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Improvement of catalyst stability during methane dehydroaromatization (MDA) on Mo/HZSM-5 comprising intracrystalline mesopores

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Improvement of catalyst stability during methane dehydroaromatization (MDA) on Mo/HZSM-5 comprising intracrystalline mesopores

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dc.contributor.author Martinez Feliu, Agustin es_ES
dc.contributor.author Peris, E. es_ES
dc.contributor.author Derewinski, M. es_ES
dc.contributor.author Burkat-Dulak, A. es_ES
dc.date.accessioned 2016-07-18T11:52:38Z
dc.date.available 2016-07-18T11:52:38Z
dc.date.issued 2011-07
dc.identifier.issn 0920-5861
dc.identifier.uri http://hdl.handle.net/10251/67740
dc.description.abstract [EN] Anew Mo/HZSM-5catalyst (3 wt% Mo, Si/Al = 26) comprising a carbon-templated zeolite having intracrystalline mesopores sizing ca. 10-20nm (HZSM-5-BP) has been prepared. For comparison purposes, an equivalent catalyst has also been prepared from a commercial zeolite (HZSM-5-ref). The materials have been extensively characterized by XRD, ICP-OES, N(2) physisorption, SEM-TEM, (27)Al MAS NMR, FTIR-pyridine, NH(3)-TPD, H(2)-TPR, TG-DTG analyses and TPO, and their catalytic activity evaluated for methane dehydroaromatization (MDA) at 700 degrees C, 1 bar, and 1500 ml/g(cat) h. The hierarchical Mo/HZSM-5-BP catalyst displayed a lower deactivation rate during MDA than the reference one, leading to a higher and stable aromatics yield at T.O.S. above 3 h, despite a higher amount of less reactive coke (associated to the zeolite acid sites) was produced in the former. We hypothesize that the enhanced tolerance to carbon deposits of the carbon-templated zeolite could be related to the intracrystalline mesopores acting as a trap for coke molecules and leaving a higher fraction of acid sites within the channels active for aromatization. es_ES
dc.description.sponsorship Financial support by the Comision Interministerial de Ciencia y Tecnologia (CICYT) of Spain through the projects CTQ2007-66614/PPQ and CTQ2006-28341-E/BQU is gratefully acknowledged. Thanks are also due to the UE Network of Excellence IDECAT (FP6 Programme, NMP3-CT-2005-011730) which promoted the collaboration between the two research institutions.
dc.language Inglés es_ES
dc.publisher Elsevier es_ES
dc.relation.ispartof Catalysis Today es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject Methane dehydroaromatization es_ES
dc.subject Mo/HZSM-5 es_ES
dc.subject Intracrystalline mesopores es_ES
dc.subject Catalyst stability es_ES
dc.title Improvement of catalyst stability during methane dehydroaromatization (MDA) on Mo/HZSM-5 comprising intracrystalline mesopores es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1016/j.cattod.2010.11.063
dc.relation.projectID info:eu-repo/grantAgreement/MEC//CTQ2007-66614/ES/NUEVOS CATALIZADORES NANOPARTICULADOS PARA PROCESOS DE CONVERSION DE GAS DE SINTESIS/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/EC/FP6/11730/EU/Integrated Design of Catalytic Nanomaterials for a Sustainable Production/IDECAT/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/MEC//CTQ2006-28341-E/ES/MATERIALES NANOESTRUCTURADOS MICRO-MESOPOROSOS COMO CATALIZADORES EFICIENTES PARA LA PRODUCCION DE DIESEL MEDIOAMBIENTALMENTE LIMPIO/
dc.rights.accessRights Cerrado es_ES
dc.contributor.affiliation Universitat Politècnica de València. Instituto Universitario Mixto de Tecnología Química - Institut Universitari Mixt de Tecnologia Química es_ES
dc.description.bibliographicCitation Martinez Feliu, A.; Peris, E.; Derewinski, M.; Burkat-Dulak, A. (2011). Improvement of catalyst stability during methane dehydroaromatization (MDA) on Mo/HZSM-5 comprising intracrystalline mesopores. Catalysis Today. 169(1):75-84. doi:10.1016/j.cattod.2010.11.063 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion http://dx.doi.org/10.1016/j.cattod.2010.11.063 es_ES
dc.description.upvformatpinicio 75 es_ES
dc.description.upvformatpfin 84 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 169 es_ES
dc.description.issue 1 es_ES
dc.relation.senia 41162 es_ES
dc.contributor.funder Comisión Interministerial de Ciencia y Tecnología
dc.contributor.funder European Commission


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