Fast screening of perfluorooctane sulfonate in
water using vortex-assisted liquid-liquid
microextraction coupled to liquid
chromatography-mass spectrometry
Δεν υπάρχει διαθέσιμη μικρογραφία
Ημερομηνία
2011
Συγγραφείς
Elefteria Psillakis
Antonio Canals
Konstantina Tyrovola
Iván P. Román
Aikaterini Papadopoulou
Τίτλος Εφημερίδας
Περιοδικό ISSN
Τίτλος τόμου
Εκδότης
Elsevier
Περίληψη
Fast screening of trace amounts of the perfluorooctane sulfonate anion (PFOS) in water samples was
performed following a simple, fast and efficient sample preparation procedure based on vortex-assisted
liquid–liquid microextraction (VALLME) prior to liquid chromatography–mass spectrometry. VALLME
initially uses vortex agitation, a mild emulsification procedure to disperse microvolumes of octanol, a
low density extractant solvent, in the aqueous sample. Microextraction under equilibrium conditions is
thus achieved within few minutes. Subsequently, centrifugation separates the two phases and restores
the initial microdrop shape of the octanol acceptor phase, which can be collected and used for liquid
chromatography–single quadrupole mass spectrometry analysis. Several experimental parameters were
controlled and the optimum conditions found were: 50L of octanol as the extractant phase; 20mL
aqueous donor samples (pH = 2); a 2 min vortex extraction time with the vortex agitator set at a 2500rpm
rotational speed; no ionic strength adjustment. Centrifugation for 2 min at 3500rpm yielded separation
of the two phases throughout this study. Enhanced extraction efficiencies were observed at low pH
which was likely due to enhanced electrostatic interaction between the negatively PFOS molecules and
the positively charged octanol/water interface. The effect of pH was reduced in the presence of sodium
chloride, likely due to electrical double layer compression. The linear response range for PFOS was from
5 to 500 ng L−1 (coefficient of determination, r2, 0.997) and the relative standard deviation for aqueous
solutions containing 10 and 500 ng L−1 PFOS were 7.4% and 6.5%, respectively. The limit of detection was
1.6 ng L−1 with an enrichment factor of approximately 250. Analysis of spiked tap, river and well water
samples revealed that matrix did not affect extraction
Περιγραφή
Λέξεις-κλειδιά
Παραπομπή
A. Papadopoulou, I. P Román, A. Canals, K. Tyrovola, E. Psillakis , 'Fast screening of perfluorooctane sulfonate in water using vortex-assisted liquid–liquid microextraction coupled to liquid chromatography–mass spectrometry " ,Anal. Chim. Acta,VOL. 691,no.1 , PP. 56–61,2011.doi :10.1016/j.aca.2011.02.043