Synthesis, electrical and dielectric properties of FeVO4 nanoparticles

The electrical and dielectric properties of FeVO₄ nanoparticles were studied at different temperatures from ambient to 200 °C. The samples were prepared by simple co-precipitation method using ferric nitrate and ammonium metavanadate as the starting precursors. The powder X-ray diffraction pattern inferred the single phase formation and triclinic structure of FeVO₄. The morphology of the particles was elucidated from SEM studies. Detailed studies on the electrical and dielectric properties of the compound were carried out by using solid state impedance spectroscopy. A maximum dc conductivity of 4.65×10⁻⁵ S cm⁻¹ was observed at the measuring temperature of 200 °C. The calculated activation energy from dc conductivity was found to be 0.28 eV. It was evident that the electrical transport process in the system was due to the hopping mechanism. The detailed dielectric studies were also carried out.     

Investigation on the performance,emissions and combustion characteristics of CRDI engine fueled with tallow methyl ester biodiesel blends with exhaust gas recirculation

This paper demonstrates the study of performance, combustion and emission characteristics of a common rail diesel injection (CRDI) engine with the influence of exhaust gas recirculation (EGR) (5, 15 and 25%) at various fuel injection pressures (400, 500 and 600 bar) under the effective load conditions (0, 25, 50, 75 and 100%). The experiments were carried out in a controlled manner using the CRDI engine fuelled with 80% (D80) diesel (98% purity) blended with 20% (B20) tallow biodiesel. The engine has been operated at a rated speed of 1500 rpm on all load conditions, fuel injection timings of 10°, 15° and 20° bTDC, fuel injection pressures of 400, 500 and 600 bar, respectively. Combustion-influenced performance characteristics such as variation of in-cylinder pressure and net heat release rate in J deg^?1 are also studied with the above operating conditions. It was observed that the usage of 20% biofuel blend shows considerable improvement in combustion, and it further enhances with an increase in the injection pressures. Besides, EGR (up to 25%) reduced significant pollutants at higher operating pressures (600 bar) at higher load conditions. It was also observed that CO₂ emission increased with increase in the % EGR with an increase in the load conditions. However, for CO emission increased up to 50% load condition and subsequently tends to decrease due to improved combustion at higher load; hence higher temperature. NO_x, smoke opacity continue to increase with the increase in pressure and the percentage increase in EGR due to its attainment of adiabatic temperature, which leads to the pathway for the Zeldovich mechanism. The present work shows light on the usage of tallow methyl ester produced from the wastes in the tannery industry as alternate biofuel operating the CRDI engines without compromising its combustion and emission characteristics to deliver the same power as petro-diesel.

     

Study of CuFe2O4–SnO2 nanocomposites by Mössbauer spectroscopy with high velocity resolution

High velocity resolution Mössbauer spectroscopy was used to study of (CuFe₂O₄)_1???x (SnO₂) _x nanocomposites (x?= 0, 1, 5, 10, 20 wt.%). Mössbauer spectra were measured at room temperature with registration in 4,096 channels and further presentation in 1,024 channels. Mössbauer spectra of CuFe₂O₄ and (CuFe₂O₄)_0.99 + (SnO₂)_0.01 were better fitted using three sextets while spectra of (CuFe₂O₄)_0.95 + (SnO₂)_0.05 and (CuFe₂O₄)_0.80 + (SnO₂)_0.20 were better fitted using four sextets and one doublet. In contrast, spectrum of (CuFe₂O₄)_0.80 + (SnO₂)_0.20 was better fitted using five sextets and one doublet. Mössbauer hyperfine parameters were related to octahedral and tetrahedral sites in copper ferrites. The presence of two different tetrahedral sites in studied ferrites and two different octahedral sites in (CuFe₂O₄)_0.80 + (SnO₂)_0.20 was supposed.     

Volume collapse phase transitions in cerium-praseodymium alloys under high pressure

Cerium-12at%Praseodymium(Ce_0.88Pr_0.12) and Ce-50at%Praseodymium(Ce_0.50Pr_0.50) alloy samples that contain a random solid-solution of Ce (4f¹ (J?=?5/2)) and Pr (4f² (J?=?4)) localized f-states have been studied by angle dispersive x-ray diffraction in a diamond anvil cell to a pressure of 65?GPa and 150?GPa respectively using a synchrotron source. Ce_0.88Pr_0.12 alloy crystallizes in a face-centered cubic (γ-phase) structure at ambient conditions, while Ce_0.50Pr_0.50 alloy crystallizes in the double hexagonal close packed (dhcp) structure at ambient conditions. Two distinct volume collapse transitions are observed in Ce_0.88Pr_0.12 alloy at 1.5?GPa and 18?GPa with volume change of 8.5% and 3% respectively. In contrast, Ce_0.50Pr_0.50 alloy shows only a single volume collapse of 5.6% at 20?GPa on phase transformation to α-Uranium structure under high pressure. Electrical transport measurements under high pressure show anomalies in electrical resistance at phase transitions for both compositions of this alloy.     

