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Journal ArticleDOI

Homogeneous and heterogeneous contributions to the catalytic oxidative dehydrogenation of ethane

Robert Burch, +1 more
- 08 Apr 1993 - 
- Vol. 97, Iss: 1, pp 49-65
TLDR
In this article, the results showed that under optimum conditions the non-catalysed reaction can be very efficient and selective, achieving a conversion of 45% at a selectivity of 73.7%, corresponding to a percentage yield of ethene of 33% and a space-time yield of 15.8 mmol/cm3 h.
Abstract
The oxidative dehydrogenation of ethane to ethene has been studied in a quartz reactor in the absence and in the presence of a range of MgO-based catalysts using a variety of gas compositions over a range of temperatures. The results show that under optimum conditions the non-catalysed reaction can be very efficient and selective. At a temperature of 600°C, using an ethane/air ratio of 1:2, a conversion of 45% was achieved at a selectivity of 73.7%, corresponding to a percentage yield of ethene of 33% and a space-time yield of ethene of 15.8 mmol/cm3 h. It was observed that none of the catalysts tested under comparable conditions gave such high yields. Reasons for this difference are discussed. Comparison with published results on the catalytic oxidative dehydrogenation of ethane suggest that the non-catalysed gas-phase reaction is competitive with the best available catalysts.

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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

Supported metal oxide and other catalysts for ethane conversion: a review

TL;DR: In this article, the structure and performance of supported metal oxide catalysts in reactions is discussed, underlining the importance of in situ characterization under reaction conditions in order to fully understand the structural and reactivity properties of the supported metal-oxide catalysts at molecular level.
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

Catalytic Cracking of Naphtha to Light Olefins

TL;DR: In this paper, a catalytic process that produces light olefins from naphtha was developed to improve the yield of the conventional steam cracker by using a newly developed zeolite-based catalyst at a reaction temperature of 650 °C.
Journal ArticleDOI

Understanding Homogeneous and Heterogeneous Contributions to the Platinum-Catalyzed Partial Oxidation of Ethane in a Short-Contact-Time Reactor

TL;DR: In this article, a computational study of the partial oxidation of ethane to ethylene in a short contact-time reactor, using a two-dimensional computational fluid dynamics model with full heat and mass transport, is presented.
References
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Journal ArticleDOI

Chemical Kinetic Data Base for Combustion Chemistry. Part I. Methane and Related Compounds

TL;DR: In this paper, the authors evaluated data on the kinetics and thermodynamic properties of species that are of importance in methanepyrolysis and combustion, including H, H2, O, O2, OH, HO2, CH2O, CH4, C2H6, HCHO, CO2, CO, HCO, CH3, CH5, CH6, CH7, CH8, CH9, CH10, CH11, CH12, CH13, CH14, CH15, CH16, CH17, CH
Journal ArticleDOI

Formation of gas-phase methyl radicals over magnesium oxide

TL;DR: In this article, the EPR spectroscopy was used to analyze the initial activity of MgO at temperatures of approximately 500/sup 0/C and showed that methyl radicals were produced on the surface, released into the gas phase, and trapped downstream in a solid argon matrix.
Journal ArticleDOI

The catalytic conversion of methane to higher hydrocarbons

TL;DR: In this article, it has been shown that at high temperatures, at atmospheric pressure and at temperatures in excess of 650°C, combined ethane and ethylene (C2) yields of 20% have been achieved.
Journal ArticleDOI

The oxidative conversion of methane to higher hydrocarbons

TL;DR: Many transition metal oxides have been evaluated as oxidative coupling catalysts for converting methane to C2 and higher hydrocarbons as mentioned in this paper, and they have been found to give 10 to 50% selectivity to higher hydro-carbons.
Journal ArticleDOI

Oxidative dehydrogenation of ethane over a lithium-promoted magnesium oxide catalyst

TL;DR: In this article, a selectivity of 75% for ethylene was obtained at 40% ethane conversion over 6.5 g of 3 wt% Li{sup +}/MgO catalyst at 600 C.
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