Pub Date : 2016-04-15DOI: 10.4236/WJNSE.2016.62009
M. Zaydan, Naoufal Yadil, Z. Boulahia, Abderrahim Wakif, R. Sehaqui
In the present work, we numerically study the laminar natural convection of a nanofluid confined in a square cavity. The vertical walls are assumed to be insulated, non-conducting, and impermeable to mass transfer. The horizontal walls are differentially heated, and the low is maintained at hot condition (sinusoidal) when the high one is cold. The objective of this work is to develop a new height accurate method for solving heat transfer equations. The new method is a Fourth Order Compact (F.O.C). This work aims to show the interest of the method and understand the effect of the presence of nanofluids in closed square systems on the natural convection mechanism. The numerical simulations are performed for Prandtl number ( ), the Rayleigh numbers varying between and for different volume fractions varies between 0% and 10% for the nanofluid (water + Cu).
{"title":"Fourth-Order Compact Formulation for the Resolution of Heat Transfer in Natural Convection of Water-Cu Nanofluid in a Square Cavity with a Sinusoidal Boundary Thermal Condition","authors":"M. Zaydan, Naoufal Yadil, Z. Boulahia, Abderrahim Wakif, R. Sehaqui","doi":"10.4236/WJNSE.2016.62009","DOIUrl":"https://doi.org/10.4236/WJNSE.2016.62009","url":null,"abstract":"In the present work, we numerically study the laminar natural convection of a nanofluid confined in a square cavity. The vertical walls are assumed to be insulated, non-conducting, and impermeable to mass transfer. The horizontal walls are differentially heated, and the low is maintained at hot condition (sinusoidal) when the high one is cold. The objective of this work is to develop a new height accurate method for solving heat transfer equations. The new method is a Fourth Order Compact (F.O.C). This work aims to show the interest of the method and understand the effect of the presence of nanofluids in closed square systems on the natural convection mechanism. The numerical simulations are performed for Prandtl number ( ), the Rayleigh numbers varying between and for different volume fractions varies between 0% and 10% for the nanofluid (water + Cu).","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70881282","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-04-15DOI: 10.4236/WJNSE.2016.62008
Mohamed I. Ebrahim, Mohamed Ahmed, Nayef H. Felemban
Adhesive layer is an essential part of tooth colored restorations which play an important role in decreasing the microleakage between the tooth and restoration material after polymerization shrinkage. The purpose of this study was to evaluate the effect of deferent adhesive system of bonding agent on microleakage of nanocomposite resin in class II cavities. Two different types of adhesive systems: universal adhesive (ExciTE) and a newly developed adhesive (Nano-Bond) and one type of light-cured resin restorative material (nanocomposite resin) were used in this study. These adhesives were applied to prepared tooth cavities by either manufactures’ instructions or by an experimental method (single or double application). Nanocomposite resin was then placed and light-cured for 40 seconds. Teeth were subjected to 500 thermal cycles between 5d microleakage was observed microscopically. The data were analyzed by a two-way ANOVA. For comparison between groups, Tukey’s post-hoc test was used. Nanoparticles reinforced adhesive system shows low microleakage in compare with universal adhesive system, and application of two adhesive layers also can decrease the microleakage. The ability of stress absorption by adhesive layer after polymerization shrinkage of restoration material will reduce the microleakage.
