Promotional Effects on the Catalytic Activity of Co-Fe Alloy Supported on Graphitic Carbon for CO[sub.2] Hydrogenation
Starting from the reported activity of Co-Fe nanoparticles wrapped onto graphitic carbon (Co-Fe@C) as CO[sub.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) elem...
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Veröffentlicht in: | Nanomaterials (Basel, Switzerland) Switzerland), 2022-09, Vol.12 (18) |
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Sprache: | eng |
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Zusammenfassung: | Starting from the reported activity of Co-Fe nanoparticles wrapped onto graphitic carbon (Co-Fe@C) as CO[sub.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[sub.2] conversion and CH[sub.4] selectivity, probably due to H[sub.2] activation and spillover on Co-Fe. At similar concentrations, Ce does not influence CO[sub.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[sub.2] conversion and CH[sub.4] selectivity remarkably, the effect being attributable to the CO[sub.2] adsorption capacity and basicity of Ca. Sulfur at a concentration of 2.1% or higher acts as a strong poison, decreasing CO[sub.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[sub.2] conversion. Overall, this study shows how promoters and poisons can alter the catalytic activity of Co/Fe@C catalysts, changing from CH[sub.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[sub.2] hydrogenation products that are wanted. |
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ISSN: | 2079-4991 2079-4991 |
DOI: | 10.3390/nano12183220 |