Electrochemical behavior of Fe(Ⅲ)in Na_(2)SiO_(3)-SiO_(2)-Fe_(2)O_(3)molten salt

The high-temperature requirement for liquid iron smelting via molten oxide electrolysis presents significant challenges.This study investigates the electrochemical reduction of Fe(Ⅲ)in a novel low-temperature electrolyte,Na_(2)SiO_(3)-SiO_(2)-Fe_(2)O_(3),utilizing cyclic voltammetry and square wave voltammetry techniques.The results show that Fe(Ⅲ)reduction occurs in two steps:Fe(Ⅲ)+e^(−)→Fe(Ⅱ),Fe(Ⅱ)+2e^(−)→Fe,and that the redox process of Fe(Ⅲ)/Fe(Ⅱ)at the tungsten electrode is an irreversible reaction controlled by diffusion.The diffusion coefficients of Fe(Ⅲ)in the molten Na_(2)SiO_(3)-SiO_(2)-Fe_(2)O_(3)in the temperature range of 1248–1278 K are between 1.86×10^(−6)cm^(2)/s and 1.58×10^(−4)cm^(2)/s.The diffusion activation energy of Fe(Ⅲ)in the molten salt is 1825.41 kJ/mol.As confirmed by XRD analysis,potentiostatic electrolysis at−0.857 V(vs.O_(2)/O_(complex)^(2-))for 6 h produces metallic iron on the cathode.

Electrochemical behavior of galena and jamesonite flotation in high alkaline pulp

In order to effectively separate galena and jamesonite and improve the recovery during the mixing flotation, the interaction mechanisms between the minerals and the collector of diethyl dithiocarbamate （DDTC） were investigated. Single mineral flotation test was organized to research the effect of pulp pH value on the flotation behavior of galena and jamesonite. Electrochemistry property of the interaction of these two minerals with DDTC was investigated by cyclic voltammetry and Tafel tests. Flotation test shows that the recovery of jamesonite in high alkaline pulp is strongly depressed by lime （Ca（OH）2）. The cyclic voltammetry and Tafel tests results show that the interaction between galena and DDTC is an electrochemical process. High pH value has little influence on the interaction between galena and DDTC, while it has great effect on jamesonite due to self-oxidation and specific adsorption of OH^- and CaOH^＋ on jamesonite surface. Non-electroactive hydroxyl compound and low-electroconductive calcium compounds cover the surface of jamesonite, which impedes electron transfer and DDTC adsorption, thus leads to very low floatability of jamesonite.

Electrochemical behavior of mesh and plate oxide coated anodes during zinc electrowinning

The catalytic performance of two oxides coated anodes （OCSs） meshes and one OCA plate was investigated in a zinc electrowinning electrolyte at 38 ℃. Their electrochemical behaviors were compared with that of a conventional Pb-0.7%Ag alloy anode. Electrochemical measurements such as cyclic voltammetric, galvanostatic, potentiodynamic, open-circuit potential （OCP） and in situ electrochemical noise measurements were considered. After 2 h of OCP test, the linear polarization shows that the corrosion current density of the Ti/（IrO2-Ta2O5） mesh electrode is the lowest （3.37μA/cm^2） among the three OCAs and shows excellent performance. Additionally, after 24 h of galvanostatic polarization at 50 mA/cm^2and 38 ℃, the Ti/MnO2mesh anode has the highest potential （1.799 V）, followed by the Ti/（IrO2-Ta2O5） plate （1.775 V） and Ti/（IrO2-Ta2O5） mesh （1.705 V） anodes. After 24 h of galvanostatic polarization followed by 16 h of decay, the linear polarization method confirms the sequence obtained after 2 h of OCP test, and the Ti/（IrO2-Ta2O5） mesh attains the lowest corrosion current density. The Ti/（IrO2-Ta2O5） mesh anode also shows better performance after 24 h of galvanostatic polarization with the overpotential lower than that of the conventional Pb-Ag anode by about 245 mV.