{"title":"Effect of Nanoparticles Reinforced Adhesive Layers on Microleakage of Tooth Restorations","authors":"Mohamed I. Ebrahim, Mohamed Ahmed, Nayef H. Felemban","doi":"10.4236/WJNSE.2016.62008","DOIUrl":"https://doi.org/10.4236/WJNSE.2016.62008","url":null,"abstract":"Adhesive layer is an essential part of tooth colored restorations which play an important role in decreasing the microleakage between the tooth and restoration material after polymerization shrinkage. The purpose of this study was to evaluate the effect of deferent adhesive system of bonding agent on microleakage of nanocomposite resin in class II cavities. Two different types of adhesive systems: universal adhesive (ExciTE) and a newly developed adhesive (Nano-Bond) and one type of light-cured resin restorative material (nanocomposite resin) were used in this study. These adhesives were applied to prepared tooth cavities by either manufactures’ instructions or by an experimental method (single or double application). Nanocomposite resin was then placed and light-cured for 40 seconds. Teeth were subjected to 500 thermal cycles between 5d microleakage was observed microscopically. The data were analyzed by a two-way ANOVA. For comparison between groups, Tukey’s post-hoc test was used. Nanoparticles reinforced adhesive system shows low microleakage in compare with universal adhesive system, and application of two adhesive layers also can decrease the microleakage. The ability of stress absorption by adhesive layer after polymerization shrinkage of restoration material will reduce the microleakage.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70881223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-04-15DOI: 10.4236/WJNSE.2016.62010
T. A. Sironmani
Nanotechnology has shown significant promise in development of drugs and drug delivery systems that can overcome all limitations and address urgent needs to improve efficacy of diagnosis and therapy of various diseases including cancer. The functionalization with neem compounds as synthesis and capping agent had shown very high anticancer activities against Gastric cancer cells in vitro. The biochemical factors like albumin, glucose, and DNA concentrations were modulated along with Protease inhibitor and Catalase activates, the various cancer specific proteins like p53, GRD 70 - 78 kDa and other proteins of sizes 35 - 40 kDa corresponding to H+K+ATPase protein etc. The apoptic activity and antiproliferative activity were demonstrated with Gastric cancer cells in vitro.
{"title":"Therapeutic Potential of Neem Synthesized Silver Nanoparticles on Human Gastric Cancer Cells in Vitro","authors":"T. A. Sironmani","doi":"10.4236/WJNSE.2016.62010","DOIUrl":"https://doi.org/10.4236/WJNSE.2016.62010","url":null,"abstract":"Nanotechnology has shown significant promise in development of drugs and drug delivery systems that can overcome all limitations and address urgent needs to improve efficacy of diagnosis and therapy of various diseases including cancer. The functionalization with neem compounds as synthesis and capping agent had shown very high anticancer activities against Gastric cancer cells in vitro. The biochemical factors like albumin, glucose, and DNA concentrations were modulated along with Protease inhibitor and Catalase activates, the various cancer specific proteins like p53, GRD 70 - 78 kDa and other proteins of sizes 35 - 40 kDa corresponding to H+K+ATPase protein etc. The apoptic activity and antiproliferative activity were demonstrated with Gastric cancer cells in vitro.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70881713","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-01-15DOI: 10.4236/WJNSE.2016.61004
V. Srinivas, A. Raghavender, K. Kumar
Bi1-xBaxFeO3 (0 ≤ x ≤ 0.3) nanopowders were synthesized using sol-gel technique. The structural and magnetic properties were investigated using X-ray diffraction, SEM and VSM. As Ba2+ doping concentration was increased, the structure of the samples changed from rhombohedral to tetragonal or monoclinic. The structural change might be an important factor for achieving the ferroelectric properties in this material. The lattice parameters were observed to increase with increase in Ba2+ concentration. All the M-H loops showed the ferromagnetic behavior. Magnetization was observed to enhance with increase in Ba concentration. The enhancement in the magnetization due to Ba2+ doping may be due to the replacement of Bi3+ ions by Ba2+ which might have resulted in the suppression of spiral spin structure.
{"title":"Effect of Ba Substitution on the Structural and Magnetic Properties of BiFeO 3","authors":"V. Srinivas, A. Raghavender, K. Kumar","doi":"10.4236/WJNSE.2016.61004","DOIUrl":"https://doi.org/10.4236/WJNSE.2016.61004","url":null,"abstract":"Bi1-xBaxFeO3 (0 ≤ x ≤ 0.3) nanopowders were synthesized using sol-gel technique. The structural and magnetic properties were investigated using X-ray diffraction, SEM and VSM. As Ba2+ doping concentration was increased, the structure of the samples changed from rhombohedral to tetragonal or monoclinic. The structural change might be an important factor for achieving the ferroelectric properties in this material. The lattice parameters were observed to increase with increase in Ba2+ concentration. All the M-H loops showed the ferromagnetic behavior. Magnetization was observed to enhance with increase in Ba concentration. The enhancement in the magnetization due to Ba2+ doping may be due to the replacement of Bi3+ ions by Ba2+ which might have resulted in the suppression of spiral spin structure.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70881433","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-01-15DOI: 10.4236/WJNSE.2016.61001
R. Thirunakaran, Gil Hwan Lew, W. Yoon
LiMn2O4 and LiCuxCryMn2-x-yO4 (x = 0.50; y = 0.05 - 0.50) powders have been synthesized via sol-gel method for the first time using Myristic acid as chelating agent. The synthesized samples have been taken to physical and electrochemical characterization such as thermo gravimetric analysis (TG/DTA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and electrochemical characterization viz., electrochemical galvanostatic cycling studies, electrochemical impedance spectroscopy (EIS) and differential capacity curves (dQ/dE). XRD patterns of LiMn2O4 and LiCuxCryMn2-x-yO4 confirm high degree of crystallinity with good phase purity. FESEM image of undoped pristine spinel lucidly depicts cauliflower morphology with good agglomerated particle size of 50 nm while 0.5-Cu doped samples depict the pebbles morphology. TEM images of the spinel LiMn2O4 and LiCu0.5Cr0.05Mn1.45O4 authenticate that all the synthesized particles via sol-gel method are nano-sized (100 nm) with spherical surface and cloudy particles morphology. The LiMn2O4 samples calcined at 850℃ deliver the high discharge capacity of 130 mA·h/g with cathodic efficiency of 88% corresponds to 94% columbic efficiency in the first cycle. Among all four compositions studied, LiCu0.5Cr0.05Mn1.45O4 delivers 124 mA·h/g during the first cycle and shows stable performance with a low capacity fade of 1.1 mA·h/g cycle over the investigated 10 cycles.
