Iranian Journal of Materials Science and Engineering

The inherent reactivity of the Al–Cu alloys is such that their use for structural, marine, and aerospace components and structures would not be possible without prior application of a corrosion resistance system. Historically these corrosion resistance coatings were based on the use of chemicals containing Cr (VI) compounds. Silane coatings are of increasing interest in industry due to their potential application for the replacement of current toxic hexavalent chromate based treatments. In this study, hydrophobic coating sol was prepared with methyltriethoxysilane (MTES), methanol (MeOH), and water (as 7M NH4OH) at a molar ratio of 1:25:4.31 respectively. The coatings were applied by a dip-technique to 2024-T3 Al alloy, and subsequently cured at room temperature and there after heat treated in an oven at 150°C. The anticorrosion properties of the coatings within 3.5 wt% NaCl solution were studied by Tafel polarization technique. The sol–gel coating exhibited good anticorrosion properties providing an adherent protection film on the Al 2024-T3 substrate. The surface properties were characterized by water contact angle measurement, scanning electron microscopy (SEM), and the composition was studied by Fourier transform infrared spectroscopy (FTIR).

In this paper, the influence of heat treatment on PH17-7 stainless steel spring was evaluated. Precipitation hardening phenomenon of  PH 17-7 steel was evaluated in three stages. First, the spring constant changes with time and temperature was evaluated. Second, the spring constant changes with respect to its original length at constant temperature and time with blocking (spring length after compression, 18 and 21 mm) were investigated.  And finally, the spring heat treatment at 480 °C for 80 min and then holding at 230 °C in oil bath for 60 min without blocking were investigated. The results showed that the use of 18 mm block have large spring constant than 21 mm block. The optimal conditions (480°C for 80 min) for this spring to reaching maximum spring constant were determined.

In this study, polyaniline-graphene composites with different nano-structures are synthesized and the behaviour of the obtained composites serving as electrode materials in electrochemical capacitors is studied. The morphology, crystal structure, and thermal stability of the composites are examined using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Thermal gravimetric analysis (TGA). Electrochemical properties are characterized by cyclic voltammetry (CV). According to the results, the obtained composites show different crystal structures and different thermal stabilities, and consequently different electrochemical capacities, when used as electrodes in electrochemical capacitors. A nano-fibre composite is shown to have a good degree of crystallization, 5.17% water content, 637oC degradation onset temperature, and 379 Fg-1 electrochemical capacity.

A homogenous TiO₂ / multi-walled carbon nanotubes(MWCNTs) composite film were prepared by electrophoretic co-deposition from organic suspension on a stainless steel substrate.  In this study, MWCNTs was incorporated to the coating because of their long structure and their capability to be functionalized by different inorganic groups on the surface. FTIR spectroscopy showed the existence of carboxylic groups on the modified carbon nanotubes surface. The effect of applied electrical fields, deposition time and concentration of nanoparticulates on coatings morphology were investigated by scanning electron microscopy. It was found that combination of MWCNTs within TiO₂ matrix eliminating micro cracks presented on TiO₂ coating. Also, by increasing the deposition voltages, micro cracks were increased. SEM observation of the coatings revealed that TiO₂/multi-walled carbon nanotubes coatings produced from optimized electric field was uniform and had good adhesive to the substrate.

Porous hollow glass microspheres have many uses, including encapsulation of active materials. In this paper a fast and facile method for fabricating porous hollow glass-microspheres was demonstrated by etching them using dilute hydrofluoric acid. Then, a highly reactive amine was infiltrated into the etched glass microspheres. Scanning electron microscopy was conducted for the hollow glass microspheres prior and post etching process. With regards to the porous hollow glass spherical sample, the spherical nature, morphology, pore diameter and the porosity were studied using scanning electron microscopy. Formation of the intact hollow glass microspheres with an open through wall porosities following phase separation and etching of the boron oxide rich phase was demonstrated using reciprocating shaker as the most suitable agitation method. The BET results indicated that the surface of the porous microspheres contained nano-pores. It is believed that the simplicity of the reported fabrication technique of micro/nano porous structure has the potential to scaling up for large scale production

Up to now, lots of materials such as active carbon, iron, manganese, zirconium, and metal oxides have been widely used for removal of dyes from contaminated water. Among these, ferrite nanoparticle is an interesting magnetic material due to its moderate saturation magnetization, excellent chemical stability and mechanical hardness. Graphene, a new class of 2D carbonaceous material with atom thick layer features, has attracted much attention recently due to its high specific surface area. Reduced graphene oxide (rGO) has also been of great interest because of its unique properties, which are similar to those of graphene, such as specific surface area, making it an ideal candidate for dye removal. Thus far, few works have been carried out on the preparation of CoFe₂O₄-rGO composite and its applications in removal of contaminants from water. In this paper, CoFe₂O₄ reduced graphene oxide nanocomposite was fabricated using hydrothermal process. During the hydrothermal process, the reduction of graphene oxide and growth of CoFe₂O₄ simultaneously occurred on the carbon basal planes under the conditions generated in the hydrothermal system. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy contaminant and UV-Vis spectroscopy as the analytical method. The experimental results suggest that this material has great potential for treating Congo red contaminated water.

In this work, the effects of co-precipitation temperature and post calcination on the magnetic properties and photocatalytic activities of ZnFe₂O₄ nanoparticles were investigated. The structure, magnetic and optical properties of zinc ferrite nanoparticles were characterized by X-ray diffraction (XRD), vibrating sample magnetometry and UV–Vis spectrophotometry techniques.  The XRD results showed that the coprecipitated as well as calcined nanoparticles are single phase with partially inverse spinel structures. The magnetization and band gap decreased with the increasing of co-precipitation temperature through the increasing of the crystallite size. However, the post calcination at 500 °C was more effective on the decreasing of magnetization and band gap. Furthermore, photocatalytic activity of zinc ferrite nanoparticles was studied by the degradation of methyl orange under UV-light irradiation. Compare with the coprecipitated ZnFe₂O₄ nanoparticles with 5% degradation of methyl orange after 5 h UV-light light radiation, the calcined ZnFe₂O₄ nanoparticles exhibited a better photocatalytic activity with 20% degradation.

In this work, we report the synthesis of silver decamolybdate, Ag₆Mo₁₀O₃₃, nanostructure by a simple mechanohemical process followed by calcination treatment using acetamide as driving agent. Morphological study by scanning electron microscopy (SEM) images revealed bundles of rods grown closely together with an average diameter of 92 nm for Ag₆Mo₁₀O₃₃ sample. Ni-substituted Ag₆Mo₁₀O₃₃ compound was prepared via introducing nickel cation to precursor system in mechanical milling step. The particle size decreased to 87 nm by incorporating nickel units in substituted polymolybdate. It was concluded that the suitable selection of reagents can direct solid phase reaction towards producing nanostructured products. This technique is easy and simple for preparation of various mixed metal oxides without using any solvents and or complex procedures. In addition, the photocatalytic activity of the prepared products was studied on the removal of 4-nitro phenol (4-NP) as organic pollutant from water. The obtained results were also discussed in detail.