Showing 109 results for Nano
H. Jafarian, H. Miyamoto,
Volume 17, Issue 1 (3-2020)
Abstract
In the present work, accumulative roll bonding (ARB) was used as an effective method for processed of nano/ultrafine grained AA6063 alloy. Microstructural characteristics indicate considerable
grain refinement leading to an average grain size of less than 200 nm after 7 ARB cycles. Texture analysis showed that 1-cycle ARB formed a strong texture near Copper component ({112}<111>). However, texture transition appeared by increasing the number of ARB cycles and after 7-cycle of ARB, the texture was mainly developed close to Rotated Cube component ({100}<110>). The results originated from mechanical properties indicated a substantial increment in strength and microhardness besides a meaningful drop of ductility after 7 ARB cycles.
M. Mahdi, A. Abdul-Hameed, B. Ali, H.f Al-Taay,
Volume 17, Issue 1 (3-2020)
Abstract
Silicon nanowires (SiNWs) are synthesized through a metal-assisted chemical etching (MACE) method using Si(100) substrates and silver (Ag) as a catalyst. Scanning electron microscope (SEM) images confirmed that length of prepared SiNWs was increased when etching time increased. The prepared SiNWs demonstrated considerably low light reflectance at a wavelength range of 200–1100 nm. The photoluminescence (PL) spectra of the grown SiNWs showed a broad emission band peaked at a wavelength of about 750 nm. A solar cell and photodetector based on heterojunction SiNWs/PEDOT:PSS were fabricated using SiNWs that prepared with different etching time and its J–V, sensitivity, and time response were investigated. The conversion efficiency of fabricated solar cell was increased from 0.39% to 0.68% when wire length decreased from 24 µm to 21 µm, respectively. However, the sensitivity of the heterojunction SiNWs/PEDOT:PSS photodetector was decreased from 53774% to 36826% when wire length decreased from 24 µm to 21 µm, respectively.
T. Mandal, D. Roy,
Volume 17, Issue 1 (3-2020)
Abstract
Magnetic iron oxide nanomaterials (MIONs) have been extensively investigated for the various important applications. Coprecipitation, hydrothermal, high temperature decomposition of organic precursors, microemulsions, polyol methods, electrochemical methods, aerosol method, sonolysis and green synthesis processes for the fabrication of MIONs have been reviewed. Different characterization methods like XRD, SEM, EDX and TEM for the as prepared MION materials have been studied. Important applications of MIONs in the field of biomedical, nanorobotics and energy devices have also been addressed in this review. Target oriented drug delivery and hyperthermia applications of MIONs have also focused
S. Manafi, S. Joughehdoust,
Volume 17, Issue 2 (6-2020)
Abstract
In this research, calcium titanate (CaTiO3) hollow crystals have been successfully prepared via hydrothermal method. Titanium tetrachloride, calcium chloride dihydrate and potassium hydroxide were used as Ti, Ca and precipitating agent, respectively. The hydrothermal synthesis was performed at different temperatures and time durations. The negative amount of the Gibbs free energy shows the reactivity of the reaction at room temperature. Characterization of CaTiO3 was carried out using scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and X-ray diffraction (XRD). The optimum condition for preparing CaTiO3 is the sample kept in an autoclave at 300 ℃ for 3 h that requires less energy and time which consists of a high degree of crystallinity. In this research, tetragonal CaTiO3 hollow crystals have been successfully prepared via hydrothermal method. TiCl4, CaCl2.2H2O, and KOH were used as Ti, Ca and precipitating agent, respectively. The hydrothermal synthesis was performed at different temperatures and time durations. Characterization of CaTiO3 was carried out using SEM, HRTEM, and XRD. The sample kept in the autoclave at 300 ℃ for 3 h well crystallized and required less energy and time for synthesis. The powder has a homogenous dispersity of crystals with the range of nanometer to micrometer sizes which makes it a good candidate as a photocatalyst material
N. Mohammed, H. F. Dagher,
Volume 17, Issue 3 (9-2020)
Abstract
Thin films of meta-cinnabar mercuric sulfide (β-HgS) nanoparticles (NPs) was prepared by pulsed laser ablation (PLA) utilizing a pellet of cinnabar mercuric sulfide (α-HgS) was immersed in distilled water (DW). Q-switched Nd:YAG laser of 1064 nm wavelengths with repetition rate (1hz) and fluency (1.5 J/cm2) applied for ablation. Structural, morphological and particle sizes of the β-HgS NPs are invastigated by analyzing XRD, AFM, SEM and TEM measurements. Their crystal structure is transformed from hexagonal (wurtzite) of the α-HgS target material to cubic (zinc blende) β-HgS NPs. The optical properties of the β-HgS NPs are measured by UV–visible spectrophotometer. The direct band gap is calculated to be (2.45eV) of small particles (4-6.2nm) moreover, the band gap value of smallest particles (1-4nm) is (3.47eV) according to the optical transmission spectra
