Kinetics of active zinc dissolution in concentrated KOH solutions

2019 ◽  
Vol 50 (2) ◽  
pp. 149-158 ◽  
Author(s):  
Laurens Reining ◽  
Marina Bockelmann ◽  
Ulrich Kunz ◽  
Thomas Turek
Keyword(s):  
1987 ◽  
Vol 118 (4) ◽  
pp. 453-462 ◽  
Author(s):  
S. A. Khalil ◽  
M. A. El-Manguch

1987 ◽  
Vol 19 (3-4) ◽  
pp. 333-344 ◽  
Author(s):  
J. P. Gould ◽  
I. B. Escovar ◽  
B. M. Khudenko

The kinetics of the cementation of cadmium by zinc have been studied over a range of solution pH values and initial cadmium concentrations. The kinetics were interpreted in terms of a model postulating a transition from a migration controlled mechanism with consequent half order kinetics to a diffusion controlled regime following first order kinetics. The conditions under which each mechanism was found to apply were consistent with the model in which the immediate reductant was hydride ion generated by the interaction of hydrogen ions with the zinc. The reaction stoichiometry was remarkable in that conditions were observed under which more than the theoretical one mole of cadmium per mole of zinc could be reduced. This was ascribed to the electrolysis of water by the induced electrochemical system. A lag in both cadmium cementation and zinc dissolution was observed in many runs. The zinc dissolution was found to commence about 25% sooner than cadmium cementation, a fact ascribed to the establishment of the reducing electrochemical system.


ChemInform ◽  
1987 ◽  
Vol 18 (27) ◽  
Author(s):  
S. A. KHALIL ◽  
M. A. EL-MANGUCH

2003 ◽  
Vol 68 (3) ◽  
pp. 207-218 ◽  
Author(s):  
Slavka Stankovic ◽  
Branimir Grgur ◽  
Nedeljko Krstajic ◽  
Milan Vojnovic

Polarization curves of the anodic dissolution reaction of zinc were determined in EDTA solutions of different total molar concentrations (0.05 0.10, 0.15 and 0.20 mol dm-3), the pH values of which were systematically varied (pH 3.0 ? 10.0). The Tafel slopes of the anodic polarization curves are close to 40 mV dec-1 at lower current densities (10-5 ? 5x10-4 A cm-2) while at higher current densities (5x10-4 ? 10-2 A cm-2) the slopes are in the range of 60 ? 120 mV dec-1. The order of the anodic reaction determined from the anodic polarization curves at lower current densities are: z+(H+) ?? 1/2 for pH < 8 and z+(H+) ??1 for pH > 8, while z+(H4Y) ??1 for all pH values of the examined EDTA solutions. On the basis of these results, two mechanisms of the zinc anodic dissolution reaction are proposed: at pH < 8 and at pH > 8. In both cases the relevant EDTA species directly participate as reactants in the anodic reaction. The dependences of the corrosion potential on pH and on total molar EDTA concentration indicate that the relevant EDTA species take part as reactants in both the cathodic (hydrogen evolution) and anodic (zinc dissolution) reactions of the zinc corrosion process.


Author(s):  
J. F. DeNatale ◽  
D. G. Howitt

The electron irradiation of silicate glasses containing metal cations produces various types of phase separation and decomposition which includes oxygen bubble formation at intermediate temperatures figure I. The kinetics of bubble formation are too rapid to be accounted for by oxygen diffusion but the behavior is consistent with a cation diffusion mechanism if the amount of oxygen in the bubble is not significantly different from that in the same volume of silicate glass. The formation of oxygen bubbles is often accompanied by precipitation of crystalline phases and/or amorphous phase decomposition in the regions between the bubbles and the detection of differences in oxygen concentration between the bubble and matrix by electron energy loss spectroscopy cannot be discerned (figure 2) even when the bubble occupies the majority of the foil depth.The oxygen bubbles are stable, even in the thin foils, months after irradiation and if van der Waals behavior of the interior gas is assumed an oxygen pressure of about 4000 atmospheres must be sustained for a 100 bubble if the surface tension with the glass matrix is to balance against it at intermediate temperatures.


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