Iranian Journal of Materials Science and Engineering

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Abstract
Gelatin (GEL) is most extensively used in various fields, particularly in therapeutics and pharmaceuticals. GEL was extracted from goat skin using hot temperature extraction process and compared with that of commercial GEL. The physico-chemical characterization and functional properties were investigated by using temperature denaturation (T_d), water-holding and fat-binding capacities (WHC and FBC), colour measurement and UV-light spectrum. In vitro biocompatibility was studied for the first time and was evaluated by blood coagulation index (BCI) and haemolytic tests for using as wounds dressing. The results revealed thermal stability of goat GEL at T_d 37°C. WHC and FBC capacities represented 2.5 and 1.2 g/ml, respectively. The hunter colour spaces a*, b* and L* showed a -0.27, -1.97 and 25.23 values, respectively. UV-Vis absorption spectrum of the goat GEL showed a maximum absorption peak at 280 nm. The in vitro anticoagulant activities of extracting GEL were higher than 70% after incubation for one hour. After being in contact with red blood cells for 1 h, the haemolysis ratio increased from to 0.46 to 1.4 when the concentration of goat GEL increased from 1 to 50 mg/ml suggesting the safety of the tested samples. These results suggest that thromboresistivity and hemocompatibility of this biopolymer retained the biological activity of our samples for biomaterial applications. According to this, goat GEL successfully competes with, and significantly could be useful for substitution of bovine in wound healing.

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In this study, for the first time, the Forsterite (Mg₂SiO₄) nanoparticles (NPs) with the size of about 25 nm were added to the phosphate-based electrolyte, and the characteristics and properties of the obtained plasma electrolytic oxidation (PEO) coating on AZ31 Mg alloy was investigated. The results of the potentiodynamic polarization measurements revealed that after one week of exposure to simulated body fluid (SBF) solution, the coating with Mg₂SiO₄ NPs possessed 12.30 kΩ cm² polarization resistance, which was more than two times greater than that of the coating without NPs. The thicker coating layer, lower wettability, and also presence of Mg₂SiO₄ NPs inside the pores were responsible for enhanced corrosion protection in the Mg₂SiO₄ NPs incorporated coating. After three weeks of immersion in SBF solution, the in-vitro bioactivity test results indicated the ability of the NPs-containing coating to form apatite (Ca/P ratio of 0.92) was weaker than the coating without NPs (Ca/P ratio of 1.17). This could be attributed to the lower wettability of the coating with NPs and supports that the addition of the nanoparticles is not beneficial to the bioactivity performance of the coating. 

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Sodium alginate (SA), brown seaweed algae, and Lignosulphonic acid (LS), a plant product, are biodegradable polymers extensively investigated for drug-controlled release. The Hydroxychloroquine sulphate (HCQ) drug, an antimalarial drug, was extensively used in the initial periods of COVID situations. The HCQ drug release from SALS beads is investigated for its control release in a simulated medium (pH1.2 and pH7.4) using different crosslinking agents such as Calcium chloride, Barium chloride and Aluminum chloride. The HCQ release has better controlled in Barium crosslinked beads. They are found to be relatively intact and stable and release the drug for more than 180 minutes in the simulated medium. Further drug entrapment studies prove very high for Ba crosslinked SALS beads. Whereas Aluminum crosslinked beads showed, inferior crosslinking and drug retention in beads is very low and starts degrading in simulated fluids. Drug release kinetics were analyzed using various kinetic model equations to discuss the order of reaction and drug-polymer mechanism.  FT-IR investigations of beads show chemical interactions between crosslinking ion and alginate blends.

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Quaternary ammonium compounds (QACs) are among the most commonly used antibacterial agents. The aim of this study was to synthesize a dimethacrylate monomer functionalized with a QAC and to study its effect on the properties of an orthodontic adhesive primer. Urethane dimethacrylate monomer functionalized with a QAC (UDMAQAC) was synthesized and then characterized by nuclear magnetic resonance spectroscopy (NMR) and Fourier transform infrared spectroscopy (FTIR). 5, 10, 15 and 20 wt% of UDMAQAC was added to an orthodontic adhesive primer (control group). FTIR analysis was used to measure the degree of conversion (DC). The bond strength of dental brackets was measured by shear bond strength (SBS) test and adhesive remaining index (ARI) was evaluated by stereomicroscope. Agar diffusion test and MTT assay were used to evaluate the antibacterial property and cell viability, respectively. Statistical analysis included one-way ANOVA with Tukey’s post hoc test and Kruskal-Wallis nonparametric test (P˂0.05). Although the obtained data did not show significant differences between the SBS and DC of different groups, but the highest values were obtained by adding 10 wt% monomer. Adding more than 10 wt% UDMAQAC resulted in significant increase in antibacterial property. The 15 and 20 wt% groups showed significantly lower cell viability

