Overview of the fundamental reactions and degradation mechanisms of NOx storage/reduction catalysts

被引:808
作者
Epling, WS
Campbell, LE
Yezerets, A
Currier, NW
Parks, JE
机构
[1] EmeraChem, Maryville, TN USA
[2] Adv Catalyst Syst, Maryville, TN USA
[3] Cummins Inc, Columbus, IN USA
[4] Oak Ridge Natl Lab, Natl Transportat Res Ctr, Knoxville, TN USA
来源
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING | 2004年 / 46卷 / 02期
关键词
emissions; NOx storage/reduction catalysts; NO oxidation; NOx release; NOx storage; catalyst;
D O I
10.1081/CR-200031932
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
Over the last several years, nitrogen oxide(s) (NOx) storage/reduction (NSR) catalysts, also referred to as NOx adsorbers or lean NOx traps, have been developed as an aftertreatment technology to reduce NOx emissions from lean-burn power sources. NSR operation is cyclic: during the lean part of the cycle, NOx are trapped on the catalyst; intermittent rich excursions are used to reduce the NOx to N2 and restore the original catalyst surface; and lean operation then resumes. This review will describe the work carried out in characterizing, developing, and understanding this catalyst technology for application in mobile exhaust-gas aftertreatment. The discussion will first encompass the reaction process fundamentals, which include five general steps involved in NOx reduction to N(2) on NSR catalysts; NO oxidation, NO(2) and NO sorption leading to nitrite and nitrate species, reductant evolution, NOx release, and finally NOx reduction to N(2). Major unresolved issues and questions are listed at the end of each of the reaction process fundamental sections. Degradation mechanisms and their effects on NSR catalyst performance are also described in relation to these generalized reactions. Since at this stage it does not appear possible to arrive at a complete and consistent mechanistic model describing the broad, existing experimental phenomenology for these processes, this review is primarily focused on summarizing and evaluating literature data and reconciling the many differences presented.
引用
收藏
页码:163 / 245
页数:83
相关论文
共 184 条
[1]   Influence of the type of reducing agent (H2, CO, C3H6 and C3H8) on the reduction of stored NOX in a Pt/BaO/Al2O3 model catalyst [J].
Abdulhamid, H ;
Fridell, E ;
Skoglundh, M .
TOPICS IN CATALYSIS, 2004, 30-1 (1-4) :161-168
[2]   Sulfur deactivation of NOx storage catalysts:: influence of exposure conditions and noble metal [J].
Amberntsson, A ;
Skoglundh, M ;
Ljungström, S ;
Fridell, E .
JOURNAL OF CATALYSIS, 2003, 217 (02) :253-263
[3]   Investigations of sulphur deactivation of NOx storage catalysts:: influence of sulphur carrier and exposure conditions [J].
Amberntsson, A ;
Skoglundh, M ;
Jonsson, M ;
Fridell, E .
CATALYSIS TODAY, 2002, 73 (3-4) :279-286
[4]   NOx release from a noble metal/BaO catalyst:: dependence on gas composition [J].
Amberntsson, A ;
Persson, H ;
Engström, P ;
Kasemo, B .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2001, 31 (01) :27-38
[5]  
Amberntsson A, 1999, STUD SURF SCI CATAL, V126, P317
[6]   Influence of platinum and rhodium composition on the NOx storage and sulphur tolerance of a barium based NOx storage catalyst [J].
Amberntsson, A ;
Fridell, E ;
Skoglundh, M .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 46 (03) :429-439
[7]  
Anderson J., 2000, STUD SURF SCI CATAL, V130, P1331
[8]   Transient surface processes of storage and conversion of NOx species on Pt-Me/Al2O3 catalysts (Me = Ba, Ce, Cu) [J].
Arena, GE ;
Bianchini, A ;
Centi, G ;
Vazzana, F .
TOPICS IN CATALYSIS, 2001, 16 (1-4) :157-164
[9]   ENVIRONMENTAL CATALYSIS [J].
ARMOR, JN .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1992, 1 (04) :221-256
[10]   CATALYTIC REDUCTION OF NITROGEN-OXIDES WITH METHANE IN THE PRESENCE OF EXCESS OXYGEN - A REVIEW [J].
ARMOR, JN .
CATALYSIS TODAY, 1995, 26 (02) :147-158