Mechanical and electrochemical characteristics in sea water of 5052-O aluminum alloy for ship

The optimum corrosion protection potentials were examined for 5052-O Al alloy,which is mainly used in ships.Various electrochemical experiments were carried out and the surface morphologies of specimens were observed by scanning electron microscopy（SEM） in order to determine the optimum corrosion protection potential to overcome pitting,corrosion,stress corrosion cracking（SCC）,and hydrogen embrittlement in sea water.An optimum protection potential range of-1.3 V to-0.7 V was determined under the application of an impressed current cathodic protection（ICCP） system.The low current densities were shown in the range of-1.3 V to-0.7 V in the electrochemical experiments and good specimen surface morphologies were observed after potentiostatic experiment.

Cavitation and electrochemical characteristics of thermal spray coating with sealing material

Steel applied in ocean environment is exposed to corrosion and cavitation and is subject to increasing damages. To prevent this, anti-corrosion thermal spray coating technique is widely used. The low-temperature thermal spray coating was performed with 85%Al-14.5%Zn-0.5%Zr for ship materials and various sealing materials were applied to improve its durability, and the electrochemical behavior and cavitation characteristics were observed. The results show that the sealing improves all the properties of the materials. Hybrid ceramic and fluoro-silicon sealing materials show good electrochemical characteristics, and the fluoro-silieon sealing material shows the best anti-cavitation characteristics.

Microstructure and electrochemical characteristics of nonstoichiometric La-rich AB_5-type alloy for Ni/MH battery electrode

The nonstoichiometric La-rich mischmetal (designated by MI)-based hydrogen storage alloy with a composition of MI(Ni0.64Co0.2Mn0.12Al0.04)(4.76) was prepared by arc melting and annealed at 1173 K for 10 h to investigate the effect of annealing treatment on the microstructure and electrochemical characteristics of the alloy. X-ray diffraction analysis showed that annealing can cause a release of the crystal lattice strain and an increase in amounts of the La2Ni7-type second phase in MI(Ni0.64Co0.20Mn0.12Al0.04)(4.76) alloy. Scanning electron microscopy and electron probe microanalysis examinations indicated that annealing leads to disappearance of the dendrite structure in the as-cast alloy, growth of crystal grain, and decrease of composition segregation. The annealing at 1173 K for 10 h flattened and extended the potential plateau and increased the maximum discharge capacity to 328 mA center dot h/g from 310 mA center dot h/g and the cycling life. The mechanism of the improvement in electrochemical characteristics was discussed based on the alloy microstructure change induced by annealing.

Phase Structure and Electrochemical Characteristics of Ml(Ni_(3.55)Co_(0.75)Mn_(0.40)Al_(0.30))_(5x)(x=0.88,0.92,0.96,1.00) Hydrogen Storage Alloys

The phase structure and electrochemical characteristics of Ml （（Ni3.55Co0.75Mn0.40Al0.30）sx （ x = 0.88, 0.92, 0.96, 1.00） hydrogen storage alloys were studied. The effect of the stoichiometric ratio on the phase structure and electrochemical characteristics was analyzed. The results of XRD reveal that all the alloys consist mainly of LaNi5 phase with the hexagonal CaCu5 structure. But a few of the diffraction peaks of La2Ni7 phase on XRD pattern are observed when x ≤ 0.92, and with decreasing x, the intensity of La2Ni7 diffraction peaks increases and the values of lattice parameters a and cell volume increase, c and c/a of LaNi5 phase decrease gradually. When x≥0.96, La2Ni7 phase disappears and the alloys become single CaCu5-type. The electrochemical tests show that the maximum discharge capacity, high rate dischargeability and low temperature dischargeability are improved to different degrees by adjusting the stoichiometric ratio.

Preparation and electrochemical characteristics of Co_3(PO_4)_2-coated LiNi_(0.8)Co_(0.2)O_2 by solid-state reaction at room temperature

LiNi0.8Co0.2O2 particles were modified by Co3（PO4）2 coating. The effects of the Co3（PO4）2 coating on the structure and electrochemical properties of the LiNi0.8Co0.2O2 cathode material were investigated. The Co3（PO4）2 coating forms a thin layer on the surface of the LiNi0.8Co0.2O2 material and a solid solution by interacting with the LiNi0.8Co0.2O2 core material during calcination at 700℃ for 4 h. Charge-discharge experiment results show that the Co3（PO4）2 coating improves the cycling stability of the LiNi0.8Co0.2O2 cathode material. The capacity retention of the pristine LiNi0.8Co0.2O2 cathode after 50 cycles is 83.6%, whereas it is 91.7% in the case of the LiNi0.8Co0.2O2 cathode coated with 1 wt.% Co3（PO4）2. Storage tests of the 4.35 V charged electrode at 60℃ after a month show that the Co3（POg）2-coated sample exhibits good storage properties compared with the pristine sample.

