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Please use this identifier to cite or link to this item: https://saber.ucv.ve/jspui/handle/10872/6134
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dc.contributor.authorAcevedo, Sócrates-
dc.contributor.authorRanaudo, María Antonieta-
dc.contributor.authorGarcía, Coromoto-
dc.contributor.authorCastillo, Jimmy-
dc.contributor.authorFernández, Alberto-
dc.date.accessioned2014-04-29T15:52:28Z-
dc.date.available2014-04-29T15:52:28Z-
dc.date.issued2003-01-16-
dc.identifier.citationEnergy Fuels, 2003, 17 (2), pp 257–261es_VE
dc.identifier.other10.1021/ef020104q-
dc.identifier.urihttp://hdl.handle.net/10872/6134-
dc.description.abstractThe adsorption kinetics of asphaltenes at the toluene - silica interface has been measured for nine solution concentrations CS (from 5 to 3000 mgL-1) Results could be adjusted to an irreversible second-order adsorption kinetics, where the adsorption rate k was strongly dependent on concentration. Thus a large reduction in k was observed when CS was increased in the studied concentration range. This rate reduction was accounted for in terms of adsorption of aggregates formed in solution. The step - wise trends observed for the adsorption isotherms of asphaltenes on mineral surfaces, could be reproduced using the above k values.es_VE
dc.language.isoenes_VE
dc.publisherEnergy & Fuel an american chemicla society Journales_VE
dc.subjectAsphalteneses_VE
dc.subjectAsfaltenoses_VE
dc.subjectAdsorptiones_VE
dc.subjectAdsorciónes_VE
dc.subjectcrude oiles_VE
dc.subjectpetróleoes_VE
dc.titleAdsorption of Asphaltenes at the Toluene-Silica Interface: A Kinetic Studyes_VE
dc.typeArticlees_VE
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