The series of Cr-Zn nano ferrites having the general composition Cr<sub>x</sub>ZnFe<sub>2-x</sub>O<sub>4</sub> (0 ≤ x ≤ 0.5) have been synthesized successfully in the nanocrystall...The series of Cr-Zn nano ferrites having the general composition Cr<sub>x</sub>ZnFe<sub>2-x</sub>O<sub>4</sub> (0 ≤ x ≤ 0.5) have been synthesized successfully in the nanocrystalline form using the sol-gel method. The samples were sintered at 900°C for 3 hours. The effect of chromium substitution on dielectric properties of Zn-ferrites is reported in this paper. The analysis of XRD patterns revealed the formation of single phase cubic spinel structure for all the Cr-Zn ferrite samples. The FTIR spectra show two strong absorption bands in the range of 400 - 600 cm<sup>-1</sup>, which corroborate the spinel structure of the samples. The average grain size was found to be in the nanometer range and of the order of 43 - 63 nm obtained using TEM images. The lattice parameter and crystallite size decrease with increase in Cr concentration (x). The investigation on dielectric constant (ε'), dissipation factor (D) and ac conductivity (σ<sub>ac</sub>) was carried out at a fixed frequency 1 kHz and in the frequency range of 100 Hz to 1 MHz at room temperature using LCR meter. The plots of dielectric constant (ε') versus frequency show the normal dielectric behavior of spinel ferrites. The value of ac conductivity (σ<sub>ac</sub>) increases with increase in frequency for all the compositions. The appearance of the peak for each composition in the dissipation factor versus frequency curve suggests the presence of relaxing dipoles in the Cr-Zn nano ferrite samples. It is also found that the shifting of the relaxation peak towards lower frequency side with an increase in chromium content (x) is due to the strengthening of dipole-dipole interactions. The composition and frequency dependence of the dielectric constant, dielectric loss and ac-conductivity are explained based on the Koop’s two-layer model, Maxwell-Wagner polarization process, and Debye relaxation theory.展开更多
Bismuth substituted cobalt nano ferrites with the chemical composition Co Bi<sub>x</sub> Fe<sub>2-x</sub> O<sub>4</sub> (x = 0.00, 0.05, 0.10, 0.15, 0.20 & 0.25) were prepared b...Bismuth substituted cobalt nano ferrites with the chemical composition Co Bi<sub>x</sub> Fe<sub>2-x</sub> O<sub>4</sub> (x = 0.00, 0.05, 0.10, 0.15, 0.20 & 0.25) were prepared by sol-gel combustion method. The phase identification of prepared samples is characterised by X-ray powder diffraction (XRD) method, which confirms the formation of a single phase fcc spinal structure. The mean crystallite sizes of all prepared samples were obtained within the range of 21 (±5) nm. Transmission Electron Microscopy (TEM) images also confirmed the crystallite size of all the synthesised samples was in nano range. With the effect of Bi<sup>3+</sup> ion substitution on spinal cobalt ferrite, the magnetic properties were investigated by using Vibration Sample Magnetometer (VSM). The obtained hysteresis (M-H) curves of all the samples were analysed under the applied magnetic field of range ± 10 K Oe at 300 K. The magnetic properties such as saturation magnetisation (M<sub>s</sub>), remnant magnetization (M<sub>r</sub>) and coercivity (H<sub>c</sub>) values are tabulated, which show a decrease in trend as the bismuth ion concentration increases. This is due to the addition of Bi<sup>3+</sup> ion in the place of Fe<sup>3+</sup> ion (octahedral site) and hence the Bi<sup>3+</sup>-Fe<sup>3+</sup> ion interaction predominates as compared with the Fe<sup>2+</sup>-Fe<sup>3+</sup> ion interaction. The data obtained from magnetic studies, the variation among the magnetic properties have been investigated for all the prepared samples.展开更多
Mixed Mg-Cr Nano ferrites having the compositional formula MgCrxFe2-xO4 (where x = 0.0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1.0) were synthesized using Citrate-Gel auto combustion method. Structural characterization was carri...Mixed Mg-Cr Nano ferrites having the compositional formula MgCrxFe2-xO4 (where x = 0.0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1.0) were synthesized using Citrate-Gel auto combustion method. Structural characterization was carried out by XRD Analysis which confirmed the formation of single phase cubic spinel structure without any impurity peak. The dielectric properties such as Dielectric constant (ε'), Dielectric Loss tangent (tan δ) and AC conductivity (σAC) of Mg-Cr nano ferrites were studied at room temperature in the frequency range of 2 Hz - 2 MHz using Agilent E4980A Precision LCR meter. The dielectric constant, loss tangent and AC conductivity shows a normal behavior with frequency. A qulitative explanation is given for composition and frequency dependance of the dielectric constant, dielectric loss tangent and AC conductivity of the nano ferrite. The loss tangent for the synthesized samples was found to be decreased from 0.09 to 0.054 in higher frequency region showing the potential applications of these materials in high frequency micro wave devices. On the basis of these results the explanation of dielectric mechanism in Mg-Cr ferrites is suggested.展开更多
