4.8 Article

Deactivation trends of Pd/SSZ-13 under the simultaneous presence of NO, CO, hydrocarbons and water for passive NOx adsorption

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 299, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.apcatb.2021.120591

关键词

Passive NOx adsorption; SSZ-13; Palladium; Ion-exchange; Low-temperature emission control; USDRIVE

资金

  1. U.S. Department of Energy's Vehicle Technologies Office (VTO)

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Pd-functionalized chabazite (Pd/SSZ-13) demonstrated varying levels of effectiveness in passive NOx adsorption (PNA) under different experimental conditions, with notable differences observed in the presence of CO and unsaturated hydrocarbons. The desorption behaviors also showed qualitative differences, with distinct desorption stages observed for different feed conditions. The presence of CO and unsaturated hydrocarbons in the feed resulted in almost complete elimination of lower temperature desorption peaks.
Pd-functionalized chabazite (Pd/SSZ-13) was evaluated for passive NOx adsorption (PNA) using low temperature combustion with diesel (LTC-D) reaction feed of the United States Driving Research and Innovation for Vehicle efficiency and Energy sustainability (U.S.DRIVE) protocol. Notably as per the protocol conditions, 12 % O2 + 6 % CO2 + 6 % H2O was flown in all cases. NO-uptake studies in the presence of the LTC-D feed showed a systematic decline with (NO:Pd)molar changing from 0.5 to 0.4 after 10 trials. Control experiments showed more pronounced decline for NO + CO case, with appreciable intial (NO:Pd)molar value of 0.4, yet comparable-to-theLTC-D-feed decline after 8 trials. CO-induced particle formation and larger extent of particle sintering was also evident from TEM analysis. Other controls did not exhibit trial-dependent deactivation as (NO:Pd)molar values were similar between trials, at 0.3, 0.2, 0.5 and 0.2 for NO, NO+H2, NO + unsaturated hydrocarbon (C2H4, C3H6) and NO + saturated HC (C3H8, C10H22) feeds respectively. In addition to these quantitative differences, desorption behaviors are qualitatively different. While only one major desorption event was observed for the full LTC-D feed, NO + CO and NO + unsaturated HC-controls, desorption occured in two distinct stages for NO, NO + saturated HCs and initial-NO+H2 trials. This arises due to inherent differences in Pd sites while exposed to these chemically distinct feeds. The presence of CO and unsaturated HCs in the feed resulted in almost complete elimination of lower, sub-200 degrees C desorption peak. The higher temperature desorption peaks, at > 300 degrees C is associated with NO strongly bound to ionic Pd sites and are prevalent under reducing conditions. Using DRIFTS also, three complexes leading to PNA are assigned, [O--N-Pd2+(OH)-Z], [O--N-Pd2+(Z2)] and [O--N-Pd2+(H2O)y-Z] with the latter being clearly observed upon water exposure. Pd/SSZ-13 showed higher hydrocarbon trapping than the SSZ-13 counterpart.

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