Chromium substituted copper ferrites via gluconate precursor route

CuFe_2−xCr_xO₄ spinel (0≤x≤2) powders were synthesized by a soft chemistry method—the gluconate multimetallic complex precursor route. The complex precursors were characterized by elemental chemical analysis, infrared (IR) and ultraviolet–visible (UV–vis) spectroscopy, thermal analysis and Mössbauer spectroscopy. The oxide powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), IR, Raman and Mössbauer spectroscopy. It was shown that the structure, morphology and magnetic properties of the obtained spinel powders depend on the concentration of Cr³⁺ ion. The XRD of the chromium substituted copper ferrite powders calcined at 700 °C/1 h indicated the formation of a cubic spinel type structure for x=0.5, 1.0 and a tetragonal structure for x=0, 0.2, 2. The crystallite size ranged from 19 nm to 39 nm. The Mössbauer spectroscopy revealed the site occupancy of iron ions, relative abundance and internal hyperfine magnetic fields in both tetrahedral and cubic CuFe_2−xCr_xO₄ spinels.     

Composition-dependent xBa(Zr0.2Ti0.8)O3-(1-x)(Ba0.7Ca0.3)TiO3 bulk ceramics for high energy storage applications

This work reports the composition dependent microstructure, dielectric, ferroelectric and energy storage properties, and the phase transitions sequence of lead free xBa(Zr_0.2Ti_0.8)O₃-(1-x)(Ba_0.7Ca_0.3)TiO₃ [xBZT-(1-x)BCT] ceramics, with x?=?0.4, 0.5 and 0.6, prepared by solid state reaction method. The XRD and Raman scattering results confirm the coexistence of rhombohedral and tetragonal phases at room temperature (RT). The temperature dependence of Raman scattering spectra, dielectric permittivity and polarization points a first phase transition from ferroelectric rhombohedral phase to ferroelectric tetragonal phase at a temperature (T_R-T) of 40?°C and a second phase transition from ferroelectric tetragonal phase - paraelectric pseudocubic phase at a temperature (T_T-C) of 110?°C. The dielectric analysis suggests that the phase transition at T_T-C is of diffusive type and the BZT-BCT ceramics are a relaxor type ferroelectric materials. The composition induced variation in the temperature dependence of dielectric losses was correlated with full width half maxima (FWHM) of A₁, E(LO) Raman mode. The saturation polarization (P_s) ≈8.3?μC/cm² and coercive fields ≈2.9?kV/cm were found to be optimum at composition x?=?0.6 and is attributed to grain size effect. It is also shown that BZT-BCT ceramics exhibit a fatigue free response up to 10⁵ cycles. The effect of a.c. electric field amplitude and temperature on energy storage density and storage efficiency is also discussed. The presence of high T_T-C (110?°C), a high dielectric constant (ε_r ≈?12,285) with low dielectric loss (0.03), good polarization (P_s ≈?8.3?μC/cm²) and large recoverable energy density (W?=?121?mJ/cm³) with an energy storage efficiency (η) of 70% at an electric field of 25?kV/cm in 0.6BZT-0.4BCT ceramics make them suitable candidates for energy storage capacitor applications.     

Microwave Synthesis and Characterization of Spinel-type Zinc Aluminate Nanoparticles

In the present work, ZnAl₂O₄ nanoparticles have been synthesized with the aid of Zn(OAc)₂·2H₂O and Al(NO₃)₃·9H₂O as starting reagents in the presence of microwave irradiation. Besides, the effect of preparation parameters such as microwave power and irradiation time on the morphology and particle size of products was studied by SEM images. The as-prepared ZnAl₂O₄ nanoparticles were characterized extensively by techniques like XRD, TEM, SEM, FT-IR, PL, and EDS. Photoluminescence studies of the ZnAl₂O₄ nanoparticles displayed quantum confinement behavior with band gap of 3.2 eV. The XRD studies showed that pure orthorhombic ZnAl₂O₄ nanoparticles have been produced after calcination.     

