Simultaneous determination of cyanogen chloride and cyanogen bromide in treated water at sub-mu g/L levels by a new solid-phase microextraction-gas chromatographic-electron-capture detection method
B. Cancho et al., Simultaneous determination of cyanogen chloride and cyanogen bromide in treated water at sub-mu g/L levels by a new solid-phase microextraction-gas chromatographic-electron-capture detection method, J CHROMAT A, 897(1-2), 2000, pp. 307-315
A headspace solid-phase microextraction (HS-SPME) procedure has been develo
ped and applied for the determination of cyanogen halides in treated water
samples at mug/L concentrations. Several SPME coatings were tested, the div
inylbenzene-Carboxen-polydimethylsiloxane fiber being the most appropriate
coating. GC-electron-capture detection was used for separation and quantita
tion. Experimental parameters such as sample volume, addition of a salt, ex
traction time and desorption conditions were studied. The optimized method
has an acceptable linearity, good precision, with RSD values <10% for both
compounds, and it is sufficiently sensitive to detect ng/L levels. HS-SPME
was compared with liquid-liquid microextraction (US Environmental Protectio
n Agency Method 551.1) for the analysis of spiked ultrapure and granular ac
tivated carbon filtered water samples. There was good agreement between the
results from both methods. Finally, the optimized procedure was applied to
determine both compounds at the Barcelona water treatment plant (N.E. Spai
n). Cyanogen chloride in treated water was <1.0 mug/L and cyanogen bromide
ranged from 3.2 to 6.4 mug/L. (C) 2000 Elsevier Science B.V. All rights res
erved.