铋、银对铅钙合金腐蚀行为的影响

针对铅钙合金产生的早期容量损失、板栅的变形长大等问题,进行添加Bi、Ag对铅钙四元合金腐蚀行为影响的研究。认为:加Ag、Bi的Pb-Ca-Sn-Al合金耐腐蚀性能大大提高,Ag含量的增加有利于腐蚀阻抗的增大,Bi含量的增大对腐蚀阻抗的提高不利;高Sn:Ca比合金的腐蚀阻抗大于低Sn:Ca比的合金,Sn含量的增大有利于腐蚀阻抗的提高,但Ca含量不宜过低,否则会降低析氢电位;加Ag合金的析氢过电位远远高于Pb-Ca-Sn-Al四元合金,适合于作免维护电池的板栅材料;加Bi合金当Bi含量为0.0192%时,析氢电位类似于铅钙合金,当Bi含量高达0.0617%时,析氢电位降低了大约200mV。

温度对X52管线钢CO_2腐蚀电化学行为影响

利用动电位极化和电化学阻抗谱技术,研究了温度(30oC,50oC,70oC)对X52管线钢在饱和CO2的NaCl溶液中腐蚀过程的影响。由实验结果得出温度升高促进腐蚀反应的阳极过程和阴极过程,使X52管线钢腐蚀速率增大而且温度对阴极过程的促进作用大于阳极,使Ecorr正向移动;同时温度升高增大了腐蚀产物的形成速率,使其在电极表面析出并以膜层的形式存在,但温度的改变并没有改变X52管线钢在此环境下的腐蚀机理。

Galvanic corrosion behavior of copper/titanium galvanic couple in artificial seawater

The corrosion behaviors of copper and copper/titanium galvanic couple （GC） in seawater were studied by electrochemical impedance spectroscopy （EIS） and electrochemical noise （EN） techniques in conjunction with scanning electron microscopy （SEM） method. The results show that the corrosion process of copper in seawater can be divided into two stages, in which corrosion resistance and SE show the same evolution trend of initial increase and subsequent decrease, while SG changes oppositely. However, the ensemble corrosion process of copper/titanium GC in seawater includes three stages, in which corrosion resistance and SE show the evolution features of initial decrease with a subsequently increase, and the final decrease again;while SG changes oppositely. The potential difference between copper and titanium in their galvanic couple can accelerate the initiation of pitting corrosion of copper, and both the minimum and maximum corrosion potentials of copper/titanium GC are much more positive than those of pure copper.

Corrosion behavior of tinplate in NaCl solution

The corrosion process of tinplate in 0.5 mol/L NaCl solution was investigated using the electrochemical impedance spectroscopy（EIS）,and the morphology and structure of the corrosion products were characterized by scanning electron microscope（SEM）,scanning probe microscopy（SPM）,X-ray diffraction（XRD） and X-ray photoelectron spectroscopy（XPS）.The results showed that the resistance of tin coating,Rc,was essentially constant but the charge transfer resistance,Rct,decreased by 2 orders of magnitude,which indicated that the tin coating was not seriously corroded while the carbon steel substrate was corroded continuously.The corrosion of tinplate in 0.5 mol/L NaCl solution was mainly the dissolution of carbon steel substrate because of the defects in the tin layer and the corrosion product was mainly γ-FeOOH.

Electrochemical and corrosion behaviors of pure Mg in neutral 1.0% NaCl solution

The corrosion behaviors and corresponding electrochemical impedance spectroscopy（EIS） and polarization curves of pure Mg in neutral 1.0% NaCl solution were investigated.The fractal dimension of EIS at different time was studied.The corrosion process and EIS evolution are divided into three stages.In the initial stage,EIS is composed of two overlapped capacitive arcs,the polarization resistance and charge transfer resistance increase rapidly with immersion time,and the corrosion rate decreases.Then,two well-defined capacitive arcs appear,and the charge transfer resistance and corrosion rate remain stable.After a long immersion time,inductive component appears in a low frequency range,the charge transfer resistance decreases and the corrosion rate increases with the immersion time.The fractal dimension obtained from the time records of EIS seems to be a promising tool for the analysis of corrosion morphology because of its direct relationship with the metal surface.

