Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2429
DC FieldValueLanguage
dc.contributor.authorDelannoy, Laurenten_US
dc.contributor.authorHassan, Nissrine Elen_US
dc.contributor.authorMusi, Andreaen_US
dc.contributor.authorNguyen Le To, Ngaen_US
dc.contributor.authorKrafft, Jean-Marcen_US
dc.contributor.authorLouis , Catherineen_US
dc.date.accessioned2020-12-23T09:13:10Z-
dc.date.available2020-12-23T09:13:10Z-
dc.date.issued2006-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2429-
dc.description.abstractIn this work, we show that if the mere procedure of impregnation of oxide supports with chloroauric acid, which is well-known to lead to large gold particles, is followed by a step of washing with ammonia, small gold particles (3−4 nm) can be obtained after a treatment of calcination at 300 °C on any type of oxide supports (alumina, titania, silica). Moreover, gold leaching is very limited during the washing step, and a large range of gold loadings (0.7−3.5 wt %) can be achieved. Elemental analysis, Raman spectroscopy, and temperature programmed desorption under argon show that this ammonia posttreatment results in the removal of chloride ligands from the coordination sphere of Au(III) precursor and their replacement by ammine ligands, leading to an ammino-hydroxo or an ammino-hydroxo-aquo gold complex and not to gold hydroxide. The Au/TiO2 catalysts prepared with this modified procedure of impregnation are almost as active as those prepared by deposition−precipitation with urea in the CO oxidation reaction performed at room temperature.en_US
dc.format.extent7 p.en_US
dc.language.isoengen_US
dc.titlePreparation of supported gold nanoparticles by a modified incipient wetness impregnation methoden_US
dc.typeJournal Articleen_US
dc.contributor.affiliationDepartment of Chemical Engineeringen_US
dc.description.volume110en_US
dc.description.issue45en_US
dc.description.startpage22471en_US
dc.description.endpage22478en_US
dc.date.catalogued2017-10-26-
dc.description.statusPublisheden_US
dc.identifier.OlibID174558-
dc.relation.ispartoftextJournal of physical chemistry Ben_US
dc.provenance.recordsourceOliben_US
Appears in Collections:Department of Chemical Engineering
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