Title: Ni supported on CaO-MgO-Al2O3 as a highly selective and stable catalyst for H2 production via the glycerol steam reforming reaction [view paper]
Journal: International Journal of Hydrogen Energy 44 (2019) 256-273.
Authors: N.D. Charisiou1, K.N. Papageridis1, L. Tzounis2, V. Sebastian3,4, S.J. Hinder5, M.A. Baker5, M. AlKetbi6, K. Polychronopoulou6, M.A. Goula1,*
Affiliations:
1Laboratory of Alternative Fuels and Environmental Catalysis (LAFEC), Department of Environmental and Pollution Control Engineering, Western Macedonia University of Applied Sciences, GR-50100, Greece
2Composite and Smart Materials Laboratory (CSML), Department of Materials Science & Engineering, University of Ioannina, GR-45110, Ioannina, Greece
3Chemical and Environmental Engineering Department & Nanoscience Institute of Aragon (INA), University of Zaragoza, Zaragoza, SP-50018, Spain
4Networking Research Center on Bioengineering, Biomaterials and Nanomedicine, CIBERBBN, 28029 Madrid, Spain
5The Surface Analysis Laboratory, Faculty of Engineering and Physical Sciences, University of Surrey, Guildford, GU2 4DL, UK
6Department of Mechanical Engineering, Khalifa University of Science and Technology, Abu Dhabi, P.O. Box 127788, UAE
ABSTRACT
A comparative study of the GSR performance for Ni/CaO-MgO-Al2O3 and Ni/Al2O3 catalysts is reported. Catalysts were synthesized applying the wet impregnation method at a constant metal loading (8 wt. %). Synthesized samples were characterized by N2 adsorption/ desorption, ICP, BET, XRD, NH3-TPD, CO2-TPD, H2-TPR, XPS and TEM, STEM-HAADF and EDS. The carbon deposited on their surface under reaction conditions was characterized by TPO, Raman and TEM. It was proven that the use of CaO-MgO as alumina modifiers leads to smaller nickel species crystallite size, increased basicity and surface amount of Ni0 phase. Thus, it increases the conversion to gaseous products favoring H2 and CO2 production to the detriment of CO formation, by enhancing the water gas-shift (WGS) reaction. No liquid products were produced by the Ni/modAl catalyst over 550oC, whereas time on stream results confirmed that deactivation can be prevented, as apart from decreasing the amount of coke deposition the nature of carbon was altered towards less graphitic and more defective structures.