Coupling dispersive liquid-liquid microextraction to inductively coupled plasma atomic emission spectrometry: An oxymoron?

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10045/68969
Información del item - Informació de l'item - Item information
Título: Coupling dispersive liquid-liquid microextraction to inductively coupled plasma atomic emission spectrometry: An oxymoron?
Autor/es: Martínez Rubio, David | Torregrosa Carretero, Daniel | Grindlay, Guillermo | Gras, Luis | Mora, Juan
Grupo/s de investigación o GITE: Espectrometría Atómica Analítica (GEAA)
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatología
Palabras clave: Metals | Sample preparation | Dispersive liquid-liquid microextraction | Flow-injection | Atomic emission spectrometry | Inductively coupled plasma
Área/s de conocimiento: Química Analítica
Fecha de publicación: 1-ene-2018
Editor: Elsevier
Cita bibliográfica: Talanta. 2018, 176: 374-381. doi:10.1016/j.talanta.2017.08.036
Resumen: Coupling dispersive liquid-liquid micro-extraction (DLLME) to inductively coupled plasma atomic emission spectrometry (ICP-AES) is usually troublesome due to the limited plasma tolerance to the organic solvents usually employed for metal extraction. This work explores different coupling strategies allowing the multi-element determination by ICP-AES of the solutions obtained after DLLME procedures. To this end, three of the most common extractant solvents in DLLME procedures (1-undecanol, 1-butyl-3-methyl-imidazolium hexafluorophosphate and chloroform) have been selected to face most of the main problems reported in DLLME-ICP-AES coupling (i.e., those arising from the high solvent viscosity and volatility). Results demonstrate that DLLME can be successfully coupled to ICP-AES after a careful optimization of the experimental conditions. Thus, elemental analysis in 1-undecanol and 1-butyl-3-methyl-imidazolium hexafluorophosphate extracts can be achieved by ICP-AES after a simple dilution step with methanol (1:0.5). Chloroform can be directly introduced into the plasma with minimum changes in the ICP-AES configuration usually employed when operating with aqueous solutions. Diluted inorganic acid solutions (1% w w−1 either nitric or hydrochloric acids) have been successfully tested for the first time as a carrier for the introduction of organic extractants in ICP-AES. The coupling strategies proposed have been successfully applied to the multi-element analysis (Al, Cu, Fe, Mn, Ni and Zn) of different water samples (i.e. marine, tap and river) by DLLME-ICP-AES.
Patrocinador/es: The authors would like to thank the Generalitat Valenciana (Project GV/2014/138) for the financial support of this work. D. Martínez and D. Torregrosa also thank the University of Alicante for the research fellowships (UAFPU2015-5998 and AII16-33).
URI: http://hdl.handle.net/10045/68969
ISSN: 0039-9140 (Print) | 1873-3573 (Online)
DOI: 10.1016/j.talanta.2017.08.036
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2017 Elsevier B.V.
Revisión científica: si
Versión del editor: http://dx.doi.org/10.1016/j.talanta.2017.08.036
Aparece en las colecciones:INV - GEAA - Artículos de Revistas

Archivos en este ítem:
Archivos en este ítem:
Archivo Descripción TamañoFormato 
Thumbnail2018_Martinez_etal_Talanta_final.pdfVersión final (acceso restringido)894,28 kBAdobe PDFAbrir    Solicitar una copia
Thumbnail2018_Martinez_etal_Talanta_accepted.pdfEmbargo 24 meses (acceso abierto: 11 ag. 2019)777,86 kBAdobe PDFAbrir    Solicitar una copia


Todos los documentos en RUA están protegidos por derechos de autor. Algunos derechos reservados.