Mixed Copper substituted Nickel nano-ferrites having the chemical formula Ni1-xCuxFe2O4 (where x = 0, 0.2, 0.4, 0.6, 0.8, 0.9 and 1.0) were synthesized by citrate gel technique. The crystal structure characterization ...Mixed Copper substituted Nickel nano-ferrites having the chemical formula Ni1-xCuxFe2O4 (where x = 0, 0.2, 0.4, 0.6, 0.8, 0.9 and 1.0) were synthesized by citrate gel technique. The crystal structure characterization and morphology were investigated by X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM). An elemental composition of the samples were studied by energy dispersive X-ray Spectroscopy (EDS). Lattice parameter, X-ray density, Volume of the Unit Cell and The values of the hopping length for octahedral (dB) and tetrahedral (dA) sites were calculated. The observed results can be explained on the basis of composition.展开更多
Co-Cr nano-ferrites, having the chemical formula CoCrxFe2-xO4 (where x = 0.0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1.0), were synthesized by the Citrate-gel auto combustion method. Synthesized powders were sintered at 500°...Co-Cr nano-ferrites, having the chemical formula CoCrxFe2-xO4 (where x = 0.0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1.0), were synthesized by the Citrate-gel auto combustion method. Synthesized powders were sintered at 500°C for 4 hours in an air and were characterized by XRD, SEM and EDS. XRD analysis showed cubic spinel structure of the ferrites and the crystallite sizes (D) were found in the range of 6 - 12 nm. The values of lattice parameter (a) decreased and X-ray density (dx) increased with the increase of Cr content. Scanning Electron Microscopic (SEM) studies revealed nano crystalline nature of the samples. An elemental composition of the samples was studied by Energy Dispersive Spectroscopy (EDS). The observed results can be explained on the basis of composition and crystal size.展开更多
A simple, multi component, one-pot method has been reported for the synthesis of poly substituted imidazoles in presence of magnetically separable and recyclable spinel nano copper ferrite as heterogeneous catalyst by...A simple, multi component, one-pot method has been reported for the synthesis of poly substituted imidazoles in presence of magnetically separable and recyclable spinel nano copper ferrite as heterogeneous catalyst by the cyclo-condensation of benzil, aromatic aldehyde, ammonium acetate and substituted amines under ultrasonic irradiation. This method of preparation has many advantages compared to those methods which are previously reported in the literature. This methodology offers simple experimental procedure, milder reaction conditions and environmentally benign approach.展开更多
A microwave irradiated magnetically separable nano cobalt ferrite catalyzed green method for the synthesis of 4-phenyl-4H-pyrano[3,2-h]quinolin-2-amine and 2-amino-4-phenyl-4H-pyrano[3,2-h] quinoline-3-carbonitrile de...A microwave irradiated magnetically separable nano cobalt ferrite catalyzed green method for the synthesis of 4-phenyl-4H-pyrano[3,2-h]quinolin-2-amine and 2-amino-4-phenyl-4H-pyrano[3,2-h] quinoline-3-carbonitrile derivatives through cyclization of aromatic aldehyde, acetonitrile/malononitrile and 8-hydoxyquinoline is developed and presented in this paper. The cubic magnetic cobalt ferrite nano particles were synthesized by sol-gel citrate precursor method and characterized by FT-IR, XRD, SEM and TEM techniques and the structures of the synthesized pyranoquinoline derivatives were assigned by IR, MASS and 1</sup>H NMR techniques. The reaction is carried out in a domestic microwave oven with a heat-resistant microwave safe glass container with a lid.展开更多
