VOx/c-Al2O3 catalyst for oxidative dehydrogenation of ethane to ethylene: desorption kinetics and catalytic activity

This study reports ethane oxidative dehydrogenation (ODH) using lattice oxygen. Ethane ODH is studied under an oxygen-free atmosphere employing a 10 wt.% VOx supported on c-Al2O3. TPR and TPO show that the prepared 10 wt.% VOx supported on c-alumina catalyst is a stable catalyst over repeated reduct...

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Detalles Bibliográficos
Autores: Al Ghamdi, S., Volpe, María Alicia, Hossain, M. M., de Lasa, H.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2013
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/13462
Acceso en línea:http://hdl.handle.net/11336/13462
Access Level:acceso abierto
Palabra clave:Nh3-Tpd Kinetics
Oxidative Dehydrogenation
Ethylene
Vanadium Oxide
Lattice Oxide
Riser Simulator
https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
Descripción
Sumario:This study reports ethane oxidative dehydrogenation (ODH) using lattice oxygen. Ethane ODH is studied under an oxygen-free atmosphere employing a 10 wt.% VOx supported on c-Al2O3. TPR and TPO show that the prepared 10 wt.% VOx supported on c-alumina catalyst is a stable catalyst over repeated reduction and oxidation cycles. XRD shows the absence of V2O5 bulk surface species and a high dispersion of VOx on the support surface. Experiments are carried out in the CREC Fluidized Bed Riser Simulator at 550–600 °C and pressures close to atmospheric conditions. Reactivity tests show that the prepared ODH catalyst displays 6.5–27.6% ethane conversion and 57.6–84.5% ethylene selectivity in the 550–600 °C range. Metal–support interaction is assessed using ammonia TPD. This provides the desorption energy for both the bare c-Al2O3 support and for the VOx/c-Al2O3 catalyst. A slightly increased desorption energy is found when using the V-loaded catalyst. This shows low metal–support interactions and as a result, a well dispersed VOx catalyst phase with high availability of lattice oxygen for ODH. These findings are confirmed with XRD, showing no changes with respect to the XRD for the c-Al2O3 alumina support. This proves that there are no other species formed due to the interaction between the VOx surface species and the Al2O3 support.