Journal
CATALYSIS TODAY
Volume 207, Issue -, Pages 13-20Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.cattod.2012.09.017
Keywords
Co-precipitation; Wet impregnation; Nickel catalyst; Diesel steam reforming
Funding
- National Science & Engineering Research Council of Canada (NSERC) Solid Oxide Fuel Cells Strategic Research Network
- Government of Canada
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gamma-Al2O3 supported Ni-Al spinel catalysts, prepared by co-precipitation and wet impregnation, were produced, analysed and tested on commercial diesel steam reforming. The study of the preparation method's effect on the catalytic activity, builds on a previously patented Ni-Al spinel (NiAl2O4) catalyst supported on alumina (Al2O3) and yttria-stabilized zirconia (YSZ). This non-noble metal-based NiAl2O4/Al2O3-YSZ catalyst demonstrated high activity for commercial diesel and biodiesel steam reforming. Diesel steam reforming experiments were performed in a fixed-bed reactor setup, with a proprietary diesel-water emulsion mixture at 760 degrees C. The two tested catalytic formulations yielded the same overall conversion while the products obtained were significantly different. Thus, the catalyst produced via the co-precipitation method (Copr) (a) suffered rapid deactivation from carbon deposition; (b) produced 5 times more methane than the catalyst produced via the wet impregnation method (Impr) and (c) showed a decreasing hydrogen production. The Impr catalyst exhibited a higher stability for diesel steam reforming with no signs of carbon formation or activity loss. The difference between Impr and Copr catalyst activities is related to the Ni-aluminates dispersion: located on the surface for the Impr catalyst, whereas located in the bulk of the Copr catalyst. In order to correlate their activities to their physicochemical properties, both new catalytic formulations presented in this work were characterized before and after steam reforming tests, using scanning electron microscopy (SEM), X-ray diffraction (XRD) as well as temperature programmed reduction (TPR). (C) 2012 Elsevier B. V. All rights reserved.
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