A. Thakur, G. Reddy,
Volume 17, Issue 3 (9-2020)
Abstract
Mercury, one of the common pollutants in water, is known to affect human health adversely upon exposure. It is released in water not only by various natural processes but also by human activities. Methods developed so far for the detection of mercuric ions in water have limitations like sensitivity range, complex setup, skillful operation etc. Silver nanoparticles, due to unique properties, have been explored by researchers to develop better detection systems. Stable silver nanoparticles can be easily synthesized by methods of green chemistry, its reaction with mercuric ion can be easily observed by changes in color and UV-Vis spectra. The absorbance data from UV-Vis spectra can also be used in quantifying mercury concentration. In this paper, stable silver nanoparticles synthesized using silver nitrate as precursor, sodium lignosulphonate (LS) as reducing and stabilizing agent under microwave radiation are explored for detection of mercuric ions in water. Formation of AgNP was confirmed by UV-Vis band at 403.5nm. The intensity of this band showed a proportional decrease with increasing Hg+2 concentration. Hg+2 ions were detected by a distinct color change at higher concentration of Hg+2 also. The limit of detection (LOD) calculated from the observed absorbance data to be 0.7 ppm.
M. T. Basha G, V. Bolleddu,
Volume 17, Issue 3 (9-2020)
Abstract
The microstructural characteristics, mechanical properties, and wear characterization of air plasma sprayed coatings obtained from Carbon nanotubes (CNTs) reinforced Al2O3-3wt%TiO2 powders were examined at different loading conditions and different percentage proportion of CNTs. The CNTs in the proportion of 2, 4, and 6wt% were used as nanofillers to modify the properties of coatings. The uniform dispersion of CNTs throughout the powder particles can be observed from the SEM micrographs. The porosity of the microstructure of the coatings was measured by image analysis. Also, the mechanical properties such as microhardness and surface roughness were measured by microhardness tester and profilometer, respectively. The wear tribometer was used to analyze the tribology of the coatings by varying different parameters. The different loading conditions used were low load (0.5 kgf), moderate load (1.0 kgf), and elevated load (1.5kgf), respectively. The microhardness showed a slight increase with an increase in the percentage of CNTs proportion. Similarly, the surface roughness value showed a decreasing trend, since the CNTs were filled in the pores. From wear tests, it was observed that the coefficient of friction and wear rate were very less at 6wt% CNTs and 1.5kgf load. This was mainly due to the bridging of CNTs in between the splats. This implies that CNTs were one of the most suitable additives for improving the microstructural and tribological characterization of the ceramic coatings.
N. Akhlaghi, G. Najafpour, M. Mohammadi,
Volume 17, Issue 4 (12-2020)
Abstract
Modification of MnFe2O4@SiO2 core-shell nanoparticles with (3-aminopropyl) triethoxysilane (APTES) was investigated. The magnetite MnFe2O4 nanoparticles with an average size of ~33 nm were synthesized through a simple co-precipitation method followed by coating with silica shell using tetraethoxysilane (TEOS); that has resulted in a high density of hydroxyl groups loaded on nanoparticles. The prepared MnFe2O4@SiO2 nanoparticles were further functionalized with APTES via silanization reaction. For having suitable surface coverage of APTES, controlled hydrodynamic size of nanoparticles with a high density of amine groups on the outer surface, the APTES silanization reaction was investigated under different reaction temperatures and reaction times. Based on dynamic light scattering (DLS) and zeta potential results, the best conditions for the formation of APTES-functionalized MnFe2O4@SiO2 nanoparticles were defined at a reaction temperature of 70 °C and the reaction time of 90 min. The effectiveness of our surface modification was established by X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), Fourier transforms infrared spectroscopy (FTIR), and vibrating sample magnetometer (VSM). The prepared magnetite nanostructure can be utilized as precursors for synthesizing multilayered core-shell nanocomposite particles for numerous applications such as medical diagnostics, drug, and enzyme immobilization, as well as molecular and cell separation.
