Showing 189 results for Tic
Farah Hanani Zulkifli, Hamid Hazrulrizawati , Fathima Shahitha Jahir Hussain, Nur Fatini Ilyana Mohamat Johari,
Volume 21, Issue 2 (6-2024)
Abstract
Researchers are increasingly focusing on green synthesis methods for silver nanoparticles due to their cost-effectiveness and reduced environmental impact. In this study, we utilized an edible bird's nest (EBN), a valuable economic resource, as the primary material for synthesizing silver nanoparticles using only water as the solvent. Metabolite profiling of the EBN extract was conducted using LC-QTOF-MS in positive mode (ESI+), revealing the presence of lipids, glycosides, peptides, polysaccharides, and disaccharides. Upon the addition of silver nitrate to the aqueous EBN extract, noticeable color changes from transparent to brown indicated the successful formation of AgNPs. Subsequent characterization of these silver nanoparticles involved UV-Visible spectroscopy, which revealed an absorption peak at 421 nm. Further characterization was carried out using FESEM, ATR-FTIR spectroscopy, and EDX analysis. The involvement of phenolic agents, proteins, and amino acids in reducing the silver particles was confirmed. The synthesized nanoparticles exhibited a spherical shape, and a particle size ranging from 10 to 20 nm. The presence of elemental silver was confirmed by a strong, intense peak around 3 keV in the EDX spectrum. To assess their potential, the antibacterial properties of the silver nanoparticles against Escherichia coli and Staphylococcus aureus were evaluated using the agar diffusion method.
Ramin Dehghani, Seyed Mojtaba Zebarjad,
Volume 21, Issue 3 (9-2024)
Abstract
Acrylic resins are one of the most important thermoplastic resins used in various industries due to their significant properties. However, they are inherently brittle and addition plasticizers to them is very common. In this study, role of both Polyethylene Glycol (PEG) and Triacetin on the mechanical properties of acrylic resin have been investigated. To do so tensile test, bending and wear tests have been performed. To achieve the optimal mixture of plasticizers, a tensile test has been carried out, and the best percentage of the mixture has been determined. Subsequently, bending and wear tests were conducted, which showed a significant increase in the bending strength of the acrylic resin after the addition of plasticizers. Furthermore, it was found that the abrasion mechanism of the resin was significantly altered compared to its pure state.
Dewi Qurrota A'yuni, Hadiantono Hadiantono, Velny Velny, Agus Subagio, Moh. Djaeni, Nandang Mufti,
Volume 21, Issue 3 (9-2024)
Abstract
Rice husk carbon by-product from the industrial combustion is a promising source to produce a vast amount of activated carbon adsorbent. This research prepared rice husk-activated carbon adsorbent by varying the concentration of potassium hydroxide solution (5, 10, 15, 20 % w/v) and activation time (2, 4, 6, 8 hours). Fourier-transform infrared spectral characterization (FTIR) indicated a significant effect before and after activation, especially the presence of hydroxyl groups. Based on the iodine adsorption, the specific surface area of the produced-activated carbon was approximately 615 m2/g. Experimental results showed that increasing potassium hydroxide concentration and activation time increases the water vapor adsorption capacity of the activated carbon. Compared with the rice husk carbon, the KOH-activated carbon enhanced the water vapor adsorption capacity to 931%. In the adsorption observation, changing the temperature from 15 to 27 ℃ caused a higher water vapor uptake onto the activated carbon. Two adsorption kinetics (pseudo-first- and pseudo-second-order models) were used to evaluate the adsorption mechanism. This research found that rice husk-activated carbon performed a higher water vapor adsorption capacity than other adsorbents (silica gel, zeolite, and commercially activated carbon).