Corrosion behavior of Hastelloy C22 coating produced by laser cladding in static and cavitation acid solution

The Hastelloy C22 coatings on Q235 steel substrate were produced by high power diode laser cladding technique. Their corrosion behaviors in static and cavitation hydrochloric, sulfuric and nitric acid solutions were investigated. The electrochemical results show that corrosion resistance of coatings in static acid solutions is higher than that in cavitation ones. In each case, coating corrosion resistance in descending order is in nitric, sulfuric and hydrochloric acid solutions. Obvious erosion-corrosion morphology and serious intercrystalline corrosion of coating are noticed in cavitation hydrochloric acid solution. This is mainly ascribed to the aggressive ions in hydrochloric acid solution and mechanical effect from cavitation bubbles collapse. While coating after corrosion test in cavitation nitric acid solution shows nearly unchanged surface morphology. The results indicate that the associated action of cavitation and property of acid solution determines the corrosion development of coating. Hastelloy C22 coating exhibits better corrosion resistance in oxidizing acid solution for the stable formation of dense oxide film on the surface.

Effects of Hg and Ga on microstructures and electrochemical corrosion behaviors of Mg anode alloys

The effects of Hg and Ga on the electrochemical corrosion behaviors of the Mg-2%Hg, Mg-2%Ga and Mg-2%Hg-2%Ga (mass fraction) alloys were investigated by measurements of polarization curves, galvanostatic tests and measurements of electrochemical impedance spectroscopy. Scanning electron microscopy, X-ray diffractometry and energy dispersive spectrometry were employed to characterize the microstructures and the corroded surface of the above alloys. The results demonstrate that the microstructure of the Mg-2%Ga alloy is solid solution and the Mg-2%Hg and Mg-2%Hg-2%Ga alloys have white second-phases at the grain boundaries. The Mg-2%Ga alloy has the worst electrochemical activity and the best corrosion resistance, showing a mean potential of -1.48 V and a corrosion current density of 0.15 mA/cm2. The Mg-2%Hg-2%Ga alloy has the best electrochemical activity and the worst corrosion resistance, showing a mean potential of -1.848 V and a corrosion current density of 2.136 mA/cm2. The activation mechanism of the Mg-Hg-Ga alloy is dissolution-deposition of the Hg and Ga atoms.

Electrochemical corrosion behavior of arc sprayed Al-Zn-Si-RE coatings on mild steel in 3.5% NaCl solution

Al-Zn-Si-RE coating with high Al content was deposited on mild steel by arc spraying. The electrochemical behavior of Al-Zn-Si-RE coating in 3.5%NaCl solution was systematically studied by potentiodynamic polarization, corrosion potential (φcor ) and electrochemical impedance spectroscopy techniques (EIS). The impedance data were fitted to appropriate equivalent circuits to explain the different electrochemical processes occurring at the electrode-electrolyte interface. The results indicate that Al-Zn-Si-RE coating reveals the similar polarization behavior as Zn-15Al coating. The coating has no passive region in the anodic polarization, but far lower corrosion current and much higher corrosion potential. Al-Zn-Si-RE coating provides effective sacrificial protection for steel substrate and the sacrificial anodic protection plays dominant role during the immersion process. In addition, theφcor evolution and EIS plots indicate that the corrosion process can be divided into five stages: pitting-dissolution-redeposition, activation corrosion, cathodic protection, physical barriers and the coating failure.

Corrosion and electrochemical behaviors of 7A09 Al-Zn-Mg-Cu alloy in chloride aqueous solution

The corrosion and electrochemical behaviors of 7A09 Al？Zn？Mg？Cu alloy were investigated in 3.5% NaCl （mass fraction） solution using complementary techniques such as scanning electron microscopy （SEM）, metallographic microscopy and electrochemical measurements. The results show that both pitting corrosion from or around the intermetallic particles and intergranular corrosion are observed after the immersion test due to the inhomogeneous nature of the microstructure of the 7A09 alloy. The preferential dissolution of the anodic Cu-depleted zone along grain boundaries is believed to be the possible cause of intergranular corrosion. The passivation and depassivation of this alloy show significant dependence of immersion time, owing to the formation and dissolution of various passive films on the sample surfaces. Furthermore, the corrosion process and corrosion mechanism were also analyzed.

