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Kinetics and mechanism of PbSO4 electroformation on Pb electrodes in H2SO4 aqueous solutions

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In this paper, the electrochemical processes related to the passivation of Pb in 5 M H2SO4 at 25°C were investigated combining a rotating ring-disk electrode, linear potential sweep voltammetry and potentiostatic pulse techniques complemented with scanning electron microscopic imaging.
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This article is published in Electrochimica Acta.The article was published on 1993-08-01 and is currently open access. It has received 32 citations till now. The article focuses on the topics: Rotating disk electrode & Passivation.

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Electrodeposition of thin sulfide films: nucleation and growth observed for Bi2S3

TL;DR: In this paper, a theoretical expression for three-dimensional progressive nucleation and growth under diffusion control was derived for the potentiostatic pulse technique for in situ studies of the early stages of Bi2S3 electrodeposition on bismuth.
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Electrochemical characterisation of expander materials

TL;DR: In this paper, a method is proposed for the characterisation of expander materials based on the comparison of the results of three different electrochemical techniques: electrochemical impedance, cyclic voltammetry and potentiostatic transients.
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Effects of surfactants on sulfation of negative active material in lead acid battery under PSOC condition

TL;DR: In this paper, the influence of surfactants types in lead-acid battery electrolyte has been investigated on the sulfation of negative active material (NAM) under high-rate partial-state-of-charge (HRPSoC) opreation.
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In-situ ellipsometric study of lead sulfate film electroformation on lead in a sulfuric acid solution

TL;DR: In this article, the process of lead sulfate film formation on a Pb electrode in 0.5 M H2SO4 has been investigated using the in-situ ellipsometric technique complemented with scanning electron microscopic imaging.
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A study of the passivation mechanism of negative plates in lead/acid batteries

TL;DR: In this article, the authors investigated the passivation mechanism of negative plates by means of linear sweep voltammetry and scanning electron microscopy and found that the reduction peak of PbSO 4 is split into two peaks on a seriously passivated negative plate.
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Potentiodynamic current/potential relations for film formation under OHMIC resistance control

TL;DR: Theoretical potentiodynamic current/potential curves for a film formation process under an ohmic resistance control are given in this article, which is compared with experimental data involving the formation of insoluble parathiocyanogen on platinum and the precipitation of a solid CuCl layer during copper dissolution in aqueous HCl solution.
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Mechanism of passivation processes of the lead sulphate electrode

TL;DR: In this paper, the passivation process of the Pb/PbSO 4 electrode was investigated by measuring the potential, capacitance and resistance during galvanostatic anodic polarization and a subsequent open-circuit period.
Journal ArticleDOI

Processes of formation of divalent lead oxide compounds on anodic oxidation of lead in sulphuric acid

TL;DR: In this article, the transformation of the Pb/PbSO 4 electrode into a lead/lead-hydroxide electrode in the potential range between −400 and −500 mV has been confirmed by galvanostatic oxidation of lead in 1 N H 2 SO 4.
Journal ArticleDOI

The electrochemical dissolution of Pb to form PbSO4 by a solution-precipitation mechanism

TL;DR: In this article, a solution-precipitation mechanism was proposed for the formation of PbSO 4 by the electrochemical oxidation of the Pb in H 2 SO 4.
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Frequently Asked Questions (11)
Q1. What are the contributions in "Kinetics and mechanism of pbs04 electroformation on pb electrodes in h2s04 aqueous solutions" ?

In this paper, the electrochemical processes related to the passivation of Pb in SM H, SO, at 25 ” C, have been investigated combining a rotating ring-disk electrode, linear potential sweep voltammetry and potentiostatic pulse techniques complemented with scanning electron microscopic imaging. 

In this case, the current baseline at the ring electrode is related to the steady current of the hydrogen evolution reaction (HER) at Es. The amount of soluble Pb(I1) species produced at the disc lowers considerably along the potential cycling. 

as the transfer of cations through the film is a slow process, the contribution of jr explains the slow decay of current following the current peak. 

It is worth noting that the cathodic current contribution to the ring electrode shows a relatively sharp and somewhat asymmetric peak at E, = -0.985 V, close to the inflection point which can be observed in the ascending branch16r, , , , , ,,: __I v: 0.02&-' (All “I 1-7~5-k--),:Orpm 1 j I---lw:500rpm ); 

As the value of ED is shifted up to E, = -0.94OV, the current transient at the ring becomes sharper, and the electroreduction charge derived from these transients diminishes (Fig 6a, b, right). 

These cations contribute to the growth of a PbSO, layer at the PbSOJsolution interface through chemical precipitation when the concentration of Pb2+ cations adjacent to the electrode exceeds the supersaturation concentration. 

On the other hand, within the H,SO, concentration and pH ranges covered in this work the kinetics of a PbSO., layer formation apparently remains independent of the solution composition, except that the aj&W2 slope increases as the pH of the electrolyte solution is decreased[22]. 

Pb(I1) soluble species produced at the Pb disc at v = 0.02OV s-l, at different values of w, could be determined through the corresponding electroreduction reaction at the Pb ring electrode. 

the value of k, related to the nonconducting PbSO, layer formation, exhibits a complex potential dependence (Table l), which at present is diilicult to interpret because of the uncontrolled precipitation of Pb2+ ions as PbSO., from the solution nearest to the electrode. 

No is the number of nuclei formed instantaneously, k is the average film growth rate constant and M, p and h are the molecular weight, the density and the average height of the PbS04 layer, respectively. 

The voltammetric anodic (4.) and cathodic (qJ apparent charge densities obtained from the first triangular potential scan depend on the surface pretreatment of Pb electrodes, but this influence practically disappears in the subsequent scans.