Miscibility studies of hydroxypropyl cellulose/poly(vinyl pyrrolidone) in dilute solutions and solid state

The miscibility of hydroxypropyl cellulose (HPC) and poly(vinyl pyrrolidone) (PVP) blends in aqueous solutions was studied using viscosity, ultrasonic velocity, and refractive index techniques at 30°C. The interaction parameters ΔB, μ, and α calculated from viscosity using Sun and Chee methods indicated the miscibility of this blend. This was further confirmed by ultrasonic and refractive index results. The HPC/PVP blend films are prepared by solution casting method and are analyzed by differential scanning calorimetry, X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopic techniques that confirmed the complete miscibility. This miscibility is due to the strong intermolecular H-bonding interactions between  OH groups of HPC and CO groups of PVP. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Non-fluorinated,room temperature curable hydrophobic coatings by sol–gel process

Non-fluorinated hydrophobic silica surfaces were generated on soda lime glass (SLG) substrates using hexamethyldisilazane (HMDS) as a surface modifying agent. Silica coatings were fabricated by dip coating of a sol derived from base catalyzed hydrolysis and condensation of tetraethoxysilane (TEOS). Two methodologies were adopted to generate the hydrophobic surface; one where the hydrophilic silica coated surface was treated by immersion into different concentrations of alcoholic solutions of HMDS varying from 2.5 wt% to 15 wt%. In the other method, HMDS was directly added to a mixture of TEOS, water, ethanol, and ammonium hydroxide and coatings were deposited using this sol by dip coating and spray coating. Water contact angles (WCA) were measured to study the effect of HMDS treatment times and concentrations on hydrophobicity in the first case, and in the second case, WCA were measured for dip and spray coated samples. UV–visible transmission, scratch resistance, and thermal stability of the coatings were determined. The WCA increased from 66 ± 2° to 125 ± 4° after the treatment of the silica coatings with HMDS. In case of coatings generated from direct addition of HMDS to silica sol, WCA varied from 145 ± 2° to 166 ± 4° for dip and spray coated surfaces respectively. Surface morphology was studied to explain the difference in hydrophobicity of coatings generated using the two methods.     

High Thermal Conductivity Polymer Composites Fabrication through Conventional and 3D Printing Processes: State-of-the-Art and Future Trends

The lifespan and the performance of flexible electronic devices and components are affected by the large accumulation of heat, and this problem must be addressed by thermally conductive polymer composite films. Therefore, the need for the development of high thermal conductivity nanocomposites has a strong role in various applications. In this article, the effect of different particle reinforcements such as single and hybrid form, coated and uncoated particles, and chemically treated particles on the thermal conductivity of various polymers are reviewed and the mechanism behind the improvement of the required properties are discussed. Furthermore, the role of manufacturing processes such as injection molding, compression molding, and 3D printing techniques in the production of high thermal conductivity polymer composites is detailed. Finally, the potential for future research is discussed, which can help researchers to work on the thermal properties enhancement for polymeric materials.     

Simulation Based Investigation of Triple Heterojunction TFET (THJ-TFET) for Low Power Applications

Silicon - We designed a new model tunnel field-effect transistor (TFET) based on Triple Heterojunction Tunnel Field Effect Transistor (THJ-TFET) is investigated and designed in this paper. This...     

Biomimetic high toughness Si3N4 ceramics with inverse-bouligand structure

Inspired by the Bouligand structure in nature, a kind of Inverse-Bouligand structure was designed. Different from the bionic Bouligand structure of a one-dimensional material unit, the inverse-Bouligand structure is obtained by stacking and twisting the ceramic layer with a parallel groove structure. The grooves arranged in parallel are first etched on the ceramic green body and then sintered after stacking and twisting. After sintering, the groove structure can still be maintained, so the resulting laminated twisted groove structure in the bulk forms an inverse-Bouligand structure, which can promote crack deflection and improve the toughness of the material during the fracture process. After testing different twist angles, the results show that when the twist angle is 15°, the toughness of the material can reach 11.22 ± 1.77 MPa m^1/2, and high strength can be guaranteed. The synergistic effect of interlayer crack deflection and regional crack twist is the main mechanism for the improvement of material toughness.     