Zn-55%Al-Si合金镀层钢丝在海水中的耐蚀性能

建立了"极化-弛豫-阻抗测量"的多周期电化学测试方法,并用此方法研究了热浸镀锌-55%铝-硅合金镀层不同组织的耐蚀性能.结果表明,锌-55%铝-硅镀层的腐蚀分为三个阶段,分别对应镀层结构中的富Zn相、富Al相和合金相,其腐蚀反应极化电阻的平均值分别为500Ω·cm^2、1000Ω·cm^2和12000Ω·cm^2,表明合金相的耐蚀性能最好.

Zn粉含量及表面沾污对环氧富Zn漆电化学行为的影响

采用腐蚀电位、电化学阻抗谱(EIS)评价了Zn粉含量以及涂层/基体界面污染程度对环氧富Zn涂层的防腐蚀性能的影响并探索了富Zn涂层的失效机制。实验结果表明,当涂层中Zn含量较少时,Zn粉没有有效的阻挡作用,通过对可能的阻抗模型的分析,认为富Zn涂层的电化学阻抗谱的低频段是由Zn^2+从金属表面穿过腐蚀产物的扩散控制,涂层/基体界面污染不仅影响了环氧富Zn涂层的防腐蚀性能的发挥,也加速了钢铁基体的腐蚀。

铬酸盐化

SY509-3-134 [篇名] Development of Cr(VI)-free treated steel sheet for electrical appliances and business machines；SY509-3-135 [篇名] Development of electroplated Zn-Ni-SiO{sub}2 composite coatings treated with a silane coupling agent to replace chromating；……

铸造金属

Improving the quality of ring castings from nitrogen-containing corrosion-resistant steels；Influence of abrasive flow machining on reducing fuel consumption, lowering emissions and increasing power；Production of Ship Propeller Steel Blades in Sand Molds with Electroslag Replenishment；Prototyping process produces sand molds, cores for castings production。

Enhanced corrosion resistance of phytic acid coated magnesium by stearic acid treatment

A green chemical conversion coating for magnesium was obtained with a phytic acid solution. The microstructure and corrosion properties of phytic acid conversion coated magnesium were further improved by soaking in stearic acid solution. The phytic acid conversion coated magnesium after soaking in the stearic acid showed no micro-cracks and the surface became very smooth. The corrosion behavior of the uncoated and coated magnesium samples was studied by electrochemical methods. The corrosion resistance of the stearic acid treated sample was much higher than that of phytic acid conversion coated magnesium or uncoated magnesium. The electrochemical results indicated that the stearic acid treated coating provided effective corrosion protection to the magnesium sample.

Initial corrosion behavior of pure zinc in simulated tropical marine atmosphereInitial corrosion behavior of pure zinc in simulated tropical marine atmosphere

The initial corrosion behavior of pure zinc in a simulated tropical marine atmosphere was investigated using gravimetric method,scanning electron microscope combined with energy dispersive spectroscopy(SEM-EDS),X-ray diffractometry(XRD),Fourier transform infrared spectrometry(FTIR)and electrochemical impedance spectroscopy(EIS).The kinetics of corrosion process is a decelerating process following the empirical equation D=At^n(n<1).The protectiveness of the corrosion product layer could be attributed to the formation of simonkolleite,Zn5(OH)8Cl2·H2O,which could inhibit the rate determining step,namely charge transfer step,of the electrochemical corrosion process.A model of the evolution process of the product layers formed on zinc was proposed.In addition,the regularity of the corrosion rate of zinc as a function of the NaCl deposition rate can be described by a power function.

Comparative investigation on copper atmospheric corrosion by electrochemical impedance and electrical resistance sensors

Electrochemical impedance(EIS)and thin electrical resistance(ER)sensors were invented for atmospheric corrosion measurement of copper(Cu)during cyclic wetting−drying/high−low temperature tests and field exposure tests.Three-month field exposure results showed that average corrosion rate of Cu measured by ER sensor was well in accordance with that by weight loss method.During cyclic wetting−drying test,EIS was proven to reflect sensitively time of wetting and drying on the surface of sensor.Although corrosion rate obtained from EIS had a similar tendency to that obtained from ER sensors,the former was more dependent on environmental humidity than the latter.When relative humidity was low than 60%,corrosion rate of Cu measured by EIS was much lower than that by weight loss method,mainly attributing to the fact that impedance sensor failed to detect corrosion current of interlaced Cu electrodes due to the breakdown of conductive passage composed of absorbed thin liquid film under low humidity condition.Promisingly,ER sensor was proven to be more suitable for atmospheric corrosion monitoring than electrochemical techniques because it could sensitively monitor thickness loss of Cu foil according to the Ohmic law,no matter how dry or wet the sensor surface is.

