-907X
1099-114X
DOI:10.1002/er.3298