Electrochemical Behavior and Specific Capacitance of Polyaniline/Silver Nanoparticle/Multi-walled Carbon Nanotube Composites

In this work, we fabricated the polyaniline/silver nanoparticle/multi-walled carbon nanotube （PANI/Ag/MWCNT） composites by in situ polymerization of aniline on the wall of Ag/MWCNTs with different aniline to Ag/MWCNT mass ratios. The chemical structure of the ternary composites was characterized by Fourier transform infrared spectroscopy, Xray diffraction, and X-ray photoelectron spectroscopy. Scanning electron microscope and high-resolution transmission electron microscopy were used to observe the morphology of the ternary composites. The results showed that the polyaniline PANI layer was prepared successfully and it covered Ag/MWCNTs completely. In addition, Ag nanoparticles between the MWCNT core and the PANI layer existed in the form of elemental crystal, which could contribute to the electrochemical performance of the composites. Then we prepared the composite electrodes and studied their electrochemical behaviors in 1 mol/L KOH. It was found that these composite electrodes had very low impedance, and exhibited lower resistance, higher electrochemical activity, and better cyclic stability compared with pure PANI electrode. Particularly, when the mass ratio of aniline to Ag/MWCNTs was 5：5, the composite electrode displayed a small equivalent series resistance （0.23 Ω） and low interfacial charge transfer resistance （〈0.25 Ω）, as well as 160 F/g of the maximum specific capacitance at a current density of 0.25 A/g in KOH solution. We could conclude that the composite material had potential applications as cathode materials for lithium batteries and supercapacitors.

Effects of chromium on the corrosion and electrochemical behaviors of ultra high strength steels

The effects of chromium on the corrosion and the electrochemical behaviors of ultra high strength steels were studied by the salt spray test and electrochemical methods. The results show that ultra high strength steels remain martensite structures and have anodic dissolution characteristic with an increase of chromium content. There is no typical passive region on the polarization curves of an ultra high strength stainless steel, AerMet 100 steel, and 300M steel. However, chromium improves the corrosion resistance of the stainless steel remarkably. It has the slowest corrosion rate in the salt spray test, one order of magnitude less than that of AerMet 100 and 300M steels. With the increase of chromium content, the polarization resistance becomes larger, the corrosion potential shifts towards the positive direction with a value of 545 mV, and the corrosion current density decreases in electrochemical measures in 3.5wt% NaCl solutions. Because of the higher content of chromium, the ultra high strength stainless steel has a better corrosion resistance than AerMet 100 and 300M steels.

Electrochemical behaviors of Zn-Fe alloy and Zn-Fe-TiO_2 composite electrodeposition

Electrochemical behaviors of Zn-Fe alloy and Zn-Fe-TiO2 composite electrodeposition in alkaline zincatesolutions were studied respectively by the methods of linear potential sweep and cyclic voltammetry. From the re-sults it can be concluded that Zn shows under potential deposition, Zn-Fe alloy codeposition is anomalous codeposi-tion and Zn-Fe alloy cathode polarization is increased with the introduction of additive. From the view point of elec-trochemistry, the reasons that the content of Fe in the Zn-Fe coating changes with the composition of the electrolyteand the process conditions altering and the relationship between the content of Fe and the appearance of the coatingare interpreted. The cathode polarization of Zn-Fe alloy codeposition is enhanced obviously with addition of additive.In the course of composite electrodeposition, TiO2 has less promotion to electrodeposition of zinc ions than to iron i-ons, while the electrodeposition of iron ions improves the content of TiO2 in composite coating, which is inagreement with the results of process experiments.

Electrochemical behavior and corrosion resistance of IrO2–ZrO2 binary oxide coatings for promoting oxygen evolution in sulfuric acid solution

In this study,we prepared Ti/IrO2–ZrO2 electrodes with different ZrO2 contents using zirconium-n-butoxide(C16H36O4Zr)and chloroiridic acid(H2IrCl6)via a sol–gel route.To explore the effect of ZrO2 content on the surface properties and electrochemical behavior of electrodes,we performed physical characterizations and electrochemical measurements.The obtained results revealed that the binary oxide coating was composed of rutile IrO2,amorphous ZrO2,and an IrO2–ZrO2 solid solution.The IrO2–ZrO2 binary oxide coatings exhibited cracked structures with flat regions.A slight incorporation of ZrO2 promoted the crystallization of the active component IrO2.However,the crystallization of IrO2 was hindered when the added ZrO2 content was greater than 30at%.The appropriate incorporation of ZrO2 enhanced the electrocatalytic performance of the pure IrO2 coating.The Ti/70at%IrO2–30at%ZrO2 electrode,with its large active surface area,improved electrocatalytic activity,long service lifetime,and especially,lower cost,is the most effective for promoting oxygen evolution in sulfuric acid solution.

