Modeling and Optimization Studies of Combined LNT-SCR Catalyst Systems

Tuesday, October 18, 2011: 1:50 PM
200 H (Minneapolis Convention Center)
Arun S. Kota, Dan Luss and Balakotaiah Vemuri, Department of Chemical and Biomolecular Engineering, University of Houston, Houston, TX

 

Abstract:

A one-dimensional two-phase model with global rate expressions for various reactions is used to study the performance of combined LNT-SCR catalyst systems. The LNT system modeled is that of Pt/BaO/Al2O3 catalyst with two different BaO storage sites, designated as fast and slow sites. LNT model includes reactions that describe NO oxidation, storage of NO2 in the form of nitrates during lean storage cycle and reduction to N2 in the subsequent rich cycle with H2 as a reductant. The SCR system considered is that of Cu-ZSM5 and the model includes NO oxidation, ammonia storage and oxidation, selective catalytic reduction of NO, NO2 and formation of N2O. Model predicts the spatio-temporal concentration profiles of reactants and products inside the channel, which gives insight into the performance of each LNT and SCR catalyst during operation. It has been found that series arrangement of alternate LNT and SCR catalyst, by dividing them into equal halves, substantially improves NOx conversion. For fixed total catalyst length as the number of divisions increase, NOx conversion increases and reaches a limit which is theoretically equivalent to that of mixed catalyst. It is also observed that for fixed length of LNT catalyst better DeNOx performance is obtained by increasing the length of SCR catalyst in the alternate arrangement. Spatio-temporal profiles indicate complete storage of NH3 on SCR catalyst which can be efficiently used to reduce NOx slipping out of LNT. Various catalyst arrangements, the effect of different catalyst loading and rich cycle time are investigated in the present work.     


Extended Abstract: File Not Uploaded
See more of this Session: Modeling and Analysis of Chemical Reactors
See more of this Group/Topical: Catalysis and Reaction Engineering Division