Microstructure and Electrochemical Characteristics of Melt-Spinning Alloy Ml(NiCoMnAl)_5

The microstructure and electrochemical characteristics of Ml(NiCoMnAl) 5 alloys prepared by both the melt spinning method and the conventional induction melting were investigated and compared. SEM and XRD studies show that the microstructure of melt spinning alloys is columnar structure. With increasing melt spinning rate, the crystal grains become finer and preferentially grow along (111)[111] direction. The melt spinning and cast alloys belong to CaCu 5 type hexagonal crystal structure. The electrochemical measurements show that the initial capacities of melt spinning alloy electrodes are all above 210 mAh·g -1 with good activation behavior, reaching their maximum capacities after two charge discharge cycles. The maximum capacity (294 mAh·g -1 ) of melt spinning (10 m·s -1 ) alloy electrodes is as the same as that of as cast alloy electrode, and stability of charge discharge cycles of all melt spinning alloy electrodes is better than that of the as cast alloy electrodes. When charged at 600 mA·g -1 , the capacity of melt spinning (10 m·s -1 ) alloy electrode could reach 65% of its maximum capacity about 45 min with high rate discharge capability; but with the cycle number increasing, the stability of its capacity is less than that electrodes of melt spinning rate.

MICROSTRUCTURE AND ELECTROCHEMICAL CHARACTERISTICS OF Zr_(0.9)Ti_(0.1)(Ni_(1.1)Mn_(0.7)V_(0.2))_x METAL HYDRIDE ELECTRODE

The crystal structure, the phase composition and the electrochemical characteristics of Zr0.9Ti0.1(Ni1.1Mn0.7V0.2)x (x=0.90, 0.95, 1.00, 1.05) alloys were investigated by means of XRD, SEM, EDS and electrochemical measurements. It was shown that all alloys are multiphase with C15 Laves phase as a main phase along with C14 phase and some secondary phases. And the amounts of the C14 phase and secondary phases in the four alloys increases with decreasing x. The results indicated that the various stoichiometric ratios have great effects on the electrochemical characteristics such as the maximum discharge capacity, discharge rate capability and self-discharge properties etc. for Zr0.9Ti0.1(Ni1.1Mn0.7 V0.2)X (x=0.90, 0.95, 1.00, 1.05) alloys. The hyper-stoichiometric Zr0.9 Ti0.1(N1.1Mn0.7 V0.20)1.05 exhibits the maximum discharge capacity of 332mAh-g-1. The C14 phase and secondary phases seems to improve discharge rate capability of the alloys.

Improvement of alkaline electrochemical characteristics of bauxite residue amendment with organic acid and gypsum

Neutralization of alkaline properties of bauxite residue(BR)by using organic acid and gypsum additions may effectively improve electrochemical properties and alleviate physicochemical barriers to ecological rehabilitation.Mineral acids,citric acid and hybrid acid–gypsum additions were compared for their potential to transform and improve zeta potential,isoelectric point(IEP),surface protonation and active alkaline-OH groups,which are critical factors for further improvement of physicochemical and biological properties later.Isoelectric points of untransformed bauxite residue and six transformed derivatives were determined by using electroacoustic methods.Electrochemical characteristics were significantly improved by the amendments used,resulting in reduced IEP and-OH groups and decreased surface protonation for transformed residues.XRD results revealed that the primary alkaline minerals of cancrinite,calcite and grossular were transformed by the treatments.The treatments of citric acid and gypsum promoted the dissolution of cancrinite.From the SEM examination,citric acid and gypsum treatments contributed to the reduction in IEP and redistribution of-OH groups on particle surfaces.The collective evidence suggested that citric acid and gypsum amendments may be used firstly to rapidly amend bauxite residues for alleviating the caustic conditions prior to the consideration of soil formation in bauxite residue.

