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The triangular potential sweep voltammetric studies on pure tin in concentrated sodium hydroxide solutions

✍ Scribed by V.S. Muralidharan; K. Thangavel; K.S. Rajagopalan


Publisher
Elsevier Science
Year
1983
Tongue
English
Weight
551 KB
Volume
28
Category
Article
ISSN
0013-4686

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✦ Synopsis


The triangular potential sweep voltammetric studies were carried out on pure tin (99.9999 %) in NaOH solutions (l-10 N). The forward scan revealed two distinguished peaks in the region -1.12 to -0.9 V US see and at faster sweep rates a single peak appeared. Oscillations were observed in the E-i curve in the potential regions of Sn/Sn(OH), or Sn(OH),/Sn(OH)., in the forward scan; and increase of stannitc concentration increased the oscillations. The non-stoichiometric nature of the passive oxide film is responsible for these oscillations. The first anodic peak potential and current dependencies on sweep rates revealed that a "pore resistance model" holds good. The appearance of a single cathodic peak at far negative potentials, compared to the anodic peak observed at higher sweep rate, was understood to be due to irreversible reduction of oxidised species formed on the fo-d scan. The fractional dependence of cathodic peak current and potential on stannite ion concentration, at constant OH-ion concentration and a Tafel slope of 60 mV decade-', suggests the reduction of stannite involves activated adsorption of Sn(OH) obeying the Temkin isotherm with its discharge as a rate-determining step. NOMENCLATURE anodic peak potential anodic peak current film formation potential resistance of the solution in the pores film density thickness of the film specific conductivity of the solution inside the pores degree of coverage of the electrode total area of the electrode resistance of the solution external to the film cathodic peak potential cathodic Desk current symme& factor number of electrons involved in the electro-chemical reaction diffusion coefficient of oxidant rate constant sweep rate concentration of the oxidant