Muddukrishnaiah Kotakonda, Sajisha V.s, Aiswarya G, Safeela Nasrin Pakkiyan, Najamol A Alungal, Mayoora Kiliyankandi K, Divya Thekke Kareth, Naheeda Ashraf Verali Parambil, Saranya Sasi Mohan, Renjini Anil Sheeba, Sarika Puthiya Veettil, Dhanish Joseph, Nishad Kakkattummal, Afsal Bin Haleem Mp, Safeera Mayyeri, Thasneem Chemban Koyilott, Nasiya Nalakath, Samuel Thavamani B, Famila Rani J, Aruna Periyasamy, Chellappa V Rajesh, Rameswari Shanmugam, Marimuthu Poornima, Tina Raju, Roshni E R, Sirajudheen Mukriyan Kallungal, Lekshmi Ms Panicker, Saranya K G, Shilpa V P,
Volume 21, Issue 3 (9-2024)
Abstract
Biogenic synthesis of papain-conjugated copper metallic Nanoparticles and their antibacterial and antifungal activities Papain metallic conjugated nanoparticles (Papain-CuNPs) were synthesised using Papain and CuSO4.5H2O. Papain-CuNPs were characterized using UV-visible spectroscopy, FT-IR, HR-TEM, XRD, FE-SEM, zeta potential, and a zeta sizer. The antibacterial activity of papain-CuNPs against human infectious microorganisms (Citrobacter spp, Pseudomonas aeruginosa and Candida albicans) was investigated. The mechanism of action of papain-CuNPs was evaluated using FE-SEM and HRTM. UV spectroscopy confirmed the plasma resonance (SPR) at 679 nm, which indicated the formation of papain-CuNPs. The FT-IR spectrum absorbance peaks at 3927, 3865, 3842, 3363, 2978, and 2900 cm-1 indicate the presence of O-H and N-H of the secondary amine, and peaks at 1643 and 1572 cm-1 represent C=O functional groups in Papain-CuNPs. EDAX analysis confirmed the presence of copper in the papain-CuNPs. The zeta potential (-42.6 mV) and zeta size (99.66 d. nm) confirmed the stability and size of the nanoparticles. XRD confirmed the crystalline nature of the papain-CuNPs. FE-SEM and HRTM showed an oval structure, and the nano particles' 16.71244–34.84793 nm. The synthesized papain-NPs showed significant antibacterial activity against clinical P. aeruginosa (15 mm). MIC 125 µg/ml) showed bactericidal activity against P. aeruginosa and the mechanism of action of Papain-NPs was confirmed using an electron microscope by observing cell damage and cell shrinking. Papain-CuNPs have significant antibacterial activity and are thus used in the treatment of P. aeruginosa infections
Ahmad Ostovari Moghaddam, Olga Zaitseva, Sergey Uporov, Rahele Fereidonnejad, Dmitry Mikhailov, Nataliya Shaburova, Evgeny Trofimov,
Volume 21, Issue 3 (9-2024)
Abstract
High entropy intermetallic compounds (HEICs) are an interesting class of materials combining the properties of multicomponent solid solutions and the ordered superlattices in a single material. In this work, microstructural and magnetic properties of (CoCuFeMnNi)Al, (CoCuFeMnNi)Zn3, (FeCoMnNiCr)3Sn2, (FeCoNiMn)3Sn2 and Cu3(InSnSbGaGe) HEICs fabricated by induction melting are studied. The magnetic properties of the HEICs was determined mainly by the nature of the magnetic momentum of the constituent elements. (CoCuFeMnNi)Al and (CoCuFeMnNi)Zn3 displayed ferromagnetic behavior at 5 K, while indicated linear dependency of magnetization vs. magnetic (i.e. paramagnetic or antiferromagnetic state) at 300 K. The magnetization of (FeCoMnNiCr)3Sn2, (FeCoNiMn)3Sn2 and Cu3(InSnSbGaGe) HEICs at 300 K exhibited a nearly linear dependency to magnetic field. Among all the investigated samples, (CoCuFeMnNi)Al exhibited the best magnetic properties with a saturation magnetization of about Ms = 6.5 emu/g and a coercivity of about Hc = 100 Oe.
Umadevi Prasanna, Vijaya Kumar Kambila, Krishna Jyothi Nadella,
Volume 21, Issue 4 (12-2024)
Abstract
The composite solid polymer electrolyte films were prepared by doping nano-sized Fe2O3 particles on PVB (Polyvinyl Butyral) complexed with NaNO3 salt by solution casting technique. FTIR, XRD, and SEM methods characterized these electrolyte films. The Fourier Transform Infrared Spectroscopy and X-ray diffraction methods reveal the structural and complexation changes occurring in the electrolytes. The surface morphology of the electrolyte film was examined using the SEM (Scanning Electron Microscope) technique. The PVB+NaNO3+Fe2O3(70:30:3%) electrolyte shows a moderate ionic conductivity of 2.51×10−5 S cm−1 at ambient temperature (303 K). AC impedance spectroscopic analysis evaluates the ionic conductivity of the produced polymer electrolyte. Wagner's polarisation technique was applied to study the charge transport characteristics in the electrolyte films. The investigation revealed that ions constituted the majority of the transport carriers. An Open Circuit Voltage (OCV) of 2.0V and a Short Circuit Current (SCC) of 0.8 mA were found in the discharge characteristics data for the cell constructed with the polymer electrolyte sample.
