Separation and Quantification of Tl(I) and Tl(III) in Fresh Water Samples

Abstract

The two oxidation states of thallium, Tl(I) and Tl(III), were quantified by IC-ICP-MS using complexation of Tl³⁺ with DTPA (penta-carboxymethyl-diethylenetriamine) and separation on a cation exchange column according to a modification of the method devised by Coetzee et al. In order to avoid successively lowered separation efficiency and loss of resolution during a run, a gradient elution was made using HCl instead of HNO₃. With an ultrasonic nebuliser instead of a V-groove nebuliser the limit of detection for Tl(I) and Tl(III) could be lowered from 25 ng/L and 3.0 ng/L to 9.0 ng/L and 0.7 ng/L, respectively, which is adequate for many fresh water systems. The stability of Tl(III) in acidic solutions was found to be concentration dependent, with an initially high reduction rate of Tl(III). Exposure of the sample to light further increased the reduction rate. Addition of DTPA (0.01 mM) and acid (HNO₃, 1%) to a sample with 1 μg/L Tl(III) stabilised the Tl(III) content for at least 48 h. Analysis of field samples showed that only acidification is inadequate to maintain the original distribution of Tl(I) and Tl(III). Internal calibration (standard addition) and correction of the analytical signal (²⁰⁵Tl) with a non-ionic internal standard (¹¹B) yielded almost quantitative recoveries of both Tl(I) and Tl(III). A scheme for field sample preparation is proposed, including sampling, storage and pre-analysis treatment.

Keywords:

• Speciation
• Thallium
• Stability
• Ion chromatography
• Mass spectrometry
• Sample preparation

ACKNOWLEDGMENTS

Thanks to Prof. B. Allard for valuable comments and The Swedish Knowledge Foundation for financial support.

Notes

^aPeak area used.

^bRatio between ¹¹B and ²⁰⁵Tl used.

^aOnly one analysis.

^bNo peak visible.

^aStock solution.

^b1% HNO₃ matrix is used.

^c5 mM ammonium acetate set to pH 3.

^dLarge vessels (120 mL).

^eSmall vessels (15 mL).

^fExposure to light.

*i.l. is the concentration at which the peak just becomes possible to integrate.