{"title":"Sol-Gel Synthesis Using Novel Chelating Agent and Electrochemical Characterization of Binary Doped LiMn 2 O 4 Spinel as Cathode Material for Lithium Rechargeable Batteries","authors":"R. Thirunakaran, Gil Hwan Lew, W. Yoon","doi":"10.4236/WJNSE.2016.61001","DOIUrl":"https://doi.org/10.4236/WJNSE.2016.61001","url":null,"abstract":"LiMn2O4 and LiCuxCryMn2-x-yO4 (x = 0.50; y = 0.05 - 0.50) powders have been synthesized via sol-gel method for the first time using Myristic acid as chelating agent. The synthesized samples have been taken to physical and electrochemical characterization such as thermo gravimetric analysis (TG/DTA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and electrochemical characterization viz., electrochemical galvanostatic cycling studies, electrochemical impedance spectroscopy (EIS) and differential capacity curves (dQ/dE). XRD patterns of LiMn2O4 and LiCuxCryMn2-x-yO4 confirm high degree of crystallinity with good phase purity. FESEM image of undoped pristine spinel lucidly depicts cauliflower morphology with good agglomerated particle size of 50 nm while 0.5-Cu doped samples depict the pebbles morphology. TEM images of the spinel LiMn2O4 and LiCu0.5Cr0.05Mn1.45O4 authenticate that all the synthesized particles via sol-gel method are nano-sized (100 nm) with spherical surface and cloudy particles morphology. The LiMn2O4 samples calcined at 850℃ deliver the high discharge capacity of 130 mA·h/g with cathodic efficiency of 88% corresponds to 94% columbic efficiency in the first cycle. Among all four compositions studied, LiCu0.5Cr0.05Mn1.45O4 delivers 124 mA·h/g during the first cycle and shows stable performance with a low capacity fade of 1.1 mA·h/g cycle over the investigated 10 cycles.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70879642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-01-15DOI: 10.4236/WJNSE.2016.61003
F. Al-Marhaby, R. Seoudi
Silver nanoparticles of various sizes were prepared at room temperature using silver nitrate as a precursor, various molar ratios of sodium citrate as a surfactant stabilizing material and sodium borohydride as a reducing agent. The morphology, distribution and sphericity of the particles were assessed in images from a transmission electron microscope (TEM). The sizes of the particles were calculated as being 9, 11 and 14 nm. The effects of the particles’ sizes on the plasmon bands were confirmed by ultraviolet-visible spectra measurements. The prepared samples were applied in photo catalysis of 4-Nitrophenol (4-NP), and the rate constant was determined as 0.05 s-1, 0.0015 s-1 and 0.00021 s-1 for particles of 9 nm, 11 nm and 14 nm, respectively. Due to their high surface energy, the smaller particle sizes were more active in the photo catalytic application.
