Showing 22 results for Nanoparticles
R. Lotfi Orimi, V. Asghari , M. Lashkarbolouki,
Volume 30, Issue 1 (6-2011)
Abstract
ZnS nanoparticles were synthesized by chemical precipitation method. As-prepared ZnS nanoparticles were found to be stabilized in the form of cubic phase. Cubic to hexagonal structural transformation was studied using X-ray diffraction (XRD). The effect of annealing temperature (100-700 ) on the band gap, particle size, and structural phase was investigated. Photoluminescence studies indicated two strong and narrow emission peaks in blue and orange regions. These two strong and narrow emission peaks were shifted to blue and red regions by increasing the annealing temperature..
M.tahriri, F. Moztarzadeh, M. Raz , M. Ashuri,
Volume 32, Issue 1 (6-2013)
Abstract
In this study, magnetite (Fe3O4) nanoparticles were synthesized by chemical co-precipitation from the solution containing iron salts in alkaline medium under N2 gas and room temperature. Magnetite nanoparticles were characterized by X- ray diffraction (XRD), Fourier transform infrared spectrometer (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermal gravimetric analysis (TGA), differential thermal analysis (DTA), Brunauer-Emmet-Teller (BET), and vibrating-sample magnetometer (VSM). The rheological properties of magnetite ferrofluid were examined by rheology apparatus. The biocompatibility and cytotoxity of magnetite nanoparticles were evaluated by 3T3 and fibroblast cells. The results showed that the Fe3O4 magnetite nanoparticles coated by polyvinyl alcohol (PVA) could be an appropriate candidate for biomedical applications.
H.r. Salehi, S. Salami, M. Atarian, O. Ozhdelnia,
Volume 32, Issue 1 (6-2013)
Abstract
Carbon fiber composite is one of the most important materials in aerospace engineering applications. For fabrication of this composite, optimum polymerization and carbonization cycles of phenolic resin were obtained [1]. Then, carbon/phenolic composite was fabricated by mixing different weight percentages of T700 carbon fiber with phenolic resin, and the flexural strength of specimens was examined.The samples were pyrolyzed at 1100°C to form high temperature phenolic matrix. Because of high porosity of samples, the composite was impregnated to increase the density and reduce porosity. The maximum flexural strength of samples was obtained with 40 wt. % of fiber. With addition of TiO2 and ZrO2 nanoparticles to carbon/phenolic composite, thermal and mechanical improvement was measured. The samples were examined by ablation test and microstructures of composites were analyzed by SEM.
F.s. Sayyedan, M.h. Fathi, H. Edris, A. Doostmohamadi, V.s., Mortazavi, F. Shirani,
Volume 33, Issue 3 (3-2015)
Abstract
The objective of this study was to synthesize glass ionomer–forsterite nanocomposite and study the effect of
incorporating forsterite nanoparticles to the ceramic part of glass ionomer cement in order to improve mechanical properties and
bioactivity. So, Forsterite nanoparticles were made by the sol-gel process using different weight percentages added to the ceramic
part of commercial GIC (Fuji II GC). X-ray diffraction (XRD) was used in order to characterize and determine grain size of the
produced forsterite nanopowder. In order to study the mechanical properties of the produced glass ionomer cement-forsterite
nanocomposite, the compressive strength (CS), three-point flexural strength (FS) and diametral tensile strength (DTS) of
specimens were measured. Statistical analysis was done by one Way ANOVA and differences were considered significant if
P‹0.05. The morphology of fracture surface of specimens was studied using scanning electron microscopy (SEM) technique.
Bioactivity of specimens was investigated by Fourier transitioned-infrared spectroscopy (FTIR), scanning electron microscopy
(SEM), and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). The results of XRD analysis confirmed the
nanocrystalline and pure forsterite synthesis. According to the mechanical properties measurements, the optimum weight
percentages of forsterite nanoparticles for enhancement of CS, FS, and DTS were obtained equal to 3, 1 and 1 wt.%, respectively.
