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

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 w...

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Veröffentlicht in:Talanta (Oxford) 2014-05, Vol.122, p.30-35
Hauptverfasser: Magnier, A., Fekete, V., Van Loco, J., Bolle, F., Elskens, M.
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Fekete, V.
Van Loco, J.
Bolle, F.
Elskens, M.
description 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 –0.60V (all potential values in the paper are given versus the Ag/AgCl, [KCl]=3M reference electrode) during 60s, and a final cupferron concentration of 4×10−4M. 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. Determination of aluminium by CLE–AdSV in beverages compared to computer simulation. [Display omitted] •Development of a sensitive method to measure electro-labile aluminium in beverages.•Assessment of complexing parameters is improved by combining titration and computer speciation modelling.•Presence of fluoride and citric acid in beverages changes Al speciation pattern.
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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 –0.60V (all potential values in the paper are given versus the Ag/AgCl, [KCl]=3M reference electrode) during 60s, and a final cupferron concentration of 4×10−4M. 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. Determination of aluminium by CLE–AdSV in beverages compared to computer simulation. 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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 –0.60V (all potential values in the paper are given versus the Ag/AgCl, [KCl]=3M reference electrode) during 60s, and a final cupferron concentration of 4×10−4M. 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. Determination of aluminium by CLE–AdSV in beverages compared to computer simulation. 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subjects Adsorption
Aluminium
Aluminum
Aluminum - analysis
Aluminum - metabolism
Beverages
Beverages - analysis
Binding, Competitive
CLE–AdSV
Computer simulation
Cupferron
Electrochemical Techniques - methods
Electrodes
Environmental Sciences
Exchange
Ligands
Speciation
Voltammetry
title Speciation study of aluminium in beverages by Competitive Ligand Exchange–Adsorptive Stripping Voltammetry
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