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Nickel Supported on AlCeO3 as a Highly Selective and Stable Catalyst for Hydrogen Production via the Glycerol Steam Reforming Reaction

Authors :
Nikolaos D. Charisiou
Georgios I. Siakavelas
Binlin Dou
Victor Sebastian
Steven J. Hinder
Mark A. Baker
Kyriaki Polychronopoulou
Maria A. Goula
Source :
Catalysts, Vol 9, Iss 5, p 411 (2019)
Publication Year :
2019
Publisher :
MDPI AG, 2019.

Abstract

In this study, a critical comparison between two low metal (Ni) loading catalysts is presented, namely Ni/Al2O3 and Ni/AlCeO3 for the glycerol steam reforming (GSR) reaction. The surface and bulk properties of the catalysts were evaluated using a plethora of techniques, such as N2 adsorption/desorption, Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP−AES), X-ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Microscopy / Energy Dispersive X-Ray Spectroscopy (SEM/EDX, Transmission Electron Microscopy (TEM), CO2 and NH3− Temperature Programmed Desorption (TPD), and Temperature Programmed Reduction (H2−TPR). Carbon deposited on the catalyst’s surfaces was probed using Temperature Programmed Oxidation (TPO), SEM, and TEM. It is demonstrated that Ce-modification of Al2O3 induces an increase of the surface basicity and Ni dispersion. These features lead to a higher conversion of glycerol to gaseous products (60% to 80%), particularly H2 and CO2, enhancement of WGS reaction, and a higher resistance to coke deposition. Allyl alcohol was found to be the main liquid product for the Ni/AlCeO3 catalyst, the production of which ceases over 700 °C. It is also highly significant that the Ni/AlCeO3 catalyst demonstrated stable values for H2 yield (2.9−2.3) and selectivity (89−81%), in addition to CO2 (75−67%) and CO (23−29%) selectivity during a (20 h) long time-on-stream study. Following the reaction, SEM/EDX and TEM analysis showed heavy coke deposition over the Ni/Al2O3 catalyst, whereas for the Ni/AlCeO3 catalyst TPO studies showed the formation of more defective coke, the latter being more easily oxidized.

Details

Language :
English
ISSN :
20734344
Volume :
9
Issue :
5
Database :
Directory of Open Access Journals
Journal :
Catalysts
Publication Type :
Academic Journal
Accession number :
edsdoj.347ae2c115d249f0b40680f3d04484c4
Document Type :
article
Full Text :
https://doi.org/10.3390/catal9050411