G. Delahay et al., N2O ORIGIN IN NO REDUCTION WITH NH3 OVER COPPER ZEOLITES, COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE II FASCICULE C-CHIMIE, 1(4), 1998, pp. 229-235
Ammonia oxidation has been studied between 298 to 800 K on zeolite NaY
and copper-based catalysts (Cu(x)-NaY, x being the exchange degree).
The main product of the reaction was N-2. The rates of NH3 conversion
in selective catalytic reduction (SCR) of NO by NH3 (NH3 + O-2 + NO) a
nd in NH3 oxidation (NH3 + O-2) were similar on Cu (195)-NaY, but diff
ered at lower temperature on Cu(76)-NaY. On Cu(25)-NaY, the rate of NH
(3 )conversion in SCR of NO was always much faster. During the SCR of
NO on Cu(76)-NaY, two waves of N(2)O( )formation were observed, while
on Cu(25)-NaY, no N2O was detected. The formation of N2O at low temper
ature was ascribed to the decomposition of ammonium nitrate formed on
CuO aggregates. The second N2O formation at a higher temperature resul
ted from the ammonia oxidation which occurred either on next-neighbour
isolated Cu2+ Or On [CuOCu](2+) dimers. (C) Academie des Sciences/Els
evier, Paris.