铝合金表面环氧涂层中水传输行为的电化学阻抗谱研究

研究了LY12铝合金/环氧涂层电极在不同浓度NaCl溶液中的电化学阻抗谱(EIS),提出了涂层电极在浸泡过程中的不同阻抗模型。通过涂层电容值的变化得出环氧涂层在NaCl溶液中浸泡初期主要发生Fick扩散,中后期发生非Fick扩散Cl^-离子的存在使水的扩散系数增大,但却抑制了水与涂层组元间的相互作用,从而抑制了水的非Fick扩散过程。阻抗参数解析表明,金属/溶液界面的电化学反应阻抗主要决定于涂层中的吸水过程,后者直接决定基体/溶液界面的电化学反应面积。

Rate Law for Photoelectrochemical Water Splitting Over CuO

Photocatalytic splitting of water over p-type semiconductors is a promising strategy for production of hydrogen.However,the determination of rate law is rarely reported.To this purpose,copper oxide(CuO)is selected as a model photocathode in this study,and the photogenerated surface charge density,interfacial charge transfer rate constant and their relation to the water reduction rate(in terms of photocurrent)were investigated by a combination of(photo)electrochemical techniques.The results showed that the charge transfer rate constant is exponential-dependent on the surface charge density,and that the photocurrent equals to the product of the charge transfer rate constant and surface charge density.The reaction is first-order in terms of surface charge density.Such an unconventional rate law contrasts with the reports in literature.The charge density-dependent rate constant results from the Fermi level pinning(i.e.,Galvani potential is the main driving force for the reaction)due to accumulation of charge in the surface states and/or Frumkin behavior(i.e.,chemical potential is the main driving force).This study,therefore,may be helpful for further investigation on the mechanism of hydrogen evolution over a CuO photocathode and for designing more efficient CuO-based photocatalysts.

Electrochemical behaviors of tantalum in anhydrous ethanol containing hydrogen sulfate ions

The electrochemical behaviors of Ta in tetrabutylammonium hydrogen sulfate（TBAHS） ethanol solutions were studied using potentiodynamic polarization,cyclic voltammetry,potentiostatic current time transient and impedance techniques.The results revealed that no active-passive transition is presented in the cyclic voltammogram,and the anodic current density increases with the increase of solution temperature,TBAHS concentration,potential scan rate and water content.The apparent activation energy is about 43.389 kJ/mol and the dissolution process is diffusion-controlled.Potentiostatic measurements showed that the current density gradually decays to a steady value when the potential is low;however,when the potential is higher than a certain value,the current density initially declines to a minimum value and then increases gradually.The resistance of passive film decreases with increasing potential,and inductive loops are presented when the potential is higher than 2.0 V.

Effects of weight-lifting or resistance exercise on breast cancer-related lymphedema:A systematic review

The purpose of this systematic review was to identify the effects of weight-lifting or resistance exercise on breast cancer-related lymphedema.Published articles written in English were retrieved from electronic databases,including ScienceDirect,PubMed,Scopus,and CINAHL databases.Hand-searches for unpublished papers were also completed.Content analysis was used to examine articles that met the inclusion criteria.Among 525 searched papers,15 papers met the inclusion criteria:13 trials evaluated weight-lifting or resistance exercise alone and two trials evaluated weight-lifting or resistance exercise plus aerobic exercise.The results of the review showed that no arm volume change was observed for either exercise modality.In addition,six included studies showed that weight-lifting or resistance exercise did not cause lymphedema or adverse events in patients at risk of breast cancer-related lymphedema.For patients with breast cancer-related lymphedema,six studies reported that change of swelling outcome measures were not significantly different between the weight-lifting or resistance exercise group and the control group.However,three included studies reported that volume of arm was significantly more reduced in the weight-lifting or resistance exercise group than those in the control group.The findings suggest that supervised resistance exercise may be safe,feasible,and beneficial in patients with breast cancer-related lymphedema or at risk for breast cancer-related lymphedema.However,the limitation of small sample size implies that further research is needed to confirm these findings.

Influence of welding speed on corrosion behaviour of friction stir welded AA5086 aluminium alloy

The plates of AA5086 aluminium alloy were joined together by friction stir welding at a fixed rotation speed of 1000 r/min various welding speeds ranging from 63 to 100 mm/min.Corrosion behavior of the parent alloy(PA),the heat affected zone(HAZ),and the weld nugget zone(WNZ)of the joints were studied in 3.5%(mass fraction)aerated aqueous Na Cl solution by potentiodynamic polarization and electrochemical impedance spectroscopy(EIS).The corrosion susceptibility of the weldments increases when the welding speed increases to 63 and 100 mm/min.However,the value of corrosion rate in the weldments is lower than that in the PA.Additionally,the corrosion current density increases with increasing the welding speed in the HAZ and the WNZ.On the contrary,the corrosion potential in the WNZ appears more positive than in the HAZ with decreasing the welding speed.The WNZ exhibits higher resistance compared to the HAZ and the PA as the welding speed decreases.The results obtained from the EIS measurements suggest that the weld regions have higher corrosion resistance than the parent alloy.With increasing the welding speed,the distribution and extent of the corroded areas in the WNZ region are lower than those of the HAZ region.In the HAZ region,in addition to the pits in the corroded area,some cracks can be seen around the corroded areas,which confirms that intergranular corrosion is formed in this area.The alkaline localized corrosion and the pitting corrosion are the main corrosion mechanisms in the corroded areas within the weld regions.Crystallographic pits are observed within the weld regions.

