http://www.cnr.it/ontology/cnr/individuo/prodotto/ID182822
Structure and reactivity in the selective oxidation of methane to formaldehyde of low-loaded FeOx/SiO2 catalysts (Articolo in rivista)
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- Label
- Structure and reactivity in the selective oxidation of methane to formaldehyde of low-loaded FeOx/SiO2 catalysts (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.jcat.2005.01.029 (literal)
- Alternative label
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- Arena F.; Gatti G.; Martra G.; Coluccia S.; Stievano L.; Spadaro L.; Famulari P.; Parmaliana A. (literal)
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- Dipartimento di Chimica Industriale e Ingegneria dei Materiali, Università degli Studi di Messina, Salita Sperone 31, 98166 S. Agata (Messina), Italy
Dipartimento di Chimica IFM and NIS Centre of Excellence, Università di Torino, Via P. Giuria 7, 10125 Torino,
Italy - UdR TO1 of INCA Interuniversity Consortium
Laboratoire de Réactivité de Surface, Université Paris VI, UMR 7609, Place Jussieu 4, 75252 Paris, France
Instituto CNR-ITAE \"Nicola Giordano\", Salita S. Lucia 39, I-98126 S. Lucia (Messina), Italy (literal)
- Titolo
- Structure and reactivity in the selective oxidation of methane to formaldehyde of low-loaded FeOx/SiO2 catalysts (literal)
- Abstract
- The structure of low-loaded (0.09-0.73 Fe wt%) FeOx/SiO2 catalysts prepared by adsorption-precipitation of Fe2+ precursor on silica
(AP) has been assessed by DR UV-Vis and Mössbauer techniques in comparison with counterpart incipient wetness (IW) systems.
Spectroscopic findings indicate the speciation of the active phase into isolated Fe3+ species, oligomeric 2-d FeOx patches, and 3-d Fe2O3
nanoparticles, characterised by decreasing interaction strength with silica carrier. The reduction pattern of the above surface structures has
been probed by temperature-programmed reduction (TPR) measurements, and a deconvolution analysis of spectra allowed the concentration
of the various surface species to be highlighted. The catalytic activity in the selective oxidation of CH4 to HCHO with oxygen (MPO)
has been systematically evaluated by batch (BR) and continuous-flow (CF) measurements in the range of 400-750 oC. Direct relationships
among Fe dispersion and specific atomic rate of CH4 conversion (FeCH4, s-1) and HCHO formation (FeHCHO, s-1) confirm the superior
catalytic performance of AP systems. After a poor reactivity of \"isolated species\" and the unselective behaviour of 3-d Fe2O3 particles,
2-d oligomeric patches feature the best catalytic pattern, owing to an optimum Fe-O bond strength. Sintering and surface reconstructuring
phenomena affect the catalyst stability during the MPO reaction. (literal)
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