Kinetic and in situ DRIFT spectroscopy studies of NO oxidation, and reduction by C3H6 in excess O2 over γ-Al2O3 and Au/γ-Al2O3

被引:13
作者
Bamwenda, GR [1 ]
Obuchi, A [1 ]
Ogata, A [1 ]
Oi, J [1 ]
Kushiyama, S [1 ]
Yagita, H [1 ]
Mizuno, K [1 ]
机构
[1] AIST, Natl Inst Resources & Environm, Tsukuba, Ibaraki 3058565, Japan
来源
SCIENCE AND TECHNOLOGY IN CATALYSIS 1998 | 1999年 / 121卷
关键词
D O I
10.1016/S0167-2991(99)80077-9
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The in situ DRIFT spectroscopy studies of NO and NO2 SCR were performed on gamma-Al2O3 and Au/gamma-Al2O3. The obtained results indicate that the initiation of NO SCR on Au/gamma-Al2O3 involves the oxidation of NO to NO2 at active centers at the interface between Au and Al2O3 followed by coupling of the NO2 or its adspecies, NOx-, with activated C3H6 on active sites on Al2O3 to form CnHmNxOy species, which are responsible for the propagation step. Its subsequent internal rearrangement and decomposition leads to the formation of N-2 and other products. Taken together, the obtained results suggest that the NO2 intermediacy benefits the NO SCR over gold catalysts as a reaction initiator or oxygen transfer agent.
引用
收藏
页码:263 / 268
页数:6
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