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Determination of As in honey samples by magnetic ionic liquid-based dispersive liquid-liquid microextraction and electrothermal atomic absorption spectrometry.
Fiorentini, Emiliano F; Canizo, Brenda V; Wuilloud, Rodolfo G.
Afiliação
  • Fiorentini EF; Laboratory of Analytical Chemistry for Research and Development (QUIANID), Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo, Instituto Interdisciplinario de Ciencias Básicas (ICB), UNCUYO-CONICET, Padre J. Contreras 1300, 5500 Mendoza, Argentina.
  • Canizo BV; Laboratory of Analytical Chemistry for Research and Development (QUIANID), Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo, Instituto Interdisciplinario de Ciencias Básicas (ICB), UNCUYO-CONICET, Padre J. Contreras 1300, 5500 Mendoza, Argentina.
  • Wuilloud RG; Laboratory of Analytical Chemistry for Research and Development (QUIANID), Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo, Instituto Interdisciplinario de Ciencias Básicas (ICB), UNCUYO-CONICET, Padre J. Contreras 1300, 5500 Mendoza, Argentina. Electronic address: rwuilloud@mendoza-conicet.gob.ar.
Talanta ; 198: 146-153, 2019 Jun 01.
Article em En | MEDLINE | ID: mdl-30876542
A dispersive liquid-liquid microextraction (DLLME) method was developed based on the application of a magnetic ionic liquid (MIL) used as extractant phase for trace As determination in honey samples by electrothermal atomic absorption spectrometry (ETAAS). The procedure was simple, efficient and did not require a centrifugation stage. The As(III) species was preconcentrated by chelation with ammonium diethyldithiophosphate under acidic conditions at 3 mol L-1 HCl, followed by the extraction of the chelated analyte with the MIL trihexyl(tetradecyl)phosphonium tetrachloroferrate (III) ([P6,6,6,14]FeCl4) and acetonitrile as dispersant. The MIL phase containing the analyte was separated simply by a magnet. The collected aliquot of the MIL phase was injected directly into the graphite furnace of ETAAS for As determination. Under optimal experimental conditions, an extraction efficiency of 99% and a sensitivity enhancement factor of 110 were obtained. The limit of detection was 12 ng L-1 As and the relative standard deviation 3.9% (at 1 µg L-1 As and n = 10), calculated from the peak height of the absorbance signals. The linear range obtained was 0.02-5.0 µg L-1. This work reports the first application of the MIL [P6,6,6,14]FeCl4 along with the DLLME technique for the determination of As in honeys.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arsênio / Líquidos Iônicos / Microextração em Fase Líquida / Mel Idioma: En Revista: Talanta Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Argentina País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arsênio / Líquidos Iônicos / Microextração em Fase Líquida / Mel Idioma: En Revista: Talanta Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Argentina País de publicação: Holanda