Flotation and electrochemical behaviors of chalcopyrite and pyrite in the presence of N-propyl-N′-ethoxycarbonyl thiourea

The characteristics of N-propyl-N′-ethoxycarbonyl thiourea（PECTU） were studied in the flotation experiments of chalcopyrite and pyrite compared with butyl xanthate（BX）. The interaction mechanism between mineral and PECTU was investigated according to zeta potential and electrochemistry measurements in the presence of PECTU. The results proved that PECTU performed a stronger ability to capture chalcopyrite and a better selectivity against pyrite. The zeta potential of chalcopyrite was positively shifted after interacting with PECTU, which indicated that the collector PECTU was obviously adsorbed on chalcopyrite surface. The cyclic voltammetry and Tafel curves results indicated that the oxidation and corrosion rates of chalcopyrite surface were limited in the presence of PECTU, while the effect of PECTU on pyrite in weak alkaline solution can be neglected basically according to the results of zeta potential and electrochemical tests.

Electrochemical behavior of microbiologically influenced corrosion on Fe_3Al in marine environment

In this article, microbiologically influenced corrosion behavior of Fe3Al intermetallie compound in microorganism culture medium has been investigated by using weight loss methods, electrochemical techniques, and electron microscopy. Polarization curves showed that a sharp electrical current peak caused by surface pitting could be observed after Fe3Al electrodes were immersed in culture medium for 15 days when the polarization potential was about -790 mV vs SCE. Based on the electrochemical impedance spectroscopy （EIS） and the equivalent circuit parameters of the associated system, the corrosion products were found to exhibit a two-layer structured feature and the microorganisms could induce pitting and erosion corrosion of the inner layer. In addition, the passivating film of the inner layer was absolutely destroyed by microbial metabolic products.

Effect of grain size on the electrochemical behavior of pure magnesium anode

Three kinds of pure magnesium anode materials with different grain sizes were prepared by extrusion at different temperatures.The grain size of each sample was calculated,then the effect of grain size on the electrochemical properties of pure magnesium anode was investigated by chemical immersion hydrogen test,potentiodynamic polarization scanning,constant current discharge and electrochemical impedance spectroscopy.As the extrusion temperature increases from 180℃ to 250℃,the average grain size of pure magnesium increases from 20m to 30m,and the pure magnesium extruded at 250℃ has the best electrochemical performance as magnesium anode,with the discharge potential of−1.571 V(vs.SCE).Plastic deformation process is a convenient method that can change the microstructure and improve the electrochemical behavior of magnesium anode.

Electrochemical behavior and electrolytic preparation of lead in eutectic NaCl−KCl melts

A novel molten salt extraction process consisting of chlorination roasting and molten salt electrolysis was proposed to develop a more efficient and environmental friendly technology for recovering lead from spent lead acid batteries(LABs).The feasibility of this process was firstly assessed based on thermodynamics fundamentals.The electrochemical behavior of Pb(II)on a tungsten electrode in the eutectic NaCl−KCl melts at 700℃ was then investigated in detail by transient electrochemical techniques.The results indicated that the reduction reaction of Pb(II)in NaCl−KCl melts was a one-step process exchanging two electrons,and it was determined to be a quasi-reversible diffusion-controlled process.Finally,potentiostatic electrolysis was carried out at−0.6 V(vs Ag/AgCl)in the NaCl−KCl−PbCl2 melts,and the obtained cathodic product was identified as pure Pb by X-ray diffraction analysis.This investigation demonstrated that it is practically feasible to produce pure Pb metal by electrochemical reduction of PbCl2 in eutectic NaCl−KCl melts,and has provided important fundamental for the further study on lead recovery from spent LABs via molten salt extraction process.

Electrochemical behavior of tantalum in ethylene carbonate and aluminum chloride solvate ionic liquid

To investigate the electrochemical reduction mechanism of Ta(Ⅴ)in ethylene carbonate and aluminum chloride(EC-AlCl3)solvate ionic liquid,cyclic voltammetry experiments were conducted on a tungsten working electrode.Four reduction peaks were observed in the cyclic voltammogram of the EC-AlCl3-TaCl5 ionic liquid.The reduction peaks at-0.55,-0.72,and-1.12 V(vs Al)were related to the reduction of Ta(Ⅴ)to tantalum metal by three stages including the formation of Ta(Ⅳ)and Ta(Ⅲ)complex ions.The reduction of Ta(Ⅲ)to tantalum metal was an irreversible diffusion-controlled reaction with a diffusion coefficient of 3.7×10^-7 cm^2/s at 323 K,and the diffusion activation energy was 77 k J/mol.Moreover,the cathode products at 323 K were characterized by scanning electron microscopy,energy-dispersive spectroscopy,and X-ray photoelectron spectroscopy.The results showed that tantalum metal and tantalum oxides were obtained by potentiostatic electrodeposition at-0.8 V for 2 h.