{"title":"Preparation and Characterization of Silver Nanoparticles and their Use in Catalytic Reduction of 4-Nitrophenol","authors":"F. Al-Marhaby, R. Seoudi","doi":"10.4236/WJNSE.2016.61003","DOIUrl":"https://doi.org/10.4236/WJNSE.2016.61003","url":null,"abstract":"Silver nanoparticles of various sizes were prepared at room temperature using silver nitrate as a precursor, various molar ratios of sodium citrate as a surfactant stabilizing material and sodium borohydride as a reducing agent. The morphology, distribution and sphericity of the particles were assessed in images from a transmission electron microscope (TEM). The sizes of the particles were calculated as being 9, 11 and 14 nm. The effects of the particles’ sizes on the plasmon bands were confirmed by ultraviolet-visible spectra measurements. The prepared samples were applied in photo catalysis of 4-Nitrophenol (4-NP), and the rate constant was determined as 0.05 s-1, 0.0015 s-1 and 0.00021 s-1 for particles of 9 nm, 11 nm and 14 nm, respectively. Due to their high surface energy, the smaller particle sizes were more active in the photo catalytic application.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70880951","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2016-01-15DOI: 10.4236/WJNSE.2016.61002
Ajinkya Nene, M. Takahashi, P. Somani
Nanoparticles of Fe3O4 and Fe are chemically synthesized by reduction of Fe(acac)3 using ascorbic acid in controlled condition. It was observed that addition of water during the chemical synthesis process yields Fe3O4 nanoparticles, whereas if the reaction is carried out in absence of water yields Fe nanoparticles—which get oxidized upon exposure to air atmosphere. Fe3O4 (15 ± 5 nm) and Fe/iron oxide nanoparticles (7 ± 1 nm) were successfully synthesized in the comparative study reported herewith. Mechanism for formation/synthesis of Fe3O4 and Fe/iron oxide nanoparticles is proposed herewith in which added water acts as an oxygen supplier. Physico-chemical characterization done by SEM, TEM, EDAX, and XPS supports the proposed mechanism.
利用抗坏血酸在可控条件下还原铁(acac)3，化学合成了Fe3O4和Fe纳米颗粒。观察到，在化学合成过程中加入水会产生Fe3O4纳米颗粒，而如果在没有水的情况下进行反应会产生Fe纳米颗粒，这些纳米颗粒在暴露于空气中会被氧化。本文成功合成了Fe3O4纳米颗粒(15±5 nm)和Fe/iron oxide纳米颗粒(7±1 nm)。本文提出了以水为供氧源的Fe3O4和Fe/氧化铁纳米颗粒的形成/合成机理。通过SEM, TEM, EDAX和XPS进行的物理化学表征支持了该机制。
{"title":"Fe<sub>3</sub>O<sub>4</sub> and Fe Nanoparticles by Chemical Reduction of Fe(acac)<sub>3</sub> by Ascorbic Acid: Role of Water","authors":"Ajinkya Nene, M. Takahashi, P. Somani","doi":"10.4236/WJNSE.2016.61002","DOIUrl":"https://doi.org/10.4236/WJNSE.2016.61002","url":null,"abstract":"Nanoparticles of Fe3O4 and Fe are chemically synthesized by reduction of Fe(acac)3 using ascorbic acid in controlled condition. It was observed that addition of water during the chemical synthesis process yields Fe3O4 nanoparticles, whereas if the reaction is carried out in absence of water yields Fe nanoparticles—which get oxidized upon exposure to air atmosphere. Fe3O4 (15 ± 5 nm) and Fe/iron oxide nanoparticles (7 ± 1 nm) were successfully synthesized in the comparative study reported herewith. Mechanism for formation/synthesis of Fe3O4 and Fe/iron oxide nanoparticles is proposed herewith in which added water acts as an oxygen supplier. Physico-chemical characterization done by SEM, TEM, EDAX, and XPS supports the proposed mechanism.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70879691","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-11-13DOI: 10.4236/WJNSE.2015.54019
M. Rezaei, A. Motamedzadegan
The effects of glycerol and sorbitol as two plasticizers on mechanical properties, water vapor permeability, thermal properties, color and capability of heat sealing of gelatin films (of phytophagous fish, bovine gelatin with high gel-forming ability, and bovine gelatin with low gel-forming ability) containing clay nanoparticles were studied in this research. For this purpose, 6 × 2 × 3 factorial experiments using the completely randomized design and comparison of the means at 95% confidence level (α = 0.05) were performed. Higher concentrations of plasticizers increased percentage elongation to the breaking point. When glycerol concentration was raised to over 20%, flexibility of the layers improved but their water vapor permeability increased. The minimum passage of water vapor was that of fish-skin gelatin films containing clay nanoparticles and 30% sorbitol, and the maximum that of bovine gelatin films with high gel-forming ability which contained nanoparticles but no plasticizers (p 0.05). All samples had heat sealing capability, and fish-skin gelatin films containing clay nanoparticles had better heat sealing capability compared with the other samples so that fish-skin gelatin films containing clay nanoparticles with 25% glycerol and 5% sorbitol had the highest flexibility and tensile strength, and remained attached to where they were heat sealed. Electron microscope images showed that films without plasticizers had uniform surfaces, but that samples containing glycerol at concentrations of over 0.20 g/g gelatin exhibited cavities between gelatin chains and that water vapor permeability in gelatin films containing clay nanoparticles.
