Iranian Journal of Materials Science and Engineering

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The structural properties of a natural clay sample (51% kaolinite) were tweaked to suit specific applications. H₂SO₄ and NaOH (1.0 M) treatment caused structural alterations and a significant release of Al ions compared to Si ions. Chemical treatment caused structural alterations, according to XRD analysis. FTIR analysis also indicated higher density of polar surface groups upon treatment which affected the corresponding dielectric behaviors. Dielectric measurements shown the suitable application of the materials either as dielectrical insulator and this dependent on the applied frequency. Acid treated kaolinite was reported to be a promising dielectric at 10 and 1000 Hz. With appropriate mass attenuation coefficients (μ/ρ) 12.098-12.182 cm²/g and a high half value layer of 10 cm at 10 keV, kaolinite and other treated forms were adequate shielding materials.

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In this study, aluminum matrix composites reinforced with Al₂O₃ and SiC nanoparticles, and graphene nanoplatelets produced by Spark Plasma Sintering (SPS) were studied. The microstructural and mechanical properties of the composites were evaluated by changing the amounts of the reinforcing materials. The SEM images showed that the reinforcing particles were more distributed in the grain boundary regions. According to the results, the addition of alumina and SiC to the matrix caused an increase in the composite density whereas the composite density decreased by adding graphene nanoplatelets. The highest relative density of 96.3% was obtained for the composite containing 2 wt% Al₂O₃. The presence of the reinforcing particles increased the hardness of all the samples compared to the pure aluminum (39 HV). The composite containing 1 wt.% Al₂O₃, 0.7 wt.% SiC, and 0.3 wt.% graphene showed the highest hardness of 79 HV. Moreover, the plastic deformation of the specimens decreased and the slope of the plastic region increased by adding the reinforcing particles to the matrix.

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In this study, CrN/ZrN multilayer nanostructured coatings with different bilayers (10, 20, and 30) were created by the cathodic arc evaporation. The electrochemical behavior of samples was evaluated by polarization and impedance spectroscopy tests in the Ringer medium and the pin on disk test was used to investigate the tribological behavior of the samples. The results of measurements showed that the electrochemical and tribological behavior of the coatings depends on the number of bilayers and by rising the number of bilayers, the coating shows higher corrosion resistance and better tribological performance. Field emission scanning electron microscopy (FE-SEM) images of the specimens after exposure to the corrosion medium showed that the number of surface cavities were formed by the coating that had the highest number of bilayers comparing with other coatings were quite fewer in number and smaller in diameter. The results of the pin on disk test showed that by increasing the number of bilayers from 10 to 30, the coefficient of friction and wear rate decreased and the 30L coating ‌showed better wear resistance.

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Copper oxide thin layers were elaborated using the sol-gel dip-coating. The thickness effect on morphological, structural, optical and electrical properties was studied. Copper chloride dihydrate was used as precursor and dissolved into methanol. The scanning electron microscopy analysis results showed that there is continuity in formation of the clusters and the nuclei with the increase of number of the dips. X-ray diffractogram showed that all the films are polycrystalline cupric oxide CuO phase with monoclinic structure with grain size in the range of 30.72 - 26.58 nm. The obtained films are clear blackin appearance, which are confirmed by the optical transmittance spectra. The optical band gap energies of the deposited films vary from 3.80 to 3.70 eV. The electrical conductivity of the films decreases from 1.90.10^-2 to 7.39.10^-3 (Ω.cm)^-1

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Recently, using calcium phosphates and at the top of them, hydroxyapatite (HA) has been considered in medical and dental applications as an artificial biomaterial due to their chemical and structural similarity to the bodychr('39')s skeletal tissues such as bone and tooth. Because of reinforcement of hydroxyapatitechr('39')s mechanical and biological properties by substitution of OH- groups by F- ions to produce fluorapaptite (FA) has been proven, in this article synthesis methods, properties and medical applications of fluorapatite and its pros and cons in comparison with hydroxyapatite have been reviewed.

