Simultaneous analysis of 23 priority volatile compounds in water by solid-phase microextraction-gas chromatography-mass spectrometry and estimation of the method's uncertainty

• Tipo: Artigo em Revista Científica Internacional
• Data: 2008

Autores

Ana Dias Guimarães (Autor) Outra; José João Carvalho (Autor) Outra; Maria de Fátima Alpendurada (Autor) FFUP; Carlos Gonçalves (Autor) FFUP

Revista

Título: International Journal of Environmental Analytical Chemistry

Vol. 88 Nº 3

Páginas: 151-164

ISSN: 0306-7319

Editora: Taylor & Francis

Classificação Científica

FOS: Ciências médicas e da saúde > Outras ciências médicas

CORDIS: Ciências da Saúde

Outras Informações

Resumo (PT): Most water contaminations with volatile organic compounds (VOCs) are traceable to leaking underground fuel reservoirs, solvent storage vessels, agricultural practices, industrial residues, and deficient wastewater treatment and disposal. In order to perform effective monitoring of such organic micropollutants in a straightforward manner, a multiresidue method for the determination of 23 VOCs (trihalomethanes (THMs), BTEX and chlorinated solvents) in water has been developed using solid-phase microextraction (SPME) and capillary gas chromatography-mass spectrometry (GC-MS). This group includes also methyl-tert-butyl ether, epichlorhydrine, and vinyl chloride which present additional analytical difficulties. Three different fibres were assayed: 7-µm polydimethylsiloxane (PDMS), 100-µm PDMS, and 75-µm Carboxen-PDMS, and the extraction conditions were optimized. The best results for the majority of the analytes and mainly for those with the lowest signals were obtained using the Carboxen-PDMS fibre after 15 min of extraction in the headspace mode at a room temperature of 20 ± 2°C. The analytical sensitivity, linearity, precision, accuracy, and uncertainties have been studied for method validation in agreement with the international standard ISO/IEC 17025:2005. The limits of detection achieved with the proposed method (0.06-0.17 µg L-1) are adequate to determine the VOCs at the restrictive levels established by the European legislation. This was a decisive achievement to enable the analysis of all VOCs listed under the drinking-water directive in a single assay. The method exhibits performance capabilities suitable for routine analysis of VOCs in drinking-water by quality-control laboratories as enforced by EU Directives. The method is currently being used for this purpose, and participation in proficiency tests was assessed, with encouraging results. <br> <br> Keywords: SPME; Water; VOCs; Epichlorydrine; Vinyl chloride; MTBE; GC-MS; Uncertainty <br> <a target="_blank" href="http://www.informaworld.com/smpp/content~db=all~content=a790621571"> Texto integral</a> <br> <br>

Abstract (EN): Most water contaminations with volatile organic compounds (VOCs) are traceable to leaking underground fuel reservoirs, solvent storage vessels, agricultural practices, industrial residues, and deficient wastewater treatment and disposal. In order to perform effective monitoring of such organic micropollutants in a straightforward manner, a multiresidue method for the determination of 23 VOCs (trihalomethanes (THMs), BTEX and chlorinated solvents) in water has been developed using solid-phase microextraction (SPME) and capillary gas chromatography-mass spectrometry (GC-MS). This group includes also methyl-tert-butyl ether, epichlorhydrine, and vinyl chloride which present additional analytical difficulties. Three different fibres were assayed: 7-µm polydimethylsiloxane (PDMS), 100-µm PDMS, and 75-µm Carboxen-PDMS, and the extraction conditions were optimized. The best results for the majority of the analytes and mainly for those with the lowest signals were obtained using the Carboxen-PDMS fibre after 15 min of extraction in the headspace mode at a room temperature of 20 ± 2°C. The analytical sensitivity, linearity, precision, accuracy, and uncertainties have been studied for method validation in agreement with the international standard ISO/IEC 17025:2005. The limits of detection achieved with the proposed method (0.06-0.17 µg L-1) are adequate to determine the VOCs at the restrictive levels established by the European legislation. This was a decisive achievement to enable the analysis of all VOCs listed under the drinking-water directive in a single assay. The method exhibits performance capabilities suitable for routine analysis of VOCs in drinking-water by quality-control laboratories as enforced by EU Directives. The method is currently being used for this purpose, and participation in proficiency tests was assessed, with encouraging results. <br> <br> Keywords: SPME; Water; VOCs; Epichlorydrine; Vinyl chloride; MTBE; GC-MS; Uncertainty <br> <a target="_blank" href="http://www.informaworld.com/smpp/content~db=all~content=a790621571"> Full text </a> <br> <br>

Idioma: Português

Tipo (Avaliação Docente): Científica