4.6 Article

Catalysts Based on Strontium Titanate Doped with Ni/Co/Cu for Dry Reforming of Methane

Journal

MATERIALS
Volume 14, Issue 23, Pages -

Publisher

MDPI
DOI: 10.3390/ma14237227

Keywords

dry reforming of methane; SrTiO3; nickel catalyst

Funding

  1. EU [POWR.03.02.00-00-I004/16]

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Two series of strontium titanates doped with Ni, Co, or Cu were prepared using the wet chemical method, with different stoichiometries. These materials were characterized for their structural properties, possibility of reduction and oxidation reactions, and catalytic properties. Ni-doped samples showed the highest catalytic activity in dry reforming of methane reaction, while Co and Cu-doped samples had minimal catalytic effects. Additionally, a decrease in methane conversion with increasing calcination temperature was observed for Ni-doped strontium titanates.
Two series of strontium titanates doped with Ni, Co, or Cu with general formula of SrTi1-xMexO3 for Sr-stoichiometric and Sr0.95Ti1-xMexO3 for Sr-non-stoichiometric materials (where Me = Ni, Co or Cu and x were 0.02 and 0.06) were obtained by the wet chemical method. The samples were calcinated at 900, 950, and 1050 degrees C and characterized in terms of their structural properties (XRD), the possibility of undergoing the reduction and oxidation reactions (TPR/TPOx), and catalytic properties. All obtained materials were multiphase and although the XRD analysis does not confirm the presence of Ni, Co, and Cu oxides (with one exception for Cu-doped sample), the TPR/TPOx profiles show reduction peaks that can be attributed to the reduction of these oxides which may at first appear in an amorphous form. Catalytic tests in dry reforming of methane reaction showed that the highest catalytic activity was achieved for Ni-doped materials (up to 90% of CH4 conversion) while Co and Cu-doped samples showed only a very slight catalytic effect. Additionally, the decrease in methane conversion with an increasing calcination temperature was observed for Ni-doped strontium titanates.

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