1,8-Dioxo-octahydroxanthenes (4a-4f) and 1,8-dioxohexahydroacridines (5a-5c) were synthesized by novel, simple and eco-friendly method with higher yields in the presence of magnetically separable nano nickel-cobalt fe...1,8-Dioxo-octahydroxanthenes (4a-4f) and 1,8-dioxohexahydroacridines (5a-5c) were synthesized by novel, simple and eco-friendly method with higher yields in the presence of magnetically separable nano nickel-cobalt ferrite catalyst (Ni0.5Co0.5Fe2O4). The former, 1,8-dioxo-octahydroxanthenes have been synthesized from dimedone and different aromatic aldehydes, while the latter from this mixture are along with ammonium acetate. The main advantage of this method is that the nano catalyst can be reused up to five reaction cycles without losing the catalytic activity.展开更多
In this paper, immobilized laccase enzyme on nano zinc ferrite was used in order to decolorize disperse dyes from single and binary systems. In this case, disperse dyes such as Disperse red 60 (DR60), Disperse blue 56...In this paper, immobilized laccase enzyme on nano zinc ferrite was used in order to decolorize disperse dyes from single and binary systems. In this case, disperse dyes such as Disperse red 60 (DR60), Disperse blue 56 (DB56) and Disperse yellow 54 (DY54) were selected as model dyes. Several parameters such as enzyme concentration, pH and dye concentration and their effect on decolorization of dyes from single and binary systems were studied. According to the experimental results, the optimized immobilized laccase enzyme concentration, reaction time and pH for decolorization of DR60, DB56 and DY54 from single and binary systems were 500 mg/L (for DR60 and DY54) and 400 mg/L (for DB56), 20 min and 3, respectively. Moreover, Dye decolorization kinetics followed Michaelis-Menten Model. Finally, the results showed that enzymatic process using immobilized laccase enzyme on nano zinc ferrite was effective method to decolorize disperse dyes from single and binary systems.展开更多
Cu-Zn ferrite nano thin films were deposited from a target of Cu-Zn ferrite onto a sapphire substrate using XeCl excimer laser operating 308 nm with an energy of 225 mJ and a frequency of 30 Hz. Films were deposited f...Cu-Zn ferrite nano thin films were deposited from a target of Cu-Zn ferrite onto a sapphire substrate using XeCl excimer laser operating 308 nm with an energy of 225 mJ and a frequency of 30 Hz. Films were deposited from the target onto sapphire (001) substrates heated to 650℃ in an oxygen atmosphere of 100 mTorr. The laser beam was incident On the target face at an angle of 45°. Studies on crystal structure were done by X-ray diffactometry (XRD). The surface texture, cross-section morphology and grain size was observed by JEOL-JSM-6400 scanning electron microscopy, atomic force microscopy (AFM) and magnetic force microscopy (MFM) [Model DI 3000, Digital instruments].展开更多
Lithium ferrite nanoparticles were synthesized by a sol-gel auto-combustion method. For prepared samples, the nanograins were increased with increasing the annealing temperature. Positron annihilation lifetime spectro...Lithium ferrite nanoparticles were synthesized by a sol-gel auto-combustion method. For prepared samples, the nanograins were increased with increasing the annealing temperature. Positron annihilation lifetime spectroscopy (PALS) was used to study defects at different sites for nanograins Li-ferrites. The analysis of the PAL spectrum indicated two lifetime components τ1 and τ2 for the annihilation of the positrons, and their corresponding relative intensities I1% and I2%. For nanoparticles Li-ferrite there are correlations between: 1) I2, τ2, annealing temperature and the total porosity (Pt) with the grain size;2) I1, μi, Ms and the homogeneity with grain size.展开更多
Mn-Zn spinel ferrites were synthesized by sol-gel method. Effects of calcined temperature on structure and particle size of MnZnFe2O4 were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM)...Mn-Zn spinel ferrites were synthesized by sol-gel method. Effects of calcined temperature on structure and particle size of MnZnFe2O4 were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM). XRD patterns indicate that the ultra fine Mn-Zn ferrite exhibits a spinel crystal structure. SEM images show that the powder fired at 900℃for 2 h has an average diameter of 60 ~ 90 nm. The particle size becomes larger with the increasing of calcined temperature and the distribution of particle becomes even more homogeneous. Sintering behaviors of synthesized ferrite powders depend on the powder characteristics and high temperatures have induced the good crystallization of particles.展开更多
