Impedance and modulus studies of Na0.9Ba0.1Nb0.9(Sn0.5Ti0.5)0.1O3 ceramic

Polycrystalline Na[Formula: see text]Ba[Formula: see text]Nb[Formula: see text](Sn[Formula: see text]Ti[Formula: see text]O3is prepared by the solid-state reaction technique. The formation of single-phase material was confirmed by an X-ray diffraction study and it was found to be a tetragonal phase at room temperature. Nyquist plots ([Formula: see text]ˆ2 versus [Formula: see text] show that the conductivity behavior is accurately represented by an equivalent circuit model which consists of a parallel combination of bulk resistance and constant phase elements (CPE). The frequency dependence of the conductivity is interpreted in terms of Jonscher’s law. The conductivity [Formula: see text] follows the Arrhenius relation. The modulus plots can be characterized by the empirical Kohlrausch–Williams–Watts (KWW), [Formula: see text] = exp([Formula: see text]/[Formula: see text] function and the value of the stretched exponent ([Formula: see text] is found to be almost independent of temperature. The near value of activation energies obtained from the analyses of modulus and conductivity data confirms that the transport is through an ion hopping mechanism dominated by the motion of the (O[Formula: see text] ions in the structure of the investigated material.

Kinetics Study of the Hydrodeoxygenation of Xylitol over a ReOx-Pd/CeO2 Catalyst

In this study, we elucidate the reaction kinetics for the simultaneous hydrodeoxygenation of xylitol to 1,2-dideoxypentitol and 1,2,5-pentanetriol over a ReOx-Pd/CeO2 (2.0 weight% Re, 0.30 weight% Pd) catalyst. The reaction was determined to be a zero-order reaction with respect to xylitol. The activation energy was elucidated through an Arrhenius relationship as well as non-Arrhenius kinetics. The Arrhenius relationship was investigated at 150–170 °C and a constant H2 pressure of 10 bar resulting in an activation energy of 48.7 ± 10.5 kJ/mol. The investigation of non-Arrhenius kinetics was conducted at 120–170 °C and a sub-Arrhenius relation was elucidated with activation energy being dependent on temperature, and ranging from 10.2–51.8 kJ/mol in the temperature range investigated. Internal and external mass transfer were investigated through evaluating the Weisz–Prater criterion and the effect of varying stirring rate on the reaction rate, respectively. There were no internal or external mass transfer limitations present in the reaction.

Irreversibility line and thermally activated flux flow in Micro-bridges of high-temperature superconductor

We have studied the electrical resistivity as a function of temperature in Micro-bridges of YBa2Cu3O7-δ deposited by laser ablation on the SrTiO3 substrate face, around superconducting transition region in different magnetic fields. The activation energy U0 was determined and discussed using the Arrhenius relation. The irreversibility line Birr and the upper critical field Bc2were obtained using 10% and 90% criteria of the normal-state resistivity value from ρ (T) curves. A phase diagram of the studied sample is constructed showing the Tg glass line and a very broad vortex-liquid phase regime.

Thermodynamics and Kinetics of Glycolytic Reactions. Part I: Kinetic Modeling Based on Irreversible Thermodynamics and Validation by Calorimetry

In systems biology, material balances, kinetic models, and thermodynamic boundary conditions are increasingly used for metabolic network analysis. It is remarkable that the reversibility of enzyme-catalyzed reactions and the influence of cytosolic conditions are often neglected in kinetic models. In fact, enzyme-catalyzed reactions in numerous metabolic pathways such as in glycolysis are often reversible, i.e., they only proceed until an equilibrium state is reached and not until the substrate is completely consumed. Here, we propose the use of irreversible thermodynamics to describe the kinetic approximation to the equilibrium state in a consistent way with very few adjustable parameters. Using a flux-force approach allowed describing the influence of cytosolic conditions on the kinetics by only one single parameter. The approach was applied to reaction steps 2 and 9 of glycolysis (i.e., the phosphoglucose isomerase reaction from glucose 6-phosphate to fructose 6-phosphate and the enolase-catalyzed reaction from 2-phosphoglycerate to phosphoenolpyruvate and water). The temperature dependence of the kinetic parameter fulfills the Arrhenius relation and the derived activation energies are plausible. All the data obtained in this work were measured efficiently and accurately by means of isothermal titration calorimetry (ITC). The combination of calorimetric monitoring with simple flux-force relations has the potential for adequate consideration of cytosolic conditions in a simple manner.

