Speciation study of aluminium in beverages by Competitive Ligand Exchange-Adsorptive Stripping Voltammetry

Etude de la spéciation de l'aluminium dans les boissons par CLE-AdSV

Magnier, A. ; Fekete, V. ; Van Loco, J. ; Bolle, F. ; Elskens, M.

Type de document
Article de revue scientifique à comité de lecture
Langue
Anglais
Affiliation de l'auteur
VRIJE UNIVERSITY BRUSSELS BEL ; WETENSCHAPPELIJK INSTITUUT VILKSGEZONDHEID BEL ; WETENSCHAPPELIJK INSTITUUT VILKSGEZONDHEID BEL ; WETENSCHAPPELIJK INSTITUUT VILKSGEZONDHEID BEL ; VRIJE UNIVERSITY BRUSSELS BEL
Année
2014
Résumé / Abstract
Competitive Ligand Exchange - Adsorptive Stripping Voltammetry (CLE-AdSV) was used for determining the speciation of aluminium in commonly consumed beverages (water, tea, infusion, coffee, orange juice, tomato juice, beer and red wine). Aluminium determination involves the adsorption of Al-complexes with the ligand cupferron onto a hanging mercury drop electrode. All samples were studied at pH 6.5 with an accumulation step at -0.60 V (all potential values in the paper are given versus the Ag/AgCl, [KCl] = 3M reference electrode) during 60 s, and a final cupferron concentration of 4 10-4 M. These conditions were used to establish (i) the concentration of electro-labile aluminium, (ii) the range of ligand concentrations and (iii) the conditional stability constants of beverage samples using titration procedures. The results based on Ruzic plots were compared to computer simulation with Visual MINTEQ. This comparison suggests that labile monomeric Al-forms and soluble organic complexes of low molecular weight can be quantified by the CLE-AdSV procedure. Overall the relative uncertainties on the determination of the electro-active Al fraction and the complexing parameters, i.e., concentration and conditional stability constant of natural ligands in the samples, are less than 15%. Thanks to these results, information on Al bioavailability in beverages was collected and discussed. This study also illustrates the value of computer simulations when complex, time-consuming voltammetric techniques are applied.
Source
Talanta, vol. 122, p. 30 - 35

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