Impedance Spectroscopic Study on Room Temperature Ionic Liquid-Water Mixtures

AC impedance spectroscopy in pure room temperature ionic liquids （RTILs） and RTIL-water mixture was measured at the temperature of range from 30 ℃ down to -30 ℃. The cations of RTILs are N,N-diethyl-N-methyl-N-（2-methoxyethyl） ammonium （[DEME]）, 1-ethyl-3-methylimidazolium （[C2mim]） and l-butyl-3-methylimidazolium （[Camim]）, the anions are tetrafluoroborate （[BF4]） and bis（trifluoromethanesulfonyl）imide （[TFSI]）. In all pure RTILs, there are two kinds of local minima in real part of the AC impedance Zreal. By adding water to [DEME][BF4] （0 mol% 〈 x 〈 94 mol%） at room temperature, the local minimum value at higher frequency decreased remarkably at the fixed frequency with increasing water concentration. Above 94 mol% H20, a quite different profile of the AC impedance spectroscopy was obtained. In addition to Zreal. temperature dependence of an imaginary part of the impedance Zimag had an isosbestic point below 94 mol%. The isosbestic point disappeared above 94 mol%. The isosbestic point in Zing reveals an interaction between [DEME][BFa] and H2O.

Corrosion behavior of 907 steel under thin electrolyte layers of artificial seawater

The corrosion behavior of 907 steel under thin electrolyte layer(TEL) has been investigated by means of cathodic polarization curve measurement, electrochemical impedance spectroscopy(EIS) and scanning electron microscopy(SEM). The results show that the cathodic diffusion current density presents the variation trend of initial increase and subsequent decrease with the decrease of TEL thickness, and the maximum deposits at 58 μm. The cotangent-hyperbolic impedance(O) is rationally first introduced to study the diffusion process of the reactants through the corrosion products layer with many permeable holes. The initial corrosion rate of 907 steel under different TEL thickness increases with the decrease of TEL thickness except that of 104 μm,whereas the corrosion rate after long time corrosion can be ranked as 104 μm﹥402 μm﹥198 μm﹥301 μm﹥bulk solution.

Monitoring the Morphology of the Bottom of Streams and Reservoirs Using Electrical Impedance Spectrometry Method

A part of the Earth＇s surface has been formed by the action of running water during geomorphological development. The flow of water is one of the ways of how particles can be eroded, transported and accumulated. If endogenous processes do not work, the surface of the continents would lower to the level close to the ocean surface and the relief would have almost no ruggedness. Recently, there have been talks about the relative classification of deviation of the present state from the ＂original＂ or ＂natural＂ one caused by anthropogeneous effects. The activity of man can manifest itself by pollution, the excessive use of water, a change in the flow regime, and the like. Research into the morphology of the river bottom and the bottom of settling tanks or dam reservoirs is systematically carried out in selected streams and reservoirs by the long-term sampling of bottom sediments. The knowledge of the sediment layer is also important. The EIS method, which was used for measuring, is new for the aforementioned applications. Possibilities of EIS method with new apparatus using for this application were tested in laboratory and in situ. On the basis of interpretation of the electrical conductivity data, a grid of depth data was acquired. These data are characterized by anomalously high and low ＂spots＂ and show morphological changes in the studied area.

Research on the Mechanism of Impedance Matching for Underwater Acoustic Transmitter based on Mathematical Modelling and Corresponding Balance Transformer

With the progress of power transmission technology, it is necessary for researchers to conduct related research on impedance matching. In this paper, we conduct research on the mechanism of impedance matching for underwater acoustic transmitter based on mathematical modelling and corresponding balance transformer. To realize underwater acoustic signal of wide band and high power emission, in addition to need the bandwidth performance good transducer array yuan, to a large extent also depends on a good matching between the transducer and amplifier. The result shows the feasibility and robustness of our designed system.

Ultra-low charge transfer resistance carbons by onepot hydrothermal method for glucose sensing

Hydrothermal carbon （HTC） is typically well- dispersed, but it remains a great challenge for HTC to become conductive. Co-doping with heteroatoms has been confirmed to be an effective strategy to significantly promote the electrical conductivity of carbon. Moreover, there is no simple and green method to construct sensitive HTC based electro- chemical biosensors until now. In this paper, N and S dual-doped carbon （NS-C） with ultra-low charge transfer resistance is easily synthesized from L-cysteine and glucose in a hydrothermal reaction system. The morphology, structural prop- erties and electrochemical properties of the as-prepared NS-C are analyzed. In comparison with the undoped hydrothermal （UC） modified glassy carbon electrode （GCE）, the charge transfer resistance of UC （476 Ω） is ten times the value of NS- C （46 Ω）. The developed biosensor shows a better performance to detect glucose in a wide concentration range （50-2500 μmol L^-1） with the detection limit of 1.77 μmol L^-1 （S/N-3） and a high sensitivity （0.0554 μA cm^-2μmol^-1 L）. The apparent Michaelis-Menten constant value of GCE/NS-C/GOx/nafion modified electrode is 0.769 mmol L^-1, indicating a high affinity of glucose oxidase to glucose. These results demonstrate that the hydrothermal method is an effective way for prepar- ing high electrical conductivity carbon with excellent performances in biosensor application.