Application of electrochemical depassivation in PRB systems to recovery Fe^0 reactivity

Permeable reactive barriers （PRBs） show remarkable Cr（VI） removal performance. However, the diminished removal rate because of mineral fouling over time is the bottleneck for application of PRBs. The present study demonstrated that electrochemical depassivation was effective for recovering the Fe^0 reactivity, and minerals can be cleaned layer by layer with no secondary ion contamination and no transformation from Cr（III） to Cr（VI）. The removal recovery rate increased with increasing electrolysis voltage before reaching the optimal electrolysis voltage, and then decreased as the electrolysis voltage further increased. The recovery effect at electrolysis voltages of 5, 10, and 15 V show the same trend as a function of electrolysis time, where recovery rate first increased and then decreased after reaching the optimal electrolysis time. The Cr（VI） removal rate significantly decreased with increasing electrolysis distance. Furthermore, Fe^0 brush meshes electrode, Fe^0 fillings, and polyvinyl chloride （PVC） meshes separators were combined to create an Electro-PRB configuration for the caisson excavation construction technique, which lays the foundation for establishment of promising Electro-PRB systems to treat Cr（VI）-contaminated groundwater.

INFLUENCE OF MAGNETIC FIELD ON ACCURACY OF ECM BY CHANGING THE CONDUCTIVITY OF ANODE FILM

The change of conductivity, thickness and scanning electron microscopy （SEM） appearance of the anode film of CrWMn in 10% NaNO3 at different anode potential either with or without the magnetic field applied are investigated by testing film resistance, galvanostatic transient and using SEM to design magnetic circuit in magnetic assisted electrochemical machining （MAECM）. The experiments show that the anode film has semi-conducting property. Compared with the situation without magnetic field applied, the resistance of the film formed at 1 .SV （anode potential） increased and decreased at 4.0V while B=0.4T and the magnetic north pole points toward anode. The SEM photo demonstrates that the magnetic field will densify the film in the passivation area and quicken dissolution of the anode metal in over-passivation area. Based on the influence of magnetic field on electrochemical machining（ECM） due to the changes of the anode film conductivity behavior, the magnetic north pole should be designed to point towards the workpiece surface that has been machined. Process experiments agree with the results of test analysis.

Effect of solution pH,Cl- concentration and temperature on electrochemical behavior of PH13-8Mo steel in acidic environments

The effect of solution pH,Cl;concentration and temperature on the electrochemical corrosion behavior of PH13-8Mo steel in acidic solution was investigated by using the electrochemical tests,scanning electron microscopy and X-ray photoelectron spectroscopy.The PH13-8Mo martensitic precipitation hardened stainless steel is in the passivity state when the pH value is above 3.0,below which the anodic polarization curves of the steel are actively dissolved.The corrosion current density gradually decreases with increasing the solution pH and decreasing Cl;concentration and solution temperature.Pits are initiated on the sample surface in the presence of the Cl;and gradually developed into uniform corrosion with increasing the Cl;concentrations.Moreover,the corrosion is more serious with an increase in solution temperature.

Insight into relationship between composition,thickness and electrochemistry behavior of oxide film formed on TA15under different potentials in 0.5 mol·L^(-1)H_(2)SO_(4)

The oxide film formed on TA15 alloy in0.5 mol·L^(-1)H_(2)SO_(4)at different applied potentials is investigated by evaluating the film formation current density,film thickness,surface film composition,valence state,and the electrochemical characteristics.The relative quantitative spectral analysis revealed by X-ray photoelectron spectroscopy(XPS)and X-ray absorption spectra(XAS)shows that the increasing applied potential promotes the formation of thick and high-valence state films.By contrasting with XAS of the reference titanium oxides,it is found that TiO_(2)within the oxide film changes from anatase type to rutile type with the potential increases to 2.00 V.The oxide film formed at passive region has better protection performance,and with the increase of applied potential,the corrosion resistance of passive film increases,whereas the ND(donor density)values obtained from the Mott-Schottky(MS)results decrease with the increasing applied potential,indicating a better uniformity and protective effect of the oxide film.Based on above facts,the model of the oxide films formed on TA15 at different applied potentials in passive region and dissolve region is proposed.Besides,the existence forms of all the TA15alloying elements under the most corrosion resistant condition are confirmed.

Role of late transition metals on pitting resistance of Zr-Ti-(Cu, Ni,Co)-Al bulk metallic glasses in 0.6 M NaCl aqueous solution

Four quanternary Zr-based bulk metallic glasses（BMGs）were selected,including the Zr_（46）Ti_2Cu_（45）Al_7,Zr_（61）Ti_2Cu_（25）Al_（12）,Zr_（55）Ti_4Ni_（22）Al_（19）and Zr_（55）Ti_2Co_（28）Al_（15）,due to their robust glass-forming ability and containing a single species of late transition metal（LTM）in compositions.Their pitting resistances in 0.6 M Na Cl aqueous solution were investigated to examine the role of LTM elements in the alloys,with electrochemical measurements,surface morphology observation and x-ray photoelectron spectrometry analysis.It is shown that in comparision with two Cu-bearing BMGs,Zr_（55）Ti_4Ni_（22）Al_（19）and Zr_（55）Ti_2Co_（28）Al_（15）BMGs exhibited significantly superior resistance to pitting.Zr_（61）Ti_2Cu_（25）Al_（12）,Zr_（55）Ti_4Ni_（22）Al_（19）and Zr_（55）Ti_2Co_（28）Al_（15）BMGs manifested distinct passivation behaviour,because of the formation of surface passive film mainly comprising of Zr O_2,Ti O_2and Al_2O_3.However,no significant differences in the electrochemical resistive properties and thicknesses of passive films were found between Zr_（61）Ti_2Cu_（25）Al_（12）and Zr_（55）Ti_4Ni_（22）Al_（19）BMGs.Nevertheless,at the passive film/metal interface,copper enrichment took place in Zr_（61）Ti_2Cu_（25）Al_（12）,whereas the nickel was slightly deficient at the interface in Zr_（55）Ti_4Ni_（22）Al_（19）.During pitting propagation,selective dissolution of the zirconium,titanium and aluminum over the copper took place in Zr_（61）Ti_2Cu_（25）Al_（12）,but it was not the case in Zr_（55）Ti_4Ni_（22）Al_（19）.For the two Cu-bearing BMGs,reduction of passive base metal elements in composition resulted in local selective dissolution,even absence of the passivation.