R.s Krishna, J. Mishra, A. Adeniji, Sh. Das, S. Mohammed Mustakim,
Volume 17, Issue 4 (12-2020)
Abstract
The field of nanomaterial has greatly advanced in the last decade following a wider range of applications in the fields of electronics, automobiles, construction, and healthcare due to its extraordinary and ever-evolving properties. Synthesis of the nanomaterial plays a crucial role in redefining the current engineering and science field. At the same time, procuring an environment-friendly end product through eco-friendly solutions and sustainable processes is the key to many global problems. Green synthesis of nanomaterials like graphene and its derivatives involves mild reaction conditions and nontoxic precursors because it is simple, cost-effective, relatively reproducible, and often results in more stable materials. This paper primarily focuses on the green synthesis of graphene and its derivatives (graphene oxide & reduced graphene oxide) and geopolymers; a green technology for preparing graphene reinforced geopolymer composites. Various methods used globally for green synthesis of graphene and geopolymer are briefly discussed and this paper tries to integrate these two areas for a green end product. Possible applications of these green composites are also discussed to provide insights on the current growth and developments.
Z. Abasali Karaj Abad, A. Nemati, A. Malek Khachatourian, M. Golmohammad,
Volume 17, Issue 4 (12-2020)
Abstract
The graphene oxide -TiO2 (GO-TiO2) and pre-reduced graphene oxide -TiO2 (rGO-TiO2) nanocomposites were fabricated successfully by hydrothermal method. The microstructure of synthesized nanocomposites was investigated using field emission scanning electron microscopy (FESEM) equipped with energy dispersive spectroscopy (EDS) analysis. Moreover, galvanostatic charge/discharge (GCD), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) methods in three electrode system were applied to evaluate electrochemical properties. The results revealed that nanoparticles distributed more uniformly on graphene sheets, at lower concentrations of TiO2. The rGO-TiO2 and GO-TiO2 nanocomposites showed 224 and 32 F/g specific capacitance at 5 mV s-1 scan rate in 1 M KOH aqueous electrolyte, respectively. The pre-reduction of graphene oxide is the main reason for the better electrochemical performance of rGO-TiO2 nanocomposite compared to GO-TiO2 nanocomposite.
S. M. Alduwaib, Muhannad M. Abd,
Volume 17, Issue 4 (12-2020)
Abstract
Graphene oxide thin layers, graphene oxide:silver nano-composite, graphene oxide:zinc oxide nano-composite and graphene oxide:zinc oxide/graphene oxide:silver bilayer were deposited by spray pyrolysis method. The synthesized thin layers were characterized using X-ray diffraction spectroscopy, field emission scanning electron microscope, energy dispersive x-ray spectroscopy and Raman spectroscopy. The optical properties and the band gap of the thin layers were also studied and calculated using the Tauc equation. Gram-negative bacterium of Escherichia coli was used to study the antibacterial properties of thin layers. The results showed that among the thin layers investigated, GO:ZnO/GO:Ag bilayer had the greatest effect on the inhibition of E. coli growth and was able to control the growth of bacterium after 2 hours.
Mohammad Ali Maghsoudlou, Reza Barbaz Isfahani, Saeed Saber-Samandari, Mojtaba Sadighi,
Volume 18, Issue 2 (6-2021)
Abstract
The low velocity impact (LVI) response of pure and glass fiber reinforced polymer composites (GFRP) with 0.1, 0.3 and 0.5 wt% of functionalized single-walled carbon nanotubes (SWCNTs) was experimentally investigated. LS-DYNA simulation was used to model the impact test of pure and incorporated GFRP with 0.3 wt% of SWCNT in order to compare experimental and numerical results of LVI tests. All tests were performed in two different levels of energy. In 30J energy, the specimen containing 0.5 wt% SWCNT was completely destructed. The results showed that the incorporated GFRP with 0.3 wt% SWCNT has the highest energy absorption and the back-face damage area of this sample was smaller than other specimens. TEM images from specimens were also analyzed and showed the incorporation of well-dispersed 0.1 and 0.3 wt% of SWCNT, while in specimens containing 0.5 wt% of CNT, tubes tended to be agglomerated which caused a drop in LVI response of the specimen. The contact time of impactor in numerical and experimental results was approximately equal; however, the maximum contact forces in LS DYNA simulation results were higher than the experimental results which could be due to the fact that in the numerical modeling, properties are considered ideal, unlike in experimental conditions.