Nazli Aharipour, Adrine Malek Khachatourian, Ali Nemati,
Volume 21, Issue 4 (12-2024)
Abstract
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.
Maryam Hajiebrahimi, Sanaz Alamdari, Omid Mirzaee,
Volume 21, Issue 4 (12-2024)
Abstract
Dual nanocomposites based on metal sulfide nanomaterials with a narrow band gap are favorable candidates for future optoelectronic applications and ionizing ray sensors. In this study, novel silver-doped zinc sulfide/ cadmium sulfide (ZnS/CdS: Ag) nanocomposites were synthesized using the cost-effective solvothermal approach. For the first time, the radiation sensitivity of the newly developed nanocomposite was assessed using a 241Am alpha source and ion beam-induced luminescence (IBIL) measurements. The ZnS/CdS: Ag nanocomposite demonstrated significant light emission in the blue-green spectrum when measured at room temperature. When exposed to alpha irradiation, the ZnS/CdS: Ag nanocomposite film displayed exceptional sensitivity compared to pure ZnS or CdS films. The FESEM images revealed a uniform distribution of semi-spherical and rod-shaped nanoparticles, with an average particle size measuring 180 nm. The results from XRD and EDX demonstrated distinct peaks corresponding to ZnS, CdS, and associated elements within the nanocomposite. The existence of several groups within the nanocomposite was confirmed through Fourier transform infrared spectroscopy. Evaluations revealed that the optical quality of the ZnS/CdS: Ag nanocomposite showed enhancement in comparison to pure ZnS and CdS. The results suggest that the ZnS/CdS: Ag nanocomposite film holds great promise for applications in optoelectronic devices and detection technologies.
Divya Bajpai Tripathy, Anita Kushwaha, Smrita Singh, Smriti Dwivedi, Anjali Gupta, Lalit Prasad, Ashutosh Chauhan,
Volume 22, Issue 2 (6-2025)
Abstract
Organosilicon compounds represent a fascinating class of molecules with diverse structures, unique bonding characteristics, and wide-ranging applications across various fields. The structural diversity of organosilicon compounds arises from the versatility of silicon, which can form a variety of chemical bonds, including single, double, and triple bonds with carbon, as well as bonds with other heteroatoms such as oxygen, nitrogen, and sulfur. This diversity enables the synthesis of an extensive range of organosilicon molecules, including silanes, siloxanes, silanols, silazanes, and silsesquioxanes, among others. The unique properties of these compounds, such as thermal stability, chemical inertness, and flexibility, make them valuable building blocks for the design of advanced materials.Organosilicon compounds find applications in diverse fields, including materials science, pharmaceuticals, electronics, and agriculture. In materials science, they are used as coatings, adhesives, sealants, and modifiers to impart desirable properties such as water repellency, thermal resistance, and biocompatibility. In the pharmaceutical industry, organosilicon compounds serve as drug delivery agents, imaging agents, and synthetic intermediates due to their biocompatibility and tunable properties. In electronics, they are employed as dielectric materials, insulators, and encapsulants in semiconductor devices. Current review aims to unlock new opportunities for the development of innovative materials and technologies with enhanced performance and functionality.
