Effect of MnO_4^- and silver content on electrochemical behaviour of Pb-Ag alloy anodes during potential decay periods

The effect of MnO4- and silver content on electrochemical behaviour of five commercial Pb-Ag alloy anodes was studied in acid zinc sulphate electrolyte with and without MnO4- ions at 38 °C during potential decay periods. When the anodes were immersed into acid zinc sulphate electrolyte without MnO4- ions, the Pb-0.72%Ag anode entered complete passivation state in the shortest time among the five anodes, followed by anodes Pb-0.67%Ag, Pb-0.60%Ag, Pb-0.58%Ag and Pb-0.29%Ag-0.1%Ca by measurement of open circuit potential. During immersion of the anodes, MnO4 ions accelerated the passivation and increased the corrosion current density of the anodes. After immersion in zinc electrolyte with MnO4-, the anode Pb-0.72%Ag had the best corrosion resistance, followed by anodes Pb-0.67%Ag, Pb-0.60%Ag, then the close anodes Pb-0.58%Ag and Pb-0.29%Ag-0.1%Ca by the electrochemical impedance spectroscopy （EIS） analysis.

ELECTROCHEMICAL BEHAVIOUR OF PHASES IN TITANIUM ALLOYS

The electrochemical behaviour,which is presented by means of anodic polarization curves.of the component phases in Ti and Ti alloys in aqueous solutions of fluorhydrie acid,chhnhydric acid and amber acid has been investigated.The results indicate that the electrochemical behaviour of the allloys depends upon the composition and the lattice type.The corrosion of x and x′phase in actire region and that of β phase in passive region are the dominant corrosion behaviour.

DIRECT ELECTROCHEMICAL BEHAVIOUR OF CYTOCHROME C AT A BARE GLASSY CARBON ELECTRODE

A reversible electron transfer between horse heart cytochrome c and a bare glassy carbon electrode was found and the dependence of direct electrochemical behaviotw on the electrode surface state was discussed.

ELECTROCHEMICAL BEHAVIOURS OF CYANOETHENYL ANILINE DERIVATIVES

The redox behaviours of the donor-acceptor model compounds, cyanoethenyl aniline derivatives were investigated by cyclic voltammetry and the mechanism of the electrode reaction was studied in detail.

THE ELECTROCHEMICAL BEHAVIOUR OF THE NEW VANADIUM BRONZE (Li_3V_5O_(15)) CATHODE IN SECONDARY LITHIUM BATTERY

A new kind of vanadium bronze with rich lithium (Li_5V_5O_(15))was prepared from Li_2CO_3 and V_2O_5 at 680℃ for 24 hrs. The charge and discharge curves of bronze electrode were determined in organic electrolyte. One mole of this material could be incorporated up to 4 mole lithium at 0.2mA/cm^2 and 1.0V cut-off voltage, corresponding capacity about 340Ah/kg. Compared with the cell of Li/Li_(1+x)V_3O_5 the cell of Li/new bronze had higher capacity, smoother discberge curve, but lower plateau voltage (about 1.8V). The cycling behaviour of this material was good. The electrode insertion reaction was controlled by the lithium diffusion process in the bronze. This new bronze could be used for low voltage rechargeable lithium battery.

Tailoring the microstructure of Mg-Al-Sn-RE alloy via friction stir processing and the impact on its electrochemical discharge behaviour as the anode for Mg-air battery

Constructing the magnesium alloy with fine grains,low density of dislocations,and weak crystal orientation is of crucial importance to enhance its comprehensive performance as the anode for Mg-air battery.However,this unique microstructure can hardly be achieved with conventional plastic deformation such as rolling or extrusion.Herein,we tailor the microstructure of Mg-Al-Sn-RE alloy by using the friction stir processing,which obviously refines the grains without increasing dislocation density or strengthening crystal orientation.The Mg-air battery with the processed Mg-Al-Sn-RE alloy as the anode exhibits higher discharge voltages and capacities than that employing the untreated anode.Furthermore,the impact of friction stir processing on the electrochemical discharge behaviour of Mg-Al-Sn-RE anode and the corresponding mechanism are also analysed according to microstructure characterization and electrochemical response.

Surface morphology and electrochemical behaviour of Ti-48Al-2Cr-2Nb alloy in low-concentration salt solution

Electrochemical machining(ECM) is becoming increasingly important for the efficient machining of parts with a large machining area. This is an addition challenge for ECM because of the very high machining current. To overcome this difficulty, a direct and effective strategy is to adopt the machining mode that uses a low-concentration electrolyte with a low current density.The purpose of this study is to reveal the electrochemical behaviour and surface morphology in low-concentration electrolyte.The polarization behavior of Ti-48Al-2Cr-2Nb is measured by linear sweep voltammetry and cyclic voltammetry curves. The ηω-j curves demonstrate the special dissolution behaviour of Ti-48Al-2Cr-2Nb at low current densities. The surface morphology,surface quality, and dissolution mechanism are analysed in three low-concentration electrolytes at different current densities after the ECM dissolution experiments. The results demonstrate that Ti-48Al-2Cr-2Nb exhibits three unique dissolution morphologies in the three solutions, and we found that the γ-TiAl phase dissolves faster than the α2-Ti3Al phase. These results also show that 1% NaCl solution is more suitable for Ti-48Al-2Cr-2Nb in ECM compared with the other two solutions, considering its good surface quality, low breakdown potential, and high material removal rate. Later, the dissolution process of the sample in 1% NaCl solution at different corrosion times is revealed. Moreover, a dissolution model is proposed for the electrochemical dissolution behaviour of Ti-48Al-2Cr-2Nb in 1% NaCl solution.

Corrosion Evolution of Low Alloy Steel in Deaerated Bicarbonate Solutions

Corrosion evolution during immersion tests （up to 43 days） of NiCu steel in deaerated 0.1 mol/L bicarbonate solutions was investigated by electrochemical measurements, scanning electron microscopy （SEM） and X-ray diffraction （XRD）. Results show that NiCu steel transformed from the anodic dissolution in the early stage of immersion to a metastable passive state in the final stage as the open-circuit potential value shifted positively, which was aroused by the precipitation of corrosion products. This process was mainly promoted by the trace amount of oxygen. Simultaneously, dominant cathodic reaction transformed from the hydrogen evolution in early stage to reduction processes of corrosion products in later stages. Possible corrosion processes were discussed with the assistance of a corresponding Pourbaix diagram.