Unique properties of Ir/ZSM-5 catalyst for NO reduction with CO in the presence of excess oxygen

被引:90
作者
Wang, AQ [1 ]
Ma, L [1 ]
Cong, Y [1 ]
Zhang, T [1 ]
Liang, DB [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
关键词
Ir/ZSM-5; Pt/ZSM-5; NO+CO+O-2; NO reduction; TPD; NOBLE-METAL CATALYSTS; NITRIC-OXIDE; OXIDATION; REMOVAL; METHANE; ZEOLITE; MIXTURES; IGNITION; STATE; FTIR;
D O I
10.1016/S0926-3373(02)00157-1
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 reduction of NO with CO in the presence of excess oxygen was investigated over different noble metal catalysts for probing the relationship between catalytic properties and adsorption behaviors. Among the four precious metal catalysts investigated, Ir/ZSM-5 was found to be the only active one for NO reduction with CO under lean conditions. With the decreasing of the Ir content, higher NO conversion and CO selectivity was obtained. Temperature-programmed reaction (TPR) studies of NO/H-2/O-2 and NO/CO/O-2 showed that the Pt/ZSM-5 was active when H-2 was used as the reductant, whereas, the Ir/ZSM-5 was active when CO was the reducing agent. This difference is due to the different mechanisms of the two reactions. Temperature-programmed desorption (TPD) of NO, CO and O-2 showed that NO could dissociate more easily over the Ir/ZSM-5 than on the Pt/ZSM-5, while the oxidation of CO by O-2 proceeded more rapidly on the Pt/ZSM-5 than on the Ir/ZSM-5. The presence of excess O-2 inhibited drastically the dissociation of NO, which is considered as the key step for the NO-CO reaction. The high dissociation rate of NO over the Ir/ZSM-5 is visualized as the key factor for its superior high activity in NO reduction with CO under lean conditions. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:319 / 329
页数:11
相关论文
共 28 条
[1]   FTIR study of the oxidation reaction of CO with O2 over bimetallic Pd-Rh/SiO2 catalysts in an oxidized state [J].
Araya, P ;
Weissmann, C .
CATALYSIS LETTERS, 2000, 68 (1-2) :33-39
[2]   An investigation of the NO/H2/O2 reaction on noble-metal catalysts at low temperatures under lean-burn conditions [J].
Burch, R ;
Coleman, MD .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1999, 23 (2-3) :115-121
[3]   A steady-state isotopic transient kinetic analysis of the NO/O2/H2 reaction over Pt/SiO2 catalysts [J].
Burch, R ;
Shestov, AA ;
Sullivan, JA .
JOURNAL OF CATALYSIS, 1999, 188 (01) :69-82
[4]   FeZSM-5: A durable SCR catalyst for NOx removal from combustion streams [J].
Feng, XB ;
Hall, WK .
JOURNAL OF CATALYSIS, 1997, 166 (02) :368-376
[5]   Studies of direct decomposition and reduction of nitrogen oxide with ethylene by supported noble metal catalysts [J].
Gervasini, A ;
Carniti, P ;
Ragaini, V .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1999, 22 (03) :201-213
[6]   OXIDATION OF CO BY O2, NO, AND MIXTURES OF O2 AND NO OVER PD(100) [J].
GRAHAM, GW ;
LOGAN, AD ;
SHELEF, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (21) :5445-5446
[7]   Effects of Pd particle size and ceria loading on NO reduction with CO [J].
Holles, JH ;
Davis, RJ ;
Murray, TM ;
Howe, JM .
JOURNAL OF CATALYSIS, 2000, 195 (01) :193-206
[8]   FTIR SPECTROSCOPY OF NITRIC-OXIDE ADSORPTION ON PD/AL2O3 - EVIDENCE OF METAL-SUPPORT INTERACTION [J].
HOOST, TE ;
OTTO, K ;
LAFRAMBOISE, KA .
JOURNAL OF CATALYSIS, 1995, 155 (02) :303-311
[9]   Performance and structure of Pt-Rh three-way catalysts: Mechanism for Pt/Rh synergism [J].
Hu, Z ;
Allen, FM ;
Wan, CZ ;
Heck, RM ;
Steger, JJ ;
Lakis, RE ;
Lyman, CE .
JOURNAL OF CATALYSIS, 1998, 174 (01) :13-21
[10]  
IWAMOTO M, 1992, P 10 INT C CAT BUD, V1285