TY - GEN
T1 - Behavior of supported, and molybdenum and gallium promoted, V-Mg-O catalysts in the oxidative dehydrogenation of n-butane
AU - Papa, J.
AU - Armas, N.
AU - Lopez Nieto, J. M.
AU - Marzuka, S.
AU - Brito, J.
AU - Rivas, H.
AU - Rosato, G.
AU - Malaver, R.
AU - Farias, A.
AU - Pedroza, R.
AU - Guaran, N.
PY - 2005
Y1 - 2005
N2 - Perhaps one of the most promising catalysts found for the n-butane oxidative dehydrogenation is a mixture of vanadium and magnesium oxides with an atomic Mg/V ratio of 4. A study was carried out to solve some of the drawbacks of this catalyst by the addition of different amounts of promoters. Catalysts tests were performed in an isothermal packed bed tubular quartz reactor operated at 1 atm, 480°-540°C, and 6-50 gcat/(moltot/min). All catalysts showed dependence with the reaction temperature and the contact time within the expected trends, and a reduced activity when they were compared to the basic catalyst (V-Mg-O). Selectivity toward dehydrogenated hydrocarbons increased with increasing contents of molybdenum; opposed variation was observed when the promoter was the gallium oxide. Molybdenum enhanced the selectivity toward butenes over the selectivity toward butadiene. The catalyst prepared supporting the V-Mg-O phase over the attrition resistant SiO 2 showed comparable levels on selectivity when compared with the non-supported one, but with a reduced activity. This is an abstract of a paper presented at the 7th World Congress of Chemical Engineering (Glasgow, Scotland 7/10-14/2005).
AB - Perhaps one of the most promising catalysts found for the n-butane oxidative dehydrogenation is a mixture of vanadium and magnesium oxides with an atomic Mg/V ratio of 4. A study was carried out to solve some of the drawbacks of this catalyst by the addition of different amounts of promoters. Catalysts tests were performed in an isothermal packed bed tubular quartz reactor operated at 1 atm, 480°-540°C, and 6-50 gcat/(moltot/min). All catalysts showed dependence with the reaction temperature and the contact time within the expected trends, and a reduced activity when they were compared to the basic catalyst (V-Mg-O). Selectivity toward dehydrogenated hydrocarbons increased with increasing contents of molybdenum; opposed variation was observed when the promoter was the gallium oxide. Molybdenum enhanced the selectivity toward butenes over the selectivity toward butadiene. The catalyst prepared supporting the V-Mg-O phase over the attrition resistant SiO 2 showed comparable levels on selectivity when compared with the non-supported one, but with a reduced activity. This is an abstract of a paper presented at the 7th World Congress of Chemical Engineering (Glasgow, Scotland 7/10-14/2005).
UR - http://www.scopus.com/inward/record.url?scp=33645163636&partnerID=8YFLogxK
M3 - Contribución a la conferencia
AN - SCOPUS:33645163636
SN - 0852954948
SN - 9780852954942
T3 - 7th World Congress of Chemical Engineering, GLASGOW2005, incorporating the 5th European Congress of Chemical Engineering
SP - 257
BT - 7th World Congress of Chemical Engineering, GLASGOW2005, incorporating the 5th European Congress of Chemical Engineering - Congress Manuscripts
T2 - 7th World Congress of Chemical Engineering, GLASGOW2005, incorporating the 5th European Congress of Chemical Engineering
Y2 - 10 July 2005 through 14 July 2005
ER -