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Promotional Effects on the Catalytic Activity of Co-Fe Alloy Supported on Graphitic Carbon for CO(2) Hydrogenation

Starting from the reported activity of Co-Fe nanoparticles wrapped onto graphitic carbon (Co-Fe@C) as CO(2) hydrogenation catalysts, the present article studies the influence of a series of metallic (Pd, Ce, Ca, Ca, and Ce) and non-metallic (S in various percentages and S and alkali metals) elements...

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Detalles Bibliográficos
Autores principales: Jurca, Bogdan, Peng, Lu, Primo, Ana, Gordillo, Alvaro, Dhakshinamoorthy, Amarajothi, Parvulescu, Vasile I., García, Hermenegildo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506583/
https://www.ncbi.nlm.nih.gov/pubmed/36145013
http://dx.doi.org/10.3390/nano12183220
Descripción
Sumario:Starting from the reported activity of Co-Fe nanoparticles wrapped onto graphitic carbon (Co-Fe@C) as CO(2) hydrogenation catalysts, the present article studies the influence of a series of metallic (Pd, Ce, Ca, Ca, and Ce) and non-metallic (S in various percentages and S and alkali metals) elements as Co-Fe@C promoters. Pd at 0.5 wt % somewhat enhances CO(2) conversion and CH(4) selectivity, probably due to H(2) activation and spillover on Co-Fe. At similar concentrations, Ce does not influence CO(2) conversion but does diminish CO selectivity. A 25 wt % Fe excess increases the Fe-Co particle size and has a detrimental effect due to this large particle size. The presence of 25 wt % of Ca increases the CO(2) conversion and CH(4) selectivity remarkably, the effect being attributable to the CO(2) adsorption capacity and basicity of Ca. Sulfur at a concentration of 2.1% or higher acts as a strong poison, decreasing CO(2) conversion and shifting selectivity to CO. The combination of S and alkali metals as promoters maintain the CO selectivity of S but notably increase the CO(2) conversion. Overall, this study shows how promoters and poisons can alter the catalytic activity of Co/Fe@C catalysts, changing from CH(4) to CO. It is expected that further modulation of the activity of Co/Fe@C catalysts can serve to drive the activity and selectivity of these materials to any CO(2) hydrogenation products that are wanted.