Tuning catalytic performances of cobalt catalysts for clean hydrogen generation via variation of the type of carbon support and catalyst post-treatment temperature

Multi-walled carbon nanotubes, three types of activated carbons, single wall carbon nanotube and reduced graphene oxides were used to synthesize nano-sized Co catalysts for H2 preparation via NH3 decomposition. Catalyst samples were characterized by number of techniques such as N2 physisorption, X-r...

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Veröffentlicht in:International journal of hydrogen energy 2014-10, Vol.39 (31), p.17573-17582
Hauptverfasser: Zhang, Hui, Alhamed, Yahia A., Al-Zahrani, Abdulrahim, Daous, Mohammad, Inokawa, Hitoshi, Kojima, Yoshitsugu, Petrov, Lachezar A.
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Sprache:eng
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Zusammenfassung:Multi-walled carbon nanotubes, three types of activated carbons, single wall carbon nanotube and reduced graphene oxides were used to synthesize nano-sized Co catalysts for H2 preparation via NH3 decomposition. Catalyst samples were characterized by number of techniques such as N2 physisorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopes (XPS), Transmission electron microscopy (TEM), CO chemisorption, temperature-programmed reduction (H2-TPR) and temperature-programmed desorption (N2-TPD). The catalytic activities of the studied catalysts for H2 production via NH3 decomposition were measured in a fixed-bed micro-reactor. Co catalyst supported on multi-wall carbon nanotubes has shown the highest catalytic activity. The Co particles size was significantly affected by the variation of the post-treatment temperature. The Co particles size in the range of 4.7–64.8 nm can be effectively controlled by varying post-treatment temperature between 230 and 700 °C. The maximum TOF of NH3 decomposition was registered on cobalt catalyst post-treated at 600 °C. [Display omitted] •Catalytic activity was much depended on the support properties of carbon materials.•Post-treatment temperature of catalysts has a great effect on cobalt particle size.•Cobalt catalyst supported on MWCNTs exhibited the best catalytic performance.
ISSN:0360-3199
1879-3487
DOI:10.1016/j.ijhydene.2014.07.183