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Magnetic ionic liquids as non-conventional extraction solvents for the determination of polycyclic aromatic hydrocarbons
dc.contributor.author | Trujillo Rodríguez, María José | |
dc.contributor.author | Nacham, Omprakash | |
dc.contributor.author | Clark, Kevin D. | |
dc.contributor.author | Pino, Veronica | |
dc.contributor.author | Anderson, Jared L. | |
dc.contributor.author | Ayala, Juan H. | |
dc.contributor.author | Afonso, Ana M. | |
dc.contributor.other | Química | |
dc.contributor.other | MAT4LL Materials for chemical analysis (https://portalciencia.ull.es/grupos/6582/detalle) | |
dc.date.accessioned | 2024-02-08T21:08:07Z | |
dc.date.available | 2024-02-08T21:08:07Z | |
dc.date.issued | 2016 | |
dc.identifier.uri | http://riull.ull.es/xmlui/handle/915/36181 | |
dc.description.abstract | This work describes the applicability of magnetic ionic liquids (MILs) in the analytical determination of a group of heavy polycyclic aromatic hydrocarbons. Three different MILs, namely, benzyltrioctylammonium bromotrichloroferrate (III) (MIL A), methoxybenzyltrioctylammonium bromotrichloroferrate (III) (MIL B), and 1,12-di(3-benzylbenzimidazolium) dodecane bis[(trifluoromethyl) sulfonyl)]imide bromotrichloroferrate (III) (MIL C), were designed to exhibit hydrophobic properties, and their performance examined in a microextraction method for hydrophobic analytes. The magnet-assisted approach with these MILs was performed in combination with high performance liquid chromatography and fluorescence detection. The study of the extraction performance showed that MIL A was the most suitable solvent for the extraction of polycyclic aromatic hydrocarbons and under optimum conditions the fast extraction step required ~20 mL of MIL A for 10 mL of aqueous sample, 24 mmol L1 NaOH, high ionic strength content of NaCl (25% (w/v)), 500 mL of acetone as dispersive solvent, and 5 min of vortex. The desorption step required the aid of an external magnetic field with a strong NdFeB magnet (the separation requires few seconds), two back-extraction steps for polycyclic aromatic hydrocarbons retained in the MIL droplet with n-hexane, evaporation and reconstitution with acetonitrile. The overall method presented limits of detection down to 5 ng L1 , relative recoveries ranging from 91.5 to 119%, and inter-day reproducibility values (expressed as relative standard derivation) lower than 16.4% for a spiked level of 0.4 mg L1 (n ¼ 9). The method was also applied for the analysis of real samples, including tap water, wastewater, and tea infusion | en |
dc.format.mimetype | application/pdf | |
dc.language.iso | en | |
dc.relation.ispartofseries | Analytica Chimica Acta. Volume 934, 31 August 2016, Pages 106-113 | |
dc.rights | Licencia Creative Commons (Reconocimiento-No comercial-Sin obras derivadas 4.0 Internacional) | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es_ES | |
dc.title | Magnetic ionic liquids as non-conventional extraction solvents for the determination of polycyclic aromatic hydrocarbons | en |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | 10.1016/j.aca.2016.06.014 | |
dc.subject.keyword | Ionic liquids | en |
dc.subject.keyword | Magnetic ionic liquids | en |
dc.subject.keyword | Magnetic-assisted microextraction | en |
dc.subject.keyword | Polycyclic aromatic hydrocarbons | en |
dc.subject.keyword | High-performance liquid chromatography | en |