The Zn0.5CuxMg0.5-xFe2O4 (where x = 0.0, 0.1, 0.2, 0.3 and 0.4) was prepared by sol-gel route and characterized in detail in terms of their structural, morphological, elemental and optical properties as a function of ...The Zn0.5CuxMg0.5-xFe2O4 (where x = 0.0, 0.1, 0.2, 0.3 and 0.4) was prepared by sol-gel route and characterized in detail in terms of their structural, morphological, elemental and optical properties as a function of Cu concentration. X-ray diffractometer (XRD) results confirmed the formation of cubic spinel-type structure with average crystallized size in the range of 30.56 to 40.58 nm. Lattice parameter was found to decrease with Cu concentration due to the smaller ionic radius of Cu2+ ion. The HR-SEM images show morphology of the samples as prismatic shaped particles in agglomeration. The elemental dispersive X-ray Spectroscopy (EDX) confirmed the elemental composition of the as-prepared spinel ferrite material with respect to the initial concentration of the synthetic composition used for the material. The Fourier transform infrared (FTIR) spectroscopy confirmed the formation of spinel ferrite and showed the characteristics absorption bands around 463, 618, 876, 1116, 1442, 1622 and 2911 cm-1. The energy band gap was calculated for the samples were found to be in the range of 4.87 to 5.30 eV.展开更多
In this study, nano ferrite materials were produced to replace costive industrial materials<span style="font-family:;" "=""> </span><span style="font-family:Verdana;"&...In this study, nano ferrite materials were produced to replace costive industrial materials<span style="font-family:;" "=""> </span><span style="font-family:Verdana;"><span style="font-size:10.0pt;font-family:" color:#943634;"=""><span style="font-family:Verdana;white-space:normal;">[1]</span></span><span style="font-size:10.0pt;font-family:;" "=""></span><span style="font-size:10.0pt;font-family:" times="" new="" roman","serif";"=""><span></span></span></span><span></span><span><span></span></span><span style="font-family:Verdana;">.</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">Ferrite nanoparticles are the interesting material due to their rich and unique physical and chemical properties. They find applications in catalysis, bio-processing, medicine, magnetic recording, adsorption, devices etc.</span><span style="font-family:;" "=""> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">Using co-participation method, five nano ferrite samples Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> (x = 0.00, 0.10, 0.20, 0.30 and 0.40) were prepared. The electrical and optical properties of the Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> samples were studied using the Ultraviolet-visible (UV-Vis) spectroscopy. The results verified that the formation of the absorption coefficient of the five samples of Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> increased with the increase of Lithium (Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">). The energy band gap of the Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> samples ranged </span></span><span style="font-family:Verdana;">from</span><span style="font-family:Verdana;"> 3.28 to 3.12</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">eV</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">[1]</span><span style="font-family:;" "=""></span><span style="font-family:" minion="" pro="" capt","serif";"=""><span></span></span><span style="font-family:Verdana;">.</span><span style="font-family:;" "=""> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">The extinction coefficient (K) for five samples of Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> increased with the increase of Lithium (Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">) at 338 nm f</span></span><span style="font-family:Verdana;">ro</span><span style="font-family:Verdana;">m 0.074 to 0.207. The high magnitude of optical conductivity is (1.34</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">×</span><span style="font-family:;" "=""> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">10</span><sup><span style="font-family:Verdana;">12</span></sup><span style="font-family:Verdana;"> sec<span style="font-size:10px;"><sup>-1</sup></span></span><span style="font-family:Verdana;">) and the maximum value of electrical conductivity is 42</span></span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">(Ω<sup>.</sup></span><span style="font-family:;" "=""><span><span style="font-family:Verdana;">cm)<span style="font-size:10px;"><sup>-1</sup></span></span><span style="font-family:Verdana;">. This may due to the electrical and optical properties of lithium.</span></span></span>展开更多
Co-precipitation is an important issue in chemical analysis, where it is often undesirable, but in some cases, it can be exploited. The Zn0.5Mn0.5−xLi2xFe2O4 nanomaterials (x = 0.0, 0.1, 0.2, 0.3 and 0.4) wa...Co-precipitation is an important issue in chemical analysis, where it is often undesirable, but in some cases, it can be exploited. The Zn0.5Mn0.5−xLi2xFe2O4 nanomaterials (x = 0.0, 0.1, 0.2, 0.3 and 0.4) was afforded by utilizing co-precipitation method. The structural and optical characteristics were analyzed for the samples employing X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR) and Ultraviolet-visible spectrophotometer (UV-Vis). XRD revealed that the structure of certain nanoparticles is a cubic spinel with space group (Fd-3m) and crystallite size in the scale 124 - 150 nm. Lattice parameter was determined to increments with Li+1 and that may occur due to the larger ionic radius of the Li1+ ion. FTIR spectroscopy confirmed the form of spinel ferrite and explicated the properties of absorption bands approximately 593, 1111, 1385, 1640, 2922 and 3430. The energy band gap was estimated for all samples with diverse ratios and was observed in the range of 2.58 - 2.52 eV.展开更多
文摘The series of Cr-Zn nano ferrites having the general composition Cr<sub>x</sub>ZnFe<sub>2-x</sub>O<sub>4</sub> (0 ≤ x ≤ 0.5) have been synthesized successfully in the nanocrystalline form using the sol-gel method. The samples were sintered at 900°C for 3 hours. The effect of chromium substitution on dielectric properties of Zn-ferrites is reported in this paper. The analysis of XRD patterns revealed the formation of single phase cubic spinel structure for all the Cr-Zn ferrite samples. The FTIR spectra show two strong absorption bands in the range of 400 - 600 cm<sup>-1</sup>, which corroborate the spinel structure of the samples. The average grain size was found to be in the nanometer range and of the order of 43 - 63 nm obtained using TEM images. The lattice parameter and crystallite size decrease with increase in Cr concentration (x). The investigation on dielectric constant (ε'), dissipation factor (D) and ac conductivity (σ<sub>ac</sub>) was carried out at a fixed frequency 1 kHz and in the frequency range of 100 Hz to 1 MHz at room temperature using LCR meter. The plots of dielectric constant (ε') versus frequency show the normal dielectric behavior of spinel ferrites. The value of ac conductivity (σ<sub>ac</sub>) increases with increase in frequency for all the compositions. The appearance of the peak for each composition in the dissipation factor versus frequency curve suggests the presence of relaxing dipoles in the Cr-Zn nano ferrite samples. It is also found that the shifting of the relaxation peak towards lower frequency side with an increase in chromium content (x) is due to the strengthening of dipole-dipole interactions. The composition and frequency dependence of the dielectric constant, dielectric loss and ac-conductivity are explained based on the Koop’s two-layer model, Maxwell-Wagner polarization process, and Debye relaxation theory.
文摘Bismuth substituted cobalt nano ferrites with the chemical composition Co Bi<sub>x</sub> Fe<sub>2-x</sub> O<sub>4</sub> (x = 0.00, 0.05, 0.10, 0.15, 0.20 & 0.25) were prepared by sol-gel combustion method. The phase identification of prepared samples is characterised by X-ray powder diffraction (XRD) method, which confirms the formation of a single phase fcc spinal structure. The mean crystallite sizes of all prepared samples were obtained within the range of 21 (±5) nm. Transmission Electron Microscopy (TEM) images also confirmed the crystallite size of all the synthesised samples was in nano range. With the effect of Bi<sup>3+</sup> ion substitution on spinal cobalt ferrite, the magnetic properties were investigated by using Vibration Sample Magnetometer (VSM). The obtained hysteresis (M-H) curves of all the samples were analysed under the applied magnetic field of range ± 10 K Oe at 300 K. The magnetic properties such as saturation magnetisation (M<sub>s</sub>), remnant magnetization (M<sub>r</sub>) and coercivity (H<sub>c</sub>) values are tabulated, which show a decrease in trend as the bismuth ion concentration increases. This is due to the addition of Bi<sup>3+</sup> ion in the place of Fe<sup>3+</sup> ion (octahedral site) and hence the Bi<sup>3+</sup>-Fe<sup>3+</sup> ion interaction predominates as compared with the Fe<sup>2+</sup>-Fe<sup>3+</sup> ion interaction. The data obtained from magnetic studies, the variation among the magnetic properties have been investigated for all the prepared samples.
文摘Mixed Mg-Cr Nano ferrites having the compositional formula MgCrxFe2-xO4 (where x = 0.0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1.0) were synthesized using Citrate-Gel auto combustion method. Structural characterization was carried out by XRD Analysis which confirmed the formation of single phase cubic spinel structure without any impurity peak. The dielectric properties such as Dielectric constant (ε'), Dielectric Loss tangent (tan δ) and AC conductivity (σAC) of Mg-Cr nano ferrites were studied at room temperature in the frequency range of 2 Hz - 2 MHz using Agilent E4980A Precision LCR meter. The dielectric constant, loss tangent and AC conductivity shows a normal behavior with frequency. A qulitative explanation is given for composition and frequency dependance of the dielectric constant, dielectric loss tangent and AC conductivity of the nano ferrite. The loss tangent for the synthesized samples was found to be decreased from 0.09 to 0.054 in higher frequency region showing the potential applications of these materials in high frequency micro wave devices. On the basis of these results the explanation of dielectric mechanism in Mg-Cr ferrites is suggested.
文摘Mixed Copper substituted Nickel nano-ferrites having the chemical formula Ni1-xCuxFe2O4 (where x = 0, 0.2, 0.4, 0.6, 0.8, 0.9 and 1.0) were synthesized by citrate gel technique. The crystal structure characterization and morphology were investigated by X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM). An elemental composition of the samples were studied by energy dispersive X-ray Spectroscopy (EDS). Lattice parameter, X-ray density, Volume of the Unit Cell and The values of the hopping length for octahedral (dB) and tetrahedral (dA) sites were calculated. The observed results can be explained on the basis of composition.
文摘Co-Cr nano-ferrites, having the chemical formula CoCrxFe2-xO4 (where x = 0.0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1.0), were synthesized by the Citrate-gel auto combustion method. Synthesized powders were sintered at 500°C for 4 hours in an air and were characterized by XRD, SEM and EDS. XRD analysis showed cubic spinel structure of the ferrites and the crystallite sizes (D) were found in the range of 6 - 12 nm. The values of lattice parameter (a) decreased and X-ray density (dx) increased with the increase of Cr content. Scanning Electron Microscopic (SEM) studies revealed nano crystalline nature of the samples. An elemental composition of the samples was studied by Energy Dispersive Spectroscopy (EDS). The observed results can be explained on the basis of composition and crystal size.
文摘A simple, multi component, one-pot method has been reported for the synthesis of poly substituted imidazoles in presence of magnetically separable and recyclable spinel nano copper ferrite as heterogeneous catalyst by the cyclo-condensation of benzil, aromatic aldehyde, ammonium acetate and substituted amines under ultrasonic irradiation. This method of preparation has many advantages compared to those methods which are previously reported in the literature. This methodology offers simple experimental procedure, milder reaction conditions and environmentally benign approach.
文摘A microwave irradiated magnetically separable nano cobalt ferrite catalyzed green method for the synthesis of 4-phenyl-4H-pyrano[3,2-h]quinolin-2-amine and 2-amino-4-phenyl-4H-pyrano[3,2-h] quinoline-3-carbonitrile derivatives through cyclization of aromatic aldehyde, acetonitrile/malononitrile and 8-hydoxyquinoline is developed and presented in this paper. The cubic magnetic cobalt ferrite nano particles were synthesized by sol-gel citrate precursor method and characterized by FT-IR, XRD, SEM and TEM techniques and the structures of the synthesized pyranoquinoline derivatives were assigned by IR, MASS and 1</sup>H NMR techniques. The reaction is carried out in a domestic microwave oven with a heat-resistant microwave safe glass container with a lid.
文摘1,8-Dioxo-octahydroxanthenes (4a-4f) and 1,8-dioxohexahydroacridines (5a-5c) were synthesized by novel, simple and eco-friendly method with higher yields in the presence of magnetically separable nano nickel-cobalt ferrite catalyst (Ni0.5Co0.5Fe2O4). The former, 1,8-dioxo-octahydroxanthenes have been synthesized from dimedone and different aromatic aldehydes, while the latter from this mixture are along with ammonium acetate. The main advantage of this method is that the nano catalyst can be reused up to five reaction cycles without losing the catalytic activity.
文摘In this paper, immobilized laccase enzyme on nano zinc ferrite was used in order to decolorize disperse dyes from single and binary systems. In this case, disperse dyes such as Disperse red 60 (DR60), Disperse blue 56 (DB56) and Disperse yellow 54 (DY54) were selected as model dyes. Several parameters such as enzyme concentration, pH and dye concentration and their effect on decolorization of dyes from single and binary systems were studied. According to the experimental results, the optimized immobilized laccase enzyme concentration, reaction time and pH for decolorization of DR60, DB56 and DY54 from single and binary systems were 500 mg/L (for DR60 and DY54) and 400 mg/L (for DB56), 20 min and 3, respectively. Moreover, Dye decolorization kinetics followed Michaelis-Menten Model. Finally, the results showed that enzymatic process using immobilized laccase enzyme on nano zinc ferrite was effective method to decolorize disperse dyes from single and binary systems.
文摘Cu-Zn ferrite nano thin films were deposited from a target of Cu-Zn ferrite onto a sapphire substrate using XeCl excimer laser operating 308 nm with an energy of 225 mJ and a frequency of 30 Hz. Films were deposited from the target onto sapphire (001) substrates heated to 650℃ in an oxygen atmosphere of 100 mTorr. The laser beam was incident On the target face at an angle of 45°. Studies on crystal structure were done by X-ray diffactometry (XRD). The surface texture, cross-section morphology and grain size was observed by JEOL-JSM-6400 scanning electron microscopy, atomic force microscopy (AFM) and magnetic force microscopy (MFM) [Model DI 3000, Digital instruments].
文摘Lithium ferrite nanoparticles were synthesized by a sol-gel auto-combustion method. For prepared samples, the nanograins were increased with increasing the annealing temperature. Positron annihilation lifetime spectroscopy (PALS) was used to study defects at different sites for nanograins Li-ferrites. The analysis of the PAL spectrum indicated two lifetime components τ1 and τ2 for the annihilation of the positrons, and their corresponding relative intensities I1% and I2%. For nanoparticles Li-ferrite there are correlations between: 1) I2, τ2, annealing temperature and the total porosity (Pt) with the grain size;2) I1, μi, Ms and the homogeneity with grain size.
基金Project supported by the Fund for Harbin Young Scholars (2005AFQXJ031)
文摘Mn-Zn spinel ferrites were synthesized by sol-gel method. Effects of calcined temperature on structure and particle size of MnZnFe2O4 were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM). XRD patterns indicate that the ultra fine Mn-Zn ferrite exhibits a spinel crystal structure. SEM images show that the powder fired at 900℃for 2 h has an average diameter of 60 ~ 90 nm. The particle size becomes larger with the increasing of calcined temperature and the distribution of particle becomes even more homogeneous. Sintering behaviors of synthesized ferrite powders depend on the powder characteristics and high temperatures have induced the good crystallization of particles.
文摘The Zn0.5CuxMg0.5-xFe2O4 (where x = 0.0, 0.1, 0.2, 0.3 and 0.4) was prepared by sol-gel route and characterized in detail in terms of their structural, morphological, elemental and optical properties as a function of Cu concentration. X-ray diffractometer (XRD) results confirmed the formation of cubic spinel-type structure with average crystallized size in the range of 30.56 to 40.58 nm. Lattice parameter was found to decrease with Cu concentration due to the smaller ionic radius of Cu2+ ion. The HR-SEM images show morphology of the samples as prismatic shaped particles in agglomeration. The elemental dispersive X-ray Spectroscopy (EDX) confirmed the elemental composition of the as-prepared spinel ferrite material with respect to the initial concentration of the synthetic composition used for the material. The Fourier transform infrared (FTIR) spectroscopy confirmed the formation of spinel ferrite and showed the characteristics absorption bands around 463, 618, 876, 1116, 1442, 1622 and 2911 cm-1. The energy band gap was calculated for the samples were found to be in the range of 4.87 to 5.30 eV.
