Potentiodynamic Polarization Curves (potentiodynamic + polarization_curve)

Distribution by Scientific Domains


Selected Abstracts


Inhibition of corrosion of AZ91 magnesium alloy in ethylene glycol solution in presence of chloride anions

MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 2 2005
E. Slavcheva
Abstract The influence of chloride ions on the corrosion of AZ91 magnesium alloy in water/ethylene glycol solutions and the inhibiting effect of lactobiono-tallowamide (LTA) were investigated using electrochemical and surface analysis methods. Potentiodynamic polarization curves in aqueous solution of ethylene glycol (50:50w%) containing 0.1 g.L,1 chloride and up to 0.5 g.L,1 LBT were obtained at room and at elevated temperatures. The chloride anions showed a distinct deteriorating effect as they caused pit initiation and accelerated the dissolution of the tested alloy. The selected organic compound demonstrated good protective properties against corrosion of AZ91 magnesium alloy and behaved as inhibitor of mixed type hindering both the cathodic and the anodic partial reactions. It showed inhibition efficiency of 77% at relatively low concentration of 0.2 g.L,1 and was considered as a promising corrosion inhibitor. The mechanism of inhibition was discussed on the basis of the electrochemical impedance spectroscopy (EIS) and XRD analysis of the surface. [source]


The electrochemical behavior of Ti-6Al-7Nb alloy with and without plasma-sprayed hydroxyapatite coating in Hank's solution

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 5 2002
I. C. Lavos-Valereto
Abstract The electrochemical behavior of Ti-6Al-7Nb alloy with and without plasma-sprayed hydroxyapatite (HA) coating was investigated in Hank's balanced salt solution at 37 °C. This behavior was evaluated by analyzing both corrosion potential variation with time curves and potentiodynamic polarization curves. The polarization curves were determined both in aerated and deaerated solutions. It was found that the corrosion potential of uncoated sample is always more noble than that of coated one. In aerated solutions the polarization curve of a coating-free alloy presents a typical passive/transpassive behavior, which is absent in the HA-coated alloy and in deaerated solution for both coated and uncoated conditions. In the latter polarization curves, the current density continuously increases with the increase of the potential. The corrosion rate determined from polarization curves is higher for HA-coated alloys, but it still can be considered negligible (less than 1 ,A/cm2). © 2002 Wiley Periodicals, Inc. J Biomed Mater Res (Appl Biomater) 63: 664,670, 2002 [source]


A block-on-ring tribocorrosion setup for combined electrochemical and friction testing

LUBRICATION SCIENCE, Issue 3 2007
M.S. Jellesen
Abstract The combined action of corrosion and wear can cause degradation of equipment, and thereby financial losses related to the renewal or repair of damaged equipment. In the food industry, metal degradation is a major concern since metal release eventually can cause health risks for consumers. This study describes a block-on-ring testing facility used to determine sliding wear, and additionally allowing for electrochemical measurements, such as potentiodynamic polarization curves and potentiostatic monitoring of current and potential. To verify the reliability and reproducibility of this block-on-ring tribocorrosion setup, the tribological and electrochemical behaviour of stainless steel sliding against a ceramic ring in sulphuric acid has been determined. Furthermore, a case taken from the food industry has been examined. The study shows that results made on the described block-on-ring testing facility are reliable and can provide improved information about material properties when the material is exposed to combined chemical and mechanical degradation. Copyright © 2007 John Wiley & Sons, Ltd. [source]


Testing procedure to obtain reliable potentiodynamic polarization curves on type 310S stainless steel in alkali carbonate melts

MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 4 2006
S. Frangini
Abstract Potentiodynamic polarization measurements have been employed to evaluate the anodic behavior of a type 310S stainless steel in the eutectic Li/K molten carbonate. In general, the electrochemical tests yield useful information to predict the stability of the oxide films formed on the surface at the initial period of corrosion, although some precaution is required in the testing procedure as the reproducibility of results is seen to be adversely affected by the passage of large currents. Especially when the steel is in a passive state, erratic results are easily observed if the corrosion layer is being damaged by uncontrolled large currents. This is because the acid-base properties of the melt are susceptible to deep changes by applied currents in the milli-ampere range resulting in hysteresis phenomena in the polarization plot. Hysteresis is caused, on one hand, by acidic dissolution of the passive layer at high anodic currents and, on the other hand, by increased melt basicity due to oxide ion build-up at high cathodic currents. An optimized testing procedure is therefore suggested that minimizes these effects by imposing a 2 mA/cm2 threshold current during polarization measurements. Moreover, the conditions for the applicability of the linear polarization technique to estimate kinetic parameters have been discussed in relationship with the corrosion mechanisms analysed by impedance spectra. It is concluded that the presence of diffusional impedance terms and formation of surface resistive films in molten carbonates may result in not reliable polarization resistance values obtained with the linear polarization. [source]