Please use this identifier to cite or link to this item:
https://scholarhub.balamand.edu.lb/handle/uob/1741
Title: | CO2 reforming of CH4 over highly active and stable yRhNix/NaY catalysts | Other Titles: | Reformage du méthane par le dioxyde de carbone sur des catalyseurs yRhNix/NaY actifs et stables | Authors: | Estephane, Jane Ayoub, Marc Safieh, Khaled Kaydouh, Marie-Nour Casale, Sandra Zakhem, Henri El |
Affiliations: | Department of Chemical Engineering Department of Chemical Engineering |
Keywords: | Dry reforming Nickel Rhodium Syngas Zeolite NaY |
Issue Date: | 2015 | Part of: | Comptes rendus chimie | Volume: | 18 | Issue: | 3 | Start page: | 277 | End page: | 282 | Abstract: | Ni7.5/NaY catalysts were prepared using two different methods, the incipient wetness impregnation method and the "two-solvent" method. These catalysts were characterised by N2 sorption, XRD, TEM and TPR. Their activity and stability in the dry reforming of methane were tested at atmospheric pressure under an equimolar mixture of methane and carbon dioxide. Three different Ni species, very small, spherical, and layers of nickel silicate were observed by TEM. The preparation by the two-solvent method led to a better dispersion of the active phase as well as to better activity and stability. These catalysts were promoted with small amounts (0.1 wt%) of rhodium. Rhodium facilitates the reducibility and greatly enhances catalytic activity. A complete conversion (100%) for CH4 and CO2 over the Rh promoted catalyst is achieved at 584 °C and 559 °C respectively, while for the non-promoted Ni7.5/NaY catalyst, only a 60% conversion rate for CH4 and CO2 is reached at the same temperatures. |
URI: | https://scholarhub.balamand.edu.lb/handle/uob/1741 | DOI: | 10.1016/j.crci.2014.08.007 | Ezproxy URL: | Link to full text | Type: | Journal Article |
Appears in Collections: | Department of Chemical Engineering |
Show full item record
SCOPUSTM
Citations
10
checked on Dec 21, 2024
Record view(s)
62
checked on Dec 22, 2024
Google ScholarTM
Check
Altmetric
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.