Daniela Pietrogiacomi

The selective catalytic reduction of NOx with CH4 on Mn-ZSM5: A comparison with Co-ZSM5 and Cu-ZSM5

The abatement of NO with CH4 in the presence of O2 was studied on Mn-ZSM5 (Mn percent exchange 2 to 75%), prepared from Na-ZSM5 by the ion-exchange method. Samples were characterised by FTIR, ESR and magnetic measurements. Both ESR and magnetic measurements showed that all manganese was present as MnII. FTIR showed the formation of carbonyls (one type only, on manganese equivalent sites). The intensity of bands from carbonyls was almost proportional to the manganese content. The selectivity for NO abatement, reaction orders in O2, NO or CH4, and apparent activation energy were independent of the manganese content, suggesting that the same surface complexes were formed on all Mn-ZSM5 catalysts. On Mn-ZSM5, turnover frequencies (molecules s−1 Mn-atom−1) for both NO abatement and CH4 reaction were nearly independent of the manganese content and close to the relevant values on Co-ZSM5 (previously investigated in our laboratory), but substantially higher than those on Cu-ZSM5 (Cu percent exchange 98%, studied for a comparison). On Mn-ZSM5, Co-ZSM5 and Cu-ZSM5, the adsorption at RT of NO+O2 or NO2 caused the formation of nitrates. The normalised intensity (per atom) of monodentate nitrate bands (∼1520 and ∼1320 cm−1) was (i) independent of the metal content, (ii) the same in Mn-ZSM5 and Co-ZSM5, and (iii) much higher in Mn-ZSM5 and Co-ZSM5 than in Cu-ZSM5. On all these catalysts, NO abatement rates were proportional to the concentration of these monodentate nitrates. On FTIR evidence, these species reacted with methane at the same temperature at which the various catalysts were active. These findings suggest a role of monodentate nitrates in the SCR reaction.

Decomposition of Nitrous Oxide on CoOX/ZrO2, CuOX/ZrO2 and FeOX/ZrO2 Catalysts

On CoOx/ZrO2, CuOx/ZrO2 and FeOx/ZrO2 catalysts, below the limits shown by characterization to have high metal dispersion, the turnover frequency for N2O decomposition is nearly independent of metal content.

No abatement with CH4 in the presence of O2 on H-ZSM5 with Si/Al = 15-200: The dependence of activity on the proton concentration

AbstractThe abatement of NO with methane in the presence of oxygen was studied on commercial H-ZSM5 samples with Si/Al = 15–200 in a conventional flow apparatus. H-ZSM5 samples were used in the acid form or after exchanging protons with sodium ions to various extents. Their catalytic activity was compared with that of commercial H-mordenite and H-Y. On all H-ZSM5 catalysts, reaction rates RNO and

IRON SPECIES IN FEOX/ZRO2 AND FEOX/SULPHATED-ZRO2 CATALYSTS

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Cobalt supported on ZrO2: Catalysts characterization and their activity for the reduction of NO with C3H6 in the presence of excess O2

(molecules s−1 g−1) increased proportionally to the proton concentration, showing that either all protons or a constant fraction of them were equally active. On sodium-exchanged H-ZSM5 samples with Si/Al = 15–17, both RNO and

THE SURFACE COMPOSITION OF CUOX/ZRO2 CATALYSTS AS DETERMINED BY FTIR, XPS,ESR SPECTROSCOPIES AND VOLUMETRIC CO ADSORPTION

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