The
development of advanced analytical methods for trace amounts
of selenium (Se) ions in wastewater become a matter of great importance
in avoiding biological and environmental burdens due to Se pollution.
In this study, a simple microanalytical methodology was developed,
enabling the rapid and highly efficient extraction, real-time monitoring
in situ, and extraction kinetic analysis of Se(IV) ions. The microscale
extraction and analysis was verified by means of fluorescence intensity
changes of fluorogenic complex 4,5-benzopiazselenol (BPS) consisting
of the coordination of Se(IV) with 2,3-diaminonaphthalene (DAN). After
the optimal BPS formation conditions, including pH, temperature, and
Se(IV)/DAN concentration ratio, were examined, the microscale extraction
of BPS was carried out under aqueous and organic two-phase parallel
flow regimes in Y-shaped microchannels. The fluorescence intensity
profiles of BPS in the organic phase were scanned in situ along the
flow direction in the microchannel by a fluorescence microscope. The
residence time dependence of the BPS concentrations could be precisely
detected in real time. The results show that the developed microsystem
has not only a detection limit of a submicromolar level for Se(IV),
which is sufficiently lower than the permeable limit concentration
of selenium in wastewater, but also a large apparent extraction rate
constant of approximately 0.3 s–1 and a short time
to reach equilibrium of approximately 20 s, compared to those of bulk-scale
extraction. This would indicate a valuable technique for elucidating
microfluidic extraction kinetics and for applying real-time, environmentally
friendly monitoring of toxic selenium ions.