Statistical analysis showed that the differences between all the groups were significant (P<0.05). SEM images and results of the
ICP-OES and FTIR tests confirmed the bioactivity of the nanocomposite. Glass ionomer-forsterite nanocomposite containing 1 to
3 wt.%-forsterite nanoparticles can be a suitable candidate for dentistry and orthopedic applications due to the improvement of
mechanical properties and bioactivity.
R. Nayerhoda, F. Asjadi, P. Seifi, M. Salimi,
Volume 34, Issue 1 (5-2015)
Abstract
In the present investigation, spherical nanoparticles of nickel ferrite with uniform structure were successfully produced by hydrothermal method in the presence of polyethylene glycol (PEG) as a polymeric surfactant at 180°C for 12 hour aging time and the effects of the synthesis time, temperature and surfactant were investigated. According to the X-ray analysis, conversion of nickel oxide and hematite to nickel ferrite was a way to produce NiFe2O4. At 140°C, agglomerated particles without specific shape were formed, but at 180°C particles were homogenous with spherical shape. Saturation magnetization increased by increasing the hydrothermal process aging time.
M.r. Saeri, M. Azizi1, R. Amooaghaie,
Volume 34, Issue 4 (3-2016)
Abstract
Bio-inspired silver nanoparticles were synthesized with the aid of a novel method, using leaves of the plant Nigella sativa. After drying the leaves in air, they were first sweltered in boiling distilled water and the liquid was filtered subsequently. The result was the brothused to reduce solutions including various concentrations of silver nitrate in a proper amount of pH. The displayed UV–visible spectra identified formation of silver nanoparticles whenever the colorless initial acclimated mixture turned brown. The centrifuged powder samples were examined using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (FESEM) and energy dispersive X-ray diffraction analysis (EDX) methods. The results clearly revealed that the final particles of precipitated powder are high purity agglomerates of silver nanoparticles. Besides, the effects of various amounts of the silver salt on particle size of nano silver were studied, using a particle size analyzer. FTIR results also indicated the role of different functional groups in the synthetic process.
S. Nikbakht Katouli, A. Doostmohammadi, F. Esmaeili,
Volume 35, Issue 1 (6-2016)
Abstract
The aim of this study was to fabricate carbon nanotube (CNT) and bioactive glass nanoparticles (BG) (at levels of
5 and 10 wt%) incorporated electrospun chitosan (CS)/polyvinyl alcohol (PVA) nanofibers for potential neural tissue engineering applications.The morphology, structure, and mechanical properties of the formed electrospun fibrous mats were characterized using scanning electron microscopy (SEM) and mechanical testing, respectively. In vitro cell culture of embryonal carcinoma stem cells (P19) were seeded onto the electrospun scaffolds. The results showed that the incorporation of CNTs and BG nanoparticles did not appreciably affect the morphology of the CS/PVA nanofibers. The maximum tensile strength (7.9 MPa) was observed in the composite sample with 5 %wt bioactive glass nanoparticles. The results suggest that BG and CNT-incorporated CS/PVA nanofibrous scaffolds with small diameters, high porosity, and promoted mechanical properties can potentially provide many possibilities for applications in the fields of neural tissue engineering and regenerative medicine.