Low-cost flame synthesized La2/3Cu3Ti4O12 electro-ceramic and extensive investigation on electrical,impedance, modulus,and optical properties

An environmentally-friendly synthesis route and low-cost starting materials are more appropriate for the production of ceramic materials at the industry level. With this concern we prepared the La_2/3Cu₃Ti₄O₁₂(LCTO), which is isostructural of CaCu₃Ti₄O₁₂ (CCTO), using the low-cost TiO₂ instead of a high-cost of titanium source (titanium isopropoxide or titanium chloride) using a low-cost wet-chemical route. Although, there are lots of synthetic methods reported for LCTO fabrication in terms of duration, cheap reagents, energy consumption, feasibility, etc. The present method is far better than the others. The prepared ceramic samples were sintered at 1050 ^°C/12 h and studied their structural, morphology and impedance, and modulus studies for further confirmation. The prepared LCTO ceramic shows the pure phase with the cubic type of morphology. The homogenous distribution of all the elements was observed through dispersive X-ray analysis. X-ray photoelectron spectroscopy studies revels that La is in +3 oxidation state, Cu is in a +2 oxidation state, and Ti is multiple (+3 and + 4) oxidation state. The LCTO ceramic displayed the very high dielectric constant (∼3852) and dielectric loss (0.322), at 1 kHz and at room temperature. Calculated the activation energy using the impedance and modulus data and it shows the superior to that of CCTO ceramic synthesized by the same method. The prepared samples exhibited Debye-type relaxation, which is evoked from the impedance and modulus studies. The calculated optical energy bandgap of LCTO (2.06 eV) is found to be lesser than that of the well-known structure of perovskites (BaTiO₃ (3.28 eV), PbTiO₃ (3.18 eV), LiNbO₃ (3.78 eV) and BiFeO₃ (2.67 eV) as well as structure of spinel CoCr₂O₄ (3.10 eV) and LuFe₂O₄ (2.18 eV)) materials.     

Chemical conversion during transient liquid-phase hot pressing of TaSi2–TaC–SiC SHS-powder

This article presents a study on the manufacturing of three-phase TaSi₂–TaC–SiC ceramics through self-propagating high-temperature synthesis (SHS) and their subsequent chemical conversion to TaC–SiC carbide composites during transient liquid-phase hot pressing (HP). The effect of carbon black doping, ranging from 0% to 7%, on the degree of chemical conversion, structure, mechanical, and thermophysical properties of the ceramics was investigated. Our results showed that the proportionate increase of carbide content and decrease of TaSi₂ content in hot-pressed samples was achieved through carbon black doping. The increase of TaSi₂ content during hot pressing led to an increase in porosity from 4.3% to 23.8%, while the density decreased from 6.3 to 4.6 g/cm³. Superior mechanical properties were obtained when SHS-powder was doped with 1.5% carbon black (HV = 15.2 GPa, K_IC = 4.8 MPa × m^1/2, and σ_bend = 331 MPa). The structure of the ceramics was characterized by a TaSi₂–SiC matrix and highly dispersed TaC grains predominantly residing inside TaSi₂, with the TaC–TaSi₂ and TaSi₂–SiC interface being incoherent, as demonstrated through TEM studies. Complete conversion of TaSi₂ to TaC and SiC was achieved through 7% carbon black doping, resulting in the hot-pressed sample consisting solely of carbide grains. Two-stage hot pressing was employed to enhance the relative density of the two-phase TaC–SiC sample, resulting in ceramics characterized by HV up to 22.3 GPa, K_IC up to 6.1 MPa × m^1/2, σ_bend up to 256 MPa, and λ up to 36 W/(m × K).