Uglal Pandit Shinde, Somnath Bhika Handge, Dharma Kisan Halwar,
Volume 22, Issue 2 (6-2025)
Abstract
This study investigates the effect of SnO2 as an additive on the structural, electrical, optical, and gas sensing properties of LaCrO3 nanoparticles. SnO2 is added into the LaCrO3 by weight percentage (1 wt. %, 3 wt. %, 5 wt. %, 7 wt. %, 9 wt. % and 11 wt. %) employing screen printing method. Initially, the nanoparticles of SnO2 and LaCrO3 separately synthesis by sol-gel method and then used for the development of thick films. LaCrO3 is used as host material while SnO2 is additive material. The structural characterizations like FESEM, EDX and XRD were carried out to investigate the morphology, elements and crystallite size respectively. The inclusion of SnO2 modifies the crystalline structure and surface morphology of LaCrO3, as revealed by structural analyses. The optical characterizations like FTIR and UV were used for the study of impact of SnO2 additive on functional group and band gap of the host material respectively. Optical studies indicate a modification in the bandgap, affecting light absorption properties and indicating changes in electronic transitions. The electrical characterizations were conducted by using half bridge method. Electrical resistivity measurements show enhanced performance, likely due to variation in charge carrier mobility induced by the SnO2 additive. Among other selected wt. % SnO2 additives, 9 wt. % SnO2 added LaCrO3 thick films shows maximum sensitivity to CH4 gas at 120oC operating temperature. The gas sensing characteristics demonstrate enhanced sensitivity, selectivity, and response time to target gases, suggesting that SnO2 doping improves the sensing capabilities of LaCrO3 nanoparticles, making them more efficient as a gas sensor. Obtained findings suggest that, SnO2 as an additive enhances the multifunctional properties of LaCrO3 nanoparticles, making them promising candidates for advanced gas sensing applications.
Ali Keramatian, Mohammad Hossein Enayati, Fatemehsadat Sayyedan, Sima Torkian,
Volume 22, Issue 2 (6-2025)
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.
Y C Goswami,
Volume 22, Issue 3 (9-2025)
Abstract
CuS nanoparticles (NPs) with dimensions in the nanometer range were synthesized using a wet chemical approach. The comprehensive characterization of these NPs involved an analysis of their structure, composition, and optical properties, primarily conducted through X-ray diffraction (XRD) analysis. The XRD pattern conclusively confirmed the presence of the hexagonal phase in the CuS particles, a result corroborated by the accompanying Raman spectrum. The investigation further determined an estimated bandgap energy of 2.05 eV for the slightly sulfur-rich CuS NPs. Notably, this energy value exceeds that of bulk CuS (1.85 eV), indicating a noticeable miniaturization effect. The novel CuS NPs exhibited outstanding photocatalytic activity in the degradation of methyl Red (MR), particularly under visible light. This impressive performance is attributed to surface-bound OH ions on the CuS nanostructures, facilitating the adsorption and acceleration of the degradation process for MR molecules under visible light irradiation. The research presented in this article highlights the significant promise and efficiency of the synthesized CuS NPs as photocatalysts. These nanoparticles are particularly responsive to stable visible light, making them highly suitable for purifying chemically contaminated wastewater. Specifically, their effectiveness in degrading stable azo dyes, exemplified by MR, underscores their potential in practical applications.
Mohammad Abdullah Al Asad, Hasan Ridoy, Md. Shuzon Ali, Mst. Jeba Maimuna,
Volume 22, Issue 3 (9-2025)
Abstract
Perovskite materials have accumulated considerable attention in recent years for their exceptional electro-optical properties, creating them rising candidates for various uses in the fields of photovoltaics, light-emitting devices, and beyond. Among these perovskite materials, CsPbI3 stands out as a notable example due to its remarkable stability, tunable bandgap, and efficient light-emitting properties. The crystal structure, composition, and introductory properties of CsPbI3 perovskite using density functional theorem (DFT) being focused. In detailed exploration of Electronic property, Elastic property, Optical property, Population analysis, and shedding light on the unique attributes of this material highlighted this study. To do above computation we have used CASTEP in Material Studio.
Salahaldin Mansur Alduwaib, Reihane Etefagh, Boshra Ghanbari Shohany,
Volume 22, Issue 3 (9-2025)
Abstract
This research is focused on the synthesis of zinc oxide nanoparticles by means of the sol-gel conventional method, followed by the formulation of a zinc oxide-polypropylene (ZnO: PP) masterbatch using a twin-screw extruder. The next step involved the fabrication of antibacterial fibers through electrospinning. The resulting Nano powders, masterbatch, and fibers were subjected to a series of characterization techniques. X-ray diffraction (XRD) was used to examine the crystalline structure, field emission scanning electron microscopy (FESEM) was employed to scrutinize the morphology of the samples, energy-dispersive X-ray spectroscopy (EDX) was adopted for elemental analysis, and Fourier-transform infrared spectroscopy (FTIR) was hired to identify the chemical bonds.