M. Rezazadeh, M.r. Saeri, F. Tirgir Malkhlifeh, A. Doostmohammdi,
Volume 35, Issue 2 (9-2016)
Abstract
The aim of the present study is to study the effects of adding diopside (CaMgSi2O6) as well as silica sulfuric acid nanoparticles to ceramic part of glass ionomer cement (GIC) in order to improve its mechanical properties. To do this, firstly, diopside (DIO) nanoparticles with chemical formula of CaMgSi2O6 were synthesized using sol-gel process and then, the structural and morphological properties of synthesized diopside nanoparticles were investigated. The results of scanning electron microscopy (SEM) and particle size analyzing (PSA) confirmed that synthesized diopside are nanoparticles and agglomerated. Besides, the result of X-ray diffraction (XRD) analyses approved the purity of diopside nanoparticles compounds. Silica sulfuric acid (SSA) nanoparticles are also prepared by chemical modification of silica nanoparticles by means of chlorosulfonic acid. Fourier transform infrared spectroscopy (FTIR) technique was used to find about the presence of the (SO3H) groups on the surface of silica sulfuric acid nanoparticles. Furthermore, various amounts (0.1, 3 and 5 wt.%) of diopside and silica sulfuric acid nanoparticles were added to the ceramic part of GIC (Fuji II GIC commercial type) to produce glass ionomer cement nanocomposites. The mechanical properties of the produced nanocomposites were measured using the compressive strength, three-point flexural strength and diametral tensile strength methods. Fourier transform infrared spectroscopy technique confirmed the presence of the (SO3H) groups on the surface of silica nanoparticles. The compressive strength, three-point flexural strength and diametral tensile strength were 42.5, 15.4 and 6 MPa, respectively, without addition. Although adding 1% silica solfonic acid improved nanocomposite mchanical properties by almost 122%, but maximum increase in nanocomposite mechanical properties was observed in the nanocomposites with 3% diposid, in which 160% increase was seen in the mechanical properties.
P. Mouchani, R. Sarraf Mamoori, N. Riahi Noori,
Volume 35, Issue 4 (2-2017)
Abstract
In this study, the parameters affecting the synthesis of silver nanoparticles were optimized by green chemical reduction method to make a conductive pattern. The raw materials used in this study, include silver nitrate as a source of
silver ions, polyvinylpyrrolidone as surface stabilizer, and glucose as the reducing agent. Effective parameters were investigated
by Taguchi statistical design, to determine the optimum conditions and achieve the smallest average particle size. Silver nanoparticles were characterized by X-ray diffraction and field emission scanning electron microscopy. The smallest particle size can be applied by solution adding rate of 0.1 ml/min, temperature 90 °C, weight ratio of glucose to silver nitrate 3 g/g and weight ratio of Polyvinylpyrrolidone to silver nitrate 3.2 g/g. According to.our expectation 20 nm silver nanoparticles were obtained in this condition. FE-SEM confirmed the above results and showed nanoparticles with a size of 25 nm. Finally, A conductive pattern was printed on a glass substrate with synthesized powder. The electrical resistance of the printed pattern was 0.088× 10 -4 Ω.cm.
A. Rostamnejadi, M. K. Esmaeilzadeh,
Volume 36, Issue 3 (11-2017)
Abstract
In this research, nanoparticles of La0.8Sr0.2MnO3 with mean crystallite size of 20 nm have been prepared by sol gel method. The sample has been characterized by X-Ray Diffraction (XRD) using Rietveld refinement, Field Emission Scanning Electron Microscope (FESEM) and Fourier Transform Infrared (FTIR) spectroscopy. The static magnetic properties such as saturation magnetization, effective magnetic moment and ferromagnetic phase fraction of the nanoparticles are determined by different techniques using magnetic hysteresis loop at room temperature. The magnetic dynamic properties of crystalls are studied by measuring AC magnetic susceptibility versus temperature at different frequencies. Néel-Brown, Vogel-Fulcher, critical slowing down models and empirical parameters are used to distinguish between superparamagnetic and superspin glass behaviour in the nanoaprticles. By fitting the experimental data with the models, relaxation time, critical view, magnetic anisotropy energy and effective magnetic anisotropy constant have been estimated. The obtained results support the presence of interacting superparamagnetic behaviour between magnetic nanoparticles of La0.8Sr0.2MnO3.
