Methane dry reforming on fibrous silica-alumina employing nanocrystals of nickel and cobalt to recognize the most efficient metal
Abstract
Presently, the production of syngas through the dry reforming of methane is a widely employed approach for reducing vast amounts of greenhouse gas emissions. Several metals, particularly transition metals support have been evaluated as active DRM catalyst systems. In this work, a comparative studies is presented between Cobalt and Nickel metals impregnated over fibrous silica-alumina (FSA) support synthesized by the hydrothermal method for dry methane reforming. The specimens were characterized via FESEM mapping, TEM, XRD, H2-TPR, XRF, N2 physisorption, and KBr-FTIR techniques. Unlike the Co/FSA, Ni/FSA displayed a higher surface area with a fine dispersion of Ni nano-crystalline and less agglomeration, and more active sites which enhanced the metal-support interaction. Approximately 0.2g of each catalyst was evaluated at 650â800 °C with a respective. CH4:CO2:N2 ratio of 1:1:2, gas hourly space velocity 30,000 mL gâ1 hâ1. The Ni/FSA demonstrated more conversion of CH4 (89%) over (67%) of Co/FSA at 800 °C. After 10 h of long-term reaction, the Ni/FSA exhibited more stability at 800 °C. TGA/DTA, Raman, and TEM results showed that spent Ni/FSA catalysts did not demonstrate signs of considerable nano-graphitic carbon or metal sintering as compared to Co/FSA catalysts, which had bigger crystallites of Co. The finding of this study would add new knowledge on reaction conditions involving and catalytic activities of the metals over the FSA.
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| Título según WOS: | ID WOS:001138906200001 Not found in local WOS DB |
| Título según SCOPUS: | Methane dry reforming on fibrous silica-alumina employing nanocrystals of nickel and cobalt to recognize the most efficient metal |
| Título de la Revista: | International Journal of Hydrogen Energy |
| Volumen: | 52 |
| Editorial: | Elsevier Ltd. |
| Fecha de publicación: | 2024 |
| Página de inicio: | 567 |
| Página final: | 579 |
| Idioma: | English |
| DOI: |
10.1016/j.ijhydene.2023.05.004 |
| Notas: | ISI, SCOPUS |