Mohammed Ruhul Amin Bhuiyan, Hayati Mamur,
Volume 18, Issue 3 (9-2021)
Abstract
Carbon-based chemical substances persistence can contribute to adverse health impacts on human lives. It is essential to overcome for treatment purposes. The semiconducting metal oxide is Zinc Oxide (ZnO), which has excellent biocompatibility, good chemical stability, selectivity, sensitivity, non-toxicity, and fast electron transfer characteristics. The ZnO nanoparticles are more efficient compared to other metal oxide materials. Thus, the nanoparticles are in the present research situation to receive increasing attention due to their potential performance of the human body to feel comfortable. The nanoparticles become more promising for biomedical applications through the development of anticancer agents to recovery different types of malignant cells in the human body. The ZnO nanoparticles can be the future potential materials for biomedical applications. The purpose of this paper is to review the cost-effective approach to synthesize the ZnO nanoparticles. Moreover, these ideas can develop for synthesized ZnO biomaterial to perform easily up-scaled in biomedical applications.
Amirhosein Paryab, Toktam Godary, Sorosh Abdollahi, Mohsen Anousheh, Adrine Malek Khachatourian,
Volume 18, Issue 3 (9-2021)
Abstract
Silicon oxycarbide (SiOC) materials derived from silicone attracted great attention for their superior high-temperature behavior. In the present study, Si(Ti)OC and Si(Ti,Al)OC nanocomposites, in which alkoxide precursors were used with the main silicone precursor, have been compared with SiOC material. Although in SiOC, C was bonded with Si in a carbon-rich SiOC phase, X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) showed that TiC was the preferred state for C atoms upon adding Ti into the system. This claim was also substantiated by Raman spectroscopy, where adding Ti into the system lowered the intensity of the D band, indicating the high affinity of C to form crystalline TiC. In the Si(Ti,Al)OC nanocomposites synthesized by adding AlCl3 into the Si(Ti)OC system, mullite nanocrystals formed a superlattice structure with TiC. UV-vis spectra of the nanocomposites showed Si(Ti,Al)OC with mullite-TiC superlattice had a larger bandgap compared with Si(Ti)OC with only TiC nanocrystals.
Farideh Golbabaie, Somayeh Farhang Dehghan, Majid Habibi Mohraz, Elham Akhlaghi Pirposhteh,
Volume 18, Issue 4 (12-2021)
Abstract
The present study aims to investigate the role of the electrostatic mechanism in the filtration process of Polyacrylonitrile nanofibers containing single-walled carbon nanotube. The nanofibers were fabricated via electrospinning using 16wt% Polyacrylonitrile polymer (PAN) solution, single-wall carbon nanotubes (SWNT) at a ratio of 99:1 along with N and N-Dimethylformamide solvents. Initial filtration efficiency was tested as per ISO 29463:2011 standard inside a test rig. An electrostatic discharge test was performed via the chemical treatment of the filter media with Isopropyl alcohol in accordance to EN779 standard. Mean initial filtration efficiency of the nanofiber media in the capturing of 100nm and 200nm particles were 95.92% ±2.74 and 97.26% ±1.11 respectively, while for particles between 80nm to 250nm, this was 96.73% ±2.74. The efficiency of the untreated media was 0.2% to 1.2% higher than the PAN/SWNT media after electron discharge using Isopropyl alcohol with an even bigger difference being observed at lower particle size ranges. After treatment with Isopropyl alcohol, the pressure drop of the filtration media was increased from 164.7 Pa to 185.3 Pa. The reduction in filtration efficiency observed after the electrostatic discharge test indicates that the electrical charge of the electrospun nanofibers is influential in its initial efficiency for removing the submicron particles.
Mohammad Jafaripour, Hassan Koohestani, Behrooz Ghasemi,
Volume 18, Issue 4 (12-2021)
Abstract
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.