Thermogravimetric analysis (TGA) indicated a three-stage weight loss process, and differential scanning calorimetry (DSC) showed a primary endothermic peak centered at about 317 °C and a pronounced exothermic peak at approximately 455 °C. XRD confirmed the hexagonal wurtzite structure of the zinc oxide nanoparticles and the presence of the alpha (α) crystal form in polypropylene. FESEM imaging revealed that the zinc oxide and masterbatch samples had a uniform size and shape, predominantly in the nanometer range with an elongated spherical morphology. The antibacterial properties of polypropylene fibers containing varying concentrations of zinc oxide, including 1.2, 2.4, and 5 wt.%, were tested against Escherichia coli and Staphylococcus aureus.
Azam Bayat,
Volume 22, Issue 3 (9-2025)
Abstract
The lindgrenite compounds [Cu3(MoO4)2(OH)2] with various architectures and high crystallinity were prepared by a simple surfactant-assisted hydrothermal method. Then, the Cu3Mo2O9 samples were prepared by calcination of the as-synthesized Cu3(MoO4)2(OH)2. The resulting samples had high crystallinity, colloidal properties, high-yield, large-scale production capability with using of nontoxic and inexpensive reagents and water as an environmentally solvent. The scanning electron microscope studies showed that the as-prepared lindgrenite nanostructures were well crystallized with rod, sheet and hollow sphere morphologies. These products were content of the Cu3(MoO4)2(OH)2 rods with diameters of about 100 nm, the Cu3(MoO4)2(OH)2 nanosheets with thickness of 30–100 nm and the Cu3(MoO4)2(OH)2 hallow spheres, consisting of a large number of nanosheets with thickness of about 40-70 nm. The Cu3Mo2O9 samples that obtained by thermal treatment of lindgrenite retained the original morphologies. Meanwhile, the photoluminescence and magnetic properties of the nanosheet samples showed super paramagnetic behavior at room temperature and in comparison with previous works, Cu3(MoO4)2(OH)2 and Cu3Mo2O9 samples synthesized by the surfactant-assisted hydrothermal method had a very obvious red-shifted PL emission and high intensity.
Yasin Mehdizadeh, Saeed Reza Allahkaram, Mohammad H.mohammad-Ebrahimi, Majid Shamsarjmand,
Volume 22, Issue 4 (12-2025)
Abstract
The present work deals with the corrosion behavior and mechanical properties of a coted AZ31 magnesium alloy through plasma electrolyte oxidation (PEO) coating process in different alkaline electrolytes based on sodium silicate (Si-coating), sodium polyphosphate (P-coating) and sodium aluminate (Al-coating). The scanning electron microscopy (SEM) equipped with the energy dispersive x-ray spectroscopy (EDX) plus x-ray diffraction were recruited to investigate the morphology, chemical composition, and phase structure of coatings, respectively. Microscopic scrutiny revealed that the coating in the phosphate electrolyte was twice as thick and the relative porosity percentage was higher than those formed in the other electrolytes. The phase analysis indicated that the MgO was present as the prevailing phase in the Al-coating and P-coating. However, the dominant phase in the Si-coating was Mg2SiO4. Electrochemical testing was examined in a solution containing 3.5.wt% sodium chloride, showing improvements in corrosion resistance of coated alloys. These investigations confirmed that the corrosion resistance of Si-coating was dramatically higher than others which could be attributed to the presence of the dense and stable Mg2SiO4 phase as well as its relatively low porosity. According to the results of tensile tests, the coated samples had lower tensile strength and elongation than the uncoated one. The tensile strength and elongation diminished upon changing the electrolyte from Al-coating to P-coating, while the yield strength was almost similar. Further analyses indicated that the drop of tensile strength and elongation could be attributed to the presence of cracks and pores in the brittle ceramic PEO coating as stress concentration regions during deformation. Those areas are created due to thermal stress during the coating process and deformation in the elastic stage.
