A comparison between Pt and Pd in NOx storage catalysts

被引:118
作者
Salasc, S
Skoglundh, M
Fridell, E [1 ]
机构
[1] Chalmers Univ Technol, Competence Ctr Catalysis, SE-41296 Gothenburg, Sweden
[2] Chalmers Univ Technol, Dept Appl Phys, SE-41296 Gothenburg, Sweden
关键词
lean burn; NOx; storage-reduction catalyst; NSR concept; platinum; palladium; barium; alumina;
D O I
10.1016/S0926-3373(01)00300-9
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 importance of Pt and I'd in noble metal-barium oxide type NO, storage catalysts was investigated. Model Pt/BaO/Al2O3 and Pd/BaO/Al2O3 catalysts were prepared and evaluated with respect to NOx storage capacity, activity towards NO reduction under lean conditions and NOx oxidation capacity using synthetic lean burn exhausts containing NO, O-2, C3H6 and N-2. The study was carried out by performing static and transient flow reactor experiments and temperature-programmed desorption studies. At 300degreesC, the Pd/BaO/Al2O3 sample shows a higher NOx storage capacity than Pt/BaO/Al2O3, i.e. more NOx is stored during the lean periods and almost all NO, is released and reduced during the subsequent rich periods. At this temperature (300 degreesC) the NO reduction is not complete during the rich phase for the Pt-based catalyst suggesting poisoning of Pt-sites by adsorbed species. At 400degreesC, Pt/BaO/Al2O3 stores slightly more NOx, than its Pd-based counterpart. XPS measurements on pre-treated catalysts, show some changes in oxidation state for Pd between the rich and lean phases. The oxidation of NO is much more limited on Pd based samples compared to Pt containing catalysts. The importance of NO2 as an intermediate in the storage of NOx as nitrate under lean conditions is confirmed in this study. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:145 / 160
页数:16
相关论文
共 50 条
[11]   C-H bond activation in hydrocarbon oxidation on heterogeneous catalysts [J].
Burch, R ;
Crittle, DJ ;
Hayes, MJ .
CATALYSIS TODAY, 1999, 47 (1-4) :229-234
[12]   MECHANISM OF THE SELECTIVE REDUCTION OF NITROGEN MONOXIDE ON PLATINUM-BASED CATALYSTS IN THE PRESENCE OF EXCESS OXYGEN [J].
BURCH, R ;
MILLINGTON, PJ ;
WALKER, AP .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1994, 4 (01) :65-94
[13]   Kinetics and mechanism of the reduction of NO by C3H8 over Pt/Al2O3 under lean-burn conditions [J].
Burch, R ;
Watling, TC .
JOURNAL OF CATALYSIS, 1997, 169 (01) :45-54
[14]   Selective reduction of NOx by hydrocarbons in excess oxygen by alumina- and silica-supported catalysts. [J].
Burch, R ;
Millington, PJ .
CATALYSIS TODAY, 1996, 29 (1-4) :37-42
[15]   SELECTIVE REDUCTION OF NITROGEN-OXIDES BY HYDROCARBONS UNDER LEAN-BURN CONDITIONS USING SUPPORTED PLATINUM-GROUP METAL-CATALYSTS [J].
BURCH, R ;
MILLINGTON, PJ .
CATALYSIS TODAY, 1995, 26 (02) :185-206
[16]   Catalyst microstructure and methane oxidation reactivity during the Pd⇆PdO transformation on alumina supports [J].
Datye, AK ;
Bravo, J ;
Nelson, TR ;
Atanasova, P ;
Lyubovsky, M ;
Pfefferle, L .
APPLIED CATALYSIS A-GENERAL, 2000, 198 (1-2) :179-196
[17]   CATALYTIC CHEMISTRY OF SUPPORTED PALLADIUM FOR COMBUSTION OF METHANE [J].
FARRAUTO, RJ ;
HOBSON, MC ;
KENNELLY, T ;
WATERMAN, EM .
APPLIED CATALYSIS A-GENERAL, 1992, 81 (02) :227-237
[18]   THERMAL-DECOMPOSITION AND REFORMATION OF PDO CATALYSTS - SUPPORT EFFECTS [J].
FARRAUTO, RJ ;
LAMPERT, JK ;
HOBSON, MC ;
WATERMAN, EM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1995, 6 (03) :263-270
[19]   NOx storage in barium-containing catalysts [J].
Fridell, E ;
Skoglundh, M ;
Westerberg, B ;
Johansson, S ;
Smedler, G .
JOURNAL OF CATALYSIS, 1999, 183 (02) :196-209
[20]   The mechanism for NOx storage [J].
Fridell, E ;
Persson, H ;
Westerberg, B ;
Olsson, L ;
Skoglundh, M .
CATALYSIS LETTERS, 2000, 66 (1-2) :71-74