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Theory of reverse scan square-wave voltammetry influenced by the kinetics of reactant adsorption (CROSBI ID 163790)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Lovrić, Milivoj ; Komorsky-Lovrić, Šebojka Theory of reverse scan square-wave voltammetry influenced by the kinetics of reactant adsorption // Central European journal of chemistry, 8 (2010), 3; 513-518. doi: 10.2478/s11532-010-0034-y

Podaci o odgovornosti

Lovrić, Milivoj ; Komorsky-Lovrić, Šebojka

engleski

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

A model of electrode reaction complicated by slow adsorption of the reactant is developed for square-wave voltammetry with inverse scan direction. The relationship between dimensionless net peak current and the logarithm of dimensionless rate constant of adsorption is a curve with the minimum and the 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 maximum, or minimum. The frequency of extreme serves for the estimation of the rate constant: log(kads/D1/2) = log( )crit + 0.5 log fcrit, where ( )crit is a critical dimensionless rate constant of adsorption. Square-wave voltammetry is sensitive to the kinetics of adsorption if kads < 102 cm/s.

Square-wave voltammetry ; Kinetics of adsorption ; Adsorption of reactant

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Podaci o izdanju

8 (3)

2010.

513-518

objavljeno

1895-1066

1644-3624

10.2478/s11532-010-0034-y

Povezanost rada

Kemija

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