Application of a central composite design to the determination of inorganic and organic arsenic species in water by liquid chromatography-hydride generation-atomic absorption spectrometry

An on-line high performance liquid chromatography - hydride generation atomic absorption spectrometry coupled system (HPLC–HG–AAS) has been used for the determination of [As (III)], [As (V)], monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA) in water samples. Four variables were taken into...

Descripción completa

Detalles Bibliográficos
Autores: Blanes, Patricia Silvia, Hunzicker, Gabriel Alejandro, Garro, Oscar Alfredo, Giménez, María Cecilia
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2009
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/62118
Acceso en línea:http://hdl.handle.net/11336/62118
Access Level:acceso abierto
Palabra clave:ARSENIC SPECIATION
CENTRAL COMPOSITE DESIGN
HIGH PERFORMANCE LIQUID CHROMATOGRAPHICS
HYDRIDE GENERATION
ATOMIC ABSORPTION SPECTROMETRY
WATER ANALYSIS
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
Descripción
Sumario:An on-line high performance liquid chromatography - hydride generation atomic absorption spectrometry coupled system (HPLC–HG–AAS) has been used for the determination of [As (III)], [As (V)], monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA) in water samples. Four variables were taken into account and a central composite design 24+* was used in the optimization of analytical conditions for the arsenic speciation method. The variables investigated were (A) mobile phase flow rate, (B) HCl concentration, (C) KI concentration, (D) NaBH4 concentration. Individual factors (A) and (B) were the most significant effects, and the optimum conditions for all factors were A = 1.2 mL min–1, B = 2.8 mol L–1, C = 1.7 % w/v, and D = 1.4 % w/v. The repeatability, stability, calibration curve and limit of detection were established. The method was applied to different kinds of waters; good recoveries of added spikes (92 – 109 %) were obtained for all analytes.