dc.creatorMartinis, Estefanía Mabel
dc.creatorEscudero, Leticia Belén
dc.creatorBerton, Paula
dc.creatorMonasterio, Romina Paula
dc.creatorFilippini, Maria Flavia Ramona
dc.creatorWuilloud, Rodolfo German
dc.date.accessioned2019-12-26T14:40:03Z
dc.date.accessioned2022-10-15T15:42:41Z
dc.date.available2019-12-26T14:40:03Z
dc.date.available2022-10-15T15:42:41Z
dc.date.created2019-12-26T14:40:03Z
dc.date.issued2011-09
dc.identifierMartinis, Estefanía Mabel; Escudero, Leticia Belén; Berton, Paula; Monasterio, Romina Paula; Filippini, Maria Flavia Ramona; et al.; Determination of inorganic selenium species in water and garlic samples with on-line ionic liquid dispersive microextraction and electrothermal atomic absorption spectrometry; Elsevier Science; Talanta; 85; 4; 9-2011; 2182-2188
dc.identifier0039-9140
dc.identifierhttp://hdl.handle.net/11336/92907
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4404384
dc.description.abstractA non-chromatographic separation and preconcentration method for Se species determination based on the use of an on-line ionic liquid (IL) dispersive microextraction system coupled to electrothermal atomic absorption spectrometry (ETAAS) is proposed. Retention and separation of the IL phase was achieved with a Florisil®-packed microcolumn after dispersive liquid-liquid microextraction (DLLME) with tetradecyl(trihexyl)phosphonium chloride IL (CYPHOS® IL 101). Selenite [Se(IV)] species was selectively separated by forming Se-ammonium pyrrolidine dithiocarbamate (Se-APDC) complex followed by extraction with CYPHOS® IL 101. The methodology was highly selective towards Se(IV), while selenate [Se(VI)] was reduced and then indirectly determined. Several factors influencing the efficiency of the preconcentration technique, such as APDC concentration, sample volume, extractant phase volume, type of eluent, elution flow rate, etc., have been investigated in detail. The limit of detection (LOD) was 15 ng L-1 and the relative standard deviation (RSD) for 10 replicates at 0.5 μg L -1 Se concentration was 5.1%, calculated with peak heights. The calibration graph was linear and a correlation coefficient of 0.9993 was achieved. The method was successfully employed for Se speciation studies in garlic extracts and water samples.
dc.languageeng
dc.publisherElsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.talanta.2011.07.065
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0039914011006588
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectIONIC LIQUID
dc.subjectLIQUID-LIQUID MICROEXTRACTION
dc.subjectPRECONCENTRATION
dc.subjectSELENIUM
dc.subjectSPECIATION
dc.subjectTETRADECYL(TRIHEXYL)PHOSPHONIUM CHLORIDE
dc.titleDetermination of inorganic selenium species in water and garlic samples with on-line ionic liquid dispersive microextraction and electrothermal atomic absorption spectrometry
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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