Role of nascent oxygen transients in N2O decomposition and selective catalytic reduction of N2O
2004; Elsevier BV; Volume: 93-95; Linguagem: Inglês
10.1016/j.cattod.2004.06.072
ISSN1873-4308
AutoresTakeshi Nobukawa, Masanori Yoshida, Satoshi Kameoka, Shin‐ichi Ito, Keiichi Tomishige, Kimio Kunimori,
Tópico(s)Catalysis and Hydrodesulfurization Studies
ResumoPulsed N2O decomposition on an 18O treated Rh/USY catalyst has been carried out to study the mechanism of O2 desorption using isotopic tracer technique. The results show that O2 desorption proceeds at 220 °C via the Langmuir–Hinshelwood (LH) mechanism, although O2-TPD measurement showed that desorption of oxygen in He gas from Rh catalyst occurred at much higher temperatures. Therefore, it was proposed that reaction-assisted desorption of O2 occurs during N2O decomposition. Reaction between N2O and CH4 over an Fe-BEA catalyst was also studied. In the pulse studies, N2O readily reacted with CH4 in the exposure of N2O+CH4 mixture above 200 °C. In the O2-TPD studies, a new O2 desorption peak appeared at the lower temperatures (300–600 °C) after N2O treatment. However, CH4 was not reactive with the new O(a) species even at 300 °C. In the FT-IR studies, the peak of FeOH was not changed in the exposure of CH4 only, but decreased in the exposure of N2O+CH4 mixture, accompanied with the formation of methoxy and formate species. A possible mechanism is discussed in terms of nascent oxygen transients (O∗(a)), which may play an important role in the activation/oxidation of CH4 at initial steps.
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