C. Dossi et al., Cu-ZSM-5 (Si/Al=66), Cu-Fe-S-1 (Si/Fe=66) and Cu-S-1 catalysts for NO decomposition: preparation, analytical characterization and catalytic activity, MICROP M M, 30(1), 1999, pp. 165-175
We prepared H-ZSM-5 (Si/Al = 66), Fe-S-1 (Si/Fe = 66), and Silicalite-1 (S-
1) according to the methods described by Bellussi and coworkers, and compar
ed their ion-exchange capacity for copper ions. The Cu-ZSM-5, Cu-Fe-S and C
u-S-1 samples thus obtained have been investigated as catalysts for the NO
decomposition reaction at 773 K. We found that using copper acetate solutio
ns with concentrations in the range 0.004 M less than or equal to[Cu2+]less
than or equal to 0.1 M, at room temperature and at 323 K, it is very easy
to prepare overexchanged Cu-ZSM-5, Cu-Fe-S-1, and Cu-S-1 catalysts. XRD and
Vis-UV DRS techniques show that after thermal treatments of the fresh samp
les in air at 823 K for 4 h no segregation of bulk CuO phase occurs, sugges
ting the presence of low nuclearity [CunOx(OH)(y)](q+) species [q=2(n-x)-y
greater than or equal to 0]. These results were confirmed by TPR studies. A
t 773 K, only Cu-ZSM-5 and Cu-Fe-S-1 catalysts showed NO decomposition acti
vity (NO 1% in He, W/F = 0.2 g s cm(-3)). Instead, the activities of Cu-S-1
and of the copper-free matrices (S-1, H-ZSM-5 and Fe-S-1) were not measura
ble under our experimental conditions. The negative results obtained with C
u-S-1 catalysts clearly demonstrate that the active sites for NO decomposit
ion in Cu-MFI catalysts consist of polynuclear ionic copper species strongl
y anchored to framework [MO4](-) species (M=Al, Fe). (C) 1999 Elsevier Scie
nce B.V. All rights reserved.