posted on 2012-11-06, 00:00authored byRuth Suárez, Burkhard Horstkotte, Carlos M. Duarte, Víctor Cerdà
A sensitive and selective automated in-syringe dispersive
liquid–liquid
microextraction (DLLME) method is presented. It was successfully applied
to the determination of aluminum in coastal seawater samples. The
complete analytical procedure including sampling, buffering, reaction
of the analyte with fluorescence reagent lumogallion (LMG), extraction,
phase separation, and quantification was completely automized and
carried out within 4 min. DLLME was done using n-hexanol
as an extracting solvent and ethanol as a dispersing solvent in a
1:8 v/v percent mixture. The Al–LMG complex was extracted by
an organic solvent and separated from the aqueous phase within the
syringe of an automated syringe pump. Two devices were specially developed
for this work. These were (a) the fluorescence detector and accompanying
flow cell for the organic phase enriched with the reaction product
and (b) a heating device integrated into the holding coil to accelerate
the slow reaction kinetics. The limits of detection (3σ) and
quantification (10σ) were 8.0 ± 0.5 nmol L–1 and 26.7 ± 1.6 nmol L–1, respectively. The
relative standard deviation for eight replicate determinations of
200 nmol L–1 Al3+ was <1.5%. The calibration
graph using the preconcentration system was linear up to 1000 nmol
L–1 with a correlation coefficient of 0.999. Ambient
concentrations of samples were quantifiable with found concentrations
ranging from 43 to 142 nmol L–1. Standard additions
gave analyte recoveries from 97% to 113% proving the general applicability
and adequateness of the analyzer system to real sample analysis.