dc.creatorROSSI, Liane M.
dc.creatorMACHADO, Giovanna
dc.date.accessioned2012-10-20T05:23:30Z
dc.date.accessioned2018-07-04T15:49:21Z
dc.date.available2012-10-20T05:23:30Z
dc.date.available2018-07-04T15:49:21Z
dc.date.created2012-10-20T05:23:30Z
dc.date.issued2009
dc.identifierJOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, v.298, n.1/Fev, p.69-73, 2009
dc.identifier1381-1169
dc.identifierhttp://producao.usp.br/handle/BDPI/31228
dc.identifier10.1016/j.molcata.2008.10.007
dc.identifierhttp://dx.doi.org/10.1016/j.molcata.2008.10.007
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1627866
dc.description.abstractThe hydrogenation of benzene and benzene derivatives was studied using Ru(0) nanoparticles prepared by a very simple method based on the in situ reduction of the commercially available precursor ruthenium dioxide under mild conditions (75 degrees C and hydrogen pressure 4atm) in imidazolium ionic liquids. Total turnovers (TTO) of 2700 mol/mol Ru were obtained for the conversion of benzene to cyclohexane under solventless conditions and TTO of 1200 mol/mol Ru were observed under ionic liquid biphasic conditions. When corrected for exposed ruthenium atoms, TTO values of 7940 (solventless) and 3530 (biphasic) were calculated for benzene hydrogenation. These reaction rates are higher than those observed for Ru nanoparticles prepared from decomposition of an organometallic precursor in similar conditions. The presence of the partially hydrogenated product cyclohexene was also detected at low conversion rates. (C) 2008 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherELSEVIER SCIENCE BV
dc.relationJournal of Molecular Catalysis A-chemical
dc.rightsCopyright ELSEVIER SCIENCE BV
dc.rightsrestrictedAccess
dc.subjectNanoparticle
dc.subjectRuthenium
dc.subjectHydrogenation
dc.subjectBenzene
dc.subjectIonic liquid
dc.titleRuthenium nanoparticles prepared from ruthenium dioxide precursor: Highly active catalyst for hydrogenation of arenes under mild conditions
dc.typeArtículos de revistas


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