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Featured researches published by Simonetta Tuti.


Applied Catalysis B-environmental | 1998

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

Maria Cristina Campa; Daniela Pietrogiacomi; Simonetta Tuti; Giovanni Ferraris; Valerio Indovina

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.


Reaction Kinetics and Catalysis Letters | 2001

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

Simonetta Tuti; Franco Pepe; Daniela Pietrogiacomi; Valerio Indovina

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.


International Journal of Hydrogen Energy | 2012

Co and Ni supported on CeO2 as selective bimetallic catalyst for dry reforming of methane

Igor Luisetto; Simonetta Tuti; Elisabetta Di Bartolomeo


Catalysis Letters | 2008

On the Catalytic Activity of Cobalt Oxide for the Steam Reforming of Ethanol

Simonetta Tuti; Franco Pepe


Applied Catalysis B-environmental | 2000

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

Daniela Pietrogiacomi; Simonetta Tuti; Maria Cristina Campa; Valerio Indovina


Applied Catalysis A-general | 2015

Ni/CeO2-Al2O3 catalysts for the dry reforming of methane: The effect of CeAlO3 content and nickel crystallite size on catalytic activity and coke resistance

Igor Luisetto; Simonetta Tuti; Chiara Battocchio; Sergio Lo Mastro; Armida Sodo


Applied Catalysis B-environmental | 1999

The catalytic activity of CuOx/ZrO2 for the abatement of NO with propene or ammonia in the presence of O2

Daniela Pietrogiacomi; Diana Sannino; Simonetta Tuti; Paolo Ciambelli; Valerio Indovina; Manlio Occhiuzzi; Franco Pepe


Journal of Physical Chemistry B | 1999

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

Valerio Indovina; Manlio Occhiuzzi; Daniela Pietrogiacomi; Simonetta Tuti


Applied Catalysis B-environmental | 2002

The catalytic activity of CuSO4/ZrO2 for the selective catalytic reduction of NOx with NH3 in the presence of excess O2

Daniela Pietrogiacomi; Diana Sannino; Alessandro Magliano; Paolo Ciambelli; Simonetta Tuti; Valerio Indovina


Applied Catalysis B-environmental | 2003

CoOx/sulphated-ZrO2 and CoSO4/ZrO2 as catalysts for the abatement of NO with C3H6 in the presence of excess O2

Daniela Pietrogiacomi; Maria Cristina Campa; Simonetta Tuti; Valerio Indovina

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Igor Luisetto

Sapienza University of Rome

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Valerio Indovina

Sapienza University of Rome

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E. Di Bartolomeo

University of Rome Tor Vergata

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Francesco Basoli

Università Campus Bio-Medico

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Chiara Battocchio

Sapienza University of Rome

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Manlio Occhiuzzi

Sapienza University of Rome

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Franco Pepe

Nuclear Regulatory Commission

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