Electrochemical hydrogen storage characteristics of as-cast and annealed La_(0.8-x)Nd_xMg_(0.2)Ni_(3.15)Co_(0.2)Al_(0.1)Si_(0.05)(x=0-0.4)alloys

The La-Mg-Ni-based A2B7-type La0.8-xNdxMg0.2Ni3.15Co0.2Al0.15 （x=0, 0.1, 0.2, 0.3, 0.4） electrode alloys were prepared by casting and annealing. The influences of partial substitution of Nd for La on the structure and electrochemical performance of the as-cast and annealed alloys were investigated. It was found that the experimental alloys consist of two major phases, （La, Mg）2Ni7 phase with the hexagonal Ce2Ni7-type structure and LaNi5 phase with the hexagonal CaCu5-type structure, as well as some residual phase LaNi3 and NdNi5. The discharge capacity and high rate discharge ability （HRD） of the as-cast and annealed alloys first increase and then decrease with Nd content growing. The as-cast and annealed alloys （x=0.3） yield the largest discharge capacities of 380.3 and 384.3 mA·h/g, respectively. The electrochemical cycle stability of the as-cast and annealed alloys markedly grows with Nd content rising. As the Nd content increase from 0 to 0.4. The capacity retaining rate （S100） at the 100th charging and discharging cycle increases from 64.98% to 85.17% for the as-cast alloy, and from 76.60% to 96.84% for the as-annealed alloy.

Composition optimization and electrochemical characteristics of Co-free Fe-containing AB_5-type hydrogen storage alloys through uniform design

In order to reduce the cost of ABs-type hydrogen storage alloys, effects of substitution of Ce for La （A side） and Fe, Mn, Al for Ni （B side） on structural and electrochemical properties of （LaCe）;（NiFeMnAl）s alloys were studied systematically. To make component uniform and operation easy, uniform design （UD） method was introduced into the study of composition optimization of Co-free Fe-containing ABs-type alloys for the first time. X-ray diffraction （XRD） results showed that the designed alloys were of single CaCus-type structure phase. The replacement of Fe had a severe effect on electrochemical capacity, and the substitution of Fe and A1 had a synergetic action among the unit cell volume, cycling stability and high rate discharge property. Interestingly, it was found that the hydrogen storage alloys with excessively high plateau pressure showed a tilted line in Nyquist plot instead of the semicircle, and the current decayed rapidly to near zero at the beginning of the step in constant potential step （CPS）, indicating that electrochemical impedance spectra （EIS） and CPS cannot accurately measure the electrochemical kinetics process of the hydrogen storage alloys with excessively high plateau pressure.

Electrochemical characteristics and synergetic effect of Ti_(0.10)Zr_(0.15)V_(0.35)Cr_(0.10)Ni_(0.30)-10 wt.%LaNi_5 hydrogen storage composite electrode

In order to improve performance of Ti-V-based solid solution alloy, electrochemical characteristics and synergetic effect of Ti0.10Zr0.15V0.35Cr0.10Ni0.30-10 wt.%LaNi5 hydrogen storage composite electrode prepared by two-step arc-melting were investigated system-atically. X-ray diffractometry （XRD） and scanning electron microscopy-energy dispersive spectroscopy （SEM-EDS） showed that the main phase of composite alloy was composed of V-based solid solution phase with a BCC structure and C14 Laves phase with hexagonal structure, while secondary phase also existed in the composite alloy. The results showed that electrochemical characteristics of the composite alloy elec-trode were significantly improved. It was suggested that synergetic effect appeared in the maximum discharge capacity of the composite alloy, synergetic effect of the discharge capacity appeared in the activation process, in the composite process, in the cyclic process, in the discharge process at low/high temperature and at different current densities, and synergetic effect existed in the charge-transfer resistance and in the ex-change current density, which seemed to be related to formation of the secondary phase.

Electrochemical Characteristics and Applications of Boron-Doped Polycrystalline Diamond Film Electrodes

The elcetrochemical characteristics of boron doped polycrystalline diamond thin film (BDF) electrode 4×4 mm 2 in size were studied using cyclic voltammetry and potentiostatic method. The diamond electrode exhibits adequate electrochemical activity and its response current changes linearly with K 3Fe(CN) 6 concentrations. The response current is proportional to the square root of the scan rate, reflecting mass transport controlled by planar diffusion. Stable mass transport can be quickly established within 4s. The BDF electrode provides good resolving power for the determination of lead and cadmium and gives satisfactory results in the analysis of pure water sample.