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Cordierite ceramics are of interest for various applications due to their properties such as low thermal expansion coefficient and high thermal shock resistance. However, due to the narrow range of sintering temperature, attempts have been made to synthesize it using different additives. In this way, titania and tialite have been added in different amounts to the initial raw material mixture (talc, kaolin, and synthetic alumina). In this research, the initial powders (talc, kaolin, and synthetic alumina) were mixed in a planetary ball mill using different amounts of TiO₂ and tialite. The mixtures were sintered at 1250, 1300, and 1350 °C for 3 h. X-ray diffractometry and fluorescence, thermal analysis, microstructural observation, density, and cold compressive strength (CCS) were used to evaluate the sintered samples. Phase analysis revealed the presence of the cordierite phase along with small amounts of spinel. With increasing sintering temperature and titania addition, the amount of spinel decreased and the amount of cordierite phase increased. The real density increased with increasing titania additive content, but at higher titania contents, microcracks were observed in the SEM micrographs. By adding 15 wt% of tialite to the initial batch, the compressive strength has been increased by 88% compared to the pure cordierite sample.

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In this investigation, a formulation was developed as a solution and thin films by combining poly (3-hexylthiophene) (P3HT) and fullerene Indene-C60 multi-adducts (ICxA) with varying solvent ratios. The formulations were prepared under ambient conditions. Morphological parameters were assessed utilizing a transmission electron microscope, scanning electron microscope  and complemented by optical microscope pictures. UV-Visible absorbance and photoluminescence (PL) measurements were implemented to investigate the optical properties of active layers The values of the energy gaps of the prepared thin films and solutions increased as the solvent ratios of chlorobenzene to stander solvent increased, as a result of the isolation of P3HT chains from their neighbours. The Raman spectra are associated with high aggregation of composition and increased conformation when the intensity ratio (IC= C/IC-C) is small and the full width at high maximum (FWHM) is low. In ambient conditions, organic photovoltaic cells (OPVs) are produced with varying solvent ratios. The device with a 30% ratio exhibited the highest performance, with a power conversion efficiency (PCE) of approximately 1%, an open circuit voltage (VOC) of 0.571 V, a short circuit current density (JSC) of 7.47 mA.cm^-2, and a fill factor (FF) of 38.6%.

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Fe₃O₄ nanoparticles (NPs) with a continuous and mesoporous silica (m-SiO₂) shell were synthesized using a one-step method, sourcing silica from rice husk ash (RHA). The rice husk was thermally treated to obtain ash, from which silica was extracted as sodium silicate and precipitated by pH reduction. This silica powder, combined with iron chloride salts, facilitated the synthesis of the core-shell NPs. Mint extract acted as a capping agent to prevent agglomeration, and CTAB (cetyltrimethylammonium bromide) was used to create the porous SiO₂ shell. X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) characterization investigated the structure, size, and shell formation. Coating integrity and suspension stability were assessed through Fourier transform infrared spectroscopy (FTIR) and dynamic light scattering (DLS). DLS analysis showed a relatively narrow particle size distribution with an average hydrodynamic size of 72.6 nm. Small-angle X-ray scattering (SAXS) provided insights into the meso- and nanoscale structure, while BET and nitrogen adsorption-desorption isotherms confirmed the mesoporous nature of the silica shell. Magnetization measurements showed superparamagnetic behavior, with specific magnetization values of 57.9 emu/g for Fe₃O₄ and 27.5 emu/g for Fe₃O₄@m-SiO₂. These results confirm the successful synthesis of superparamagnetic magnetite NPs with a mesoporous silica coating from RHA.
 

