Journals / Turkish Journal of Chemistry / 2010 / Cilt: 34 - Sayı: 6
Nile Blue-hexacyanoferrate carbon paste modified electrode as an amperometric sensor for determination of hydrazine
- Journal
- Turkish Journal of Chemistry
- Pages
- 901–910
- DOI
- —
Abstract
The main problem associated with metal hexacyanoferrates (MHCFs) is their instability at high pH values. We synthesized a new Prussian Blue analogue, Nile-Blue hexacyanoferrate (NBHCF), that remains stable in 0.2 M KOH. A carbon paste (CPE) chemically modified electrode (ME) containing NBHCF was prepared as a stable electrochemical sensor for measuring hydrazine. A detailed characterization of the electrochemical and electrocatalytic behavior of NBHCF was performed using cyclic voltammetric, chronoamperometric, differential pulse voltammetric (DPV) and hydrodynamic amperometric methods. The NBHCF-modified electrode produced reproducible redox peaks and resulted in a linear increase in the oxidation signal of hydrazine with increasing concentration of hydrazine in the range of 0.1-6.0 mM (in hydrodynamic amperometry method (HDA)). The electrode detection limit was 40 m M and possessed a surface coverage of G = 2.0 \times 10-8 mol cm-2.
Özet
The main problem associated with metal hexacyanoferrates (MHCFs) is their instability at high pH values. We synthesized a new Prussian Blue analogue, Nile-Blue hexacyanoferrate (NBHCF), that remains stable in 0.2 M KOH. A carbon paste (CPE) chemically modified electrode (ME) containing NBHCF was prepared as a stable electrochemical sensor for measuring hydrazine. A detailed characterization of the electrochemical and electrocatalytic behavior of NBHCF was performed using cyclic voltammetric, chronoamperometric, differential pulse voltammetric (DPV) and hydrodynamic amperometric methods. The NBHCF-modified electrode produced reproducible redox peaks and resulted in a linear increase in the oxidation signal of hydrazine with increasing concentration of hydrazine in the range of 0.1-6.0 mM (in hydrodynamic amperometry method (HDA)). The electrode detection limit was 40 m M and possessed a surface coverage of G = 2.0 \times 10-8 mol cm-2.