Kinetic study of redox reaction of Ce4+ ions with hypophosphite by means of vibrating platinum electrode

1977 ◽  
Vol 42 (8) ◽  
pp. 2332-2342
Author(s):  
Ľ. Treindl ◽  
J. Hatala
Sensor Review ◽  
2018 ◽  
Vol 38 (3) ◽  
pp. 335-344 ◽  
Author(s):  
Ilhem Ghodbane ◽  
Rochdi Kherrrat ◽  
Saida Zougar ◽  
Rim Lamari ◽  
Redouane Haddadji ◽  
...  

PurposeThe purpose of this work is to explore electrical properties of an electrochemical sensor designed for the detection of malachite green (MG) present in an aqueous solution.Design/methodology/approachThe present sensor consists in the spatial coupling of a polymeric membrane and an ion-sensitive electrode (platinum electrode). The preparation of the polymeric membrane involves the incorporation of an ionophore (D2HPA), a polymer (polyvinylchloride [PVC]) and a plasticizer (dioctyl phthalate [DOP]). Several techniques have been used to characterize this sensor: the cyclic voltammetry, the electrochemical impedance spectroscopy and the optical microscopy. The sensibility, the selectivity and the kinetic study of a modified platinum electrode have been evaluated by cyclic voltammetry.FindingsThe obtained results reveal the possibility of a linear relationship between the current of reduction peaks and MG concentration. A linear response was obtained in a wide-concentration range that stretches from 10−5to 10−13mol L−1, with a good correlation coefficient (0.976) and a good detection limit of 5.74 × 10−14mol L−1(a signal-to-noise ratio of 3). In addition, the voltammetric response of modified electrode can be enhanced by adding a layer of Nafion membrane. Under this optimal condition, a linear relationship was obtained, with a correlation coefficient of 0.986 and a detection limit of 1.92 × 10−18mol L−1.Originality/valueIn the present research, a convenient, inexpensive and reproducible method for the detection of MG was developed. The developed sensor is capable of competing against the conventional techniques in terms of speed, stability and economy.


1972 ◽  
Vol 37 (3) ◽  
pp. 762-767 ◽  
Author(s):  
Ľ. Adamčíková ◽  
Ľ. Treindl
Keyword(s):  

1982 ◽  
Vol 47 (11) ◽  
pp. 2831-2837 ◽  
Author(s):  
Ľudovít Treindl ◽  
Vasil Dorovský

Oxidation of α-ketoglutaric acid with Ce(IV) ions in a solution of sulphuric acid is a reaction of the first order with respect to both Ce(IV) ions and substrate, is acid catalysed, and its rate is proportional to the reciprocal square of the equilibrium HSO4- concentration. From the temperature dependence of the rate constant in 1.5M-H2SO4, the activation parameters were determined as ΔH##f = 57 kJ/mol and ΔS##f = -45 J mol-1 K-1. The redox reaction proper consists apparently of two steps: in the first one, the enol form of α-ketoglutaric acid reacts with Ce(IV) ions with the formation of the corresponding radical; in the second one, the latter is oxidized further with Ce(IV) to give malonic and succinic acids. Conditions are indicated under which α-ketoglutaric acid serves as substrate for the Belousov-Zhabotinskii oscillation reaction in the presence of Ce(IV)-Ce(III) redox catalyst. Oscillations of Ce(IV) and Br2 concentrations, shifted in phase, can be recorded polarographically with a rotating platinum electrode.


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