Application of liquid–liquid–liquid microextraction and high-performance liquid chromatography for the determination of alkylphenols and bisphenol-A in water

✍ Scribed by Che-Yi Lin; Ming-Ren Fuh; Shang-Da Huang

• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 201 KB
• Volume: 34
• Category: Article
• ISSN: 1615-9306
• DOI: 10.1002/jssc.201000727

✦ Synopsis

Abstract

A method termed liquid–liquid–liquid microextraction (LLLME) was utilized to extract 4‐t‐butylphenol, 4‐t‐octylphenol, 4‐n‐nonylphenol, and bisphenol‐A from water. The extracted target analytes were separated and quantified by high‐performance liquid chromatography using a fluorescence detector. In LLLME, the donor phase (i.e. water sample) was made weakly acidic by adding monobasic potassium phosphate (KH~2~PO~4~); the organic phase adopted was 4‐chlorotoluene; the acceptor phase (i.e. enriched extract) was 0.2 M tetraethylammonium hydroxide dissolved in ethylene glycol. This study solves a problem associated with the surface activity of long‐chain alkylphenolate ions, permitting LLLME to extract long‐chain alkylphenols. Experimental conditions such as acceptor phase composition, organic phase identity, acceptor phase volume, sample agitation, extraction time, and salt addition were optimized. The relative standard deviation (RSD, 2.0–5.8%), coefficient of determination (r^2^ 0.9977–0.9999), and detection limit (0.017–0.0048 ng/mL) of the proposed method were achieved under the selected optimized conditions. The method was successfully applied to analyses of lake and tap water samples, and the relative recoveries of target analytes from the spiked lake and tap water samples were 92.8–106.3 and 93.6–105.6%, respectively. The results obtained with the proposed method confirm this microextraction technique to be reliable for the monitoring of alkylphenols and bisphenol‐A in water samples.