Parviz Parviz Mohamadian Samim, Arash Fattah-Alhosseini, Hassan Elmkhah, Omid Imantalab,
Volume 19, Issue 1 (3-2022)
Abstract
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.
Tashi Tenzin, Amrinder Kaur,
Volume 19, Issue 2 (6-2022)
Abstract
Green synthesis refers to the synthesis of nanoparticles using plants and microorganisms. It is preferred over conventional methods as its sustainable, eco-friendly, cost effective and rapid method. The phytochemicals and enzymes present in plants and microorganisms respectively acts as the reducing and capping agent for the synthesis of nanoparticles. Phytochemicals and enzymes have the ability to reduce precursor metal ions into nanoparticles. As the conventional methods involve the use of high energy and toxic chemicals which are harmful to both environment and organisms, these synthesis methods are discouraged. Of the nanoparticles, gold nanoparticles (AuNPs) and silver nanoparticles (AgNPs) have gained lots of attention owing to their multiple applications and less toxicity. In addition, various in-vitro studies have reported the antimicrobial activity of AgNPs and AuNPs against various microbes. This particular review portrays the methods of nanoparticles synthesis, components of green synthesis, mechanism of green synthesis, antimicrobial activity, other applications and various factors affecting the green synthesis of AgNPs and AuNPs.
Fiza Ur Rehman, Syeda Sohaila Naz, Muhammad Junaid Dar, Annum Malik, Maimoona Qindeel, Francesco Baino, Fazli Wahid, Abbas Rahdar, Saeeda Munir, Sara Qaisar, Kifayat Ullah Shah, Mahtab Razlansari,
Volume 19, Issue 2 (6-2022)
Abstract
Neoplastic cells have co-opted inflammatory receptors and signaling molecules that potentiate inflammation. Activated inflammatory pathways lead to neo-angiogenesis, lymph-angiogenesis, immunosuppression, tumor growth, proliferation and metastasis. This cancer-sustaining inflammation is a critical target to arrest cancer growth. Multiple drug resistance, high cost, low oral bioavailability and serious side effects have rendered conventional cytotoxic chemotherapeutics less impressive. The aim of this research was to achieve cancer debulking and proliferation prevention by limiting ‘cancer-sustaining’ tumor niche inflammation through non-conventional oral approach employing anti-inflammatory agents and avoiding conventional cytotoxic agents. Synergistic anti-inflammatory agents, i.e. celecoxib as selective COX-2 inhibitor and montelukast as cysteinyl leukotriene receptor antagonist, were selected. Silver nanoparticles (AgNPs) were used as nanocarriers because of their efficient synergistic anti-neoplastic effects and excellent oral drug delivery potential. Specifically, selected drugs were co-conjugated onto AgNPs. Synthesized nanoparticles were then surface-modified with poly(vinyl alcohol) to control particle size, avoid opsonization/preferred cellular uptake and improve dispersion. Surface plasmon resonance analysis, particle size analysis, DSC, TGA, XRD, FTIR and LIBS analysis confirmed the successful conjugation of drugs and efficient polymer coating with high loading efficiency. In-vitro, the nanoparticles manifested best and sustained release in moderately acidic (pH 4.5) milieu enabling passive tumor targeting potential. In-vivo, synthesized nanoparticles exhibited efficient dose-dependent anti-inflammatory activity reducing the dose up to 25-fold. The formulation also manifested hemo-compatibility, potent anti-denaturation activity and dose-dependent in-vitro and in-vivo anti-cancer potential against MCF-7 breast cancer and Hep-G2 liver cancer cell lines in both orthotopic and subcutaneous xenograft cancer models. The anti-inflammatory nanoparticles manifested tumor specific release potential exhibiting selective cytotoxicity at cancerous milieu with slightly acidic environment and activated inflammatory pathways. The formulation displayed impressive oral bioavailability, sustained release, negligible cytotoxicity against THLE-2 normal human hepatocytes, low toxicity (high LD50) and wide therapeutic window. Results suggest promise of developed nanomaterials as hemo-compatible, potent, cheaper, less-toxic oral anti-inflammatory and non-conventional anti-cancer agents.
Pooyan Soroori, Saeid Baghshahi, Arghavan Kazemi, Nastaran Riahi Noori, Saba Payrazm, Amirtaymour Aliabadizadeh,
Volume 19, Issue 3 (9-2022)
Abstract
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 149o. 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.
