dc.creatorJACOBS, Gary
dc.creatorRIBEIRO, Mauro C.
dc.creatorMA, Wenping
dc.creatorJI, Yaying
dc.creatorKHALID, Syed
dc.creatorSUMODJO, Paulo T. A.
dc.creatorDAVIS, Burtron H.
dc.date.accessioned2012-10-20T05:23:13Z
dc.date.accessioned2018-07-04T15:49:08Z
dc.date.available2012-10-20T05:23:13Z
dc.date.available2018-07-04T15:49:08Z
dc.date.created2012-10-20T05:23:13Z
dc.date.issued2009
dc.identifierAPPLIED CATALYSIS A-GENERAL, v.361, n.1/Fev, p.137-151, 2009
dc.identifier0926-860X
dc.identifierhttp://producao.usp.br/handle/BDPI/31181
dc.identifier10.1016/j.apcata.2009.04.007
dc.identifierhttp://dx.doi.org/10.1016/j.apcata.2009.04.007
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1627819
dc.description.abstractCo/Al(2)O(3) Fischer-Tropsch synthesis catalysts promoted with different quantities of Group 11 metals (Cu, Ag, Au) were characterized and tested. The presence of relatively small quantities of such metals enhanced Co reducibility and, in the cases of Ag and Au, improved the surface Co metal active site densities. EXAFS experiments with the most loaded catalyst samples show that only Co-Co and Me-Me (Me = Cu, Ag and Au) coordination could be observed. This suggests that the greater fraction of the metals form different phases. However, the reduction promoting effect of the Group 11 metal is severely hampered once the catalyst receives a mild passivation treatment following primary reduction. An explanation in terms of promoter segregation during primary reduction is proposed. At lower promoter levels (0.83%Ag and 1.51%Au) and higher Ag levels (2.76%), significant gains in Co active site densities were achieved resulting in improved CO conversion levels relative to the unpromoted catalyst. Moreover, slight decreases in light product (e.g., CH(4)) selectivity and slight increases in C(5)+ selectivity were achieved. At high Au loading (5.05%), however, too much Au was loaded which, although significantly increasing the fraction of Co reduced, blocked Co surface sites and resulted in decreased Co conversion rates. While Cu facilitated Co reduction, the increased fraction of reduced Co did not translate to improved active site densities. It appears that a fraction of Cu tended to cover the rim of Co clusters, resulting in decreases in CO conversion rates and detrimental increases in light product selectivity. (C) 2009 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherELSEVIER SCIENCE BV
dc.relationApplied Catalysis A-general
dc.rightsCopyright ELSEVIER SCIENCE BV
dc.rightsrestrictedAccess
dc.subjectCo
dc.subjectCobalt
dc.subjectCu
dc.subjectCopper
dc.subjectAg
dc.subjectSilver
dc.subjectAu
dc.subjectGold
dc.subjectAl(2)O(3)
dc.subjectAlumina
dc.subjectSyngas
dc.subjectSynthesis gas
dc.subjectFischer-Tropsch synthesis
dc.subjectFT
dc.subjectGas to liquids
dc.subjectGTL
dc.subjectPromoters
dc.subjectReducibility
dc.subjectEXAFS
dc.subjectXANES
dc.titleGroup 11 (Cu, Ag, Au) promotion of 15%Co/Al(2)O(3) Fischer-Tropsch synthesis catalysts
dc.typeArtículos de revistas


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