4.8 Article

Hydrogen production by glycerol steam reforming catalyzed by Ni-promoted Fe/Mg-bearing metallurgical wastes

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 219, Issue -, Pages 183-193

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcatb.2017.07.039

Keywords

Industrial waste; Nickel catalyst; Solid-state impregnation; Glycerol steam reforming; Catalyst stability

Funding

  1. Fonds de recherche du Quebec - Nature et technologies (FRQNT)
  2. Natural Sciences and Engineering Research Council of Canada (NSERC)

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The present work investigates the catalytic potential of a Ni-promoted Fe/Mg containing metallurgical waste for sustainable hydrogen production by glycerol steam reforming (GSR). The catalyst (Ni-UGS) was prepared through solid-state impregnation of Ni into the structure of metallurgical residue. Ni incorporation led to the formation of (Ni,Mg)O solid solution, (NiFe2O4) and/or a nickel iron mixed oxide (NixFe1-xO). GSR performed in a fixed bed reactor at T= 580 degrees C, P = 1 atm, steam to carbon ratio (S/C) of 3, and gas hourly space velocity (GHSV) of 20,600 cm(3) (STP)gcat(-1) h(-1) led to a glycerol conversion to gaseous (X-g) of 87%, H-2 yield (Y-H2) of 79%, and H-2/CO molar ratio of 5.5. The catalytic performance of Ni-UGS containing 11.7 wt.% Ni was found to be superior to that of an alumina supported Ni-based commercial steam reforming catalyst with higher Ni content (29.8 wt.%): X-g = 86%, Y-H2 = 71%, and H-2/CO molar ratio of 4.1. A stable performance during 48 h on stream was also obtained by using the Ni-UGS catalyst. Characterization of the used catalyst confirmed the low formation rate (similar to 2.7 mgcoke g(cat)(-1) h(-1)) of filamentous type carbon. The promising obtained results were mainly attributed to (i) superior dispersion of Ni particles due to the formation of (Ni,Mg)O solid solution and (ii) the presence of active magnesium and iron oxide species (e.g., MgO, Fe3O4, MgFe2O4 and (MgO)(FeO) solid solution) in the Ni-UGS catalyst which stimulate the water gas shift reaction and coke gasification. Regeneration by an oxidative treatment of the used catalyst in air was examined and analysis of the regenerated catalyst revealed complete coke removal together with recovery of initial crystalline phases. (C) 2017 Elsevier B.V. All rights reserved.

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