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Mn-based mixed oxides for low temperature NOx adsorber applications

  • Yaying Ji
  • , Dongyan Xu
  • , Mark Crocker
  • , Joseph R. Theis
  • , Christine Lambert
  • , Agustin Bueno-Lopez
  • , Deb Harris
  • , Dave Scapens

Producción científica: Articlerevisión exhaustiva

29 Citas (Scopus)

Resumen

Pd-promoted ternary oxides of the type Mn-Ce-Zr and Mn-Pr-Zr were characterized and evaluated for low temperature NOx storage applications such as diesel vehicle cold starts. While X-ray diffraction data were in all cases consistent with the formation of solid solutions, Mn/Zr and Mn/Ce(Pr) ratios found by XPS were consistently higher than the bulk values, indicative of an enrichment of Mn at the surface of the solids. Both sets of Pd-promoted mixed oxides showed remarkably high NOx storage efficiency in the range 80–160 °C, while a 1.8% Pd/Mn(27)-Ce(7)-Zr catalyst showed excellent NOx storage in simulated cold start experiments. Moreover, ramping the temperature to 370 °C in these experiments, simulating higher speed operation, resulted in near complete purging of stored NOx from the catalyst. NOx storage efficiency in isothermal storage experiments was found to improve with increasing Mn content for the 1%Pd/Mn(x)-Ce(7)-Zr series (x = 9, 18, 27 wt.%), DRIFTS measurements showing that relative to Ce-Zr mixed oxides, Mn incorporation favored NOx storage as nitrate. During temperature programmed desorption (TPD) two main desorption events were observed, corresponding to decomposition of nitrites (up to 200 °C), followed by loss of nitrates (⁓200–400 °C). Nitrates stored on Pd/Mn-Ce(Pr)-Zr mixed oxides desorbed during TPD at lower temperatures than for CeO2-ZrO2 mixed oxides, a finding attributed to the lower basicity of Mn compared to Ce. Hydrothermal aging of 1.8%Pd/Mn(27)-Ce(7)-Zr at 700 °C reduced NOx storage efficiency, although the catalyst was still able to store significant amounts of NOx. However, catalyst sulfation led to a large decrease in NOx storage efficiency and the efficiency could not be completely recovered with lean or rich desulfations at high temperatures.

Idioma originalEnglish
Páginas (desde-hasta)90-101
Número de páginas12
PublicaciónApplied Catalysis A: General
Volumen567
DOI
EstadoPublished - oct 25 2018

Nota bibliográfica

Publisher Copyright:
© 2018 Elsevier B.V.

Financiación

The authors thank Shelley Hopps for XRD measurements. This project was funded by the National Science Foundation and the U.S. Department of Energy (DOE) under award no. CBET-1258742 . However, any opinions, findings, conclusions, or recommendations expressed herein are those of the authors and do not necessarily reflect the views of the DOE. The authors thank Shelley Hopps for XRD measurements. This project was funded by the National Science Foundation and the U.S. Department of Energy (DOE) under award no. CBET-1258742. However, any opinions, findings, conclusions, or recommendations expressed herein are those of the authors and do not necessarily reflect the views of the DOE.

FinanciadoresNúmero del financiador
National Science Foundation Arctic Social Science Program
U.S. Department of Energy EPSCoRCBET-1258742

    ASJC Scopus subject areas

    • Catalysis
    • Process Chemistry and Technology

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