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Synthesis, acid properties and catalysis by niobium oxide nanostructured materials

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Synthesis, acid properties and catalysis by niobium oxide nanostructured materials

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dc.contributor.author Marín García, Mª Luisa es_ES
dc.contributor.author Hallett-Tapley, Geniece L. es_ES
dc.contributor.author Impellizzeri, Stefania es_ES
dc.contributor.author Fasciani, Chiara es_ES
dc.contributor.author Simoncelli, Sabrina es_ES
dc.contributor.author Netto-Ferreira, Jose Carlos es_ES
dc.contributor.author Scaiano, Juan C. es_ES
dc.date.accessioned 2016-03-04T11:47:25Z
dc.date.available 2016-03-04T11:47:25Z
dc.date.issued 2014
dc.identifier.issn 2044-4753
dc.identifier.uri http://hdl.handle.net/10251/61430
dc.description.abstract Several forms of niobium oxide were prepared, including nanostructured mesoporous materials, and their acidity properties were comprehensively investigated and compared with commercially available materials. The composites were characterized by a variety of techniques, including XRD, TEM, N-2 adsorption and Hammett acid indicator studies. The acidity of the niobium oxide derivatives was also investigated by the ability of the materials to successfully promote the halochromic ring-opening of an oxazine-coumarin probe that was specifically designed for use in fluorescence imaging studies. The ring-opening reaction was easily monitored using UV-visible, fluorescence and NMR spectroscopy. Single molecule microscopy was employed to gain a more in-depth understanding of the niobium oxide acid catalysis pathway. Using this technique, the rate of niobium oxide mediated protonation was estimated to be 1.8 x 10(-13) mol m(-2) s(-1). Single molecule analysis was also used to obtain a detailed map of Bronsted acid sites on the niobium oxide surface. The active sites, located by multiple blinking events, do not seem to be localized on any area of the material, but rather randomly distributed throughout the solid state surface. As the reaction proceeds, the sites with the highest acidity and accessibility are gradually consumed, making the next tier of acid sites available for reaction. The phenomenon was more closely characterized by using time lapsed reactivity maps. es_ES
dc.description.sponsorship The authors wish to thank the Natural Sciences and Engineering Research Council (NSERC) and the Canada Research Chairs program. The University of Ottawa International Office provided grants to study niobium. M. L. Marin thanks the financial support of the Generalitat Valenciana (BEST/2012/233). Thanks are due to the Government of Canada and NSERC for a Banting Postdoctoral Fellowship to S. Impellizzeri and a Vanier Sholarship to C. Fasciani. S. Simoncelli acknowledges a DFAIT fellowship from ELAP (Emerging Leaders in the Americas Program) to support her visit to Canada. en_EN
dc.language Inglés es_ES
dc.publisher Royal Society of Chemistry es_ES
dc.relation.ispartof Catalysis Science and Technology es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject 5-HYDROXYMETHYL-2-FURALDEHYDE es_ES
dc.subject DEHYDRATION es_ES
dc.subject PHOSPHATE es_ES
dc.subject SILICA es_ES
dc.subject.classification QUIMICA ORGANICA es_ES
dc.subject.classification QUIMICA ANALITICA es_ES
dc.title Synthesis, acid properties and catalysis by niobium oxide nanostructured materials es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1039/c4cy00238e
dc.relation.projectID info:eu-repo/grantAgreement/GVA//BEST%2F2012%2F233/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Departamento de Química - Departament de Química 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 Marín García, ML.; Hallett-Tapley, GL.; Impellizzeri, S.; Fasciani, C.; Simoncelli, S.; Netto-Ferreira, JC.; Scaiano, JC. (2014). Synthesis, acid properties and catalysis by niobium oxide nanostructured materials. Catalysis Science and Technology. 4(9):3044-3052. https://doi.org/10.1039/c4cy00238e es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion http://dx.doi.org/10.1039/c4cy00238e es_ES
dc.description.upvformatpinicio 3044 es_ES
dc.description.upvformatpfin 3052 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 4 es_ES
dc.description.issue 9 es_ES
dc.relation.senia 279828 es_ES
dc.identifier.eissn 2044-4761
dc.contributor.funder Government of Canada es_ES
dc.contributor.funder Generalitat Valenciana es_ES
dc.contributor.funder University of Ottawa es_ES
dc.contributor.funder Natural Sciences and Engineering Research Council of Canada es_ES
dc.contributor.funder Foreign Affairs and International Trade Canada


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