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Journal ArticleDOI

Homogeneous and heterogeneous contributions to the oxidative dehydrogenation of propane on oxide catalysts

Robert Burch, +1 more
- 01 Jul 1993 - 
- Vol. 100, Iss: 1, pp 111-130
TLDR
In this paper, a variety of oxide-based catalysts have been prepared, characterised, and tested in the oxidative dehydrogenation reaction and it has been found that with these catalysts, the maximum selectivity to propene at a specific conversion of propane is never higher than can be obtained in the absence of a catalyst.
Abstract
The pyrolysis and the oxidative dehydrogenation of propane have been investigated in a quartz reactor. It has been found that by optimising the propane/air ratio it has been possible to obtain very high yields of propene and ethene. A variety of oxide-based catalysts have been prepared, characterised, and tested in the oxidative dehydrogenation reaction. It has been found that with these catalysts, the maximum selectivity to propene at a specific conversion of propane is never higher than can be obtained in the absence of a catalyst. The results also show no obvious correlation between catalytic properties and the presence of specific crystalline phases. It is suggested that lower than optimum selectivities to propene may arise because of the presence in the catalysts of small, but undetected, amounts of pure V 2 O 5 . Comparison with other published work suggests that there is an upper limit on the yield of propene which can be obtained for a purely heterogeneously catalysed reaction. A combination of homogeneous and heterogeneous contributions to the oxidative dehydrogenation reaction may provide a means of obtaining even higher yields of propene.

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Citations
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Journal ArticleDOI

Oxidative dehydrogenation of ethane and propane : How far from commercial implementation?

TL;DR: In this article, a review examines the recent literature on the oxidative dehydrogenation (ODH) of ethane and propane, which aims for the synthesis of the corresponding alkenes.
Journal ArticleDOI

The oxidative dehydrogenation of ethane and propane as an alternative way for the production of light olefins

Fabrizio Cavani, +1 more
- 23 Jun 1995 - 
TL;DR: The main aspects of ethane and propane oxydehydrogenation are discussed in this article, where the performance of various catalysts described in the literature has been compared and compared.
Journal ArticleDOI

On the partial oxidation of propane and propylene on mixed metal oxide catalysts

TL;DR: In this paper, the authors analyzed the literature data reported on the partial oxidation of propane to organic compounds (acrolein, acrylic acid and acrylonitrile) over mixed metal oxides, mainly magnesium vanadates, vanadia bismuth molybdates and vanadia antimony.
Book ChapterDOI

Oxidative Dehydrogenation of Light (C2 to C4) Alkanes

Abstract: Publisher Summary This chapter summarizes the data and current understanding regarding the oxidative dehydrogenation reaction of alkanes. The reaction mechanism, the nature of the catalysts, and factors that determine selectivity for dehydrogenation versus formation of oxygen-containing products are discussed in the chapter. From the pattern of product distribution in the oxidation of C 2 to C 6 alkanes obtained with supported vanadium oxide, orthovanadates of cations of different reduction potentials, and vanadates of different bonding units of VO x in the active sites, it is shown that the selectivities can be explained by the probability of the surface alkyl species (or the surface alkene formed from the alkyl) to react with a reactive surface lattice oxygen. Catalysts for which this occurs with a high probability would show low selectivities. This probability increases for vanadates that have low heats of removal of lattice oxygen, which are those that contain easily reducible cations in the active sites and for vanadates whose active sites can bind the surface alkyl species (or alkene) in a way that bring the surface intermediate close to the reactive lattice oxygen. The dependence of selectivity for dehydrogenation on the conversion of alkane shows that for the more selective catalysts known, the reaction proceeds with a sequential mechanism.
Journal ArticleDOI

Selective oxidation of light alkanes: interaction between the catalyst and the gas phase on different classes of catalytic materials

Fabrizio Cavani, +1 more
- 29 Jul 1999 - 
TL;DR: In this article, the role of the redox properties of transition metal oxide-based systems, and the contribution of radical-type, homogeneous and heterogeneously-initiated homogeneous reactions over nonreducible metal oxide catalysts are examined.
References
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Journal Article

Selective oxidative dehydrogenation of propane over V-Mg-O catalysts

TL;DR: Vanadium-magnesium oxides were found to be active and selective catalysts for the oxidative dehydrogenation of propane to propene as discussed by the authors, achieving a selectivity of up to 65% at 10% conversion, but decreased with increasing conversion.
Journal ArticleDOI

Oxidative dehydrogenation of propane over VMgO catalysts

TL;DR: In this paper, a dynamic model of the working catalyst favored by the corner-sharing VO 4 tetrahedra of the V 2 O 7 4− units was proposed for dehydrogenation of propane to propene.
Journal ArticleDOI

On the NiMoO4 oxidative dehydrogenation of propane to propene : some physical correlations with the catalytic activity

TL;DR: In this paper, the α-and β-phases of NiMoO4 have been investigated with different techniques (X-ray diffraction, electrical conductivity, IR spectroscopy) in order to tentatively rationalise the different catalytic activities observed in the oxidative dehydrogenation of propane to propene.
Journal ArticleDOI

The effect of potassium in the preparation of magnesium orthovanadate and pyrovanadate on the oxidative dehydrogenation of propane and butane

TL;DR: In this article, the catalytic properties of mixed oxides of vanadium and magnesium in the oxidative dehydrogenation of propane and butane were compared with two different methods, with or without the use of K.
Journal ArticleDOI

Generation of gaseous radicals by a VMgO catalyst during oxidative dehydrogenation of propane

TL;DR: In this paper, a VMg-mg-O catalyst for possible gas-phase reactions initiated by the desorption of reactive intermediates from the catalyst surface was studied and it was found that the conversions of propane at 556 and 570°C in the void volume positioned immediately downstream of the catalyst were higher than those in the same void volume located upstream of the catalytic surface.
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