Showing 2 results for Enayati
A. Shahcheraghi, F. Dehghani, K. Raeissi, A. Saatchi, M. H. Enayati,
Volume 10, Issue 1 (march 2013)
Abstract
Abstract: Mg2Ni alloy and Mg2Ni–x wt% TiO2 (x = 3, 5 and 10 wt %) composites are prepared by mechanical alloying. The produced alloy and composites are characterized as the particles with nanocrystalline/amorphous structure. The effects of TiO2 on hydrogen storage properties are investigated using anodic polarization and electrochemical impedance spectroscopy. It is demonstrated that the initial discharge capacity and exchange current density of hydrogen are increased by adding 5wt% TiO2, while the cycle stability and bulk hydrogen diffusivity don’t change. It is found that the charge transfer resistance of Mg2Ni–5wt% TiO2 composite is lower than that of Mg2Ni alloy. On the other hand, the hydrogen oxidation during the discharge process proceeds more easily on the electrode surface containing TiO2 additive.
Ali Keramatian, Mohammad Hossein Enayati, Fatemehsadat Sayyedan, Sima Torkian,
Volume 21, Issue 0 (IN PRESS 2024)
Abstract
The aim of this study was to investigate the effect of current density on the microstructure of electrodeposited Ni–WC–TiC composite coatings on 304 stainless steel and compare the corrosion resistance of the coating and substrate in a 3.5 wt.% sodium chloride solution. A Watts nickel bath was employed under direct current (DC) conditions. Microstructure, elemental composition, and phase composition analyses were conducted using scanning electron microscopy (SEM) equipped with energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD), respectively. The results revealed that the coating formed at a current density of 40 mA/cm² exhibited a denser microstructure with higher cohesion and uniformity compared to coatings produced at other current densities. The corrosion resistance of the coating and substrate was evaluated using Tafel and electrochemical impedance spectroscopy (EIS) analyses. The corrosion test results indicated that the substrate exhibited superior corrosion resistance compared to the coating. Based on the dynamic polarization test plots, the corrosion mechanism of the substrate is active-quasi passive, with a pseudo-passive layer forming on the sample which remains stable within the potential range of -0.17 to 0.17 V. Beyond this potential range, the sample becomes susceptible to pitting. In the coated sample, the corrosion behavior is similar to that of the substrate, with the exception that the pseudo-passive layer remains stable within a narrower potential range of -0.19 to 0.08 V.
