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1.
Environ Pollut ; 183: 143-50, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23639471

RESUMEN

Tropospheric ozone is a secondary pollutant whose primary sources are volatile organic compounds and nitrogen oxides. The national standard is exceeded on a third of summer days in some areas of the Chilean Metropolitan Region (MR). This study reports normalized springtime experimental emissions factors (EF) for biogenic volatile organic compounds from tree species corresponding to approximately 31% of urban trees in the MR. A Photochemical Ozone Creation Index (POCI) was calculated using Photochemical Ozone Creation Potential of quantified terpenes. Ten species, natives and exotics, were analysed using static enclosure technique. Terpene quantification was performed using GC-FID, thermal desorption, cryogenic concentration and automatic injection. Observed EF and POCI values for terpenes from exotic species were 78 times greater than native values; within the same family, exotic EF and POCI values were 28 and 26 times greater than natives. These results support reforestation with native species for improved urban pollution management.


Asunto(s)
Contaminantes Atmosféricos/análisis , Monitoreo del Ambiente , Árboles/fisiología , Compuestos Orgánicos Volátiles/análisis , Chile , Ciudades , Óxidos de Nitrógeno/análisis , Ozono/análisis , Terpenos/análisis
2.
Talanta ; 103: 361-70, 2013 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-23200400

RESUMEN

The possibility of simultaneously determining seven concerned heavy polycyclic aromatic hydrocarbons (PAHs) of the US-EPA priority pollutant list, in extra virgin olive and sunflower oils was examined using unfolded partial least-squares with residual bilinearization (U-PLS/RBL) and parallel factor analysis (PARAFAC). Both of these methods were applied to fluorescence excitation emission matrices. The compounds studied were benzo[a]anthracene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenz[a,h]anthracene, benzo[g,h,i]perylene and indeno[1,2,3-c,d]-pyrene. The analysis was performed using fluorescence spectroscopy after a microwave assisted liquid-liquid extraction and solid-phase extraction on silica. The U-PLS/RBL algorithm exhibited the best performance for resolving the heavy PAH mixture in the presence of both the highly complex oil matrix and other unpredicted PAHs of the US-EPA list. The obtained limit of detection for the proposed method ranged from 0.07 to 2 µg kg(-1). The predicted U-PLS/RBL concentrations were satisfactorily compared with those obtained using high-performance liquid chromatography with fluorescence detection. A simple analysis with a considerable reduction in time and solvent consumption in comparison with chromatography are the principal advantages of the proposed method.


Asunto(s)
Análisis de los Mínimos Cuadrados , Aceites de Plantas/análisis , Hidrocarburos Policíclicos Aromáticos/análisis , Espectrometría de Fluorescencia , Cromatografía Líquida de Alta Presión , Estudios de Factibilidad , Extracción Líquido-Líquido , Microondas , Aceite de Oliva , Extracción en Fase Sólida , Aceite de Girasol
3.
Talanta ; 100: 439-46, 2012 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-23141362

RESUMEN

The potential of microwave-assisted liquid-liquid and solid phase extraction coupled with fluorescence spectroscopy and employing one- to three-way spectral data was assessed in terms of their capacity for the rapid detection of heavy polycyclic aromatic hydrocarbons (PAHs) in olive and sunflower oils. Tocopherols and pigments groups (chlorophyll and pheophytin) present in oil matrices were the main interference compounds in the detection of PAHs using fluorescence spectroscopy. Partial spectral overlap and inner-filter effects were observed in the emission range of the analytes. The effectiveness of removing these interferences using solid phase extraction (silica, C18 and graphitized carbon black) was examined. Solid phase extraction with silica was the most effective method for the removal of pigments and tocopherol and allowed for the detection of PAHs in edible oils using fluorescence spectroscopy. The limit of detection was observed to depend on the use of one-, two- or three-way fluorescence spectral data in the range of 0.8 to 7.0 µg kg(-1). The individual recoveries of PAHs following the microwave-assisted L-L extraction and SPE with silica were assessed using HPLC-FD with satisfactory results.


Asunto(s)
Extracción Líquido-Líquido/métodos , Microondas , Aceites de Plantas/química , Hidrocarburos Policíclicos Aromáticos/análisis , Hidrocarburos Policíclicos Aromáticos/aislamiento & purificación , Extracción en Fase Sólida/métodos , Contaminación de Alimentos/análisis , Aceite de Oliva , Espectrometría de Fluorescencia , Aceite de Girasol
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