Szczegóły publikacji
Opis bibliograficzny
A novel catalytic adsorptive stripping voltammetric method for the determination of germanium ultratraces in the presence of chloranilic acid and the V(IV)$\cdot$HEDTA complex / Jerzy ZARĘBSKI, Andrzej BOBROWSKI, Agnieszka KRÓLICKA, Julia GONCIARCZYK, Vasiliki Manolopoulou, Anastasios Economou // Journal of Solid State Electrochemistry ; ISSN 1432-8488. — 2020 — vol. 24 iss. 11–12 spec. iss.: dedicated to the 65th birthday of Fritz Scholz on July 4th, 2020, s. 2891–2899. — Bibliogr. s. 2898–2899, Abstr. — Publikacja dostępna online od: 2020-07-11
Autorzy (6)
- AGHZarębski Jerzy
- AGHBobrowski Andrzej
- AGHKrólicka Agnieszka
- AGHGonciarczyk Julia
- Manolopoulou Vasiliki
- Economou Anastasios
Słowa kluczowe
Dane bibliometryczne
| ID BaDAP | 129588 |
|---|---|
| Data dodania do BaDAP | 2020-11-06 |
| Tekst źródłowy | URL |
| DOI | 10.1007/s10008-020-04669-0 |
| Rok publikacji | 2020 |
| Typ publikacji | artykuł w czasopiśmie |
| Otwarty dostęp |  |
| Creative Commons | |
| Czasopismo/seria | Journal of Solid State Electrochemistry |
Abstract
A novel, sensitive catalytic adsorptive stripping voltammetric procedure which can be used to determine trace amounts of germanium is described. The method is based on the interfacial accumulation of the complex formed by Ge(IV) and the product of the reduction of chloranilic acid on the hanging mercury drop electrode or the renewable silver amalgam film electrode, and its subsequent reduction from the adsorbed state followed by the catalytic action of the V(IV)center dot HEDTA complex. The presence of V(IV)center dot HEDTA greatly enhances the adsorptive stripping response of Ge. The reduction of the Ge(IV) in the presence of chloranilic acid and V(IV)center dot HEDTA was investigated in detail and the effects of pH, electrolyte composition, and instrumental parameters were studied. Under optimal conditions, the catalytic peak current of germanium exhibited good linearity for Ge(IV) concentrations in the range of 0.75-60 nM (for 60 s of accumulation at -0.1 V,r(2)= 0.995) and a low limit of detection (LOD = 0.085 nM). The procedure was successfully applied to determine Ge in water samples.
