The inhibition process of steel against corrosion in 1.0 M HCl using natural honey in the presence and absence of 0.1 M KI was studied at 25–55 °C utilizing a potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) measurements and gravimetric method. Corresponding surfaces of steel were examined by SEM and EDX techniques. The obtained data demonstrated that inhibition efficiency increased by increasing both natural honey dose and environment temperature. Synergism parameter values were found more than one indicating that the inhibition efficiency of natural honey enhanced by an addition of KI due to synergism. The adsorption of natural honey in the presence and absence of iodide ions on the steel surface was found to follow Langmuir adsorption isotherm.
The effect of chloride ion concentration and pH of solution on the corrosion behavior of aluminum alloy AA7075 coated with phenyltrimethoxysilane (PTMS) immersed in aqueous solutions of NaCl is reported. Potentiodynamic polarization, linear polarization, open circuit potential, and weight loss measurements were performed. The surface of samples was examined using SEM and optical microscopy. Elemental characterization of the coating by secondary ion mass spectrometry indicates an intermediate layer between coating and aluminum alloy surface. The corrosion behavior of the aluminum alloy AA7075 depends on chloride concentration and pH of solution. In acidic or neutral solutions, general and pitting corrosion occur simultaneously. On the contrary, exposure to alkaline solutions results in general corrosion only. Results further reveal that aluminum alloy AA7075 is susceptible to pitting corrosion in all chloride solutions with concentrations between 0.05 M and 2 M NaCl; an increase in the chloride concentration slightly shifted both the pitting and corrosion potentials to more active values. Linear polarization resistance measurements show a substantially improved corrosion resistance value in case of samples coated with PTMS as compared to uncoated samples in both neutral (pH=7), acidic (pH=0.85 and 3), and alkaline chloride solutions (pH=10 and 12.85). The higher corrosion resistance of the aluminum alloy coated with PTMS can be attributed to the hydrophobic coating which acts as a barrier and prevents chloride ion penetration and subsequent reaction with the aluminum alloy.
Novel poly(glycidyl methacrylate)-grafted Nafion-phosphoric acid membranes for direct-oxidation methanol fuel cells were prepared with a potassium persulfate chemical initiation system for the first time. The introduced epoxy groups were converted to amine groups through a reaction with ethylenediamine, which consequently doped with phosphoric acid (APO 3 H) groups. The latter significantly contributed to enhancing the ionexchange capacity, mechanical properties, and thermal stability. Factors affecting the modification steps were studied. Changes in the chemical and morphological structure were verified through Fourier transform infrared spectroscopy, TGA, and scanning electron microscopy characterization. Various grafting percentages (GP%'s) up to 32.31% were obtained. As a result, the thickness of the grafted membranes increased. Furthermore, the methanol permeability of the modified membranes was reduced with increasing grafted polymer content compared with that of the Nafion membrane. An 83.64% reduction in the methanol permeability was obtained with a polymer grafted content of 18.27%. Finally, the efficiency factor for all of the modified Nafion membranes was enhanced compared with that of Nafion. A fourfold improvement was obtained with membranes with a GP% of 18.27% as a maximum value. Such promising results nominate the used technique as a one for the improvement of Nafion membrane efficiency.
Nanocrystalline metal ferrite MFe 2 O 4 (M=Cu, Zn, and Ni) thin films have been synthesized via electrodeposition-anodization process. Electrodeposited (M)Fe 2 alloys were obtained from aqueous sulfate bath. The formed alloys were electrochemically oxidized (anodized) in aqueous (1 M KOH) solution, at room temperature, to the corresponding hydroxides. The parameters controlling the current efficiency of the electrodeposition of (M)Fe 2 alloys such as the bath composition and the current density were studied and optimized. The anodized (M)Fe 2 alloy films were annealed in air at 400°C for 2 h. The results revealed the formation of three ferrite thin films were formed. The crystallite sizes of the produced films were in the range between 45 and 60 nm. The microstructure of the formed film was ferrite type dependent. The corrosion behavior of ferrite thin films in different pH solutions was investigated using open circuit potential (OCP) and potentiodynamic polarization measurements. The open circuit potential indicates that the initial potential E im of ZnFe 2 O 4 thin films remained constant for a short time, then sharply increased in the less negative direction in acidic and alkaline medium compared with Ni and Cu ferrite films. The values of the corrosion current density I corr were higher for the ZnFe 2 O 4 films at pH values of 1 and 12 compared with that of NiFe 2 O 4 and CuFe 2 O 4 which were higher only at pH value 1. The corrosion rate was very low for the three ferrite films when immersion in the neutral medium. The surface morphology recommended that Ni and Cu ferrite films were safely used in neutral and alkaline medium, whereas Zn ferrite film was only used in neutral atmospheres.
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