Search

We report a novel system to analyze atmospheric nitrophenols (NPs). Pain or air sample extracts (1 mL) are pre-concentrated on a narrow bore (2 mm) aliphatic anion exchanger. In the absence of strong retention of NPs exhibited by aromatic ion exchangers, retained NPs are eluted as a plug by injection of 100 [micro]L of 0.1 M [Na.sub.2]S[O.sub.4] on to a short (2 x 50 mm) reverse phase C-18 column packed with 2.2 [micro]m particles. The salt plug passes through the C-18 column unretained while the NPs are separated by an ammonium acetate buffered methanol--water eluent, compatible with mass spectrometry (MS). The eluted NPs are measured with a long path Teflon AF-based liquid core waveguide (0.15 x 1420 mm) illuminated by a 403 nm light emitting diode and detected by a monolithic photodiode-operational amplifier. The waveguide is rendered chemically active by suspending it over concentrated ammonia that permeates into the lumen. The NPs ionize to the yellow anion form ([[lambda].sub.max] ~ 400 nm). The separation of 4-nitrophenol, 2,4-dinitrophenol, 2-methyl-4-nitrophenol, 3-methyl-4-nitrophenol, and 2-nitrophenol (these are the dominant NPs, typically in that order, in both rain and air of Houston and Arlington, TX, confirmed by tandem MS) takes just over 5 min with respective S/N = 3 limits of detection (LODs) of 60, 12, 30, 67, and 23 pg/mL compared to MS/MS LODs of 20, 49, 11, 20, and 210 pg/mL. Illustrative air and rain data are presented. 10.1021/ac101015y