文摘In this study, nano ferrite materials were produced to replace costive industrial materials<span style="font-family:;" "=""> </span><span style="font-family:Verdana;"><span style="font-size:10.0pt;font-family:" color:#943634;"=""><span style="font-family:Verdana;white-space:normal;">[1]</span></span><span style="font-size:10.0pt;font-family:;" "=""></span><span style="font-size:10.0pt;font-family:" times="" new="" roman","serif";"=""><span></span></span></span><span></span><span><span></span></span><span style="font-family:Verdana;">.</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">Ferrite nanoparticles are the interesting material due to their rich and unique physical and chemical properties. They find applications in catalysis, bio-processing, medicine, magnetic recording, adsorption, devices etc.</span><span style="font-family:;" "=""> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">Using co-participation method, five nano ferrite samples Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> (x = 0.00, 0.10, 0.20, 0.30 and 0.40) were prepared. The electrical and optical properties of the Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> samples were studied using the Ultraviolet-visible (UV-Vis) spectroscopy. The results verified that the formation of the absorption coefficient of the five samples of Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> increased with the increase of Lithium (Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">). The energy band gap of the Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> samples ranged </span></span><span style="font-family:Verdana;">from</span><span style="font-family:Verdana;"> 3.28 to 3.12</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">eV</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">[1]</span><span style="font-family:;" "=""></span><span style="font-family:" minion="" pro="" capt","serif";"=""><span></span></span><span style="font-family:Verdana;">.</span><span style="font-family:;" "=""> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">The extinction coefficient (K) for five samples of Zn</span><sub><span style="font-family:Verdana;">0.5</span></sub><span style="font-family:Verdana;">Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">Mg</span><sub><span style="font-family:Verdana;">0.5-x</span></sub><span style="font-family:Verdana;">Fe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">O</span><sub><span style="font-family:Verdana;">4</span></sub><span style="font-family:Verdana;"> increased with the increase of Lithium (Li</span><sub><span style="font-family:Verdana;">2x</span></sub><span style="font-family:Verdana;">) at 338 nm f</span></span><span style="font-family:Verdana;">ro</span><span style="font-family:Verdana;">m 0.074 to 0.207. The high magnitude of optical conductivity is (1.34</span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">×</span><span style="font-family:;" "=""> </span><span style="font-family:;" "=""><span style="font-family:Verdana;">10</span><sup><span style="font-family:Verdana;">12</span></sup><span style="font-family:Verdana;"> sec<span style="font-size:10px;"><sup>-1</sup></span></span><span style="font-family:Verdana;">) and the maximum value of electrical conductivity is 42</span></span><span style="font-family:;" "=""> </span><span style="font-family:Verdana;">(Ω<sup>.</sup></span><span style="font-family:;" "=""><span><span style="font-family:Verdana;">cm)<span style="font-size:10px;"><sup>-1</sup></span></span><span style="font-family:Verdana;">. This may due to the electrical and optical properties of lithium.</span></span></span>
文摘Co-precipitation is an important issue in chemical analysis, where it is often undesirable, but in some cases, it can be exploited. The Zn0.5Mn0.5−xLi2xFe2O4 nanomaterials (x = 0.0, 0.1, 0.2, 0.3 and 0.4) was afforded by utilizing co-precipitation method. The structural and optical characteristics were analyzed for the samples employing X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR) and Ultraviolet-visible spectrophotometer (UV-Vis). XRD revealed that the structure of certain nanoparticles is a cubic spinel with space group (Fd-3m) and crystallite size in the scale 124 - 150 nm. Lattice parameter was determined to increments with Li+1 and that may occur due to the larger ionic radius of the Li1+ ion. FTIR spectroscopy confirmed the form of spinel ferrite and explicated the properties of absorption bands approximately 593, 1111, 1385, 1640, 2922 and 3430. The energy band gap was estimated for all samples with diverse ratios and was observed in the range of 2.58 - 2.52 eV.