Marzieh Akbari, Fatemeh Dabbagh Kashani, Seyed Mohammad Mirkazemi,
Volume 22, Issue 4 (12-2025)
Abstract
CIGS solar cells are currently very high-efficiency thin-film solar cells. With regard to higher efficiency in solar cells, research is being conducted on the influence of both light scattering and plasmonic resonances due to metallic nano-structures. This article discusses the assessment of the incorporate plasmonic nanostructures on the absorber layer of a 1000 nm CIGS solar cell, in terms of light absorption and device performance. It is noted that decisions on material, size, and surface coverage (Occupied Factor) were important considerations that affected the performance. Opto-electrical assessment was used to investigate absorption, charge-carrier generation, current density-voltage response, power-voltage properties, and total efficiency. Using simulations, we discovered the aluminum nanosphere arrays (200 nm diameter, Occupied Factor 0.64) at the top of the absorber layer yielded the maximum efficiency (26.14%). This was shown by the resonances, and near-field distribution garnered from the nanospheres boost charge carrier generation, diminished recombination losses, and increased charge separation. Collectively, these raised the performance of the CIGS solar cells in this research and suggested hope for moving CIGS and potentially other photovoltaics forward using nanoscale plasmonic resonances.
Mohammad J. Rezaei, Mohammad Sedighi,
Volume 22, Issue 4 (12-2025)
Abstract
The investigation of the mechanical response and microstructural evolution of engineering materials at the micro-scale under macro-scale loading poses a significant challenge in mechanical engineering, particularly in the fields of material forming and materials science. This critical has been addressed using a computational crystal plasticity tool known as DAMASK (Düsseldorf Advanced Material Simulation Kit). DAMASK is a multi-scale computational framework developed for modeling the deformation of crystalline materials by employing the principles of continuum mechanics and crystal plasticity. This software is widely recognized within the scientific community for its high flexibility and capability to simulate complex material behavior under various loading conditions. In this study, the DAMASK code—a finite element crystal plasticity software—was employed to analyze a representative volume element (RVE) containing 1000 grains under tensile loading. By applying a random initial texture to aluminum grade 1050, the microstructural evolution of the material under the specified loading conditions was evaluated. The results indicate the formation of <111> and <100> fiber textures in the (111) crystallographic plane of the FCC-structured material, which are consistent with observations obtained from EBSD experiments.
Vyacheslav Sirota, Sergey Savotchenko, Valeriya Strokova, Daniil Podgornyi, Marina Kovaleva, Sergey V Zaitsev, Аnton S Churikov,
Volume 22, Issue 4 (12-2025)
Abstract
The surface properties of metal-ceramic coatings based on titanium dioxide are described in dependence on the detonation spraying conditions. It is found that such properties as surface roughness, surface thickness and its hydrophobicity can be controlled in the production process by selecting certain values of the technological parameters of the spraying process. The optimal values of the technological parameters of detonation spraying, ensuring maximum hydrophobicity of the produced coatings are determined. The roughness of the coating surface and the coating thickness depend on the speed of the nozzle passage in accordance with the inverse power law. The roughness and the contact angle depend on spray distance in accordance with a parabolic law. New equations are obtained that can be useful for predicting the characteristics of the coating surface, as well as for determining the optimal mode of spraying the coating, ensuring its best hydrophobicity.
Khashayar Zamani, Majid Tavoosi, Ali Ghasemi,
Volume 22, Issue 4 (12-2025)
Abstract
The present work, set out with the aim of studying the effect of in-situ precipitation of TiO2 form Ti3C2Tx MXene phase on the electromagnetic (EM) behavior of Ti3C2/TiO2 composites. In this regard, Ti3C2Tx MXene phase was synthesized using HF acidic etching of Ti3AlC2 MAX phase and the in-situ precipitation of TiO2 phase within Ti3C2 sheets was followed by controlled annealing in temperature range of 500-800 oC for 2 h. The phase and structural characteristics of prepared composites were investigated using X-ray diffraction (XRD), scanning electron microscope (SEM) and differential thermal analysis. The electromagnetic behavior of samples was also analyzed using vector network analyzer (VNA). The results showed that by performing the controlled annealing process of Ti3C2Tx MXene phase, it is possible to in-situ formation of TiO2 phase and form the Ti3C2/TiO2 composites. The electromagnetic behavior of Ti3C2/TiO2 composites is in direct relation with the percentage of TiO2 phase deposited within Ti3C2 sheets during annealing process. The reflection loss (RL) changed from -7.98 to -21.28 dB (within frequency range of 1-18 GHz) with increasing in annealing temperature from 500 to 800 oC as well as increasing the size and percentage of formed TiO2 particles.
