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dc.contributor.authorPalhares, Luciana Boaventura-
dc.contributor.authorSantos, Claudio Gouvea dos-
dc.contributor.authorHunter, Timothy-
dc.date.accessioned2018-03-13T14:42:34Z-
dc.date.available2018-03-13T14:42:34Z-
dc.date.issued2016-
dc.identifier.citationPALHARES, L. B.; SANTOS, C. G. dos; HUNTER, T. Study of citric acid dispersant in the settling behavior of slate powder suspensions. International Journal of Mineral Processing, v. 150, p. 39-46, maio 2016. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0301751616300436>. Acesso em: 15 set. 2017.pt_BR
dc.identifier.issn0301-7516-
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/9604-
dc.description.abstractThe behavior of aqueous suspensions of slate stabilizedwith citric acidwas investigated using sedimentation and rheological techniques. In order to determine the more effective dispersing agent concentration and the maximum loading of solids, a series of 12 suspensions were prepared with citric acid content between 0.5 and 2.5% w/v and solid percentages of 40, 55 and 70%. Light scattering techniques were used to obtain sedimentation data and particle size distribution; flow curves were obtained with a rheometer. The results indicated that the interaction between particle surfaces could either induce flocculation, at higher citric acid concentrations, or enhance the stabilization, at low dispersant concentration and pH values around 6. The highest sediment bed density was obtained for suspensions with 40% slate powder and 1.0% citric acid. This behavior was explained on the basis of the carboxyl groups of citric acid promoting higher dispersion of the particles resulting in lower settling rate, better stability and enhanced compact sediment bed.pt_BR
dc.language.isoen_USpt_BR
dc.rightsrestritopt_BR
dc.subjectSlate powderpt_BR
dc.subjectSuspensionspt_BR
dc.subjectSedimentation techniquespt_BR
dc.titleStudy of citric acid dispersant in the settling behavior of slate powder suspensions.pt_BR
dc.typeArtigo publicado em periodicopt_BR
dc.identifier.uri2http://www.sciencedirect.com/science/article/pii/S0301751616300436pt_BR
dc.identifier.doihttps://doi.org/10.1016/j.minpro.2016.03.005-
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