Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/6669
Title: A comparative study of zirconia supported nickel and/or ruthenium catalysts for glycerol steam reforming
Authors: Dahdah, Eliane
Estephane, Jane 
Gennequin, Cedric
El Khoury, Bilal
Aboukaïs, Antoine
Abi-Aad, Edmond
Aouad, Samer 
Affiliations: Department of Chemistry 
Department of Chemical Engineering 
Department of Chemistry 
Keywords: Glycerol
Hydrogen
Nickel
Reforming
Ruthenium
Zirconia
Issue Date: 2023-05
Publisher: Elsevier
Part of: Sustainable Chemistry and Pharmacy
Volume: 32
Abstract: 
The physico-chemical properties of Ni, Ru, Ru–Ni monoclinic ZrO2 catalysts were studied and their catalytic activities in the glycerol steam reforming reaction (GSR) were compared. The catalysts were prepared by the wet impregnation method, calcined at 600 °C and characterized using XRD, BET, H2-TPR and CO2-TPD techniques. The XRD analyses revealed varying crystallite sizes depending on the active phase nature and composition. The H2-TPR analyses demonstrated that the reducibility of the active metal oxide species and its dispersion were affected by the active phase composition. The CO2-TPD analyses revealed that surface modification following impregnation modified the basic properties of the catalysts. The catalytic activity tests (T = 400–700 °C, WGFR 9:1, flow rate of 0.025 mL/min) showed that the nickel based catalysts were active while the ruthenium based catalyst was inactive. Combining ruthenium and nickel over zirconia led to smaller Ni particle sizes and a better metal dispersion both of which contributed to higher H2 yields and an increased coke resistance. During 24 h on stream, the combined Ru–Ni/ZrO2 catalyst maintained a higher total glycerol conversion compared to the Ni/ZrO2 catalyst. Only filamentous coke was identified on the spent catalysts after the stability tests. For a higher water to glycerol feed ratio (WGFR 46:1), encapsulating coke was formed over Ru–Ni/ZrO2 leading to the blockage of active sites and a more rapid catalyst deactivation.
URI: https://scholarhub.balamand.edu.lb/handle/uob/6669
DOI: 10.1016/j.scp.2023.101019
Ezproxy URL: Link to full text
Type: Journal Article
Appears in Collections:Department of Chemistry
Department of Chemical Engineering

Show full item record

SCOPUSTM   
Citations

2
checked on Apr 13, 2024

Record view(s)

29
checked on Apr 17, 2024

Google ScholarTM

Check

Dimensions Altmetric

Dimensions Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.