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     Zinc Oxide (ZnO) nanorods and titanium dioxide (TiO₂) nanostructures thin films were prepared onto glass substrates by the chemical bath deposition (CBD) method. The ZnO was structured as nanorods (NRs) while TiO₂ was formed as nanoflowers plate as confirmed by Field-Emission Scanning Electron Microscope (FESEM) images. The ZnO/Fe₃O₄ and TiO₂/Fe₃O₄ nanostructures thin films were prepared via drop-casting Fe₃O₄ NPs onto the grown ZnO and TiO₂ nanostructures thin films. The diameter of Fe₃O₄ NPs was deposited onto ZnO NRs thin films and TiO₂ nanostructures thin films was ranged from 8nm to 59nm with dominated range between 10nm to 30 nm.  The crystalline structure of prepared samples was investigated through X-ray diffraction (XRD) method. However, the particles size of Fe₃O₄  was estimated  by XRD as well as FESEM images was around 22 nm. The photocatalytic activity of the as-prepared ZnO/Fe₃O₄ and TiO₂/Fe₃O₄ nanostructures thin films was investigated against methylene blue (MB) dye at room temperature with a pH value of 10 under different exposure time by visible light. The photodegradation rate of MB dye by ZnO/Fe₃O₄ and TiO₂/Fe₃O₄ nanostructures thin films was higher than that obtained by ZnO and TiO₂ nanostructures thin films. The best photodegradation rate of MB dye was 100% after exposure time of 180 min was obtained by ZnO/Fe₃O₄ nanostructures thin film whereas it was 82% for TiO₂/Fe₃O₄ nanostructures thin films after exposure time of  240 min.  
 

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The goal of the present study is to prepare a room temperature cured hydrophobic and self-cleaning nano-coating for power line insulators. As a result, the installed insulators operating in power lines can be coated without being removed from the circuit and without the need to cut off power. For this purpose, hydrophobic silica nanoparticles were synthesized by sol-gel method using TEOS and HMDS. The synthesized hydrophobic silica nanoparticles were characterized by XRD, FTIR, SEM, and TEM analyses to investigate phase formation, particle size, and morphology. Then the surface of the insulator was cleaned and sprayed by Ultimeg binder solution, an air-dried insulating coating, as the base coating. Then the hydrophobic nano-silica powder was sprayed on the binder coated surface and left to be air-cured at room temperature. After drying the coating, the contact angle was measured to be 149^o. Pull-off test was used to check the adhesion strength of the hydrophobic coating to the base insulator. To evaluate the effect of environmental factors, UV resistance and fog-salt corrosion tests were conducted. The results showed that 150 hours of UV radiation, equivalent to 9 months of placing the samples in normal conditions, did not have any significant effect on reducing the hydrophobicity of the applied coatings.

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Background: Superhydrophobic materials which have contact angle higher than 150°, considering their widespread applications, are very important for researchers.
Method: In this research, silica nanopowder was synthesized successfully using inexpensive sodium silicate source and very simple and facile method. Synthesis of hydrophobic solution was carried out by sol-gel method. The surface modification of silica nanopowder was performed using different silane/siloxane polymers and was deposited on glass slides. For characterization of the samples XRD, FESEM, EDX, TEM, FTIR, and Raman analysis were used.
Results: The XRD result shows a very wide peak at 2q = 24.7° which indicates the amorphous nature of the silica particles. The results of the performed characteristics confirm the synthesis of silica nanopowder with the size of less than 25 nm. The EDX spectrum shows that only Si and O elements are present in the structure and no impurities are visible. The contact angle between water droplet and thin films was measured and the effect of different synthesis parameters on the contact angle was studied. Among the studied polymers and solvents, the most hydrophobicity was obtained using TMCS polymer and xylene solvent. The optimized sample has a maximum contact angle of 150.8°.
Conclusion: The synthesized thin films have superhydrophobic properties and the method used in this research can be developed for use in industrial applications.

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The present study used a hydrothermal technique to synthesize undoped and Mn2+ doped CdS/Zn3(PO4)2 semiconducting nanocomposite materials. Powder X-ray diffraction, scanning electron microscopy, UV-Vis diffuse reflectance spectrometer, Fourier transform-Infrared Spectroscopy-FT-IR, and photoluminescence techniques were employed to study structural, optical, and luminescence properties of produced nanocomposites. The hexagonal structure of CdS and the monoclinic structure of Zn3(PO4)2 are both reflected in the powder X-ray diffraction spectra. When Mn2+ ions are present in the host lattice, a lattice distortion occurs, causing a phase change from the phase of γ-Zn3(PO4)2 to the β-phase of Zn3(PO4)2, without affecting the hexagonal phase of CdS. The average crystallite size of produced nanocomposites was 22-25 nm, and also calculated the lattice strain and dislocation density to better understand internal deformation of the samples. The FT-IR spectra were used to investigate the molecular vibrations and functional groups in the samples. The surface morphology of the nanocomposites is hexagonal spheres on rectangular shaped nano-flakes, and the interatomic distance between the hexagonal spheres is decreased as the doping concentration increases, forming a rod-like structure on the flakes. EDAX results confirm the presence of various relevant elements in the prepared samples. The quantum confinement of produced samples reduces as the Mn2+ doping concentration in the host lattice increases. The photoluminescence results demonstrate shallow trapped states due to the transition: d-d (4T1 → 6A1) of the tetrahedrally coordinated Mn2+ states and the impact of Mn2+ ions exhibiting several peaks in the UV-Visible region (365-634 nm) generating RGB (Red, Green, Blue) luminescence. Color coordinates and CCT values were calculated using the CIE diagram, and color correlated temperatures in the range of 2513–7307 K were discovered, which might be used in solid state lighting applications.

