In this study, the electrochemical behavior of Mg–9Al–0.5Zn, Mg–9Al–0.7Zn, and Mg–9Al–1.0Zn electrodes in a 0.7 mol L−1 NaCl solution is evaluated by using potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and potentiostatic oxidation. The utilization efficiencies of these materials are also determined. The results show that the Mg–9Al–1.0Zn alloy has the highest corrosion resistance and that Mg–9Al–0.5Zn displays the largest discharge current in the 0.7 mol L −1 NaCl solution at 25°C. In addition, the utilization efficiencies of the alloys decrease as follows: Mg–9Al–1.0Zn > Mg–9Al–0.7Zn > Mg–9Al–0.5Zn. This study illustrates that doping Zn into Mg‐Al electrodes increases the corrosion resistance and utilization efficiency but decreases the discharge activity of Mg–Al–Zn anodes when the Zn content is between 0.5% and 1.0%.
Etching treatment for acrylonitrile butadiene styrene (ABS) resin and electroless nickel plating process have been studied. The ABS first was etched in a chromium‐free potassium permanganate etching system with different etching times. Scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FT‐IR), and hydrophilicity test showed that the ABS is of moderate and homogeneous hole size after being etched at a temperature of 65 °C with 6 g L−1 potassium permanganate for 20 min. Then electroless nickel process was performed by immersing the ABS into in a Ni plating bath at 45 °C for 20 min at a pH of 8.5–9.5. The coating was even, dense, and reveals good corrosion resistance. In addition, the nickel plating adhesion strength reached 2.73 MPa. Therefore, the excellent performance of the KMnO4‐H2SO4‐H3PO4‐H2O etching system may replace the traditional chromic anhydride‐sulfuric acid etching system as an environmentally friendly process.
We report on the electrochemical performance of Mg‐14Li‐3Al‐1Gd electrodes prepared by the accumulation roll bonding technique in a 0.7 M NaCl solution. To explore the effects of adding different concentrations of Na2SnO3 to 0.7 M NaCl solutions, potentiodynamic polarization, potentiostatic oxidation, electrochemical impedance spectroscopy, and scanning electron microscopy were utilized. The results show that the addition of Na2SnO3 to a 0.7 M NaCl solution increases the corrosion potential of the Mg‐14Li‐3Al‐1Gd electrodes. Samples with 0.1 mM Na2SnO3 retained the highest discharging current density and lowest polarization resistance of all the specimens. Electrodes in an electrolyte solution mixed with 0.1 mM Na2SnO3 presented a larger active reaction area, deeper channels, and higher discharging currents than those with other additive concentrations. In conclusion, to improve the electrochemical behavior of Mg‐14Li‐3Al‐1Gd electrodes in a 0.7 M NaCl solution, the optimal concentration of Na2SnO3 is 0.1 mM.
In this paper, Al 2 O 3 /cerium oxide composite films were prepared on the surface of aluminum by anodic oxidation and chemical solution deposition. The aluminum was firstly anodized in sulfuric acid, then treated with different concentrations of Ce(NO 3 ) 3 · 6H 2 O solution at different temperatures. X-ray diffraction (XRD), energy dispersive spectrometer (EDS), scanning electron microscope (SEM), electrochemical impedance spectroscopy (EIS), and electrochemical polarization tests were used to characterize the properties of the composite films. The results indicate that the Al 2 O 3 /cerium oxide composite films successfully form on 1060Al alloy, and the best condition of film-forming is 2 g/L Ce(NO 3 ) 3 · 6H 2 O and 50°C. Al 2 O 3 /cerium oxide composite film under this condition has a uniform, smooth, and pyknotic surface topography and optimal corrosion resistance. The corrosion density at that time is 1.106 × 10 −6 A/cm 2 and the corrosion potential is −0.458 V. K E Y W O R D SAl 2 O 3 /cerium oxide composite films, aluminum, Ce(NO 3 ) 3 · 6H 2 O, corrosion resistance, temperature
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