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   <subfield code="a">Application of adsorptive stripping voltammetry for indirect measurement of nonelectroactive ions using competitive complex formation reactions</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Joseph Wang, Božidar Grabarić]</subfield>
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   <subfield code="a">It is shown that adsorptive stripping voltammetry can be used for indirect determinations of non-electroactive species. Determination of fluoride was selected to demonstrate this concept which can be used in environmental, clinical and other applications. The fluoride determination is based on competitive complex formation reactions between zirconium and organic ligands, viz. Alizarin Red S (ARS) and Acid Alizarin Violet N (AAVN) and fluoride ions in acidic media (0.1M HNO3 or HClO4). Free ARS ligand is adsorbable on mercury electrode and its voltammetric peak increases with fluoride concentration due to ARS displacement from the Zr-ARS complexes with fluoride forming more stable Zr-fluoride complexes. Using AAVN as a ligand Zr-AAVN complexes are adsorbable on a mercury electrode and the voltammetric peak decreases with increasing fluoride concentration due to formation of more stable Zr-fluoride complexes. The sensitivity of the method is down to 0.1 μM of fluoride. Overall fluoride recovery from synthetic water samples at micromolar concentration level was within 1% of the concentration added, with overall reproducibility of 5 independent measurements of ± 2.5% and ± 1.8% with ARS and AAVN ligand, respectively. Some interferences possibly present in water have been investigated.</subfield>
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   <subfield code="a">fluoride determination</subfield>
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   <subfield code="a">zirconium determination</subfield>
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