Surfactant-enhanced liquid-liquid microextraction coupled to micro-solid phase extraction onto highly hydrophobic magnetic nanoparticles

dc.contributor.authorGiannoulis, K. M.en
dc.contributor.authorGiokas, D. L.en
dc.contributor.authorZhu, Q.en
dc.contributor.authorTsogas, G. Z.en
dc.contributor.authorVlessidis, A. G.en
dc.contributor.authorPan, Q. M.en
dc.date.accessioned2015-11-24T16:48:49Z
dc.date.available2015-11-24T16:48:49Z
dc.identifier.issn0026-3672-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9372
dc.rightsDefault Licence-
dc.subjectdispersive liquid-liquid microextractionen
dc.subjecthighly hydrophobic magnetic nanoparticlesen
dc.subjectmagnetic solid-phase dispersionen
dc.subjectmetal chelatesen
dc.subjectcadmiumen
dc.subjectatomic absorption spectrometryen
dc.subjectatomic-absorption-spectrometryen
dc.subjectenvironmental water samplesen
dc.subjectorganic-compoundsen
dc.subjectdrop microextractionen
dc.subjectpreconcentrationen
dc.subjectseparationen
dc.subjectsolidificationen
dc.subjectoptimizationen
dc.subjectleaden
dc.titleSurfactant-enhanced liquid-liquid microextraction coupled to micro-solid phase extraction onto highly hydrophobic magnetic nanoparticlesen
heal.abstractWe are presenting a simplified alternative method for dispersive liquid-liquid microextraction (DLLME) by resorting to the use of surfactants as emulsifiers and micro solid-phase extraction (mu-SPE). In this combined procedure, DLLME of hydrophobic components is initially accomplished in a mixed micellar/microemulsion extractant phase that is prepared by rapidly mixing a non-ionic surfactant and 1-octanol in aqueous medium. Then, and in contrast to classic DLLME, the extractant phase is collected by highly hydrophobic polysiloxane-coated core-shell Fe2O3@C magnetic nanoparticles. Hence, the sample components are the target analyte in the DLLME which, in turn, becomes the target analyte of the mu-SPE step. This 2-step approach represents a new and simple DLLME procedure that lacks tedious steps such as centrifugation, thawing, or delicate collection of the extractant phase. As a result, the analytical process is accelerated and the volume of the collected phase does not depend on the volume of the extraction solvent. The method was applied to extract cadmium in the form of its pyrrolidine dithiocarbamate chelate from spiked water samples prior to its determination by FAAS. Detection limits were brought down to the low mu g L-1 levels by preconcentrating 10 mL samples with satisfactory recoveries (96.0-108.0 %).en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1007/s00604-013-0987-6-
heal.identifier.secondary<Go to ISI>://000320862100006-
heal.identifier.secondaryhttp://download.springer.com/static/pdf/185/art%253A10.1007%252Fs00604-013-0987-6.pdf?auth66=1381994825_160d20c750615f1d0d3f077ae51b6712&ext=.pdf-
heal.journalNameMicrochimica Actaen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2013-
heal.publisherSpringer Verlag (Germany)en
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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