Solvent Microextraction with Simultaneous Back-Extraction for Sample Cleanup and Preconcentration:  Quantitative Extraction

• Published in: Analytical chemistry (Washington) 1998-09, Vol.70 (18), p.3912-3919
• Main Authors: Ma, Minhui, Cantwell, Frederick F
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Chemical and thermal methods; Chemistry; Exact sciences and technology; Solvents
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac980174n

A solvent microextraction technique has been developed to perform simultaneous forward- and back-extraction across a microliter-size organic liquid membrane. The organic liquid membrane phase (o), consisting of 40 or 80 μL of n-octane, is layered over 0.5 or 1.0 mL of aqueous sample phase (a1) contained in a 1- or 2-mL microreaction vial and is stabilized against mechanical disruption by a small Teflon ring, even when the a1 phase is stirred at a speed of 2000 rpm. A 0.1- or 0.2-mL aqueous receiving phase (a2) is layered over the o phase. After extraction for a prescribed time, an aliquot of the a2 phase is injected directly into an HPLC for quantification. The technique is efficient and selective for ionizable compounds. In 30 min, the model compounds, mephentermine and 2-phenylethylamine, in the a1 phase buffered at pH 13 are 100% and 90% extracted, respectively, into the a2 phase buffered at pH 2.1. A kinetic model has been developed, based on the Whitman two-film theory, to describe the extraction process and has been verified experimentally. The technique is promising for routine applications because of its simplicity, reproducibility, selectivity, overall sample preparation time, and quantitative extraction of compounds with relatively small distribution coefficients with submilliliter volumes of aqueous back-extractant.