Determination of uranium in environmental matrices by chelation ion chromatography using a high performance substrate dynamically modified with 2,6-pyridinedicarboxylic acid
Mj. Shaw et al., Determination of uranium in environmental matrices by chelation ion chromatography using a high performance substrate dynamically modified with 2,6-pyridinedicarboxylic acid, CHROMATOGR, 51(11-12), 2000, pp. 695-700
Chelation ion chromatography, involving a high efficiency neutral polystyre
ne-divinylbenzene resin dynamically coated with 2,6-pyridinedicarboxylic ac
id, has been developed as a novel technique for the quantitative determinat
ion of uranium in complex matrices. An isocratic separation method, using a
n eluent consisting of 1M KNO3, 0.5M HNO3 and 0.1 mM 2,6-pyridinedicarboxyl
ic acid, allowed the uranyl ion to elute away from matrix interferences in
under ten minutes. Detection was achieved using an Arsenate III post column
reaction system. Good recoveries were obtained from spiked mineral water a
nd sea water and the standard addition curves produced good linearity (r(2)
> 0.997) with a detection limit, calculated as twice baseline noise, of 20
mu g L-1. The procedure was applied to the determination of trace uranium
in standard reference water and sediment samples. The results obtained comp
ared well with the certified values for uranium.