Discharge properties and electrochemical behaviors of AZ80-La-Gd magnesium anode for Mg-air battery

In this work,the discharge properties and electrochemical behaviors of as-cast AZ80-La-Gd anode for Mg-air battery have been investigated and compared with the AZ80 anode.The microstructure evolution,electrochemical behaviors and surface morphologies after discharge have been discussed to connect the discharge properties.The results indicate that the modified AZ80-La-Gd is an outstanding candidate for anode for Mg-air batter,which has high cell voltage,stable discharge curves,good specific capacity and energy,and good anodic efficiency.It exhibits the best anodic efficiency,specific capacity and energy of 76.45%,1703.6 mAh·g^(-1)and 2186.3 mWh·g^(-1),respectively,which are20.24%,18.92%and 25.71%higher than values for AZ80 anode.Such excellent discharge performance is attributed to the Al-RE particles.They refine the Mg_(17)Al_(12)phase and therefore improve the self-corrosion resistance and desorption ability of AZ80 anode.

Effect of yttrium and calcium additions on electrochemical behaviors and discharge performance of AZ80 anodes for Mg-air battery

The effects of yttrium(Y)and yttrium+calcium(Y+Ca)additions on the electrochemical properties and discharge performance of the as-extruded Mg−8Al−0.5Zn−0.2Mn(AZ80)anodes for Mg−air batteries were investigated.The results show that the addition of 0.2 wt.%Y increased the corrosion resistance and discharge activity of AZ80 anode.This was attributed to the fine and sphericalβ-Mg_17)Al_(12) phases dispersing evenly in AZ80+0.2Y alloy,which suppressed the localized corrosion and severe“chunk effect”,and facilitated the rapid activation ofα-Mg.Combinative addition of 0.2 wt.%Y and 0.15 wt.%Ca generated grain refinement and a reduction of theβ-Mg_17)Al_(12) phase,resulting in a further enhancement in discharge voltage.However,the incorporation of Ca in Mg_17)Al_(12) and Al_(2)Y compounds compromised the corrosion resistance and anodic efficiency of AZ80+0.2Y+0.15Ca anode.Consequently,AZ80+0.2Y anode exhibited excellent overall discharge performance,with the peak discharge capacity and anodic efficiency of 1525 mA·h·g^(−1) and 67%at 80 mA/cm^(2),13%and 14%higher than those of AZ80 anode,respectively.

Electrochemical behavior of gold and its associated minerals in alkaline thiourea solutions

Electrochemical measurements were conducted to study the electrochemical behavior of gold （Au） and its commonly associated minerals in alkaline thiourea solutions. The results indicated that without addition of any stabilizer, selective dissolution of Au from stibnite and pyrite was only possible at relatively low thiourea concentrations. As Na2SiO3 was added, pyrite started to become active and an oxida- tion peak appeared; the oxidation peaks of axsenopyrite and chalcocite appeared earlier thaxl that of Au. The chalcocite peak shifted in the positive direction and the peak current increased. Stibnite did not show an oxidation peak and its current was nearly zero. Adding Na2SiO3 favored the selective dissolution of Au when its minerals were associated with chalcocite and stibinte. At pH 12, the Au anode dissolution peak current increased with stabilizer concentration. At 0.38 and 0.42 V and for Na2SiO3 concentration below 0.09 M, the current density continuously increased with Na2SiO3 concentration. The Na2SiO3 concentration had to be adequate to stabilize thiourea. When the potential was higher than 0.42 V, the surface of the Au electrode started to passivate. With an additional increase in potential, the presence of Na2SiO3 could not stop the inevitable decomposition of thiourea.

Effect of thermo-mechanical processing on microstructure and electrochemical behavior of Ti-Nb-Zr-V new metastable β titanium biomedical alloy

The influence of thermo-mechanical processing (TMP) on the microstructure and the electrochemical behavior of new metastableβ alloy Ti?20.6Nb?13.6Zr?0.5V (TNZV) was investigated. The TMP included hot working in belowβ transus, solution heat treatments at the same temperature and different cooling rates in addition to aging. Depending upon the TMP conditions, a wide range of microstructures with varying spatial distributions and morphologies of equiaxed/elongatedα andβ phases were attained, allowing for a wide range of electrochemical properties to be achieved. The corrosion behavior of the studied alloy was evaluated in a Ringer’s solution at 37 °C via open circuit potential?time and potentiodynamic polarization measurements.

