Takayanagi Toshio, Yamashita Hiroki, Motomizu Shoji, Musijowski Jacek, Trojanowicz Marek
Graduate School of Natural Science and Technology, Okayama University, 3-1-1 Tsushimanaka, Okayama 700-8530, Japan.
Talanta. 2008 Feb 15;74(5):1224-30. doi: 10.1016/j.talanta.2007.08.026. Epub 2007 Aug 30.
Perfluorinated surfactants of heptafluorobutylate and pentadecafluorooctanoate ions were adsorbed on an activated charcoal cartridge and decomposed with sodium biphenyl (SBP) reagent to form inorganic fluoride ion. The fluoride ion thus formed was determined by flow injection analysis (FIA) using quercetin-Zr complex as a fluorimetric reagent, where lambda(ex) and lambda(em) were 422 and 491 nm, respectively. The limit of detection for fluoride ion by the FIA system was developed to 1.1 x 10(-6)M (signal to noise ratio of three), when 50% (v/v) tetrahydrofuran (THF) was used as a dissolving solvent for quercetin. The perfluorinated surfactants in the sample solution were quantitatively adsorbed on the cartridge containing 100mg of activated charcoal and were decomposed with 0.5 mL of sodium biphenyl reagent after drying thoroughly by flowing through dry nitrogen gas. The fluoride ion formed was recovered with 3 mL of purified water as an eluent, and it was determined by the fluorimetric flow injection system. The blank fluorescence signal accompanied during the adsorption/decomposition on the cartridge was reduced by washing the activated charcoal with acetone. The blank signal was also observed from dimethoxyethane, which was used in sodium biphenyl reagent. When 600 mL sample solution was used and 200 times enrichment was applied, the heptafluorobutylate and pentadecafluorooctanoate ions at the concentrations of 2.1 microg L(-1) were quantitatively recovered as fluoride ion, and the limit of detections for the perfluorinated surfactants were 0.3 and 0.3 microgL(-1) for the two perfluorinated surfactants, respectively (3 sigma of the blank signal).
全氟丁酸盐和十五氟辛酸根离子的全氟表面活性剂吸附在活性炭柱上,并用联苯钠(SBP)试剂分解以形成无机氟离子。由此形成的氟离子通过流动注射分析(FIA),使用槲皮素 - 锆络合物作为荧光试剂进行测定,其中激发波长(λex)和发射波长(λem)分别为422和491nm。当使用50%(v/v)四氢呋喃(THF)作为槲皮素的溶解溶剂时,FIA系统对氟离子的检测限提高到1.1×10⁻⁶M(信噪比为3)。样品溶液中的全氟表面活性剂定量吸附在含有100mg活性炭的柱上,在通过干燥氮气彻底干燥后,用0.5mL联苯钠试剂分解。形成的氟离子用3mL纯化水作为洗脱剂回收,并通过荧光流动注射系统进行测定。通过用丙酮洗涤活性炭,减少了柱上吸附/分解过程中伴随的空白荧光信号。在联苯钠试剂中使用的二甲氧基乙烷也观察到了空白信号。当使用600mL样品溶液并进行200倍富集时,浓度为2.1μg L⁻¹的全氟丁酸盐和十五氟辛酸根离子作为氟离子被定量回收,两种全氟表面活性剂的全氟表面活性剂检测限分别为0.3和0.3μg L⁻¹(空白信号的3σ)。