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The nature of ruthenium sulfide clusters encaged in a Y zeolite

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dc.contributor.author Moraweck, B en
dc.contributor.author Bergeret, G en
dc.contributor.author Cattenot, M en
dc.contributor.author Kougionas, V en
dc.contributor.author Geantet, C en
dc.contributor.author Portefaix, J-L en
dc.contributor.author Zotin, JL en
dc.contributor.author Breysse, M en
dc.date.accessioned 2014-03-01T01:46:15Z
dc.date.available 2014-03-01T01:46:15Z
dc.date.issued 1997 en
dc.identifier.issn 00219517 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/24876
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-0002413359&partnerID=40&md5=90238a7a72b26517e6da124aee70c1df en
dc.title The nature of ruthenium sulfide clusters encaged in a Y zeolite en
heal.type journalArticle en
heal.publicationDate 1997 en
heal.abstract Catalysts of ruthenium sulfide supported in a dealuminated KY zeolite were prepared by ion exchange and subsequent sulfidation using several atmospheres containing sulfur. They were characterized by means of HREM, EDX, TPR, and EXAFS. The activity for the tetralin hydrogenation, carried out in presence of large amounts of H2S (1.85%), was very high and roughly 300 times the activity (expressed per metal atom) of an industrial NiMo/Al2O3 hydrotreating catalyst. A simple modeling of the results obtained by the physicochemical techniques suggests that the active phase consists of clusters of less than 50 ruthenium atoms of a ruthenium sulfide-like phase with very small domains of ruthenium metal. © 1997 Academic Press, Inc. en
heal.journalName Journal of Catalysis en
dc.identifier.volume 165 en
dc.identifier.issue 1 en
dc.identifier.spage 45 en
dc.identifier.epage 56 en


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