Back to Search Start Over

NiCe/γ-Al2O3 coated onto cordierite monoliths applied to Oxidative Dehydrogenation of Ethane (ODE).

Authors :
Brussino, P.
Bortolozzi, J.P
Milt, V.G.
Banús, E.D.
Ulla, M.A.
Source :
Catalysis Today. Sep2016, Vol. 273, p259-265. 7p.
Publication Year :
2016

Abstract

The present work investigates the preparation of NiCe/γ-Al 2 O 3 coated cordierite monoliths for oxidative dehydrogenation of ethane (ODE) reaction through a two steps procedure: the primer deposition of a γ-Al 2 O 3 coating consisting in a mixture of micro and nanoparticles via the washcoating method and the latter incorporation of the active phase by impregnation. Moreover, a modification in these two steps was made: the suppression of some calcination steps to save energy in the manufacture process. The structured catalysts, named as Ni(X)Ce(Y)-M, where X = 13 or 19 wt%. Ni and Y = 5 or 8 wt%. Ce respectively, with respect to the alumina loading, were characterized by SEM/EDX, XRD, FTIR, LRS and XPS, and their catalytic activity was tested in the ODE reaction. Furthermore, their mechanical resistance to vibration was studied. Similar results corresponding to the un-promoted system are also presented for comparison. It was found that the co-impregnation of nickel and cerium was affected by the suppression of some calcinations: a preferential absorption of Ce rather than Ni occurred, generating at the end a catalytic coating with a higher Ce/Ni ratio than that of the precursor solution and a lower Ni loading than that of Ni(13)-M. On the other side, in the NiCe-based catalysts the properties of the active sites remained the same despite the increment in the active phase, at a fixed Ce/Ni nominal atomic ratio of 0.17. In the case of the Ni(19)Ce(8)-M system, although the Ni/Al atomic ratios were found lower than those of the nominal ones by EDX and XPS and ethylene selectivity decayed, ethane conversion resulted markedly higher, leading to an improved ethylene yield. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09205861
Volume :
273
Database :
Academic Search Index
Journal :
Catalysis Today
Publication Type :
Academic Journal
Accession number :
115977521
Full Text :
https://doi.org/10.1016/j.cattod.2016.02.055