Biological,antibacterial activities and electrochemical behavior of borided commercially pure titanium in BSA-containing PBS

The effects of boride coating on the bioactivity, antibacterial activity, and electrochemical behavior of commercially pure titanium(CP-Ti) in phosphate buffer solution(PBS) with bovine serum albumin(BSA) were studied. The grazing incidence X-ray diffraction(GIXRD) pattern confirmed the formation of a Ti B/Ti B2 coating via boriding process. Scanning electron microscopy(SEM) observation indicated that the Ti B2 cross-linked particles covered the Ti B whiskers. Water contact angle measurements revealed that boriding led to the formation of a surface with intermediate water affinity. Potentiodynamic polarization(PDP) assays demonstrated that the Ti B/Ti B2 coating had acceptable passivation behavior in BSA-containing PBS. Electrochemical impedance spectroscopy(EIS) measurements revealed that the passivation behavior of the CP-Ti and the borided samples was improved by increasing exposure time. Based on the Mott-Schottky(M-S) tests, it was realized that the charge carriers of passive films of both samples decreased with increasing exposure time in BSA-containing PBS. The bioactivity test results in a simulated body fluid showed that the Ti B/Ti B2 coating switched the CP-Ti from bioinert to bioactive material. Finally, the antibacterial activity test of the Ti B/Ti B2 coating against Escherichia coli and Staphylococcus aureus indicated 99% antibacterial activity.

Electrochemical behaviors of Bi (Ⅲ) in dimethylsulfoxide

Cyclic voltammetry, chronoamperometry and chronopotentiometry were used toinvestigate the electrochemical behaviors of Bi(III) in Bi(NO_3)_3-LiClO_4-DMSO (dimethylsulfoxide)system on Pt and Cu electrodes. Experimental results indicated that the electroreducation of Bi(III)to Bi(0) was irreversible on Pt and Cu electrodes. The diffusion coefficient and electron transfercoefficient of Bi(III) in 0.01 mol.L^(-1) Bi(NO_3)_3-0.l mol.L^(-1) LiClO_4-DMSO system at 303 Kwere 1.75 X 10^(-6) cm^2.s^1 and 0.147 respectively.

Influence of heat treatment on microstructure and electrochemical behaviors of Mg-Zn binary alloys prepared by gas-phase alloying technique

Mg-Zn binary alloys fabricated by the gas-phase alloying technique under vacuum condition were investigated in the state of initial state and after heat treatment for the microstructure and electrochemical behaviors.Different from the traditional Mg-Zn alloys preparation methods,alloys prepared by gas-phase alloying have a large number of intermetallic compounds,such as MgZn,Mg7Zn3 and MgZn2.After solution treatment,the boundary of the eutectic disappeared and the size ofα-Mg increased from 100μm to 150μm.At the same time,the value of the resistance of charge transfer increased,which indicates that the resistance of the charge transfer and the corrosion resistance of the alloys increased.After artificial aging treatment,the distribution ofα-Mg was more uniform and its size was reduced to about 50μm,and there was new eutectic structure formed.The newly formed eutectic structure forms galvanic cells with the alloy matrix,which makes the corrosion resistance of the alloy weaken.

Study on the electrochemical behavior of Mg and Al ions in LiCl-KCl melt and preparation of Mg-Al alloy

The electrochemical behavior of Mg^(2+)and Al^(3+)in LiCl-KCl(mass 4:1)melt at 973 K was studied on a Mo electrode systematically by cyclic voltammetry,square wave voltammetry and chronopotentiometry.The results showed that the reductions of Mg^(2+)and Al^(3+)were reversible processes controlled by the rate of the mass transfer.When Mg^(2+)and Al^(3+)coexisted in LiCl-KCl melt,they had no significant effect on the reduction potential of each other.The equilibrium potentials of Mg^(2+)/Mg and Al^(3+)/Al were obtained by open circuit potential method.Their apparent standard potentials were also calculated in this system and the values were-2.52 V vs Cl_(2)/Cl^(−),-1.66 V vs Cl_(2)/Cl^(−),respectively.Correspondingly,the apparent Gibbs free energies of Mg^(2+)/Mg and Al^(3+)/Al were-485.71 kJ/mol^(-1),-480.78 kJ/mol^(-1).Finally,potentiostatic electrolysis was performed on a Mo electrode in LiCl-KCl-MgCl_(2)-AlCl_(3)(the mass ratio of MgCl_(2) to AlCl_(3) was 10:1)melt at different potentials.The components of the deposits were characterized by scanning electron microscope and energy dispersive spectroscopy.The study revealed that the content of Al in the deposit decreased as the overpotential increased and Al tended to segregate at the grain boundaries.