Structure-activity relationships in NH3-SCR over Cu-SSZ-13 as probed by reaction kinetics and EPR studies

被引:428
作者
Gao, Feng [1 ]
Walter, Eric D. [1 ]
Karp, Eric M. [1 ]
Luo, Jinyong [1 ]
Tonkyn, Russell G. [1 ]
Kwak, Ja Hun [1 ]
Szanyi, Janos [1 ]
Peden, Charles H. F. [1 ]
机构
[1] Pacific NW Natl Lab, Inst Integrated Catalysis, POB 999, Richland, WA 99352 USA
关键词
Selective catalytic reduction; Cu-SSZ-13; Electron paramagnetic resonance; Temperature-programmed reduction; Reaction kinetics; Mass-transfer limitation; SELECTIVE CATALYTIC-REDUCTION; ISOLATED CU2+ IONS; NITRIC-OXIDE; NOX REDUCTION; ZEOLITE; LOCATION; CHEMISTRY; DIFFUSION; AMMONIA; SITES;
D O I
10.1016/j.jcat.2012.12.020
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
Cu-SSZ-13 catalysts with various Cu loadings were prepared via aqueous solution ion-exchange. The hydrated samples were characterized with Electron Paramagnetic Resonance (EPR). Cu2+ ion coordination numbers were obtained by analyzing the hyperfine structures, while Cu-Cu distances were estimated from line broadening of the EPR features. By examining EPR and temperature-programmed reduction (TPR) results, two Cu2+ ion locations are suggested. Standard NH3-SCR, as well as non-selective NH3 oxidation reaction with O-2, were carried out over these catalysts at high-space velocities. For the SCR reaction, intra-particle diffusion limitations are found. The kinetic data allow for reactant diffusivities to be estimated. However, clear structure-activity relationships for the SCR reaction cannot be derived due to this diffusion limitation. The slower NH3 oxidation reaction, on the other hand, is kinetically limited at low temperatures, and, therefore allows for a correlation between Cu2+ ion location and reaction kinetics to be made. Published by Elsevier Inc.
引用
收藏
页码:20 / 29
页数:10
相关论文
共 43 条
[1]   The State of the Art in Selective Catalytic Reduction of NOx by Ammonia Using Metal-Exchanged Zeolite Catalysts [J].
Brandenberger, Sandro ;
Kroecher, Oliver ;
Tissler, Arno ;
Althoff, Roderik .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 2008, 50 (04) :492-531
[2]  
Broach R.W., 2010, ZEOLITES IND SEPARAT
[3]   CATION SITE LOCATION IN HYDRATED CHABAZITES - CRYSTAL-STRUCTURE OF BARIUM-EXCHANGED AND CADMIUM-EXCHANGED CHABAZITES [J].
CALLIGARIS, M ;
NARDIN, G .
ZEOLITES, 1982, 2 (03) :200-204
[4]   NATURE OF ACTIVE SPECIES IN COPPER-BASED CATALYSTS AND THEIR CHEMISTRY OF TRANSFORMATION OF NITROGEN-OXIDES [J].
CENTI, G ;
PERATHONER, S .
APPLIED CATALYSIS A-GENERAL, 1995, 132 (02) :179-259
[5]  
Chen N.Y., 1994, Molecular transport and reaction in zeolites
[6]   TPD study of mordenite-type zeolites for selective catalytic reduction of NO by NH3 [J].
Choi, EY ;
Nam, IS ;
Kim, YG .
JOURNAL OF CATALYSIS, 1996, 161 (02) :597-604
[7]   Confirmation of Isolated Cu2+ Ions in SSZ-13 Zeolite as Active Sites in NH3-Selective Catalytic Reduction [J].
Deka, Upakul ;
Juhin, Amelie ;
Eilertsen, Einar A. ;
Emerich, Hermann ;
Green, Mark A. ;
Korhonen, Satu T. ;
Weckhuysen, Bert M. ;
Beale, Andrew M. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (07) :4809-4818
[8]   MOLECULAR-DYNAMICS STUDIES ON ZEOLITES .4. DIFFUSION OF METHANE IN SILICALITE [J].
DEMONTIS, P ;
FOIS, ES ;
SUFFRITTI, GB ;
QUARTIERI, S .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (10) :4329-4334
[9]   Kinetic and mechanistic study of NOx reduction by NH3 over H-form zeolites .1. Kinetic and mechanistic insights into NO reduction over H-ZSM-5 [J].
Eng, J ;
Bartholomew, CH .
JOURNAL OF CATALYSIS, 1997, 171 (01) :14-26
[10]   The ammonia selective catalytic reduction activity of copper-exchanged small-pore zeolites [J].
Fickel, Dustin W. ;
D'Addio, Elizabeth ;
Lauterbach, Jochen A. ;
Lobo, Raul F. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2011, 102 (3-4) :441-448