Effects of Lattice O Atom Coordination and Pore Confinement on Selectivity Limitations for Ethane Oxidative Dehydrogenation Catalyzed by Vanadium-Oxo Species

2019 ◽  
Vol 123 (46) ◽  
pp. 28168-28191 ◽  
Author(s):  
Yilang Liu ◽  
Leelavathi Annamalai ◽  
Prashant Deshlahra
ACS Catalysis ◽  
2016 ◽  
Vol 6 (7) ◽  
pp. 4775-4781 ◽  
Author(s):  
Mimoun Aouine ◽  
Thierry Epicier ◽  
Jean-Marc M. Millet

2020 ◽  
Vol 63 (19-20) ◽  
pp. 1754-1764
Author(s):  
Daniel Melzer ◽  
Gerhard Mestl ◽  
Klaus Wanninger ◽  
Andreas Jentys ◽  
Maricruz Sanchez-Sanchez ◽  
...  

AbstractThe pathways of ethane oxidative dehydrogenation and total combustion have been elucidated for M1 phase type Mo–V oxide catalysts with different metal composition. The ethane oxidation mechanism is not affected by the presence of Te or Nb. Conversely, the selectivity is strongly affected by stoichiometry of M1 catalysts. This is attributed to the facile oxidation of ethene to COx upon formation of unselective VOx species in the absence of Te and Nb.


2000 ◽  
Vol 61 (1-4) ◽  
pp. 87-92 ◽  
Author(s):  
Yumin Liu ◽  
Peijun Cong ◽  
Robert D. Doolen ◽  
Howard W. Turner ◽  
W.Henry Weinberg

2016 ◽  
Vol 6 (18) ◽  
pp. 6953-6964 ◽  
Author(s):  
Ştefan-Bogdan Ivan ◽  
Ionel Popescu ◽  
Ioana Fechete ◽  
François Garin ◽  
Vasile I. Pârvulescu ◽  
...  

Adding P to NiO leads to a decrease of ethane conversion with an increase in ODH selectivity.


Author(s):  
Gulsun Karamullaoglu ◽  
Timur Dogu

Oxidative dehydrogenation of ethane to ethylene was investigated over Chromia and Cr-V mixed oxide catalysts synthesized following a complexation procedure. With an O2/C2H6 feed ratio of 0.17, Chromia exhibited a total conversion value of about 0.20 at 447°C (at a space time of 0.24 s.g/mL) with an ethylene selectivity of 0.82. Chromia catalyst was more active than Cr-V mixed oxide at temperatures as low as 200°C. Pulse-response experiments carried out with ethane pulses injected into O2-He indicated the presence of at least two different sites for the formation of CO2 and H2O over Chromia catalyst. In the dynamic experiments carried out with the Cr-V mixed oxide catalyst and by injecting O2 pulses into a gas stream containing a mixture of C2H6 and He, formation of CO rather than C2H4 was favored. Results of the dynamic runs carried out without gas phase oxygen strengthened the conclusion of lattice oxygen participation in the selective oxidation of ethane reaction through a redox mechanism.


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