Electrochemical reduction characteristics and mechanism of nitrobenzene compounds in the catalyzed Fe-Cu process

The reduction of the nitrobenzene compounds （NBCs） by the catalyzed Fe-Cu process and the relationship between the electrochemical reduction characteristics of NBCs at copper electrode and reduction rate were studied in alkaline medium（pH=11）. The catalyzed Fe-Cu process was found more effective on degradation of NBCs compared to Master Builder＇s iron. The reduction rate by the catalyzed Fe-Cu process decreased in the following order： nitrobenzene 〉4-chloro-nitrobenzene ≥m-dinitrobenzene ：〉 4-nitrophenol ≥2,4-dinitrotoluene 〉2-nitrophenol. The reduction rate by Master Builder＇s iron decreased in the following order： m-dinitrobenzene ≥4-chloro-nitrobenzene 〉4-nitrophenol 〉2,4-dinitrotoluene ≈nitrobenzene 〉2-nitrophenol. NBCs were reduced directly on the surface of copper rather than by the hydrogen produced at cathode in the catalyzed Fe-Cu process. The reduction was realized by the hydrogen produced at cathode and Fe（OH）2 in Master Builder＇s iron, It is an essential difference in reaction mechanisms between these two technologies. For this reason, the reduction by the catalyzed Fe-Cu depended greatly on NBC＇s electron withdrawing ability.

Effects of Ti and Co on the Electrochemical Characteristics of MgNi-Based Alloy Electrodes

Mg-based hydrogen storage alloys MgNi, Mg0.9Ti0.1Ni and Mg0.9Ti0.1Ni0.9Co0.1 were successfully prepared by means of mechanical alloying （MA）. The structure and the electrochemical characteristics of these Mg-based materials were also studied. The results of X-ray diffraction （XRD） and scanning electron microscopy （SEM） show that the main phases of the alloys exhibit amorphous structures, and trace of Ni co-exists. The charge-discharge cycle tests indicate these alloys have good electrochemical active characteristics. And the cycle stability of Ti and Co doped alloy was better than that of MgNi alloy. After 50 cycle charge-discharge, the discharge capacity of the Mg0.9Ti0.1Ni0.9Co0.1 alloy was much better than that of MgNi and Mg0.9Ti0.1Ni alloys. The discharge capacity of Mg0.9Ti0.1Ni0.9Co0.1 was 102.8% higher than that of MgNi alloy, and 45.49% higher than that of the Mg0.9Ti0.1Ni alloy. During the process of charge-discharge cycle test, the main reason for the electrode capacity fading is the corrosion of Mg to Mg（OH）2 on the surface of alloys. The Tafel polarization test indicates Ti and Co improve the anticorrosion in an alkaline solution. The EIS results suggest that proper amount of Ti and Co doping improve the electrochemical catalytical activity on the Mg-based alloy surface significantly.

Structures and electrochemical hydrogen storage performance of Si added A_2B_7-type alloy electrodes

In order to ameliorate the electrochemical hydrogen storage performance of La-Mg-Ni system A2B7-type electrode alloys, a small amount of Si was added. The La0.8Mg0.2Ni3.3Co0.2Six （x=0-0.2） electrode alloys were prepared by casting and annealing. The effects of adding Si on the structure and electrochemical hydrogen storage characteristics of the alloys were investigated systematically. The results indicate that the as-cast and annealed alloys hold multiple structures, involving two major phases of （La, Mg）2Ni7 with a Ce2Ni7-type hexagonal structure and LaNi5 with a CaCu5-type hexagonal structure as well as one residual phase LaNi3. The addition of Si results in a decrease in （La, Mg）2Ni7 phase and an increase in LaNi5 phase without changing the phase structure of the alloys. What is more, it brings on an obvious effect on electrochemical hydrogen storage characteristics of the alloys. The discharge capacities of the as-cast and annealed alloys decline with the increase of Si content, but their cycle stabilities clearly grow under the same condition. Furthermore, the measurements of the high rate discharge ability, the limiting current density, hydrogen diffusion coefficient as well as electrochemical impedance spectra all indicate that the electrochemical kinetic properties of the electrode alloys first increase and then decrease with the rising of Si content.

Influence of pretreatment process on structure, morphology and electrochemical properties of Li[Ni_(1/3)Co_(1/3)Mn_(1/3)]O_2 cathode material

The layered Li[Ni1/3Mn1/3Co1/3]O2 was separately synthesized by pretreatment process of ball mill method and solution phase route, using [Ni1/3Co1/3Mn1/3]3O4 and lithium hydroxide as raw materials. The physical and electrochemical behaviors of Li[Ni1/3Mn1/3Co1/3]O2 were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, field emission scanning electron microscopy （FESEM） and electrochemical charge/discharge cycling tests. The results show that the difference in pretreatment process results in the difference in compound Li[Ni1/3Co1/3Mn1/3]O2 structure, morphology and the electrochemical characteristics. The Li[Ni1/3Mn1/3Co1/3]O2 prepared by solution phase route maintains the uniform spherical morphology of the [Ni1/3Co1/3Mn1/3]3O4, and it exhibits a higher capacity retention and better rate capability than that prepared by ball mill method. The initial discharge capacity of this sample reaches 178 mA-h/g and the capacity retention after 50 cycles is 98.7% at a current density of 20 mA/g. Moreover, it delivers high discharge capacity of 135 mA-h/g at a current density of 1 000 mA/g.