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In this work, the addition of a combination of Graphene Oxide Nanoplatelets (GONPs) and Ground
Granulated Blast Furnace Slag (GGBFS) was studied as admixture in concrete. Tests on physical and mechanical
properties and chloride permeability were conducted. GGBFS was replaced with Ordinary Portland Cement (OPC)
and it was determined that GGBFS Up to 50% by weight improves the physical and mechanical properties of
concrete. GONPs with an optimal amount of 50% by weight of GGBFS were added to the concrete and the physical
and mechanical properties of the samples were determined. It was observed that the addition of GONPs was effective
in improving the mechanical strength and physical properties of specimens. The results indicated that addition of
0.1 wt.% GO and 50 wt.% GGBFS would increase the compressive strength of the concrete sample up to 42.7%
during 28 days and 46% during 90 days compared to OPC. Concrete with a combination of 0.1 wt.% GONPs and
50 wt.% GGBFS witnessed an increase in its flexural strength up to 58.5% during 28 days and 59.2% during 90
days. The results indicated that by adding 0.1 wt.% GO and 50 wt.%, concrete chloride permeability decreased
substantially 72% for 90 day cured samples compared to OPC. GONPs as an alternative to cement up to 0.1% by
weight can accelerate the formation of C-S-H gel, thereby increasing the strength and improving the resistance of
water absorption and chloride permeability. The effects of pozolanic reaction in the concrete leading to the filling
of the pores were significant factors in the proposed curtailment mechanism

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The aims of this research were to evaluate the effects of different thermomechanical treatments on the microstructure and investigate some of the mechanical properties of a TWIP steel rich in Mn & Al. So, a block of a TWIP steel with nominal composition Fe-17.5Mn-1.36Al-0.8C was cast and then subjected to hot rolling followed by cold rolling and heat treatment. Cold rolling was performed before heat treatment in order to reduce the grain size and improve the tensile and fatigue properties. X-ray diffraction technique was used before and after the heat treatment to evaluate the possibility of any phase formation. No sign of martensitic transformation after cold deformation was observed. However, by increasing the amount of cold deformation, the number of mechanical twins and slip band increased resulted to an increase in hardness and strength. The best tensile and fatigue result were obtained after 47% thickness reduction and annealing at 715˚C for 10 min. Under these conditions, the mean grain size reduced from 138 to 9 μm resulted to an increase in yield strength from 395 to 510 MPa, and the fatigue life improvement from the mean life of 10200 for the cast sample to 21500 cycles for the treated sample, when these samples underwent fatigue tests at a stress range of 650 MPa and R=0. In addition, the diameter and depth of dimples in fracture surfaces decreased by reducing the grain size but the fracture mode was remained ductile and adequate plastic deformation occurred before failure.
 

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The effect of Strain-Induced Melt-Activated (SIMA) Process, ultrasonic treatment (UST) and Al-5Ti-1B refiner on the microstructure and globularity of Al–15%Mg2Si composite was studied. Deformation of 25% were used. After deformation the samples were heated at 560, 580 and 595 °C for 5, 10, 20 and 40 min. The composite was treated with different amounts of the Ti concentrations and ultrasonic treatment with different power. Microstructural study was carried out on the alloy. It was observed that SIMA process, ultrasonic treatment and Al-5Ti-1B refiner has caused the globular morphology of Mg2Si particles. The results showed that for the desired microstructures of the alloy during SIMA process, the optimum temperature and time are 595 °C and 20 min respectively. Optimum amount of Ti refiner is 1 wt.% and power for UST is 1800W. After applying the SIMA process, Al-5Ti-1B master alloy and ultrasonic treatment, the strength and engagement have increased. This means that tensile strength increases from 251 MPa to 303 MPa and elongation percentage improves from 2.1 to 3.4, respectively.
 