S. Yousefi, B. Ghasemi, M. Tajalli, A. Asghari,
Volume 36, Issue 4 (3-2018)
Abstract
In this paper, high purity magnesium hydroxide nanoplates were successfully synthesized by using brine rich in magnesium ions as precursor and NaOH as precipitating agent without using dispersant agent in the room temoerature. The study and characterization of various properties of obtained nanopowder was carried out by X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive X-ray Fluorescence Spectrometer (EDX), Fourier Transform Infrared Spectrophotometer (FTIR) and Ultraviolet–visible spectroscopy (UV-Vis). The FESEM and XRD analysis results showed that magnesium hydroxide powder had nanoplates with the average crystallite size 17.1nm and no impurity; that was in agreement with the result of EDX and FTIR perfectly. Furthermore, optical characteristics of magnesium hydroxide nanoplates by UV-Vis spectroscopy showed an optical band gap of 5.5 eV. This wide band gap can be a useful innovation in optoelectronic sub-micron devices.
E. Shirani, A. Razmjou,
Volume 36, Issue 4 (3-2018)
Abstract
The significance of producing superhydrophobic surfaces through modification of surface chemistry and structure is in preventing or delaying biofilm formation. This is done to improve biocompatibility and chemical and biological properties of the surface by creating micro-nano multilevel rough structure; and to decrease surface free energy by Fault Tolerant Control Strategy (FTCS) . Here, we produced a superhydrophobic surface through TiO2 coating and flurosilanization methods. Then, in order to evaluate the physicochemical properties of the modified surfaces, they were characterized by Scanning Electron Microscope (SEM), Fourier Transform Infrared Spectroscopy (FTIR), Contact Angle (CA), cell viability assay (using Hela and MCF-7 cancer cell lines as well as non-cancerous human fibroblast cells) by MTT, Bovine Serum Abumin (BSA) protein adsorption using Bradford and bacterial adhesion assay (Staphylococcus aureus and Staphylococcus epidermidis) using microtiter. Results showed that contact angle and surface energey of superhydrophobic modified surface increased to 150° and decreased to 5.51 mj/m2, respectively due to physicochemical modifications of the surface. In addition, the results showed a substantial reduction in protein adsorption and bacterial cell adhesion in superhydrophobic surface.
Sh. Tavakoli Dehaghi, S. Darvishi, Sh. Nemati, M. Kharaziha,
Volume 37, Issue 3 (12-2018)
Abstract
Abstract: With the advances in the development of biomaterials for tissue replacement, the attention of scientists has been focused on the improvement of clinical implant properties. In this regard, despite the appropriate properties of the stainless steel, the application of stainless steel as implants has been limited due to the weak corrosion resistivity. The purpose of this paper was preparation and characterization of hydrophobic polydimethylsiloxane (PDMS)-SiO2-CuO nanocomposite coating on the 316L stainless steel surface. The 316L stainless steel was coated by SiO2 nanoparticles (20 wt. %), CuO nanoparticles (0.5, 1 and 2 wt. %) and biocompatible PDMS. In this research, x-ray diffraction (XRD) and scanning electron microscopy (SEM) were applied to characterize the coating. Moreover, the roughness and water contact angle of the coatings consisting of various amounts of CuO nanopowder were estimated. Finally, the effects of various amounts of the CuO nanopowder on the corrosion resistivity of nanocomposite coatings were investigated. XRD patterns confirmed the presence of crystalline CuO nanoparticles on the substrate. Due to the non-crystalline nature of silica nanoparticles and the semi-crystalline PDMS polymer, no peak confirming the presence of these phases was detected on the XRD pattern of the nanocomposite coating. SEM images showed the formation of a lotus leaf-like layer on the surface of the nanocomposite coating containing 1 and 2 wt. % CuO. Moreover, water contact angle evolution revealed that while contact angle was 81 degree without CuO nanoparticles, it was enhanced to 146 degree in the presence of 1 wt. % CuO. Moreover, the corrosion study showed the nanocomposite containing 2 wt.% CuO had the best corrosion resistance, the corrosion current density of 2.1E-7 A.cm-2, and the corrosion potential of 0.22 V.