How do high-voltage cathode and PEO electrolyte get along well?EIS analysis mechanism&potentiometric control strategy

PEO-based all-solid-state electrolytes are extensively utilized and researched owing to their exceptional safety,low-mass-density,and cost-effectiveness.However,the low oxidation potential of PEO makes the interface problem with the high-voltage cathode extremely severe.In this work,the impedance of PEO-based all-solid-state batteries with high-voltage cathode(NCM811)was studied at different potentials.The Nyquist plots displayed a gyrate arc at low-frequencies for NCM811/PEO interface.Based on the kinetic modeling,it was deduced that there is a decomposition reaction of PEO-matrix in addition to de-embedded reaction of NCM811,and the PEO intermediate product(dehydra-PEO)adsorbed on the electrode surface leading to low-frequency inductive arcs.Furthermore,the distribution of relaxation time shows the dehydra-PEO results in the kinetic tardiness of the charge transfer process in the temporal dimension.Hence,an artificial interface layer(CEI_(x))was modified on the surface of NCM811 to regulate the potential of cathode/electrolyte interface to prevent the high-voltage deterioration of PEO.NCM/CEI_(x)/PEO batteries exhibit capacity retentions of 96.0%,84.6%,and 76.8%after undergoing 100 cycles at cut-off voltages of 4.1,4.2,and 4.3 V,respectively.Therefore,here the failure mechanism of high-voltage PEO electrolyte is investigated by EIS and a proposed solving strategy is presented.

Effect of electrolyte concentration on low-temperature electrochemical properties of LaNi_5 alloy electrodes at 233 K

The effect of KOH electrolyte concentration on low-temperature electrochemical properties of LaNi5 alloy electrodes at 233 K was studied. The results indicated that the electrolyte concentration had great influence on discharge capacity and discharge voltage plateau of LaNi5 alloy electrode at 233 K, and the highest discharge capacity and discharge voltage plateau were both obtained at 6 mol/L KOH. When the KOH electrolyte concentration changed from 5 to 9 mol/L at 233 K, the high rate discharge ability （HRD） had the same change tendency as the diffusion coefficient, but the exchange current density did not change significantly, which implied that hydrogen diffusion was the control step at low temperature 233 K for discharge process of LaNi5 alloy electrode.

Microstructures and Electrochemical Properties of Cobalt-Free LaNi_(4.0)Al_(0.2)Fe_(0.4)Cu_(0.4-x)Sn_x (x=0～0.4) Electrode Alloys Prepared by Casting

The microstructure, hydriding performance, and electrochemical properties of LaNi4.0Ai0.2Fe0.4Cu0.4-x Snx（x = 0- 0.4） hydrogen storage alloys prepared by casting were investigated using XRD, SEM, pressure-composition isotherms, and electrochemical measurements. Substitution of Sn for Cu leads to the precipitation of LaNiSn phase. With increasing amount of tin substitution, cell volume, plateau pressures, and discharge capacities of the alloys decrease, whereas the cycle life of the alloys improves.

Electrochemical Behavior of Antimierobial Stainless Steel Bearing Copper in Sulfate Reducing Bacterial Medium

The electrochemical characteristic of antimicrobial stainless steel bearing copper NSSAM3 in sulfate reducing bacterial （SRB） was investigated by electrochemical impedance spectroscopy （EIS） and potentiodynamic polarization. The results show that inoculation of SRB into the culture medium significantly affects the anodic polarization behavior of NSSAM3 and accelerates anodic depolarization process, however, it has little effect on cathodic polarization curves of NSSAM3. Under the same exposure time, the anodic polarization curves of NSSAM3 in culture medium with SRB are in anodic active dissolution state when anodic polarization potential value is below 0 V（SCE）, whose anodic polarization current density is bigger than that of in culture medium without SRB. Moreover, when the concentration of Cu^2＋ in SRB medium increases, anodic polarization current density of NSSAM3 decreases and polarization resistance increases with increasing time. Scanning electron microscope （SEM） observations indicate that SRB unevenly attaches on the surface of NSSAM3, and induces the sensitivity to local corrosion.