scholarly journals Effect of Hydrogen and Absence of Passive Layer on Corrosive Properties of Aluminum Alloys

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1580 ◽  
Author(s):  
Paweł P. Włodarczyk ◽  
Barbara Włodarczyk

This paper reports the results of research on the effect of hydrogen permeation and the absence of passive layers on the variations in the corrosive properties of aluminum alloys. The study demonstrated that such variations contribute to the deterioration of corrosive properties, which in turn contributes to shortening the reliability time associated with the operation of aluminum alloy structures. The analysis involved structural aluminum alloys: EN AW-1050A, EN AW-5754, and EN AW-6060. It was demonstrated that the absorption of hydrogen by the analyzed alloys led to the shift of the electrode potential to the negative side. The built hydrogen corrosion cells demonstrate in each case the formation of electromotive force (EMF) cells. The initial EMF value of the cell and its duration depends on the duration of hydrogenation. As a result of removing the passive layers, the electrode potential also changes to the negative side. Following the removal of the passive layer from one of the electrodes, the cells also generated a galvanic (metal) cell. The duration of such a cell is equivalent to the time of restoration of the passive layer. The formation of such hydrogen and metal galvanic cells changes the electrochemical properties of aluminum alloys, therefore deteriorates the corrosive properties of aluminum alloys.

1930 ◽  
Vol 3 (5) ◽  
pp. 473-489
Author(s):  
A. Norman Shaw ◽  
H. E. Reilley

A detailed procedure for the maintenance of a standard of voltage to within one or two parts in a million is described.In so far as these investigations have proceeded, neutral saturated cells have been found to be superior to acid cells as independent standards for a period of many years, though the latter are preferable for purposes of ordinary precision or shorter periods. The recommended code of procedure is briefly as follows: a number of cells should be constructed according to standard specifications with the new requirements of uniformity of container and speed of preparation, and observations made upon them every few days for a period of three months. The differences in electromotive force (at constant temperature) should be determined between each cell in the group and any one of them chosen arbitrarily as reference cell, and certain new selection and rejection rules applied. In accordance with these rules a cell should be rejected: (a) if its deviation from the mean electromotive force of the group has increased or decreased by 10 microvolts or more during the preceding two weeks; or (b) if it differs in electromotive force from the mean of the group by more than 10 +d microvolts where d is the mean deviation of the cells of the group. If d exceeds 20 microvolts the entire group should be considered untrustworthy. The selected cells should be observed for three additional months, the rejection rules again applied and if a specified proportion survive elimination, the initial reference mean of the laboratory may be established.At intervals of several months additional groups of cells, neutral and acid, should be constructed and exchanges made with laboratories possessing cells of known characteristics. Analysis of the resulting observations determines: (a) the constants in the aging* equation for the reference batch, and (b) the difference between the initial reference mean of the laboratory and the estimated value of the international reference mean.Examples of the analysis of cell observations are given, illustrating the establishment of the initial reference mean, the recapture of this value when the aging coefficients are known, and the preliminary determination of the aging equation for a given group of cells. The use of the aging equation is found to be the essential feature in the attainment of increased precision.A summary of data on standard cells is included.