{"title":"The Effect of Plasticizers on Mechanical Properties and Water Vapor Permeability of Gelatin-Based Edible Films Containing Clay Nanoparticles","authors":"M. Rezaei, A. Motamedzadegan","doi":"10.4236/WJNSE.2015.54019","DOIUrl":"https://doi.org/10.4236/WJNSE.2015.54019","url":null,"abstract":"The effects of glycerol and sorbitol as two plasticizers on mechanical properties, water vapor permeability, thermal properties, color and capability of heat sealing of gelatin films (of phytophagous fish, bovine gelatin with high gel-forming ability, and bovine gelatin with low gel-forming ability) containing clay nanoparticles were studied in this research. For this purpose, 6 × 2 × 3 factorial experiments using the completely randomized design and comparison of the means at 95% confidence level (α = 0.05) were performed. Higher concentrations of plasticizers increased percentage elongation to the breaking point. When glycerol concentration was raised to over 20%, flexibility of the layers improved but their water vapor permeability increased. The minimum passage of water vapor was that of fish-skin gelatin films containing clay nanoparticles and 30% sorbitol, and the maximum that of bovine gelatin films with high gel-forming ability which contained nanoparticles but no plasticizers (p 0.05). All samples had heat sealing capability, and fish-skin gelatin films containing clay nanoparticles had better heat sealing capability compared with the other samples so that fish-skin gelatin films containing clay nanoparticles with 25% glycerol and 5% sorbitol had the highest flexibility and tensile strength, and remained attached to where they were heat sealed. Electron microscope images showed that films without plasticizers had uniform surfaces, but that samples containing glycerol at concentrations of over 0.20 g/g gelatin exhibited cavities between gelatin chains and that water vapor permeability in gelatin films containing clay nanoparticles.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2015-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70879732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-11-13DOI: 10.4236/WJNSE.2015.54013
M. Khalid Hossain, J. Ferdous, M. Haque, A. Hakim
Iron-based amorphous alloys have attracted technological and scientific interests due to their excellent soft magnetic properties. The typical nanocrystalline alloy with the composition of Fe73.5Cu1Nb3Si13.5B9 known as FINEMENT has been studied for structural properties analysis. Recently, it is found that after proper annealing the amorphous alloy like Fe73.5Cu1Nb3Si13.5B9 has a transition to the nanocrystalline state, thus exhibiting good magnetic properties. The alloy in the form of ribbon of 10 mm width and 25mm thickness with the composition of Fe73.5Cu1Nb3Si13.5B9 was prepared by rapid quenching method. The prepared ribbon sample has been annealed for 30 min in a controlled way in the temperature range 490℃ - 680℃. By analyzing X-ray diffraction (XRD) patterns, various structural parameters such as lattice parameters, grain size and silicon content of the nanocrystalline Fe(Si) grains, crystallization behavior and nanocrystalline phase formation have been investigated. In the nanocrystalline state, Cu helps the nucleation of α-Fe(Si) grains while Nb controls their growth, Si and B has been used as glass forming materials. Thus on the residual amorphous, the nanometric Fe(Si) grains develops. From broadening of fundamental peaks, the optimum grain size has been determined in the range of 7 - 23 nm.
