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Effects of potassium addition on the acidity and reducibility of chromia/alumina dehydrogenation catalysts (Articolo in rivista)
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- Effects of potassium addition on the acidity and reducibility of chromia/alumina dehydrogenation catalysts (Articolo in rivista) (literal)
- Anno
- 2003-01-01T00:00:00+01:00 (literal)
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- E. Rombi (a); M.G. Cutrufello (a); V. Solinas (a); S. De Rossi (b); G. Ferraris (b); A. Pistone (c) (literal)
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- ISI Web of Science (WOS) (literal)
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- a) Dipartimento di Scienze Chimiche, Università di Cagliari, Complesso Universitario di Monserrato, S.S. 554 Bivio per Sestu, 09042 Monserrato (CA), Italy
b) IMIP CNR Sezione Materiali Inorganici e Catalisi Eterogenea c/o Dipartimento di Chimica, Università \"La Sapienza\", P.le Aldo Moro 5, 00185 Rome, Italy
c) Dipartimento di Chimica Industriale ed Ingegneria dei Materiali, Università di Messina, Salita Sperone 31, 98166 S. Agata di Messina (Me), Italy (literal)
- Titolo
- Effects of potassium addition on the acidity and reducibility of chromia/alumina dehydrogenation catalysts (literal)
- Abstract
- Dehydrogenation catalysts based on chromia supported on gamma-alumina, containing about 6wt.% of chromium and increasing
amounts of potassium (up to 1.8 wt.%), were prepared and characterised by means of several techniques, such asN2 adsorption
at 77 K, X-ray powder diffraction (XRPD), UV-Vis diffuse reflectance spectroscopy (DRS), electron paramagnetic resonance
(EPR), temperature programmed reduction (TPR), microcalorimetry and chemical analyses. The catalytic behaviour of the
samples was investigated in the propane dehydrogenation reaction at 813K and the effect of potassium loading was examined.
The addition of increasing amounts of the alkali metal, as expected, determined a general decrease in the surface acidity. The
sites strength distribution was greatly influenced, due to the fact that, at loadings above 0.5 wt.%, potassium preferentially
caused the disappearance of weak and medium acid sites. EPR showed a decrease of CrIII species (especially alfa-Cr2O3) on
potassium increasing. TPR profiles of the K-containing samples showed the presence of two reduction peaks, ascribable to
two different kinds of CrVI surface species with a different reduction behaviour. All catalysts showed a maximum of activity
as a function of time-on-stream, due to reduction of CrVI to CrIII species in the first reaction period, and then a decrease, due
to deactivation by coking. Propene selectivity was high in all cases and was positively affected by the presence of potassium
in concentrations up to 1 wt.%. (literal)
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