A. Razmjou, F. Noorisafa, N. Emami,
Volume 37, Issue 4 (3-2019)
Abstract
Polyurethane polymer plays an important role in health care, and it is widely used in medical devices and instruments. However, the low biocompatibility and biofilm formation on the surface can be regarded as a challenging issue. Engineering the wetting capability of the surface is an effective way to increase the biodegradability of polymer surfaces with sufficient bulk properties. In this study, the surface modification of polyurethane sheets by a thin layer of polyethylene glycol and trapping of titanium dioxide nanoparticles were carried out by means of physical and chemical changes on the surface to enhance the biocompatibility. The physicochemical properties of the modified surfaces were determined using fourier-transform infrared (FTIR) spectroscopy , scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and contact angle and free surface energy measurement. The biocompatibility of the modified levels was evaluated using the MTT toxicity test on cervical cancer cells (HeLA), bacterial adhesion, biofilm formation, and the protein absorption assay by the Bradford method. A thin, autoclave able and inexpensive thin layer with a solid and stable roughening structure was created covalently on the surface of the polyurethane plates for biological and medical applications. The results, therefore, showed that apart from antibacterial activity, the modified sample also had the ability to reduce the biofilm formation, such that the maximum biofilm attachment inhibition in the first 24 hours was 94% higher than that of the modified sample.
F. Mohammadi Bodaghabadi, M. R. Loghman Estarki, M. Ramazani, A. Alhaji,
Volume 38, Issue 3 (12-2019)
Abstract
In this research, synthesis of lithium fluoride (LiF) nanoparticles by fluorolytic sol-gel method has been studied. Moreover, the effect of lithium ion to fluorine source molar ratio and calcination temperature on particle size and phase of LiF nanoparticles were investigated. Lithium acetate (C2H3LiO2), trifluoroacetic acid (TFA), ethylene glycol monobutyl ether and oleic acid were used as sources of Li+ and F- ions, solvent and growth inhibitor, respectively. Thermal and X-ray diffraction (XRD) analyses as well as field emission scanning electron microscopy (FESEM) were used to investigate thermal behavior of the primary gel and to determine the phase and morphology of samples, respectively. The results showed that the 2: 1 molar ratio of Li+/ TFA and the calcination temperature of 400 °C result in LiF nanoparticles with a mean particle size of 80-100 nm.
F. Davar, Z. Enteshari,
Volume 39, Issue 1 (5-2020)
Abstract
In this research, Zinc oxide nanoparticles with semi-spherical morphology were synthesized by modified sol-gel method using rosemary extract as a stabilizing agent. The effect of the amount of rosemary extract and calcination temperature on size and shape of the particles was investigated. The samples were characterized by X-ray diffraction (XRD), infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and elemental analysis (EDX). X-ray diffraction results showed hexagonal structure (wurtzite phase) of zinc oxide. According to the SEM results semi-spherical nanoparticles of 18 nm in size were obtained using 75 ml of rosemary extract. The photocatalytic activity of the modified ZnO nanoparticles was investigated for degradation of the methylene blue dye solution. The results showed 96.87% of dye degradation in the 135 min that confirmed suitable efficiency of as-synthesized nanoparticles in the photocatalytic degradation process of dyes.
A. H. Kianfar, N. Eskandari, M. A. Arayesh,
Volume 39, Issue 2 (8-2020)
Abstract
In this research the synthesis of [Co(Salen)(PPh3)(H2O)]4[Fe(CN)6] and [Co(Salophen)(PPh3)(H2O)]4[Fe(CN)6] schiff base complexes was reported. Co3O4/CoFe2O4 magnetic nanoparticles were prepared by calcination of these complexes at 500, 550 and 600°C. Precursor complexes were identified by FT-IR and UV-Vis spectroscopy and their thermal behavior was studied via TG/DTA. Nanomagnetic samples were characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), and Fourier Transform Infrared Spectroscopy (FT-IR). Magnetic properties of the synthesized nanoparticles were studied using Vibrating Sample Magnetometer (VSM). Magnetic parameters such as saturation magnetization (Ms), remanent magnetization (Mr), coercive field (Hc) and squareness ratio (SQ = Mr/Ms) were determined at room temperature. Stoichiometry and approximate composition of the prepared samples were studied by Electron Diffraction X-ray spectroscopy (EDX). The prepared nanocomposites could be useful in some practical applications due to their high magnetization, good chemical stability and dispersion.
