Autor: |
Huawang Zhao, Xiaoyin Chen, Alexander J. Hill, Guohua Jing, Yongdan Li, Johannes W. Schwank |
Přispěvatelé: |
University of Michigan, Ann Arbor, Huaqiao University, Industrial chemistry, Department of Chemical and Metallurgical Engineering, Aalto-yliopisto, Aalto University |
Rok vydání: |
2023 |
Předmět: |
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Zdroj: |
Chemical Engineering Journal. 452:139507 |
ISSN: |
1385-8947 |
DOI: |
10.1016/j.cej.2022.139507 |
Popis: |
Publisher Copyright: © 2022 The Author(s) Pd/SSZ-13 catalysts were investigated for the simultaneous storage of NO and C3H6 at 100 °C. The effects of the state of Pd species on co-adsorption and release were studied under simulated exhaust conditions. The catalysts were characterized by NH3-TPD, XRD, and TEM for Pd2+ and PdO species. NO adsorption/release behavior is impacted by the nature of reactants and the NO storage capacity at 100 °C was enhanced by simultaneous NO + C3H6 adsorption. DRIFTs results showed that Pd2+ provides the adsorption sites for NO + C3H6 to form Pd2+(NO)(C3H6), which alleviates the inhibition effect of H2O on NO adsorption on Pd ions. Different release behaviors, which are discussed in light of the chemistry of NO and C3H6 adsorption and effect of intermediate CO, depend on whether NO was adsorbed alone or together with C3H6. The mechanistic pathways during different stages of NO + C3H6 co-adoption and release are proposed. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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