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To overcome deactivation of Pd-based catalysts at high temperatures, we herein design a novel pathway by introducing a certain amount of CoO to the supported Au-Pd alloy nanoparticles (NPs) to generate high-performance Au-Pd-xCoO/three-dimensionally ordered macroporous (3DOM) Co3O4 (x is the Co/Pd molar ratio) catalysts. The doping of CoO induced the formation of PdO-CoO active sites, which was beneficial for the improvement in adsorption and activation of CH4 and catalytic performance. The Au-Pd-0.40CoO/3DOM Co3O4 sample performed the best (T-90% = 341 degrees C at a space velocity of 20 000 mL Deactivation of the 3DOM Co3O4-supported Au-Pd, Pd-CoO, and Au-Pd-xCoO nanocatalysts resulting from water vapor addition was due to the formation and accumulation of hydroxyl on the catalyst surface, whereas deactivation of the Pd-CoO/3DOM Co3O4 catalyst at high temperatures (680-800 degrees C) might be due to decomposition of the PdOy active phase into aggregated Pd-0 NPs. The Au-Pd-xCoO/3DOM Co3O4 nanocatalysts exhibited better thermal stability and water tolerance ability compared to the 3DOM Co3O4-supported Au-Pd and Pd-CoO nanocatalysts. We believe that the supported Au-Pd-xCoO nanomaterials are promising catalysts in practical applications for organic combustion.
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ENVIRONMENTAL SCIENCE & TECHNOLOGY
ISSN: 0013-936X
Year: 2017
Issue: 4
Volume: 51
Page: 2271-2279
1 1 . 4 0 0
JCR@2022
ESI Discipline: ENVIRONMENT/ECOLOGY;
ESI HC Threshold:228
CAS Journal Grade:1
Cited Count:
WoS CC Cited Count: 66
SCOPUS Cited Count: 67
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 10