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Study of the origin of the deactivation of a Pt/CeO2 catalyst during reverse water gas shift (RWGS) reaction
被引:175
作者:
Goguet, A
Meunier, F
Breen, JP
Burch, R
Petch, MI
Ghenciu, AF
机构:
[1] Queens Univ Belfast, Sch Chem, Belfast BT9 5AG, Antrim, North Ireland
[2] Johnson Matthey Fuel Cells, Reading RG4 9NH, Berks, England
[3] Johnson Matthey Fuel Cells, W Chester, PA 19380 USA
关键词:
deactivation;
ceria;
reverse water gas shift;
Pt;
temperature-programmed oxidation;
carbon deposition;
active site;
D O I:
10.1016/j.jcat.2004.06.011
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The effect of carbon deposition in the deactivation of a 2% Pt/CeO2 under RWGS conditions was investigated via an accelerated ageing procedure consisting of measuring the catalyst activity (under 1% CO2, 4% H-2, 300 degreesC) before and after exposure to CO, CO2, H-2, or CH4 at 400 C. Exposure to CO led to severe deactivation while exposure to CO2, CH4, or H-2 led to moderate or no deactivation. Additional activity measurements performed before and after exposure to CO followed by subsequent temperature-programmed oxidation (TPO) showed that exposure to increasing amounts of CO led to increased deposits of carbon and deactivation. No evidence for metal sintering was found. Additional TPO following catalyst exposure to RWGS conditions evidenced the deposition of carbonaceous deposits under the RWGS reactant mix. (C) 2004 Elsevier Inc. All rights reserved.
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页码:382 / 392
页数:11
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