Chromatographic Determination of Nanomolar Cyanate Concentrations in Estuarine and Sea Waters by Precolumn Fluorescence DerivatizationClick to copy article linkArticle link copied!
Abstract

Recent studies suggest that cyanate (OCN–) is a potentially important source of reduced nitrogen (N) available to support the growth of aquatic microbes and, thus, may play a role in aquatic N cycling. However, aquatic OCN– distributions have not been previously described because of the lack of a suitable assay for measuring OCN– concentrations in natural waters. Previous methods were designed to quantify OCN– in aqueous samples with much higher reduced N concentrations (micromolar levels) than those likely to be found in natural waters (nanomolar levels). We have developed a method to quantify OCN– in dilute, saline environments. In the method described here, OCN– in aqueous solution reacts with 2-aminobenzoic acid to produce a highly fluorescent derivative, 2,4-quinazolinedione, which is then quantified using high performance liquid chromatography. Derivatization conditions were optimized to simultaneously minimize the reagent blank and maximize 2,4-quinazolinedione formation (>90% reaction yield) in estuarine and seawater matrices. A limit of detection (LOD) of 0.4 nM was achieved with only minor matrix effects. We applied this method to measure OCN– concentrations in estuarine and seawater samples from the Chesapeake Bay and coastal waters from the mid-Atlantic region. OCN– concentrations ranged from 0.9 to 41 nM. We determined that OCN– concentrations were stable in 0.2 μm filtered seawater samples stored at −80 °C for up to nine months.
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