1878 ◽  
Vol 27 (185-189) ◽  
pp. 196-238 ◽  

The contact theory of voltaic action seems to have undergone no development since the date of Sir W. Thomson’s experiment, which consisted in connecting a plate of zinc and a plate of copper by means, of a drop of water, when it was found that the metals were brought to the same electric potential, although when metallically connected they were at different potentials. He believed that any electrolyte would behave in exactly the same way as the water of his experiment, equalizing the potentials of any two metals connected by it. The electromotive force of a simple cell, ought, in accordance with the theory, to be equal to the difference of potentials between zinc and copper in; contact. A test founded on this deduction was very difficult to apply, because there was no exact determination of the difference of potential of zinc and copper in contact, Sir W. Thomson, in his experiment, having really measured the difference of potential between air at the surface of a zinc plate, and air at the surface of a copper plate. In the absence of this test, the equality of the electromotive forces of simple cells in which zinc and copper are the metals (the liquids being water, dilute sulphuric acid, and sulphate of zinc) was held as a proof of the theory. Now it is known that when two pieces of the same metal are dipped into any two liquids, which are diffusing into one another, a difference of potentials is established between the metals, and the electromotive force of a cell of this kind can in no way depend on a difference of potentials due to metallic contact. So that although in such a cell there is an action which is somewhat the same as the action in a simple voltaic cell, the theory took no account of it whatever. In fact, the explanation of voltaic action given in the latest treatises on electricity is felt to be incomplete, even by the writers of such treatises, and the present investigation has been entered upon in consequence. Sir W. Thomson’s result, and our own experiments lead us to magine that when zinc and copper are immersed in water there are three successive states to be noticed:—At the instant of immersion the zinc and copper may be reduced to the same potential, so that the electromotive force of the voltaic cell E is equal to the difference of potential ZC — between zinc and copper in contact; the zinc now becomes negative to the copper, so that E reaches a limit which is greater than ZC — ; lastly, if a current passes, polarization occurs and the zinc becomes gradually less negative to the copper, E diminishing, therefore, from its maximum value# But when a saturated solution of zinc sulphate is employed instead of water, the first state, if it exists at all, exists for so short a time that practically, zinc and copper in zinc sulphate are never at the same potential. Thus (see Table X ) when care is taken to keep the zinc and copper in a water cell well insulated from one another, E is found to increase from a value very little greater than ZC — , the electromotive force of contact of zinc and copper, to a limit, but in a zinc sulphate cell no such great increase is observed.


1996 ◽  
Vol 458 ◽  
Author(s):  
R. J. Racicot ◽  
S. C. Yang ◽  
R. Brown

ABSTRACTEvidence for the formation of a passive layer between a conductive polymer coating and aluminum alloy surfaces is reported Experimental results from electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) on aluminum alloys coated with a novel double strand conductive polymer coating based on polyaniline reveal the evidence for the formation of passive layer. The key results are: (1) Modeling of EIS data is best fit with a three RC circuit, indicating a third interface between the polymer coating and the alloy's surface; (2) EIS testing in acidic salt solutions shows the conductive polymer coating performs differently and better than a typical anodized or chromáte conversion coating indicating a possibly different interface layer than a typical aluminum oxide and (3) SEM studies of the aluminum surface, after the polymer film is removed, indicates that this interfacial layer has a dense and smooth “oxide type” surface morphology. The experimental results are consistent with a mechanism in which the conducting polymer serves as a surface conversion agent that oxidizes the aluminum metal surface to form a passive layer.


It is well known that the so-called "oxygen electrode" does not behave in a thermodynamically reversible manner. The decomposition voltage of water has been calculated thermodynamically from various calorimetric and solubility data by Lewis, Nernst and von Wartenberg, Brönsted and Lewis and Randall. The final critical value given by the last-named authors is 1.227 volt at 25ºC., which should therefore be the e. m. f. of a cell consisting of a reversible hydrogen electrode and a reversible oxygen electrode immersed in the same electrolyte, both gases being at 760 mm. pressure. In practice this value has never been obtained. Smale found that the e. m. f. of the hydrogen-oxygen cell, though independent of the p H of the electrolyte, was only 1.07-1.08 volt. Wilsmore obtained a value of 1.07 volt, rising to 1.12 volt if the cell were allowed to stand for stand for some days, while a similar result, 1.06 volt, was obtained by Crotogino. More recently, Richards has reported 0.979 volt, and Furman also obtains a value of about 0.98 volt. Since it is well established that the hydrogen electrode bahaves in a perfectly reversible manner in accord with thermodynamic laws, the discrepancy between the "theoretical" and experimental e. m. f. of the hydrogen-oxygen cell must have its origin in the oxygen electrode. It is in fact experimentally found that oxygen electrodes, whether set up with bright or plantinized plantium, ( a ) tend to be irreproducible, ( b ) do not obey the thermodynamic relation between electrode potential and partial pressure of oxygen, and ( c ) are readily polarized even by minute currents, thus failing to conform with any of the criteria of reversibility.


2004 ◽  
Vol 2004 (0) ◽  
pp. 105-106
Author(s):  
Ryusuke AKAGI ◽  
Takahiro IZUMI ◽  
Goroh ITOH ◽  
Nobuhide ITOH ◽  
Yuzo SASAKI

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