T. Rajabi, M. Vahedi, S. K. Sadrnezhaad,
Volume 39, Issue 2 (8-2020)
Abstract
Zinc/zinc oxide nanoparticles are used in an increasing number of medical and industrial applications due to their attractive physical, chemical and antibacterial properties. Therefore, achieving a simple and beneficial way to produce them is an important aspect. In this study, zinc/zinc oxide nanopowders were synthesized by fast electric discharges between two electrodes of (a) a spark device in distilled water medium and (b) a handmade high-voltage ignition machine in argon gas medium. The resulting powders were characterized by x-ray diffraction (XRD), dynamic light scattering (DLS) and field emission electron microscopy (FESEM). Using the spark device in distilled water, a mixture of zinc crystals with an average diameter of 11.28 nm and zinc oxide crystals with an average diameter of 22.22 nm was produced. However, using the handmade device in argon, zinc crystals with an average diameter of 7.5 nm were obtained and subsequently oxidized due to their extremely high activity. The production rate of the high voltage discharge method was lower than other conventional methods. On the other hand, its ability in reducing the size and increasing the particle activity was higher than other methods.
A. Zamani, M. R. Loghman Estraki, S. R. Hosseini, M. Ramezani, A. Al-Haji,
Volume 39, Issue 3 (12-2020)
Abstract
The aim of the study was to investigate the effect of temperature, time, pH, capping agent concentration (mercaptoacetic acid), Zn to Se and Se to reducing agent (NaBH4) mole ratios on morphology, phase developments and size of zinc selenide nanoparticles prepared by hydrothermal method. Characterization of zinc selenide nanoparticles was performed by Field Emission Electron Microscopy (FESEM), Energy Dispersive X-ray Spectrometry (EDS), X-ray Diffraction (XRD), Induced Coupled Plasma Spectrometry (ICP), Fourier Transform Infrared spectroscopy (FTIR) and Simultaneous Thermal Analysis (STA). The results of EDS showed that the ratio of atomic percentage of Zn to Se in the optimized zinc selenide nanoparticles is 1: 1 and elements are evenly distributed in the nanoparticles. Based on the results of FTIR and STA thermal analyses, MAA as the stabilizing agent binds to and stabilizes zinc selenide nanoparticles. Finally, fine nanoparticles of zinc selenide with narrow size distribution, spherical shape and cubic crystal structure were obtained at the minimum temperature (130 °C) and processing time (15 hours) with the least amount of reducing and capping agents compared to previous researches.
S. Borhani Esfahani, H. R. Salimi Jazi, M. H. Fathi, A. Ershad Langroudi, M. Khoshnam,
Volume 40, Issue 1 (5-2021)
Abstract
In this research, a kind of environmentally-friendly inorganic-organic hybrid nanocomposite coating based on silica containing titania/silica core/shell nanoparticles was synthesized and characterized for conservation of facade tiles in historical buildings. The matrix of the composite was prepared by sol-gel process via two methods of ultrasonic and reflux stirring. Tetraethyl orthosilicate (TEOS) and poly-dimethyl siloxane hydroxy-terminated (PDMS-OH) were used for the formation of silica network and creation of flexibility and hydrophobicity, respectively. Titania nanoparticles were used in the form of titania/silica core/shell as ultraviolet absorber. The synthesized nanocomposite was applied on the microscope slides and tiles by dip coating technique. The properties of nanoparticles and coatings were characterized by Fourier-transform infrared spectroscopy (FTIR), Transmission electron microscopy (TEM) and water contact angle measurement. The results revealed that formation of titania/silica core/shell structure was successful. The investigation of PDMS content effect on transparency, cohesion and hydrophobicity of the coating confirmed that the optimum content of this siloxane was around 20 wt.%. In general, the results showed that the silica-based hybrid nanocomposite reinforced with TiO2/SiO2 core/shell nanoparticles could produce a transparent and hydrophobic coating for tile and glass protection.
