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Authordc.contributor.authorFolch Cano, Christian
Authordc.contributor.authorOlea Azar, Claudioes_CL
Authordc.contributor.authorSpeisky Cosoy, Hernánes_CL
Admission datedc.date.accessioned2014-02-12T19:55:05Z
Available datedc.date.available2014-02-12T19:55:05Z
Publication datedc.date.issued2013
Cita de ítemdc.identifier.citationColloids and Surfaces A: Physicochem. Eng. Aspects 418 (2013) 105–111en_US
Identifierdc.identifier.otherdoi 10.1016/j.colsurfa.2012.11.017
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/124103
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractIn this studywefindthe possible structural factors that can determine the adsorption process ofsomepure phenolic compounds (PC) onto polyvinylpolypyrrolidone (PVPP), analyzing their adsorption isotherms by using the Langmuir and the Freundlich theories. In this perspective, the adsorption capacity of short size PC would depend on the number and availability of its hydroxyl groups. To intermediate molecular size PC, the improvement in the adsorption capacity presumably depends on its resemblance with the resveratrol molecule. To large size PC, the adsorption capacity was considerably high due to hydroxyl groups disposed in different spatial orientations with respect to the plane. Thermodynamic analyses showed that adsorption onto PVPP of some pure PC correspond to a physisorption process that was spontaneous and enthalpically-driven for PC like catechin (C) and entropically-driven for PC like epigallocatechin gallate (EGCG) and gallic acid (GA). These results implicate potential selective adsorption uses of PVPP.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevieren_US
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Keywordsdc.subjectPolyvinylpolypyrrolidoneen_US
Títulodc.titleStructural and thermodynamic factors on the adsorption process of phenolic compounds onto polyvinylpolypyrrolidoneen_US
Document typedc.typeArtículo de revistaen_US


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile