Biomaterials & Biodevices
Venâncio Alves Amaral; Juliana Ferreira de Souza; Thais Francine Ribeiro Alves; Fernando Batain; Kessi Marie de Moura Crescencio; Daniel Komatsu; Marco Vinicius Chaud
Abstract
The chemical processing of polymeric mixtures is a promising alternative for designing materials with new characteristics for biomedical applications. This work proposed to produce and characterize polymeric mixtures obtained using polyethylene glycol (PEG400 or PEG4000) with poly (L-co-D, L lactic acid)/PLDLA ...
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The chemical processing of polymeric mixtures is a promising alternative for designing materials with new characteristics for biomedical applications. This work proposed to produce and characterize polymeric mixtures obtained using polyethylene glycol (PEG400 or PEG4000) with poly (L-co-D, L lactic acid)/PLDLA for biomedical use. The mixtures were prepared by the casting method. Characterizations were performed by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), mechanical properties (perforation, resilience, elastic modulus, plastic deformation, tensile strength and mucoadhesion) and in vitro biodisintegration studies. The results obtained by FTIR and DSC suggest that the chemical interactions that generate the mixtures between the polymers occurred through hydrogen bonds and/or dipole-dipole interactions. Chemical interactions created compounds that were more hydrophilic and had different rearrangements when using PEG400 or PEG4000 in the mixture. The mechanical tests showed changes in the resistance of the materials, highlighting the exponential value of plastic deformation of PLDLA/PEG400, significantly increasing the plasticity of this structure by 111-fold about PLDLA/PEG4000. In the biodisintegration study, after 120 hours, greater mass loss was observed for PLDLA/PEG4000 (68.82 ± 1.46%). Hydrolytic disintegration did not influence pH values, which remained between 7.34 and 7.41 during the study. In conclusion, these mixtures can provide valuable characteristics to produce a biocompatible biomedical device with properties to support tissue regeneration, where the issue of plastic deformation is necessary in collaboration with the formation of pores, after PEG dissolution in vivo.
Environmental & Green Materials
Marian Catalin Grosu; Emilia Visileanu; Alexandra Gabriela Ene; Razvan Victor Scarlat; Virgil Emanuel Marinescu
Abstract
This paper presents the polypropylene (PP) micro-nano particles (MNPs) exposure routes of textile industry personnel and analyses the characteristics of such particles collected in and outside the workplaces. A Laser Aerosol Spectrometer set was used to determine: the total suspended particles (TSP), ...
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This paper presents the polypropylene (PP) micro-nano particles (MNPs) exposure routes of textile industry personnel and analyses the characteristics of such particles collected in and outside the workplaces. A Laser Aerosol Spectrometer set was used to determine: the total suspended particles (TSP), PM10, PM2.5, PM1 fractions (µm/m3), and the total number of particles (TC) (1/l) from the air. Specific methods for descriptive statistics were used to characterize the particle populations. Mean, dispersion and standard deviation, median and quartiles, skewness and kurtosis for asymmetry, and highlighting the cases in which they should be performed were calculated. The box plots and histograms graphs for TSP, PM10, PM2.5, and PM1, TC variables. The comparative analysis of the results led to the identification of the fraction of the particles with the highest value concentration in the air. The particles were collected on quartz and polycarbonate filters with gold membrane using TECORA and GilAirPlus pumps. The mass of particles collected was determined by weighing the filters before and after collection, using an electronic balance. Characterization of PP dust collected by analysis: Optical microscope, Scanning Electron Microscopy, µRaman spectroscopy, FTIR, and TG-DSC allowed the identification of the shape, size, and structural footprint of PP particles.
Ceramic Composite
G. Upender; V. Chandra Mouli; V. Sreenivasulu; Praveena Kuruva; M. Prasad
Abstract
The new tellurite glasses with chemical composition 64TeO2-15CdO-(20-x) ZnO-xLi2O-1V2O5 (x= 0, 5, 10, 15 and 20 mol %) were synthesized by traditional melt quench hardening method. The glass samples showed broad humps of typical amorphous phase in the X- ray diffraction patterns. The physical properties ...
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The new tellurite glasses with chemical composition 64TeO2-15CdO-(20-x) ZnO-xLi2O-1V2O5 (x= 0, 5, 10, 15 and 20 mol %) were synthesized by traditional melt quench hardening method. The glass samples showed broad humps of typical amorphous phase in the X- ray diffraction patterns. The physical properties of glass samples such as density (ρ), molar volume (Vm), oxygen packing density (OPD), refractive index (n), molar refractivity (Rm) and metallization parameter (M) were estimated. The Fourier transform infrared spectroscopy (FTIR) studies exhibited that replacement of ZnO by Li2O forms significantly some basic structural units of TeO4, TeO3/TeO3+1 and ZnO4. Differential scanning calorimetry (DSC) was employed to find out the glass transition temperature (Tg) and thermal stability ( ). The optical enthrallment studies exhibited that the cut-off wavelength (λ) decreases while optical energy gap (Eopt) and Urbach energy ( ) values increases with an increase an escalation of Li2O content. This tellurite glasses possess an important use such as sensor devices, storage of data system and industrial applications etc.
Composite Materials
Rajnish Raj; Pooja Lohia; D. K. Dwivedi
Abstract
The traditional melt-quench technique was used to synthesize non-oxide (Ga2Ge)100-x(Ga3Sb2)x (x = 15, 30, 45, 60) glass alloys. The vacuum thermal evaporation unit was used to obtain thin films of prepared sample for investigation of optical properties. SEM, XRD and DSC technique were used to find the ...
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The traditional melt-quench technique was used to synthesize non-oxide (Ga2Ge)100-x(Ga3Sb2)x (x = 15, 30, 45, 60) glass alloys. The vacuum thermal evaporation unit was used to obtain thin films of prepared sample for investigation of optical properties. SEM, XRD and DSC technique were used to find the thermal and structural properties of the materials. The linear properties like optical bandgap, extinction coefficient for prepared samples have been studied in present paper of Ge-Ga-Sb for application of optoelectronics. The impurities present in the prepared thin films were defined by FTIR transmittance spectra. The extinction coefficient (k) value decreases with increase in Sb concentration while absorption coefficient (α). It was noticed that value of energy bandgap (Eg) derived from Tauc’s plot varies from 2.9 eV to 1.25 eV. Urbach energy is inversely proportional to the bandgap of the materials. As the Sb concentration increases the band gap goes on decreases which result the increase in Urbach energy. Mott and Davis model has been used for explaining decrease in energy gap of prepared glassy alloys.
M.B. Lava; Uday M. Muddapur; B. Nagaraj
Abstract
Biosynthesis of gold nanoparticles is one among the best and cheap economical viable process, which is environmental friendly. The purpose of this study is to synthesis the gold nanoparticles using Lobelia nicotianifolia leaf extract and to investigate its biological activities. The synthesized gold ...
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Biosynthesis of gold nanoparticles is one among the best and cheap economical viable process, which is environmental friendly. The purpose of this study is to synthesis the gold nanoparticles using Lobelia nicotianifolia leaf extract and to investigate its biological activities. The synthesized gold nanoparticles were characterized by UV-vis spectroscopy, TEM, SAED, FTIR and XRD, the nanoparticles produced at maximum absorbance 532 nm. The Characterization study proved that the size and shape of AuNPs were spherical in shape, with an average size of 80 nm. Synthesized AuNPs were evaluated for various in-vitro biological studies.
Ramakanta Naik
Abstract
The nano multilayered thin films of Sb/As2S3 metal chalcogenide were prepared by thermal evaporation technique under high vacuum. The optical parameters such as optical band gap, tauc parameter, urbach energy were determined from the transmission spectra using Fourier Transform Infrared Spectroscopy. ...
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The nano multilayered thin films of Sb/As2S3 metal chalcogenide were prepared by thermal evaporation technique under high vacuum. The optical parameters such as optical band gap, tauc parameter, urbach energy were determined from the transmission spectra using Fourier Transform Infrared Spectroscopy. These properties are greatly influenced by the thickness of the nano layered Sb/As2S3 thin film. The Small Angle X-ray diffraction study reveals the amorphous nature of these films. The analysis reveals that the optical band gap decreases with increase in thickness due to Sb metal. The tauc parameter and urbach energy supports the optical property change. Such type of dependence is attributed to quantum size effect in semiconductors.
K. Kaviyarasu; M. Jayachandran; M. Maaza; E. Manikandan; J. Kennedy
Abstract
The electronics industry is heavily reliant on the use of silicon in devices ranging from solar panels to circuitry. This is of growing concern due to the environmental impact of sourcing and refining the material. Thus, a green source of silicon is of vital importance to meet the growing demand for ...
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The electronics industry is heavily reliant on the use of silicon in devices ranging from solar panels to circuitry. This is of growing concern due to the environmental impact of sourcing and refining the material. Thus, a green source of silicon is of vital importance to meet the growing demand for silicon in the industry. Rice husk represents an abundant source of nano silica. Currently the husk is considered a waste product that is separated from the grain during the milling process. Several methods have been trailed to extract the nano silica from rice husk. This paper reviews these current methods and presents suggestions of innovative research directions for processing techniques. This work reveals that the structural nature of superfine silica from rice husk ash is independent of the purification method, but dependent on the incineration temperature used. The paper concludes by advocating the physic-chemical process for producing high purity reactive nanosilica from rice husk. This method has the advantage of having high volume production versatility and being environmentally friendly. However, control of the morphology, shape, size, crystalline structure and chemical composition of rice husk nanostructures remains a challenge in the development of 3D nanopores arrays controllable by synthesis methods. We hope this article can provide the reader with snapshots of the recent development and future challenges.
Yesodaran Sangeetha; Sankaran Meenakshi; Chandrasekaran Sairam Sundaram
Abstract
The inhibition performance of water soluble chitin (WSC) and its synergistic inhibition with potassium iodide (KI) in 1 M HCl was studied using gravimetric and electrochemical measurements. From gravimetric measurement it is inferred that there is an increase in inhibition efficiency with the increased ...
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The inhibition performance of water soluble chitin (WSC) and its synergistic inhibition with potassium iodide (KI) in 1 M HCl was studied using gravimetric and electrochemical measurements. From gravimetric measurement it is inferred that there is an increase in inhibition efficiency with the increased addition of inhibitor and it further stepped up to a higher value in the presence of 0.1 % KI. Polarization studies revealed that there is mixed mode of inhibition by WSC. Impedance study suggested the adsorption of the inhibitor at the interface between mild steel and acidic solution. The adsorption of inhibitor followed Frumkin isotherm. Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray (EDX) confirmed the co- adsorption of KI with WSC on the mild steel surface. Fourier Transform Infra-red (FTIR), Atomic Force Microscopy (AFM) and X- ray Diffraction (XRD) indicated the formation of protective film by the inhibitor on the surface of mild steel.
Mayank Pandey; Girish M. Joshi; Kalim Deshmukh; Jamil Ahmad
Abstract
Polyvinyl alcohol (PVA) and Polyvinyl Pyrrolidone (PVP) based polymer electrolytes for different loading wt% of CdCl2 were prepared by solution casting. The structural complexation was confirmed and interlayer spacing (d) was evaluated by using X-ray diffraction (XRD) study. The chemical bonding between ...
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Polyvinyl alcohol (PVA) and Polyvinyl Pyrrolidone (PVP) based polymer electrolytes for different loading wt% of CdCl2 were prepared by solution casting. The structural complexation was confirmed and interlayer spacing (d) was evaluated by using X-ray diffraction (XRD) study. The chemical bonding between polymer and salt was identified by using Fourier transform infrared spectroscopy (FTIR) technique. The FTIR peak at 3402.43 cm -1 in addition of PVP in PVA/CdCl2 composite demonstrates the grafting between two polymers. The presence of ionic bright channels and variation in morphology for different loading wt% of CdCl2 was confirmed by scanning electron microscope (SEM) and was also verified by Atomic force microscopy (AFM) micrographs. The analysis of impedance spectroscopy represented by semicircular pattern is driven by conduction mechanism and correlated with electrical conductivity. The enhanced AC conductivity of polymer electrolyte is directly proportional to frequency (50Hz-1MHz). The maximum value of DC conductivity 1.65x10 -5 S/m evaluated from Arrhenius plots and attribute to high mobility of free charges at higher temperature. The evaluated results of structural, morphological and electrical properties of present composites make the present research good for electrochemical devices.
B.S. Bhau; Sneha Ghosh; Sangeeta Puri; B. Borah; D.K. Sarmah; Raju Khan
Abstract
Synthesis of nanoparticles from various biological systems has been reported, but among all, biosynthesis of nanoparticles from plants is considered as the most suitable method. The use of plant material not only makes the process eco-friendly but also the abundance makes it more economical. The aim ...
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Synthesis of nanoparticles from various biological systems has been reported, but among all, biosynthesis of nanoparticles from plants is considered as the most suitable method. The use of plant material not only makes the process eco-friendly but also the abundance makes it more economical. The aim of this study was to investigate the ability of this plant to synthesis gold nanoparticles and study the properties of the nanoparticles thus produced. Antimicrobial activity and medicinal values of Nepenthes khasiana fascinated us to utilize it for biosynthesis of gold nanoparticles. The synthesized gold nanoparticles were characterized by UV-vis spectrophotometry, Scanning Electron Microscopy, X-ray Diffraction, Fourier Transform Infra-red Spectroscopy and Transmission Electron Microscopy. Different time intervals for the reaction with aqueous chloroauric acid solution increase in the absorbance with time and became constant giving a maximum absorbance at 599.78 nm at three hours of incubation. The results from XRD, TEM and SEM supports the biosynthesis of triangular and spherical shaped Gold nanoparticles between 50nm to 80 nm. In this study, the antimicrobial property of the AuNPS was exploited against human pathogenic micro-organisms. The results of TEM, SEM, FT-IR, UV-VIS and XRD confirm that the leaves extract of N. Khasiana can be used to produce Gold nanoparticles with significant amount of antimicrobial activity.
Niyaz Parvin Shaik; N. V. Poornachandra Rao; K. V. R. Murthy
Abstract
Pure LaPO4 and LaPO4: Eu (0.5 mol %) Ce (0.5 mol %) phosphors were synthesized by the solid-state reaction method. X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), photoluminescence (PL) spectra and the particle size analysis were used to characterize ...
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Pure LaPO4 and LaPO4: Eu (0.5 mol %) Ce (0.5 mol %) phosphors were synthesized by the solid-state reaction method. X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), photoluminescence (PL) spectra and the particle size analysis were used to characterize these samples. The XRD results reveal that the synthesized LaPO4:Eu (0.5 mol%) Ce (0.5 mol%) phosphors are well crystalline and assigned to the monoclinic structure with a main (120) diffraction peak. The calculated crystallite size of pure LaPO4 and LaPO4:Eu, Ce phosphors were 67.6nm and 64nm respectively. Upon excitation at 254nm wavelength, the emission spectrum of pure LaPO4 phosphor emits a maximum intensity peak at 470 (blue) nm. In the emission spectrum of LaPO4:Eu 3+ Ce 3+ phosphor, the low contributions of the red (613nm) 5D0-7F2 emissions and the high intensity of the orange-red (589nm)5D0-7F1 emission results in high color purities.The most intense emissions appearing in the 580-620nm region is responsible for the strong orange-red luminescence observed in the Eu,Ce doped LaPO4 phosphor whose CIE colour coordinates are x = 0.57 and y = 0.43.Thus the prepared phosphors can be used as an orange-red emitting material in the field of illuminations and display devices.
Vishal R. Panse; N.S. Kokode; S.J. Dhoble
Abstract
In this paper we present luminescence results on Tb 3+ doped Sr2(BO3)Cl green phosphor. The vibrational properties of Sr2(BO3)Cl phosphor was studied by Fourier transform infrared spectroscopy. Photoluminescence studies have been carried out to understand the mechanism of excitation and the corresponding ...
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In this paper we present luminescence results on Tb 3+ doped Sr2(BO3)Cl green phosphor. The vibrational properties of Sr2(BO3)Cl phosphor was studied by Fourier transform infrared spectroscopy. Photoluminescence studies have been carried out to understand the mechanism of excitation and the corresponding emission in the as prepared phosphor. As the Tb 3+ ion is commonly used as an activator for the green emission, the excitation and emission spectra indicate that this phosphor can be effectively excited by 380 nm, to exhibit bright green emission centered at 546 nm corresponding to the f→f transition of Tb3 +ions.
Seema Sharma; Rashmi Rani; Radheshyam Rai; T. S. Natarajan
Abstract
One dimensional nanofibers of organic and inorganic materials have been used in filters, optoelectronic devices, sensors etc. It is difficult to obtain ultra fine fibers of inorganic materials having lengths in the order of millimeter as they tend to break during formation due to thermal and other mechanical ...
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One dimensional nanofibers of organic and inorganic materials have been used in filters, optoelectronic devices, sensors etc. It is difficult to obtain ultra fine fibers of inorganic materials having lengths in the order of millimeter as they tend to break during formation due to thermal and other mechanical stresses. In this study, we have investigated the mechanism to prevent the defect formation and the breaking of CuO nanofibers by using optimized heat flow rates. CuO nanofibers were obtained by heat treating the poly(vinyl acetate) PVA composite fibers formed by electrospinning. The morphology and structural characteristics of prepared samples were investigated by Scanning electron microscopy, Transmission electron microscopy and X-ray diffraction. It was found that the morphology of the composite and annealed nanofibers could be influenced by the concentration of the polymer content. A lower concentration favors the formation of defects along the fiber and the number of defects reduces when the concentration is increased.
Pradip Z. Zambare; K. V. R. Murthy;O. H. Mahajan; K. D. Girase
Abstract
In this paper we report Strontium Cerium Oxide (Sr2CeO4) blue phosphor was synthesized via solid state reaction method using strontium carbonate SrCO3 and cerium oxide CeO2 as raw materials. The samples were characterized by Thermo analytical techniques (TG, DTA, DTG and DSC) in nitrogen atmosphere, ...
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In this paper we report Strontium Cerium Oxide (Sr2CeO4) blue phosphor was synthesized via solid state reaction method using strontium carbonate SrCO3 and cerium oxide CeO2 as raw materials. The samples were characterized by Thermo analytical techniques (TG, DTA, DTG and DSC) in nitrogen atmosphere, Fourier transformation infrared (FTIR) spectroscopy, and Photoluminescence at room temperature. Thermal analysis indicates that Sr2CeO4 phosphor can be prepared at temperature higher than 1100 °C. In excitation spectra two excitation peaks were located at 262 and 399 nm respectively. The emission spectrum was a broad band peaking at 470 nm, which was suitable for the doping of rare earth ions. The color co-ordinates for the pure Sr2CeO4 were x = 0.1918 and y = 0.2483. This material has potential for applications in the field of emission devices.
A. Kumar;Somik Banerjee
Abstract
Structural and conformational modifications in conducting polymer nanostructures viz., Polyaniline (PAni) nanofibers induced by swift heavy ion (SHI) irradiation have been investigated employing TEM, XRD, UV-Vis, FTIR and micro-Raman spectroscopy. Upon interaction with the highly energetic ions, PAni ...
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Structural and conformational modifications in conducting polymer nanostructures viz., Polyaniline (PAni) nanofibers induced by swift heavy ion (SHI) irradiation have been investigated employing TEM, XRD, UV-Vis, FTIR and micro-Raman spectroscopy. Upon interaction with the highly energetic ions, PAni nanofibers are fragmented and get amorphized. The local range of order is found to decrease with a corresponding increase in the concentration of point defects and dislocations leading to the enhancement in strain. Vibrational spectra of the pristine and SHI irradiated PAni nanofibers studied using FTIR and micro-Raman (μR) spectroscopy indicate conformational changes in PAni nanofibers upon SHI irradiation. Loss of π-stacking due to the enhancement in the torsion angle between Cring-N-Cring upon irradiation is indicative of strong electrostatic interaction between the electron rich C-N site in the aromatic rings of PAni chains and the ion beam. The most significant variation in PAni nanofibers upon SHI irradiation is the transformation of para di-substituted benzene (benzenoid) structure of PAni into the quinone di-imine (quinoid) structures; a phenomenon that has been simultaneously observed in both the FTIR and Raman spectra. The presence of two main peaks representing the same structures in PAni nanofibers in both the Raman and IR spectra is because of the presence of delocalized sp2 phases and local disorder in PAni nanofibers, which gives rise to electrical and mechanical fluctuations that destroy the symmetry rules.
Surender Kumar; Tukaram J. Shinde; Pramod N. Vasambekar
Abstract
Powder diffraction, Fourier transform infrared spectroscopy and scanning electron microscopy were used to characterize the spinel structure of nanocrystalline Ferrites with composition Mn1-xZnxFe2O4 (x = 0.2, 0.4, 0.6 and 0.8) prepared by oxalate coprecipitation technique and followed by microwave heating ...
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Powder diffraction, Fourier transform infrared spectroscopy and scanning electron microscopy were used to characterize the spinel structure of nanocrystalline Ferrites with composition Mn1-xZnxFe2O4 (x = 0.2, 0.4, 0.6 and 0.8) prepared by oxalate coprecipitation technique and followed by microwave heating of precursors. Effect of composition on the lattice constant, x-ray density, crystallite size was studied. Crystallite size and x-ray density increases with increase in Zinc content. The face centered cubic spinel structure has undergone deviation from ideality. A correlation exists between splitting of infrared absorption bands and lowering of composition dependent crystalline symmetry. This preparation technique could be used for synthesis of materials which use microwave transparent precursors.
Saruchi Surbhi; Praveen Aghamkar; Sushil Kumar
Abstract
Nanomaterials and nanostructures have received steadily growing interests as a result of their peculiar and fascinating properties and applications. Neodymia-silica nanocomposites were prepared by sol-gel route followed by calcination. The samples were prepared with different concentration of dopant ...
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Nanomaterials and nanostructures have received steadily growing interests as a result of their peculiar and fascinating properties and applications. Neodymia-silica nanocomposites were prepared by sol-gel route followed by calcination. The samples were prepared with different concentration of dopant (Nd2O3) and calcined in a programmable furnace at 1000 °C for 5 h. The structural evolution of samples was investigated by employing techniques such as XRD, FTIR and TEM. X-ray diffraction patterns showed that the samples were nanocrystalline and the size of crystallites has been determined using Debye-Scherrer relation. The FTIR spectra confirmed the presence of functional groups of prepared material. The particle size of samples was also estimated through TEM analysis. It has been observed that crystallinity as well as particle size of the samples increases with increase in dopant concentration.
Gagan Dixit; J.P. Singh; R.C. Srivastava; H.M. Agrawal; R.J. Chaudhary
Abstract
In the present work, structural, morphological, magnetic and optical properties of nickel ferrite thin films having different thickness are reported. All the films were deposited on Si (100) substrate by pulsed laser deposition technique. Thicknesses of the films determined by x-ray reflectivity vary ...
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In the present work, structural, morphological, magnetic and optical properties of nickel ferrite thin films having different thickness are reported. All the films were deposited on Si (100) substrate by pulsed laser deposition technique. Thicknesses of the films determined by x-ray reflectivity vary from 62 to 176nm as the deposition time varies from 16 min to 40 min. The films were characterised by x-ray diffractogram, Fourier transform infrared (FTIR) and Raman spectroscopy for structural and phase confirmation. FTIR and Raman spectra confirm mixed spinel nature of nickel ferrite. Surface morphology is studied by Atomic force microscopy. All the films have granular nature. Magnetic properties were studied by vibrating sample magnetometer and magnetic hysteresis curves were recorded for all the films at room temperature and at10K. At 10K, saturation magnetisation was found to increase while coercivity deceases with thickness. The results are explained on the basis of anisotropy induced by cation inversion and strain. Optical properties were studied by UV-vis reflectance spectra. The value of optical band gap (5.7eV) was found to be independent of thickness of the film.
S.B. Raut; S.J. Dhoble; R.G. Atram
Abstract
A new blue emitting material containing quinoline is designed, synthesized and characterized. The material has been prepared by well-known reaction such as Friedlander condensation reaction at 140 °C. The blended thin films of Trichloro-DPQ with poly (methyl methacrylate) (PMMA) at different weight ...
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A new blue emitting material containing quinoline is designed, synthesized and characterized. The material has been prepared by well-known reaction such as Friedlander condensation reaction at 140 °C. The blended thin films of Trichloro-DPQ with poly (methyl methacrylate) (PMMA) at different weight % concentrations such as 10, 5, 1 and 0.1 weight % have been prepared. The structural characterization has been done by FTIR spectra. The synthesized polymeric compound demonstrates emission in blue region at 460 nm in powder form. At different weight % concentrations, there is emission at 444 nm with varying intensity. The light emitting and optoelectronic property of polymeric compound may find application in electroluminescence, OLED and sensors.
Abstract
Swift Heavy Ion (SHI) irradiation induces chemical and structural changes in polymers by evolving various gases and gaseous fragments. The evolution of gases as a result of chain scissoring and bond breaking leads to cross-linking and cluster formation. Study of the evolved gases helps in understanding ...
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Swift Heavy Ion (SHI) irradiation induces chemical and structural changes in polymers by evolving various gases and gaseous fragments. The evolution of gases as a result of chain scissoring and bond breaking leads to cross-linking and cluster formation. Study of the evolved gases helps in understanding the various chemical and structural changes occurring within the polymer under the effect of SHI irradiation. In the present work, Poly (o-toluidine) (PoT), a derivative of polyaniline, is prepared by chemical oxidation polymerization and is blended with polyvinylchloride (PVC) to achieve self supported films. These PoT-PVC blend films were irradiated by 60 MeV Si 5+ ions at different fluences and evolved gases were monitored on-line by Residual Gas Analyzer (RGA). Pre and post irradiation FTIR, UV-Visible absorption and XRD studies have been carried out on these films to observe the changes in chemical/structural and optical properties. An effort has been made to correlate the evolved gases and structural properties after irradiation.Copyright © 2011 VBRI press.
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