4.8 Article

Pd-promoted WO3-ZrO2 for low temperature NOx storage

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 264, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2019.118499

关键词

Passive NOx adsorber; Tungstated zirconia; DRIFTS; Palladium; Cations; Nitrosyl complex

资金

  1. National Science Foundation [CBET-1258742]
  2. U.S. Department of Energy (DOE) [CBET-1258742]
  3. British Council under the Global Innovation Initiative
  4. Center for Understanding and Control of Acid Gas-Induced Evolution of Materials for Energy (UNCAGE-ME), an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Basic Energy Sciences

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Pd-promoted ZrO2 and WO3-ZrO2 (W-Zr) were investigated for low temperature NOx adsorption and release. Pd-promoted W-Zr exhibited high NOx storage efficiency at short storage times, subsequently releasing similar to 95% of the stored NOx upon thermal ramping to 350 degrees C. DRIFTS studies demonstrated that Pd increased nitrate formation relative to nitrite during NOx storage on both Pd-Zr and Pd-W-Zr. Moreover, Pd sites on Pd-W-Zr played a major role in NOx storage, the ad-species being readily removed by 350 degrees C. From NO- and CO-DRIFTS data, it is inferred that Pd on the acidic W-Zr support was present as mainly cationic species, and was therefore able to adsorb NO, whereas on ZrO2 Pd was not able to directly store NOx. Co-feeding CO with NO resulted in increased NOx storage capacity for Pd-W-Zr, which on the basis of DRIFTS measurements is attributed to the formation of Pd2+ (CO)(NO) complexes.

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