The influence of gas phase reactions on the design criteria for catalysts for lean NOx reduction with dimethyl ether
Artikel i vetenskaplig tidskrift, 2009

In the selective catalytic reduction (SCR) of NO by dimethyl ether (DME), the formation of unexpectedly high amounts of NO2 over 300 degrees C has previously been reported, In this study, we explain this phenomenon by radical reactions initiated by DME and O-2, during which DME is partly oxidized and NO2 is formed in the presence of NO. For the design criteria of a DME-SCR catalyst, these gas phase reactions have mainly three consequences: (i) another type of reducing agent than that fed into the reactor reaches the catalyst. (ii) no activation of the reducing agent such as partial oxidation is required, and (iii) several of the proposed intermediate species for HC-SCP, e.g. NO2, HONO, CH3-NO2, and CH3-NO form already in the gas phase. An efficient DME-SCR catalyst should thus have high selectivity for reduction of NO, predominately by partially oxidized Cl-compounds, and it should not have particularly strong oxidizing properties to avoid non-selective oxidation of these Cl-compounds. These two requirements appear to be reasonable well met by the acidic zeolite H-ZSM-5.

H-ZSM-5

reducing agent

Gas phase reaction

nitric-oxide

Dimethyl ether

selective reduction

kinetics

Radical

zeolite

oxygen

nitrogen-oxides

dme

low-temperature oxidation

NOx-reduction

mechanism

Författare

Stefanie Tamm

Chalmers, Kemi- och bioteknik, Teknisk ytkemi

Kompetenscentrum katalys (KCK)

Hanna Härelind Ingelsten

Chalmers, Kemi- och bioteknik, Teknisk ytkemi

Kompetenscentrum katalys (KCK)

Magnus Skoglundh

Chalmers, Kemi- och bioteknik, Teknisk ytkemi

Kompetenscentrum katalys (KCK)

Anders Palmqvist

Kompetenscentrum katalys (KCK)

Chalmers, Kemi- och bioteknik, Teknisk ytkemi

Applied Catalysis B: Environmental

0926-3373 (ISSN) 1873-3883 (eISSN)

Vol. 91 1-2 234-241

Drivkrafter

Hållbar utveckling

Styrkeområden

Nanovetenskap och nanoteknik

Transport

Energi

Materialvetenskap

Ämneskategorier

Fysik

DOI

10.1016/j.apcatb.2009.05.030

Mer information

Senast uppdaterat

2018-11-05