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ZrO₂ is commonly incorporated into ceramic glass substrates to enhance radiopacity, mechanical strength, and chemical durability. Experience has shown that the crystallization of tetragonal zirconia in glass will have a greater effect on the mechanical properties of ceramic glass. To achieve optimal properties in zirconia, stabilizing oxides are often added to enhance its structural and mechanical qualities. In this research, in order to stabilize the tetragonal phase of zirconia, MgO and CeO₂ were added to the glass ceramic composition of the Li₂O-SiO₂-ZrO₂ system and the desired dental substrate was synthesized through the sinter process. The behavior of sintering and crystallization of basic and optimized glass was investigated using HSM and DTA thermal analysis, respectively. The results showed that the optimal sinter temperature, heat press and heat treatment are equal to 730°C, 900°C and 825°C, respectively. Then, in order to determine the crystallization behavior of the prepared samples, X-ray diffraction and microstructure images were used. The results also showed that the presence of the main Li₂ZrSi₆O₁₅ phase crystallizes at a temperature of 825°C in the base sample and the sample containing ceria. Also, due to early formation of MgSiO₃ crystals, magnesia prevents sintering and formation of Li₂ZrSi₆O₁₅ phase and stability of tetragonal zirconia phase. In the sample containing ceria, during crystallization, ZrO₂ entered its crystal structure and led to the stability of the tetragonal zirconia phase at room temperature.

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In this work, the effect of variation of the non-ideality coefficient of the p-n-junction volt-ampere (I-V) characteristic located in the strong microwave field on the differential resistance, diffusion capacitance and differential conductance is studied. Here, it is shown that the p-n junction I-V characteristics increases with the value of the non-ideality coefficient, whether the differential resistance is in a strong microwave field or a weak microwave field. Diffusion capacitance and differential conductance are shown to decrease with increasing value of non-ideality coefficient.
 

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Celestite ore, the primary mineral for producing strontium compounds, particularly strontium carbonate, is processed using the black ash method, which involves carbothermic reduction, water leaching, and carbonation. This study aims to investigate the combined effect of mechanical activation and additional graphite on the recovery rate and purity of strontium carbonate. Celestite ore with a strontium sulfate content of 79% was obtained from the Dasht-e-Kavir mine. Acid washing with 10% hydrochloric acid significantly reduced carbonate impurities, resulting in a celestite purity of 96.9%. Mixtures of celestite and graphite with varying amounts of graphite were prepared with and without milling. The mixtures were roasted at 900 °C for 1 hour to form strontium sulfide, followed by hot water leaching. After filtration, sodium carbonate was added to the leachate containing SrS, resulting in the formation and precipitation of white strontium carbonate crystals. The results showed that the addition of graphite increased the recovery rate in unmilled specimens. However, the recovery rate decreased significantly when 1 and 10 hours of milling were applied in the presence of excess graphite. Conversely, in the absence of additional graphite, milling for 1 and 10 hours increased the strontium recovery rate to over 95%. Furthermore, the analysis of strontium carbonate obtained from the sample with the highest recovery rate showed a purity of over 99.9%.

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In this research, Lanthanum (La)-doped Strontium Titanate (STO) with the formula of Sr_1-xLa_xT_iO₃ (LSTO; x=0, 0.03, 0.05, and 0.07) powders have been successfully fabricated by co-precipitation route. The impacts of La³⁺ on the structural, microstructure, band-gap, and photocatalytic activity for the degradation of organic pollutants, in this case, methylene blue, under UV exposure, were reported in detail. The formation of undoped and La-doped STO samples with cubic perovskite structures was confirmed by X-ray Diffraction (XRD) results. The presence of La doping affected the microstructure morphology by producing LSTO powders with a larger specific surface area. Besides, the UV absorption of the LSTO powders was enhanced due to the narrowed band gap caused by La³⁺ dopants. Accordingly, an improvement in photocatalytic activity applied for the photodegradation of methylene blue solution was exhibited by the LSTO samples.

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In this study, the hot deformation and dynamic recrystallization behavior of low carbon steel containing 21 ppm boron was investigated. After homogenizing the samples at 1250 ℃ for 1-hour, hot compression tests were conducted at temperatures ranging from 850 ℃ to 1150 ℃ and strain rates from 0.01 to 10 s⁻¹, resulting in strain-stress flow curves. Following corrections, calculations and modeling were performed based on Arrhenius equations. Among them, the hyperbolic sine relationship provided the most accurate estimate and was selected as the valid model for the applied strain range. According to this model, the deformation activation energy (Q), was determined to be 293.37 KJ/mol. Additionally, critical and peak stress and strain values were obtained for each temperature and strain rate, and power relationships were established to describe their variation with respect to the Zener-Hollomon parameter (Z). Recrystallization fractions were derived by comparing the hypothetical recovery curves with the material flow curves, and the results were successfully modeled using the Kolmogorov-Johnson-Mehl-Avrami (KJMA) equation. The Avrami exponent was measured at approximately 2, indicating that nucleation predominantly occurred at grain boundaries. Microstructural analysis revealed that at higher Z values, recrystallization occurred along with a fraction of elongated grains, while lower Z values resulted in a greater fraction of equiaxed dynamic recrystallization (DRX) grains. The average grain sizes after compression tests at 950 ℃, 1050 ℃, and 1150 ℃ were measured as 21.9 µm, 30.4 µm, and 33.6 µm respectively at a strain rate of 0.1 s⁻¹, and 17.7 µm, 28.7 µm, and 31.3 µm at 1 s⁻¹. The overall microstructure displayed a more uniform grain size distribution with increasing deformation temperature.

