Sorbent-packed needle microextraction trap for benzene, toluene, ethylbenzene, and xylenes determination in aqueous samples

A needle trap (NT) device filled with Carbopack X as a sorbent material is evaluated for the static headspace analysis of benzene, toluene, ethylbenzene, and xylene (BTEX) compounds in aqueous samples. Injection parameters used with the NT device (e.g. volume of carrier gas and time to open the spli...

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Detalles Bibliográficos
Autores: De Crom, Jorn, Claeys, Sara, Godayol Boix, Anna, Alonso Roura, Mònica, Anticó i Daró, Ma. Enriqueta, Sánchez Navarro, Juan Manuel
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2010
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10256/26036
Acceso en línea:http://hdl.handle.net/10256/26036
Access Level:acceso abierto
Palabra clave:Adsorció
Separació (Tecnologia)
Adsorption
Separation (Technology)
Compostos orgànics volàtils
Volatile organic compounds
Descripción
Sumario:A needle trap (NT) device filled with Carbopack X as a sorbent material is evaluated for the static headspace analysis of benzene, toluene, ethylbenzene, and xylene (BTEX) compounds in aqueous samples. Injection parameters used with the NT device (e.g. volume of carrier gas and time to open the split valve) are evaluated to determine the mechanism involved during the desorption and transferring of the target compounds into the GC column. Furthermore, different parameters affecting the adsorption capacity of the sorbent are studied (e.g. sampling time and temperature, headspace/sample volume ratio, salting-out, and stirring). The evaluation of the method with aqueous samples shows that repeatability and recoveries with the NT device are equivalent to those obtained using solid-phase microextraction with a carboxen/PDMS (CAR/PDMS) coating. LODs obtained with flame ionization detection are in the range of 10-25 μg/L, and in the range of hundredths of μg/L with MS detection. The method developed is satisfactorily applied to the analysis of aqueous samples obtained from wastewater treatment plants