Effect of 2-mercaptobenzothiazole concentration on sour-corrosion behavior of API X60 pipeline steel:Electrochemical parameters and adsorption mechanism

We investigated the effect of the 2-mercaptobenzothiazole concentration on the sour-corrosion behavior of API X60 pipeline steel in an environment containing H_(2)S at 25°C and in the presence of 0,2.5,5.0,7.5,and 10.0 g/L of 2-mercaptobenzothiazole inhibitor.To examine this behavior,we conducted open-circuit potential(OCP),potentiodynamic polarization,and electrochemical impedance spectroscopy(EIS)tests.Energy dispersive spectroscopy and scanning electron microscopy were also used to analyze the corrosion products.The results of the OCP and potentiodynamic polarization tests revealed that 2-mercaptobenzothiazole reduces the speed of both the anodic and cathodic reactions.An assessment of the Gibbs free energy of the inhibitor(△G_(ads)^(■))indicated that its value was less than-20 kJ·mol^(-1)and greater than-40 k J·mol^(-1).Therefore,the adsorption of 2-mercaptobenzothiazole onto the surface of the API X60 pipeline steel occurs both physically and chemically,the latter of which is particularly intentional.In addition,as the△G_(ads)^(■)dsvalue was negative,we could conclude that the adsorption of 2-mercaptobenzothiazole onto the surface of the pipeline steel occurs spontaneously.The EIS results indicate that with the increase in the 2-mercaptobenzothiazole inhibitor concentration,the corrosion resistance of API X60 steel increases.An analysis of the corrosion products revealed that iron sulfide compounds form on the surface.In summary,the results showed that an increase in the inhibitor concentration results in a decrease in the corrosion rate and an increase in inhibitory efficiency.Additionally,we found that the 2-mercaptobenzothiazole adsorption process on the API X60 steel surfaces in an H2 S-containing environment follows the Langmuir adsorption isotherm and occurs spontaneously.

CHRONOABSORPTOMETRY FOR THE DETERMINATION OF KINETIC PARAMETERS OF ELECTRON TRANSFER REACTIONS USING LONG-OPTICAL-PATH ELECTROCHEMICAL CELL

A single potential step chronoabsorptometric method for the determination of ki- netic parameters of simple quasi-reversible reactions is described.It is verified by determining the kinetic parameters for the electroreduction of ferricyanide.A long-optical-path electro- chemical cell with a plug-in electrode is used.The thickness of solution layer is 0.55 mm

New Inclusion Assessment Method in Aluminum Alloys——Electrochemical Method for Inclusion Assessment

The existence of inclusion influences the properties of aluminum alloy castings,from which the castings will face scrapping under severe condition.Great efforts on the inclusions in aluminum alloy were made and many inclusion assessment methods were put forward.However,most of the current methods are characterized by time consuming and expensive equipment cost,which limits the application in aluminum industry.Since the aluminum properties are sensitive to the inclusion,this paper tries to establish a new kind of inclusion assessment method.The inclusions were introduced to aluminum melts by adding aluminum scraps.The samples with different inclusion contents were prepared.The microstructure contained inclusions was observed.The inclusion was automatically identified with an image analyzer by setting different grey threshold value,and the inclusion content was obtained.The image analysis shows that inclusions wreck the continuity of the alloy matrix seriously,and the inclusion area percentage increases with the increasing of aluminum scraps.The high and low polarization measurements were conducted in 3.5 wt% NaCl aqueous solution at the temperature of 25 ℃.The electrochemical parameters of the testing materials,such as corrosion potential E k,corrosion current density I k and the linear polarization resistance R p,were obtained.The polarization measurement results show that the linear polarization resistances decrease,the corrosion potentials move towards more negative direction,and the corrosion current densities increase with the increasing of inclusion content.The theoretical analysis of the inclusion content and the corrosion current density was performed.The existence of inclusions makes the microstructure form corrosion microcells between the alloy matrix and inclusions.The impressed current can accelerate the current velocity or corrosion current density.The regression model of the inclusion contents vs.the corrosion current density was obtained.This model can be used to quantitatively analyze the inclusion content in aluminum alloys on the basis of inclusion sensitivity to the inclusion content.It is confirmed that the electrochemical method for inclusion assessment （EcMIA） is simple and reliable,which can provide a new solution for inclusion assessment in aluminum alloy.

Control of repair effect and hydrogen embrittlement risk by parameters optimization for BIEM

Bidirectional electromigration rehabilitation(BIEM)is a novel electrochemical rehabilitation method involving the injection of inhibitors into steel bar surface.The BIEM effect and hydrogen embrittlement(HE)risk depend on the electrochemical parameters(current density and duration)and operating condition(stress level and concrete cover thickness)of reinforced concrete structures.Experiments were performed in this study to investigate the relationships between the aforementioned factors.For a small current density group,a linear relationship was established between electric flux and chloride extraction.For a large current density group,the reasonable current density,stress level,and treatment time were obtained.Finally,the querying method of electrochemical parameters combined with treatment time and current density was proposed.

Influence of ammonium sulfate on the corrosion behavior of AZ31 magnesium alloy in chloride environment

Electrochemical corrosion of AZ31 magnesium alloy in the NH_(4)^(+)-SO_(4)2−-Cl−environment is studied.Effect of NH_(4)^(+)overshadows that of Cl−as the(NH_(4))_(2)SO_(4) concentration is 0.005 M or higher,yielding an evolution from localized corrosion to uniform corrosion.Acceleration effect of NH_(4)^(+)can be attributed to that(i)NH_(4)^(+)dissolves the inner MgO and hinders the precipitation of Mg(OH)_(2) and(ii)the buffering ability of NH_(4)^(+)provides H+,enhances the hydrogen evolution,and expedites the corrosion process.The latter is demonstrated as the dominant factor with the results in unbuffered and buffered environments.The severe corrosion and hydrogen process in NH_(4)^(+)-containing solution results in a high Hads coverage and yields an inductive loop within the low frequency.Meanwhile,SO_(4)^(2−)is helpful in generating cracked but partially protective corrosion products,while Cl−could broaden the corrosion area beneath the corrosion product.

Effect of Ca2+ and Mg2+ on CO2 Corrosion Behavior of Tube Steel

Effects of Ca2+ and Mg2+ on the CO2 corrosion behaviors of tube steel were studied in simulated oil-field environment.The influence of Ca2+and Mg2+ on the corrosion rate and morphologies of corrosion product layer was determined by scanning electron microscope and measuring mass loss.Potentiodynamic polarization and impedance spectroscopy were used to investigate the change of electrochemical characteristic parameters of corrosion product layer and corrosion dynamic process.The results show that with Ca2+ and Mg2+ in electrolyte,the morphologies and microstructures of corrosion product layer changed obviously,thus affecting the corrosion process.