{"title":"Development of Nanostructure Formation of Fe73.5Cu1Nb3Si13.5B9 Alloy from Amorphous State on Heat Treatment","authors":"M. Khalid Hossain, J. Ferdous, M. Haque, A. Hakim","doi":"10.4236/WJNSE.2015.54013","DOIUrl":"https://doi.org/10.4236/WJNSE.2015.54013","url":null,"abstract":"Iron-based amorphous alloys have attracted technological and scientific interests due to their excellent soft magnetic properties. The typical nanocrystalline alloy with the composition of Fe73.5Cu1Nb3Si13.5B9 known as FINEMENT has been studied for structural properties analysis. Recently, it is found that after proper annealing the amorphous alloy like Fe73.5Cu1Nb3Si13.5B9 has a transition to the nanocrystalline state, thus exhibiting good magnetic properties. The alloy in the form of ribbon of 10 mm width and 25mm thickness with the composition of Fe73.5Cu1Nb3Si13.5B9 was prepared by rapid quenching method. The prepared ribbon sample has been annealed for 30 min in a controlled way in the temperature range 490℃ - 680℃. By analyzing X-ray diffraction (XRD) patterns, various structural parameters such as lattice parameters, grain size and silicon content of the nanocrystalline Fe(Si) grains, crystallization behavior and nanocrystalline phase formation have been investigated. In the nanocrystalline state, Cu helps the nucleation of α-Fe(Si) grains while Nb controls their growth, Si and B has been used as glass forming materials. Thus on the residual amorphous, the nanometric Fe(Si) grains develops. From broadening of fundamental peaks, the optimum grain size has been determined in the range of 7 - 23 nm.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2015-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70879273","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2015-11-13DOI: 10.4236/WJNSE.2015.54016
N. Kumar, K. Kumar
A series of Bismuth doped Cobalt nanoferrites of chemical composition CoBixFe2-xO4 (where x = 0.00, 0.05, 0.10, 0.15, 0.20 & 0.25) were prepared by sol-gel combustion method and calcinated at 600℃. The structural and morphological studies were carried out by using X-ray diffraction (XRD), Scanning Electron Microscope (SEM), Transmission Electron Microscopy (TEM), Energy Dispersive Spectroscopy (EDS) and Fourier Transform Infrared (FT-IR) spectra showing the single phase spinal structure. The X-ray diffraction (XRD) analysis confirmed a single phase fcc crystal. The crystallite size of all the compositions was calculated using Debye-Scherrer equation and found in the range of 17 to 26 nm. The lattice parameters were found to be decreased as Bi3+ ion doping increases. The surface morphology was studied by Scanning Electron Microscope (SEM) and particle size was confirmed by Transmission Electron Microscopy (TEM). The EDS plots revealed existence of no extra peaks other than constituents of the taken up composition. The Fourier Transform Infrared (FT-IR) studies were made in the frequency range 350 - 900 cm-1 and observed two strong absorption peaks. The frequency band is found at 596 cm-1 where as the lower frequency band at 393 cm-1. It is clearly noticed that the two prominent absorption bands were slightly shifted towards higher frequency side with the increase of Bi3+ ion concentration.
{"title":"Synthesis and Structural Properties of Bismuth Doped Cobalt Nanoferrites Prepared by Sol-Gel Combustion Method","authors":"N. Kumar, K. Kumar","doi":"10.4236/WJNSE.2015.54016","DOIUrl":"https://doi.org/10.4236/WJNSE.2015.54016","url":null,"abstract":"A series of Bismuth doped Cobalt nanoferrites of chemical composition CoBixFe2-xO4 (where x = 0.00, 0.05, 0.10, 0.15, 0.20 & 0.25) were prepared by sol-gel combustion method and calcinated at 600℃. The structural and morphological studies were carried out by using X-ray diffraction (XRD), Scanning Electron Microscope (SEM), Transmission Electron Microscopy (TEM), Energy Dispersive Spectroscopy (EDS) and Fourier Transform Infrared (FT-IR) spectra showing the single phase spinal structure. The X-ray diffraction (XRD) analysis confirmed a single phase fcc crystal. The crystallite size of all the compositions was calculated using Debye-Scherrer equation and found in the range of 17 to 26 nm. The lattice parameters were found to be decreased as Bi3+ ion doping increases. The surface morphology was studied by Scanning Electron Microscope (SEM) and particle size was confirmed by Transmission Electron Microscopy (TEM). The EDS plots revealed existence of no extra peaks other than constituents of the taken up composition. The Fourier Transform Infrared (FT-IR) studies were made in the frequency range 350 - 900 cm-1 and observed two strong absorption peaks. The frequency band is found at 596 cm-1 where as the lower frequency band at 393 cm-1. It is clearly noticed that the two prominent absorption bands were slightly shifted towards higher frequency side with the increase of Bi3+ ion concentration.","PeriodicalId":66816,"journal":{"name":"纳米科学与工程(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2015-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70879551","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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