The effect of changing the gas composition on soot oxidation over DPF and SCR-coated filters
Artikel i vetenskaplig tidskrift, 2018

In this study, we have investigated the effect of changing the gas feed composition on soot oxidation over diesel particulate filter (DPF) and SCR-coated filter during temperature ramp experiments from 200 to 750 degrees C. For DPF, the increasing NO2/NOx ratio promoted soot oxidation across a fairly low temperature range (200-500 degrees C) and, in addition, soot oxidation was enhanced by water. Interestingly, the presence of NH3 in the gas feed inhibited the soot oxidation under various feed compositions for the DPF. Moreover, ammonia oxidation was also observed over the filter and based on these experiments together with experiments without soot, we conclude that ammonia oxidation is actually occurring on soot particles and that the interaction of the ammonia with the soot is inhibiting soot oxidation. Further, fast and NO2 SCR reactions were found to occur on soot particles, while no reactions with NO under standard SCR conditions was observed. Thus, the NH3 and NO2 molecules are interacting with the soot. When comparing the DPF and SCR-filter we found that the SCR material enhanced the soot oxidation under standard and fast SCR conditions, because of the fact that soot oxidation was inhibited by NH3 and would be rapidly consumed under SCR reactions with the Cu-zeolite in the SCR-filter. Furthermore, during fast SCR conditions, because NO2 is consumed during fast SCR reaction for the SCR-filter, the opposite results were found where soot oxidation occurred at lower temperature for the DPF. (c) 2017 Elsevier B.V. All rights reserved.

Soot oxidation

Copper zeolite

SCR-coated filter

DPF

Exhaust aftertreatment

Författare

Oana Mihai

Chalmers, Kemi och kemiteknik, Kemiteknik, Kemisk reaktionsteknik

Marie Stenfeldt

Volvo Cars

Louise Olsson

Chalmers, Kemi och kemiteknik, Kemiteknik

Catalysis Today

0920-5861 (ISSN)

Vol. 306 243-250

Ämneskategorier

Oorganisk kemi

Materialkemi

Annan kemi

DOI

10.1016/j.cattod.2017.03.005