Corrosion resistance of Ti and Ti-Pd alloy in phosphate buffered saline solutions with and without H_2O_2 addition

Corrosion resistance of pure titanium（Grade 2） and Ti-Pd alloy（Grade 7） was studied using the electrochemical techniques of potentiodynamic measurements and electrochemical impedance spectroscopy（EIS）.Measurements were performed at the temperature of 36.6 ℃ in two solutions：PBS solution with pH of 7.4 simulating conditions of healthy human body,and PBS solution with pH of 5.2 and with the addition of hydrogen peroxide（0.015 mol/L） simulating the inflammatory state.It is found that,Ti Grade 7 can be a good candidate as a material for orthopedic implant application,because its corrosion resistance in the PBS solution containing H2O2 is better（lower corrosion current densities） than that of pure titanium.

Corrosion performance of high pressure die-cast Al-6Si-3Ni and Al-6Si-3Ni-2Cu alloys in aqueous NaCl solution

The corrosion performance of high pressure die-cast Al？6Si？3Ni （SN63） and Al-6Si-3Ni-2Cu （SNC632） alloys in 3.5%（mass fraction） NaCl solution was investigated. X-ray diffraction （XRD） and microstructural studies revealed the presence of singlephase Si and binary Al3Ni/Al3Ni2 phases along the grain boundary. Besides, the single Cu phase was also identified at the grainboundaries of the SNC632 alloy. Electrochemical corrosion results revealed that, the SNC632 alloy exhibited nobler shift incorrosion potential （φcorr）, lower corrosion current density （Jcorr） and higher corrosion resistance compared to the SN63 alloy.Equivalent circuit curve fitting analysis of electrochemical impedance spectroscopy （EIS） results revealed the existence of twointerfaces between the electrolyte and substrate. The surface layer and charge transfer resistance （Rct） of the SNC632 alloy was higherthan that of the SN63 alloy. Immersion corrosion test results also confirmed the lower corrosion rate of the SNC632 alloy andsubstantiated the electrochemical corrosion results. Cu addition improved the corrosion resistance, which was mainly attributed to theabsence of secondary Cu containing intermetallic phases in the SNC632 alloy and Cu presented as single phase.

Effect of micro arc oxidation treatment on localized corrosion behaviour of AA7075 aluminum alloy in 3.5% NaCl solution

Alumina coating was formed on AA7075 aluminum alloy by micro arc oxidation（MAO） method and its corrosion and stress corrosion cracking（SCC） behaviors were examined in 3.5%（mass fraction） NaCl solution.Electrochemical impedance spectroscopy（EIS） was used to evaluate the degradation of the coating as a function of immersion time and was modeled with appropriate equivalent circuits.Constant load stress corrosion cracking（SCC） results followed by post-test metallographic observations demonstrated the usefulness of MAO coating to avoid the premature failure of the alloy due to severe localized corrosion initiated by Cu-and Fe-rich intermetallic phases.

Surface nanostructure modification of Al substrates by N^+ ion implantation and their corrosion inhibition

The influence of implantation of N+ions of different energies on the nanostructure of7049Al substrates and the corrosioninhibition of produced Al samples in a3.5%NaCl solution was studied.The X-ray diffraction(XRD)results confirmed the formationof AlN as a result of N+ion implantation.The atomic force microscope(AFM)results showed that grains of larger scale are formedby increasing N+energy which can be due to heat accumulation in the sample during implantation causing higher rate of diffusion inthe sample,hence decreasing the number of defects.Corrosion resistance of the samples was studied by the electrochemicalimpedance spectroscopy(EIS)measurements.Results showed that corrosion resistance of implanted Al increases with increasing N+ion energy.The equivalent circuits for the N+implanted Al samples with different energies were obtained,using the EIS data whichshowed strong dependence of the equivalent circuit elements on the surface morphology of the samples.Finally,the relationshipbetween corrosion inhibition and equivalent circuit elements was investigated.