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In this study, we thoroughly examine β-Bi₂O₃ thin films as potential photocatalysts. We produced these films using an environmentally friendly Sol Gel method that is also cost-effective. Our research focuses on how different precursor concentrations, ranging from 0.1 M to 0.4 M, affect the photocatalytic performance of these films. We conducted a comprehensive set of tests to analyze various aspects of the films, including their structure, morphology, topography, optical properties, wettability, and photocatalytic capabilities. These tests provided us with a well-rounded understanding of the films' characteristics. To assess their photocatalytic efficiency, we used Methylene Blue (MB) as a contaminant and found that the films, particularly those with a 0.1 M concentration, achieved an impressive 99.9% degradation of MB within four hours. The 0.1 M film had a crystalline size of 39.7 nm, an indirect band gap of 2.99 eV, and a contact angle of 51.37°. Our findings suggest that β-Bi₂O₃ films, especially the 0.1 M variant, have promising potential for treating effluents from complex industrial dye processes. This research marks a significant step in utilizing sustainable materials to address pollution and environmental remediation challenges.

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Natural-reinforced hybrid composites, called "eco-materials," are becoming increasingly important for protecting the environment and eliminating waste problems. In this study, hybrid biocomposites were produced by the colloidal mixing method using seashell (SS) as natural waste, two graphene derivatives (graphene oxide (GO) and reduced graphene oxide (RGO)) as filler material, and polyvinyl chloride (PVC) as the polymer matrix. The crystallization and mechanical properties of hybrid biocomposites were examined based on their thermal properties using TGA and DSC analysis. In comparison to PVC/GO and PVC/RGO composites with identical weight percentages of GO and RGO, the PVC/GO composite exhibited superior thermal stability and crystallinity, resulting in elevated hardness values for the same composite. These results were attributed to the better interaction of GO with PVC due to the higher number of oxygen-containing functional groups in GO than in RGO. However, the PVC/RGO/SS hybrid biocomposites exhibited superior properties than PVC/GO/SS hybrid biocomposites. The greatest crystallinity values were 39.40% for PVC/RGO/SS-20 compared to PVC/RGO at 20 wt% SS content and 29.21% for PVC/GO/SS-20 compared to PVC/GO. The PVC/RGO/SS-20 hybrid biocomposite showed the greatest gain in hardness value, up 18.47% compared to the PVC/RGO composite. No significant change was observed in the melting and weight loss temperatures as the SS content increased; however, the crystallinity and glass transition temperatures in hybrid biocomposites increased as the SS content increased. All analysis results demonstrated the achievement of SS-graphene-PVC interactions, suggesting that SS waste could enhance the thermal and mechanical properties of composite production.

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In this research study, a composite coating of Ni-Co/SiC-CeO₂ was prepared on a copper substrate using the pulse electrodeposition technique. The effects of electrodeposition parameters, including current density, duty cycle, and frequency, on the properties of the prepared coating were investigated. The selected current density values were 0.1, 0.2, and 0.3 A/cm², the duty cycle options were 10, 20, and 30%, and the frequency values were 10, 100, and 1000 Hz. Increasing the current density enhanced the microhardness of the coating but reduced its corrosion resistance. This behavior can be attributed to the grain refinement occurring within the coating as the current density increases. On the other hand, an increase in duty cycle resulted in a decrease in microhardness, which can be attributed to a decrease in the concentration of nanoparticles within the coating. The lower corrosion resistance observed at higher duty cycles could be attributed to the decrease in off-time, causing the pulse electrodeposition conditions to approach a DC (direct current) state. Furthermore, higher frequencies were found to be associated with increased microhardness and improved corrosion resistance of the coatings. The coatings with the highest corrosion resistance exhibited a corrosion current density of 0.29 µA/cm² and a polarization resistance of 1063 Ω.cm² in a 3.5% NaCl solution. These coatings were prepared using a current density of 0.2 A/cm², a duty cycle of 10%, and a frequency of 1000 Hz.