Electrochemical study of the pitting corrosion of aluminium and its alloys—III. The role of bonded water and the kinetics of formation and reformation of a passive layer

1993 ◽  
Vol 38 (17) ◽  
pp. 2541-2546 ◽  
Author(s):  
L. Tomcsányi ◽  
Zs. Nagy ◽  
J. Somlai ◽  
J. Borszéki
Keyword(s):  
Pitting Corrosion ◽  
Passive Layer ◽  
Electrochemical Study ◽  
Kinetics Of Formation ◽  
Kinetics Of

scholarly journals Studies on Pitting Corrosion of Al–Cu–Li Alloys Part III: Passivation Kinetics of AA2098–T851 Based on the Point Defect Model

Materials ◽  
2019 ◽  
Vol 12 (12) ◽  
pp. 1912 ◽  
Author(s):  
Elmira Ghanbari ◽  
Alireza Saatchi ◽  
Xiaowei Lei ◽  
Digby D. Macdonald
Keyword(s):  
Barrier Layer ◽  
Potential Model ◽  
Electrochemical Impedance ◽  
Passive Layer ◽  
Charge Carriers ◽  
Theoretical Interpretation ◽  
Defect Model ◽  
Kinetics Of Formation ◽  
Kinetics Of

In this paper, the passivation kinetics of AA2098–T851 was investigated by a fundamental theoretical interpretation of experimental results based on the mixed potential model (MPM). The steady state passive layer formed on the AA2098–T851 in NaHCO3 solution in a CO2 atmosphere upon potentiostatic stepping in the anodic direction followed by stepping in the opposite direction was explored. Potentials were selected in a way that both anodic passive dissolution of the metal and hydrogen evolution reaction (HER) occur, thereby requiring the MPM for interpretation. Optimization of the MPM on the experimental electrochemical impedance spectroscopy (EIS) data measured after each potentiostatic step revealed the important role of the migration of Al interstitials in determining the kinetics of passive layer formation and dissolution. More importantly, it is shown that the inequalities of the kinetics of formation and dissolution of the passive layer as observed in opposite potential stepping directions lead to the irreversibility of the passivation process. Finally, by considering the Butler–Volmer (B–V) equation for the cathodic reaction (HER) in the MPM, and assuming the quantum mechanical tunneling of the charge carriers across the barrier layer of the passive film, it was shown that the HER was primarily controlled by the slow electrochemical discharge of protons at the barrier layer/solution (outer layer) interface.

Role of ionic strength in the kinetics of formation of the monochelate of nickel(II) with heptane-3,5-dione

1992 ◽  
Vol 24 (4) ◽  
pp. 359-368 ◽  
Author(s):  
María Luisa Moyá ◽  
Amalia Rodriguez ◽  
Francisco Sánchez ◽  
Carlos Blanco ◽  
Michael J. Hynes
Keyword(s):  
Ionic Strength ◽  
Kinetics Of Formation ◽  
Kinetics Of

An Evaluation of the Plane Strain Compression Test. III. Experimental Study of the Friction Test: The Role of the Metallurgical Parameters of Die and Sheet

1982 ◽  
Vol 104 (4) ◽  
pp. 538-544 ◽  
Author(s):  
F. Delamare ◽  
J. Kubie´
Keyword(s):  
Experimental Study ◽  
Shear Stress ◽  
Chemical Nature ◽  
Marked Effect ◽  
Friction Test ◽  
Good Reliability ◽  
Plane Strain Compression Test ◽  
Kinetics Of Formation ◽  
Kinetics Of

This paper deals with the influence of the metallurgical parameters of dies and sheet on the friction shear-stress which could be measured by P.S.C.T. The metallurgical parameters of the dies have a marked effect on the kinetics of formation of transfer layers. The metallurgical parameters of the sheet have an effect both on the kinetics of formation, and the chemical nature of the transfer layers. Many parameters must be controlled to have good reliability in PSCT. Then the results can be correlated with boundary lubrication in cold rolling.

Electrochemical Study of cis-Cyanoaquobis(ethylenediamine)chromium(III) Ion and Its Adducts with Hg(II) and Ag(I)

1993 ◽  
Vol 58 (2) ◽  
pp. 328-334 ◽  
Author(s):  
Miroslav Rievaj ◽  
Elena Korgová ◽  
Dušan Bustin
Keyword(s):  
Electrochemical Properties ◽  
Acid Hydrolysis ◽  
Electrochemical Study ◽  
Factors Affecting ◽  
Kinetics Of Formation ◽  
Kinetics Of

The paper describes voltammetric and polarographic properties of the cis-cyanoaquobis(ethylenediamine)chromium(III) complex and the kinetics of its acid hydrolysis. The reactions of this complex with Hg(II) and Ag(I) ions were studied. Formation of di- and trinuclear adducts was found. Linkage isomerisation of CN bridging group in these adducts (Cr-NC-Hg and Cr-NC-Ag) was proposed on the basis of their electrochemical properties. The kinetics of formation and decomposition of [Cr(CN)(en)2(H2O)]2+ adducts with Hg(II) and Ag(I) are described and the factors affecting them are discussed.

Kinetics of Formation and Dissolution of Weak Polyelectrolyte Multilayers:  Role of Salt and Free Polyions

Langmuir ◽  
2002 ◽  
Vol 18 (14) ◽  
pp. 5607-5612 ◽  
Author(s):  
D. Kovacevic ◽  
S. van der Burgh ◽  
A. de Keizer ◽  
M. A. Cohen Stuart
Keyword(s):  
Polyelectrolyte Multilayers ◽  
Kinetics Of Formation ◽  
Kinetics Of

Kinetic- or Thermodynamic-Growth Formation of Pd Nanocrystals: a combined TEM-DLS Approach

2008 ◽  
Vol 1087 ◽  
Author(s):  
Gilles Berhault ◽  
Marta Bausach
Keyword(s):  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Growth Kinetics ◽  
Palladium Nanoparticles ◽  
Theory Model ◽  
Collision Theory ◽  
Kinetics Of Formation ◽  
Growth Formation ◽  
Kinetics Of

AbstractThe kinetics of formation of palladium nanoparticles with well-defined morphologies (rods, cubes, MTP icosahedra, bipyramids) was studied using a combination of TEM and dynamic light scattering (DLS). The present study was focused on the role of the concentration and the size of seeds on both the kinetics of growth and the morphology distribution. Results clearly emphasize the role of the seed concentration (and not the size) on the growth kinetics in agreement with a collision theory model.

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