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A simple model catalyst study to distinguish the roles of different oxygen species in propane and soot combustion
It is important yet difficult to distinguish the specific roles of superficial Oxn- and interfacial lattice oxygen in catalytic combustion, especially over catalysts consisting of reducible metal oxides. In this study, based on the comparison of two natural counterparts with similar structure — CeO2...
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Published in: | Applied catalysis. B, Environmental Environmental, 2022-08, Vol.310, p.121331, Article 121331 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | It is important yet difficult to distinguish the specific roles of superficial Oxn- and interfacial lattice oxygen in catalytic combustion, especially over catalysts consisting of reducible metal oxides. In this study, based on the comparison of two natural counterparts with similar structure — CeO2 (an Oxn- generator) and Pr6O11 (a lattice oxygen contributor), it is suggested that the catalytic combustion of propane under lean-burn conditions followed a typical Mars-van Krevelen mechanism, in which catalyst lattice oxygen represented the dominant reactive phases while superficial Oxn- played negligible roles. As for soot combustion, adsorbed Oxn- represented more sustainable oxidants than lattice oxygen (drained easily at the beginning of the reactions). Such a comparison is readily achieved and widely applicable, which may shed light on the identification of dominant reactive phases for various oxidation reactions over oxide-based catalysts.
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•Pr6O11 with higher lattice oxygen mobility oxidized propane faster than did CeO2.•The defects-induced Oxn- worked as the key soot oxidizer over CeO2.•Pr6O11 deactivated with the draining of its lattice oxygen by soot.•The catalytic combustion of propane followed a typical Mars-van Krevelen mechanism.•Soot ignition followed a Mars-van Krevelen-like mechanism with open redox cycles. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2022.121331 |