Please use this identifier to cite or link to this item: http://ricaxcan.uaz.edu.mx/jspui/handle/20.500.11845/2029
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dc.contributor265859es_ES
dc.coverage.spatialGlobales_ES
dc.creatorElizondo Álvarez, Martha Araceli-
dc.creatorDávila Pulido, Gloria Ivone-
dc.creatorBello Teodoro, Simón-
dc.creatorUribe Salas, Alejandro-
dc.date.accessioned2020-07-27T19:28:59Z-
dc.date.available2020-07-27T19:28:59Z-
dc.date.issued2019-
dc.identifierinfo:eu-repo/semantics/publishedVersiones_ES
dc.identifier.issn0008-4433es_ES
dc.identifier.issn1879-1395es_ES
dc.identifier.urihttp://ricaxcan.uaz.edu.mx/jspui/handle/20.500.11845/2029-
dc.description.abstractIn the concentrators of a Mexican mining company has been observed that the pH of the flotation has a significant effect on the galena recovery: the increase of pH from 7.5 to 9.5 in the Pb/Cu flotation circuit, resulted in a decrease of about 10% of lead recovery. In the present investigation, experimental models and techniques were developed to study the effect of pH on xanthate and di-isobutyl dithiophosphinate adsorption onto galena. The results obtained by UV / Vis spectroscopy showed that once galena surface has been slightly oxidised by the dissolved oxygen of the aqueous suspension, adsorption of both surfactants increases significantly, being adversely affected by the increase of pH from 5.5 to 9.5. Microflotation measurements performed for both surfactants support these findings. Thermodynamic simulation of the system suggests that the observed behaviour is due to the nature of the solid species formed on the galena surface at the particular pH: lead sulfate (PbSO4) under neutral and slightly acid conditions, and the basic sulfate (2PbO·PbSO4) under neutral and slightly alkaline conditions, as well as to their respective solubility. Infrared spectrometry confirmed the occurrence of sulfate onto galena particles, with a higher concentration for the acid pre-conditioning compared to the alkaline pre-conditioning.es_ES
dc.language.isoenges_ES
dc.publisherTaylor & Francises_ES
dc.relationhttps://www.tandfonline.com/doi/abs/10.1080/00084433.2018.1514202?journalCode=ycmq20es_ES
dc.relation.ispartofwww.tandfonline.com/toc/ycmq20/currentes_ES
dc.relation.urigeneralPublices_ES
dc.rightsAtribución-NoComercial-CompartirIgual 3.0 Estados Unidos de América*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.sourceCanadian Metallurgical Quarterly Vol. 58, No. 1, pp. 107-115es_ES
dc.subject.classificationINGENIERIA Y TECNOLOGIA [7]es_ES
dc.subject.otherGalenaes_ES
dc.subject.otherXanthatees_ES
dc.subject.otherDithiophosphinatees_ES
dc.subject.otherAdsorptiones_ES
dc.titleRole of pH on the adsorption of xanthate and dithiophosphinate onto galenaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
Appears in Collections:*Documentos Académicos*-- M. en C. e Ing. de los Materiales

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