Crystal Growth,Structure, Resistivity,Magnetic, and Photoelectric Properties of One‐Dimensional Selenometallate Ba2BiFeSe5

Low‐dimensional materials have attracted extensive research interest in recent years owing to their interesting structural chemistry and physical properties, which will greatly deepen our knowledge of these materials and could lead to additional breakthroughs in the future. Herein we have synthesized and characterized Ba₂BiFeSe₅, which adopts a quasi‐one‐dimensional structure and possesses some fascinating physical properties. The sharp divergences between the field‐cooled (FC) and the zero‐field‐cooled (ZFC) data and the rather small magnetic moment per Fe³⁺ (0.07 μ_B) strongly suggest that the title compound is weakly ferromagnetic with a high magnetic transition temperature above room temperature, which is controlled by competing super‐exchange interactions within and between [FeBiSe₅]_∞ anionic ladders. Moreover, with its narrow bandgap of 0.95 eV, Ba₂BiFeSe₅ shows photoelectric properties with a photocurrent density of approximately 30 mA cm² at 5 V. Our study demonstrates that Ba₂FeBiSe₅ might be a new type of multifunctional material that deserves further investigation.     

Extraction of palladium from nitric acid medium by commercial resins with phosphinic acid,methylene thiol and isothiouronium moieties attached to polystyrene-divinylbenzene

Summary Commercially available polystyrene-divinylbenzene (PS-DVB) resins functionalized with isothiouronium (Tulsion CH-95), phosphinic acid (Tulsion CH-96) and methylene thiol (Tulsion CH-97) moieties have been used for separating palladium from nitric acid medium. Extraction of palladium has been studied as a function of time, concentration of nitric acid and palladium. The distribution coefficients (K_d, ml/g) of palladium on sulfur based resins (Tulsion CH-95 and Tulsion CH-97) are higher (5000-10⁴ml/g in 0.1M nitric acid) than on Tulsion CH-96 resin and decrease with increasing concentration of nitric acid. The initial rate of extraction of palladium by Tulsion CH-95 and Tulsion CH-97 resins was very rapid and the time required for the establishment of equilibrium was a function of palladium concentration in the aqueous phase. The rate data could be fitted by a second order rate equation and the magnitude of rate constant for the extraction of palladium by these resins (~10²M^-1. min^-1) decreased in the order of: Tulsion CH-95 > Tulsion CH-97 > Tulsion CH-96. The extraction isotherms of Tulsion CH-95 were fitted by Langmuir adsorption model and the coefficients were obtained by regression. The extraction capacity of palladium on Tulsion CH-95 was found to be ~20 mg/g at 3M nitric acid. Column experiments have been conducted and the data were fitted using Thomas model. A column utilization of 75% was achieved for the extraction of palladium by Tulsion CH-95 resin.     

Comparison of the hydration and diffusion of protons in perfluorosulfonic acid membranes with molecular dynamics simulations. scui@utk.edu

Classical molecular dynamics (MD) simulations were performed to determine the hydrated morphology and hydronium ion diffusion coefficients in two different perfluorosulfonic acid (PFSA) membranes as functions of water content. The structural and transport properties of 1143 equivalent weight (EW) Nafion, with its relatively long perfluoroether side chains, are compared to the short-side-chain (SSC) PFSA ionomer at an EW of 977. The separation of the side chains was kept uniform in both ionomers consisting of -(CF 2) 15- units in the backbone, and the degree of hydration was varied from 5 to 20 weight % water. The MD simulations indicated that the distribution of water clusters is more dispersed in the SSC ionomer, which leads to a more connected water-channel network at the low water contents. This suggests that the SSC ionomer may be more inclined to form sample-spanning aqueous domains through which transport of water and protons may occur. The diffusion coefficients for both hydronium ions and water molecules were calculated at hydration levels of 4.4, 6.4, 9.6, and 12.8 H 2O/SO 3H for each ionomer. When compared to experimental proton diffusion coefficients, this suggests that as the water content is increased the contribution of proton hopping to the overall proton diffusion increases.     

A molecular dynamics study of a nafion polyelectrolyte membrane and the aqueous phase structure for proton transport

A molecular dynamics simulation study of hydrated Nafion at water contents ranging from 5 to 20 wt % was performed to examine the structure and dynamics of the hydrated polyelectrolyte system. The simulations show that the system forms segregated hydrophobic regions consisting primarily of the polymer backbone and hydrophilic regions with an inhomogeneous water distribution. We find that the water clustering strongly depends on the water content. At low water content, only isolated small water clusters are formed. As the water content increases, it becomes increasingly possible that a predominant majority of water molecules form a single cluster, suggesting that the hydrophilic regions become connected. We characterize the atomic structures formed within the system by various atomic pair correlation functions. The water structure factor shows a peak at q values corresponding to an intercluster distance about 2.5 nm and greater. With increasing water content, the distance moves to larger values, consistent with findings from scattering experiments. We find that the degree of solvation of hydronium ions by water molecules is a strong function of water content. At 5 wt %, a majority of the hydronium ions are hydrated by no more than two water molecules, prohibiting structural diffusion. As water content increases, the hydronium ions continue to become increasingly hydrated, resulting in structures capable of forming eigen ions, a necessary step in structural diffusion. Addressing the experimentally observed fact that conductivity in these membranes abruptly drops near 5 wt %, we find that both the local structure of the poorly hydrated hydronium ions and the disconnected nature of the global morphology of the water nanonetwork at low water content should contribute to poor conductivity.