2010
DOI: 10.1016/j.jcat.2009.10.025
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Activity, selectivity, and adsorbed reaction intermediates/reaction side products in the selective methanation of CO in reformate gases on supported Ru catalysts

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Cited by 113 publications
(106 citation statements)
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References 56 publications
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“…Adsorbed OH bands appear in the 3500-3750 cm -1 range for all three catalysts [15,56]. The intensities for the bands were higher for the Mo-containing catalysts than for the non-promoted sample, indicating that more OH was available on the Mo-containing catalyst for CHx gasification to CO, and could promote the OH gasification route rather than through O only, even if carbon was formed on the Ni catalyst.…”
Section: Page 22 Of 53mentioning
confidence: 95%
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“…Adsorbed OH bands appear in the 3500-3750 cm -1 range for all three catalysts [15,56]. The intensities for the bands were higher for the Mo-containing catalysts than for the non-promoted sample, indicating that more OH was available on the Mo-containing catalyst for CHx gasification to CO, and could promote the OH gasification route rather than through O only, even if carbon was formed on the Ni catalyst.…”
Section: Page 22 Of 53mentioning
confidence: 95%
“…At all three times a distinguishable difference between the three catalysts was observed for the bands ranging from 1760 -2094 cm -1 , which are attributed to molecular CO adsorption. Bands in the 2100-2000 cm -1 region are assigned to linear CO adsorption, which is favored over isolated metal sites (corners and edges), while bands in the 1900-1800 cm -1 range are most likely a contribution of bridging CO, adsorbed on more flat and extensive metal sites [53,55,56]. For the 15Ni and the 0.1Mo catalysts, within the first 5 min of the reaction, CO was adsorbed more on the less reactive flat sites.…”
Section: Co and Propane Adsorptionmentioning
confidence: 99%
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“…Therefore, CO 2 dissociation and subsequent methanation is the only pathwayf or CO 2 conversion that has to be considered herein. [16] Also, in this case, we first performed ar eference measurement in dry SR-ref 100 (Table 3), compared with 9.9 10 À6 mol g Ru À1 s…”
Section: Activation Of Ru/al 2 O 3 Underwet Conditionsmentioning
confidence: 99%
“…These Ru species were proposed to result from oxidative rupture of Ru-Ru bonds and, by some authors, identified as oxidized Ru nþ sites. [29] In Ru/Al 2 O 3 and Ru/SiO 2 catalysts this signal was accompanied by a peak at 2135 cm À1 .…”
Section: Co-drifts-qms Characterizationmentioning
confidence: 93%