Thermophysical and Transport Properties of the BaCl2-CsCl High Temperature Ionic Liquid Mixtures

High temperature ionic liquids (HTILs) densities and transport properties for mixtures BaCl2‑CsCl, x(BaCl2) = 0-1, have been studied as a function of composition and temperature. In terms of Arrhenius theory, the temperature correlation of all measured properties was made and discussed. Thermodynamic properties (isothermal compressibility, molecular volume, lattice energy, heat capacity, molar Gibbs energy, enthalpy and entropy) were derived for all the studied HTILs from experimental data. The viscosity isotherms show negative deviations from linearity, while conductivity isotherms have positive deviations which may be related to the formation of highly negative changed ion associated species. The evolution of the excess quantities: viscosity deviation (Δη), excess molar viscosity (ΔEη), excess molar conductivity (ΔEκ), show a very good parallelism. The linear behavior between conductivity and viscosity was determined using the fractional Walden rule and the average slope was found far from unity.

CALCULATION OF THE TEMPERATURES OF THE CHEMICAL REACTIONS OF THE IRON STEPPED RECOVERY FROM HEMATITE WITH CO GAS AND GASIFICATION OF SOLID CARBON ACCORDING EXISTING FORMULAS AND BY STANDARD VALUES OF ENTHALPY AND ENTROPY OF SUBSTANCES

The article presents the results of a thermodynamic assessment of the possibility of chemical reactions of the stepped recovery of iron from hematite with a recovering gas CO, as well as the Bell-Boudoir chemical reaction. It has been established that for each of the indicated chemical reactions there is a certain temperature (called by the author as "boundary temperature"), up to or above which CO gas cannot be a recovering agent for lower iron oxide from higher or the metallic iron itself from wustite, as well as gasification of solid carbon; while the recovery of Fe3O4 from Fe2O3 is theoretically possible at any temperatures above 0 ° C, the recovery of FeO from Fe3O4 and the gasification of solid carbon are theoretically possible above certain temperatures (i.e. at elevated and high temperatures), and the recovery of iron from FeO is below a certain temperature (i.e. at low temperatures). The numerical values of the boundary temperatures for the reactions of iron recovery and its lower oxides, as well as the reaction of gasification of solid carbon are given; graphical dependences of the Gibbs free energy of the indicated chemical reactions on temperature are made according to the equations available in metallurgical literary sources, and according to the expressions derived in the article by the author.

Adsorption of Gas-Phase Cyclohexanone on Atmospheric Water Films

The fate of atmospheric volatile organic compounds (VOCs) strongly depends on the partitioning processes on the surface of aerosols, which are coated with a thin water film. However, the behavior of VOCs in the aqueous film of aerosols is difficult to measure. In this work, the interfacial partition constant of cyclohexanone was determined using a novel flow-tube reactor. A thin, aqueous film placed in the reactor was exposed to cyclohexanone gas. The subsequent partitioning was measured using chromatography techniques. The quality control tests were first conducted to ensure the accuracy of the adsorption experiments. The cyclohexanone concentration was then plotted as a function of film thickness to obtain the partitioning constants. As the thickness of the water film decreased, the aqueous concentration of cyclohexanone increased, indicating that surface adsorption played a dominant role in the uptake of cyclohexanone. According to the temperature dependence of the interfacial partition constant, the solvation enthalpy and entropy of cyclohexanone were obtained. The results of this study would help to elucidate the effect of atmospheric water film on the gas–aerosol partitioning of VOCs, and thus can help to better understand the fate of VOCs in the atmosphere.

On the Jumps of Volume, Enthalpy and Entropy at the Melting Point, the Thermal Conductivity and Thermal Diffusivity for F.C.C. Au: the Temperature- and Pressure-Dependences

The melting temperature, the jumps of volume, enthalpy and entropy at the melting point, the isothermal compressibility, the thermal expansion coefficient, the heat capacity at constant volume, the Grüneisen parameter, the Debye temperature, the electrical resistivity, the thermal conductivity, and the thermal diffusivity for defective and perfect f.c.c. metals are studied by combining the statistical moment method (SMM), the limiting condition of the absolute stability of the crystalline state, the Clapeyron–Clausius equation, the Debye model, the Grüneisen equation, the Wiedemann–Franz law, and the Mott equation. Numerical calculations are carried out for Au under high temperature and pressure. The calculated melting curve of Au is in good agreement with experiments and other calculations. Obtained results are predictive and orient towards new experiments.

Adsorption Isotherm and Activation Energy of Inhibition of Alkaloids on Mild Steel Surface in Acidic Medium

Alkaloids as green inhibitors were extracted from three different plants Rhynchostylis retusa, Artimesia vulgaris,and Solanum tuberosum. Weight loss measurement in mild steel has been carried out in the presence and absence of green inhibitors individually in an acidic medium. Weight loss measurements at different temperatures are used to calculate thermodynamic parameters. The weight loss measurements at different concentrations are used to find adsorption isotherm and found that it obeys Langmuir adsorption isotherm with R2 values 1, 1, 0.996 for three inhibitors. Activation energy, enthalpy, and entropy of the three inhibitors have been calculated. It is found that the value of all these parameters increased in the addition of inhibitors. The free energy of the system is calculated and found (-17.46 kJ mol-1) indicating that the adsorption process is spontaneous and there is physical adsorption at the MS-Inhibitor interface.

Chemical Thermodynamics

Chemical Thermodynamics discusses the fundamental laws of thermodynamics along with their relationships to heat, work, enthalpy, entropy, and temperature. Predicting the direction of a spontaneous change and calculating the change in entropy of a reaction are core concepts. The relationship between entropy, free energy and work is covered. The Gibbs free energy is used quantitatively to predict if reactions or processes are going to be exothermic and spontaneous or endothermic under the stated conditions. Also explored are the enthalpy and entropy changes during a phase change. Finally the Gibbs free energy of a chemical reaction is related to its equilibrium constant and the temperature.