“…5). Similar results have also been found on palladium pentacyanonitrosylferrate modified aluminum electrode 14 and on Co(II) porphyrin modified carbon paste electrode 17 for nitrite electrocatalytic oxidation. The pH-independent result seems to be inconsistent with the pH-dependent characteristic of the nitrite oxidation reaction to nitrate.…”
Section: No2 -+ 2h + + E -⎯→ No + H2osupporting
confidence: 84%
“…Figure 6 illustrates the cyclic voltammograms at lower concentration range and the corresponding calibration curve. The detection limit (S/N = 3) is estimated to be 2.4 × 10 -6 M, lower than that on the palladium pentacyanonitrosylferrate-modified aluminum electrode 14 and the 3-mercaptopropanoic-modified gold electrode. 34 …”
Section: Calibration Curve For Nitrite Determinationmentioning
“…5). Similar results have also been found on palladium pentacyanonitrosylferrate modified aluminum electrode 14 and on Co(II) porphyrin modified carbon paste electrode 17 for nitrite electrocatalytic oxidation. The pH-independent result seems to be inconsistent with the pH-dependent characteristic of the nitrite oxidation reaction to nitrate.…”
Section: No2 -+ 2h + + E -⎯→ No + H2osupporting
confidence: 84%
“…Figure 6 illustrates the cyclic voltammograms at lower concentration range and the corresponding calibration curve. The detection limit (S/N = 3) is estimated to be 2.4 × 10 -6 M, lower than that on the palladium pentacyanonitrosylferrate-modified aluminum electrode 14 and the 3-mercaptopropanoic-modified gold electrode. 34 …”
Section: Calibration Curve For Nitrite Determinationmentioning
“…As shown in , r = 0.999). The detection limit (S/N = 3) for nitrite is 2.00 × 10 −6 M. The linear dynamic range and detection limit obtained at the present poly(methylene blue)-modified GC electrode without the incorporation of nanostructured materials are clearly comparable to those reported in the literature, [7][8][9][10][11][12][13][14] which is a distinctive advantage of the present method.…”
Section: Resultssupporting
confidence: 81%
“…Many methods such as spectrophotometry, 3,4 chromatography, 5,6 and electrochemical sensors, [7][8][9][10][11][12][13][14][15][16] have been developed for nitrite determination. Among those methods, electrochemical methods are most favorable in terms of simplicity, speed, and cost effectiveness.…”
Electrochemical characteristics of nitrite ion were investigated at a poly(methylene blue)-modified glassy carbon electrode by cyclic voltammetry and differential pulse voltammetry. The poly(methylene blue)-modified glassy carbon electrode exhibited enhanced anodic signals for nitrite. The effects of key parameters on the detection of nitrite were evaluated at the modified electrode, such as pH, accumulation time, and scan rate. Under optimum condition, the chemically modified electrode can detect nitrite in the concentration range 2.0 × 10 −6 to 5.0 × 10 −4 M with the detection limit of 2.0 × 10 −6 M and a correlation coefficient of 0.999. The detection of nitrite using the chemically modified electrode was not affected by common ions such as Na2− and H 2 PO 4 − . The modified electrode showed good stability and reproducibility. The practical application of the present method was successfully applied to the determination of nitrite ion in cabbage samples.
“…[1][2][3][4][5][6][7][8][9][10] The metal pentacyanonitrosylferrate (MPCNF), a class of polynuclear mixed valence compounds, also have attracted much attention for the preparation of thin films on electrodes in the last years. [11][12][13][14][15][16][17][18][19][20] The MPCNF modified electrodes used for electrocatalytic oxidation of iodide, 11 nitrite, 12 sulfite, 13,14 hydrazine, 16,18 and ascorbic acid 20 and in this studies, M at MPCNF modified electrode was Ni, 11,18,20 Pd, 12,15 Co, 13,16 They act as mediators in electron transfer from substrate to electrode materials, and the most important feature of the chemically modified electrodes (CMEs), are the electrocatalysis of slow electron transfer reactions. The MEs enhance the rate of electron transfer by reducing the over potential associated with a reaction, therefore such electrocatalysis enables a high current density (i.e.…”
An electroactive thin film of Cobalt pentacyanonitrosylferrate (CoPCNF) was electrodeposited on a glassy carbon electrode by cyclic voltammetry. The modified electrode exhibits good electrocatalytic activity toward oxidation of thiosulfate. The electrocatalytic oxidation of thiosulfate at glassy carbon electrode modified with CoPCNF as a working electrode has been studied by using cyclic voltammetry, rotating disk electrode (RDE) voltammetry and chronoamperometry in a solution of 0.25 mol L -1 KNO 3 as a supporting electrolyte. A Tafel plot, derived from voltammograms indicated a one-electron charge transfer process, at rate determining step in the catalytic oxidation of thiosulfate. The kinetics of catalytic reaction was investigated and the average value of the rate constant (k), for the catalytic reaction and the diffusion coefficient (D) were evaluated by different approaches for thiosulfate and found to be (5.61 ± 0.14) ×10 2 (mol L -1 ) -1 s -1 and (6.59 ± 0.70) ×10 -6 cm 2 s -1 respectively.
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