Determination of rate constant of quasi-reversible electrode reaction by mechanical square wave polarography

1981 ◽  
Vol 53 (7) ◽  
pp. 1006-1011 ◽  
Author(s):  
Feng. Qiang-Sheng ◽  
Lin. Sin-rhu
Keyword(s):  
Rate Constant ◽  
Electrode Reaction ◽  
Square Wave

scholarly journals Theory of reverse scan square-wave voltammetry influenced by the kinetics of reactant adsorption

2010 ◽  
Vol 8 (3) ◽  
pp. 513-518 ◽  
Author(s):  
Milivoj Lovrić ◽  
Šebojka Komorsky-Lovrić
Keyword(s):  
Rate Constant ◽  
Square Wave Voltammetry ◽  
Electrode Reaction ◽  
Peak Current ◽  
Kinetics Of Adsorption ◽  
Square Wave ◽  
Wave Voltammetry ◽  
Reverse Scan ◽  
The Relationship ◽  
Kinetics Of

AbstractA model of electrode reaction complicated by slow adsorption of the reactant is developed for square-wave voltammetry with inverse scan direction. The relationship between the dimensionless net peak current and the logarithm of dimensionless rate constant of adsorption is a curve with a minimum and a maximum. For this reason the ratio of real net peak current and the square-root of frequency is a non-linear function of the logarithm of frequency and exhibits either a maximum or a minimum. The frequency of extreme serves for the estimation of the rate constant: log(k ads /D 1/2 ) = log(k*ads )crit + 0.5 log f crit , where (k*ads )crit is a critical dimensionless rate constant of adsorption. Square-wave voltammetry is sensitive to the kinetics of adsorption if k ads 2 cm s−1

Temperature-dependence of electrochemical kinetic parameters: Electrode reaction of the Zn(Hg)/Zn(II) system

1982 ◽  
Vol 47 (5) ◽  
pp. 1433-1443 ◽  
Author(s):  
S. Kang ◽  
K. Matsuda ◽  
R. Tamamushi
Keyword(s):  
Aqueous Solutions ◽  
Temperature Dependence ◽  
Kinetic Parameters ◽  
Rate Constant ◽  
Activation Parameters ◽  
Electrode Reaction ◽  
Thermodynamic Quantities ◽  
Empirical Correlations ◽  
Square Wave ◽  
Different Temperatures

The electrochemical kinetic parameters of the D.M.E./Zn(II) electrode reaction in aqueous solutions containing perchlorate, nitrate, chloride and bromide ions were measured at different temperatures (5-50 °C) by the modified square-wave polarographic technique. The Arrhenius activation parameters and thermodynamic quantities of the electrode reaction were determined from the temperature dependence of the rate constant and conditional potential, respectively. Empirical correlations were observed between some pairs of kinetic and thermodynamic quantities.

Determination of rate constants of redox reactions of second order from current-less potential-time curves by a simplified graphical-numerical method

1983 ◽  
Vol 48 (5) ◽  
pp. 1358-1367 ◽  
Author(s):  
Antonín Tockstein ◽  
František Skopal
Keyword(s):  
Numerical Method ◽  
Explicit Form ◽  
Rate Constant ◽  
Optimization Algorithm ◽  
Rate Constants ◽  
Redox Reactions ◽  
Second Order ◽  
Wide Region ◽  
Recurrent Formula

A method for constructing curves is proposed that are linear in a wide region and from whose slopes it is possible to determine the rate constant, if a parameter, θ, is calculated numerically from a rapidly converging recurrent formula or from its explicit form. The values of rate constants and parameter θ thus simply found are compared with those found by an optimization algorithm on a computer; the deviations do not exceed ±10%.

Regeneration Mechanism Studied by Potential-Time Response to Sinusoidal Current-Time Function

1997 ◽  
Vol 62 (10) ◽  
pp. 1511-1526
Author(s):  
María-Luisa Alcaraz ◽  
Ángela Molina
Keyword(s):  
Kinetic Parameters ◽  
Rate Constant ◽  
Theoretical Study ◽  
Time Function ◽  
Time Response ◽  
Current Time ◽  
Regeneration Mechanism ◽  
Sinusoidal Current ◽  
Regeneration Processes

A theoretical study of the potential-time response to sinusoidal current applied to static and dynamic electrodes for regeneration processes is presented. Methods for determination of the regeneration fraction, rate constant of the chemical reaction and heterogeneous kinetic parameters are proposed.

Isopotential points in square-wave voltammetry of reversible electrode reactions

2009 ◽  
Vol 74 (10) ◽  
pp. 1489-1501 ◽  
Author(s):  
Marina Zelić ◽  
Milivoj Lovrić
Keyword(s):  
Square Wave Voltammetry ◽  
Electrode Reaction ◽  
Time Model ◽  
Model Calculations ◽  
Square Wave ◽  
Electrode Reactions ◽  
Wave Voltammetry ◽  
Electron Transfer Processes ◽  
Diagnostic Criterion ◽  
First Time

Isopotential points in square-wave voltammetry are described for the first time. Model calculations and real measurements (performed with UO22+ and Eu3+ in perchlorate and bromide solutions, respectively) indicate that such an intersection could be observed when backward components of the net response, resulting from an increase in frequency or reactant concentration, are presented together. The electrode reaction should be fully reversible because quasireversible or slower electron transfer processes give the isopoints only at increasing reactant concentrations but not at increasing square-wave frequencies. The effect could be used as an additional diagnostic criterion for recognition of reversible electrode reactions where products remain dissolved in the electrolyte solution.

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