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Elsevier, Journal of Chromatography A, 2(910), p. 301-309

DOI: 10.1016/s0021-9673(00)01242-5

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Sensitive and selective ion chromatographic method for the determination of trace beryllium in water samples

Journal article published in 2001 by Wasim Bashir, Brett Paull ORCID
This paper is available in a repository.
This paper is available in a repository.

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Abstract

A selective and sensitive ion chromatographic method has been developed for the determination of beryllium in a number of water samples at low-microg/l concentrations. The separation was performed on a 250x4.0 mm I.D. iminodiacetic acid functionalised silica gel column. Chromatographed Be(II) was detected using visible detection at 590 nm following post-column reaction with chrome azurol S (CAS). The optimum separation and derivatisation conditions were studied in detail. The optimum eluent conditions were found to be 0.4 M KNO3, adjusted to pH 2.5 using HNO3, with optimum post-column detection being achieved using a solution containing 0.26 mM CAS, 2% Triton X-100, 50 mM 2-(N-morpholino)ethanesulfonic acid, pH 6.0. Under the above conditions, the concentration detection limit for Be(II) was found to be 3 microg/l in a standard solution and 4 microg/l in a typical tap water sample, using a 250 microl injection. The method was linear over the investigated range of 10 microg/l to 10 mg/l and highly reproducible. The method was successfully applied to a number of water samples of varying matrix complexity, including simulated seawater, and also to a natural freshwater certified reference material NIST 1640.