Methane dry reforming on fibrous silica-alumina employing nanocrystals of nickel and cobalt to recognize the most efficient metal

Sofi, M. H. M.

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 650–800 °C with a respective. CH4:CO2:N2 ratio of 1:1:2, gas hourly space velocity 30,000 mL g?1 h?1. 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. © 2023 Hydrogen Energy Publications LLC

Más información

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