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Considering the widespread use of aluminum composites in various industries and the emergence of nanomaterials such as graphene and boron nitrite (BN) with their unique properties, aluminum-based nanocomposite reinforced by the graphene-BN hybrid was fabricated at different percentages. For this purpose, the graphene-BN hybrid was prepared and subjected to wet milling along with the aluminum powder. The mechanical properties of the final nanocomposite which was consolidated using the spark plasma sintering (SPS) method were examined. Aluminum-based composite specimens containing 1 wt.% graphene–0 wt.% BN (AGB1), 0.95 wt.% graphene–0.05 wt.% BN (AGB2), 0.90 wt.% graphene–0.1 wt.% BN (AGB3), and 0.85 wt.% graphene–0.15 wt.% BN (AGB4) were fabricated and compared with non-reinforced aluminum (AGB0). The hardness values of 48.1, 51.1, 56.2, 54.1, and 43.6 Hv were obtained for AGB0, AGB1, AGB2, AGB3, and AGB4, respectively. Additionally, tensile strengths of these specimens were 67.2, 102.1, 129.5, 123.7, and 114.7 MPa, respectively. According to the results of the hardness and tensile tests, it was revealed that the AGB2 specimen had the highest tensile strength (93% higher than AGB0 and 27% higher than AGB1) and hardness (17% higher than AGB0 and 10% higher than AGB1).

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1. In this article, the effect of graphite on iron-silicon interactions was investigated. It was found that, as graphite enters the iron structure, it permits further development of iron-silicon reactions. It was found that in the stoichiometric ratio of 1:0.5 of iron and silicon, when graphite is added to the system, simultaneously with the reaction of iron and silicon to form Fe₃Si₅, some amount of carbon can be dissolved in the iron and lead to more diffusion in iron and more iron silicide production. Silicon also reacts with carbon and produces SiC. The more amount of carbon entered into the system, the more growth of SiC occurs, while the production of other iron silicide phases, namely FeSi and Fe₃Si preceded. Finally diffused carbon into the iron reaches a definite amount that can form Fe₃C. In the stoichiometric ratio of 1:1 of iron and silicon, the formation of FeSi and SiC phases is observable. At the same time, the diffusion of carbon occurs in the same as the previous stoichiometric ratio. In the stoichiometric ratio of 1:2 of iron and silicon, compared with the stoichiometric ratio of 1:1, a larger amount of silicon is available and, the FeSi₂ phase can form in addition to FeSi

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This study was undertaken to investigate the influence of graphene nano sheets on the structural characteristics and dry sliding wear behaviour of Al-5Cu-1Mg aluminium alloy. The optimum amount of GNPs for proper grain refining was selected as 0.5 wt.%. T6 heat treatment was applied for all specimens before wear testing. Significant improvements in wear properties were obtained with the addition of GNPs combined with T6 heat treatment. Dry sliding wear performance of the alloy was examined in normal atmospheric conditions. The experimental results showed that the T6 heat treatment considerably improved the resistance of Al-5Cu-1Mg aluminium alloy to the dry sliding wear. The results showed that dry sliding wear performance of without T6 microstructure specimens was a lower value than that of with T6 specimens.
 

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In this study, poly(3-hexylthiophene) (P3HT) and fullerene Indene-C₆₀ multi-adducts (ICxA) were blended to create a formulation as a solution and thin films, which were prepared under ambient conditions. The optical properties of various compositional ratios were studied using UV-Visible absorbance and photoluminescence (Pl) measurements. The energy gaps of the prepared thin films and solutions were determined, and their values increased with increasing fullerene ratio because of the isolation of P3HT chains from their neighbors. Intensity ratio (I_C=C/I_C-C) with a small value in addition to a low value of full width at high maximum (FWHM) of Raman spectra are associated with increased conformation and high aggregation of composition. Furthermore, according to X-ray diffraction  (XRD) results the 1:0.8 and 1:0.6 ratios have the largest crystallite sizes in comparison to the other ratios. The highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) levels for blends by electrochemical measurements were determined, which are sandwiched between those of the pure materials. In ambient conditions, binary organic photovoltaic cells (OPVs) at different ratios of the photoactive layer were evaluated. The device with a ratio of 1:0.6 had the best performance, with power conversion efficiency (PCE) of 1.21 %, open circuit voltage (V_OC) of 0.53 V, short circuit current density (J_SC) of  5.71 mA.cm^-2, and fill factor (FF) of 39.5 % at a small V_loss of 1.39 V.