Dependence of Electrical Properties on Frequency and Temperature for Novel Cyclopentenone Derivatives

Electrical properties of some new cyclopentenone derivatives have been studied. The structures of prepared samples were characterized by (UV), (XRD) and (SEM). The dependence of electrical properties such as σdc , σac , ɛ' and ɛ'' on frequency and temperature were studied at frequency range from 50 Hz to 5 MHz and the temperature range from 25oC to 140oC. It was found that, ɛ' decreased with increasing frequency while it increases with increasing temperatures within the used ranges. Moreover, dielectric constant is structural dependent which is obvious from the variation of dielectric constant for each sample. Ac-electrical conductivity increased with increasing frequency which was attributed to the polarization of the charge carriers. The temperature dependence of dc-electrical conductivity show typical Arrhenius relation for the three prepared samples. The activation energy calculated from Arrhenius equation and the results are discussed in detailed.

Influence of High Conductive Magnetite Impurity on the Electrical Conductivity of Dry Olivine Aggregates at High Temperature and High Pressure

The electrical conductivity of dry sintered olivine aggregates with various contents of magnetite (0, 3, 5, 7, 10, 20, and 100 vol. %) was measured at temperatures of 873–1273 K and a pressure of 2.0 GPa within a frequency range of 0.1–106 Hz. The changes of the electrical conductivity of the samples with temperature followed an Arrhenius relation. The electrical conductivity of the sintered olivine aggregates increased as the magnetite-bearing content increased, and the activation enthalpy decreased, accordingly. When the content of interconnected magnetite was higher than the percolation threshold (~5 vol. %), the electrical conductivity of the samples was markedly enhanced. As the pressure increased from 1.0 to 3.0 GPa, the electrical conductivity of the magnetite-free olivine aggregates decreased, whereas the electrical conductivity of the 5 vol. % magnetite-bearing sample increased. Furthermore, the activation energy and activation volume of the 5 vol. % magnetite-bearing sintered olivine aggregates at atmospheric pressure were calculated to be 0.16 ± 0.04 eV and −1.50 ± 0.04 cm3/mole respectively. Due to the high value of percolation threshold (~5 vol. %) in the magnetite impurity sample, our present results suggest that regional high conductivity anomalies in the deep Earth’s interior cannot be explained by the presence of the interconnected magnetite-bearing olivine aggregates.

Experimental study on the electrical conductivity of quartz andesite at high temperature and high pressure: evidence of grain boundary transport

In this study, the grain boundary conductivity of quartz andesite was in situ measured under conditions of 0.5–2.0 GPa and 723–973 K using a YJ-3000t multi-anvil press and Solartron-1260 Impedance/Gain-phase Analyzer. Experimental results indicate that grain interior transport controls the higher frequencies (102–106 Hz), whereas the grain boundary process dominates the lower frequencies (10−1–102 Hz). At a given pressure and temperature range, the relationship between log σ and 1/T conforms to an Arrhenius relation. As temperature increased, both of the grain boundary and grain interior conductivities of quartz andesite increased. Under increasing pressure, however, both of the grain boundary and grain interior conductivities of the sample decreased. By the virtue of the dependence of grain boundary conductivity on pressure, the activation enthalpy and the activation volume were calculated at 0.77–1.03 eV and 5.29 ± 1.94 cm3 mol−1, respectively. Furthermore, the small polaron conduction mechanism between the ferrous and ferric ion is also discussed.

Influence of Temperature on the Electrochemical Characteristics of Ti-6Al-4V

Titanium is not only the most widely used biomaterial for medical implants, but with its very good mechanical properties, corrosion resistance and low density is also applicated in many sectors of industry (aerospace, military, aviation, machinery, energetics, chemicals, etc.). In this paper it is described the influence of temperature on the electrochemical characteristics of Ti-6Al-4V alloy. The surface was mechanically grinded and polished by chemical-mechanical process. Basic electrochemical characteristics were determined by potentiodynamic tests in 0.1M NaCl solution at different temperatures. The obtained results were analysed by the Tafel-extrapolation method. Finally, a modified Arrhenius relation was used for determination of activation energy. The activation energy of grinded and chemical-mechanical polished surface is nearly three times higher than activation energy of only grinded surface.