Abstract
Fully ion-exchanged Pd/SSZ-13 model passive NOx adsorbers (PNA) exhibit significant NOx storage capability, achieving NOx-to-Pd ratios of 1, and NOx desorption at higher temperatures, where downstream NOx reduction catalysts are active, under simulated exhaust conditions. However, CO has been found to induce PNA degradation, which limits the potential for practical application. In this study, in an attempt to understand the consequences of limiting CO exposure, we integrated a model Pt/Al2O3 diesel oxidation catalyst (DOC) with a Pd/SSZ-13 PNA and performed NOx adsorption and temperature-programmed desorption (TPD) cycles with the PNA, the DOC, and the DOC+PNA integrated system. Despite the high initial NOx-to-Pd ratio, Pd/SSZ-13 experienced significant degradation over 15 adsorption and desorption cycles when including CO, with the NOx-to-Pd ratio dropping from 0.98 to 0.75. CO oxidation over the DOC+PNA integrated system lights off at significantly lower temperature compared to the PNA, limiting the PNA CO exposure at temperatures above 200 °C. As a result, the durability of the DOC+PNA integrated system is enhanced, and only a 0.02 decrease in NOx-to-Pd ratio was observed over the 15 test cycles. A further benefit with integration of the PNA with the DOC was a lower temperature NOx release, within a more practical temperature window. This is due to the enhanced oxidation activity of the DOC+PNA integrated system and consequently an early onset of NO2 formation, which was found to trigger the low temperature NOx release. Low temperature NOx adsorption and TPD experiments with controlled exposure of CO and NO2 reveal two types of NOx storage mechanisms, one of which is destabilized by the presence of NO2, leading to the evolution of a lower temperature NOx release. Overall, integrating the PNA with a highly active low temperature CO oxidation catalyst was beneficial by lowering the NOx release temperature window and leading to significantly less NOx capacity loss.
